Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9989407 16 68730609 intergenic variant C/A;G;T snv 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs11191439
AS3MT ; BORCS7-ASMT
0.851 0.120 10 102878966 missense variant T/A;C snv 9.2E-02 6
rs9527
BORCS7-ASMT ; BORCS7
10 102863821 3 prime UTR variant C/T snv 0.21 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs12919719
CDH1
16 68788438 intron variant C/G snv 0.25 1
rs7196495
CDH1
16 68739957 intron variant C/G;T snv 1
rs7196661
CDH1
16 68740009 intron variant C/T snv 0.80 1
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1540087
FOLR1
1.000 0.080 11 72190447 5 prime UTR variant G/A snv 3.8E-02 2
rs61735836
FTCD-AS1 ; FTCD
21 46152973 missense variant C/T snv 5.7E-02 5.6E-02 3
rs4925
GSTO1
0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs11191979
GSTO1
10 104265109 intron variant T/C snv 0.23 1
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs2297235
GSTO2
0.752 0.320 10 104274733 5 prime UTR variant A/G snv 0.22 11
rs157077
GSTO2
1.000 0.080 10 104278136 intron variant T/C snv 0.45 0.53 3
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43 6
rs1133400
INPP5A
1.000 0.080 10 132645884 missense variant A/G snv 0.22 0.18 4
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49