rs36056065
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TGGTAAGT;TGGTAAGT) | 0 | common in clinvar |
Make rs36056065(-;-) |
Make rs36056065(-;GTAAGTTG) |
Make rs36056065(GTAAGTTG;GTAAGTTG) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 160139876 |
Gene | SLC22A1 |
is a | snp |
is | mentioned by |
dbSNP | rs36056065 |
dbSNP (classic) | rs36056065 |
ClinGen | rs36056065 |
ebi | rs36056065 |
HLI | rs36056065 |
Exac | rs36056065 |
Gnomad | rs36056065 |
Varsome | rs36056065 |
LitVar | rs36056065 |
Map | rs36056065 |
PheGenI | rs36056065 |
Biobank | rs36056065 |
1000 genomes | rs36056065 |
hgdp | rs36056065 |
ensembl | rs36056065 |
geneview | rs36056065 |
scholar | rs36056065 |
rs36056065 | |
pharmgkb | rs36056065 |
gwascentral | rs36056065 |
openSNP | rs36056065 |
23andMe | rs36056065 |
SNPshot | rs36056065 |
SNPdbe | rs36056065 |
MSV3d | rs36056065 |
GWAS Ctlg | rs36056065 |
Max Magnitude | 0 |
[PMID 22735389] Association of genetic variation in the organic cation transporters OCT1, OCT2 and multidrug and toxin extrusion 1 transporter protein genes with the gastrointestinal side effects and lower BMI in metformin-treated type 2 diabetes patients
ClinVar | |
---|---|
Risk | rs36056065(-;-) |
Alt | rs36056065(-;-) |
Reference | Rs36056065(TGGTAAGT;TGGTAAGT) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | SLC22A1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000006.11:g.160560908_160560915delGTAAGTTG |
CLNSRC | |
CLNACC | RCV000455695.1, |