rs146880270
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs146880270(C;T) |
Make rs146880270(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 32438312 |
Gene | DMD |
is a | snp |
is | mentioned by |
dbSNP | rs146880270 |
dbSNP (classic) | rs146880270 |
ClinGen | rs146880270 |
ebi | rs146880270 |
HLI | rs146880270 |
Exac | rs146880270 |
Gnomad | rs146880270 |
Varsome | rs146880270 |
LitVar | rs146880270 |
Map | rs146880270 |
PheGenI | rs146880270 |
Biobank | rs146880270 |
1000 genomes | rs146880270 |
hgdp | rs146880270 |
ensembl | rs146880270 |
geneview | rs146880270 |
scholar | rs146880270 |
rs146880270 | |
pharmgkb | rs146880270 |
gwascentral | rs146880270 |
openSNP | rs146880270 |
23andMe | rs146880270 |
SNPshot | rs146880270 |
SNPdbe | rs146880270 |
MSV3d | rs146880270 |
GWAS Ctlg | rs146880270 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs146880270(A;A) rs146880270(T;T) |
Alt | rs146880270(A;A) rs146880270(T;T) |
Reference | Rs146880270(C;C) |
Significance | Other |
Disease | Duchenne muscular dystrophy |
Variation | info |
Gene | DMD |
CLNDBN | Duchenne muscular dystrophy |
Reversed | 0 |
HGVS | NC_000023.10:g.32456429C>A |
CLNSRC | |
CLNACC | RCV000196412.1, |