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rs80359386

From SNPedia

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


Make rs80359386(-;-)
ReferenceGRCh38 38.1/142
Chromosome13
Position32337813
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359386
ebirs80359386
HLIrs80359386
Exacrs80359386
Varsomers80359386
Maprs80359386
PheGenIrs80359386
hapmaprs80359386
1000 genomesrs80359386
hgdprs80359386
ensemblrs80359386
gopubmedrs80359386
geneviewrs80359386
scholarrs80359386
googlers80359386
pharmgkbrs80359386
gwascentralrs80359386
openSNPrs80359386
23andMers80359386
23andMe allrs80359386
SNP Nexus

SNPshotrs80359386
SNPdbers80359386
MSV3drs80359386
GWAS Ctlgrs80359386
Max Magnitude6
rs80359386, also known as 3686delA, c.3458_3458delA and p.Lys1153Argfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359386(;)
Alt rs80359386(;)
Reference rs80359386(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911950delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113182.1,