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rs121964980

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964980(A;A)
Make rs121964980(A;G)
ReferenceGRCh37 37.1/132
Chromosome9
Position6554768
GeneGLDC
is asnp
is mentioned by
dbSNPrs121964980
ebirs121964980
HLIrs121964980
Exacrs121964980
Varsomers121964980
Maprs121964980
PheGenIrs121964980
hapmaprs121964980
1000 genomesrs121964980
hgdprs121964980
ensemblrs121964980
gopubmedrs121964980
geneviewrs121964980
scholarrs121964980
googlers121964980
pharmgkbrs121964980
gwascentralrs121964980
openSNPrs121964980
23andMers121964980
23andMe allrs121964980
SNP Nexus

SNPshotrs121964980
SNPdbers121964980
MSV3drs121964980
GWAS Ctlgrs121964980
Max Magnitude0
OMIM238300
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121964980(A;A)
Alt rs121964980(A;A)
Reference rs121964980(G;G)
Significance Pathogenic
Disease Non-ketotic hyperglycinemia
Variation info
Gene GLDC
CLNDBN Non-ketotic hyperglycinemia
Reversed 1
HGVS NC_000009.11:g.6554768C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012770.24,