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rs878854933

From SNPedia

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


Make rs878854933(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093929
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878854933
dbSNP (old)rs878854933
ClinGenrs878854933
ebirs878854933
HLIrs878854933
Exacrs878854933
Gnomadrs878854933
Varsomers878854933
Maprs878854933
PheGenIrs878854933
Biobankrs878854933
1000 genomesrs878854933
hgdprs878854933
ensemblrs878854933
gopubmedrs878854933
geneviewrs878854933
scholarrs878854933
googlers878854933
pharmgkbrs878854933
gwascentralrs878854933
openSNPrs878854933
23andMers878854933
23andMe allrs878854933
SNP Nexus

SNPshotrs878854933
SNPdbers878854933
MSV3drs878854933
GWAS Ctlgrs878854933
Max Magnitude6
ClinVar
Risk rs878854933(-;-)
Alt rs878854933(-;-)
Reference Rs878854933(AG;AG)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not provided
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 not provided
Reversed 1
HGVS NC_000017.10:g.41245946_41245947delCT
CLNSRC
CLNACC RCV000227100.1, RCV000256582.2, RCV000482387.1,