Disease: Alopecia, Male Pattern
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs76972608 0.807 0.080 12 130078818 intergenic variant A/T snv 0.13 7
rs78003935 0.807 0.080 1 170372381 upstream gene variant T/A;G snv 0.25 7
rs79437808 0.807 0.080 8 108585572 intron variant C/T snv 1.3E-02 7
rs9287638 0.807 0.080 2 238785990 downstream gene variant C/A snv 0.40 7
rs9357047 0.807 0.080 6 9327323 intergenic variant T/A;C snv 7
rs6152
AR
0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28 9
rs12565727
C1orf127
0.807 0.080 1 10973025 intron variant A/G snv 0.31 7
rs2095921
C1orf127
0.807 0.080 1 10973265 intron variant C/G;T snv 7
rs7542354
C1orf127
0.807 0.080 1 10980328 intron variant G/A snv 0.37 7
rs13021718
DPY30 ; MEMO1
0.807 0.080 2 31956355 intron variant G/A snv 0.15 7
rs12902958
DRAIC
0.807 0.080 15 69747915 intron variant G/A snv 7.7E-02 7
rs7177657
DRAIC
0.807 0.080 15 69749354 intron variant T/C snv 8.7E-02 7
rs1422798
EBF1
0.807 0.080 5 158893869 intron variant C/G snv 0.32 7
rs62385385
EBF1
0.807 0.080 5 158940241 intron variant T/A snv 0.32 7
rs77767830
EIF3E
0.807 0.080 8 108256167 intron variant A/T snv 2.5E-02 7
rs10888690
FAF1
0.807 0.080 1 50494849 intron variant T/A;C snv 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
rs4690116
FGF5
0.807 0.080 4 80285223 intron variant T/A snv 0.59 7
rs7680591
FGF5
0.807 0.080 4 80276795 intron variant T/A snv 0.58 7
rs2073963
HDAC9
0.807 0.080 7 18838251 intron variant T/G snv 0.43 7
rs71530654
HDAC9
0.807 0.080 7 18857365 intron variant A/G snv 0.43 7
rs756853
HDAC9
0.925 0.080 7 18850377 intron variant G/A snv 0.56 2
rs7801037
HDAC9
0.807 0.080 7 18857888 intron variant C/A;G;T snv 7
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38