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rs80358818

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358818(A;A)
Make rs80358818(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326569
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358818
ebirs80358818
HLIrs80358818
Exacrs80358818
Varsomers80358818
Maprs80358818
PheGenIrs80358818
hapmaprs80358818
1000 genomesrs80358818
hgdprs80358818
ensemblrs80358818
gopubmedrs80358818
geneviewrs80358818
scholarrs80358818
googlers80358818
pharmgkbrs80358818
gwascentralrs80358818
openSNPrs80358818
23andMers80358818
23andMe allrs80358818
SNP Nexus

SNPshotrs80358818
SNPdbers80358818
MSV3drs80358818
GWAS Ctlgrs80358818
Max Magnitude0
ClinVar
Risk rs80358818(A,T;A,T)
Alt rs80358818(A,T;A,T)
Reference rs80358818(G;G)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32900706G>A; NC_000013.10:g.32900706G>T
CLNSRC ClinVar
CLNACC RCV000044782.2, RCV000077365.3, RCV000044783.2, RCV000113840.1, RCV000166163.1,