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rs878854356

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854356(G;G)
Make rs878854356(G;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position151404910
GeneVMA21
is asnp
is mentioned by
dbSNPrs878854356
ebirs878854356
HLIrs878854356
Exacrs878854356
Varsomers878854356
Maprs878854356
PheGenIrs878854356
hapmaprs878854356
1000 genomesrs878854356
hgdprs878854356
ensemblrs878854356
gopubmedrs878854356
geneviewrs878854356
scholarrs878854356
googlers878854356
pharmgkbrs878854356
gwascentralrs878854356
openSNPrs878854356
23andMers878854356
23andMe allrs878854356
SNP Nexus

SNPshotrs878854356
SNPdbers878854356
MSV3drs878854356
GWAS Ctlgrs878854356
Max Magnitude0
ClinVar
Risk rs878854356(G;G)
Alt rs878854356(G;G)
Reference rs878854356(T;T)
Significance Pathogenic
Disease Myopathy
Variation info
Gene VMA21
CLNDBN Myopathy, X-linked, with excessive autophagy
Reversed 0
HGVS NC_000023.10:g.150573382T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000190832.2,