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rs80359737

From SNPedia

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


Make rs80359737(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379776
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359737
ebirs80359737
HLIrs80359737
Exacrs80359737
Varsomers80359737
Maprs80359737
PheGenIrs80359737
hapmaprs80359737
1000 genomesrs80359737
hgdprs80359737
ensemblrs80359737
gopubmedrs80359737
geneviewrs80359737
scholarrs80359737
googlers80359737
pharmgkbrs80359737
gwascentralrs80359737
openSNPrs80359737
23andMers80359737
23andMe allrs80359737
SNP Nexus

SNPshotrs80359737
SNPdbers80359737
MSV3drs80359737
GWAS Ctlgrs80359737
Max Magnitude6
rs80359737, also known as 9208del4, c.8980_8983delTCAG and p.Ser2994_Asp2995?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359737(;)
Alt rs80359737(;)
Reference rs80359737(TCAG;TCAG)
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.32953913_32953916delTCAG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045680.2, RCV000114027.1,