rs794727030

Orientation

minus

Stabilized

minus

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

Make rs794727030(A;G)

Make rs794727030(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32644315

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs794727030
dbSNP (classic)	rs794727030
ClinGen	rs794727030
ebi	rs794727030
HLI	rs794727030
Exac	rs794727030
Gnomad	rs794727030
Varsome	rs794727030
LitVar	rs794727030
Map	rs794727030
PheGenI	rs794727030
Biobank	rs794727030
1000 genomes	rs794727030
hgdp	rs794727030
ensembl	rs794727030
geneview	rs794727030
scholar	rs794727030
google	rs794727030
pharmgkb	rs794727030
gwascentral	rs794727030
openSNP	rs794727030
23andMe	rs794727030
SNPshot	rs794727030
SNPdbe	rs794727030
MSV3d	rs794727030
GWAS Ctlg	rs794727030

Max Magnitude

0

ClinVar
Risk	rs794727030(G;G)
Alt	rs794727030(G;G)
Reference	Rs794727030(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.32662432T>C
CLNSRC
CLNACC	RCV000174087.1, RCV000174088.1,