Genetic background for MALIGNANT BOWEL CANCER

Test covers the analysis of
zmian genetycznych w84 genach related:

  • adenocarcinoma of the pivotal type,

  • medullary carcinoma,

  • microadenocarcinoma,

  • mucinous adenocarcinoma,

  • serrated adenocarcinoma,

  • signet cell carcinoma,

  • adenocarcinoma,

  • spindle cell carcinoma,

  • squamous cell carcinoma.

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4,690.00 zł

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Why is it worth testing?

The waiting time for the result is only 4 weeks

The analysis always includes genetic changes within exons, introns and promoters of genes and in mitochondrial DNA

Always an additional test included in the price

Consultation with specialist and written interpretation of the result

Each result is reanalysed every 6 months .

Rough data from sequencing are made available on request.

Colorectal cancer develops quite slowly, its symptoms depend on the location of the tumour and its stage.

“Rak jelita grubego jest trzecim najczęściej występującym nowotworem na świecie. Jest to trzeci najczęstszy nowotwór złośliwy u mężczyzn i drugi u kobiet.

In 2020, more than 1.9 million new cases were recorded.

Nowotwór jelita cienkiego występuje dość rzadko.

For a long time it does not give any symptoms, so it is most often diagnosed by chance

The most common symptoms of bowel cancers are:

♦ blood in the stool,

♦ changes in the colour of the stool (very dark stools),

♦ rectal bleeding,

♦ problems with defecation,

♦ anaemia,

♦ stomachache,

♦ constipation,

♦ nausea and vomiting,

♦ weight loss,

♦ diarrhoea.

 

About 12% of men and 10% of women die of malignant bowel cancer in Poland.

In Poland, in 2020, the mortality rate is:

18,53/100,000 people

(9th place in the world)

Females : 13,39/100,000 people

Dla mężczyzn: 26,11/100 000 osób

Risk factors:

♦ smoking tobacco products,

♦ age over 50,

♦ niska aktywność fizyczna,

♦ diet based on red meat,

♦ spożywanie wysokoprocentowego alkoholu,

♦ obesity,

♦ polyps of the intestine,

♦ inflammatory bowel disease,

♦ genetic load.

Badanie obejmuje analizę zmian genetycznych (SNP) w 84 genes:

Ostatnia aktualizacja bazy: 2023.11.18

GENCHOROBA
AAGABORPHA:79501,OMIM:148600
ADA2OMIM:615688,ORPHA:820,ORPHA:124,OMIM:182410
APCORPHA:261584,OMIM:135290,ORPHA:247806,ORPHA:873,ORPHA:3258,OMIM:175100,OMIM:114550,OMIM:619182,ORPHA:79665,ORPHA:99818,OMIM:613659,OMIM:114500
ATMOMIM:208900,OMIM:114480,ORPHA:440437,ORPHA:100,ORPHA:52416
AXIN2ORPHA:401911,ORPHA:99798,OMIM:608615,OMIM:114500
BLMOMIM:210900,ORPHA:125
BMPR1AORPHA:329971,OMIM:174900,OMIM:610069,ORPHA:157794,ORPHA:440437,ORPHA:79076
BRCA1ORPHA:84,OMIM:114480,ORPHA:145,ORPHA:1333,ORPHA:70567,OMIM:617883,ORPHA:168829,OMIM:604370
BRCA2ORPHA:84,ORPHA:1333,ORPHA:654,ORPHA:440437,OMIM:613347,OMIM:155255,OMIM:605724,OMIM:612555,OMIM:114480,ORPHA:145,ORPHA:70567,OMIM:176807,OMIM:613029,OMIM:194070
BUB1ORPHA:1052,OMIM:620183,OMIM:114500
BUB1BOMIM:257300,ORPHA:1052,OMIM:176430,OMIM:114500
BUB3ORPHA:1052
C1SORPHA:75392,OMIM:613783,OMIM:617174
CDKN2AOMIM:155755,ORPHA:1333,ORPHA:524,ORPHA:1501,ORPHA:618,OMIM:155601,OMIM:606719
CEP57OMIM:614114,ORPHA:1052
CHEK2ORPHA:145,ORPHA:524,OMIM:609265,ORPHA:440437,OMIM:176807,ORPHA:668,OMIM:259500
COL14A1ORPHA:79501
ENGORPHA:231160,ORPHA:774,ORPHA:329971,OMIM:187300
EPCAMOMIM:613244,OMIM:613217,ORPHA:92050,ORPHA:144
FAN1OMIM:614817,ORPHA:144
FLCNORPHA:122,OMIM:610883,OMIM:173600,OMIM:135150,OMIM:144700,ORPHA:2903,OMIM:114500
FOXE1ORPHA:95713,OMIM:241850,ORPHA:1226,ORPHA:319487,OMIM:616534
GATA1ORPHA:67044,OMIM:300835,OMIM:314050,OMIM:301083,ORPHA:124,ORPHA:231393,OMIM:159595,ORPHA:79277,OMIM:300367
GREM1ORPHA:157794
HABP2OMIM:616535,ORPHA:319487,OMIM:188050
HEATR3ORPHA:124,OMIM:620072
KITOMIM:273300,OMIM:172800,OMIM:606764,ORPHA:280794,ORPHA:2884,ORPHA:280785,OMIM:154800,OMIM:601626,ORPHA:79455,ORPHA:44890,ORPHA:98849
KRASOMIM:600268,OMIM:108010,ORPHA:2612,ORPHA:2396,OMIM:163200,OMIM:615278,ORPHA:1333,OMIM:211980,ORPHA:648,OMIM:613659,OMIM:260350,OMIM:614470,OMIM:609942,OMIM:114480,OMIM:601626,ORPHA:144,OMIM:109800,ORPHA:3339,ORPHA:1340
MAD1L1OMIM:620189,OMIM:176807
MBD4OMIM:619975,OMIM:606660
MDM2OMIM:618681,ORPHA:524,ORPHA:99971
MINPP1OMIM:619527,OMIM:188470,ORPHA:319487,ORPHA:284339
MLH1OMIM:609310,OMIM:158320,ORPHA:144,OMIM:276300
MLH3OMIM:614385,ORPHA:144,OMIM:608089,OMIM:114500
MSH2OMIM:120435,OMIM:619096,OMIM:158320,ORPHA:144
MSH3ORPHA:480536,OMIM:617100,OMIM:608089
MSH6OMIM:619097,ORPHA:144,OMIM:614350,OMIM:608089
MUTYHOMIM:608456,ORPHA:440437,OMIM:613659,ORPHA:247798
NTHL1ORPHA:454840,OMIM:616415
PALB2ORPHA:84,OMIM:610832,ORPHA:145,ORPHA:1333
PALLDORPHA:1333,OMIM:606856
PDGFRAORPHA:199306,OMIM:175510,OMIM:607685,ORPHA:44890
PIK3CAOMIM:155500,OMIM:612918,ORPHA:276280,OMIM:182000,ORPHA:60040,ORPHA:2495,ORPHA:221061,OMIM:211980,ORPHA:99802,OMIM:602501,OMIM:613659,OMIM:114500,OMIM:162900,OMIM:615108,OMIM:114480,OMIM:114550,OMIM:613089,ORPHA:168984,ORPHA:144,OMIM:167000,OMIM:619538,ORPHA:201
PMS1OMIM:120435,ORPHA:144
PMS2ORPHA:144,OMIM:614337,OMIM:619101
POLD1OMIM:612591,OMIM:615381,ORPHA:440437,ORPHA:447877
POLEORPHA:85173,OMIM:615139,ORPHA:440437,OMIM:615083,OMIM:618336,ORPHA:447877
PTENORPHA:397596,ORPHA:137608,ORPHA:2969,OMIM:607174,ORPHA:101070,OMIM:605309,ORPHA:210548,ORPHA:744,OMIM:158350,ORPHA:65285,ORPHA:145,OMIM:613028,ORPHA:109,ORPHA:79076,OMIM:176807,ORPHA:201
RABL3OMIM:618680,ORPHA:1333
RNF43OMIM:617108,ORPHA:157798
RPL11OMIM:612562,ORPHA:124
RPL15ORPHA:124,OMIM:615550
RPL18OMIM:618310,ORPHA:124
RPL26ORPHA:124,OMIM:614900
RPL27OMIM:617408,ORPHA:124
RPL31ORPHA:124
RPL35ORPHA:124,OMIM:618312
RPL35AORPHA:124,OMIM:612528
RPL5ORPHA:124,OMIM:612561
RPL8ORPHA:124
RPL9ORPHA:124
RPS10ORPHA:124,OMIM:613308
RPS15AORPHA:124,OMIM:618313
RPS17ORPHA:124,OMIM:612527
RPS19ORPHA:124,OMIM:105650
RPS20ORPHA:124,ORPHA:440437
RPS24ORPHA:124,OMIM:610629
RPS26ORPHA:124,OMIM:613309
RPS27ORPHA:124,OMIM:617409
RPS28ORPHA:124,OMIM:606164
RPS29ORPHA:124,OMIM:615909
RPS7ORPHA:124,OMIM:612563
SDHAOMIM:614165,OMIM:619259,ORPHA:3208,OMIM:613642,ORPHA:29072,ORPHA:154,ORPHA:44890,OMIM:252011
SDHBORPHA:97286,OMIM:115310,ORPHA:3208,OMIM:606764,ORPHA:29072,ORPHA:44890,OMIM:619224,ORPHA:201,ORPHA:276621,OMIM:606864
SDHCORPHA:97286,OMIM:606764,OMIM:605373,ORPHA:29072,ORPHA:44890,ORPHA:201,OMIM:606864
SEMA4AORPHA:1872,ORPHA:440437,OMIM:610282,OMIM:610283,ORPHA:791
SH3KBP1OMIM:300310
SMAD4ORPHA:2588,ORPHA:774,ORPHA:329971,ORPHA:91387,OMIM:174900,ORPHA:1333,OMIM:175050,OMIM:139210,OMIM:260350
SMAD7OMIM:612229
STK11OMIM:155600,OMIM:175200,OMIM:273300,ORPHA:2869,OMIM:260350
TGFBR2ORPHA:91387,ORPHA:60030,OMIM:610168,ORPHA:99977,OMIM:133239,ORPHA:144,OMIM:614331
TP53ORPHA:1333,OMIM:202300,ORPHA:524,ORPHA:96253,ORPHA:668,ORPHA:3318,OMIM:260500,OMIM:260350,OMIM:259500,OMIM:114500,OMIM:137800,OMIM:151623,OMIM:114480,OMIM:114550,ORPHA:2807,ORPHA:145,OMIM:618165,ORPHA:1501,OMIM:607107
TRIP13OMIM:617598,ORPHA:1052,ORPHA:654,OMIM:619011
TSR2OMIM:300946,ORPHA:124

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