rs765445866

Orientation

plus

Stabilized

plus

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

Make rs765445866(A;A)

Make rs765445866(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32364626

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs765445866
dbSNP (classic)	rs765445866
ClinGen	rs765445866
ebi	rs765445866
HLI	rs765445866
Exac	rs765445866
Gnomad	rs765445866
Varsome	rs765445866
LitVar	rs765445866
Map	rs765445866
PheGenI	rs765445866
Biobank	rs765445866
1000 genomes	rs765445866
hgdp	rs765445866
ensembl	rs765445866
geneview	rs765445866
scholar	rs765445866
google	rs765445866
pharmgkb	rs765445866
gwascentral	rs765445866
openSNP	rs765445866
23andMe	rs765445866
SNPshot	rs765445866
SNPdbe	rs765445866
MSV3d	rs765445866
GWAS Ctlg	rs765445866

Max Magnitude

0

ClinVar
Risk	rs765445866(A;A) rs765445866(T;T)
Alt	rs765445866(A;A) rs765445866(T;T)
Reference	Rs765445866(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	0
HGVS	NC_000023.10:g.32382743C>A
CLNSRC
CLNACC	RCV000466883.1,