rs398124049

Orientation

minus

Stabilized

minus

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

Make rs398124049(-;-)

Make rs398124049(-;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31729739

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124049
dbSNP (classic)	rs398124049
ClinGen	rs398124049
ebi	rs398124049
HLI	rs398124049
Exac	rs398124049
Gnomad	rs398124049
Varsome	rs398124049
LitVar	rs398124049
Map	rs398124049
PheGenI	rs398124049
Biobank	rs398124049
1000 genomes	rs398124049
hgdp	rs398124049
ensembl	rs398124049
geneview	rs398124049
scholar	rs398124049
google	rs398124049
pharmgkb	rs398124049
gwascentral	rs398124049
openSNP	rs398124049
23andMe	rs398124049
SNPshot	rs398124049
SNPdbe	rs398124049
MSV3d	rs398124049
GWAS Ctlg	rs398124049

Max Magnitude

0

ClinVar
Risk	rs398124049(-;-)
Alt	rs398124049(-;-)
Reference	Rs398124049(C;C)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.31747856delG
CLNSRC	ClinVar
CLNACC	RCV000080763.3,