rs777864641

Orientation

plus

Stabilized

plus

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

Make rs777864641(C;T)

Make rs777864641(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32348504

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs777864641
dbSNP (classic)	rs777864641
ClinGen	rs777864641
ebi	rs777864641
HLI	rs777864641
Exac	rs777864641
Gnomad	rs777864641
Varsome	rs777864641
LitVar	rs777864641
Map	rs777864641
PheGenI	rs777864641
Biobank	rs777864641
1000 genomes	rs777864641
hgdp	rs777864641
ensembl	rs777864641
geneview	rs777864641
scholar	rs777864641
google	rs777864641
pharmgkb	rs777864641
gwascentral	rs777864641
openSNP	rs777864641
23andMe	rs777864641
SNPshot	rs777864641
SNPdbe	rs777864641
MSV3d	rs777864641
GWAS Ctlg	rs777864641

Max Magnitude

0

ClinVar
Risk	rs777864641(A;A) rs777864641(G;G) rs777864641(T;T)
Alt	rs777864641(A;A) rs777864641(G;G) rs777864641(T;T)
Reference	Rs777864641(C;C)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	0
HGVS	NC_000023.10:g.32366621C>A
CLNSRC	Quest Diagnostics
CLNACC	RCV000201039.1,