rs1060502647

Orientation

minus

Stabilized

minus

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

Make rs1060502647(-;-)

Make rs1060502647(-;AC)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32364635

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502647
dbSNP (classic)	rs1060502647
ClinGen	rs1060502647
ebi	rs1060502647
HLI	rs1060502647
Exac	rs1060502647
Gnomad	rs1060502647
Varsome	rs1060502647
LitVar	rs1060502647
Map	rs1060502647
PheGenI	rs1060502647
Biobank	rs1060502647
1000 genomes	rs1060502647
hgdp	rs1060502647
ensembl	rs1060502647
geneview	rs1060502647
scholar	rs1060502647
google	rs1060502647
pharmgkb	rs1060502647
gwascentral	rs1060502647
openSNP	rs1060502647
23andMe	rs1060502647
SNPshot	rs1060502647
SNPdbe	rs1060502647
MSV3d	rs1060502647
GWAS Ctlg	rs1060502647

Max Magnitude

0

ClinVar
Risk	rs1060502647(-;-)
Alt	rs1060502647(-;-)
Reference	Rs1060502647(AC;AC)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32382752_32382753delGT
CLNSRC
CLNACC	RCV000473975.1,