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rs863223534

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223534(A;A)
Make rs863223534(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127826587
GeneENG
is asnp
is mentioned by
dbSNPrs863223534
ebirs863223534
HLIrs863223534
Exacrs863223534
Varsomers863223534
Maprs863223534
PheGenIrs863223534
hapmaprs863223534
1000 genomesrs863223534
hgdprs863223534
ensemblrs863223534
gopubmedrs863223534
geneviewrs863223534
scholarrs863223534
googlers863223534
pharmgkbrs863223534
gwascentralrs863223534
openSNPrs863223534
23andMers863223534
23andMe allrs863223534
SNP Nexus

SNPshotrs863223534
SNPdbers863223534
MSV3drs863223534
GWAS Ctlgrs863223534
Max Magnitude0
ClinVar
Risk rs863223534(A;A)
Alt rs863223534(A;A)
Reference rs863223534(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ENG
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130588866C>T
CLNSRC
CLNACC RCV000195747.1,