Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909089

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909089(A;A)
Make rs121909089(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position10793833
GeneDNM2
is asnp
is mentioned by
dbSNPrs121909089
ebirs121909089
HLIrs121909089
Exacrs121909089
Varsomers121909089
Maprs121909089
PheGenIrs121909089
hapmaprs121909089
1000 genomesrs121909089
hgdprs121909089
ensemblrs121909089
gopubmedrs121909089
geneviewrs121909089
scholarrs121909089
googlers121909089
pharmgkbrs121909089
gwascentralrs121909089
openSNPrs121909089
23andMers121909089
23andMe allrs121909089
SNP Nexus

SNPshotrs121909089
SNPdbers121909089
MSV3drs121909089
GWAS Ctlgrs121909089
Max Magnitude0
OMIM602378
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909089(A,T;A,T)
Alt rs121909089(A,T;A,T)
Reference rs121909089(G;G)
Significance Pathogenic
Disease Myopathy not provided
Variation info
Gene DNM2
CLNDBN Myopathy, centronuclear, 1 Myopathy, centronuclear not provided
Reversed 0
HGVS NC_000019.9:g.10904509G>A; NC_000019.9:g.10904509G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007702.3, RCV000145900.1, RCV000236677.1,