Have questions? Visit https://www.reddit.com/r/SNPedia

rs80359679

From SNPedia

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


Make rs80359679(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357886
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359679
ebirs80359679
HLIrs80359679
Exacrs80359679
Varsomers80359679
Maprs80359679
PheGenIrs80359679
hapmaprs80359679
1000 genomesrs80359679
hgdprs80359679
ensemblrs80359679
gopubmedrs80359679
geneviewrs80359679
scholarrs80359679
googlers80359679
pharmgkbrs80359679
gwascentralrs80359679
openSNPrs80359679
23andMers80359679
23andMe allrs80359679
SNP Nexus

SNPshotrs80359679
SNPdbers80359679
MSV3drs80359679
GWAS Ctlgrs80359679
Max Magnitude6
rs80359679, also known as 7990delA, c.7762_7762delA and p.Ile2588Tyrfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359679(;)
Alt rs80359679(;)
Reference rs80359679(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32932023delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045307.3, RCV000113814.1,