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rs587777767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777767(A;A)
Make rs587777767(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position119030538
GeneNANOS1
is asnp
is mentioned by
dbSNPrs587777767
ebirs587777767
HLIrs587777767
Exacrs587777767
Varsomers587777767
Maprs587777767
PheGenIrs587777767
hapmaprs587777767
1000 genomesrs587777767
hgdprs587777767
ensemblrs587777767
gopubmedrs587777767
geneviewrs587777767
scholarrs587777767
googlers587777767
pharmgkbrs587777767
gwascentralrs587777767
openSNPrs587777767
23andMers587777767
23andMe allrs587777767
SNP Nexus

SNPshotrs587777767
SNPdbers587777767
MSV3drs587777767
GWAS Ctlgrs587777767
Max Magnitude0
ClinVar
Risk rs587777767(A;A)
Alt rs587777767(A;A)
Reference rs587777767(G;G)
Significance Pathogenic
Disease Spermatogenic failure 12
Variation info
Gene NANOS1
CLNDBN Spermatogenic failure 12
Reversed 0
HGVS NC_000010.10:g.120790050G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000055619.2,