Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs10096777
RP1L1
8 10660990 intron variant G/A snv 0.61 2
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs10832417
KCNQ1OT1 ; KCNQ1
11 2631427 non coding transcript exon variant T/G snv 0.32 3
rs10850411 12 114949991 intergenic variant T/C snv 0.34 1
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs11023906
SOX6
11 16302860 intron variant G/A snv 0.17 3
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs11158609
NEDD8 ; NEDD8-MDP1
14 24219608 intron variant G/A snv 0.89 2
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs1133322
COX5A
15 74920016 3 prime UTR variant A/G snv 0.38 2
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs11693319
CCDC141
2 178873542 3 prime UTR variant C/G;T snv 2
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs12705959
FOXP2
7 114358191 intron variant C/T snv 0.39 2
rs12899430
COX5A
15 74936759 intron variant T/C snv 0.37 2
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 5
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs13178964 5 105011948 intron variant A/G snv 0.17 2
rs13255193
FAM167A
8 11451683 intron variant T/C snv 0.47 2