Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4400605 1 159370626 intron variant T/C snv 0.47 2
rs4446959 1 159387894 intron variant T/A;C snv 2
rs4517343 1 159369216 intron variant A/G snv 0.47 2
rs4537549 1 159369246 intron variant C/A;G snv 2
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 2
rs6660102 1 159241274 intergenic variant G/T snv 0.34 2
rs6677678 1 159369730 intron variant C/T snv 0.47 2
rs6687840 1 159372649 intron variant C/T snv 0.47 2
rs6692378 1 159369451 intron variant T/C snv 0.54 2
rs6702853 1 159372620 intron variant T/A snv 0.46 2
rs863013 1 159230230 regulatory region variant G/T snv 0.23 2
rs9378212 0.925 0.160 6 32477914 upstream gene variant C/G;T snv 2
rs9405112 1.000 0.120 6 32477823 upstream gene variant G/A;T snv 2
rs9782926 1 159353602 intron variant T/A snv 0.35 2
rs10437339 1 159740595 intergenic variant C/G;T snv 1
rs10437340 1 159741019 intergenic variant G/C snv 0.40 1
rs10489849 1 159226975 regulatory region variant C/A;T snv 1
rs10494326 1 159679910 intergenic variant C/T snv 5.3E-02 1
rs10521222 16 51124799 intergenic variant C/T snv 3.2E-02 1
rs10751037 11 81025386 intron variant C/G;T snv 1
rs10789192 1 65660087 intergenic variant G/A snv 0.43 1
rs10888935 1 55595278 intron variant T/A snv 0.52 1
rs10908733 1 159534264 downstream gene variant T/A;C snv 1
rs11208711 1 65682163 intergenic variant G/T snv 0.43 1
rs11265177 1 159356044 intron variant A/G snv 0.16 1