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rs80359774

From SNPedia

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


Make rs80359774(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32398189
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359774
dbSNP (old)rs80359774
ClinGenrs80359774
ebirs80359774
HLIrs80359774
Exacrs80359774
Varsomers80359774
Maprs80359774
PheGenIrs80359774
Biobankrs80359774
1000 genomesrs80359774
hgdprs80359774
ensemblrs80359774
gopubmedrs80359774
geneviewrs80359774
scholarrs80359774
googlers80359774
pharmgkbrs80359774
gwascentralrs80359774
openSNPrs80359774
23andMers80359774
23andMe allrs80359774
SNP Nexus

SNPshotrs80359774
SNPdbers80359774
MSV3drs80359774
GWAS Ctlgrs80359774
Max Magnitude6
ClinVar
Risk rs80359774(-;-)
Alt rs80359774(-;-)
Reference Rs80359774(T;T)
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.32972326delT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045884.2, RCV000114152.3, RCV000482822.1,