Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs727503054 0.756 0.179 15 48420752 missense variant A/G,T snp 1.6E-05 14
rs137854480 0.744 0.179 15 48537629 missense variant G/A snp 10
rs111401431 0.756 0.179 15 48468097 missense variant G/A snp 9
rs113871094 0.769 0.179 15 48465820 stop gained G/A snp 8
rs193922228 0.769 0.179 15 48430736 missense variant A/G snp 8
rs397515757 0.769 0.179 15 48515382 splice region variant C/T snp 8
rs193922219 0.784 0.214 15 48446701 splice region variant C/A,T snp 7
rs137854467 0.821 0.214 15 48600217 missense variant G/A snp 6
rs140598 0.821 0.143 15 48487333 missense variant G/A,C snp 3.2E-02 1.8E-02 5
rs137854464 0.846 0.179 15 48425483 missense variant C/T snp 4
rs387906623 0.878 0.143 15 48460258 missense variant C/T snp 4
rs137854478 0.923 0.143 15 48488233 missense variant C/T snp 3
rs794728228 1.000 0.143 15 48468064 stop gained G/A snp 3
rs1057519320 0.923 0.143 15 48444574 stop gained G/A snp 2
rs113001196 1.000 0.143 15 48432947 stop gained G/A snp 2
rs137854456 1.000 0.143 15 48487365 missense variant C/A,G,T snp 4.0E-06; 4.0E-05 6.4E-05 2
rs137854457 1.000 0.143 15 48428423 stop gained C/G,T snp 2
rs137854465 1.000 0.143 15 48488230 missense variant A/G snp 2
rs137854468 0.923 0.143 15 48487396 missense variant C/T snp 2
rs137854472 1.000 0.143 15 48488448 missense variant T/C snp 8.0E-06 2
rs137854477 1.000 0.143 15 48489979 missense variant C/T snp 2
rs137854481 1.000 0.143 15 48488481 missense variant C/T snp 2
rs147195031 1.000 0.143 15 48420780 missense variant G/A snp 2
rs25403 0.923 0.179 15 48613073 missense variant G/A snp 2
rs267606798 0.923 0.143 15 48465825 missense variant C/T snp 2