rs398124003

Orientation

minus

Stabilized

minus

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

Make rs398124003(-;-)

Make rs398124003(-;CTCA)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32310182

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124003
dbSNP (classic)	rs398124003
ClinGen	rs398124003
ebi	rs398124003
HLI	rs398124003
Exac	rs398124003
Gnomad	rs398124003
Varsome	rs398124003
LitVar	rs398124003
Map	rs398124003
PheGenI	rs398124003
Biobank	rs398124003
1000 genomes	rs398124003
hgdp	rs398124003
ensembl	rs398124003
geneview	rs398124003
scholar	rs398124003
google	rs398124003
pharmgkb	rs398124003
gwascentral	rs398124003
openSNP	rs398124003
23andMe	rs398124003
SNPshot	rs398124003
SNPdbe	rs398124003
MSV3d	rs398124003
GWAS Ctlg	rs398124003

Max Magnitude

0

ClinVar
Risk	rs398124003(-;-)
Alt	rs398124003(-;-)
Reference	Rs398124003(CTCA;CTCA)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32328299_32328302delTGAG
CLNSRC	ClinVar
CLNACC	RCV000080680.3,