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

rs863223535

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223535(C;C)
Make rs863223535(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127825693
GeneENG
is asnp
is mentioned by
dbSNPrs863223535
ebirs863223535
HLIrs863223535
Exacrs863223535
Varsomers863223535
Maprs863223535
PheGenIrs863223535
hapmaprs863223535
1000 genomesrs863223535
hgdprs863223535
ensemblrs863223535
gopubmedrs863223535
geneviewrs863223535
scholarrs863223535
googlers863223535
pharmgkbrs863223535
gwascentralrs863223535
openSNPrs863223535
23andMers863223535
23andMe allrs863223535
SNP Nexus

SNPshotrs863223535
SNPdbers863223535
MSV3drs863223535
GWAS Ctlgrs863223535
Max Magnitude0
ClinVar
Risk rs863223535(C;C)
Alt rs863223535(C;C)
Reference rs863223535(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ENG
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130587972A>G
CLNSRC
CLNACC RCV000200037.1,