rs128626233

Orientation

minus

Stabilized

minus

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

Make rs128626233(C;T)

Make rs128626233(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32849736

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs128626233
dbSNP (classic)	rs128626233
ClinGen	rs128626233
ebi	rs128626233
HLI	rs128626233
Exac	rs128626233
Gnomad	rs128626233
Varsome	rs128626233
LitVar	rs128626233
Map	rs128626233
PheGenI	rs128626233
Biobank	rs128626233
1000 genomes	rs128626233
hgdp	rs128626233
ensembl	rs128626233
geneview	rs128626233
scholar	rs128626233
google	rs128626233
pharmgkb	rs128626233
gwascentral	rs128626233
openSNP	rs128626233
23andMe	rs128626233
SNPshot	rs128626233
SNPdbe	rs128626233
MSV3d	rs128626233
GWAS Ctlg	rs128626233

Max Magnitude

0

OMIM	300377
Desc
Variant	0029
Related	also

ClinVar
Risk	rs128626233(T;T)
Alt	rs128626233(T;T)
Reference	Rs128626233(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32867853G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011990.11,