Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs149617956 0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 32