rs1060502639

Orientation

minus

Stabilized

minus

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

Make rs1060502639(C;T)

Make rs1060502639(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32485057

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502639
dbSNP (classic)	rs1060502639
ClinGen	rs1060502639
ebi	rs1060502639
HLI	rs1060502639
Exac	rs1060502639
Gnomad	rs1060502639
Varsome	rs1060502639
LitVar	rs1060502639
Map	rs1060502639
PheGenI	rs1060502639
Biobank	rs1060502639
1000 genomes	rs1060502639
hgdp	rs1060502639
ensembl	rs1060502639
geneview	rs1060502639
scholar	rs1060502639
google	rs1060502639
pharmgkb	rs1060502639
gwascentral	rs1060502639
openSNP	rs1060502639
23andMe	rs1060502639
SNPshot	rs1060502639
SNPdbe	rs1060502639
MSV3d	rs1060502639
GWAS Ctlg	rs1060502639

Max Magnitude

0

ClinVar
Risk	rs1060502639(T;T)
Alt	rs1060502639(T;T)
Reference	Rs1060502639(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32503174G>A
CLNSRC
CLNACC	RCV000474172.1,