rs267606770

Orientation

minus

Stabilized

minus

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

Make rs267606770(G;T)

Make rs267606770(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32501821

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs267606770
dbSNP (classic)	rs267606770
ClinGen	rs267606770
ebi	rs267606770
HLI	rs267606770
Exac	rs267606770
Gnomad	rs267606770
Varsome	rs267606770
LitVar	rs267606770
Map	rs267606770
PheGenI	rs267606770
Biobank	rs267606770
1000 genomes	rs267606770
hgdp	rs267606770
ensembl	rs267606770
geneview	rs267606770
scholar	rs267606770
google	rs267606770
pharmgkb	rs267606770
gwascentral	rs267606770
openSNP	rs267606770
23andMe	rs267606770
SNPshot	rs267606770
SNPdbe	rs267606770
MSV3d	rs267606770
GWAS Ctlg	rs267606770

Max Magnitude

0

ClinVar
Risk	rs267606770(T;T)
Alt	rs267606770(T;T)
Reference	Rs267606770(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32519938C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011975.17,