rs1060502659

Orientation

minus

Stabilized

minus

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

Make rs1060502659(-;-)

Make rs1060502659(-;AC)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31875217

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502659
dbSNP (classic)	rs1060502659
ClinGen	rs1060502659
ebi	rs1060502659
HLI	rs1060502659
Exac	rs1060502659
Gnomad	rs1060502659
Varsome	rs1060502659
LitVar	rs1060502659
Map	rs1060502659
PheGenI	rs1060502659
Biobank	rs1060502659
1000 genomes	rs1060502659
hgdp	rs1060502659
ensembl	rs1060502659
geneview	rs1060502659
scholar	rs1060502659
google	rs1060502659
pharmgkb	rs1060502659
gwascentral	rs1060502659
openSNP	rs1060502659
23andMe	rs1060502659
SNPshot	rs1060502659
SNPdbe	rs1060502659
MSV3d	rs1060502659
GWAS Ctlg	rs1060502659

Max Magnitude

0

ClinVar
Risk	rs1060502659(-;-)
Alt	rs1060502659(-;-)
Reference	Rs1060502659(AC;AC)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31893334_31893335delGT
CLNSRC
CLNACC	RCV000456686.1,