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

rs878853285

From SNPedia

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


Make rs878853285(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43051119
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878853285
dbSNP (old)rs878853285
ClinGenrs878853285
ebirs878853285
HLIrs878853285
Exacrs878853285
Gnomadrs878853285
Varsomers878853285
Maprs878853285
PheGenIrs878853285
Biobankrs878853285
1000 genomesrs878853285
hgdprs878853285
ensemblrs878853285
gopubmedrs878853285
geneviewrs878853285
scholarrs878853285
googlers878853285
pharmgkbrs878853285
gwascentralrs878853285
openSNPrs878853285
23andMers878853285
23andMe allrs878853285
SNP Nexus

SNPshotrs878853285
SNPdbers878853285
MSV3drs878853285
GWAS Ctlgrs878853285
Max Magnitude6
ClinVar
Risk rs878853285(-;-)
Alt rs878853285(-;-)
Reference Rs878853285(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41203136delT
CLNSRC
CLNACC RCV000225450.2,