rs16917546
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16917546(C;C) |
Make rs16917546(C;T) |
Make rs16917546(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 10 |
Position | 62637778 |
Gene | LOC105378327, ZNF365 |
is a | snp |
is | mentioned by |
dbSNP | rs16917546 |
dbSNP (classic) | rs16917546 |
ClinGen | rs16917546 |
ebi | rs16917546 |
HLI | rs16917546 |
Exac | rs16917546 |
Gnomad | rs16917546 |
Varsome | rs16917546 |
LitVar | rs16917546 |
Map | rs16917546 |
PheGenI | rs16917546 |
Biobank | rs16917546 |
1000 genomes | rs16917546 |
hgdp | rs16917546 |
ensembl | rs16917546 |
geneview | rs16917546 |
scholar | rs16917546 |
rs16917546 | |
pharmgkb | rs16917546 |
gwascentral | rs16917546 |
openSNP | rs16917546 |
23andMe | rs16917546 |
SNPshot | rs16917546 |
SNPdbe | rs16917546 |
MSV3d | rs16917546 |
GWAS Ctlg | rs16917546 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28177523] Association between genetic variation within vitamin D receptor-DNA binding sites and risk of basal cell carcinoma.