rs797044764

Orientation

minus

Stabilized

minus

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

Make rs797044764(-;T)

Make rs797044764(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

31820036

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs797044764
dbSNP (classic)	rs797044764
ClinGen	rs797044764
ebi	rs797044764
HLI	rs797044764
Exac	rs797044764
Gnomad	rs797044764
Varsome	rs797044764
LitVar	rs797044764
Map	rs797044764
PheGenI	rs797044764
Biobank	rs797044764
1000 genomes	rs797044764
hgdp	rs797044764
ensembl	rs797044764
geneview	rs797044764
scholar	rs797044764
google	rs797044764
pharmgkb	rs797044764
gwascentral	rs797044764
openSNP	rs797044764
23andMe	rs797044764
SNPshot	rs797044764
SNPdbe	rs797044764
MSV3d	rs797044764
GWAS Ctlg	rs797044764

Max Magnitude

0

ClinVar
Risk	rs797044764(T;T)
Alt	rs797044764(T;T)
Reference	Rs797044764(-;-)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy Becker muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy Becker muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31838154dupA
CLNSRC
CLNACC	RCV000179072.1, RCV000179073.1,