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rs80357216

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80357216(C;C)
Make rs80357216(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43047684
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357216
ebirs80357216
HLIrs80357216
Exacrs80357216
Varsomers80357216
Maprs80357216
PheGenIrs80357216
hapmaprs80357216
1000 genomesrs80357216
hgdprs80357216
ensemblrs80357216
gopubmedrs80357216
geneviewrs80357216
scholarrs80357216
googlers80357216
pharmgkbrs80357216
gwascentralrs80357216
openSNPrs80357216
23andMers80357216
23andMe allrs80357216
SNP Nexus

SNPshotrs80357216
SNPdbers80357216
MSV3drs80357216
GWAS Ctlgrs80357216
Max Magnitude0
ClinVar
Risk rs80357216(C;C)
Alt rs80357216(C;C)
Reference rs80357216(T;T)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41199701A>G
CLNSRC ClinVar
CLNACC RCV000048990.2, RCV000112653.1,