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
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1265538677 0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10