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rs267606639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606639(A;G)
Make rs267606639(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position99900712
GeneAGL
is asnp
is mentioned by
dbSNPrs267606639
ebirs267606639
HLIrs267606639
Exacrs267606639
Varsomers267606639
Maprs267606639
PheGenIrs267606639
hapmaprs267606639
1000 genomesrs267606639
hgdprs267606639
ensemblrs267606639
gopubmedrs267606639
geneviewrs267606639
scholarrs267606639
googlers267606639
pharmgkbrs267606639
gwascentralrs267606639
openSNPrs267606639
23andMers267606639
23andMe allrs267606639
SNP Nexus

SNPshotrs267606639
SNPdbers267606639
MSV3drs267606639
GWAS Ctlgrs267606639
Max Magnitude0
ClinVar
Risk rs267606639(G;G)
Alt rs267606639(G;G)
Reference rs267606639(A;A)
Significance Pathogenic
Disease Glycogen storage disease IIIc
Variation info
Gene AGL
CLNDBN Glycogen storage disease IIIc
Reversed 0
HGVS NC_000001.10:g.100366268A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001166.3,