Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs180177033
rs180177033
1.000 0.080 7 140781620 missense variant A/C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 10 2006 2015
dbSNP: rs1414714315
rs1414714315
1.000 0.080 3 89413239 missense variant A/C snv 8.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs63751121
rs63751121
1.000 0.080 2 47799840 missense variant A/C snv 1.6E-05 4.9E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs63750449
rs63750449
0.925 0.120 3 37047640 missense variant A/C;G;T snv 3.5E-03; 8.4E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 11 1996 2008
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 0.975 10 2004 2020
dbSNP: rs556554798
rs556554798
1.000 0.080 12 20916077 missense variant A/C;G;T snv 4.0E-06; 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs63750389
rs63750389
0.925 0.160 2 47800532 missense variant A/G snv 8.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 12 1999 2012
dbSNP: rs63750650
rs63750650
1.000 0.080 3 37017518 missense variant A/G snv 2.5E-04 1.3E-04
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 11 1996 2008
dbSNP: rs63750718
rs63750718
1.000 0.080 3 37047589 missense variant A/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 11 1996 2008
dbSNP: rs63749982
rs63749982
1.000 0.080 2 47475121 missense variant A/G snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 4 1998 2005
dbSNP: rs63750716
rs63750716
0.925 0.160 2 47410232 missense variant A/G snv 4.7E-04 1.3E-04
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 4 1998 2005
dbSNP: rs1277170270
rs1277170270
1.000 0.080 7 41965163 missense variant A/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs1345352474
rs1345352474
1.000 0.080 19 43997278 missense variant A/G snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs143528650
rs143528650
1.000 0.080 10 125721229 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs1442893893
rs1442893893
1.000 0.080 11 111753514 missense variant A/G snv 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs1451414636
rs1451414636
1.000 0.080 X 91835629 missense variant A/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs63751009
rs63751009
1.000 0.080 2 47799548 missense variant A/G snv 1.2E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs63751450
rs63751450
1.000 0.080 2 47800391 missense variant A/G snv 8.4E-05 4.2E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs63751612
rs63751612
0.925 0.120 3 37047520 missense variant A/G snv 1.2E-04 6.3E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs767108156
rs767108156
1.000 0.080 6 44233520 missense variant A/G snv 8.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs776537988
rs776537988
1.000 0.080 11 130473277 missense variant A/G snv 3.6E-05 5.6E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs997506328
rs997506328
1.000 0.080 16 20799983 missense variant A/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs121913279
rs121913279
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.820 1.000 2 2005 2016
dbSNP: rs34374438
rs34374438
1.000 0.080 2 47800544 missense variant A/T snv 3.9E-04 3.5E-04
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 12 1999 2012
dbSNP: rs63750804
rs63750804
1.000 0.080 2 47801075 missense variant A/T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0