Skip to main content
. Author manuscript; available in PMC: 2016 May 1.
Published in final edited form as: J Pediatr. 2015 Mar 11;166(5):1152–1157.e6. doi: 10.1016/j.jpeds.2015.01.044

Table 2.

Association of eight candidate SNPs with NBS IRT values in 111 subjects from Colorado.

SNP Chromosome Positiona Gene Risk Alleleb Risk Allele Frequency P value β (95% CI) R2
rs7512462 1 204166218 SLC26A9 T 0.57 1.16 × 10−3 −49 (−78, −20) 0.09
rs4077468 1 204181380 SLC26A9 T 0.55 7.20 × 10−3 −38 (−66, −11) 0.06
rs12047830 1 204183322 SLC26A9 C 0.50 1.92 × 10−3 −47 (−77, −18) 0.08
rs7419153 1 204183932 SLC26A9 T 0.37 0.02 −34 (−63, −5) 0.05
rs17563161 5 550624 SLC9A3 T 0.28 0.50 13 (−24, 49) 0.00
rs12839137 X 115479578 SLC6A14 C 0.84 0.87 −3 (−39, 32) 0.00
rs5905283 X 115479909 SLC6A14 C 0.63 0.21 −16 (−42, 10) 0.01
rs3788766 X 115480867 SLC6A14 T 0.73 0.41 −12 (−40, 17) 0.01

CI, Confidence Interval

a

: Based on Genome Reference Consortium Human Reference 37/Human Genome 19.

b

: Meconium ileus risk allele from Sun et al16.