rs145068530
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs145068530(A;G) |
Make rs145068530(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 132384178 |
Gene | SLC22A5 |
is a | snp |
is | mentioned by |
dbSNP | rs145068530 |
dbSNP (classic) | rs145068530 |
ClinGen | rs145068530 |
ebi | rs145068530 |
HLI | rs145068530 |
Exac | rs145068530 |
Gnomad | rs145068530 |
Varsome | rs145068530 |
LitVar | rs145068530 |
Map | rs145068530 |
PheGenI | rs145068530 |
Biobank | rs145068530 |
1000 genomes | rs145068530 |
hgdp | rs145068530 |
ensembl | rs145068530 |
geneview | rs145068530 |
scholar | rs145068530 |
rs145068530 | |
pharmgkb | rs145068530 |
gwascentral | rs145068530 |
openSNP | rs145068530 |
23andMe | rs145068530 |
SNPshot | rs145068530 |
SNPdbe | rs145068530 |
MSV3d | rs145068530 |
GWAS Ctlg | rs145068530 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs145068530(G;G) |
Alt | rs145068530(G;G) |
Reference | Rs145068530(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC22A5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.131719870A>G |
CLNSRC | |
CLNACC | RCV000434160.1, |