rs1060502643

Orientation

minus

Stabilized

minus

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

Make rs1060502643(A;A)

Make rs1060502643(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32438240

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502643
dbSNP (classic)	rs1060502643
ClinGen	rs1060502643
ebi	rs1060502643
HLI	rs1060502643
Exac	rs1060502643
Gnomad	rs1060502643
Varsome	rs1060502643
LitVar	rs1060502643
Map	rs1060502643
PheGenI	rs1060502643
Biobank	rs1060502643
1000 genomes	rs1060502643
hgdp	rs1060502643
ensembl	rs1060502643
geneview	rs1060502643
scholar	rs1060502643
google	rs1060502643
pharmgkb	rs1060502643
gwascentral	rs1060502643
openSNP	rs1060502643
23andMe	rs1060502643
SNPshot	rs1060502643
SNPdbe	rs1060502643
MSV3d	rs1060502643
GWAS Ctlg	rs1060502643

Max Magnitude

0

ClinVar
Risk	rs1060502643(A;A)
Alt	rs1060502643(A;A)
Reference	Rs1060502643(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32456357C>T
CLNSRC
CLNACC	RCV000475286.1,