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

rs267606640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606640(A;A)
Make rs267606640(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position99913557
GeneAGL
is asnp
is mentioned by
dbSNPrs267606640
ebirs267606640
HLIrs267606640
Exacrs267606640
Varsomers267606640
Maprs267606640
PheGenIrs267606640
hapmaprs267606640
1000 genomesrs267606640
hgdprs267606640
ensemblrs267606640
gopubmedrs267606640
geneviewrs267606640
scholarrs267606640
googlers267606640
pharmgkbrs267606640
gwascentralrs267606640
openSNPrs267606640
23andMers267606640
23andMe allrs267606640
SNP Nexus

SNPshotrs267606640
SNPdbers267606640
MSV3drs267606640
GWAS Ctlgrs267606640
Max Magnitude0
ClinVar
Risk rs267606640(A;A)
Alt rs267606640(A;A)
Reference rs267606640(G;G)
Significance Pathogenic
Disease Glycogen storage disease IIIa
Variation info
Gene AGL
CLNDBN Glycogen storage disease IIIa
Reversed 0
HGVS NC_000001.10:g.100379113G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001167.3,