rs1057524037

Orientation

minus

Stabilized

minus

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

Make rs1057524037(C;C)

Make rs1057524037(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

31206610

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1057524037
dbSNP (classic)	rs1057524037
ClinGen	rs1057524037
ebi	rs1057524037
HLI	rs1057524037
Exac	rs1057524037
Gnomad	rs1057524037
Varsome	rs1057524037
LitVar	rs1057524037
Map	rs1057524037
PheGenI	rs1057524037
Biobank	rs1057524037
1000 genomes	rs1057524037
hgdp	rs1057524037
ensembl	rs1057524037
geneview	rs1057524037
scholar	rs1057524037
google	rs1057524037
pharmgkb	rs1057524037
gwascentral	rs1057524037
openSNP	rs1057524037
23andMe	rs1057524037
SNPshot	rs1057524037
SNPdbe	rs1057524037
MSV3d	rs1057524037
GWAS Ctlg	rs1057524037

Max Magnitude

0

ClinVar
Risk	rs1057524037(A;A) rs1057524037(C;C)
Alt	rs1057524037(A;A) rs1057524037(C;C)
Reference	Rs1057524037(T;T)
Significance	Pathogenic
Disease	not specified Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	not specified Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31224727A>G; NC_000023.10:g.31224727A>T
CLNSRC
CLNACC	RCV000436463.1, RCV000456408.1,