rs794727322

Orientation

minus

Stabilized

minus

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

Make rs794727322(-;-)

Make rs794727322(-;AA)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32491297

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs794727322
dbSNP (classic)	rs794727322
ClinGen	rs794727322
ebi	rs794727322
HLI	rs794727322
Exac	rs794727322
Gnomad	rs794727322
Varsome	rs794727322
LitVar	rs794727322
Map	rs794727322
PheGenI	rs794727322
Biobank	rs794727322
1000 genomes	rs794727322
hgdp	rs794727322
ensembl	rs794727322
geneview	rs794727322
scholar	rs794727322
google	rs794727322
pharmgkb	rs794727322
gwascentral	rs794727322
openSNP	rs794727322
23andMe	rs794727322
SNPshot	rs794727322
SNPdbe	rs794727322
MSV3d	rs794727322
GWAS Ctlg	rs794727322

Max Magnitude

0

ClinVar
Risk	rs794727322(-;-)
Alt	rs794727322(-;-)
Reference	Rs794727322(AA;AA)
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.32509414_32509415delTT
CLNSRC
CLNACC	RCV000176068.1, RCV000176069.1,