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rs387906755

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906755(A;A)
Make rs387906755(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position91298023
GeneAUH
is asnp
is mentioned by
dbSNPrs387906755
ebirs387906755
HLIrs387906755
Exacrs387906755
Varsomers387906755
Maprs387906755
PheGenIrs387906755
hapmaprs387906755
1000 genomesrs387906755
hgdprs387906755
ensemblrs387906755
gopubmedrs387906755
geneviewrs387906755
scholarrs387906755
googlers387906755
pharmgkbrs387906755
gwascentralrs387906755
openSNPrs387906755
23andMers387906755
23andMe allrs387906755
SNP Nexus

SNPshotrs387906755
SNPdbers387906755
MSV3drs387906755
GWAS Ctlgrs387906755
Max Magnitude0
ClinVar
Risk rs387906755(A;A)
Alt rs387906755(A;A)
Reference rs387906755(G;G)
Significance Pathogenic
Disease 3-Methylglutaconic aciduria not provided
Variation info
Gene AUH
CLNDBN 3-Methylglutaconic aciduria not provided
Reversed 1
HGVS NC_000009.11:g.94060305C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022982.3, RCV000196605.1,