rs1057518207

Orientation

minus

Stabilized

minus

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

Make rs1057518207(A;A)

Make rs1057518207(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32545158

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1057518207
dbSNP (classic)	rs1057518207
ClinGen	rs1057518207
ebi	rs1057518207
HLI	rs1057518207
Exac	rs1057518207
Gnomad	rs1057518207
Varsome	rs1057518207
LitVar	rs1057518207
Map	rs1057518207
PheGenI	rs1057518207
Biobank	rs1057518207
1000 genomes	rs1057518207
hgdp	rs1057518207
ensembl	rs1057518207
geneview	rs1057518207
scholar	rs1057518207
google	rs1057518207
pharmgkb	rs1057518207
gwascentral	rs1057518207
openSNP	rs1057518207
23andMe	rs1057518207
SNPshot	rs1057518207
SNPdbe	rs1057518207
MSV3d	rs1057518207
GWAS Ctlg	rs1057518207

Max Magnitude

0

ClinVar
Risk	rs1057518207(A;A)
Alt	rs1057518207(A;A)
Reference	Rs1057518207(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DMD
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.32563275C>T
CLNSRC
CLNACC	RCV000414740.1,