rs398123952

Orientation

minus

Stabilized

minus

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

Make rs398123952(C;C)

Make rs398123952(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

X

Position

32816564

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123952
dbSNP (classic)	rs398123952
ClinGen	rs398123952
ebi	rs398123952
HLI	rs398123952
Exac	rs398123952
Gnomad	rs398123952
Varsome	rs398123952
LitVar	rs398123952
Map	rs398123952
PheGenI	rs398123952
Biobank	rs398123952
1000 genomes	rs398123952
hgdp	rs398123952
ensembl	rs398123952
geneview	rs398123952
scholar	rs398123952
google	rs398123952
pharmgkb	rs398123952
gwascentral	rs398123952
openSNP	rs398123952
23andMe	rs398123952
SNPshot	rs398123952
SNPdbe	rs398123952
MSV3d	rs398123952
GWAS Ctlg	rs398123952

Max Magnitude

0

ClinVar
Risk	rs398123952(A;A) rs398123952(C;C)
Alt	rs398123952(A;A) rs398123952(C;C)
Reference	Rs398123952(G;G)
Significance	Other
Disease	not provided Duchenne muscular dystrophy Becker muscular dystrophy not specified
Variation	info
Gene	DMD
CLNDBN	not provided Duchenne muscular dystrophy Becker muscular dystrophy not specified
Reversed	1
HGVS	NC_000023.10:g.32834681C>G; NC_000023.10:g.32834681C>T
CLNSRC
CLNACC	RCV000080612.3, RCV000268554.1, RCV000360895.1, RCV000363943.1,