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rs781580050

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs781580050(C;T)
Make rs781580050(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position99861520
GeneAGL
is asnp
is mentioned by
dbSNPrs781580050
ebirs781580050
HLIrs781580050
Exacrs781580050
Varsomers781580050
Maprs781580050
PheGenIrs781580050
hapmaprs781580050
1000 genomesrs781580050
hgdprs781580050
ensemblrs781580050
gopubmedrs781580050
geneviewrs781580050
scholarrs781580050
googlers781580050
pharmgkbrs781580050
gwascentralrs781580050
openSNPrs781580050
23andMers781580050
23andMe allrs781580050
SNP Nexus

SNPshotrs781580050
SNPdbers781580050
MSV3drs781580050
GWAS Ctlgrs781580050
Max Magnitude0
ClinVar
Risk rs781580050(T;T)
Alt rs781580050(T;T)
Reference rs781580050(C;C)
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.100327076C>T
CLNSRC
CLNACC RCV000169056.1,