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rs80359673

From SNPedia

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


Make rs80359673(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357803
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359673
ebirs80359673
HLIrs80359673
Exacrs80359673
Varsomers80359673
Maprs80359673
PheGenIrs80359673
hapmaprs80359673
1000 genomesrs80359673
hgdprs80359673
ensemblrs80359673
gopubmedrs80359673
geneviewrs80359673
scholarrs80359673
googlers80359673
pharmgkbrs80359673
gwascentralrs80359673
openSNPrs80359673
23andMers80359673
23andMe allrs80359673
SNP Nexus

SNPshotrs80359673
SNPdbers80359673
MSV3drs80359673
GWAS Ctlgrs80359673
Max Magnitude6
rs80359673, also known as 7907delTT, c.7679_7680delTT and p.Phe2560Serfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359673(;)
Alt rs80359673(;)
Reference rs80359673(TT;TT)
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.32931940_32931941delTT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045281.2, RCV000077406.3,