rs1060502656

Orientation

minus

Stabilized

minus

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

Make rs1060502656(A;A)

Make rs1060502656(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32287702

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502656
dbSNP (classic)	rs1060502656
ClinGen	rs1060502656
ebi	rs1060502656
HLI	rs1060502656
Exac	rs1060502656
Gnomad	rs1060502656
Varsome	rs1060502656
LitVar	rs1060502656
Map	rs1060502656
PheGenI	rs1060502656
Biobank	rs1060502656
1000 genomes	rs1060502656
hgdp	rs1060502656
ensembl	rs1060502656
geneview	rs1060502656
scholar	rs1060502656
google	rs1060502656
pharmgkb	rs1060502656
gwascentral	rs1060502656
openSNP	rs1060502656
23andMe	rs1060502656
SNPshot	rs1060502656
SNPdbe	rs1060502656
MSV3d	rs1060502656
GWAS Ctlg	rs1060502656

Max Magnitude

0

ClinVar
Risk	rs1060502656(A;A)
Alt	rs1060502656(A;A)
Reference	Rs1060502656(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32305819C>T
CLNSRC
CLNACC	RCV000469689.1,