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rs121434586

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434586(C;T)
Make rs121434586(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position49026719
GeneIMPDH2
is asnp
is mentioned by
dbSNPrs121434586
ebirs121434586
HLIrs121434586
Exacrs121434586
Varsomers121434586
Maprs121434586
PheGenIrs121434586
hapmaprs121434586
1000 genomesrs121434586
hgdprs121434586
ensemblrs121434586
gopubmedrs121434586
geneviewrs121434586
scholarrs121434586
googlers121434586
pharmgkbrs121434586
gwascentralrs121434586
openSNPrs121434586
23andMers121434586
23andMe allrs121434586
SNP Nexus

SNPshotrs121434586
SNPdbers121434586
MSV3drs121434586
GWAS Ctlgrs121434586
Max Magnitude0
OMIM146691
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434586(T;T)
Alt rs121434586(T;T)
Reference rs121434586(C;C)
Significance Other
Disease Impdh2 enzyme activity
Variation info
Gene IMPDH2
CLNDBN Impdh2 enzyme activity, variation in
Reversed 1
HGVS NC_000003.11:g.49064152G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015958.26,