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rs80359676

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359676(-;-)
Make rs80359676(A;A)
ReferenceGRCh38 38.1/142
Chromosome13
Position32357843
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359676
ebirs80359676
HLIrs80359676
Exacrs80359676
Varsomers80359676
Maprs80359676
PheGenIrs80359676
hapmaprs80359676
1000 genomesrs80359676
hgdprs80359676
ensemblrs80359676
gopubmedrs80359676
geneviewrs80359676
scholarrs80359676
googlers80359676
pharmgkbrs80359676
gwascentralrs80359676
openSNPrs80359676
23andMers80359676
23andMe allrs80359676
SNP Nexus

SNPshotrs80359676
SNPdbers80359676
MSV3drs80359676
GWAS Ctlgrs80359676
Max Magnitude6
rs80359676, also known as 7947insA, c.7719_7720insA and p.Leu2573_Trp2574?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359676(A;A)
Alt rs80359676(A;A)
Reference rs80359676(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32931980dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113808.1,