rs756949497

Orientation

plus

Stabilized

plus

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

Make rs756949497(G;T)

Make rs756949497(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32484925

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs756949497
dbSNP (classic)	rs756949497
ClinGen	rs756949497
ebi	rs756949497
HLI	rs756949497
Exac	rs756949497
Gnomad	rs756949497
Varsome	rs756949497
LitVar	rs756949497
Map	rs756949497
PheGenI	rs756949497
Biobank	rs756949497
1000 genomes	rs756949497
hgdp	rs756949497
ensembl	rs756949497
geneview	rs756949497
scholar	rs756949497
google	rs756949497
pharmgkb	rs756949497
gwascentral	rs756949497
openSNP	rs756949497
23andMe	rs756949497
SNPshot	rs756949497
SNPdbe	rs756949497
MSV3d	rs756949497
GWAS Ctlg	rs756949497

Max Magnitude

0

ClinVar
Risk	rs756949497(A;A) rs756949497(T;T)
Alt	rs756949497(A;A) rs756949497(T;T)
Reference	Rs756949497(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	0
HGVS	NC_000023.10:g.32503042G>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201047.2,