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rs118203964

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118203964(C;C)
Make rs118203964(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position99916492
GeneAGL, LOC101930120
is asnp
is mentioned by
dbSNPrs118203964
ebirs118203964
HLIrs118203964
Exacrs118203964
Varsomers118203964
Maprs118203964
PheGenIrs118203964
hapmaprs118203964
1000 genomesrs118203964
hgdprs118203964
ensemblrs118203964
gopubmedrs118203964
geneviewrs118203964
scholarrs118203964
googlers118203964
pharmgkbrs118203964
gwascentralrs118203964
openSNPrs118203964
23andMers118203964
23andMe allrs118203964
SNP Nexus

SNPshotrs118203964
SNPdbers118203964
MSV3drs118203964
GWAS Ctlgrs118203964
Max Magnitude0
OMIM610860
Desc
Variant0009
Relatedalso
ClinVar
Risk rs118203964(C;C)
Alt rs118203964(C;C)
Reference rs118203964(G;G)
Significance Pathogenic
Disease Glycogen storage disease IIIa
Variation info
Gene AGL
CLNDBN Glycogen storage disease IIIa
Reversed 0
HGVS NC_000001.10:g.100382048G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001161.3,