rs863225001

Orientation

minus

Stabilized

minus

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

Make rs863225001(C;T)

Make rs863225001(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32364605

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863225001
dbSNP (classic)	rs863225001
ClinGen	rs863225001
ebi	rs863225001
HLI	rs863225001
Exac	rs863225001
Gnomad	rs863225001
Varsome	rs863225001
LitVar	rs863225001
Map	rs863225001
PheGenI	rs863225001
Biobank	rs863225001
1000 genomes	rs863225001
hgdp	rs863225001
ensembl	rs863225001
geneview	rs863225001
scholar	rs863225001
google	rs863225001
pharmgkb	rs863225001
gwascentral	rs863225001
openSNP	rs863225001
23andMe	rs863225001
SNPshot	rs863225001
SNPdbe	rs863225001
MSV3d	rs863225001
GWAS Ctlg	rs863225001

Max Magnitude

0

ClinVar
Risk	rs863225001(T;T)
Alt	rs863225001(T;T)
Reference	Rs863225001(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32382722G>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201095.1,