rs1060502621

Orientation

minus

Stabilized

minus

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

Make rs1060502621(C;T)

Make rs1060502621(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31627681

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502621
dbSNP (classic)	rs1060502621
ClinGen	rs1060502621
ebi	rs1060502621
HLI	rs1060502621
Exac	rs1060502621
Gnomad	rs1060502621
Varsome	rs1060502621
LitVar	rs1060502621
Map	rs1060502621
PheGenI	rs1060502621
Biobank	rs1060502621
1000 genomes	rs1060502621
hgdp	rs1060502621
ensembl	rs1060502621
geneview	rs1060502621
scholar	rs1060502621
google	rs1060502621
pharmgkb	rs1060502621
gwascentral	rs1060502621
openSNP	rs1060502621
23andMe	rs1060502621
SNPshot	rs1060502621
SNPdbe	rs1060502621
MSV3d	rs1060502621
GWAS Ctlg	rs1060502621

Max Magnitude

0

ClinVar
Risk	rs1060502621(T;T)
Alt	rs1060502621(T;T)
Reference	Rs1060502621(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31645798G>A
CLNSRC
CLNACC	RCV000477000.1,