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rs878854355

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854355(A;G)
Make rs878854355(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position151405064
GeneVMA21
is asnp
is mentioned by
dbSNPrs878854355
ebirs878854355
HLIrs878854355
Exacrs878854355
Varsomers878854355
Maprs878854355
PheGenIrs878854355
hapmaprs878854355
1000 genomesrs878854355
hgdprs878854355
ensemblrs878854355
gopubmedrs878854355
geneviewrs878854355
scholarrs878854355
googlers878854355
pharmgkbrs878854355
gwascentralrs878854355
openSNPrs878854355
23andMers878854355
23andMe allrs878854355
SNP Nexus

SNPshotrs878854355
SNPdbers878854355
MSV3drs878854355
GWAS Ctlgrs878854355
Max Magnitude0
ClinVar
Risk rs878854355(G;G)
Alt rs878854355(G;G)
Reference rs878854355(A;A)
Significance Pathogenic
Disease Myopathy
Variation info
Gene VMA21
CLNDBN Myopathy, X-linked, with excessive autophagy
Reversed 0
HGVS NC_000023.10:g.150573536A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000190831.2,