Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934576 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 64
rs121912664 0.667 0.357 17 7670699 missense variant C/A,G,T snp 1.2E-05 31
rs121913343 0.638 0.464 17 7673803 missense variant G/A,T snp 1.2E-05 30
rs397516436 0.647 0.393 17 7674894 stop gained G/A,C snp 30
rs587778720 0.647 0.321 17 7674893 missense variant C/A,G,T snp 4.0E-06 29
rs786201057 0.673 0.357 17 7675995 missense variant G/A,C,T snp 3.2E-05 23
rs1057520003 0.685 0.286 17 7675996 missense variant T/G snp 20
rs863224451 0.692 0.429 17 7673796 stop gained C/A,G,T snp 20
rs876660754 0.699 0.321 17 7675095 missense variant C/A,T snp 19
rs587780073 0.699 0.286 17 7674262 missense variant T/C,G snp 18
rs1057519747 0.715 0.250 17 7675094 missense variant A/C,G,T snp 17
rs587781991 0.715 0.214 17 7675208 missense variant C/A,T snp 17
rs747342068 0.707 0.393 17 7675218 missense variant T/C,G snp 4.0E-06 17
rs1057519983 0.715 0.357 17 7673797 missense variant A/G snp 16
rs1057519996 0.724 0.321 17 7675217 splice acceptor variant T/A,C,G snp 15
rs866775781 0.724 0.321 17 7675216 splice acceptor variant C/A,G snp 15
rs864622237 0.724 0.214 17 7674263 missense variant A/C,G,T snp 14
rs1057519975 0.744 0.214 17 7675209 missense variant A/C,G,T snp 13
rs121912667 0.878 0.107 17 7673766 missense variant T/A snp 3
rs1131691023 1.000 0.071 17 7675142 missense variant A/G snp 2