rs1057524291

Orientation

minus

Stabilized

minus

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

Make rs1057524291(C;T)

Make rs1057524291(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32411763

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1057524291
dbSNP (classic)	rs1057524291
ClinGen	rs1057524291
ebi	rs1057524291
HLI	rs1057524291
Exac	rs1057524291
Gnomad	rs1057524291
Varsome	rs1057524291
LitVar	rs1057524291
Map	rs1057524291
PheGenI	rs1057524291
Biobank	rs1057524291
1000 genomes	rs1057524291
hgdp	rs1057524291
ensembl	rs1057524291
geneview	rs1057524291
scholar	rs1057524291
google	rs1057524291
pharmgkb	rs1057524291
gwascentral	rs1057524291
openSNP	rs1057524291
23andMe	rs1057524291
SNPshot	rs1057524291
SNPdbe	rs1057524291
MSV3d	rs1057524291
GWAS Ctlg	rs1057524291

Max Magnitude

0

ClinVar
Risk	rs1057524291(T;T)
Alt	rs1057524291(T;T)
Reference	Rs1057524291(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DMD
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.32429880G>A
CLNSRC
CLNACC	RCV000430460.1,