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rs387906757

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906757(A;T)
Make rs387906757(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position91214377
GeneAUH
is asnp
is mentioned by
dbSNPrs387906757
ebirs387906757
HLIrs387906757
Exacrs387906757
Varsomers387906757
Maprs387906757
PheGenIrs387906757
hapmaprs387906757
1000 genomesrs387906757
hgdprs387906757
ensemblrs387906757
gopubmedrs387906757
geneviewrs387906757
scholarrs387906757
googlers387906757
pharmgkbrs387906757
gwascentralrs387906757
openSNPrs387906757
23andMers387906757
23andMe allrs387906757
SNP Nexus

SNPshotrs387906757
SNPdbers387906757
MSV3drs387906757
GWAS Ctlgrs387906757
Max Magnitude0
ClinVar
Risk rs387906757(T;T)
Alt rs387906757(T;T)
Reference rs387906757(A;A)
Significance Pathogenic
Disease 3-Methylglutaconic aciduria
Variation info
Gene AUH
CLNDBN 3-Methylglutaconic aciduria
Reversed 1
HGVS NC_000009.11:g.93976659T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022984.4,