rs398123830

Orientation

minus

Stabilized

minus

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

Make rs398123830(G;T)

Make rs398123830(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32645101

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123830
dbSNP (classic)	rs398123830
ClinGen	rs398123830
ebi	rs398123830
HLI	rs398123830
Exac	rs398123830
Gnomad	rs398123830
Varsome	rs398123830
LitVar	rs398123830
Map	rs398123830
PheGenI	rs398123830
Biobank	rs398123830
1000 genomes	rs398123830
hgdp	rs398123830
ensembl	rs398123830
geneview	rs398123830
scholar	rs398123830
google	rs398123830
pharmgkb	rs398123830
gwascentral	rs398123830
openSNP	rs398123830
23andMe	rs398123830
SNPshot	rs398123830
SNPdbe	rs398123830
MSV3d	rs398123830
GWAS Ctlg	rs398123830

Max Magnitude

0

ClinVar
Risk	rs398123830(T;T)
Alt	rs398123830(T;T)
Reference	Rs398123830(G;G)
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.32663218C>A
CLNSRC	HGMD
CLNACC	RCV000080410.4, RCV000173789.1, RCV000173790.1,