Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs114780236
WDPCP
1.000 0.080 2 63561915 intron variant G/A snv 1
rs619824
WBP1L
0.925 0.080 10 102821531 intron variant A/C snv 0.50 2
rs684232
VPS53
0.925 0.080 17 715725 intron variant T/C snv 0.46 2
rs2359612
VKORC1
0.851 0.120 16 31092475 intron variant A/G snv 0.66 7
rs779805
VHL
0.851 0.120 3 10141653 5 prime UTR variant G/A;C snv 4
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2107301
VDR
0.807 0.120 12 47861787 intron variant G/A snv 0.26 7
rs11574143
VDR
0.827 0.200 12 47841134 downstream gene variant C/T snv 0.11 5
rs2238135
VDR
0.882 0.160 12 47884407 intron variant C/G snv 0.26 4
rs11168314
VDR
0.925 0.080 12 47936846 intron variant G/A snv 0.23 2
rs2239182
VDR
0.925 0.080 12 47861628 intron variant T/C snv 0.51 2
rs2408876
VDR
0.925 0.080 12 47879782 intron variant T/A;C snv 2
rs7299460
VDR
0.925 0.080 12 47902485 intron variant C/T snv 0.43 2
rs10187424
VAMP8
0.925 0.080 2 85567174 intron variant T/A;C snv 2
rs3731827
VAMP8
1.000 0.080 2 85578945 intron variant T/C snv 0.47 1
rs1529916
USP7
0.851 0.120 16 8897333 intron variant G/A snv 0.26 4
rs9469899
UHRF1BP1
1.000 0.080 6 34825347 intron variant G/A snv 0.46 1