rs398123987

Orientation

minus

Stabilized

minus

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

Make rs398123987(-;T)

Make rs398123987(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32362799

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123987
dbSNP (classic)	rs398123987
ClinGen	rs398123987
ebi	rs398123987
HLI	rs398123987
Exac	rs398123987
Gnomad	rs398123987
Varsome	rs398123987
LitVar	rs398123987
Map	rs398123987
PheGenI	rs398123987
Biobank	rs398123987
1000 genomes	rs398123987
hgdp	rs398123987
ensembl	rs398123987
geneview	rs398123987
scholar	rs398123987
google	rs398123987
pharmgkb	rs398123987
gwascentral	rs398123987
openSNP	rs398123987
23andMe	rs398123987
SNPshot	rs398123987
SNPdbe	rs398123987
MSV3d	rs398123987
GWAS Ctlg	rs398123987

Max Magnitude

0

ClinVar
Risk	rs398123987(T;T)
Alt	rs398123987(T;T)
Reference	Rs398123987(-;-)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32380917dupA
CLNSRC	ClinVar
CLNACC	RCV000080654.3,