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rs397515746

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515746(A;A)
Make rs397515746(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154420038
GeneTAZ
is asnp
is mentioned by
dbSNPrs397515746
ebirs397515746
HLIrs397515746
Exacrs397515746
Varsomers397515746
Maprs397515746
PheGenIrs397515746
hapmaprs397515746
1000 genomesrs397515746
hgdprs397515746
ensemblrs397515746
gopubmedrs397515746
geneviewrs397515746
scholarrs397515746
googlers397515746
pharmgkbrs397515746
gwascentralrs397515746
openSNPrs397515746
23andMers397515746
23andMe allrs397515746
SNP Nexus

SNPshotrs397515746
SNPdbers397515746
MSV3drs397515746
GWAS Ctlgrs397515746
Max Magnitude0
ClinVar
Risk rs397515746(A;A)
Alt rs397515746(A;A)
Reference rs397515746(G;G)
Significance Probable-Pathogenic
Disease 3-Methylglutaconic aciduria type 2
Variation info
Gene TAZ
CLNDBN 3-Methylglutaconic aciduria type 2
Reversed 0
HGVS NC_000023.10:g.153648377G>A
CLNSRC ClinVar
CLNACC RCV000035097.2,