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rs587783594

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783594(A;A)
Make rs587783594(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position10793851
GeneDNM2
is asnp
is mentioned by
dbSNPrs587783594
ebirs587783594
HLIrs587783594
Exacrs587783594
Varsomers587783594
Maprs587783594
PheGenIrs587783594
hapmaprs587783594
1000 genomesrs587783594
hgdprs587783594
ensemblrs587783594
gopubmedrs587783594
geneviewrs587783594
scholarrs587783594
googlers587783594
pharmgkbrs587783594
gwascentralrs587783594
openSNPrs587783594
23andMers587783594
23andMe allrs587783594
SNP Nexus

SNPshotrs587783594
SNPdbers587783594
MSV3drs587783594
GWAS Ctlgrs587783594
Max Magnitude0
ClinVar
Risk rs587783594(A;A)
Alt rs587783594(A;A)
Reference rs587783594(T;T)
Significance Probable-Pathogenic
Disease Myopathy
Variation info
Gene DNM2
CLNDBN Myopathy, centronuclear
Reversed 0
HGVS NC_000019.9:g.10904527T>A
CLNSRC
CLNACC RCV000145901.1,