Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs7848647 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs292001 0.807 0.320 1 22638465 intron variant G/A snv 0.54 6