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rs10500783

From SNPedia

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Make rs10500783(C;C)
Make rs10500783(C;T)
Make rs10500783(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position13552067
is asnp
is mentioned by
dbSNPrs10500783
ebirs10500783
HLIrs10500783
Exacrs10500783
Varsomers10500783
Maprs10500783
PheGenIrs10500783
hapmaprs10500783
1000 genomesrs10500783
hgdprs10500783
ensemblrs10500783
gopubmedrs10500783
geneviewrs10500783
scholarrs10500783
googlers10500783
pharmgkbrs10500783
gwascentralrs10500783
openSNPrs10500783
23andMers10500783
23andMe allrs10500783
SNP Nexus

SNPshotrs10500783
SNPdbers10500783
MSV3drs10500783
GWAS Ctlgrs10500783
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26339419OA-icon.png] Association between promoter region genetic variants of PTH SNPs and serum 25(OH)-vitamin D level