Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117902240
HAS2-AS1
1.000 0.080 8 121918402 intron variant T/G snv 7.6E-03 2
rs149702363
LOC101929006
0.925 0.120 6 29257248 intron variant T/G snv 3.8E-02 2
rs150814685 0.925 0.120 6 28728995 upstream gene variant T/G snv 3.4E-02 2
rs2381712 0.925 0.080 2 145387450 intergenic variant T/G snv 0.52 2
rs1031509
STAT4
1.000 0.080 2 191145463 intron variant T/G snv 0.64 1
rs10975416 1.000 0.080 9 6051924 intron variant T/G snv 0.17 1
rs11048317
MIR4302
1.000 0.080 12 25875474 upstream gene variant T/G snv 0.19 1
rs11735820
EPHA5
1.000 0.080 4 65633298 intron variant T/G snv 0.33 1
rs12718488 1.000 0.080 11 76655646 intron variant T/G snv 0.33 1
rs1300030496
KIDINS220
1.000 0.080 2 8731757 missense variant T/G snv 4.0E-06 1
rs17642749 1.000 0.080 10 117887745 intergenic variant T/G snv 5.6E-02 1
rs350729
LOC105369165
1.000 0.080 2 52756635 intron variant T/G snv 0.66 1
rs4697177
KCNIP4
1.000 0.080 4 20758466 intron variant T/G snv 0.73 1
rs59294057 1.000 0.080 8 21649156 intergenic variant T/G snv 6.2E-02 1
rs62626322 1.000 0.080 10 6073676 upstream gene variant T/G snv 9.6E-02 1
rs6691738 1.000 0.080 1 173182897 downstream gene variant T/G snv 0.44 1
rs7224314
PITPNC1
1.000 0.080 17 67390098 intron variant T/G snv 0.26 1
rs7599706 1.000 0.080 2 236897044 intergenic variant T/G snv 0.11 1
rs76833157 1.000 0.080 2 163945275 intron variant T/G snv 4.1E-02 1
rs7686660 1.000 0.080 4 143082006 intron variant T/G snv 0.34 1
rs77000868 1.000 0.080 10 9028714 intergenic variant T/G snv 2.6E-02 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs770460061
GSTP1
0.742 0.240 11 67585239 missense variant T/C;G snv 4.0E-06; 1.2E-05 14