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rs80357043

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80357043(C;T)
Make rs80357043(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43067628
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357043
ebirs80357043
HLIrs80357043
Exacrs80357043
Varsomers80357043
Maprs80357043
PheGenIrs80357043
hapmaprs80357043
1000 genomesrs80357043
hgdprs80357043
ensemblrs80357043
gopubmedrs80357043
geneviewrs80357043
scholarrs80357043
googlers80357043
pharmgkbrs80357043
gwascentralrs80357043
openSNPrs80357043
23andMers80357043
23andMe allrs80357043
SNP Nexus

SNPshotrs80357043
SNPdbers80357043
MSV3drs80357043
GWAS Ctlgrs80357043
Max Magnitude0
ClinVar
Risk rs80357043(T;T)
Alt rs80357043(T;T)
Reference rs80357043(C;C)
Significance Pathogenic
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.41219645G>A
CLNSRC Database of BRCA1 and BRCA2 sequence variants that have been clinically reclassified by a quantitative integrated evaluation
CLNACC RCV000048750.2, RCV000112476.2,