Skip to main content
. 2012 Aug 6;7(8):e42734. doi: 10.1371/journal.pone.0042734

Table 1. Genetic variants discovered in FGFR1OP2/wit3.0 gene by direct sequencing (n = 24).

Region SNP number SNP Name Position variation Allele Frequency HWE
Promoter rs2306852 −17552A/G chr12:27089540 A/G A∶G = 0.979∶0.021 1
Promoter rs2279351 −16542 A/C chr12:27090550 A/C A∶C = 0.938∶0.063 1
Promoter ss518063498 −16161∼16150CA/− chr12:27090931–27090942 CA/INS [6][7] = 0.958∶0.042* 1
Promoter rs78054962 −15988C/T chr12:27091104 C/T T∶C = 0.958∶0.042 1
Exon2 ss518063493 E6E chr12:27107109 G/A G∶A = 0.979∶0.021 1
Intron2 ss518063913 IVS2+7∼11T/− chr12:27107233–27107237 T/del T∶- = 0.979∶0.021** 1
Exon4 ss518063476 M113T chr12:27110618 C/T T∶C = 0.979∶0.021 1
*

[6] has six copies and [7] has seven copies of CA;

**

T/del refer to [ttttt/tttt].