rs12610022
From SNPedia
Orientation | plus |
Make rs12610022(A;A) |
Make rs12610022(A;G) |
Make rs12610022(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 19 |
Position | 7135281 |
Gene | INSR |
is a | snp |
is | mentioned by |
dbSNP | rs12610022 |
dbSNP (classic) | rs12610022 |
ClinGen | rs12610022 |
ebi | rs12610022 |
HLI | rs12610022 |
Exac | rs12610022 |
Gnomad | rs12610022 |
Varsome | rs12610022 |
LitVar | rs12610022 |
Map | rs12610022 |
PheGenI | rs12610022 |
Biobank | rs12610022 |
1000 genomes | rs12610022 |
hgdp | rs12610022 |
ensembl | rs12610022 |
geneview | rs12610022 |
scholar | rs12610022 |
rs12610022 | |
pharmgkb | rs12610022 |
gwascentral | rs12610022 |
openSNP | rs12610022 |
23andMe | rs12610022 |
SNPshot | rs12610022 |
SNPdbe | rs12610022 |
MSV3d | rs12610022 |
GWAS Ctlg | rs12610022 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 30664342] Sequencing of the insulin receptor (INSR) gene reveals association between gene variants in exon and intron 13 and schizoaffective disorder.