rs863224989

Orientation

minus

Stabilized

minus

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

Make rs863224989(A;G)

Make rs863224989(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32823389

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863224989
dbSNP (classic)	rs863224989
ClinGen	rs863224989
ebi	rs863224989
HLI	rs863224989
Exac	rs863224989
Gnomad	rs863224989
Varsome	rs863224989
LitVar	rs863224989
Map	rs863224989
PheGenI	rs863224989
Biobank	rs863224989
1000 genomes	rs863224989
hgdp	rs863224989
ensembl	rs863224989
geneview	rs863224989
scholar	rs863224989
google	rs863224989
pharmgkb	rs863224989
gwascentral	rs863224989
openSNP	rs863224989
23andMe	rs863224989
SNPshot	rs863224989
SNPdbe	rs863224989
MSV3d	rs863224989
GWAS Ctlg	rs863224989

Max Magnitude

0

ClinVar
Risk	rs863224989(G;G)
Alt	rs863224989(G;G)
Reference	Rs863224989(A;A)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32841506T>C
CLNSRC	Quest Diagnostics
CLNACC	RCV000201171.1,