rs771937610
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs771937610(A;A) |
Make rs771937610(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 130494984 |
Gene | ASS1, LOC105376294 |
is a | snp |
is | mentioned by |
dbSNP | rs771937610 |
dbSNP (classic) | rs771937610 |
ClinGen | rs771937610 |
ebi | rs771937610 |
HLI | rs771937610 |
Exac | rs771937610 |
Gnomad | rs771937610 |
Varsome | rs771937610 |
LitVar | rs771937610 |
Map | rs771937610 |
PheGenI | rs771937610 |
Biobank | rs771937610 |
1000 genomes | rs771937610 |
hgdp | rs771937610 |
ensembl | rs771937610 |
geneview | rs771937610 |
scholar | rs771937610 |
rs771937610 | |
pharmgkb | rs771937610 |
gwascentral | rs771937610 |
openSNP | rs771937610 |
23andMe | rs771937610 |
SNPshot | rs771937610 |
SNPdbe | rs771937610 |
MSV3d | rs771937610 |
GWAS Ctlg | rs771937610 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs771937610(A;A) |
Alt | rs771937610(A;A) |
Reference | Rs771937610(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ASS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.133370371G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000185788.2, |