rs128625227

Orientation

minus

Stabilized

minus

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

Make rs128625227(G;T)

Make rs128625227(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32484931

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs128625227
dbSNP (classic)	rs128625227
ClinGen	rs128625227
ebi	rs128625227
HLI	rs128625227
Exac	rs128625227
Gnomad	rs128625227
Varsome	rs128625227
LitVar	rs128625227
Map	rs128625227
PheGenI	rs128625227
Biobank	rs128625227
1000 genomes	rs128625227
hgdp	rs128625227
ensembl	rs128625227
geneview	rs128625227
scholar	rs128625227
google	rs128625227
pharmgkb	rs128625227
gwascentral	rs128625227
openSNP	rs128625227
23andMe	rs128625227
SNPshot	rs128625227
SNPdbe	rs128625227
MSV3d	rs128625227
GWAS Ctlg	rs128625227

Max Magnitude

0

OMIM	300377
Desc
Variant	0003
Related	also

ClinVar
Risk	rs128625227(T;T)
Alt	rs128625227(T;T)
Reference	Rs128625227(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32503048C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011960.9,