rs1057524825

Orientation

minus

Stabilized

minus

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

Make rs1057524825(G;T)

Make rs1057524825(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32342150

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1057524825
dbSNP (classic)	rs1057524825
ClinGen	rs1057524825
ebi	rs1057524825
HLI	rs1057524825
Exac	rs1057524825
Gnomad	rs1057524825
Varsome	rs1057524825
LitVar	rs1057524825
Map	rs1057524825
PheGenI	rs1057524825
Biobank	rs1057524825
1000 genomes	rs1057524825
hgdp	rs1057524825
ensembl	rs1057524825
geneview	rs1057524825
scholar	rs1057524825
google	rs1057524825
pharmgkb	rs1057524825
gwascentral	rs1057524825
openSNP	rs1057524825
23andMe	rs1057524825
SNPshot	rs1057524825
SNPdbe	rs1057524825
MSV3d	rs1057524825
GWAS Ctlg	rs1057524825

Max Magnitude

0

ClinVar
Risk	rs1057524825(T;T)
Alt	rs1057524825(T;T)
Reference	Rs1057524825(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DMD
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.32360267C>A
CLNSRC
CLNACC	RCV000431150.1,