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rs80359425

From SNPedia

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


Make rs80359425(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32325166
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359425
ebirs80359425
HLIrs80359425
Exacrs80359425
Varsomers80359425
Maprs80359425
PheGenIrs80359425
hapmaprs80359425
1000 genomesrs80359425
hgdprs80359425
ensemblrs80359425
gopubmedrs80359425
geneviewrs80359425
scholarrs80359425
googlers80359425
pharmgkbrs80359425
gwascentralrs80359425
openSNPrs80359425
23andMers80359425
23andMe allrs80359425
SNP Nexus

SNPshotrs80359425
SNPdbers80359425
MSV3drs80359425
GWAS Ctlgrs80359425
Max Magnitude6
rs80359425, also known as 635delA, c.407_407delA and p.Asn136Ilefs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359425(;)
Alt rs80359425(;)
Reference rs80359425(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32899303delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031457.5, RCV000044342.2, RCV000131981.2,