rs763542069
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs763542069(A;A) |
Make rs763542069(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 40364361 |
Gene | ADSL |
is a | snp |
is | mentioned by |
dbSNP | rs763542069 |
dbSNP (classic) | rs763542069 |
ClinGen | rs763542069 |
ebi | rs763542069 |
HLI | rs763542069 |
Exac | rs763542069 |
Gnomad | rs763542069 |
Varsome | rs763542069 |
LitVar | rs763542069 |
Map | rs763542069 |
PheGenI | rs763542069 |
Biobank | rs763542069 |
1000 genomes | rs763542069 |
hgdp | rs763542069 |
ensembl | rs763542069 |
geneview | rs763542069 |
scholar | rs763542069 |
rs763542069 | |
pharmgkb | rs763542069 |
gwascentral | rs763542069 |
openSNP | rs763542069 |
23andMe | rs763542069 |
SNPshot | rs763542069 |
SNPdbe | rs763542069 |
MSV3d | rs763542069 |
GWAS Ctlg | rs763542069 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763542069(A;A) |
Alt | rs763542069(A;A) |
Reference | Rs763542069(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ADSL |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.40760365G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000186690.1, |