rs1060502632

Orientation

minus

Stabilized

minus

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

Make rs1060502632(-;-)

Make rs1060502632(-;AGGA)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32365108

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502632
dbSNP (classic)	rs1060502632
ClinGen	rs1060502632
ebi	rs1060502632
HLI	rs1060502632
Exac	rs1060502632
Gnomad	rs1060502632
Varsome	rs1060502632
LitVar	rs1060502632
Map	rs1060502632
PheGenI	rs1060502632
Biobank	rs1060502632
1000 genomes	rs1060502632
hgdp	rs1060502632
ensembl	rs1060502632
geneview	rs1060502632
scholar	rs1060502632
google	rs1060502632
pharmgkb	rs1060502632
gwascentral	rs1060502632
openSNP	rs1060502632
23andMe	rs1060502632
SNPshot	rs1060502632
SNPdbe	rs1060502632
MSV3d	rs1060502632
GWAS Ctlg	rs1060502632

Max Magnitude

0

ClinVar
Risk	rs1060502632(-;-)
Alt	rs1060502632(-;-)
Reference	Rs1060502632(AGGA;AGGA)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32383225_32383228delTCCT
CLNSRC
CLNACC	RCV000461657.1,