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rs80359522

From SNPedia

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


Make rs80359522(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339932
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359522
dbSNP (old)rs80359522
ClinGenrs80359522
ebirs80359522
HLIrs80359522
Exacrs80359522
Gnomadrs80359522
Varsomers80359522
Maprs80359522
PheGenIrs80359522
Biobankrs80359522
1000 genomesrs80359522
hgdprs80359522
ensemblrs80359522
gopubmedrs80359522
geneviewrs80359522
scholarrs80359522
googlers80359522
pharmgkbrs80359522
gwascentralrs80359522
openSNPrs80359522
23andMers80359522
23andMe allrs80359522
SNP Nexus

SNPshotrs80359522
SNPdbers80359522
MSV3drs80359522
GWAS Ctlgrs80359522
Max Magnitude6
rs80359522, also known as 5805del4, c.5577_5580delTAAA and p.Ile1859_Lys1860?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359522(-;-)
Alt rs80359522(-;-)
Reference Rs80359522(TAAA;TAAA)
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.32914069_32914072delTAAA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044685.2, RCV000113446.3,