Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223537

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223537(C;T)
Make rs863223537(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127825822
GeneENG
is asnp
is mentioned by
dbSNPrs863223537
ebirs863223537
HLIrs863223537
Exacrs863223537
Varsomers863223537
Maprs863223537
PheGenIrs863223537
hapmaprs863223537
1000 genomesrs863223537
hgdprs863223537
ensemblrs863223537
gopubmedrs863223537
geneviewrs863223537
scholarrs863223537
googlers863223537
pharmgkbrs863223537
gwascentralrs863223537
openSNPrs863223537
23andMers863223537
23andMe allrs863223537
SNP Nexus

SNPshotrs863223537
SNPdbers863223537
MSV3drs863223537
GWAS Ctlgrs863223537
Max Magnitude0
ClinVar
Risk rs863223537(T;T)
Alt rs863223537(T;T)
Reference rs863223537(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ENG
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130588101G>A
CLNSRC
CLNACC RCV000199857.1,