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

rs80359456

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359456(-;-)
Make rs80359456(A;A)
ReferenceGRCh38 38.1/142
Chromosome13
Position32338900
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359456
ebirs80359456
HLIrs80359456
Exacrs80359456
Varsomers80359456
Maprs80359456
PheGenIrs80359456
hapmaprs80359456
1000 genomesrs80359456
hgdprs80359456
ensemblrs80359456
gopubmedrs80359456
geneviewrs80359456
scholarrs80359456
googlers80359456
pharmgkbrs80359456
gwascentralrs80359456
openSNPrs80359456
23andMers80359456
23andMe allrs80359456
SNP Nexus

SNPshotrs80359456
SNPdbers80359456
MSV3drs80359456
GWAS Ctlgrs80359456
Max Magnitude6
rs80359456, also known as 4773insA, c.4545_4546insA and p.Lys1515_Ile1516?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359456(A;A)
Alt rs80359456(A;A)
Reference rs80359456(;)
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.32913038dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044435.2, RCV000113317.1,