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rs771961377

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771961377(C;T)
Make rs771961377(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position99861538
GeneAGL
is asnp
is mentioned by
dbSNPrs771961377
ebirs771961377
HLIrs771961377
Exacrs771961377
Varsomers771961377
Maprs771961377
PheGenIrs771961377
hapmaprs771961377
1000 genomesrs771961377
hgdprs771961377
ensemblrs771961377
gopubmedrs771961377
geneviewrs771961377
scholarrs771961377
googlers771961377
pharmgkbrs771961377
gwascentralrs771961377
openSNPrs771961377
23andMers771961377
23andMe allrs771961377
SNP Nexus

SNPshotrs771961377
SNPdbers771961377
MSV3drs771961377
GWAS Ctlgrs771961377
Max Magnitude0
ClinVar
Risk rs771961377(T;T)
Alt rs771961377(T;T)
Reference rs771961377(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.100327094C>T
CLNSRC
CLNACC RCV000169437.1,