rs104894789

Orientation

minus

Stabilized

minus

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

Make rs104894789(C;T)

Make rs104894789(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

31182784

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs104894789
dbSNP (classic)	rs104894789
ClinGen	rs104894789
ebi	rs104894789
HLI	rs104894789
Exac	rs104894789
Gnomad	rs104894789
Varsome	rs104894789
LitVar	rs104894789
Map	rs104894789
PheGenI	rs104894789
Biobank	rs104894789
1000 genomes	rs104894789
hgdp	rs104894789
ensembl	rs104894789
geneview	rs104894789
scholar	rs104894789
google	rs104894789
pharmgkb	rs104894789
gwascentral	rs104894789
openSNP	rs104894789
23andMe	rs104894789
SNPshot	rs104894789
SNPdbe	rs104894789
MSV3d	rs104894789
GWAS Ctlg	rs104894789

Max Magnitude

0

OMIM	300377
Desc
Variant	0036
Related	also

ClinVar
Risk	rs104894789(T;T)
Alt	rs104894789(T;T)
Reference	Rs104894789(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31200901G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011993.1,