rs863224982

Orientation

minus

Stabilized

minus

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

Make rs863224982(C;C)

Make rs863224982(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32595877

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224982
dbSNP (classic)	rs863224982
ClinGen	rs863224982
ebi	rs863224982
HLI	rs863224982
Exac	rs863224982
Gnomad	rs863224982
Varsome	rs863224982
LitVar	rs863224982
Map	rs863224982
PheGenI	rs863224982
Biobank	rs863224982
1000 genomes	rs863224982
hgdp	rs863224982
ensembl	rs863224982
geneview	rs863224982
scholar	rs863224982
google	rs863224982
pharmgkb	rs863224982
gwascentral	rs863224982
openSNP	rs863224982
23andMe	rs863224982
SNPshot	rs863224982
SNPdbe	rs863224982
MSV3d	rs863224982
GWAS Ctlg	rs863224982

Max Magnitude

0

ClinVar
Risk	rs863224982(C;C)
Alt	rs863224982(C;C)
Reference	Rs863224982(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32613994C>G
CLNSRC	Quest Diagnostics
CLNACC	RCV000201056.1,