rs1060502615

Orientation

minus

Stabilized

minus

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

Make rs1060502615(A;T)

Make rs1060502615(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32454659

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502615
dbSNP (classic)	rs1060502615
ClinGen	rs1060502615
ebi	rs1060502615
HLI	rs1060502615
Exac	rs1060502615
Gnomad	rs1060502615
Varsome	rs1060502615
LitVar	rs1060502615
Map	rs1060502615
PheGenI	rs1060502615
Biobank	rs1060502615
1000 genomes	rs1060502615
hgdp	rs1060502615
ensembl	rs1060502615
geneview	rs1060502615
scholar	rs1060502615
google	rs1060502615
pharmgkb	rs1060502615
gwascentral	rs1060502615
openSNP	rs1060502615
23andMe	rs1060502615
SNPshot	rs1060502615
SNPdbe	rs1060502615
MSV3d	rs1060502615
GWAS Ctlg	rs1060502615

Max Magnitude

0

ClinVar
Risk	rs1060502615(T;T)
Alt	rs1060502615(T;T)
Reference	Rs1060502615(A;A)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32472776T>A
CLNSRC
CLNACC	RCV000473410.1,