Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs66904256
ABCB4
0.882 0.080 7 87439777 missense variant T/A snv 2
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 1
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 2
rs863223904
ALAS2
0.827 0.200 X 55014829 missense variant C/T snv 6.1E-06 1
rs116350678
AXIN1
1.000 0.080 16 298233 missense variant C/T snv 4.8E-03 2.3E-02 1
rs117208012
AXIN1
1.000 0.080 16 297063 missense variant C/A;T snv 8.0E-06; 1.6E-02 1
rs779951904
AXIN1
1.000 0.080 16 310055 missense variant G/A snv 2.0E-05 1.4E-05 1
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs121913385
CDKN2A
0.763 0.240 9 21971112 missense variant G/A;C snv 1
rs144479038
CDKN3
1.000 0.080 14 54411612 missense variant A/G snv 3.4E-04 2.4E-04 1
rs760687800
CDKN3
1.000 0.080 14 54411563 missense variant C/A;G snv 4.0E-06; 2.4E-05 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
rs121913413
CTNNB1
0.763 0.240 3 41224634 missense variant C/A;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
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 1
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 1
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 1
rs1413975856
CTNNB1
1.000 0.080 3 41224579 missense variant A/C snv 7.0E-06 1
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 1
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 1