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rs869025299

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025299(C;T)
Make rs869025299(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position12897377
GeneGCDH
is asnp
is mentioned by
dbSNPrs869025299
ebirs869025299
HLIrs869025299
Exacrs869025299
Varsomers869025299
Maprs869025299
PheGenIrs869025299
hapmaprs869025299
1000 genomesrs869025299
hgdprs869025299
ensemblrs869025299
gopubmedrs869025299
geneviewrs869025299
scholarrs869025299
googlers869025299
pharmgkbrs869025299
gwascentralrs869025299
openSNPrs869025299
23andMers869025299
23andMe allrs869025299
SNP Nexus

SNPshotrs869025299
SNPdbers869025299
MSV3drs869025299
GWAS Ctlgrs869025299
Max Magnitude0
ClinVar
Risk rs869025299(T;T)
Alt rs869025299(T;T)
Reference rs869025299(C;C)
Significance Probable-Pathogenic
Disease Glutaric aciduria
Variation info
Gene GCDH
CLNDBN Glutaric aciduria, type 1
Reversed 0
HGVS NC_000019.9:g.13008191C>T
CLNSRC
CLNACC RCV000207408.1,