Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113