rs267606771

Orientation

minus

Stabilized

minus

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

Make rs267606771(G;T)

Make rs267606771(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32448611

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs267606771
dbSNP (classic)	rs267606771
ClinGen	rs267606771
ebi	rs267606771
HLI	rs267606771
Exac	rs267606771
Gnomad	rs267606771
Varsome	rs267606771
LitVar	rs267606771
Map	rs267606771
PheGenI	rs267606771
Biobank	rs267606771
1000 genomes	rs267606771
hgdp	rs267606771
ensembl	rs267606771
geneview	rs267606771
scholar	rs267606771
google	rs267606771
pharmgkb	rs267606771
gwascentral	rs267606771
openSNP	rs267606771
23andMe	rs267606771
SNPshot	rs267606771
SNPdbe	rs267606771
MSV3d	rs267606771
GWAS Ctlg	rs267606771

Max Magnitude

0

ClinVar
Risk	rs267606771(T;T)
Alt	rs267606771(T;T)
Reference	Rs267606771(G;G)
Significance	Pathogenic
Disease	Becker muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Becker muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32466728C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012031.17,