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
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1805377 0.689 0.480 5 83353124 splice acceptor variant G/A snv 0.23 0.25 19
rs1805329 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 15
rs1056503 0.851 0.200 5 83353158 synonymous variant T/A;G snv 4.0E-06; 0.23 4