Disease: Alopecia, Male Pattern
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2073963
HDAC9
0.807 0.080 7 18838251 intron variant T/G snv 0.43 7
rs2095921
C1orf127
0.807 0.080 1 10973265 intron variant C/G;T snv 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
rs34800162
SLC14A2
0.807 0.080 18 45228094 intron variant T/G snv 0.32 7
rs34991987
LOC105375343
0.807 0.080 7 69130240 downstream gene variant A/-;AA delins 7
rs35892873
KLF15
0.807 0.080 3 126350105 intron variant C/T snv 0.33 7
rs3781452
FAM53B
0.807 0.080 10 124666560 intron variant C/T snv 0.60 7
rs3781458
FAM53B
0.807 0.080 10 124655362 intron variant C/A;G;T snv 7
rs4679956
LOC107986047
0.807 0.080 3 151937074 intergenic variant C/A;T snv 7
rs4690116
FGF5
0.807 0.080 4 80285223 intron variant T/A snv 0.59 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
rs6047844
LINC01432
0.807 0.080 20 22056937 intron variant T/C snv 0.54 7
rs62060349 0.807 0.080 17 57153807 intergenic variant T/C snv 0.37 7
rs62385385
EBF1
0.807 0.080 5 158940241 intron variant T/A snv 0.32 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
rs68088846
LOC102724584 ; RUNX1
0.807 0.080 21 34835870 intron variant G/A snv 0.27 7
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