rs4965598
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4965598(C;C) |
Make rs4965598(C;T) |
Make rs4965598(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 100219409 |
Gene | ADAMTS17 |
is a | snp |
is | mentioned by |
dbSNP | rs4965598 |
dbSNP (classic) | rs4965598 |
ClinGen | rs4965598 |
ebi | rs4965598 |
HLI | rs4965598 |
Exac | rs4965598 |
Gnomad | rs4965598 |
Varsome | rs4965598 |
LitVar | rs4965598 |
Map | rs4965598 |
PheGenI | rs4965598 |
Biobank | rs4965598 |
1000 genomes | rs4965598 |
hgdp | rs4965598 |
ensembl | rs4965598 |
geneview | rs4965598 |
scholar | rs4965598 |
rs4965598 | |
pharmgkb | rs4965598 |
gwascentral | rs4965598 |
openSNP | rs4965598 |
23andMe | rs4965598 |
SNPshot | rs4965598 |
SNPdbe | rs4965598 |
MSV3d | rs4965598 |
GWAS Ctlg | rs4965598 |
GMAF | 0.236 |
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 | 4E-13 |
Odds Ratio | .03 [NR] unit decrease |