Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12868495 13 34067425 intergenic variant G/A snv 2.3E-02 2
rs138485827 4 72166226 intergenic variant C/T snv 5.0E-02 2
rs1410656 13 46968386 intergenic variant T/C snv 0.97 2
rs1526692 4 71713007 intergenic variant A/G snv 0.41 2
rs156299
LOC107986777
7 24185113 intergenic variant T/G snv 0.53 2
rs1607741 4 71853316 intergenic variant G/C snv 0.65 2
rs17767445 4 71879550 intergenic variant G/A snv 0.20 2
rs2207173
LOC105372568
20 22824423 intergenic variant G/A snv 0.72 2
rs6730714 2 222184302 intergenic variant G/A;T snv 2
rs719700 12 45635426 intergenic variant T/C snv 1.8E-02 2
rs79761689 4 72005565 intergenic variant T/C snv 3.7E-02 2
rs79666294 5 155047146 regulatory region variant C/T snv 2.2E-02 2
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs2302190
MTMR4
17 58507147 missense variant T/A;C snv 0.24 3
rs8018720
SEC23A
14 39086981 missense variant G/C;T snv 0.80; 1.1E-04 2
rs12800438
NADSYN1
1.000 0.080 11 71459957 non coding transcript exon variant G/A;T snv 5
rs7938885
NADSYN1
11 71458997 non coding transcript exon variant T/C snv 0.59 2
rs117913124
CYP2R1
11 14879385 synonymous variant G/A snv 1.7E-02 1.6E-02 2
rs2277458
GEMIN2 ; LOC105370459
14 39114277 5 prime UTR variant A/G snv 0.80 0.83 2
rs4944062
NADSYN1
11 71476248 3 prime UTR variant G/A;T snv 2
rs11586313 1 152917994 TF binding site variant G/A;C snv 0.51 2
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs2060793
CYP2R1
0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 11
rs17467825 0.925 0.080 4 71739800 downstream gene variant A/G snv 0.22 4