rs727503844

Orientation

minus

Stabilized

minus

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

Make rs727503844(C;T)

Make rs727503844(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

32468704

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs727503844
dbSNP (classic)	rs727503844
ClinGen	rs727503844
ebi	rs727503844
HLI	rs727503844
Exac	rs727503844
Gnomad	rs727503844
Varsome	rs727503844
LitVar	rs727503844
Map	rs727503844
PheGenI	rs727503844
Biobank	rs727503844
1000 genomes	rs727503844
hgdp	rs727503844
ensembl	rs727503844
geneview	rs727503844
scholar	rs727503844
google	rs727503844
pharmgkb	rs727503844
gwascentral	rs727503844
openSNP	rs727503844
23andMe	rs727503844
SNPshot	rs727503844
SNPdbe	rs727503844
MSV3d	rs727503844
GWAS Ctlg	rs727503844

Max Magnitude

0

ClinVar
Risk	rs727503844(T;T)
Alt	rs727503844(T;T)
Reference	Rs727503844(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy Becker muscular dystrophy Dilated cardiomyopathy 3B not provided
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy Becker muscular dystrophy Dilated cardiomyopathy 3B not provided
Reversed	1
HGVS	NC_000023.10:g.32486821G>A
CLNSRC	HGMD
CLNACC	RCV000152954.3, RCV000152955.3, RCV000176399.1, RCV000493636.1,