Disease: Androgenetic Alopecia
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
rs5934505 0.776 0.120 X 8945785 intergenic variant T/A;C snv 10
rs12373124
SPPL2C ; MAPT-AS1
0.790 0.120 17 45846853 synonymous variant T/C snv 0.15 0.14 9
rs6152
AR
0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28 9
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32 7
rs10888690
FAF1
0.807 0.080 1 50494849 intron variant T/A;C snv 7
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
rs111668293
TBX15
0.807 0.080 1 118896200 intron variant G/- del 0.12 7
rs115182912 0.807 0.080 3 126274431 intron variant G/A snv 1.5E-02 7
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40 7
rs1160312
LINC01432
0.807 0.080 20 22069865 intron variant A/G snv 0.55 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
rs12565727
C1orf127
0.807 0.080 1 10973025 intron variant A/G snv 0.31 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
rs12902958
DRAIC
0.807 0.080 15 69747915 intron variant G/A snv 7.7E-02 7
rs13021718
DPY30 ; MEMO1
0.807 0.080 2 31956355 intron variant G/A snv 0.15 7
rs13405699 0.807 0.080 2 173740905 intergenic variant C/A;G;T snv 7
rs1422798
EBF1
0.807 0.080 5 158893869 intron variant C/G snv 0.32 7
rs1819008
LOC105373757
0.807 0.080 2 176833154 intron variant C/A;T snv 0.49 7
rs201563 0.807 0.080 20 22019643 intergenic variant C/T snv 0.49 7