rs10773568
This is a intron variant variant in the TMEM132C gene.
▶Research that mentions this SNP (1)
▶Genome-wide association study in Han Chinese identifies three novel loci for human heightMeta-analysisN=8,415Yongchen Hao et al.(2013)· Human Genetics
A meta-analysis of genome-wide association studies in 6,534 Han Chinese subjects identified three novel loci for human height at rs12612930 (ZNF638), rs11021504 (MAML2), and rs11082671 (C18orf12) reaching genome-wide significance (P < 5 × 10⁻⁸), along with confirmation of two previously reported loci (CS and CYP19A1). The study provided supporting evidence for 35 SNPs from previous GWAS and demonstrates substantial genetic overlap between Asian and European populations for this complex trait.
About TMEM132C
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
View all TMEM132C variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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