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rs587783597

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783597(C;C)
Make rs587783597(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position10823868
GeneDNM2
is asnp
is mentioned by
dbSNPrs587783597
ebirs587783597
HLIrs587783597
Exacrs587783597
Varsomers587783597
Maprs587783597
PheGenIrs587783597
hapmaprs587783597
1000 genomesrs587783597
hgdprs587783597
ensemblrs587783597
gopubmedrs587783597
geneviewrs587783597
scholarrs587783597
googlers587783597
pharmgkbrs587783597
gwascentralrs587783597
openSNPrs587783597
23andMers587783597
23andMe allrs587783597
SNP Nexus

SNPshotrs587783597
SNPdbers587783597
MSV3drs587783597
GWAS Ctlgrs587783597
Max Magnitude0
ClinVar
Risk rs587783597(C;C)
Alt rs587783597(C;C)
Reference rs587783597(T;T)
Significance Pathogenic
Disease Myopathy
Variation info
Gene DNM2
CLNDBN Myopathy, centronuclear
Reversed 0
HGVS NC_000019.9:g.10934544T>C
CLNSRC
CLNACC RCV000145909.1,