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rs1006150317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position12891875
GeneGCDH
is asnp
is mentioned by
dbSNPrs1006150317
dbSNP (old)rs1006150317
ClinGenrs1006150317
ebirs1006150317
HLIrs1006150317
Exacrs1006150317
Gnomadrs1006150317
Varsomers1006150317
Maprs1006150317
PheGenIrs1006150317
Biobankrs1006150317
1000 genomesrs1006150317
hgdprs1006150317
ensemblrs1006150317
gopubmedrs1006150317
geneviewrs1006150317
scholarrs1006150317
googlers1006150317
pharmgkbrs1006150317
gwascentralrs1006150317
openSNPrs1006150317
23andMers1006150317
23andMe allrs1006150317
SNP Nexus

SNPshotrs1006150317
SNPdbers1006150317
MSV3drs1006150317
GWAS Ctlgrs1006150317
Max Magnitude0
ClinVar
Risk rs1006150317(T;T)
Alt rs1006150317(T;T)
Reference Rs1006150317(G;G)
Significance Probable-Pathogenic
Disease Glutaric aciduria
Variation info
Gene
CLNDBN Glutaric aciduria, type 1
Reversed 0
HGVS NC_000019.9:g.13002689G>T
CLNSRC
CLNACC RCV000412281.1,