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rs121909092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909092(A;A)
Make rs121909092(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position10793829
GeneDNM2
is asnp
is mentioned by
dbSNPrs121909092
ebirs121909092
HLIrs121909092
Exacrs121909092
Varsomers121909092
Maprs121909092
PheGenIrs121909092
hapmaprs121909092
1000 genomesrs121909092
hgdprs121909092
ensemblrs121909092
gopubmedrs121909092
geneviewrs121909092
scholarrs121909092
googlers121909092
pharmgkbrs121909092
gwascentralrs121909092
openSNPrs121909092
23andMers121909092
23andMe allrs121909092
SNP Nexus

SNPshotrs121909092
SNPdbers121909092
MSV3drs121909092
GWAS Ctlgrs121909092
Max Magnitude0
OMIM602378
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909092(A;A)
Alt rs121909092(A;A)
Reference rs121909092(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene DNM2
CLNDBN Myopathy, centronuclear, 1 Myopathy, centronuclear
Reversed 0
HGVS NC_000019.9:g.10904505G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007705.2, RCV000145898.1,