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

rs80359568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359568(-;-)
Make rs80359568(A;A)
ReferenceGRCh38 38.1/142
Chromosome13
Position32340574
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359568
ebirs80359568
HLIrs80359568
Exacrs80359568
Varsomers80359568
Maprs80359568
PheGenIrs80359568
hapmaprs80359568
1000 genomesrs80359568
hgdprs80359568
ensemblrs80359568
gopubmedrs80359568
geneviewrs80359568
scholarrs80359568
googlers80359568
pharmgkbrs80359568
gwascentralrs80359568
openSNPrs80359568
23andMers80359568
23andMe allrs80359568
SNP Nexus

SNPshotrs80359568
SNPdbers80359568
MSV3drs80359568
GWAS Ctlgrs80359568
Max Magnitude6
rs80359568, also known as 6447insA, c.6219_6220insA and p.Leu2073_His2074?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359568(A;A)
Alt rs80359568(A;A)
Reference rs80359568(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914711dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113550.1,