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rs878853295

From SNPedia

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


Make rs878853295(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43063344
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878853295
dbSNP (old)rs878853295
ClinGenrs878853295
ebirs878853295
HLIrs878853295
Exacrs878853295
Gnomadrs878853295
Varsomers878853295
Maprs878853295
PheGenIrs878853295
Biobankrs878853295
1000 genomesrs878853295
hgdprs878853295
ensemblrs878853295
gopubmedrs878853295
geneviewrs878853295
scholarrs878853295
googlers878853295
pharmgkbrs878853295
gwascentralrs878853295
openSNPrs878853295
23andMers878853295
23andMe allrs878853295
SNP Nexus

SNPshotrs878853295
SNPdbers878853295
MSV3drs878853295
GWAS Ctlgrs878853295
Max Magnitude6
ClinVar
Risk rs878853295(-;-)
Alt rs878853295(-;-)
Reference Rs878853295(AA;AA)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41215361_41215362delTT
CLNSRC
CLNACC RCV000225514.1,