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rs80358842

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358842(A;A)
Make rs80358842(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340413
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358842
ebirs80358842
HLIrs80358842
Exacrs80358842
Varsomers80358842
Maprs80358842
PheGenIrs80358842
hapmaprs80358842
1000 genomesrs80358842
hgdprs80358842
ensemblrs80358842
gopubmedrs80358842
geneviewrs80358842
scholarrs80358842
googlers80358842
pharmgkbrs80358842
gwascentralrs80358842
openSNPrs80358842
23andMers80358842
23andMe allrs80358842
SNP Nexus

SNPshotrs80358842
SNPdbers80358842
MSV3drs80358842
GWAS Ctlgrs80358842
Max Magnitude0
ClinVar
Risk rs80358842(A,T;A,T)
Alt rs80358842(A,T;A,T)
Reference rs80358842(G;G)
Significance Untested
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914550G>A; NC_000013.10:g.32914550G>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000113521.2, RCV000129466.2, RCV000160106.2, RCV000044828.2,