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rs80357465

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80357465(A;G)
Make rs80357465(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071032
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357465
ebirs80357465
HLIrs80357465
Exacrs80357465
Varsomers80357465
Maprs80357465
PheGenIrs80357465
hapmaprs80357465
1000 genomesrs80357465
hgdprs80357465
ensemblrs80357465
gopubmedrs80357465
geneviewrs80357465
scholarrs80357465
googlers80357465
pharmgkbrs80357465
gwascentralrs80357465
openSNPrs80357465
23andMers80357465
23andMe allrs80357465
SNP Nexus

SNPshotrs80357465
SNPdbers80357465
MSV3drs80357465
GWAS Ctlgrs80357465
Max Magnitude0
ClinVar
Risk rs80357465(G;G)
Alt rs80357465(G;G)
Reference rs80357465(A;A)
Significance Probable-non-pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome Breast cancer not specified
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome Breast cancer not specified
Reversed 1
HGVS NC_000017.10:g.41223049T>C
CLNSRC Ambry Genetics ClinVar University of Washington
CLNACC RCV000048682.4, RCV000112414.1, RCV000130592.2, RCV000148406.1, RCV000212187.1,