rs1060502627

Orientation

minus

Stabilized

minus

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

Make rs1060502627(A;A)

Make rs1060502627(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32518024

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502627
dbSNP (classic)	rs1060502627
ClinGen	rs1060502627
ebi	rs1060502627
HLI	rs1060502627
Exac	rs1060502627
Gnomad	rs1060502627
Varsome	rs1060502627
LitVar	rs1060502627
Map	rs1060502627
PheGenI	rs1060502627
Biobank	rs1060502627
1000 genomes	rs1060502627
hgdp	rs1060502627
ensembl	rs1060502627
geneview	rs1060502627
scholar	rs1060502627
google	rs1060502627
pharmgkb	rs1060502627
gwascentral	rs1060502627
openSNP	rs1060502627
23andMe	rs1060502627
SNPshot	rs1060502627
SNPdbe	rs1060502627
MSV3d	rs1060502627
GWAS Ctlg	rs1060502627

Max Magnitude

0

ClinVar
Risk	rs1060502627(A;A)
Alt	rs1060502627(A;A)
Reference	Rs1060502627(T;T)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32536141A>T
CLNSRC
CLNACC	RCV000472980.1,