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rs587777031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCT;CCT) 0 common in clinvar
Make rs587777031(-;-)
Make rs587777031(-;CTC)
Make rs587777031(CTC;CTC)
ReferenceGRCh38 38.1/142
Chromosome10
Position119030041
GeneNANOS1
is asnp
is mentioned by
dbSNPrs587777031
ebirs587777031
HLIrs587777031
Exacrs587777031
Varsomers587777031
Maprs587777031
PheGenIrs587777031
hapmaprs587777031
1000 genomesrs587777031
hgdprs587777031
ensemblrs587777031
gopubmedrs587777031
geneviewrs587777031
scholarrs587777031
googlers587777031
pharmgkbrs587777031
gwascentralrs587777031
openSNPrs587777031
23andMers587777031
23andMe allrs587777031
SNP Nexus

SNPshotrs587777031
SNPdbers587777031
MSV3drs587777031
GWAS Ctlgrs587777031
Max Magnitude0
ClinVar
Risk rs587777031(;)
Alt rs587777031(;)
Reference rs587777031(CCT;CCT)
Significance Pathogenic
Disease Spermatogenic failure 12
Variation info
Gene NANOS1
CLNDBN Spermatogenic failure 12
Reversed 0
HGVS NC_000010.10:g.120789553_120789555delCTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000055617.2,