Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 10