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rs587777768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs587777768(CG;TA)
Make rs587777768(TA;TA)
ReferenceGRCh38 38.1/142
Chromosome10
Position119030627
GeneNANOS1
is asnp
is mentioned by
dbSNPrs587777768
ebirs587777768
HLIrs587777768
Exacrs587777768
Varsomers587777768
Maprs587777768
PheGenIrs587777768
hapmaprs587777768
1000 genomesrs587777768
hgdprs587777768
ensemblrs587777768
gopubmedrs587777768
geneviewrs587777768
scholarrs587777768
googlers587777768
pharmgkbrs587777768
gwascentralrs587777768
openSNPrs587777768
23andMers587777768
23andMe allrs587777768
SNP Nexus

SNPshotrs587777768
SNPdbers587777768
MSV3drs587777768
GWAS Ctlgrs587777768
Max Magnitude0
ClinVar
Risk rs587777768(TA;TA)
Alt rs587777768(TA;TA)
Reference rs587777768(CG;CG)
Significance Pathogenic
Disease Spermatogenic failure 12
Variation info
Gene NANOS1
CLNDBN Spermatogenic failure 12
Reversed 0
HGVS NC_000010.10:g.120790139_120790140delCGinsTA
CLNSRC OMIM Allelic Variant
CLNACC RCV000055619.2,