rs1060502620

Orientation

minus

Stabilized

minus

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

Make rs1060502620(-;-)

Make rs1060502620(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31932180

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502620
dbSNP (classic)	rs1060502620
ClinGen	rs1060502620
ebi	rs1060502620
HLI	rs1060502620
Exac	rs1060502620
Gnomad	rs1060502620
Varsome	rs1060502620
LitVar	rs1060502620
Map	rs1060502620
PheGenI	rs1060502620
Biobank	rs1060502620
1000 genomes	rs1060502620
hgdp	rs1060502620
ensembl	rs1060502620
geneview	rs1060502620
scholar	rs1060502620
google	rs1060502620
pharmgkb	rs1060502620
gwascentral	rs1060502620
openSNP	rs1060502620
23andMe	rs1060502620
SNPshot	rs1060502620
SNPdbe	rs1060502620
MSV3d	rs1060502620
GWAS Ctlg	rs1060502620

Max Magnitude

0

ClinVar
Risk	rs1060502620(-;-)
Alt	rs1060502620(-;-)
Reference	Rs1060502620(A;A)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31950297delT
CLNSRC
CLNACC	RCV000470659.1,