rs878854366

Orientation

minus

Stabilized

minus

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

Make rs878854366(-;-)

Make rs878854366(-;AG)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

31169486

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs878854366
dbSNP (classic)	rs878854366
ClinGen	rs878854366
ebi	rs878854366
HLI	rs878854366
Exac	rs878854366
Gnomad	rs878854366
Varsome	rs878854366
LitVar	rs878854366
Map	rs878854366
PheGenI	rs878854366
Biobank	rs878854366
1000 genomes	rs878854366
hgdp	rs878854366
ensembl	rs878854366
geneview	rs878854366
scholar	rs878854366
google	rs878854366
pharmgkb	rs878854366
gwascentral	rs878854366
openSNP	rs878854366
23andMe	rs878854366
SNPshot	rs878854366
SNPdbe	rs878854366
MSV3d	rs878854366
GWAS Ctlg	rs878854366

Max Magnitude

0

ClinVar
Risk	rs878854366(-;-)
Alt	rs878854366(-;-)
Reference	Rs878854366(AG;AG)
Significance	Probable-Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31187603_31187604delCT
CLNSRC
CLNACC	RCV000226304.1,