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rs121964977

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121964977(C;T)
Make rs121964977(T;T)
ReferenceGRCh37 37.1/132
Chromosome9
Position6553420
GeneGLDC
is asnp
is mentioned by
dbSNPrs121964977
ebirs121964977
HLIrs121964977
Exacrs121964977
Varsomers121964977
Maprs121964977
PheGenIrs121964977
hapmaprs121964977
1000 genomesrs121964977
hgdprs121964977
ensemblrs121964977
gopubmedrs121964977
geneviewrs121964977
scholarrs121964977
googlers121964977
pharmgkbrs121964977
gwascentralrs121964977
openSNPrs121964977
23andMers121964977
23andMe allrs121964977
SNP Nexus

SNPshotrs121964977
SNPdbers121964977
MSV3drs121964977
GWAS Ctlgrs121964977
Max Magnitude0
OMIM238300
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121964977(T;T)
Alt rs121964977(T;T)
Reference rs121964977(C;C)
Significance Pathogenic
Disease Non-ketotic hyperglycinemia
Variation info
Gene GLDC
CLNDBN Non-ketotic hyperglycinemia
Reversed 1
HGVS NC_000009.11:g.6553420G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012767.22,