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

rs80359681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359681(-;-)
Make rs80359681(A;A)
ReferenceGRCh38 38.1/142
Chromosome13
Position32357915
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359681
ebirs80359681
HLIrs80359681
Exacrs80359681
Varsomers80359681
Maprs80359681
PheGenIrs80359681
hapmaprs80359681
1000 genomesrs80359681
hgdprs80359681
ensemblrs80359681
gopubmedrs80359681
geneviewrs80359681
scholarrs80359681
googlers80359681
pharmgkbrs80359681
gwascentralrs80359681
openSNPrs80359681
23andMers80359681
23andMe allrs80359681
SNP Nexus

SNPshotrs80359681
SNPdbers80359681
MSV3drs80359681
GWAS Ctlgrs80359681
Max Magnitude6
rs80359681, also known as 8019insA, c.7791_7792insA and p.Lys2597_Glu2598?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359681(A;A)
Alt rs80359681(A;A)
Reference rs80359681(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32932052dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113818.1,