rs863224979

Orientation

minus

Stabilized

minus

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

Make rs863224979(C;T)

Make rs863224979(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32644139

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224979
dbSNP (classic)	rs863224979
ClinGen	rs863224979
ebi	rs863224979
HLI	rs863224979
Exac	rs863224979
Gnomad	rs863224979
Varsome	rs863224979
LitVar	rs863224979
Map	rs863224979
PheGenI	rs863224979
Biobank	rs863224979
1000 genomes	rs863224979
hgdp	rs863224979
ensembl	rs863224979
geneview	rs863224979
scholar	rs863224979
google	rs863224979
pharmgkb	rs863224979
gwascentral	rs863224979
openSNP	rs863224979
23andMe	rs863224979
SNPshot	rs863224979
SNPdbe	rs863224979
MSV3d	rs863224979
GWAS Ctlg	rs863224979

Max Magnitude

0

ClinVar
Risk	rs863224979(T;T)
Alt	rs863224979(T;T)
Reference	Rs863224979(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32662256G>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201050.1,