rs6717918
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6717918(C;C) |
Make rs6717918(C;T) |
Make rs6717918(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 232290400 |
Gene | DIS3L2 |
is a | snp |
is | mentioned by |
dbSNP | rs6717918 |
dbSNP (classic) | rs6717918 |
ClinGen | rs6717918 |
ebi | rs6717918 |
HLI | rs6717918 |
Exac | rs6717918 |
Gnomad | rs6717918 |
Varsome | rs6717918 |
LitVar | rs6717918 |
Map | rs6717918 |
PheGenI | rs6717918 |
Biobank | rs6717918 |
1000 genomes | rs6717918 |
hgdp | rs6717918 |
ensembl | rs6717918 |
geneview | rs6717918 |
scholar | rs6717918 |
rs6717918 | |
pharmgkb | rs6717918 |
gwascentral | rs6717918 |
openSNP | rs6717918 |
23andMe | rs6717918 |
SNPshot | rs6717918 |
SNPdbe | rs6717918 |
MSV3d | rs6717918 |
GWAS Ctlg | rs6717918 |
GMAF | 0.4683 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19570815] A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation