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rs878854950

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854950(A;G)
Make rs878854950(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43082577
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878854950
ebirs878854950
HLIrs878854950
Exacrs878854950
Varsomers878854950
Maprs878854950
PheGenIrs878854950
hapmaprs878854950
1000 genomesrs878854950
hgdprs878854950
ensemblrs878854950
gopubmedrs878854950
geneviewrs878854950
scholarrs878854950
googlers878854950
pharmgkbrs878854950
gwascentralrs878854950
openSNPrs878854950
23andMers878854950
23andMe allrs878854950
SNP Nexus

SNPshotrs878854950
SNPdbers878854950
MSV3drs878854950
GWAS Ctlgrs878854950
Max Magnitude0
ClinVar
Risk rs878854950(G;G)
Alt rs878854950(G;G)
Reference rs878854950(A;A)
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.41234594T>C
CLNSRC
CLNACC RCV000231953.1,