Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs879745047
NHLRC1
1.000 0.080 6 18121825 missense variant A/G snv 4.0E-06 1.4E-05 1
rs137852916
EPM2A
1.000 0.080 6 145635451 missense variant C/T snv 2.0E-05 1.4E-05 1
rs769301934
NHLRC1
1.000 0.080 6 18122171 missense variant C/T snv 3.6E-05 2.8E-05 1
rs387907571
DNAJC13
0.827 0.080 3 132477995 missense variant A/G snv 4.2E-06 3.5E-05 6
rs587776542
NHLRC1
0.925 0.080 6 18122138 frameshift variant CT/- del 4.9E-05 2
rs28940576
NHLRC1
0.925 0.080 6 18122402 missense variant G/C snv 1.1E-04 8.4E-05 2
rs514492
VCP
0.882 0.160 9 35062975 splice region variant C/T snv 0.75 0.75 3