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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].