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rs28897698

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs28897698(G;T)
Make rs28897698(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43047685
GeneBRCA1
is asnp
is mentioned by
dbSNPrs28897698
ebirs28897698
HLIrs28897698
Exacrs28897698
Varsomers28897698
Maprs28897698
PheGenIrs28897698
hapmaprs28897698
1000 genomesrs28897698
hgdprs28897698
ensemblrs28897698
gopubmedrs28897698
geneviewrs28897698
scholarrs28897698
googlers28897698
pharmgkbrs28897698
gwascentralrs28897698
openSNPrs28897698
23andMers28897698
23andMe allrs28897698
SNP Nexus

SNPshotrs28897698
SNPdbers28897698
MSV3drs28897698
GWAS Ctlgrs28897698
Max Magnitude0
ClinVar
Risk rs28897698(T;T)
Alt rs28897698(T;T)
Reference rs28897698(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 not provided Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41199702C>A; NC_000017.10:g.41199702C>T
CLNSRC ClinVar
CLNACC RCV000048988.2, RCV000112651.1, RCV000235944.1, RCV000230445.1,