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rs80357462

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80357462(C;G)
Make rs80357462(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43057083
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357462
ebirs80357462
HLIrs80357462
Exacrs80357462
Varsomers80357462
Maprs80357462
PheGenIrs80357462
hapmaprs80357462
1000 genomesrs80357462
hgdprs80357462
ensemblrs80357462
gopubmedrs80357462
geneviewrs80357462
scholarrs80357462
googlers80357462
pharmgkbrs80357462
gwascentralrs80357462
openSNPrs80357462
23andMers80357462
23andMe allrs80357462
SNP Nexus

SNPshotrs80357462
SNPdbers80357462
MSV3drs80357462
GWAS Ctlgrs80357462
Max Magnitude0
ClinVar
Risk rs80357462(G;G)
Alt rs80357462(G;G)
Reference rs80357462(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 not provided
Reversed 1
HGVS NC_000017.10:g.41209100G>C
CLNSRC ClinVar
CLNACC RCV000048881.4, RCV000112578.1, RCV000212197.1,