Disease: Oligospermia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10842262
SOX5
0.851 0.040 12 24031610 intron variant G/C snv 0.43 5
rs4474514
KITLG
0.827 0.240 12 88560182 intron variant G/A snv 0.65 6
rs995030
KITLG
0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67 9
rs12870438
EPSTI1
0.925 0.040 13 42906069 intron variant G/A snv 0.27 3
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs175080
MLH3
0.776 0.240 14 75047125 missense variant G/A snv 0.40 0.43 9
rs7174015
USP8
0.925 0.040 15 50424871 intron variant G/A;T snv 3
rs188541504
THEG
0.925 0.040 19 374362 missense variant C/T snv 8.0E-05 4.9E-05 3
rs2228611
DNMT1
0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs6080550
LOC100289473
0.851 0.040 20 1778944 intron variant C/G;T snv 9.6E-02 5
rs553509
H2BW1
0.925 0.040 X 104013293 missense variant T/C snv 0.38 3