rs863225015

Orientation

minus

Stabilized

minus

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

Make rs863225015(-;-)

Make rs863225015(-;CAAA)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

31323615

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863225015
dbSNP (classic)	rs863225015
ClinGen	rs863225015
ebi	rs863225015
HLI	rs863225015
Exac	rs863225015
Gnomad	rs863225015
Varsome	rs863225015
LitVar	rs863225015
Map	rs863225015
PheGenI	rs863225015
Biobank	rs863225015
1000 genomes	rs863225015
hgdp	rs863225015
ensembl	rs863225015
geneview	rs863225015
scholar	rs863225015
google	rs863225015
pharmgkb	rs863225015
gwascentral	rs863225015
openSNP	rs863225015
23andMe	rs863225015
SNPshot	rs863225015
SNPdbe	rs863225015
MSV3d	rs863225015
GWAS Ctlg	rs863225015

Max Magnitude

0

ClinVar
Risk	rs863225015(-;-)
Alt	rs863225015(-;-)
Reference	Rs863225015(CAAA;CAAA)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31341732_31341735delTTTG
CLNSRC	Quest Diagnostics
CLNACC	RCV000201037.1,