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rs28897758

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28897758(G;G)
Make rs28897758(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394734
GeneBRCA2
is asnp
is mentioned by
dbSNPrs28897758
ebirs28897758
HLIrs28897758
Exacrs28897758
Varsomers28897758
Maprs28897758
PheGenIrs28897758
hapmaprs28897758
1000 genomesrs28897758
hgdprs28897758
ensemblrs28897758
gopubmedrs28897758
geneviewrs28897758
scholarrs28897758
googlers28897758
pharmgkbrs28897758
gwascentralrs28897758
openSNPrs28897758
23andMers28897758
23andMe allrs28897758
SNP Nexus

SNPshotrs28897758
SNPdbers28897758
MSV3drs28897758
GWAS Ctlgrs28897758
Max Magnitude0
ClinVar
Risk rs28897758(G;G)
Alt rs28897758(G;G)
Reference rs28897758(T;T)
Significance Untested
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32968871T>C; NC_000013.10:g.32968871T>G
CLNSRC ClinVar
CLNACC RCV000198262.1, RCV000031813.5, RCV000045787.3, RCV000162632.1,