rs863224998

Orientation

minus

Stabilized

minus

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

Make rs863224998(G;T)

Make rs863224998(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32386378

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224998
dbSNP (classic)	rs863224998
ClinGen	rs863224998
ebi	rs863224998
HLI	rs863224998
Exac	rs863224998
Gnomad	rs863224998
Varsome	rs863224998
LitVar	rs863224998
Map	rs863224998
PheGenI	rs863224998
Biobank	rs863224998
1000 genomes	rs863224998
hgdp	rs863224998
ensembl	rs863224998
geneview	rs863224998
scholar	rs863224998
google	rs863224998
pharmgkb	rs863224998
gwascentral	rs863224998
openSNP	rs863224998
23andMe	rs863224998
SNPshot	rs863224998
SNPdbe	rs863224998
MSV3d	rs863224998
GWAS Ctlg	rs863224998

Max Magnitude

0

ClinVar
Risk	rs863224998(T;T)
Alt	rs863224998(T;T)
Reference	Rs863224998(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32404495C>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201102.1,