rs10500784
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10500784(A;A) |
Make rs10500784(A;C) |
Make rs10500784(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 13552278 |
is a | snp |
is | mentioned by |
dbSNP | rs10500784 |
dbSNP (classic) | rs10500784 |
ClinGen | rs10500784 |
ebi | rs10500784 |
HLI | rs10500784 |
Exac | rs10500784 |
Gnomad | rs10500784 |
Varsome | rs10500784 |
LitVar | rs10500784 |
Map | rs10500784 |
PheGenI | rs10500784 |
Biobank | rs10500784 |
1000 genomes | rs10500784 |
hgdp | rs10500784 |
ensembl | rs10500784 |
geneview | rs10500784 |
scholar | rs10500784 |
rs10500784 | |
pharmgkb | rs10500784 |
gwascentral | rs10500784 |
openSNP | rs10500784 |
23andMe | rs10500784 |
SNPshot | rs10500784 |
SNPdbe | rs10500784 |
MSV3d | rs10500784 |
GWAS Ctlg | rs10500784 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
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[PMID 26339419] Association between promoter region genetic variants of PTH SNPs and serum 25(OH)-vitamin D level