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rs80357061

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;T) 6 BRCA1 variant reported to be pathogenic for breast cancer
(T;T) 0 Normal


Make rs80357061(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43067616
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357061
dbSNP (classic)rs80357061
ClinGenrs80357061
ebirs80357061
HLIrs80357061
Exacrs80357061
Gnomadrs80357061
Varsomers80357061
LitVarrs80357061
Maprs80357061
PheGenIrs80357061
Biobankrs80357061
1000 genomesrs80357061
hgdprs80357061
ensemblrs80357061
geneviewrs80357061
scholarrs80357061
googlers80357061
pharmgkbrs80357061
gwascentralrs80357061
openSNPrs80357061
23andMers80357061
SNPshotrs80357061
SNPdbers80357061
MSV3drs80357061
GWAS Ctlgrs80357061
Max Magnitude6

aka c.5066T>G (p.Met1689Arg)


ClinVar
Risk rs80357061(C;C) rs80357061(G;G)
Alt rs80357061(C;C) rs80357061(G;G)
Reference Rs80357061(T;T)
Significance Other
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41219633A>C; NC_000017.10:g.41219633A>G
CLNSRC UniProtKB (protein)
CLNACC RCV000031206.5, RCV000048755.3, RCV000163023.2, RCV000048754.2, RCV000112480.1,