rs794727567

Orientation

minus

Stabilized

minus

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

Make rs794727567(-;-)

Make rs794727567(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32386461

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs794727567
dbSNP (classic)	rs794727567
ClinGen	rs794727567
ebi	rs794727567
HLI	rs794727567
Exac	rs794727567
Gnomad	rs794727567
Varsome	rs794727567
LitVar	rs794727567
Map	rs794727567
PheGenI	rs794727567
Biobank	rs794727567
1000 genomes	rs794727567
hgdp	rs794727567
ensembl	rs794727567
geneview	rs794727567
scholar	rs794727567
google	rs794727567
pharmgkb	rs794727567
gwascentral	rs794727567
openSNP	rs794727567
23andMe	rs794727567
SNPshot	rs794727567
SNPdbe	rs794727567
MSV3d	rs794727567
GWAS Ctlg	rs794727567

Max Magnitude

0

ClinVar
Risk	rs794727567(-;-)
Alt	rs794727567(-;-)
Reference	Rs794727567(T;T)
Significance	Pathogenic
Disease	Becker muscular dystrophy Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Becker muscular dystrophy Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32404578delA
CLNSRC
CLNACC	RCV000177739.1, RCV000177740.1,