Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10038271
HAVCR1
1.000 0.040 5 157043390 intron variant C/T snv 0.16 1
rs10127016
KANTR
1.000 0.040 X 53122914 intron variant G/T snv 1
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11095197
TAB3
1.000 0.040 X 30958830 intron variant C/T snv 0.28 1
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs12387999
ZNF630
1.000 0.040 X 48035670 intron variant G/A snv 5.0E-02 1
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs1336698
FGF14
1.000 0.040 13 102211398 intron variant C/T snv 0.85 1
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs16910534
LOC105378313
1.000 0.040 10 57337568 intergenic variant C/T snv 3.1E-02 1
rs17140937 1.000 0.040 7 118148430 intergenic variant T/C snv 6.0E-02 1
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14