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rs121434589

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434589(A;A)
Make rs121434589(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position10535137
GeneMYH2
is asnp
is mentioned by
dbSNPrs121434589
ebirs121434589
HLIrs121434589
Exacrs121434589
Varsomers121434589
Maprs121434589
PheGenIrs121434589
hapmaprs121434589
1000 genomesrs121434589
hgdprs121434589
ensemblrs121434589
gopubmedrs121434589
geneviewrs121434589
scholarrs121434589
googlers121434589
pharmgkbrs121434589
gwascentralrs121434589
openSNPrs121434589
23andMers121434589
23andMe allrs121434589
SNP Nexus

SNPshotrs121434589
SNPdbers121434589
MSV3drs121434589
GWAS Ctlgrs121434589
Max Magnitude0
OMIM160740
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434589(A;A)
Alt rs121434589(A;A)
Reference rs121434589(G;G)
Significance Pathogenic
Disease Inclusion body myopathy 3
Variation info
Gene MYH2 MYHAS
CLNDBN Inclusion body myopathy 3
Reversed 1
HGVS NC_000017.10:g.10438454C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015199.26,