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rs80359632

From SNPedia

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


Make rs80359632(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32346892
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359632
ebirs80359632
HLIrs80359632
Exacrs80359632
Varsomers80359632
Maprs80359632
PheGenIrs80359632
hapmaprs80359632
1000 genomesrs80359632
hgdprs80359632
ensemblrs80359632
gopubmedrs80359632
geneviewrs80359632
scholarrs80359632
googlers80359632
pharmgkbrs80359632
gwascentralrs80359632
openSNPrs80359632
23andMers80359632
23andMe allrs80359632
SNP Nexus

SNPshotrs80359632
SNPdbers80359632
MSV3drs80359632
GWAS Ctlgrs80359632
Max Magnitude6
rs80359632, also known as 7231del5, c.7003_7007delTTTCG and p.Phe2335_Arg2336?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359632(;)
Alt rs80359632(;)
Reference rs80359632(TTTCG;TTTCG)
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.32921029_32921033delTTTCG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045106.2, RCV000113683.1,