Have questions? Visit https://www.reddit.com/r/SNPedia

rs80357132

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80357132(C;C)
Make rs80357132(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063888
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357132
ebirs80357132
HLIrs80357132
Exacrs80357132
Varsomers80357132
Maprs80357132
PheGenIrs80357132
hapmaprs80357132
1000 genomesrs80357132
hgdprs80357132
ensemblrs80357132
gopubmedrs80357132
geneviewrs80357132
scholarrs80357132
googlers80357132
pharmgkbrs80357132
gwascentralrs80357132
openSNPrs80357132
23andMers80357132
23andMe allrs80357132
SNP Nexus

SNPshotrs80357132
SNPdbers80357132
MSV3drs80357132
GWAS Ctlgrs80357132
Max Magnitude0
ClinVar
Risk rs80357132(C;C)
Alt rs80357132(C;C)
Reference rs80357132(T;T)
Significance Probable-Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41215905A>G
CLNSRC ClinVar
CLNACC RCV000048808.3, RCV000112502.1,