rs398124100

Orientation

minus

Stabilized

minus

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

Make rs398124100(A;G)

Make rs398124100(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31204120

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124100
dbSNP (classic)	rs398124100
ClinGen	rs398124100
ebi	rs398124100
HLI	rs398124100
Exac	rs398124100
Gnomad	rs398124100
Varsome	rs398124100
LitVar	rs398124100
Map	rs398124100
PheGenI	rs398124100
Biobank	rs398124100
1000 genomes	rs398124100
hgdp	rs398124100
ensembl	rs398124100
geneview	rs398124100
scholar	rs398124100
google	rs398124100
pharmgkb	rs398124100
gwascentral	rs398124100
openSNP	rs398124100
23andMe	rs398124100
SNPshot	rs398124100
SNPdbe	rs398124100
MSV3d	rs398124100
GWAS Ctlg	rs398124100

Max Magnitude

0

ClinVar
Risk	rs398124100(G;G)
Alt	rs398124100(G;G)
Reference	Rs398124100(A;A)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31222237T>C
CLNSRC	ClinVar
CLNACC	RCV000080854.4, RCV000179670.1, RCV000179671.1,