rs1060502653

Orientation

minus

Stabilized

minus

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

Make rs1060502653(-;-)

Make rs1060502653(-;GTAGACCTTT)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31204113

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502653
dbSNP (classic)	rs1060502653
ClinGen	rs1060502653
ebi	rs1060502653
HLI	rs1060502653
Exac	rs1060502653
Gnomad	rs1060502653
Varsome	rs1060502653
LitVar	rs1060502653
Map	rs1060502653
PheGenI	rs1060502653
Biobank	rs1060502653
1000 genomes	rs1060502653
hgdp	rs1060502653
ensembl	rs1060502653
geneview	rs1060502653
scholar	rs1060502653
google	rs1060502653
pharmgkb	rs1060502653
gwascentral	rs1060502653
openSNP	rs1060502653
23andMe	rs1060502653
SNPshot	rs1060502653
SNPdbe	rs1060502653
MSV3d	rs1060502653
GWAS Ctlg	rs1060502653

Max Magnitude

0

ClinVar
Risk	rs1060502653(-;-)
Alt	rs1060502653(-;-)
Reference	Rs1060502653(GTAGACCTTT;GTAGACCTTT)
Significance	Probable-Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31222230_31222239delAAAGGTCTAC
CLNSRC
CLNACC	RCV000467852.1,