rs863225004

Orientation

minus

Stabilized

minus

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

Make rs863225004(C;T)

Make rs863225004(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32343232

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863225004
dbSNP (classic)	rs863225004
ClinGen	rs863225004
ebi	rs863225004
HLI	rs863225004
Exac	rs863225004
Gnomad	rs863225004
Varsome	rs863225004
LitVar	rs863225004
Map	rs863225004
PheGenI	rs863225004
Biobank	rs863225004
1000 genomes	rs863225004
hgdp	rs863225004
ensembl	rs863225004
geneview	rs863225004
scholar	rs863225004
google	rs863225004
pharmgkb	rs863225004
gwascentral	rs863225004
openSNP	rs863225004
23andMe	rs863225004
SNPshot	rs863225004
SNPdbe	rs863225004
MSV3d	rs863225004
GWAS Ctlg	rs863225004

Max Magnitude

0

ClinVar
Risk	rs863225004(T;T)
Alt	rs863225004(T;T)
Reference	Rs863225004(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32361349G>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201117.1,