Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057517243

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517243(-;-)
Make rs1057517243(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99861696
GeneAGL
is asnp
is mentioned by
dbSNPrs1057517243
dbSNP (old)rs1057517243
ClinGenrs1057517243
ebirs1057517243
HLIrs1057517243
Exacrs1057517243
Gnomadrs1057517243
Varsomers1057517243
Maprs1057517243
PheGenIrs1057517243
Biobankrs1057517243
1000 genomesrs1057517243
hgdprs1057517243
ensemblrs1057517243
gopubmedrs1057517243
geneviewrs1057517243
scholarrs1057517243
googlers1057517243
pharmgkbrs1057517243
gwascentralrs1057517243
openSNPrs1057517243
23andMers1057517243
23andMe allrs1057517243
SNPshotrs1057517243
SNPdbers1057517243
MSV3drs1057517243
GWAS Ctlgrs1057517243
Max Magnitude0
ClinVar
Risk rs1057517243(-;-)
Alt rs1057517243(-;-)
Reference Rs1057517243(G;G)
Significance Pathogenic
Disease Glycogen storage disease type III
Variation info
Gene AGL
CLNDBN Glycogen storage disease type III
Reversed 0
HGVS NC_000001.10:g.100327252delG
CLNSRC
CLNACC RCV000409554.1,