rs34354104
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs34354104(C;C) |
Make rs34354104(C;T) |
Make rs34354104(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 14 |
Position | 24238273 |
Gene | GMPR2 |
is a | snp |
is | mentioned by |
dbSNP | rs34354104 |
dbSNP (classic) | rs34354104 |
ClinGen | rs34354104 |
ebi | rs34354104 |
HLI | rs34354104 |
Exac | rs34354104 |
Gnomad | rs34354104 |
Varsome | rs34354104 |
LitVar | rs34354104 |
Map | rs34354104 |
PheGenI | rs34354104 |
Biobank | rs34354104 |
1000 genomes | rs34354104 |
hgdp | rs34354104 |
ensembl | rs34354104 |
geneview | rs34354104 |
scholar | rs34354104 |
rs34354104 | |
pharmgkb | rs34354104 |
gwascentral | rs34354104 |
openSNP | rs34354104 |
23andMe | rs34354104 |
SNPshot | rs34354104 |
SNPdbe | rs34354104 |
MSV3d | rs34354104 |
GWAS Ctlg | rs34354104 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.