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rs80357202

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80357202(A;A)
Make rs80357202(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091477
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357202
ebirs80357202
HLIrs80357202
Exacrs80357202
Varsomers80357202
Maprs80357202
PheGenIrs80357202
hapmaprs80357202
1000 genomesrs80357202
hgdprs80357202
ensemblrs80357202
gopubmedrs80357202
geneviewrs80357202
scholarrs80357202
googlers80357202
pharmgkbrs80357202
gwascentralrs80357202
openSNPrs80357202
23andMers80357202
23andMe allrs80357202
SNP Nexus

SNPshotrs80357202
SNPdbers80357202
MSV3drs80357202
GWAS Ctlgrs80357202
Max Magnitude0
ClinVar
Risk rs80357202(A,T;A,T)
Alt rs80357202(A,T;A,T)
Reference rs80357202(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41243494C>A; NC_000017.10:g.41243494C>T
CLNSRC ClinVar Ambry Genetics
CLNACC RCV000077137.2, RCV000048426.2, RCV000112235.1, RCV000132305.2,