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rs80359436

From SNPedia

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


Make rs80359436(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338613
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359436
ebirs80359436
HLIrs80359436
Exacrs80359436
Varsomers80359436
Maprs80359436
PheGenIrs80359436
hapmaprs80359436
1000 genomesrs80359436
hgdprs80359436
ensemblrs80359436
gopubmedrs80359436
geneviewrs80359436
scholarrs80359436
googlers80359436
pharmgkbrs80359436
gwascentralrs80359436
openSNPrs80359436
23andMers80359436
23andMe allrs80359436
SNP Nexus

SNPshotrs80359436
SNPdbers80359436
MSV3drs80359436
GWAS Ctlgrs80359436
Max Magnitude6
rs80359436, also known as 4486delG, c.4258_4258delG and p.Asp1420Ilefs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359436(;)
Alt rs80359436(;)
Reference rs80359436(G;G)
Significance Other
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32912750delG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044378.2, RCV000077322.5, RCV000165445.1,