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rs80359800

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80359800(C;C)
Make rs80359800(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363194
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359800
ebirs80359800
HLIrs80359800
Exacrs80359800
Varsomers80359800
Maprs80359800
PheGenIrs80359800
hapmaprs80359800
1000 genomesrs80359800
hgdprs80359800
ensemblrs80359800
gopubmedrs80359800
geneviewrs80359800
scholarrs80359800
googlers80359800
pharmgkbrs80359800
gwascentralrs80359800
openSNPrs80359800
23andMers80359800
23andMe allrs80359800
SNP Nexus

SNPshotrs80359800
SNPdbers80359800
MSV3drs80359800
GWAS Ctlgrs80359800
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs80359800(A,C,G;A,C,G)
Alt rs80359800(A,C,G;A,C,G)
Reference rs80359800(T;T)
Significance Probable-non-pathogenic
Disease not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32937331T>A; NC_000013.10:g.32937331T>C; NC_000013.10:g.32937331T>G
CLNSRC ClinVar
CLNACC RCV000045376.5, RCV000163206.1, RCV000195381.3, RCV000045377.2, RCV000113852.1, RCV000160146.2,