rs1060502648

Orientation

minus

Stabilized

minus

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

Make rs1060502648(-;-)

Make rs1060502648(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31209627

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502648
dbSNP (classic)	rs1060502648
ClinGen	rs1060502648
ebi	rs1060502648
HLI	rs1060502648
Exac	rs1060502648
Gnomad	rs1060502648
Varsome	rs1060502648
LitVar	rs1060502648
Map	rs1060502648
PheGenI	rs1060502648
Biobank	rs1060502648
1000 genomes	rs1060502648
hgdp	rs1060502648
ensembl	rs1060502648
geneview	rs1060502648
scholar	rs1060502648
google	rs1060502648
pharmgkb	rs1060502648
gwascentral	rs1060502648
openSNP	rs1060502648
23andMe	rs1060502648
SNPshot	rs1060502648
SNPdbe	rs1060502648
MSV3d	rs1060502648
GWAS Ctlg	rs1060502648

Max Magnitude

0

ClinVar
Risk	rs1060502648(-;-)
Alt	rs1060502648(-;-)
Reference	Rs1060502648(T;T)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31227744delA
CLNSRC
CLNACC	RCV000457661.1,