rs863224992

Orientation

minus

Stabilized

minus

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

Make rs863224992(C;G)

Make rs863224992(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32468669

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224992
dbSNP (classic)	rs863224992
ClinGen	rs863224992
ebi	rs863224992
HLI	rs863224992
Exac	rs863224992
Gnomad	rs863224992
Varsome	rs863224992
LitVar	rs863224992
Map	rs863224992
PheGenI	rs863224992
Biobank	rs863224992
1000 genomes	rs863224992
hgdp	rs863224992
ensembl	rs863224992
geneview	rs863224992
scholar	rs863224992
google	rs863224992
pharmgkb	rs863224992
gwascentral	rs863224992
openSNP	rs863224992
23andMe	rs863224992
SNPshot	rs863224992
SNPdbe	rs863224992
MSV3d	rs863224992
GWAS Ctlg	rs863224992

Max Magnitude

0

ClinVar
Risk	rs863224992(G;G)
Alt	rs863224992(G;G)
Reference	Rs863224992(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32486786G>C
CLNSRC	Quest Diagnostics
CLNACC	RCV000201111.1,