rs146071084

Orientation

plus

Stabilized

plus

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

Make rs146071084(A;T)

Make rs146071084(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32454660

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs146071084
dbSNP (classic)	rs146071084
ClinGen	rs146071084
ebi	rs146071084
HLI	rs146071084
Exac	rs146071084
Gnomad	rs146071084
Varsome	rs146071084
LitVar	rs146071084
Map	rs146071084
PheGenI	rs146071084
Biobank	rs146071084
1000 genomes	rs146071084
hgdp	rs146071084
ensembl	rs146071084
geneview	rs146071084
scholar	rs146071084
google	rs146071084
pharmgkb	rs146071084
gwascentral	rs146071084
openSNP	rs146071084
23andMe	rs146071084
SNPshot	rs146071084
SNPdbe	rs146071084
MSV3d	rs146071084
GWAS Ctlg	rs146071084

Max Magnitude

0

ClinVar
Risk	rs146071084(T;T)
Alt	rs146071084(T;T)
Reference	Rs146071084(A;A)
Significance	Pathogenic
Disease	not provided Duchenne muscular dystrophy Becker muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	not provided Duchenne muscular dystrophy Becker muscular dystrophy
Reversed	0
HGVS	NC_000023.10:g.32472777A>T
CLNSRC
CLNACC	RCV000080587.3, RCV000176660.2, RCV000176661.2,