rs1060502634

Orientation

minus

Stabilized

minus

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

Make rs1060502634(A;A)

Make rs1060502634(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32644963

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502634
dbSNP (classic)	rs1060502634
ClinGen	rs1060502634
ebi	rs1060502634
HLI	rs1060502634
Exac	rs1060502634
Gnomad	rs1060502634
Varsome	rs1060502634
LitVar	rs1060502634
Map	rs1060502634
PheGenI	rs1060502634
Biobank	rs1060502634
1000 genomes	rs1060502634
hgdp	rs1060502634
ensembl	rs1060502634
geneview	rs1060502634
scholar	rs1060502634
google	rs1060502634
pharmgkb	rs1060502634
gwascentral	rs1060502634
openSNP	rs1060502634
23andMe	rs1060502634
SNPshot	rs1060502634
SNPdbe	rs1060502634
MSV3d	rs1060502634
GWAS Ctlg	rs1060502634

Max Magnitude

0

ClinVar
Risk	rs1060502634(A;A)
Alt	rs1060502634(A;A)
Reference	Rs1060502634(G;G)
Significance	Probable-Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32663080C>T
CLNSRC
CLNACC	RCV000458031.1,