Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs267606921 0.882 0.160 1 114713941 missense variant G/A snv 3
rs267606920 0.882 0.160 1 114713911 missense variant C/T snv 7.0E-06 2