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rs786204481

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204481(A;A)
Make rs786204481(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position99884119
GeneAGL
is asnp
is mentioned by
dbSNPrs786204481
ebirs786204481
HLIrs786204481
Exacrs786204481
Varsomers786204481
Maprs786204481
PheGenIrs786204481
hapmaprs786204481
1000 genomesrs786204481
hgdprs786204481
ensemblrs786204481
gopubmedrs786204481
geneviewrs786204481
scholarrs786204481
googlers786204481
pharmgkbrs786204481
gwascentralrs786204481
openSNPrs786204481
23andMers786204481
23andMe allrs786204481
SNP Nexus

SNPshotrs786204481
SNPdbers786204481
MSV3drs786204481
GWAS Ctlgrs786204481
Max Magnitude0
ClinVar
Risk rs786204481(A;A)
Alt rs786204481(A;A)
Reference rs786204481(G;G)
Significance Probable-Pathogenic
Disease Glycogen storage disease type III
Variation info
Gene AGL
CLNDBN Glycogen storage disease type III
Reversed 0
HGVS NC_000001.10:g.100349675G>A
CLNSRC
CLNACC RCV000169136.1,