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rs875989810

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989810(G;T)
Make rs875989810(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position49528426
GeneERCC6, ERCC6-PGBD3
is asnp
is mentioned by
dbSNPrs875989810
ebirs875989810
HLIrs875989810
Exacrs875989810
Varsomers875989810
Maprs875989810
PheGenIrs875989810
hapmaprs875989810
1000 genomesrs875989810
hgdprs875989810
ensemblrs875989810
gopubmedrs875989810
geneviewrs875989810
scholarrs875989810
googlers875989810
pharmgkbrs875989810
gwascentralrs875989810
openSNPrs875989810
23andMers875989810
23andMe allrs875989810
SNP Nexus

SNPshotrs875989810
SNPdbers875989810
MSV3drs875989810
GWAS Ctlgrs875989810
Max Magnitude0
ClinVar
Risk rs875989810(T;T)
Alt rs875989810(T;T)
Reference rs875989810(G;G)
Significance Pathogenic
Disease Premature ovarian failure 11
Variation info
Gene ERCC6-PGBD3 ERCC6
CLNDBN Premature ovarian failure 11
Reversed 1
HGVS NC_000010.10:g.50736472C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000211122.1,