Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1511412 1.000 0.080 3 138994862 regulatory region variant A/G;T snv 1
rs873549 1.000 0.080 1 222098425 intron variant C/T snv 0.75 1
rs11130248 1.000 0.080 3 50314769 upstream gene variant A/G snv 0.10 1
rs8032158 1.000 0.080 15 55902679 intron variant T/A;C snv 1
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 1