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rs776977863

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776977863(A;A)
Make rs776977863(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position99900717
GeneAGL
is asnp
is mentioned by
dbSNPrs776977863
ebirs776977863
HLIrs776977863
Exacrs776977863
Varsomers776977863
Maprs776977863
PheGenIrs776977863
hapmaprs776977863
1000 genomesrs776977863
hgdprs776977863
ensemblrs776977863
gopubmedrs776977863
geneviewrs776977863
scholarrs776977863
googlers776977863
pharmgkbrs776977863
gwascentralrs776977863
openSNPrs776977863
23andMers776977863
23andMe allrs776977863
SNP Nexus

SNPshotrs776977863
SNPdbers776977863
MSV3drs776977863
GWAS Ctlgrs776977863
Max Magnitude0
ClinVar
Risk rs776977863(A,G;A,G)
Alt rs776977863(A,G;A,G)
Reference rs776977863(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.100366273C>G
CLNSRC
CLNACC RCV000169313.1,