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rs863223542

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223542(A;A)
Make rs863223542(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127818715
GeneENG
is asnp
is mentioned by
dbSNPrs863223542
ebirs863223542
HLIrs863223542
Exacrs863223542
Varsomers863223542
Maprs863223542
PheGenIrs863223542
hapmaprs863223542
1000 genomesrs863223542
hgdprs863223542
ensemblrs863223542
gopubmedrs863223542
geneviewrs863223542
scholarrs863223542
googlers863223542
pharmgkbrs863223542
gwascentralrs863223542
openSNPrs863223542
23andMers863223542
23andMe allrs863223542
SNP Nexus

SNPshotrs863223542
SNPdbers863223542
MSV3drs863223542
GWAS Ctlgrs863223542
Max Magnitude0
ClinVar
Risk rs863223542(A;A)
Alt rs863223542(A;A)
Reference rs863223542(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ENG
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130580994C>T
CLNSRC
CLNACC RCV000198224.1,