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rs369973784

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs369973784(A;G)
Make rs369973784(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position99916398
GeneAGL, LOC101930120
is asnp
is mentioned by
dbSNPrs369973784
ebirs369973784
HLIrs369973784
Exacrs369973784
Varsomers369973784
Maprs369973784
PheGenIrs369973784
hapmaprs369973784
1000 genomesrs369973784
hgdprs369973784
ensemblrs369973784
gopubmedrs369973784
geneviewrs369973784
scholarrs369973784
googlers369973784
pharmgkbrs369973784
gwascentralrs369973784
openSNPrs369973784
23andMers369973784
23andMe allrs369973784
SNP Nexus

SNPshotrs369973784
SNPdbers369973784
MSV3drs369973784
GWAS Ctlgrs369973784
Max Magnitude0
ClinVar
Risk rs369973784(G;G)
Alt rs369973784(G;G)
Reference rs369973784(A;A)
Significance Other
Disease Glycogen storage disease IIIb Glycogen storage disease IIIa Glycogen storage disease type III
Variation info
Gene AGL
CLNDBN Glycogen storage disease IIIb Glycogen storage disease IIIa Glycogen storage disease type III
Reversed 0
HGVS NC_000001.10:g.100381954A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001157.3, RCV000001158.3, RCV000020379.4,