rs878854355

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs878854355(A;G)

Make rs878854355(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

151405064

Gene

VMA21

is a	snp
is	mentioned by
dbSNP	rs878854355
dbSNP (classic)	rs878854355
ClinGen	rs878854355
ebi	rs878854355
HLI	rs878854355
Exac	rs878854355
Gnomad	rs878854355
Varsome	rs878854355
LitVar	rs878854355
Map	rs878854355
PheGenI	rs878854355
Biobank	rs878854355
1000 genomes	rs878854355
hgdp	rs878854355
ensembl	rs878854355
geneview	rs878854355
scholar	rs878854355
google	rs878854355
pharmgkb	rs878854355
gwascentral	rs878854355
openSNP	rs878854355
23andMe	rs878854355
SNPshot	rs878854355
SNPdbe	rs878854355
MSV3d	rs878854355
GWAS Ctlg	rs878854355

Max Magnitude

0

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	RCV000190831.3,