rs1057518834

Orientation

minus

Stabilized

minus

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

Make rs1057518834(-;-)

Make rs1057518834(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32849737

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1057518834
dbSNP (classic)	rs1057518834
ClinGen	rs1057518834
ebi	rs1057518834
HLI	rs1057518834
Exac	rs1057518834
Gnomad	rs1057518834
Varsome	rs1057518834
LitVar	rs1057518834
Map	rs1057518834
PheGenI	rs1057518834
Biobank	rs1057518834
1000 genomes	rs1057518834
hgdp	rs1057518834
ensembl	rs1057518834
geneview	rs1057518834
scholar	rs1057518834
google	rs1057518834
pharmgkb	rs1057518834
gwascentral	rs1057518834
openSNP	rs1057518834
23andMe	rs1057518834
SNPshot	rs1057518834
SNPdbe	rs1057518834
MSV3d	rs1057518834
GWAS Ctlg	rs1057518834

Max Magnitude

0

ClinVar
Risk	rs1057518834(-;-)
Alt	rs1057518834(-;-)
Reference	Rs1057518834(G;G)
Significance	Probable-Pathogenic
Disease	Decreased body weight EMG: myopathic abnormalities Exercise-induced muscle cramps Exercise-induced muscle fatigue Exercise-induced muscle stiffness Exercise-induced myalgia Exercise-induced rhabdomyolysis Myopathy Short stature
Variation	info
Gene	DMD
CLNDBN	Decreased body weight EMG: myopathic abnormalities Exercise-induced muscle cramps Exercise-induced muscle fatigue Exercise-induced muscle stiffness Exercise-induced myalgia Exercise-induced rhabdomyolysis Myopathy Short stature
Reversed	1
HGVS	NC_000023.10:g.32867854delC
CLNSRC
CLNACC	RCV000414800.1,