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rs121909091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909091(C;T)
Make rs121909091(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position10798543
GeneDNM2
is asnp
is mentioned by
dbSNPrs121909091
ebirs121909091
HLIrs121909091
Exacrs121909091
Varsomers121909091
Maprs121909091
PheGenIrs121909091
hapmaprs121909091
1000 genomesrs121909091
hgdprs121909091
ensemblrs121909091
gopubmedrs121909091
geneviewrs121909091
scholarrs121909091
googlers121909091
pharmgkbrs121909091
gwascentralrs121909091
openSNPrs121909091
23andMers121909091
23andMe allrs121909091
SNP Nexus

SNPshotrs121909091
SNPdbers121909091
MSV3drs121909091
GWAS Ctlgrs121909091
Max Magnitude0
OMIM602378
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909091(T;T)
Alt rs121909091(T;T)
Reference rs121909091(C;C)
Significance Pathogenic
Disease Myopathy
Variation info
Gene DNM2
CLNDBN Myopathy, centronuclear, 1 Myopathy, centronuclear
Reversed 0
HGVS NC_000019.9:g.10909219C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007704.2, RCV000145902.1,