rs727503830

Orientation

minus

Stabilized

minus

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

Make rs727503830(A;T)

Make rs727503830(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32380549

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs727503830
dbSNP (classic)	rs727503830
ClinGen	rs727503830
ebi	rs727503830
HLI	rs727503830
Exac	rs727503830
Gnomad	rs727503830
Varsome	rs727503830
LitVar	rs727503830
Map	rs727503830
PheGenI	rs727503830
Biobank	rs727503830
1000 genomes	rs727503830
hgdp	rs727503830
ensembl	rs727503830
geneview	rs727503830
scholar	rs727503830
google	rs727503830
pharmgkb	rs727503830
gwascentral	rs727503830
openSNP	rs727503830
23andMe	rs727503830
SNPshot	rs727503830
SNPdbe	rs727503830
MSV3d	rs727503830
GWAS Ctlg	rs727503830

Max Magnitude

0

ClinVar
Risk	rs727503830(T;T)
Alt	rs727503830(T;T)
Reference	Rs727503830(A;A)
Significance	Pathogenic
Disease	not provided Duchenne muscular dystrophy Becker muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	not provided Duchenne muscular dystrophy Becker muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32398666T>A
CLNSRC
CLNACC	RCV000152893.2, RCV000177781.1, RCV000177782.1,