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rs201095702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201095702(C;T)
Make rs201095702(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position124500326
GeneNR5A1
is asnp
is mentioned by
dbSNPrs201095702
ebirs201095702
HLIrs201095702
Exacrs201095702
Varsomers201095702
Maprs201095702
PheGenIrs201095702
hapmaprs201095702
1000 genomesrs201095702
hgdprs201095702
ensemblrs201095702
gopubmedrs201095702
geneviewrs201095702
scholarrs201095702
googlers201095702
pharmgkbrs201095702
gwascentralrs201095702
openSNPrs201095702
23andMers201095702
23andMe allrs201095702
SNP Nexus

SNPshotrs201095702
SNPdbers201095702
MSV3drs201095702
GWAS Ctlgrs201095702
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs201095702(T;T)
Alt rs201095702(T;T)
Reference rs201095702(C;C)
Significance Pathogenic
Disease Spermatogenic failure 8
Variation info
Gene NR5A1
CLNDBN Spermatogenic failure 8
Reversed 0
HGVS NC_000009.11:g.127262605C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022777.18,