TC2N, tandem C2 domains, nuclear, 123036

N. diseases: 17; N. variants: 17
Disease: Body Height ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1548817
rs1548817
Entrez Id: 123036
Gene Symbol: TC2N
TC2N
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019