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rs878853658

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853658(-;-)
Make rs878853658(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position127854289
GeneENG
is asnp
is mentioned by
dbSNPrs878853658
ebirs878853658
HLIrs878853658
Exacrs878853658
Varsomers878853658
Maprs878853658
PheGenIrs878853658
hapmaprs878853658
1000 genomesrs878853658
hgdprs878853658
ensemblrs878853658
gopubmedrs878853658
geneviewrs878853658
scholarrs878853658
googlers878853658
pharmgkbrs878853658
gwascentralrs878853658
openSNPrs878853658
23andMers878853658
23andMe allrs878853658
SNP Nexus

SNPshotrs878853658
SNPdbers878853658
MSV3drs878853658
GWAS Ctlgrs878853658
Max Magnitude0
ClinVar
Risk rs878853658(;)
Alt rs878853658(;)
Reference rs878853658(A;A)
Significance Pathogenic
Disease Osler hemorrhagic telangiectasia syndrome
Variation info
Gene ENG
CLNDBN Osler hemorrhagic telangiectasia syndrome
Reversed 1
HGVS NC_000009.11:g.130616568delT
CLNSRC
CLNACC RCV000228918.1,