Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11586313 1 152917994 TF binding site variant G/A;C snv 0.51 2
rs117300835 11 15097429 intergenic variant G/A snv 7.6E-03 2
rs12287212 11 14428315 intergenic variant C/A snv 0.31 2
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
rs148189294 4 71575200 downstream gene variant G/A snv 2.6E-02 2
rs1526692 4 71713007 intergenic variant A/G snv 0.41 2
rs1607741 4 71853316 intergenic variant G/C snv 0.65 2
rs17767445 4 71879550 intergenic variant G/A snv 0.20 2
rs6730714 2 222184302 intergenic variant G/A;T snv 2
rs719700 12 45635426 intergenic variant T/C snv 1.8E-02 2
rs79666294 5 155047146 regulatory region variant C/T snv 2.2E-02 2
rs79761689 4 72005565 intergenic variant T/C snv 3.7E-02 2
rs10745742
AMDHD1
12 95964751 intron variant C/T snv 0.48 2
rs55665837
COPB1
11 14473503 intron variant C/G;T snv 2
rs117913124
CYP2R1
11 14879385 synonymous variant G/A snv 1.7E-02 1.6E-02 2
rs185378533
FLJ42102
11 71422087 intron variant A/G snv 0.68 2
rs843005
GC
4 71750610 intron variant C/A;T snv 2
rs2277458
GEMIN2 ; LOC105370459
14 39114277 5 prime UTR variant A/G snv 0.80 0.83 2
rs3819817
HAL
12 95984993 intron variant C/T snv 0.50 2
rs2207173
LOC105372568
20 22824423 intergenic variant G/A snv 0.72 2
rs156299
LOC107986777
7 24185113 intergenic variant T/G snv 0.53 2
rs4423214
NADSYN1
11 71462208 intron variant C/T snv 0.58 2
rs4944062
NADSYN1
11 71476248 3 prime UTR variant G/A;T snv 2