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rs878853657

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853657(C;C)
Make rs878853657(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position127826586
GeneENG
is asnp
is mentioned by
dbSNPrs878853657
ebirs878853657
HLIrs878853657
Exacrs878853657
Varsomers878853657
Maprs878853657
PheGenIrs878853657
hapmaprs878853657
1000 genomesrs878853657
hgdprs878853657
ensemblrs878853657
gopubmedrs878853657
geneviewrs878853657
scholarrs878853657
googlers878853657
pharmgkbrs878853657
gwascentralrs878853657
openSNPrs878853657
23andMers878853657
23andMe allrs878853657
SNP Nexus

SNPshotrs878853657
SNPdbers878853657
MSV3drs878853657
GWAS Ctlgrs878853657
Max Magnitude0
ClinVar
Risk rs878853657(C;C)
Alt rs878853657(C;C)
Reference rs878853657(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.130588865C>G
CLNSRC
CLNACC RCV000231233.1,