rs398124060

Orientation

minus

Stabilized

minus

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

Make rs398124060(-;-)

Make rs398124060(-;TA)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31627825

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124060
dbSNP (classic)	rs398124060
ClinGen	rs398124060
ebi	rs398124060
HLI	rs398124060
Exac	rs398124060
Gnomad	rs398124060
Varsome	rs398124060
LitVar	rs398124060
Map	rs398124060
PheGenI	rs398124060
Biobank	rs398124060
1000 genomes	rs398124060
hgdp	rs398124060
ensembl	rs398124060
geneview	rs398124060
scholar	rs398124060
google	rs398124060
pharmgkb	rs398124060
gwascentral	rs398124060
openSNP	rs398124060
23andMe	rs398124060
SNPshot	rs398124060
SNPdbe	rs398124060
MSV3d	rs398124060
GWAS Ctlg	rs398124060

Max Magnitude

0

ClinVar
Risk	rs398124060(-;-)
Alt	rs398124060(-;-)
Reference	Rs398124060(TA;TA)
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.31645942_31645943delTA
CLNSRC	HGMD
CLNACC	RCV000080778.4, RCV000179165.1, RCV000179166.1,