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
rs137854889
ZMPSTE24
0.742 0.440 1 40290871 frameshift variant T/-;TT delins 31
rs10273639
PRSS1
0.776 0.280 7 142749077 upstream gene variant T/A;C snv 9
rs200527106
TLR4
0.925 0.120 9 117712902 missense variant G/A;C snv 4.0E-06 3
rs2412930 1.000 0.120 4 58722063 intergenic variant A/G snv 0.85 1
rs13380717
LOC105371393
1.000 0.120 16 86870529 intergenic variant A/G snv 0.33 1