rs1060502641

Orientation

minus

Stabilized

minus

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

Make rs1060502641(C;C)

Make rs1060502641(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31968337

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502641
dbSNP (classic)	rs1060502641
ClinGen	rs1060502641
ebi	rs1060502641
HLI	rs1060502641
Exac	rs1060502641
Gnomad	rs1060502641
Varsome	rs1060502641
LitVar	rs1060502641
Map	rs1060502641
PheGenI	rs1060502641
Biobank	rs1060502641
1000 genomes	rs1060502641
hgdp	rs1060502641
ensembl	rs1060502641
geneview	rs1060502641
scholar	rs1060502641
google	rs1060502641
pharmgkb	rs1060502641
gwascentral	rs1060502641
openSNP	rs1060502641
23andMe	rs1060502641
SNPshot	rs1060502641
SNPdbe	rs1060502641
MSV3d	rs1060502641
GWAS Ctlg	rs1060502641

Max Magnitude

0

ClinVar
Risk	rs1060502641(C;C)
Alt	rs1060502641(C;C)
Reference	Rs1060502641(T;T)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31986454A>G
CLNSRC
CLNACC	RCV000473580.1,