rs34343821
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs34343821(A;A) |
Make rs34343821(A;G) |
Make rs34343821(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 4 |
Position | 153636464 |
Gene | KIAA0922 |
is a | snp |
is | mentioned by |
dbSNP | rs34343821 |
dbSNP (classic) | rs34343821 |
ClinGen | rs34343821 |
ebi | rs34343821 |
HLI | rs34343821 |
Exac | rs34343821 |
Gnomad | rs34343821 |
Varsome | rs34343821 |
LitVar | rs34343821 |
Map | rs34343821 |
PheGenI | rs34343821 |
Biobank | rs34343821 |
1000 genomes | rs34343821 |
hgdp | rs34343821 |
ensembl | rs34343821 |
geneview | rs34343821 |
scholar | rs34343821 |
rs34343821 | |
pharmgkb | rs34343821 |
gwascentral | rs34343821 |
openSNP | rs34343821 |
23andMe | rs34343821 |
SNPshot | rs34343821 |
SNPdbe | rs34343821 |
MSV3d | rs34343821 |
GWAS Ctlg | rs34343821 |
Max Magnitude | 0 |
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.