rs128626232

Orientation

minus

Stabilized

minus

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

Make rs128626232(C;T)

Make rs128626232(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32545310

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs128626232
dbSNP (classic)	rs128626232
ClinGen	rs128626232
ebi	rs128626232
HLI	rs128626232
Exac	rs128626232
Gnomad	rs128626232
Varsome	rs128626232
LitVar	rs128626232
Map	rs128626232
PheGenI	rs128626232
Biobank	rs128626232
1000 genomes	rs128626232
hgdp	rs128626232
ensembl	rs128626232
geneview	rs128626232
scholar	rs128626232
google	rs128626232
pharmgkb	rs128626232
gwascentral	rs128626232
openSNP	rs128626232
23andMe	rs128626232
SNPshot	rs128626232
SNPdbe	rs128626232
MSV3d	rs128626232
GWAS Ctlg	rs128626232

Max Magnitude

0

OMIM	300377
Desc
Variant	0023
Related	also

ClinVar
Risk	rs128626232(T;T)
Alt	rs128626232(T;T)
Reference	Rs128626232(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32563427G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011984.17,