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rs587776491

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776491(C;T)
Make rs587776491(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position43063873
GeneBRCA1
is asnp
is mentioned by
dbSNPrs587776491
ebirs587776491
HLIrs587776491
Exacrs587776491
Varsomers587776491
Maprs587776491
PheGenIrs587776491
hapmaprs587776491
1000 genomesrs587776491
hgdprs587776491
ensemblrs587776491
gopubmedrs587776491
geneviewrs587776491
scholarrs587776491
googlers587776491
pharmgkbrs587776491
gwascentralrs587776491
openSNPrs587776491
23andMers587776491
23andMe allrs587776491
SNP Nexus

SNPshotrs587776491
SNPdbers587776491
MSV3drs587776491
GWAS Ctlgrs587776491
Max Magnitude0
ClinVar
Risk rs587776491(T;T)
Alt rs587776491(T;T)
Reference rs587776491(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 0
HGVS NC_000017.11:g.43063873C>T
CLNSRC ClinVar
CLNACC RCV000144212.1,