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rs387906756

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906756(A;A)
Make rs387906756(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position91296026
GeneAUH
is asnp
is mentioned by
dbSNPrs387906756
ebirs387906756
HLIrs387906756
Exacrs387906756
Varsomers387906756
Maprs387906756
PheGenIrs387906756
hapmaprs387906756
1000 genomesrs387906756
hgdprs387906756
ensemblrs387906756
gopubmedrs387906756
geneviewrs387906756
scholarrs387906756
googlers387906756
pharmgkbrs387906756
gwascentralrs387906756
openSNPrs387906756
23andMers387906756
23andMe allrs387906756
SNP Nexus

SNPshotrs387906756
SNPdbers387906756
MSV3drs387906756
GWAS Ctlgrs387906756
Max Magnitude0
ClinVar
Risk rs387906756(A;A)
Alt rs387906756(A;A)
Reference rs387906756(G;G)
Significance Pathogenic
Disease 3-Methylglutaconic aciduria
Variation info
Gene AUH
CLNDBN 3-Methylglutaconic aciduria
Reversed 1
HGVS NC_000009.11:g.94058308C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022983.3,