rs7571816
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs7571816(A;G) |
| Make rs7571816(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 232212354 |
| Gene | DIS3L2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7571816 |
| dbSNP (classic) | rs7571816 |
| ClinGen | rs7571816 |
| ebi | rs7571816 |
| HLI | rs7571816 |
| Exac | rs7571816 |
| Gnomad | rs7571816 |
| Varsome | rs7571816 |
| LitVar | rs7571816 |
| Map | rs7571816 |
| PheGenI | rs7571816 |
| Biobank | rs7571816 |
| 1000 genomes | rs7571816 |
| hgdp | rs7571816 |
| ensembl | rs7571816 |
| geneview | rs7571816 |
| scholar | rs7571816 |
| rs7571816 | |
| pharmgkb | rs7571816 |
| gwascentral | rs7571816 |
| openSNP | rs7571816 |
| 23andMe | rs7571816 |
| SNPshot | rs7571816 |
| SNPdbe | rs7571816 |
| MSV3d | rs7571816 |
| GWAS Ctlg | rs7571816 |
| GMAF | 0.1965 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
| GWAS snp | |
|---|---|
| PMID | [PMID 20189936] |
| Trait | Height |
| Title | A genome-wide association study in 19,633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci |
| Risk Allele | A |
| P-val | 9E-9 |
| Odds Ratio | 0.06 [0.04-0.08] cm increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
