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rs80357003

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80357003(C;T)
Make rs80357003(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092940
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357003
ebirs80357003
HLIrs80357003
Exacrs80357003
Varsomers80357003
Maprs80357003
PheGenIrs80357003
hapmaprs80357003
1000 genomesrs80357003
hgdprs80357003
ensemblrs80357003
gopubmedrs80357003
geneviewrs80357003
scholarrs80357003
googlers80357003
pharmgkbrs80357003
gwascentralrs80357003
openSNPrs80357003
23andMers80357003
23andMe allrs80357003
SNP Nexus

SNPshotrs80357003
SNPdbers80357003
MSV3drs80357003
GWAS Ctlgrs80357003
Max Magnitude0
ClinVar
Risk rs80357003(G,T;G,T)
Alt rs80357003(G,T;G,T)
Reference rs80357003(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41244957G>A; NC_000017.10:g.41244957G>C
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000047890.2, RCV000111898.1, RCV000132326.2, RCV000047889.2, RCV000132313.2,