Disease: Oligospermia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11204546
OR2W3
0.925 0.040 1 247896410 missense variant T/C;G snv 0.58; 4.0E-06 3
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2477686
PLCH2
0.807 0.040 1 2461209 intron variant G/C snv 0.64 7
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs55763075
MTHFR ; C1orf167
0.827 0.120 1 11790377 3 prime UTR variant C/T snv 2.1E-05 6
rs6166
FSHR
0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 17
rs121918346
DAZL
0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06 5
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs4647269
MLH1
0.925 0.040 3 37016100 intron variant C/T snv 0.35 2
rs786203623
MLH1
0.925 0.040 3 37017520 missense variant T/A;C snv 2
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2075789
MSH5-SAPCD1 ; LOC105375020 ; MSH5
0.882 0.120 6 31740551 missense variant C/T snv 0.13 9.1E-02 6
rs724078 0.925 0.040 6 29521271 intergenic variant G/A snv 0.41 3
rs10269148
STRA8
0.925 0.040 7 135230056 upstream gene variant C/A;G snv 2
rs1059060
PMS2
0.925 0.040 7 5977709 missense variant T/A;C snv 3
rs1248142939
PMS2
0.925 0.040 7 5992006 missense variant G/A snv 2
rs17420802
PMS2
0.925 0.040 7 5977709 missense variant T/A;C snv 2.5E-04 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs587781908
PMS2
0.925 0.040 7 6005973 missense variant A/G snv 1.2E-05 2
rs763468927
PMS2
0.925 0.040 7 5977755 missense variant G/A snv 4.0E-06 7.0E-06 2
rs864622096
PMS2
0.925 0.040 7 5986916 missense variant G/A snv 2
rs12348
TUSC1
0.925 0.040 9 25677217 3 prime UTR variant T/C snv 0.44 3
rs7867029
LOC107987083
0.925 0.040 9 78405502 intergenic variant G/C snv 0.22 3