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rs80359095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359095(G;T)
Make rs80359095(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370528
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359095
ebirs80359095
HLIrs80359095
Exacrs80359095
Varsomers80359095
Maprs80359095
PheGenIrs80359095
hapmaprs80359095
1000 genomesrs80359095
hgdprs80359095
ensemblrs80359095
gopubmedrs80359095
geneviewrs80359095
scholarrs80359095
googlers80359095
pharmgkbrs80359095
gwascentralrs80359095
openSNPrs80359095
23andMers80359095
23andMe allrs80359095
SNP Nexus

SNPshotrs80359095
SNPdbers80359095
MSV3drs80359095
GWAS Ctlgrs80359095
Max Magnitude0
ClinVar
Risk rs80359095(T;T)
Alt rs80359095(T;T)
Reference rs80359095(G;G)
Significance Untested
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.32944665G>T
CLNSRC ClinVar
CLNACC RCV000045524.2, RCV000113936.1,