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rs730880018

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880018(C;G)
Make rs730880018(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position91353299
is asnp
is mentioned by
dbSNPrs730880018
ebirs730880018
HLIrs730880018
Exacrs730880018
Varsomers730880018
Maprs730880018
PheGenIrs730880018
hapmaprs730880018
1000 genomesrs730880018
hgdprs730880018
ensemblrs730880018
gopubmedrs730880018
geneviewrs730880018
scholarrs730880018
googlers730880018
pharmgkbrs730880018
gwascentralrs730880018
openSNPrs730880018
23andMers730880018
23andMe allrs730880018
SNP Nexus

SNPshotrs730880018
SNPdbers730880018
MSV3drs730880018
GWAS Ctlgrs730880018
Max Magnitude0
ClinVar
Risk rs730880018(G;G)
Alt rs730880018(G;G)
Reference rs730880018(C;C)
Significance Pathogenic
Disease Premature ovarian failure 9
Variation info
Gene HFM1
CLNDBN Premature ovarian failure 9
Reversed 0
HGVS NC_000001.10:g.91818856C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000114368.2,