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rs45469092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45469092(C;T)
Make rs45469092(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379479
GeneBRCA2
is asnp
is mentioned by
dbSNPrs45469092
ebirs45469092
HLIrs45469092
Exacrs45469092
Varsomers45469092
Maprs45469092
PheGenIrs45469092
hapmaprs45469092
1000 genomesrs45469092
hgdprs45469092
ensemblrs45469092
gopubmedrs45469092
geneviewrs45469092
scholarrs45469092
googlers45469092
pharmgkbrs45469092
gwascentralrs45469092
openSNPrs45469092
23andMers45469092
23andMe allrs45469092
SNP Nexus

SNPshotrs45469092
SNPdbers45469092
MSV3drs45469092
GWAS Ctlgrs45469092
Max Magnitude0
ClinVar
Risk rs45469092(G,T;G,T)
Alt rs45469092(G,T;G,T)
Reference rs45469092(C;C)
Significance Probable-non-pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not provided Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32953616C>G; NC_000013.10:g.32953616C>T
CLNSRC ClinVar
CLNACC RCV000045656.2, RCV000114015.1, RCV000031776.7, RCV000034469.1, RCV000045657.3, RCV000163016.1,