rs863225012

Orientation

minus

Stabilized

minus

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

Make rs863225012(A;A)

Make rs863225012(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

31507314

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863225012
dbSNP (classic)	rs863225012
ClinGen	rs863225012
ebi	rs863225012
HLI	rs863225012
Exac	rs863225012
Gnomad	rs863225012
Varsome	rs863225012
LitVar	rs863225012
Map	rs863225012
PheGenI	rs863225012
Biobank	rs863225012
1000 genomes	rs863225012
hgdp	rs863225012
ensembl	rs863225012
geneview	rs863225012
scholar	rs863225012
google	rs863225012
pharmgkb	rs863225012
gwascentral	rs863225012
openSNP	rs863225012
23andMe	rs863225012
SNPshot	rs863225012
SNPdbe	rs863225012
MSV3d	rs863225012
GWAS Ctlg	rs863225012

Max Magnitude

0

ClinVar
Risk	rs863225012(A;A)
Alt	rs863225012(A;A)
Reference	Rs863225012(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31525431C>T
CLNSRC	Quest Diagnostics
CLNACC	RCV000201027.1,