Table 3.
SNPs with suggestive associations (COHORT1, n = 794)
| SNP ID | Gene | Chromosome | Physical Location (bp) | eGFR Pa | Renal Survival Pb | Alleles | Reference Allele | RAFc | HapMap RAFd | HWE P | Marker Missing (%) | GenCall Scoree |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3750940 | DKK3 | 11 | 11979474 | 0.00019 | 0.22 | A/G | G | 0.20 | 0.21 | 0.56 | 0.24 | 0.82 |
| rs7104941 | DKK3 | 11 | 11977192 | 0.0027 | 0.27 | G/A | A | 0.19 | 0.17 | 0.24 | 0.24 | 0.74 |
| rs12575803 | DKK3 | 11 | 11981152 | 0.00019 | 0.55 | C/A | A | 0.14 | 0.14 | 0.59 | 0.48 | 0.92 |
| rs875588 | RHEB | 7 | 150799763 | 0.0017 | 0.27 | G/A | A | 0.48 | 0.48 | 0.57 | 0.12 | 0.83 |
| rs3753151 | RHEB | 7 | 150815918 | 0.0051 | 0.30 | G/A | A | 0.53 | 0.57 | 0.37 | 0.72 | 0.78 |
| rs6972955 | RHEB | 7 | 150802595 | 0.0022 | 0.47 | C/A | A | 0.44 | 0.48 | 0.95 | 0.24 | 0.81 |
| rs6546365 | PPP3R1 | 2 | 68328790 | 0.0015 | 0.012 | G/A | A | 0.48 | 0.43 | 0.67 | 1.10 | 0.77 |
| rs1693869 | CALM2 | 2 | 47255568 | 0.23 | 0.0034 | G/C | C | 0.12 | 0.13 | 0.80 | 0.00 | 0.86 |
| rs815802 | CALM2 | 2 | 47245553 | 0.72 | 0.0046 | A/G | G | 0.09 | 0.08 | 0.43 | 0.24 | 0.86 |
| rs2206593 | PTGS2 | 1 | 184909052 | 0.53 | 0.0016 | G/A | A | 0.08 | 0.06 | 0.69 | 0.60 | 0.85 |
| rs3917225 | IL1R1 | 2 | 102135734 | 0.21 | 0.0019 | A/G | G | 0.48 | 0.46 | 0.83 | 0.24 | 0.86 |
| rs4150471 | ERCC3 | 2 | 127751009 | 0.52 | 0.0036 | G/A | A | 0.28 | 0.23 | 1.00 | 0.36 | 0.90 |
HWE, Hardy-Weinberg equilibrium; RAF, reference allele frequency.
aAdjusted for age, MDS dimensions C1 through C4, and family relationship by GEE.
bCox proportional hazards model was used for renal survival (absence of ESRD) analysis; adjusted for MDS dimensions C1 through C4 and family relationship.
cRAF was derived from a random draw of one genotyped individual from each family.
dRAF from the HapMap database for European population.
eThe GenCall scores ≥0.7 indicate well-behaving genotypes.