rs1060502629

Orientation

minus

Stabilized

minus

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

Make rs1060502629(A;A)

Make rs1060502629(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32573796

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502629
dbSNP (classic)	rs1060502629
ClinGen	rs1060502629
ebi	rs1060502629
HLI	rs1060502629
Exac	rs1060502629
Gnomad	rs1060502629
Varsome	rs1060502629
LitVar	rs1060502629
Map	rs1060502629
PheGenI	rs1060502629
Biobank	rs1060502629
1000 genomes	rs1060502629
hgdp	rs1060502629
ensembl	rs1060502629
geneview	rs1060502629
scholar	rs1060502629
google	rs1060502629
pharmgkb	rs1060502629
gwascentral	rs1060502629
openSNP	rs1060502629
23andMe	rs1060502629
SNPshot	rs1060502629
SNPdbe	rs1060502629
MSV3d	rs1060502629
GWAS Ctlg	rs1060502629

Max Magnitude

0

ClinVar
Risk	rs1060502629(A;A)
Alt	rs1060502629(A;A)
Reference	Rs1060502629(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32591913C>T
CLNSRC
CLNACC	RCV000469346.1,