rs1060502637

Orientation

minus

Stabilized

minus

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

Make rs1060502637(G;T)

Make rs1060502637(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32411914

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502637
dbSNP (classic)	rs1060502637
ClinGen	rs1060502637
ebi	rs1060502637
HLI	rs1060502637
Exac	rs1060502637
Gnomad	rs1060502637
Varsome	rs1060502637
LitVar	rs1060502637
Map	rs1060502637
PheGenI	rs1060502637
Biobank	rs1060502637
1000 genomes	rs1060502637
hgdp	rs1060502637
ensembl	rs1060502637
geneview	rs1060502637
scholar	rs1060502637
google	rs1060502637
pharmgkb	rs1060502637
gwascentral	rs1060502637
openSNP	rs1060502637
23andMe	rs1060502637
SNPshot	rs1060502637
SNPdbe	rs1060502637
MSV3d	rs1060502637
GWAS Ctlg	rs1060502637

Max Magnitude

0

ClinVar
Risk	rs1060502637(T;T)
Alt	rs1060502637(T;T)
Reference	Rs1060502637(G;G)
Significance	Probable-Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32430031C>A
CLNSRC
CLNACC	RCV000465065.1,