rs6569648
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6569648(C;C) |
Make rs6569648(C;T) |
Make rs6569648(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 130027974 |
Gene | L3MBTL3 |
is a | snp |
is | mentioned by |
dbSNP | rs6569648 |
dbSNP (classic) | rs6569648 |
ClinGen | rs6569648 |
ebi | rs6569648 |
HLI | rs6569648 |
Exac | rs6569648 |
Gnomad | rs6569648 |
Varsome | rs6569648 |
LitVar | rs6569648 |
Map | rs6569648 |
PheGenI | rs6569648 |
Biobank | rs6569648 |
1000 genomes | rs6569648 |
hgdp | rs6569648 |
ensembl | rs6569648 |
geneview | rs6569648 |
scholar | rs6569648 |
rs6569648 | |
pharmgkb | rs6569648 |
gwascentral | rs6569648 |
openSNP | rs6569648 |
23andMe | rs6569648 |
SNPshot | rs6569648 |
SNPdbe | rs6569648 |
MSV3d | rs6569648 |
GWAS Ctlg | rs6569648 |
GMAF | 0.1212 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | Height |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height |
Risk Allele | T |
P-val | 1E-21 |
Odds Ratio | 0.04 [NR] unit decrease |
[PMID 21757498] Adult height variants affect birth length and growth rate in children.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 6
- 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