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rs80358622

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358622(G;T)
Make rs80358622(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32316497
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358622
ebirs80358622
HLIrs80358622
Exacrs80358622
Varsomers80358622
Maprs80358622
PheGenIrs80358622
hapmaprs80358622
1000 genomesrs80358622
hgdprs80358622
ensemblrs80358622
gopubmedrs80358622
geneviewrs80358622
scholarrs80358622
googlers80358622
pharmgkbrs80358622
gwascentralrs80358622
openSNPrs80358622
23andMers80358622
23andMe allrs80358622
SNP Nexus

SNPshotrs80358622
SNPdbers80358622
MSV3drs80358622
GWAS Ctlgrs80358622
Max Magnitude0
ClinVar
Risk rs80358622(T;T)
Alt rs80358622(T;T)
Reference rs80358622(G;G)
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.32890634G>T
CLNSRC ClinVar
CLNACC RCV000044268.2, RCV000113040.1,