rs727503858

Orientation

minus

Stabilized

minus

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

Make rs727503858(G;G)

Make rs727503858(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

32491415

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs727503858
dbSNP (classic)	rs727503858
ClinGen	rs727503858
ebi	rs727503858
HLI	rs727503858
Exac	rs727503858
Gnomad	rs727503858
Varsome	rs727503858
LitVar	rs727503858
Map	rs727503858
PheGenI	rs727503858
Biobank	rs727503858
1000 genomes	rs727503858
hgdp	rs727503858
ensembl	rs727503858
geneview	rs727503858
scholar	rs727503858
google	rs727503858
pharmgkb	rs727503858
gwascentral	rs727503858
openSNP	rs727503858
23andMe	rs727503858
SNPshot	rs727503858
SNPdbe	rs727503858
MSV3d	rs727503858
GWAS Ctlg	rs727503858

Max Magnitude

0

ClinVar
Risk	rs727503858(G;G)
Alt	rs727503858(G;G)
Reference	Rs727503858(T;T)
Significance	Pathogenic
Disease	Becker muscular dystrophy Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Becker muscular dystrophy Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32509532A>C
CLNSRC
CLNACC	RCV000152999.3, RCV000153000.3, RCV000153001.3,