rs1057517960

Orientation

minus

Stabilized

minus

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

Make rs1057517960(A;A)

Make rs1057517960(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32595756

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1057517960
dbSNP (classic)	rs1057517960
ClinGen	rs1057517960
ebi	rs1057517960
HLI	rs1057517960
Exac	rs1057517960
Gnomad	rs1057517960
Varsome	rs1057517960
LitVar	rs1057517960
Map	rs1057517960
PheGenI	rs1057517960
Biobank	rs1057517960
1000 genomes	rs1057517960
hgdp	rs1057517960
ensembl	rs1057517960
geneview	rs1057517960
scholar	rs1057517960
google	rs1057517960
pharmgkb	rs1057517960
gwascentral	rs1057517960
openSNP	rs1057517960
23andMe	rs1057517960
SNPshot	rs1057517960
SNPdbe	rs1057517960
MSV3d	rs1057517960
GWAS Ctlg	rs1057517960

Max Magnitude

0

ClinVar
Risk	rs1057517960(A;A)
Alt	rs1057517960(A;A)
Reference	Rs1057517960(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DMD
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.32613873C>T
CLNSRC
CLNACC	RCV000413562.1,