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rs80357116

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80357116(A;A)
Make rs80357116(A;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43106465
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357116
ebirs80357116
HLIrs80357116
Exacrs80357116
Varsomers80357116
Maprs80357116
PheGenIrs80357116
hapmaprs80357116
1000 genomesrs80357116
hgdprs80357116
ensemblrs80357116
gopubmedrs80357116
geneviewrs80357116
scholarrs80357116
googlers80357116
pharmgkbrs80357116
gwascentralrs80357116
openSNPrs80357116
23andMers80357116
23andMe allrs80357116
SNP Nexus

SNPshotrs80357116
SNPdbers80357116
MSV3drs80357116
GWAS Ctlgrs80357116
Max Magnitude0
ClinVar
Risk rs80357116(A,G;A,G)
Alt rs80357116(A,G;A,G)
Reference rs80357116(T;T)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41258482A>C; NC_000017.10:g.41258482A>T
CLNSRC ClinVar
CLNACC RCV000047692.2, RCV000112002.1, RCV000047691.2, RCV000112001.1,