rs863225008

Orientation

minus

Stabilized

minus

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

Make rs863225008(G;T)

Make rs863225008(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

31836813

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863225008
dbSNP (classic)	rs863225008
ClinGen	rs863225008
ebi	rs863225008
HLI	rs863225008
Exac	rs863225008
Gnomad	rs863225008
Varsome	rs863225008
LitVar	rs863225008
Map	rs863225008
PheGenI	rs863225008
Biobank	rs863225008
1000 genomes	rs863225008
hgdp	rs863225008
ensembl	rs863225008
geneview	rs863225008
scholar	rs863225008
google	rs863225008
pharmgkb	rs863225008
gwascentral	rs863225008
openSNP	rs863225008
23andMe	rs863225008
SNPshot	rs863225008
SNPdbe	rs863225008
MSV3d	rs863225008
GWAS Ctlg	rs863225008

Max Magnitude

0

ClinVar
Risk	rs863225008(T;T)
Alt	rs863225008(T;T)
Reference	Rs863225008(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31854930C>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201085.1,