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rs28897746

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28897746(C;C)
Make rs28897746(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363259
GeneBRCA2
is asnp
is mentioned by
dbSNPrs28897746
ebirs28897746
HLIrs28897746
Exacrs28897746
Varsomers28897746
Maprs28897746
PheGenIrs28897746
hapmaprs28897746
1000 genomesrs28897746
hgdprs28897746
ensemblrs28897746
gopubmedrs28897746
geneviewrs28897746
scholarrs28897746
googlers28897746
pharmgkbrs28897746
gwascentralrs28897746
openSNPrs28897746
23andMers28897746
23andMe allrs28897746
SNP Nexus

SNPshotrs28897746
SNPdbers28897746
MSV3drs28897746
GWAS Ctlgrs28897746
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs28897746(C;C)
Alt rs28897746(C;C)
Reference rs28897746(T;T)
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.32937396T>C
CLNSRC ClinVar
CLNACC RCV000045405.2, RCV000113861.1,