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