Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72653758
ABCC6
0.925 0.160 16 16202113 missense variant A/C snv 4.0E-06 2
rs199473573
SCN5A
0.925 0.120 3 38604007 missense variant A/C snv 1.6E-05 7.0E-06 2
rs121908550
SCN4A
0.925 0.160 17 63941984 missense variant A/C snv 2
rs137852523
L1CAM
0.925 0.200 X 153870948 missense variant A/C snv 2
rs750779804
SMPD1
0.925 0.160 11 6391813 missense variant A/C snv 8.0E-06 2
rs367968666
GBA
0.882 0.120 1 155237458 missense variant A/C snv 2.4E-04 1.6E-04 2
rs376710410
GLB1
0.827 0.160 3 33065551 missense variant A/C snv 2.7E-05 5.6E-05 2
rs756134838
HGD
1.000 0.080 3 120647015 missense variant A/C snv 8.0E-06 1
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 1
rs104894836
HNRNPH2 ; RPL36A-HNRNPH2 ; GLA
1.000 0.160 X 101407738 missense variant A/C snv 1
rs104894838
RPL36A-HNRNPH2 ; GLA
1.000 0.160 X 101400699 missense variant A/C snv 1
rs869312158
RPL36A-HNRNPH2 ; GLA
1.000 0.160 X 101398419 missense variant A/C snv 1
rs869312138
GLA ; RPL36A-HNRNPH2 ; HNRNPH2
1.000 0.160 X 101407797 missense variant A/C snv 1
rs373661718
PAX6
1.000 0.080 11 31790836 missense variant A/C snv 1
rs1323541164
TSC1
1.000 0.120 9 132921834 missense variant A/C snv 1
rs56087561
BRCA2
1.000 0.080 13 32339425 missense variant A/C snv 2.2E-04 2.2E-04 1
rs11571747
BRCA2
1.000 0.080 13 32371035 missense variant A/C snv 1.1E-03 1.5E-03 1
rs397508869
BRCA1
1.000 0.080 17 43094138 missense variant A/C snv 1
rs121918683
MYC ; CASC11
1.000 0.160 8 127738519 missense variant A/C snv 1
rs1566734
PTPRJ
0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 1
rs121909242
PPARG
0.925 0.080 3 12416825 missense variant A/C snv 1
rs137852231
F9
1.000 0.080 X 139541085 splice acceptor variant A/C snv 1
rs137852229
F9
1.000 0.080 X 139537158 missense variant A/C snv 1
rs1414714315
EPHA3
1.000 0.080 3 89413239 missense variant A/C snv 8.0E-06 1
rs180177033
BRAF
1.000 0.080 7 140781620 missense variant A/C snv 1