rs794727323

Orientation

minus

Stabilized

minus

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

Make rs794727323(G;T)

Make rs794727323(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32491420

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs794727323
dbSNP (classic)	rs794727323
ClinGen	rs794727323
ebi	rs794727323
HLI	rs794727323
Exac	rs794727323
Gnomad	rs794727323
Varsome	rs794727323
LitVar	rs794727323
Map	rs794727323
PheGenI	rs794727323
Biobank	rs794727323
1000 genomes	rs794727323
hgdp	rs794727323
ensembl	rs794727323
geneview	rs794727323
scholar	rs794727323
google	rs794727323
pharmgkb	rs794727323
gwascentral	rs794727323
openSNP	rs794727323
23andMe	rs794727323
SNPshot	rs794727323
SNPdbe	rs794727323
MSV3d	rs794727323
GWAS Ctlg	rs794727323

Max Magnitude

0

ClinVar
Risk	rs794727323(T;T)
Alt	rs794727323(T;T)
Reference	Rs794727323(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy Becker muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy Becker muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32509537C>A
CLNSRC
CLNACC	RCV000176079.1, RCV000379286.1,