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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs4696480 0.716 0.400 4 153685974 intron variant T/A snv 0.45 19