rs398123963

Orientation

minus

Stabilized

minus

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

Make rs398123963(-;T)

Make rs398123963(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32386349

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123963
dbSNP (classic)	rs398123963
ClinGen	rs398123963
ebi	rs398123963
HLI	rs398123963
Exac	rs398123963
Gnomad	rs398123963
Varsome	rs398123963
LitVar	rs398123963
Map	rs398123963
PheGenI	rs398123963
Biobank	rs398123963
1000 genomes	rs398123963
hgdp	rs398123963
ensembl	rs398123963
geneview	rs398123963
scholar	rs398123963
google	rs398123963
pharmgkb	rs398123963
gwascentral	rs398123963
openSNP	rs398123963
23andMe	rs398123963
SNPshot	rs398123963
SNPdbe	rs398123963
MSV3d	rs398123963
GWAS Ctlg	rs398123963

Max Magnitude

0

ClinVar
Risk	rs398123963(T;T)
Alt	rs398123963(T;T)
Reference	Rs398123963(-;-)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32404467dupA
CLNSRC	ClinVar
CLNACC	RCV000080625.3,