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rs121964974

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964974(G;T)
Make rs121964974(T;T)
ReferenceGRCh37 37.1/132
Chromosome9
Position6588417
GeneGLDC
is asnp
is mentioned by
dbSNPrs121964974
ebirs121964974
HLIrs121964974
Exacrs121964974
Varsomers121964974
Maprs121964974
PheGenIrs121964974
hapmaprs121964974
1000 genomesrs121964974
hgdprs121964974
ensemblrs121964974
gopubmedrs121964974
geneviewrs121964974
scholarrs121964974
googlers121964974
pharmgkbrs121964974
gwascentralrs121964974
openSNPrs121964974
23andMers121964974
23andMe allrs121964974
SNP Nexus

SNPshotrs121964974
SNPdbers121964974
MSV3drs121964974
GWAS Ctlgrs121964974
Max Magnitude0
OMIM238300
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121964974(T;T)
Alt rs121964974(T;T)
Reference rs121964974(G;G)
Significance Pathogenic
Disease Non-ketotic hyperglycinemia
Variation info
Gene GLDC
CLNDBN Non-ketotic hyperglycinemia
Reversed 1
HGVS NC_000009.11:g.6588417C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012762.22,