Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4132699
SEMA4D
0.925 0.120 9 89421512 intron variant A/C snv 0.43 2
rs3858092
LOC105376157
1.000 0.120 9 95529166 regulatory region variant A/C snv 0.29 1
rs7566780 0.882 0.120 2 16548089 intron variant A/C;G snv 3
rs2283487 0.925 0.120 16 3919885 intergenic variant A/C;G snv 2
rs4791774
NTN1
0.882 0.240 17 9028802 intron variant A/C;G snv 2
rs28689133
LOC105376157
1.000 0.120 9 95531283 intergenic variant A/C;G snv 0.28 1
rs6126344
SALL4
0.925 0.120 20 51790963 missense variant A/C;T snv 0.35; 8.0E-06 2
rs6072081
LOC102724968
0.851 0.120 20 40632414 intergenic variant A/G snv 0.49 3
rs72728734
CCDC26
0.882 0.120 8 128921474 intron variant A/G snv 0.13 3
rs1038294
COL8A1
0.925 0.120 3 99784884 intron variant A/G snv 0.82 2
rs1588366
TANC2
0.925 0.120 17 62999067 regulatory region variant A/G snv 0.23 2
rs1838105
GOSR2 ; LRRC37A2
0.925 0.120 17 46931569 non coding transcript exon variant A/G snv 0.63 2
rs1907989 0.925 0.120 4 4817198 upstream gene variant A/G snv 0.36 2
rs6585429
VAX1
0.925 0.120 10 117133720 3 prime UTR variant A/G snv 0.68 2
rs7552
CYRIA
0.882 0.120 2 16552660 splice region variant A/G snv 0.44 2
rs188681640
LINC02476
1.000 0.120 7 119506105 intron variant A/G snv 2.4E-03 1
rs28434654
LOC105376157
1.000 0.120 9 95524196 intergenic variant A/G snv 0.28 1
rs74819164 1.000 0.120 2 147748280 intergenic variant A/G snv 7.0E-02 1
rs80004662
LOC102724542
1.000 0.120 2 81798061 intergenic variant A/G snv 6.1E-02 1
rs7554547 0.925 0.120 1 11913831 non coding transcript exon variant A/G;T snv 2
rs957448
VIRMA
0.925 0.120 8 94529074 synonymous variant A/G;T snv 0.33 2
rs6740960
C2orf91
0.925 0.120 2 41954539 intron variant A/T snv 0.61 2
rs11597348
OPALIN
1.000 0.120 10 96354046 intron variant A/T snv 7.9E-02 1
rs12175475
PRKN
1.000 0.120 6 162250424 intron variant A/T snv 2.1E-02 1
rs12543318 0.882 0.120 8 87856112 intergenic variant C/A snv 0.68 3