rs61752479
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs61752479(A;A) |
Make rs61752479(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 114688633 |
Gene | AMPD1 |
is a | snp |
is | mentioned by |
dbSNP | rs61752479 |
dbSNP (classic) | rs61752479 |
ClinGen | rs61752479 |
ebi | rs61752479 |
HLI | rs61752479 |
Exac | rs61752479 |
Gnomad | rs61752479 |
Varsome | rs61752479 |
LitVar | rs61752479 |
Map | rs61752479 |
PheGenI | rs61752479 |
Biobank | rs61752479 |
1000 genomes | rs61752479 |
hgdp | rs61752479 |
ensembl | rs61752479 |
geneview | rs61752479 |
scholar | rs61752479 |
rs61752479 | |
pharmgkb | rs61752479 |
gwascentral | rs61752479 |
openSNP | rs61752479 |
23andMe | rs61752479 |
SNPshot | rs61752479 |
SNPdbe | rs61752479 |
MSV3d | rs61752479 |
GWAS Ctlg | rs61752479 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61752479(A;A) |
Alt | rs61752479(A;A) |
Reference | Rs61752479(G;G) |
Significance | Probable-non-pathogenic |
Disease | not provided |
Variation | info |
Gene | AMPD1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.115231254G>A |
CLNSRC | ClinVar Emory University GTR |
CLNACC | RCV000416093.2, |