Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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