rs6091737
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6091737(C;C) |
Make rs6091737(C;T) |
Make rs6091737(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 53733353 |
is a | snp |
is | mentioned by |
dbSNP | rs6091737 |
dbSNP (classic) | rs6091737 |
ClinGen | rs6091737 |
ebi | rs6091737 |
HLI | rs6091737 |
Exac | rs6091737 |
Gnomad | rs6091737 |
Varsome | rs6091737 |
LitVar | rs6091737 |
Map | rs6091737 |
PheGenI | rs6091737 |
Biobank | rs6091737 |
1000 genomes | rs6091737 |
hgdp | rs6091737 |
ensembl | rs6091737 |
geneview | rs6091737 |
scholar | rs6091737 |
rs6091737 | |
pharmgkb | rs6091737 |
gwascentral | rs6091737 |
openSNP | rs6091737 |
23andMe | rs6091737 |
SNPshot | rs6091737 |
SNPdbe | rs6091737 |
MSV3d | rs6091737 |
GWAS Ctlg | rs6091737 |
GMAF | 0.2971 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20705733![]() |
Trait | |
Title | Common Variants in the Calcium Sensing Receptor Gene are Associated with Total Serum Calcium Levels |
Risk Allele | T |
P-val | 0.000006 |
Odds Ratio | 0.02 [NR] unit decrease |