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rs878854353

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854353(G;G)
Make rs878854353(G;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position151404909
GeneVMA21
is asnp
is mentioned by
dbSNPrs878854353
ebirs878854353
HLIrs878854353
Exacrs878854353
Varsomers878854353
Maprs878854353
PheGenIrs878854353
hapmaprs878854353
1000 genomesrs878854353
hgdprs878854353
ensemblrs878854353
gopubmedrs878854353
geneviewrs878854353
scholarrs878854353
googlers878854353
pharmgkbrs878854353
gwascentralrs878854353
openSNPrs878854353
23andMers878854353
23andMe allrs878854353
SNP Nexus

SNPshotrs878854353
SNPdbers878854353
MSV3drs878854353
GWAS Ctlgrs878854353
Max Magnitude0
ClinVar
Risk rs878854353(G;G)
Alt rs878854353(G;G)
Reference rs878854353(T;T)
Significance Pathogenic
Disease Myopathy
Variation info
Gene VMA21
CLNDBN Myopathy, X-linked, with excessive autophagy
Reversed 0
HGVS NC_000023.10:g.150573381T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000190829.2,