rs1057519180

Orientation

minus

Stabilized

minus

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

Make rs1057519180(-;G)

Make rs1057519180(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

33020152

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1057519180
dbSNP (classic)	rs1057519180
ClinGen	rs1057519180
ebi	rs1057519180
HLI	rs1057519180
Exac	rs1057519180
Gnomad	rs1057519180
Varsome	rs1057519180
LitVar	rs1057519180
Map	rs1057519180
PheGenI	rs1057519180
Biobank	rs1057519180
1000 genomes	rs1057519180
hgdp	rs1057519180
ensembl	rs1057519180
geneview	rs1057519180
scholar	rs1057519180
google	rs1057519180
pharmgkb	rs1057519180
gwascentral	rs1057519180
openSNP	rs1057519180
23andMe	rs1057519180
SNPshot	rs1057519180
SNPdbe	rs1057519180
MSV3d	rs1057519180
GWAS Ctlg	rs1057519180

Max Magnitude

0

ClinVar
Risk	rs1057519180(G;G)
Alt	rs1057519180(G;G)
Reference	Rs1057519180(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DMD
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.33038270dupC
CLNSRC
CLNACC	RCV000415825.1,