Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3784730
ST8SIA2
0.851 0.120 15 92443898 intron variant A/G snv 0.44 6
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs1800692
TNFRSF1A
0.925 0.120 12 6333180 missense variant A/G snv 0.64 0.71 5
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs1131692040
SNORA70 ; RPL10
0.882 0.160 X 154399844 missense variant A/G snv 4
rs561077
GPR50
0.882 0.080 X 151181177 missense variant A/G snv 0.43 0.45 4
rs3027407
MAOA
0.925 0.040 X 43745594 3 prime UTR variant A/G snv 3
rs769402060
CYP1B1-AS1 ; CYP1B1
0.925 0.120 2 38075022 missense variant A/G snv 3.3E-05 4.2E-05 3
rs11795613
NLGN3
0.925 0.120 X 71147478 intron variant A/G snv 2
rs3825251
DAO
0.925 0.040 12 108894208 intron variant A/G snv 0.18 2
rs1276905604
GLRA2
1.000 0.040 X 14581319 missense variant A/G snv 9.5E-06 1
rs1484207450
POGZ
1.000 0.040 1 151405155 missense variant A/G snv 7.0E-06 1
rs1557909821
POGZ
1.000 0.040 1 151427999 missense variant A/G snv 1
rs1568820
LANCL2
1.000 0.040 7 55413206 intron variant A/G snv 0.33 1
rs194085 1.000 0.040 5 9591303 intergenic variant A/G snv 0.15 1
rs2078178
CLEC7A ; LOC105369655
1.000 0.040 12 10123963 intron variant A/G snv 0.55 1
rs2158836
LAMB1
1.000 0.040 7 107940394 non coding transcript exon variant A/G snv 0.63 0.64 1
rs2241694
CAMK2A
1.000 0.040 5 150223045 missense variant A/G snv 0.92 0.94 1
rs34714481
ZNF804A ; LOC105373780
1.000 0.040 2 184597742 intron variant A/G snv 0.12 1
rs3759292
AVPR1A
1.000 0.040 12 63153533 intron variant A/G snv 2.4E-02 1
rs731276
SEZ6L
1.000 0.040 22 26374424 intron variant A/G snv 0.47 1
rs74336682
SHANK2
1.000 0.040 11 70586855 intron variant A/G snv 5.6E-02 1
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs1085308043
PTEN
0.763 0.200 10 87925511 splice acceptor variant A/G;T snv 12
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12