rs863225011

Orientation

minus

Stabilized

minus

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

Make rs863225011(C;T)

Make rs863225011(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

31627852

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863225011
dbSNP (classic)	rs863225011
ClinGen	rs863225011
ebi	rs863225011
HLI	rs863225011
Exac	rs863225011
Gnomad	rs863225011
Varsome	rs863225011
LitVar	rs863225011
Map	rs863225011
PheGenI	rs863225011
Biobank	rs863225011
1000 genomes	rs863225011
hgdp	rs863225011
ensembl	rs863225011
geneview	rs863225011
scholar	rs863225011
google	rs863225011
pharmgkb	rs863225011
gwascentral	rs863225011
openSNP	rs863225011
23andMe	rs863225011
SNPshot	rs863225011
SNPdbe	rs863225011
MSV3d	rs863225011
GWAS Ctlg	rs863225011

Max Magnitude

0

ClinVar
Risk	rs863225011(T;T)
Alt	rs863225011(T;T)
Reference	Rs863225011(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy Becker muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy Becker muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31645969G>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201174.2, RCV000348940.1,