Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204678

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204678(-;-)
Make rs786204678(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position99876558
GeneAGL
is asnp
is mentioned by
dbSNPrs786204678
ebirs786204678
HLIrs786204678
Exacrs786204678
Varsomers786204678
Maprs786204678
PheGenIrs786204678
hapmaprs786204678
1000 genomesrs786204678
hgdprs786204678
ensemblrs786204678
gopubmedrs786204678
geneviewrs786204678
scholarrs786204678
googlers786204678
pharmgkbrs786204678
gwascentralrs786204678
openSNPrs786204678
23andMers786204678
23andMe allrs786204678
SNP Nexus

SNPshotrs786204678
SNPdbers786204678
MSV3drs786204678
GWAS Ctlgrs786204678
Max Magnitude0
ClinVar
Risk rs786204678(;)
Alt rs786204678(;)
Reference rs786204678(G;G)
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.100342114delG
CLNSRC
CLNACC RCV000169486.1,