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

rs80359278

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
(A;A) 0 common in clinvar


Make rs80359278(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332785
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359278
ebirs80359278
HLIrs80359278
Exacrs80359278
Varsomers80359278
Maprs80359278
PheGenIrs80359278
hapmaprs80359278
1000 genomesrs80359278
hgdprs80359278
ensemblrs80359278
gopubmedrs80359278
geneviewrs80359278
scholarrs80359278
googlers80359278
pharmgkbrs80359278
gwascentralrs80359278
openSNPrs80359278
23andMers80359278
23andMe allrs80359278
SNP Nexus

SNPshotrs80359278
SNPdbers80359278
MSV3drs80359278
GWAS Ctlgrs80359278
Max Magnitude6
rs80359278, also known as 1535delA, c.1307_1307delA and p.Lys436Argfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359278(;)
Alt rs80359278(;)
Reference rs80359278(A;A)
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.32906922delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000043777.2, RCV000112905.1,