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rs863223536

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223536(A;T)
Make rs863223536(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127818832
GeneENG
is asnp
is mentioned by
dbSNPrs863223536
ebirs863223536
HLIrs863223536
Exacrs863223536
Varsomers863223536
Maprs863223536
PheGenIrs863223536
hapmaprs863223536
1000 genomesrs863223536
hgdprs863223536
ensemblrs863223536
gopubmedrs863223536
geneviewrs863223536
scholarrs863223536
googlers863223536
pharmgkbrs863223536
gwascentralrs863223536
openSNPrs863223536
23andMers863223536
23andMe allrs863223536
SNP Nexus

SNPshotrs863223536
SNPdbers863223536
MSV3drs863223536
GWAS Ctlgrs863223536
Max Magnitude0
ClinVar
Risk rs863223536(T;T)
Alt rs863223536(T;T)
Reference rs863223536(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ENG
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130581111T>A
CLNSRC
CLNACC RCV000198335.1,