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rs80359644

From SNPedia

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


Make rs80359644(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355107
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359644
ebirs80359644
HLIrs80359644
Exacrs80359644
Varsomers80359644
Maprs80359644
PheGenIrs80359644
hapmaprs80359644
1000 genomesrs80359644
hgdprs80359644
ensemblrs80359644
gopubmedrs80359644
geneviewrs80359644
scholarrs80359644
googlers80359644
pharmgkbrs80359644
gwascentralrs80359644
openSNPrs80359644
23andMers80359644
23andMe allrs80359644
SNP Nexus

SNPshotrs80359644
SNPdbers80359644
MSV3drs80359644
GWAS Ctlgrs80359644
Max Magnitude6
rs80359644, also known as 7482delAG, c.7254_7255delAG and p.Arg2418_Val2419SerTerfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359644(;)
Alt rs80359644(;)
Reference rs80359644(AG;AG)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32929244_32929245delAG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045177.2, RCV000113741.1, RCV000220840.1,