rs863224991

Orientation

minus

Stabilized

minus

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

Make rs863224991(-;T)

Make rs863224991(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32823369

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224991
dbSNP (classic)	rs863224991
ClinGen	rs863224991
ebi	rs863224991
HLI	rs863224991
Exac	rs863224991
Gnomad	rs863224991
Varsome	rs863224991
LitVar	rs863224991
Map	rs863224991
PheGenI	rs863224991
Biobank	rs863224991
1000 genomes	rs863224991
hgdp	rs863224991
ensembl	rs863224991
geneview	rs863224991
scholar	rs863224991
google	rs863224991
pharmgkb	rs863224991
gwascentral	rs863224991
openSNP	rs863224991
23andMe	rs863224991
SNPshot	rs863224991
SNPdbe	rs863224991
MSV3d	rs863224991
GWAS Ctlg	rs863224991

Max Magnitude

0

ClinVar
Risk	rs863224991(T;T)
Alt	rs863224991(T;T)
Reference	Rs863224991(-;-)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32841487dupA
CLNSRC	Quest Diagnostics
CLNACC	RCV000201042.1,