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rs7800847

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs7800847(A;A)
Make rs7800847(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position144401541
GeneNOBOX
is asnp
is mentioned by
dbSNPrs7800847
ebirs7800847
HLIrs7800847
Exacrs7800847
Varsomers7800847
Maprs7800847
PheGenIrs7800847
hapmaprs7800847
1000 genomesrs7800847
hgdprs7800847
ensemblrs7800847
gopubmedrs7800847
geneviewrs7800847
scholarrs7800847
googlers7800847
pharmgkbrs7800847
gwascentralrs7800847
openSNPrs7800847
23andMers7800847
23andMe allrs7800847
SNP Nexus

SNPshotrs7800847
SNPdbers7800847
MSV3drs7800847
GWAS Ctlgrs7800847
Max Magnitude0
ClinVar
Risk rs7800847(A;A)
Alt rs7800847(A;A)
Reference rs7800847(G;G)
Significance Pathogenic
Disease Premature ovarian failure 5
Variation info
Gene NOBOX
CLNDBN Premature ovarian failure 5
Reversed 0
HGVS NC_000007.13:g.144098634G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000154191.3,