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rs587777032

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCG;CCG) 0 common in clinvar
Make rs587777032(-;-)
Make rs587777032(-;GCC)
Make rs587777032(GCC;GCC)
ReferenceGRCh38 38.1/142
Chromosome10
Position119030318
GeneNANOS1
is asnp
is mentioned by
dbSNPrs587777032
ebirs587777032
HLIrs587777032
Exacrs587777032
Varsomers587777032
Maprs587777032
PheGenIrs587777032
hapmaprs587777032
1000 genomesrs587777032
hgdprs587777032
ensemblrs587777032
gopubmedrs587777032
geneviewrs587777032
scholarrs587777032
googlers587777032
pharmgkbrs587777032
gwascentralrs587777032
openSNPrs587777032
23andMers587777032
23andMe allrs587777032
SNP Nexus

SNPshotrs587777032
SNPdbers587777032
MSV3drs587777032
GWAS Ctlgrs587777032
Max Magnitude0
ClinVar
Risk rs587777032(;)
Alt rs587777032(;)
Reference rs587777032(CCG;CCG)
Significance Pathogenic
Disease Spermatogenic failure 12
Variation info
Gene NANOS1
CLNDBN Spermatogenic failure 12
Reversed 0
HGVS NC_000010.10:g.120789830_120789832delGCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000055618.2,