rs863224993

Orientation

minus

Stabilized

minus

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

Make rs863224993(C;T)

Make rs863224993(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32463444

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224993
dbSNP (classic)	rs863224993
ClinGen	rs863224993
ebi	rs863224993
HLI	rs863224993
Exac	rs863224993
Gnomad	rs863224993
Varsome	rs863224993
LitVar	rs863224993
Map	rs863224993
PheGenI	rs863224993
Biobank	rs863224993
1000 genomes	rs863224993
hgdp	rs863224993
ensembl	rs863224993
geneview	rs863224993
scholar	rs863224993
google	rs863224993
pharmgkb	rs863224993
gwascentral	rs863224993
openSNP	rs863224993
23andMe	rs863224993
SNPshot	rs863224993
SNPdbe	rs863224993
MSV3d	rs863224993
GWAS Ctlg	rs863224993

Max Magnitude

0

ClinVar
Risk	rs863224993(T;T)
Alt	rs863224993(T;T)
Reference	Rs863224993(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32481561G>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201074.1,