present in Gene: FTCDNL1
present in Chromosome: 2
Position on Chromosome: 199812203
Alleles of this Variant: A/C
rs7605378 in
FTCDNL1 gene and
Osteoporosis
PMID 21573128 2011 Through these staged association studies followed by resequencing and linkage disequilibrium mapping, we identified a single nucleotide polymorphism (SNP), rs7605378 associated with osteoporosis.