rs763595926
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TCAC;TCAC) | 0 | common in clinvar |
Make rs763595926(-;-) |
Make rs763595926(-;TCAC) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 20 |
Position | 44626448 |
Gene | ADA |
is a | snp |
is | mentioned by |
dbSNP | rs763595926 |
dbSNP (classic) | rs763595926 |
ClinGen | rs763595926 |
ebi | rs763595926 |
HLI | rs763595926 |
Exac | rs763595926 |
Gnomad | rs763595926 |
Varsome | rs763595926 |
LitVar | rs763595926 |
Map | rs763595926 |
PheGenI | rs763595926 |
Biobank | rs763595926 |
1000 genomes | rs763595926 |
hgdp | rs763595926 |
ensembl | rs763595926 |
geneview | rs763595926 |
scholar | rs763595926 |
rs763595926 | |
pharmgkb | rs763595926 |
gwascentral | rs763595926 |
openSNP | rs763595926 |
23andMe | rs763595926 |
SNPshot | rs763595926 |
SNPdbe | rs763595926 |
MSV3d | rs763595926 |
GWAS Ctlg | rs763595926 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763595926(-;-) |
Alt | rs763595926(-;-) |
Reference | Rs763595926(TCAC;TCAC) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ADA |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.43255089_43255092delTCAC |
CLNSRC | |
CLNACC | RCV000481952.1, |