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rs878853659

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853659(A;A)
Make rs878853659(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position127843246
GeneENG
is asnp
is mentioned by
dbSNPrs878853659
ebirs878853659
HLIrs878853659
Exacrs878853659
Varsomers878853659
Maprs878853659
PheGenIrs878853659
hapmaprs878853659
1000 genomesrs878853659
hgdprs878853659
ensemblrs878853659
gopubmedrs878853659
geneviewrs878853659
scholarrs878853659
googlers878853659
pharmgkbrs878853659
gwascentralrs878853659
openSNPrs878853659
23andMers878853659
23andMe allrs878853659
SNP Nexus

SNPshotrs878853659
SNPdbers878853659
MSV3drs878853659
GWAS Ctlgrs878853659
Max Magnitude0
ClinVar
Risk rs878853659(A;A)
Alt rs878853659(A;A)
Reference rs878853659(G;G)
Significance Pathogenic
Disease Osler hemorrhagic telangiectasia syndrome
Variation info
Gene ENG
CLNDBN Osler hemorrhagic telangiectasia syndrome
Reversed 1
HGVS NC_000009.11:g.130605525C>T
CLNSRC
CLNACC RCV000232191.1,