rs886044495

Orientation

plus

Stabilized

plus

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

Chromosome

X

Position

33020134

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs886044495
dbSNP (classic)	rs886044495
ClinGen	rs886044495
ebi	rs886044495
HLI	rs886044495
Exac	rs886044495
Gnomad	rs886044495
Varsome	rs886044495
LitVar	rs886044495
Map	rs886044495
PheGenI	rs886044495
Biobank	rs886044495
1000 genomes	rs886044495
hgdp	rs886044495
ensembl	rs886044495
geneview	rs886044495
scholar	rs886044495
google	rs886044495
pharmgkb	rs886044495
gwascentral	rs886044495
openSNP	rs886044495
23andMe	rs886044495
SNPshot	rs886044495
SNPdbe	rs886044495
MSV3d	rs886044495
GWAS Ctlg	rs886044495

Max Magnitude

0

ClinVar
Risk	rs886044495(-;-)
Alt	rs886044495(-;-)
Reference	Rs886044495(CTTAC;CTTAC)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	0
HGVS	NC_000023.10:g.33038251_33038255delCTTAC
CLNSRC
CLNACC	RCV000312151.1,