Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs25487 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 119
rs11540654 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 117
rs77375493 0.504 0.536 9 5073770 missense variant G/A,T snp 3.5E-04 2.9E-04 106
rs1695 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 100
rs1052133 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 77
rs121913279 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 68
rs861539 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 60
rs1042522 0.563 0.643 17 7676154 stop gained G/C,T snp 0.67 0.62 56
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 56
rs25489 0.587 0.571 19 43552260 stop lost C/G,T snp 8.5E-06; 7.1E-02 3.2E-05; 5.5E-02 48
rs104894230 0.615 0.464 11 534288 missense variant C/A,G,T snp 42
rs11554290 0.618 0.464 1 114713908 missense variant T/A,C,G snp 36
rs121913254 0.647 0.429 1 114713909 missense variant G/A,C,T snp 33
rs121913274 0.626 0.286 3 179218304 missense variant A/C,G,T snp 33
rs121913233 0.657 0.429 11 533874 missense variant T/A,C,G snp 25
rs121913255 0.662 0.357 1 114713907 missense variant T/A,G snp 25
rs2853669 0.724 0.179 5 1295234 TF binding site variant A/G snp 0.24 16
rs121913403 0.707 0.250 3 41224622 missense variant C/A,G,T snp 15
rs121913409 0.734 0.250 3 41224646 missense variant C/A,G,T snp 14
rs28931588 0.724 0.179 3 41224606 missense variant G/A,C,T snp 13
rs121913396 0.734 0.179 3 41224607 missense variant A/C,G,T snp 12
rs2282679
GC
0.744 0.286 4 71742666 intron variant T/G snp 0.22 11
rs121913407 0.769 0.250 3 41224645 missense variant T/C,G snp 10
rs397514606 0.769 0.214 1 243695714 missense variant C/T snp 9