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Table 2 Position and allele distribution of all FLNB variants genotyped in this and our previous study

From: Conditional testing of multiple variants associated with bone mineral density in the FLNB gene region suggests that they represent a single association signal

SNP Chromosome position* Location* Major/minor allele Minor allele frequency (%)
rs11720285 57961370 5' of TSS A/C 25.1
rs7637505 57968393 5' of TSS A/T 29.4
rs6445938 57974822 5' of TSS A/G 23.1
rs11130605 57989169 5' of TSS C/T 39.2
rs6798382 57991811 5' of TSS G/A 28.6
rs4681772 57992512 5' of TSS A/G 32.1
rs1658351 58013573 Intron 1 A/G 33.5
rs1718481 58025903 Intron 1 G/A 42.7
rs704529 58036651 Intron 1 A/G 36.2
rs839230 58036792 Intron 1 G/A 36.2
rs9809315 58050265 Intron 1 C/T 30.2
rs9822918 58057684 Intron 1 C/A 44.6
rs2177153 58092346 Intron 11 A/G 31.8
rs1131356 58109162 Exon 21, Asp > Asn G/A 22.9
rs12632456 58118555 Exon 26, Val > Met G/A 23.2
rs2001972 58123249 Intron 28 C/A 37.6
rs4284952 58126223 Intron 29 C/A 34.6
rs4234386 58150433 Intron 43 G/A 24.4
  1. *Relative to GenBank reference sequence NM_001457, Genome Build 37.5.
  2. Variant genotyped in our previous study [24].