Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
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
rs11574143
VDR
0.827 0.200 12 47841134 downstream gene variant C/T snv 0.11 5
rs11168287
VDR
0.882 0.160 12 47891631 intron variant G/A snv 0.56 3
rs11574079
VDR
1.000 0.080 12 47858947 intron variant C/T snv 1.7E-03 1
rs3819545
VDR
1.000 0.080 12 47871223 intron variant A/G snv 0.36 1