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

rs80359385

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359385(-;-)
Make rs80359385(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position32337808
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359385
ebirs80359385
HLIrs80359385
Exacrs80359385
Varsomers80359385
Maprs80359385
PheGenIrs80359385
hapmaprs80359385
1000 genomesrs80359385
hgdprs80359385
ensemblrs80359385
gopubmedrs80359385
geneviewrs80359385
scholarrs80359385
googlers80359385
pharmgkbrs80359385
gwascentralrs80359385
openSNPrs80359385
23andMers80359385
23andMe allrs80359385
SNP Nexus

SNPshotrs80359385
SNPdbers80359385
MSV3drs80359385
GWAS Ctlgrs80359385
Max Magnitude6
rs80359385, also known as 3681insT, c.3453_3454insT and p.Ile1151_Leu1152?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359385(T;T)
Alt rs80359385(T;T)
Reference rs80359385(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911946dupT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113179.1,