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rs730880309

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880309(A;A)
Make rs730880309(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position91216107
GeneAUH
is asnp
is mentioned by
dbSNPrs730880309
ebirs730880309
HLIrs730880309
Exacrs730880309
Varsomers730880309
Maprs730880309
PheGenIrs730880309
hapmaprs730880309
1000 genomesrs730880309
hgdprs730880309
ensemblrs730880309
gopubmedrs730880309
geneviewrs730880309
scholarrs730880309
googlers730880309
pharmgkbrs730880309
gwascentralrs730880309
openSNPrs730880309
23andMers730880309
23andMe allrs730880309
SNP Nexus

SNPshotrs730880309
SNPdbers730880309
MSV3drs730880309
GWAS Ctlgrs730880309
Max Magnitude0
ClinVar
Risk rs730880309(A;A)
Alt rs730880309(A;A)
Reference rs730880309(G;G)
Significance Pathogenic
Disease 3-Methylglutaconic aciduria
Variation info
Gene AUH
CLNDBN 3-Methylglutaconic aciduria
Reversed 1
HGVS NC_000009.11:g.93978389C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009624.3,