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rs786205861

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205861(C;T)
Make rs786205861(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position12896913
GeneGCDH
is asnp
is mentioned by
dbSNPrs786205861
ebirs786205861
HLIrs786205861
Exacrs786205861
Varsomers786205861
Maprs786205861
PheGenIrs786205861
hapmaprs786205861
1000 genomesrs786205861
hgdprs786205861
ensemblrs786205861
gopubmedrs786205861
geneviewrs786205861
scholarrs786205861
googlers786205861
pharmgkbrs786205861
gwascentralrs786205861
openSNPrs786205861
23andMers786205861
23andMe allrs786205861
SNP Nexus

SNPshotrs786205861
SNPdbers786205861
MSV3drs786205861
GWAS Ctlgrs786205861
Max Magnitude0
ClinVar
Risk rs786205861(T;T)
Alt rs786205861(T;T)
Reference rs786205861(C;C)
Significance Probable-Pathogenic
Disease Glutaric aciduria
Variation info
Gene GCDH
CLNDBN Glutaric aciduria, type 1
Reversed 0
HGVS NC_000019.9:g.13007727C>T
CLNSRC
CLNACC RCV000171557.1,