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rs80356883

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80356883(A;T)
Make rs80356883(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43106533
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80356883
ebirs80356883
HLIrs80356883
Exacrs80356883
Varsomers80356883
Maprs80356883
PheGenIrs80356883
hapmaprs80356883
1000 genomesrs80356883
hgdprs80356883
ensemblrs80356883
gopubmedrs80356883
geneviewrs80356883
scholarrs80356883
googlers80356883
pharmgkbrs80356883
gwascentralrs80356883
openSNPrs80356883
23andMers80356883
23andMe allrs80356883
SNP Nexus

SNPshotrs80356883
SNPdbers80356883
MSV3drs80356883
GWAS Ctlgrs80356883
Max Magnitude0
ClinVar
Risk rs80356883(T;T)
Alt rs80356883(T;T)
Reference rs80356883(A;A)
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.41258550T>A
CLNSRC ClinVar
CLNACC RCV000047439.2, RCV000111861.1,