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rs80357474

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80357474(C;C)
Make rs80357474(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049188
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357474
ebirs80357474
HLIrs80357474
Exacrs80357474
Varsomers80357474
Maprs80357474
PheGenIrs80357474
hapmaprs80357474
1000 genomesrs80357474
hgdprs80357474
ensemblrs80357474
gopubmedrs80357474
geneviewrs80357474
scholarrs80357474
googlers80357474
pharmgkbrs80357474
gwascentralrs80357474
openSNPrs80357474
23andMers80357474
23andMe allrs80357474
SNP Nexus

SNPshotrs80357474
SNPdbers80357474
MSV3drs80357474
GWAS Ctlgrs80357474
Max Magnitude0
ClinVar
Risk rs80357474(C,G;C,G)
Alt rs80357474(C,G;C,G)
Reference rs80357474(T;T)
Significance Untested
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000017.10:g.41201205A>C; NC_000017.10:g.41201205A>G
CLNSRC ClinVar Ambry Genetics
CLNACC RCV000083070.2, RCV000048948.3, RCV000112624.1, RCV000132201.2, RCV000236823.1,