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rs797044909

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044909(A;G)
Make rs797044909(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position151403744
GeneVMA21
is asnp
is mentioned by
dbSNPrs797044909
ebirs797044909
HLIrs797044909
Exacrs797044909
Varsomers797044909
Maprs797044909
PheGenIrs797044909
hapmaprs797044909
1000 genomesrs797044909
hgdprs797044909
ensemblrs797044909
gopubmedrs797044909
geneviewrs797044909
scholarrs797044909
googlers797044909
pharmgkbrs797044909
gwascentralrs797044909
openSNPrs797044909
23andMers797044909
23andMe allrs797044909
SNP Nexus

SNPshotrs797044909
SNPdbers797044909
MSV3drs797044909
GWAS Ctlgrs797044909
Max Magnitude0
ClinVar
Risk rs797044909(G;G)
Alt rs797044909(G;G)
Reference rs797044909(A;A)
Significance Pathogenic
Disease Inborn genetic diseases Myopathy
Variation info
Gene VMA21
CLNDBN Inborn genetic diseases Myopathy, X-linked, with excessive autophagy
Reversed 0
HGVS NC_000023.10:g.150572216A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000190737.1, RCV000190828.2,