rs398123985

Orientation

minus

Stabilized

minus

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

Make rs398123985(A;C)

Make rs398123985(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32809613

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123985
dbSNP (classic)	rs398123985
ClinGen	rs398123985
ebi	rs398123985
HLI	rs398123985
Exac	rs398123985
Gnomad	rs398123985
Varsome	rs398123985
LitVar	rs398123985
Map	rs398123985
PheGenI	rs398123985
Biobank	rs398123985
1000 genomes	rs398123985
hgdp	rs398123985
ensembl	rs398123985
geneview	rs398123985
scholar	rs398123985
google	rs398123985
pharmgkb	rs398123985
gwascentral	rs398123985
openSNP	rs398123985
23andMe	rs398123985
SNPshot	rs398123985
SNPdbe	rs398123985
MSV3d	rs398123985
GWAS Ctlg	rs398123985

Max Magnitude

0

ClinVar
Risk	rs398123985(C;C)
Alt	rs398123985(C;C)
Reference	Rs398123985(A;A)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32827730T>G
CLNSRC	ClinVar
CLNACC	RCV000080652.3,