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rs786204655

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204655(-;-)
Make rs786204655(-;A)
Make rs786204655(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position99915448
GeneAGL, LOC101930120
is asnp
is mentioned by
dbSNPrs786204655
ebirs786204655
HLIrs786204655
Exacrs786204655
Varsomers786204655
Maprs786204655
PheGenIrs786204655
hapmaprs786204655
1000 genomesrs786204655
hgdprs786204655
ensemblrs786204655
gopubmedrs786204655
geneviewrs786204655
scholarrs786204655
googlers786204655
pharmgkbrs786204655
gwascentralrs786204655
openSNPrs786204655
23andMers786204655
23andMe allrs786204655
SNP Nexus

SNPshotrs786204655
SNPdbers786204655
MSV3drs786204655
GWAS Ctlgrs786204655
Max Magnitude0
ClinVar
Risk rs786204655(A;A)
Alt rs786204655(A;A)
Reference rs786204655(;)
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.100381004dupA
CLNSRC
CLNACC RCV000169447.1,