rs863224983

Orientation

minus

Stabilized

minus

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

Make rs863224983(C;T)

Make rs863224983(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32573786

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224983
dbSNP (classic)	rs863224983
ClinGen	rs863224983
ebi	rs863224983
HLI	rs863224983
Exac	rs863224983
Gnomad	rs863224983
Varsome	rs863224983
LitVar	rs863224983
Map	rs863224983
PheGenI	rs863224983
Biobank	rs863224983
1000 genomes	rs863224983
hgdp	rs863224983
ensembl	rs863224983
geneview	rs863224983
scholar	rs863224983
google	rs863224983
pharmgkb	rs863224983
gwascentral	rs863224983
openSNP	rs863224983
23andMe	rs863224983
SNPshot	rs863224983
SNPdbe	rs863224983
MSV3d	rs863224983
GWAS Ctlg	rs863224983

Max Magnitude

0

ClinVar
Risk	rs863224983(T;T)
Alt	rs863224983(T;T)
Reference	Rs863224983(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32591903G>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201018.1,