Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10835979 11 4374955 upstream gene variant G/A snv 0.88 1
rs10837540 11 5193183 intergenic variant T/A snv 0.53 1
rs10837593 11 5210667 downstream gene variant C/T snv 0.79 1
rs11035045 11 4994711 upstream gene variant C/T snv 0.33 1
rs11968814 1.000 0.080 6 71067268 intergenic variant G/A snv 4.4E-02 1
rs12103880 17 9795025 intron variant G/A snv 0.26 1
rs12282135 11 5094898 downstream gene variant T/C snv 0.19 1
rs12294758 11 5093962 downstream gene variant G/A;T snv 1
rs12468946 2 60443342 upstream gene variant A/G snv 0.51 1
rs12805212 11 5205088 splice donor variant G/A snv 0.17 1
rs12997266 2 60422008 intron variant G/A snv 0.37 1
rs1455958 11 5105947 downstream gene variant C/A snv 0.18 1
rs1694676 11 5552601 intron variant T/A;G snv 1
rs172748 11 5512609 intron variant T/C snv 0.42 1
rs1823636 11 4254774 intergenic variant C/G;T snv 1
rs201286260 11 5205088 splice donor variant -/A ins 1
rs2033467 5 151660065 downstream gene variant C/T snv 0.53 1
rs2034836 11 5039561 downstream gene variant A/G snv 0.30 1
rs2034839 11 5039711 downstream gene variant G/A snv 0.52 1
rs243061 2 60396563 intron variant T/C snv 0.29 1
rs243062 2 60396541 intron variant G/A snv 0.29 1
rs2445248 11 5026828 intergenic variant G/A snv 0.43 1
rs2445252 11 5030232 intergenic variant G/A;C snv 1
rs2499935 11 5088664 upstream gene variant C/G snv 0.36 1
rs2499983 11 5040205 downstream gene variant C/G;T snv 1