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rs80359725

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
(A;A) 0 common in clinvar


Make rs80359725(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376713
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359725
ebirs80359725
HLIrs80359725
Exacrs80359725
Varsomers80359725
Maprs80359725
PheGenIrs80359725
hapmaprs80359725
1000 genomesrs80359725
hgdprs80359725
ensemblrs80359725
gopubmedrs80359725
geneviewrs80359725
scholarrs80359725
googlers80359725
pharmgkbrs80359725
gwascentralrs80359725
openSNPrs80359725
23andMers80359725
23andMe allrs80359725
SNP Nexus

SNPshotrs80359725
SNPdbers80359725
MSV3drs80359725
GWAS Ctlgrs80359725
Max Magnitude6
rs80359725, also known as 8904delA, c.8676_8676delA and p.Arg2892Serfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359725(;)
Alt rs80359725(;)
Reference rs80359725(A;A)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32950850delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045599.2, RCV000113986.1,