Disease: Alopecia, Male Pattern
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6945541
LOC105375343
0.807 0.080 7 69146973 intron variant C/T snv 0.68 7
rs7061504
OPHN1
0.807 0.080 X 68143959 intron variant A/G snv 0.23 7
rs71421546
LOC100129455 ; HOXD-AS2
0.807 0.080 2 176127129 intron variant C/A;T snv 7
rs71530654
HDAC9
0.807 0.080 7 18857365 intron variant A/G snv 0.43 7
rs7177657
DRAIC
0.807 0.080 15 69749354 intron variant T/C snv 8.7E-02 7
rs7349332
WNT10A
0.807 0.080 2 218891661 intron variant C/G;T snv 7
rs74333950
WNT10A ; LOC107984111
0.807 0.080 2 218881570 intron variant T/G snv 0.13 7
rs7542354
C1orf127
0.807 0.080 1 10980328 intron variant G/A snv 0.37 7
rs756853
HDAC9
0.925 0.080 7 18850377 intron variant G/A snv 0.56 2
rs7642536
MRPS22
0.807 0.080 3 139313491 intron variant T/C snv 0.12 7
rs7680591
FGF5
0.807 0.080 4 80276795 intron variant T/A snv 0.58 7
rs77767830
EIF3E
0.807 0.080 8 108256167 intron variant A/T snv 2.5E-02 7
rs7801037
HDAC9
0.807 0.080 7 18857888 intron variant C/A;G;T snv 7
rs79437808 0.807 0.080 8 108585572 intron variant C/T snv 1.3E-02 7
rs7974900
LOC105369705 ; SSPN ; LOC105369704
0.807 0.080 12 26275744 intron variant T/A;C snv 7
rs8085664
SLC14A2
0.807 0.080 18 45234191 intron variant C/A;T 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
rs12558842 0.925 0.080 X 67261958 intergenic variant C/A;G snv 2
rs13405699 0.807 0.080 2 173740905 intergenic variant C/A;G;T snv 7
rs1998076 0.925 0.080 20 21899407 intergenic variant A/G snv 0.64 2
rs201563 0.807 0.080 20 22019643 intergenic variant C/T snv 0.49 7
rs201571 0.925 0.080 20 22032876 intergenic variant C/T snv 0.60 2
rs2180439 0.807 0.080 20 21872462 intergenic variant C/T snv 0.58 7
rs2497938 0.807 0.080 X 67343176 intergenic variant T/C snv 0.37 7