rs2229431
From SNPedia
Orientation | minus |
Make rs2229431(C;C) |
Make rs2229431(C;T) |
Make rs2229431(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 19 |
Position | 7141764 |
Gene | INSR |
is a | snp |
is | mentioned by |
dbSNP | rs2229431 |
dbSNP (classic) | rs2229431 |
ClinGen | rs2229431 |
ebi | rs2229431 |
HLI | rs2229431 |
Exac | rs2229431 |
Gnomad | rs2229431 |
Varsome | rs2229431 |
LitVar | rs2229431 |
Map | rs2229431 |
PheGenI | rs2229431 |
Biobank | rs2229431 |
1000 genomes | rs2229431 |
hgdp | rs2229431 |
ensembl | rs2229431 |
geneview | rs2229431 |
scholar | rs2229431 |
rs2229431 | |
pharmgkb | rs2229431 |
gwascentral | rs2229431 |
openSNP | rs2229431 |
23andMe | rs2229431 |
SNPshot | rs2229431 |
SNPdbe | rs2229431 |
MSV3d | rs2229431 |
GWAS Ctlg | rs2229431 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 30664342] Sequencing of the insulin receptor (INSR) gene reveals association between gene variants in exon and intron 13 and schizoaffective disorder.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 19
- Has genotype
- Has population
- On chip 23andMe v3
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Affy GenomeWide 6
- On chip 23andMe v1
- On chip 23andMe v2
- On chip FTDNA
- On chip FTDNA2
- On chip 23andMe v4
- On chip Ancestry v2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d