rs1060502636

Orientation

minus

Stabilized

minus

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

Make rs1060502636(A;A)

Make rs1060502636(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32518098

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502636
dbSNP (classic)	rs1060502636
ClinGen	rs1060502636
ebi	rs1060502636
HLI	rs1060502636
Exac	rs1060502636
Gnomad	rs1060502636
Varsome	rs1060502636
LitVar	rs1060502636
Map	rs1060502636
PheGenI	rs1060502636
Biobank	rs1060502636
1000 genomes	rs1060502636
hgdp	rs1060502636
ensembl	rs1060502636
geneview	rs1060502636
scholar	rs1060502636
google	rs1060502636
pharmgkb	rs1060502636
gwascentral	rs1060502636
openSNP	rs1060502636
23andMe	rs1060502636
SNPshot	rs1060502636
SNPdbe	rs1060502636
MSV3d	rs1060502636
GWAS Ctlg	rs1060502636

Max Magnitude

0

ClinVar
Risk	rs1060502636(A;A)
Alt	rs1060502636(A;A)
Reference	Rs1060502636(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32536215C>T
CLNSRC
CLNACC	RCV000458271.1,