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

rs878854934

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854934(-;-)
Make rs878854934(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093732
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878854934
ebirs878854934
HLIrs878854934
Exacrs878854934
Varsomers878854934
Maprs878854934
PheGenIrs878854934
hapmaprs878854934
1000 genomesrs878854934
hgdprs878854934
ensemblrs878854934
gopubmedrs878854934
geneviewrs878854934
scholarrs878854934
googlers878854934
pharmgkbrs878854934
gwascentralrs878854934
openSNPrs878854934
23andMers878854934
23andMe allrs878854934
SNP Nexus

SNPshotrs878854934
SNPdbers878854934
MSV3drs878854934
GWAS Ctlgrs878854934
Max Magnitude0
ClinVar
Risk rs878854934(;)
Alt rs878854934(;)
Reference rs878854934(T;T)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41245749delA
CLNSRC
CLNACC RCV000231278.1,