rs763936813

Orientation

plus

Stabilized

plus

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

Make rs763936813(C;C)

Make rs763936813(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

X

Position

32595765

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs763936813
dbSNP (classic)	rs763936813
ClinGen	rs763936813
ebi	rs763936813
HLI	rs763936813
Exac	rs763936813
Gnomad	rs763936813
Varsome	rs763936813
LitVar	rs763936813
Map	rs763936813
PheGenI	rs763936813
Biobank	rs763936813
1000 genomes	rs763936813
hgdp	rs763936813
ensembl	rs763936813
geneview	rs763936813
scholar	rs763936813
google	rs763936813
pharmgkb	rs763936813
gwascentral	rs763936813
openSNP	rs763936813
23andMe	rs763936813
SNPshot	rs763936813
SNPdbe	rs763936813
MSV3d	rs763936813
GWAS Ctlg	rs763936813

Max Magnitude

0

ClinVar
Risk	rs763936813(A;A) rs763936813(C;C)
Alt	rs763936813(A;A) rs763936813(C;C)
Reference	Rs763936813(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	0
HGVS	NC_000023.10:g.32613882G>A
CLNSRC
CLNACC	RCV000351927.1,