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rs77587352

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs77587352(A;A)
Make rs77587352(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position144401890
GeneNOBOX
is asnp
is mentioned by
dbSNPrs77587352
ebirs77587352
HLIrs77587352
Exacrs77587352
Varsomers77587352
Maprs77587352
PheGenIrs77587352
hapmaprs77587352
1000 genomesrs77587352
hgdprs77587352
ensemblrs77587352
gopubmedrs77587352
geneviewrs77587352
scholarrs77587352
googlers77587352
pharmgkbrs77587352
gwascentralrs77587352
openSNPrs77587352
23andMers77587352
23andMe allrs77587352
SNP Nexus

SNPshotrs77587352
SNPdbers77587352
MSV3drs77587352
GWAS Ctlgrs77587352
Max Magnitude0
ClinVar
Risk rs77587352(A;A)
Alt rs77587352(A;A)
Reference rs77587352(C;C)
Significance Pathogenic
Disease Premature ovarian failure 5
Variation info
Gene NOBOX
CLNDBN Premature ovarian failure 5
Reversed 0
HGVS NC_000007.13:g.144098983C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000154190.4,