rs398124036

Orientation

minus

Stabilized

minus

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

Make rs398124036(A;A)

Make rs398124036(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31929602

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398124036
dbSNP (classic)	rs398124036
ClinGen	rs398124036
ebi	rs398124036
HLI	rs398124036
Exac	rs398124036
Gnomad	rs398124036
Varsome	rs398124036
LitVar	rs398124036
Map	rs398124036
PheGenI	rs398124036
Biobank	rs398124036
1000 genomes	rs398124036
hgdp	rs398124036
ensembl	rs398124036
geneview	rs398124036
scholar	rs398124036
google	rs398124036
pharmgkb	rs398124036
gwascentral	rs398124036
openSNP	rs398124036
23andMe	rs398124036
SNPshot	rs398124036
SNPdbe	rs398124036
MSV3d	rs398124036
GWAS Ctlg	rs398124036

Max Magnitude

0

ClinVar
Risk	rs398124036(A;A) rs398124036(T;T)
Alt	rs398124036(A;A) rs398124036(T;T)
Reference	Rs398124036(G;G)
Significance	Pathogenic
Disease	not specified Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	not specified Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31947719C>A; NC_000023.10:g.31947719C>T
CLNSRC	HGMD
CLNACC	RCV000178628.1, RCV000080743.4, RCV000178629.1, RCV000178630.1,