Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs9282858
SRD5A2
0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 16
rs3827760
RANBP2 ; EDAR
0.752 0.160 2 108897145 missense variant A/G snv 0.15 5.9E-02 11
rs5934505 0.776 0.120 X 8945785 intergenic variant T/A;C snv 10
rs6152
AR
0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28 9
rs12373124
SPPL2C ; MAPT-AS1
0.790 0.120 17 45846853 synonymous variant T/C snv 0.15 0.14 9
rs17833789 0.807 0.080 17 57153267 intergenic variant C/A snv 0.37 8
rs10930758 0.807 0.080 2 176897100 intergenic variant A/G;T snv 7
rs11037975 0.807 0.080 11 44389312 intergenic variant C/A;G snv 7
rs115182912 0.807 0.080 3 126274431 intron variant G/A snv 1.5E-02 7
rs11684254 0.807 0.080 2 238787252 downstream gene variant C/G snv 0.44 7
rs12083887 0.807 0.080 1 118339066 regulatory region variant A/G snv 0.62 7
rs12214131 0.807 0.080 6 105760046 intron variant G/A snv 0.29 7
rs1262557 0.807 0.080 6 126733443 intron variant C/T snv 0.51 7
rs12702271 0.807 0.080 7 46904161 intron variant C/T snv 0.20 7
rs13405699 0.807 0.080 2 173740905 intergenic variant C/A;G;T snv 7
rs201563 0.807 0.080 20 22019643 intergenic variant C/T snv 0.49 7
rs2180439 0.807 0.080 20 21872462 intergenic variant C/T snv 0.58 7
rs246180 0.807 0.080 16 14298066 upstream gene variant C/A;T snv 7
rs2497938 0.807 0.080 X 67343176 intergenic variant T/C snv 0.37 7
rs4718886 0.807 0.080 7 69433703 upstream gene variant A/G snv 0.27 7
rs58788673 0.807 0.080 7 46864701 intergenic variant -/CA ins 0.22 7
rs62060349 0.807 0.080 17 57153807 intergenic variant T/C snv 0.37 7
rs6625163 0.807 0.080 X 67291142 intergenic variant G/A snv 0.62 7
rs6752754 0.807 0.080 2 6429434 intergenic variant A/G snv 0.15 7