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rs878854403

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854403(A;A)
Make rs878854403(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position49516282
GeneERCC6, PGBD3
is asnp
is mentioned by
dbSNPrs878854403
ebirs878854403
HLIrs878854403
Exacrs878854403
Varsomers878854403
Maprs878854403
PheGenIrs878854403
hapmaprs878854403
1000 genomesrs878854403
hgdprs878854403
ensemblrs878854403
gopubmedrs878854403
geneviewrs878854403
scholarrs878854403
googlers878854403
pharmgkbrs878854403
gwascentralrs878854403
openSNPrs878854403
23andMers878854403
23andMe allrs878854403
SNP Nexus

SNPshotrs878854403
SNPdbers878854403
MSV3drs878854403
GWAS Ctlgrs878854403
Max Magnitude0
ClinVar
Risk rs878854403(A;A)
Alt rs878854403(A;A)
Reference rs878854403(G;G)
Significance Pathogenic
Disease Premature ovarian failure 11
Variation info
Gene ERCC6 PGBD3
CLNDBN Premature ovarian failure 11
Reversed 1
HGVS NC_000010.10:g.50724328C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000211123.1,