rs1057518284

Orientation

minus

Stabilized

minus

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

Make rs1057518284(-;AG)

Make rs1057518284(AG;AG)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32463504

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1057518284
dbSNP (classic)	rs1057518284
ClinGen	rs1057518284
ebi	rs1057518284
HLI	rs1057518284
Exac	rs1057518284
Gnomad	rs1057518284
Varsome	rs1057518284
LitVar	rs1057518284
Map	rs1057518284
PheGenI	rs1057518284
Biobank	rs1057518284
1000 genomes	rs1057518284
hgdp	rs1057518284
ensembl	rs1057518284
geneview	rs1057518284
scholar	rs1057518284
google	rs1057518284
pharmgkb	rs1057518284
gwascentral	rs1057518284
openSNP	rs1057518284
23andMe	rs1057518284
SNPshot	rs1057518284
SNPdbe	rs1057518284
MSV3d	rs1057518284
GWAS Ctlg	rs1057518284

Max Magnitude

0

ClinVar
Risk	rs1057518284(AG;AG)
Alt	rs1057518284(AG;AG)
Reference	Rs1057518284(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DMD
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.32481622_32481623dupCT
CLNSRC
CLNACC	RCV000412908.1,