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.
] 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


