rs1060502623

Orientation

minus

Stabilized

minus

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

Make rs1060502623(A;T)

Make rs1060502623(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32343226

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502623
dbSNP (classic)	rs1060502623
ClinGen	rs1060502623
ebi	rs1060502623
HLI	rs1060502623
Exac	rs1060502623
Gnomad	rs1060502623
Varsome	rs1060502623
LitVar	rs1060502623
Map	rs1060502623
PheGenI	rs1060502623
Biobank	rs1060502623
1000 genomes	rs1060502623
hgdp	rs1060502623
ensembl	rs1060502623
geneview	rs1060502623
scholar	rs1060502623
google	rs1060502623
pharmgkb	rs1060502623
gwascentral	rs1060502623
openSNP	rs1060502623
23andMe	rs1060502623
SNPshot	rs1060502623
SNPdbe	rs1060502623
MSV3d	rs1060502623
GWAS Ctlg	rs1060502623

Max Magnitude

0

ClinVar
Risk	rs1060502623(T;T)
Alt	rs1060502623(T;T)
Reference	Rs1060502623(A;A)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32361343T>A
CLNSRC
CLNACC	RCV000457870.1,