rs398123869

Orientation

minus

Stabilized

minus

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

Make rs398123869(-;AAGT)

Make rs398123869(AAGT;AAGT)

Reference

GRCh38 38.1/141

Chromosome

X

Position

32565790

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs398123869
dbSNP (classic)	rs398123869
ClinGen	rs398123869
ebi	rs398123869
HLI	rs398123869
Exac	rs398123869
Gnomad	rs398123869
Varsome	rs398123869
LitVar	rs398123869
Map	rs398123869
PheGenI	rs398123869
Biobank	rs398123869
1000 genomes	rs398123869
hgdp	rs398123869
ensembl	rs398123869
geneview	rs398123869
scholar	rs398123869
google	rs398123869
pharmgkb	rs398123869
gwascentral	rs398123869
openSNP	rs398123869
23andMe	rs398123869
SNPshot	rs398123869
SNPdbe	rs398123869
MSV3d	rs398123869
GWAS Ctlg	rs398123869

Max Magnitude

0

ClinVar
Risk	rs398123869(AAGT;AAGT)
Alt	rs398123869(AAGT;AAGT)
Reference	Rs398123869(-;-)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 3B
Variation	info
Gene	DMD
CLNDBN	Dilated cardiomyopathy 3B
Reversed	1
HGVS	NC_000023.10:g.32583908_32583911dupACTT
CLNSRC	ClinVar
CLNACC	RCV000080471.3,