rs863224999

Orientation

minus

Stabilized

minus

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

Make rs863224999(C;T)

Make rs863224999(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32380626

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224999
dbSNP (classic)	rs863224999
ClinGen	rs863224999
ebi	rs863224999
HLI	rs863224999
Exac	rs863224999
Gnomad	rs863224999
Varsome	rs863224999
LitVar	rs863224999
Map	rs863224999
PheGenI	rs863224999
Biobank	rs863224999
1000 genomes	rs863224999
hgdp	rs863224999
ensembl	rs863224999
geneview	rs863224999
scholar	rs863224999
google	rs863224999
pharmgkb	rs863224999
gwascentral	rs863224999
openSNP	rs863224999
23andMe	rs863224999
SNPshot	rs863224999
SNPdbe	rs863224999
MSV3d	rs863224999
GWAS Ctlg	rs863224999

Max Magnitude

0

ClinVar
Risk	rs863224999(T;T)
Alt	rs863224999(T;T)
Reference	Rs863224999(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy not provided
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy not provided
Reversed	1
HGVS	NC_000023.10:g.32398743G>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201158.1, RCV000255348.1,