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rs10500784

From SNPedia

Orientationplus
Stabilizedplus
Make rs10500784(A;A)
Make rs10500784(A;C)
Make rs10500784(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position13552278
is asnp
is mentioned by
dbSNPrs10500784
dbSNP (classic)rs10500784
ClinGenrs10500784
ebirs10500784
HLIrs10500784
Exacrs10500784
Gnomadrs10500784
Varsomers10500784
LitVarrs10500784
Maprs10500784
PheGenIrs10500784
Biobankrs10500784
1000 genomesrs10500784
hgdprs10500784
ensemblrs10500784
geneviewrs10500784
scholarrs10500784
googlers10500784
pharmgkbrs10500784
gwascentralrs10500784
openSNPrs10500784
23andMers10500784
SNPshotrs10500784
SNPdbers10500784
MSV3drs10500784
GWAS Ctlgrs10500784
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 26339419OA-icon.png] Association between promoter region genetic variants of PTH SNPs and serum 25(OH)-vitamin D level