rs794727575

Orientation

minus

Stabilized

minus

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

Make rs794727575(A;G)

Make rs794727575(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32380682

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs794727575
dbSNP (classic)	rs794727575
ClinGen	rs794727575
ebi	rs794727575
HLI	rs794727575
Exac	rs794727575
Gnomad	rs794727575
Varsome	rs794727575
LitVar	rs794727575
Map	rs794727575
PheGenI	rs794727575
Biobank	rs794727575
1000 genomes	rs794727575
hgdp	rs794727575
ensembl	rs794727575
geneview	rs794727575
scholar	rs794727575
google	rs794727575
pharmgkb	rs794727575
gwascentral	rs794727575
openSNP	rs794727575
23andMe	rs794727575
SNPshot	rs794727575
SNPdbe	rs794727575
MSV3d	rs794727575
GWAS Ctlg	rs794727575

Max Magnitude

0

ClinVar
Risk	rs794727575(G;G)
Alt	rs794727575(G;G)
Reference	Rs794727575(A;A)
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.32398799T>C
CLNSRC
CLNACC	RCV000177779.1, RCV000177780.1,