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rs786204595

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204595(-;-)
Make rs786204595(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position99915424
GeneAGL, LOC101930120
is asnp
is mentioned by
dbSNPrs786204595
ebirs786204595
HLIrs786204595
Exacrs786204595
Varsomers786204595
Maprs786204595
PheGenIrs786204595
hapmaprs786204595
1000 genomesrs786204595
hgdprs786204595
ensemblrs786204595
gopubmedrs786204595
geneviewrs786204595
scholarrs786204595
googlers786204595
pharmgkbrs786204595
gwascentralrs786204595
openSNPrs786204595
23andMers786204595
23andMe allrs786204595
SNP Nexus

SNPshotrs786204595
SNPdbers786204595
MSV3drs786204595
GWAS Ctlgrs786204595
Max Magnitude0
ClinVar
Risk rs786204595(;)
Alt rs786204595(;)
Reference rs786204595(A;A)
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.100380980delA
CLNSRC
CLNACC RCV000169345.1,