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rs878853153

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853153(C;G)
Make rs878853153(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position12893604
GeneGCDH
is asnp
is mentioned by
dbSNPrs878853153
ebirs878853153
HLIrs878853153
Exacrs878853153
Varsomers878853153
Maprs878853153
PheGenIrs878853153
hapmaprs878853153
1000 genomesrs878853153
hgdprs878853153
ensemblrs878853153
gopubmedrs878853153
geneviewrs878853153
scholarrs878853153
googlers878853153
pharmgkbrs878853153
gwascentralrs878853153
openSNPrs878853153
23andMers878853153
23andMe allrs878853153
SNP Nexus

SNPshotrs878853153
SNPdbers878853153
MSV3drs878853153
GWAS Ctlgrs878853153
Max Magnitude0
ClinVar
Risk rs878853153(G;G)
Alt rs878853153(G;G)
Reference rs878853153(C;C)
Significance Pathogenic
Disease Glutaric aciduria
Variation info
Gene GCDH
CLNDBN Glutaric aciduria, type 1
Reversed 0
HGVS NC_000019.9:g.13004418C>G
CLNSRC
CLNACC RCV000224005.1,