rs1060502626

Orientation

minus

Stabilized

minus

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

Make rs1060502626(A;A)

Make rs1060502626(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31147274

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502626
dbSNP (classic)	rs1060502626
ClinGen	rs1060502626
ebi	rs1060502626
HLI	rs1060502626
Exac	rs1060502626
Gnomad	rs1060502626
Varsome	rs1060502626
LitVar	rs1060502626
Map	rs1060502626
PheGenI	rs1060502626
Biobank	rs1060502626
1000 genomes	rs1060502626
hgdp	rs1060502626
ensembl	rs1060502626
geneview	rs1060502626
scholar	rs1060502626
google	rs1060502626
pharmgkb	rs1060502626
gwascentral	rs1060502626
openSNP	rs1060502626
23andMe	rs1060502626
SNPshot	rs1060502626
SNPdbe	rs1060502626
MSV3d	rs1060502626
GWAS Ctlg	rs1060502626

Max Magnitude

0

ClinVar
Risk	rs1060502626(A;A)
Alt	rs1060502626(A;A)
Reference	Rs1060502626(G;G)
Significance	Probable-Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31165391C>T
CLNSRC
CLNACC	RCV000464915.1,