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
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1194611372 0.763 0.320 1 152032679 missense variant A/C snv 9
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4