rs128626231

Orientation

minus

Stabilized

minus

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

Make rs128626231(G;G)

Make rs128626231(G;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32849753

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs128626231
dbSNP (classic)	rs128626231
ClinGen	rs128626231
ebi	rs128626231
HLI	rs128626231
Exac	rs128626231
Gnomad	rs128626231
Varsome	rs128626231
LitVar	rs128626231
Map	rs128626231
PheGenI	rs128626231
Biobank	rs128626231
1000 genomes	rs128626231
hgdp	rs128626231
ensembl	rs128626231
geneview	rs128626231
scholar	rs128626231
google	rs128626231
pharmgkb	rs128626231
gwascentral	rs128626231
openSNP	rs128626231
23andMe	rs128626231
SNPshot	rs128626231
SNPdbe	rs128626231
MSV3d	rs128626231
GWAS Ctlg	rs128626231

Max Magnitude

0

OMIM	300377
Desc
Variant	0020
Related	also

ClinVar
Risk	rs128626231(G;G)
Alt	rs128626231(G;G)
Reference	Rs128626231(T;T)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32867870A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011979.11,