rs863224976

Orientation

minus

Stabilized

minus

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

Make rs863224976(G;G)

Make rs863224976(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

31169584

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224976
dbSNP (classic)	rs863224976
ClinGen	rs863224976
ebi	rs863224976
HLI	rs863224976
Exac	rs863224976
Gnomad	rs863224976
Varsome	rs863224976
LitVar	rs863224976
Map	rs863224976
PheGenI	rs863224976
Biobank	rs863224976
1000 genomes	rs863224976
hgdp	rs863224976
ensembl	rs863224976
geneview	rs863224976
scholar	rs863224976
google	rs863224976
pharmgkb	rs863224976
gwascentral	rs863224976
openSNP	rs863224976
23andMe	rs863224976
SNPshot	rs863224976
SNPdbe	rs863224976
MSV3d	rs863224976
GWAS Ctlg	rs863224976

Max Magnitude

0

ClinVar
Risk	rs863224976(G;G)
Alt	rs863224976(G;G)
Reference	Rs863224976(T;T)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31187701A>C
CLNSRC	Quest Diagnostics
CLNACC	RCV000201187.1,