rs794727097

Orientation

minus

Stabilized

minus

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

Make rs794727097(-;-)

Make rs794727097(-;TCAC)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32595823

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs794727097
dbSNP (classic)	rs794727097
ClinGen	rs794727097
ebi	rs794727097
HLI	rs794727097
Exac	rs794727097
Gnomad	rs794727097
Varsome	rs794727097
LitVar	rs794727097
Map	rs794727097
PheGenI	rs794727097
Biobank	rs794727097
1000 genomes	rs794727097
hgdp	rs794727097
ensembl	rs794727097
geneview	rs794727097
scholar	rs794727097
google	rs794727097
pharmgkb	rs794727097
gwascentral	rs794727097
openSNP	rs794727097
23andMe	rs794727097
SNPshot	rs794727097
SNPdbe	rs794727097
MSV3d	rs794727097
GWAS Ctlg	rs794727097

Max Magnitude

0

ClinVar
Risk	rs794727097(-;-)
Alt	rs794727097(-;-)
Reference	Rs794727097(TCAC;TCAC)
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.32613940_32613943delGTGA
CLNSRC
CLNACC	RCV000174531.1, RCV000174532.1,