rs128625226

Orientation

minus

Stabilized

minus

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

Make rs128625226(G;T)

Make rs128625226(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32454796

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs128625226
dbSNP (classic)	rs128625226
ClinGen	rs128625226
ebi	rs128625226
HLI	rs128625226
Exac	rs128625226
Gnomad	rs128625226
Varsome	rs128625226
LitVar	rs128625226
Map	rs128625226
PheGenI	rs128625226
Biobank	rs128625226
1000 genomes	rs128625226
hgdp	rs128625226
ensembl	rs128625226
geneview	rs128625226
scholar	rs128625226
google	rs128625226
pharmgkb	rs128625226
gwascentral	rs128625226
openSNP	rs128625226
23andMe	rs128625226
SNPshot	rs128625226
SNPdbe	rs128625226
MSV3d	rs128625226
GWAS Ctlg	rs128625226

Max Magnitude

0

OMIM	300377
Desc
Variant	0001
Related	also

ClinVar
Risk	rs128625226(T;T)
Alt	rs128625226(T;T)
Reference	Rs128625226(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32472913C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011958.11,