rs1060502661

Orientation

minus

Stabilized

minus

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

Make rs1060502661(C;T)

Make rs1060502661(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32545250

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502661
dbSNP (classic)	rs1060502661
ClinGen	rs1060502661
ebi	rs1060502661
HLI	rs1060502661
Exac	rs1060502661
Gnomad	rs1060502661
Varsome	rs1060502661
LitVar	rs1060502661
Map	rs1060502661
PheGenI	rs1060502661
Biobank	rs1060502661
1000 genomes	rs1060502661
hgdp	rs1060502661
ensembl	rs1060502661
geneview	rs1060502661
scholar	rs1060502661
google	rs1060502661
pharmgkb	rs1060502661
gwascentral	rs1060502661
openSNP	rs1060502661
23andMe	rs1060502661
SNPshot	rs1060502661
SNPdbe	rs1060502661
MSV3d	rs1060502661
GWAS Ctlg	rs1060502661

Max Magnitude

0

ClinVar
Risk	rs1060502661(T;T)
Alt	rs1060502661(T;T)
Reference	Rs1060502661(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32563367G>A
CLNSRC
CLNACC	RCV000466434.1,