rs121913157
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121913157(A;A) |
Make rs121913157(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 7120739 |
Gene | INSR |
is a | snp |
is | mentioned by |
dbSNP | rs121913157 |
dbSNP (classic) | rs121913157 |
ClinGen | rs121913157 |
ebi | rs121913157 |
HLI | rs121913157 |
Exac | rs121913157 |
Gnomad | rs121913157 |
Varsome | rs121913157 |
LitVar | rs121913157 |
Map | rs121913157 |
PheGenI | rs121913157 |
Biobank | rs121913157 |
1000 genomes | rs121913157 |
hgdp | rs121913157 |
ensembl | rs121913157 |
geneview | rs121913157 |
scholar | rs121913157 |
rs121913157 | |
pharmgkb | rs121913157 |
gwascentral | rs121913157 |
openSNP | rs121913157 |
23andMe | rs121913157 |
SNPshot | rs121913157 |
SNPdbe | rs121913157 |
MSV3d | rs121913157 |
GWAS Ctlg | rs121913157 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913157(A;A) |
Alt | rs121913157(A;A) |
Reference | Rs121913157(G;G) |
Significance | Pathogenic |
Disease | Insulin resistance |
Variation | info |
Gene | INSR |
CLNDBN | Insulin resistance |
Reversed | 1 |
HGVS | NC_000019.9:g.7120750C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000015824.25, |