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rs80359262

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359262(-;-)
Make rs80359262(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position32319115
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359262
ebirs80359262
HLIrs80359262
Exacrs80359262
Varsomers80359262
Maprs80359262
PheGenIrs80359262
hapmaprs80359262
1000 genomesrs80359262
hgdprs80359262
ensemblrs80359262
gopubmedrs80359262
geneviewrs80359262
scholarrs80359262
googlers80359262
pharmgkbrs80359262
gwascentralrs80359262
openSNPrs80359262
23andMers80359262
23andMe allrs80359262
SNP Nexus

SNPshotrs80359262
SNPdbers80359262
MSV3drs80359262
GWAS Ctlgrs80359262
Max Magnitude6
rs80359262, also known as 334insT, c.106_107insT and p.Ser36?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359262(T;T)
Alt rs80359262(T;T)
Reference rs80359262(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32893252dupT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113135.1,