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rs878854935

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878854935(-;-)
Make rs878854935(-;T)
Make rs878854935(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093607
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878854935
ebirs878854935
HLIrs878854935
Exacrs878854935
Varsomers878854935
Maprs878854935
PheGenIrs878854935
hapmaprs878854935
1000 genomesrs878854935
hgdprs878854935
ensemblrs878854935
gopubmedrs878854935
geneviewrs878854935
scholarrs878854935
googlers878854935
pharmgkbrs878854935
gwascentralrs878854935
openSNPrs878854935
23andMers878854935
23andMe allrs878854935
SNP Nexus

SNPshotrs878854935
SNPdbers878854935
MSV3drs878854935
GWAS Ctlgrs878854935
Max Magnitude0
ClinVar
Risk rs878854935(T;T)
Alt rs878854935(T;T)
Reference rs878854935(;)
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.41245625dupA
CLNSRC
CLNACC RCV000234131.1,