rs1057520764
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1057520764(C;T) |
Make rs1057520764(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 32342264 |
Gene | DMD |
is a | snp |
is | mentioned by |
dbSNP | rs1057520764 |
dbSNP (classic) | rs1057520764 |
ClinGen | rs1057520764 |
ebi | rs1057520764 |
HLI | rs1057520764 |
Exac | rs1057520764 |
Gnomad | rs1057520764 |
Varsome | rs1057520764 |
LitVar | rs1057520764 |
Map | rs1057520764 |
PheGenI | rs1057520764 |
Biobank | rs1057520764 |
1000 genomes | rs1057520764 |
hgdp | rs1057520764 |
ensembl | rs1057520764 |
geneview | rs1057520764 |
scholar | rs1057520764 |
rs1057520764 | |
pharmgkb | rs1057520764 |
gwascentral | rs1057520764 |
openSNP | rs1057520764 |
23andMe | rs1057520764 |
SNPshot | rs1057520764 |
SNPdbe | rs1057520764 |
MSV3d | rs1057520764 |
GWAS Ctlg | rs1057520764 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057520764(T;T) |
Alt | rs1057520764(T;T) |
Reference | Rs1057520764(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DMD |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000023.10:g.32360381G>A |
CLNSRC | |
CLNACC | RCV000424485.1, |