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rs16917546

From SNPedia

Orientationplus
Stabilizedplus
Make rs16917546(C;C)
Make rs16917546(C;T)
Make rs16917546(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position62637778
GeneLOC105378327, ZNF365
is asnp
is mentioned by
dbSNPrs16917546
dbSNP (old)rs16917546
ClinGenrs16917546
ebirs16917546
HLIrs16917546
Exacrs16917546
Gnomadrs16917546
Varsomers16917546
Maprs16917546
PheGenIrs16917546
Biobankrs16917546
1000 genomesrs16917546
hgdprs16917546
ensemblrs16917546
gopubmedrs16917546
geneviewrs16917546
scholarrs16917546
googlers16917546
pharmgkbrs16917546
gwascentralrs16917546
openSNPrs16917546
23andMers16917546
23andMe allrs16917546
SNPshotrs16917546
SNPdbers16917546
MSV3drs16917546
GWAS Ctlgrs16917546
Max Magnitude
? (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.