rs10500783
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10500783(C;C) |
Make rs10500783(C;T) |
Make rs10500783(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 13552067 |
is a | snp |
is | mentioned by |
dbSNP | rs10500783 |
dbSNP (classic) | rs10500783 |
ClinGen | rs10500783 |
ebi | rs10500783 |
HLI | rs10500783 |
Exac | rs10500783 |
Gnomad | rs10500783 |
Varsome | rs10500783 |
LitVar | rs10500783 |
Map | rs10500783 |
PheGenI | rs10500783 |
Biobank | rs10500783 |
1000 genomes | rs10500783 |
hgdp | rs10500783 |
ensembl | rs10500783 |
geneview | rs10500783 |
scholar | rs10500783 |
rs10500783 | |
pharmgkb | rs10500783 |
gwascentral | rs10500783 |
openSNP | rs10500783 |
23andMe | rs10500783 |
SNPshot | rs10500783 |
SNPdbe | rs10500783 |
MSV3d | rs10500783 |
GWAS Ctlg | rs10500783 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26339419] Association between promoter region genetic variants of PTH SNPs and serum 25(OH)-vitamin D level