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rs878853293

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;T) 6 BRCA1 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs878853293(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43074436
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878853293
dbSNP (old)rs878853293
ClinGenrs878853293
ebirs878853293
HLIrs878853293
Exacrs878853293
Gnomadrs878853293
Varsomers878853293
Maprs878853293
PheGenIrs878853293
Biobankrs878853293
1000 genomesrs878853293
hgdprs878853293
ensemblrs878853293
gopubmedrs878853293
geneviewrs878853293
scholarrs878853293
googlers878853293
pharmgkbrs878853293
gwascentralrs878853293
openSNPrs878853293
23andMers878853293
23andMe allrs878853293
SNP Nexus

SNPshotrs878853293
SNPdbers878853293
MSV3drs878853293
GWAS Ctlgrs878853293
Max Magnitude6
ClinVar
Risk rs878853293(-;-)
Alt rs878853293(-;-)
Reference Rs878853293(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41226453delA
CLNSRC
CLNACC RCV000225462.2,