Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31