rs1060502645

Orientation

minus

Stabilized

minus

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

Make rs1060502645(G;T)

Make rs1060502645(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32365187

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502645
dbSNP (classic)	rs1060502645
ClinGen	rs1060502645
ebi	rs1060502645
HLI	rs1060502645
Exac	rs1060502645
Gnomad	rs1060502645
Varsome	rs1060502645
LitVar	rs1060502645
Map	rs1060502645
PheGenI	rs1060502645
Biobank	rs1060502645
1000 genomes	rs1060502645
hgdp	rs1060502645
ensembl	rs1060502645
geneview	rs1060502645
scholar	rs1060502645
google	rs1060502645
pharmgkb	rs1060502645
gwascentral	rs1060502645
openSNP	rs1060502645
23andMe	rs1060502645
SNPshot	rs1060502645
SNPdbe	rs1060502645
MSV3d	rs1060502645
GWAS Ctlg	rs1060502645

Max Magnitude

0

ClinVar
Risk	rs1060502645(T;T)
Alt	rs1060502645(T;T)
Reference	Rs1060502645(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32383304C>A
CLNSRC
CLNACC	RCV000463648.1,