rs886044402
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | X |
Position | 32390103 |
Gene | DMD |
is a | snp |
is | mentioned by |
dbSNP | rs886044402 |
dbSNP (classic) | rs886044402 |
ClinGen | rs886044402 |
ebi | rs886044402 |
HLI | rs886044402 |
Exac | rs886044402 |
Gnomad | rs886044402 |
Varsome | rs886044402 |
LitVar | rs886044402 |
Map | rs886044402 |
PheGenI | rs886044402 |
Biobank | rs886044402 |
1000 genomes | rs886044402 |
hgdp | rs886044402 |
ensembl | rs886044402 |
geneview | rs886044402 |
scholar | rs886044402 |
rs886044402 | |
pharmgkb | rs886044402 |
gwascentral | rs886044402 |
openSNP | rs886044402 |
23andMe | rs886044402 |
SNPshot | rs886044402 |
SNPdbe | rs886044402 |
MSV3d | rs886044402 |
GWAS Ctlg | rs886044402 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886044402(A;A) |
Alt | rs886044402(A;A) |
Reference | Rs886044402(G;G) |
Significance | Pathogenic |
Disease | Duchenne muscular dystrophy |
Variation | info |
Gene | DMD |
CLNDBN | Duchenne muscular dystrophy |
Reversed | 0 |
HGVS | NC_000023.10:g.32408220G>A |
CLNSRC | |
CLNACC | RCV000296982.1, |