rs775933965
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs775933965(A;A) |
Make rs775933965(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 45366406 |
Gene | GATM |
is a | snp |
is | mentioned by |
dbSNP | rs775933965 |
dbSNP (classic) | rs775933965 |
ClinGen | rs775933965 |
ebi | rs775933965 |
HLI | rs775933965 |
Exac | rs775933965 |
Gnomad | rs775933965 |
Varsome | rs775933965 |
LitVar | rs775933965 |
Map | rs775933965 |
PheGenI | rs775933965 |
Biobank | rs775933965 |
1000 genomes | rs775933965 |
hgdp | rs775933965 |
ensembl | rs775933965 |
geneview | rs775933965 |
scholar | rs775933965 |
rs775933965 | |
pharmgkb | rs775933965 |
gwascentral | rs775933965 |
openSNP | rs775933965 |
23andMe | rs775933965 |
SNPshot | rs775933965 |
SNPdbe | rs775933965 |
MSV3d | rs775933965 |
GWAS Ctlg | rs775933965 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775933965(A;A) |
Alt | rs775933965(A;A) |
Reference | Rs775933965(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | GATM |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.45658604G>A |
CLNSRC | |
CLNACC | RCV000187602.1, |