rs863225000

Orientation

minus

Stabilized

minus

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

Make rs863225000(-;-)

Make rs863225000(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32365127

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863225000
dbSNP (classic)	rs863225000
ClinGen	rs863225000
ebi	rs863225000
HLI	rs863225000
Exac	rs863225000
Gnomad	rs863225000
Varsome	rs863225000
LitVar	rs863225000
Map	rs863225000
PheGenI	rs863225000
Biobank	rs863225000
1000 genomes	rs863225000
hgdp	rs863225000
ensembl	rs863225000
geneview	rs863225000
scholar	rs863225000
google	rs863225000
pharmgkb	rs863225000
gwascentral	rs863225000
openSNP	rs863225000
23andMe	rs863225000
SNPshot	rs863225000
SNPdbe	rs863225000
MSV3d	rs863225000
GWAS Ctlg	rs863225000

Max Magnitude

0

ClinVar
Risk	rs863225000(-;-)
Alt	rs863225000(-;-)
Reference	Rs863225000(A;A)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32383244delT
CLNSRC	Quest Diagnostics
CLNACC	RCV000201034.1,