rs1057520764

Orientation

minus

Stabilized

minus

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

Make rs1057520764(C;T)

Make rs1057520764(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32342264

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1057520764
dbSNP (classic)	rs1057520764
ClinGen	rs1057520764
ebi	rs1057520764
HLI	rs1057520764
Exac	rs1057520764
Gnomad	rs1057520764
Varsome	rs1057520764
LitVar	rs1057520764
Map	rs1057520764
PheGenI	rs1057520764
Biobank	rs1057520764
1000 genomes	rs1057520764
hgdp	rs1057520764
ensembl	rs1057520764
geneview	rs1057520764
scholar	rs1057520764
google	rs1057520764
pharmgkb	rs1057520764
gwascentral	rs1057520764
openSNP	rs1057520764
23andMe	rs1057520764
SNPshot	rs1057520764
SNPdbe	rs1057520764
MSV3d	rs1057520764
GWAS Ctlg	rs1057520764

Max Magnitude

0

ClinVar
Risk	rs1057520764(T;T)
Alt	rs1057520764(T;T)
Reference	Rs1057520764(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DMD
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.32360381G>A
CLNSRC
CLNACC	RCV000424485.1,