Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113