Have questions? Visit https://www.reddit.com/r/SNPedia

rs28897751

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28897751(C;C)
Make rs28897751(C;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position32370445
GeneBRCA2
is asnp
is mentioned by
dbSNPrs28897751
ebirs28897751
HLIrs28897751
Exacrs28897751
Varsomers28897751
Maprs28897751
PheGenIrs28897751
hapmaprs28897751
1000 genomesrs28897751
hgdprs28897751
ensemblrs28897751
gopubmedrs28897751
geneviewrs28897751
scholarrs28897751
googlers28897751
pharmgkbrs28897751
gwascentralrs28897751
openSNPrs28897751
23andMers28897751
23andMe allrs28897751
SNP Nexus

SNPshotrs28897751
SNPdbers28897751
MSV3drs28897751
GWAS Ctlgrs28897751
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs28897751(C;C)
Alt rs28897751(C;C)
Reference rs28897751(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.32944582T>C
CLNSRC ClinVar
CLNACC RCV000045498.2, RCV000113921.1,