rs1741344
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1741344(C;C) |
Make rs1741344(C;T) |
Make rs1741344(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 4121153 |
Gene | LOC101929155 |
is a | snp |
is | mentioned by |
dbSNP | rs1741344 |
dbSNP (classic) | rs1741344 |
ClinGen | rs1741344 |
ebi | rs1741344 |
HLI | rs1741344 |
Exac | rs1741344 |
Gnomad | rs1741344 |
Varsome | rs1741344 |
LitVar | rs1741344 |
Map | rs1741344 |
PheGenI | rs1741344 |
Biobank | rs1741344 |
1000 genomes | rs1741344 |
hgdp | rs1741344 |
ensembl | rs1741344 |
geneview | rs1741344 |
scholar | rs1741344 |
rs1741344 | |
pharmgkb | rs1741344 |
gwascentral | rs1741344 |
openSNP | rs1741344 |
23andMe | rs1741344 |
SNPshot | rs1741344 |
SNPdbe | rs1741344 |
MSV3d | rs1741344 |
GWAS Ctlg | rs1741344 |
GMAF | 0.3053 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | T |
P-val | 3E-9 |
Odds Ratio | 0.0200 [NR] meters decrease |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 20
- 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 NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d