Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs764255410
ACVR2A
1.000 0.080 2 147918546 missense variant G/A snv 1
rs566841339
ASIC4-AS1 ; SPEG
1.000 0.080 2 219489128 missense variant G/A snv 2.8E-05 2.8E-05 1
rs747576071
AXL
1.000 0.080 19 41243665 missense variant C/T snv 1.6E-05 7.0E-06 1
rs752802257
BMPR1A
1.000 0.080 10 86923490 missense variant G/A snv 8.0E-06 7.0E-06 1
rs200035802
BMPR1B
1.000 0.080 4 95104516 missense variant G/A snv 1.7E-04 1.5E-04 1
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 2
rs781375003
BRDT
1.000 0.080 1 91964700 missense variant C/T snv 8.3E-06 7.0E-06 1
rs144130246
BRSK1
1.000 0.080 19 55302746 missense variant C/T snv 1.2E-05 1
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 1
rs121913385
CDKN2A
0.763 0.240 9 21971112 missense variant G/A;C snv 1
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 4
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 3
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 2
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 2
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 2
rs121913399
CTNNB1
0.724 0.200 3 41224612 missense variant G/A;C snv 1
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 1
rs1366698690
DCLK1
1.000 0.080 13 36125860 missense variant C/T snv 1
rs771803475
EPHA10
1.000 0.080 1 37761806 missense variant C/T snv 4.0E-06 2.8E-05 1
rs922655349
EPHA2
1.000 0.080 1 16131867 missense variant C/T snv 1
rs1338928289
EPHB1
1.000 0.080 3 135201571 missense variant G/A snv 4.0E-06 7.0E-06 1
rs762016655
EPHB4
1.000 0.080 7 100805514 missense variant G/A;C snv 2.2E-05; 5.5E-06 1
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 1
rs1057519893
ERBB3
0.790 0.160 12 56085070 missense variant G/A;T snv 1
rs146710304
ERN1
1.000 0.080 17 64054300 missense variant G/A;T snv 1.6E-05 1.4E-05 1