RCN3, reticulocalbin 3, 57333

N. diseases: 8; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34459162
rs34459162
Entrez Id: 57333
Gene Symbol: RCN3
RCN3
CUI: C0202025
Disease:
Fructosamine measurement
C 0.700 GeneticVariation GWASCAT Among whites, rs34459162, a novel missense single nucleotide polymorphism (SNP) in <i>RCN3</i>, was associated with fructosamine (<i>P</i> = 5.3 × 10<sup>-9</sup>) and rs1260236, a known diabetes-related missense mutation in <i>GCKR</i>, was associated with percent glycated albumin (<i>P</i> = 5.9 × 10<sup>-9</sup>) and replicated in CARDIA. 29844224 2018