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rs772871471

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772871471(C;C)
Make rs772871471(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position6587249
GeneGLDC
is asnp
is mentioned by
dbSNPrs772871471
ebirs772871471
HLIrs772871471
Exacrs772871471
Varsomers772871471
Maprs772871471
PheGenIrs772871471
hapmaprs772871471
1000 genomesrs772871471
hgdprs772871471
ensemblrs772871471
gopubmedrs772871471
geneviewrs772871471
scholarrs772871471
googlers772871471
pharmgkbrs772871471
gwascentralrs772871471
openSNPrs772871471
23andMers772871471
23andMe allrs772871471
SNP Nexus

SNPshotrs772871471
SNPdbers772871471
MSV3drs772871471
GWAS Ctlgrs772871471
Max Magnitude0
ClinVar
Risk rs772871471(C;C)
Alt rs772871471(C;C)
Reference rs772871471(G;G)
Significance Probable-Pathogenic
Disease Non-ketotic hyperglycinemia
Variation info
Gene GLDC
CLNDBN Non-ketotic hyperglycinemia
Reversed 0
HGVS NC_000009.11:g.6587249G>C
CLNSRC
CLNACC RCV000198720.1,