Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 6
rs16850073
CXCL6
4 73838282 3 prime UTR variant C/T snv 0.29 5
rs17128183 0.882 0.120 14 55112795 intergenic variant A/G snv 0.57 5
rs2250417
BCO2
1.000 0.080 11 112214593 intron variant T/C snv 0.44 5
rs2274273
DLGAP5
0.882 0.120 14 55147918 downstream gene variant G/A snv 0.40 5
rs2280401
SNORD35B ; RPS11
19 49496752 intron variant G/A snv 0.12 5
rs4985726
TNFRSF13B
0.925 0.120 17 16960324 intron variant C/G snv 0.11 5
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 4
rs3783641
GCH1
0.882 0.120 14 54893421 intron variant T/A;C snv 0.25 4
rs4273077
TNFRSF13B
0.925 0.160 17 16945825 intron variant A/G snv 0.13 4
rs514708
ABO
9 133258352 intron variant C/T snv 0.29 4
rs626035
ABO
9 133259603 intron variant T/G snv 0.28 4
rs641943
ABO
9 133258323 intron variant A/G snv 0.29 4
rs641959
ABO
9 133258308 intron variant A/C snv 0.29 4
rs7025162 1.000 0.080 9 133290774 regulatory region variant T/C snv 0.82 4
rs8176714
ABO
9 133257791 intron variant G/A snv 0.26 4
rs10265221
PRKAG2
7 151717243 intron variant T/A;C snv 3
rs10466351 11 92964815 upstream gene variant C/T snv 0.48 3
rs10483639 1.000 0.040 14 54839739 downstream gene variant G/C snv 0.26 3
rs12741825 1 159700355 downstream gene variant C/T snv 0.24 3
rs14399
SLC16A10
6 111222741 3 prime UTR variant C/A snv 0.32 3
rs1986734
SHROOM3
1.000 0.120 4 76499631 intron variant C/T snv 0.43 3
rs1998848
NDRG2 ; TPPP2 ; MIR6717
1.000 0.040 14 21024070 5 prime UTR variant G/A snv 1.6E-02 3
rs2040771 22 19174422 downstream gene variant C/A;T snv 3