rs1060502633

Orientation

minus

Stabilized

minus

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

Make rs1060502633(C;T)

Make rs1060502633(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31478129

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502633
dbSNP (classic)	rs1060502633
ClinGen	rs1060502633
ebi	rs1060502633
HLI	rs1060502633
Exac	rs1060502633
Gnomad	rs1060502633
Varsome	rs1060502633
LitVar	rs1060502633
Map	rs1060502633
PheGenI	rs1060502633
Biobank	rs1060502633
1000 genomes	rs1060502633
hgdp	rs1060502633
ensembl	rs1060502633
geneview	rs1060502633
scholar	rs1060502633
google	rs1060502633
pharmgkb	rs1060502633
gwascentral	rs1060502633
openSNP	rs1060502633
23andMe	rs1060502633
SNPshot	rs1060502633
SNPdbe	rs1060502633
MSV3d	rs1060502633
GWAS Ctlg	rs1060502633

Max Magnitude

0

ClinVar
Risk	rs1060502633(T;T)
Alt	rs1060502633(T;T)
Reference	Rs1060502633(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31496246G>A
CLNSRC
CLNACC	RCV000470018.1,