rs765338121
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs765338121(A;A) |
Make rs765338121(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 130489341 |
Gene | ASS1 |
is a | snp |
is | mentioned by |
dbSNP | rs765338121 |
dbSNP (classic) | rs765338121 |
ClinGen | rs765338121 |
ebi | rs765338121 |
HLI | rs765338121 |
Exac | rs765338121 |
Gnomad | rs765338121 |
Varsome | rs765338121 |
LitVar | rs765338121 |
Map | rs765338121 |
PheGenI | rs765338121 |
Biobank | rs765338121 |
1000 genomes | rs765338121 |
hgdp | rs765338121 |
ensembl | rs765338121 |
geneview | rs765338121 |
scholar | rs765338121 |
rs765338121 | |
pharmgkb | rs765338121 |
gwascentral | rs765338121 |
openSNP | rs765338121 |
23andMe | rs765338121 |
SNPshot | rs765338121 |
SNPdbe | rs765338121 |
MSV3d | rs765338121 |
GWAS Ctlg | rs765338121 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs765338121(A;A) |
Alt | rs765338121(A;A) |
Reference | Rs765338121(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ASS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.133364728G>A |
CLNSRC | |
CLNACC | RCV000493705.1, |