rs863224980

Orientation

minus

Stabilized

minus

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

Make rs863224980(A;A)

Make rs863224980(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32644131

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224980
dbSNP (classic)	rs863224980
ClinGen	rs863224980
ebi	rs863224980
HLI	rs863224980
Exac	rs863224980
Gnomad	rs863224980
Varsome	rs863224980
LitVar	rs863224980
Map	rs863224980
PheGenI	rs863224980
Biobank	rs863224980
1000 genomes	rs863224980
hgdp	rs863224980
ensembl	rs863224980
geneview	rs863224980
scholar	rs863224980
google	rs863224980
pharmgkb	rs863224980
gwascentral	rs863224980
openSNP	rs863224980
23andMe	rs863224980
SNPshot	rs863224980
SNPdbe	rs863224980
MSV3d	rs863224980
GWAS Ctlg	rs863224980

Max Magnitude

0

ClinVar
Risk	rs863224980(A;A)
Alt	rs863224980(A;A)
Reference	Rs863224980(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32662248C>T
CLNSRC	Quest Diagnostics
CLNACC	RCV000201140.1,