Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1430452530 0.851 0.160 14 61721518 missense variant A/G snv 4.0E-06 5
rs1467453450 0.882 0.080 9 105506513 missense variant A/G snv 7.0E-06 4
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2075786 0.790 0.360 5 1266195 intron variant A/G snv 0.55 8
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs4809957 0.763 0.240 20 54154632 3 prime UTR variant A/G snv 0.29 10
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs62514004 0.790 0.240 8 133190246 upstream gene variant A/G snv 0.28 8
rs7158663 0.827 0.240 14 100853087 non coding transcript exon variant A/G snv 0.42 9
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8