SNP ID | Location/Functional effect | Minor allele | Minor allele n (freq) |
---|---|---|---|
NR1I2 rs12721601T>C | Previously reported, Intron 1 | C | 1 (0.016) |
NR1I2 rs59371185G>A | Previously reported, Exon 2, Glu18Lys | A | 1 (0.016) |
NR1I2 rs12721613C>T | Previously reported, Exon 2, Pro27Ser | T | 4 (0.064) |
NR1I2 rs1464603C>T | Previously reported, Intron 2, Disrupts HNF1 TFB site | T | 1 (0.016) |
NR1I2 rs1464602C>T | Previously reported, Intron 2 | T | 20 (0.313) |
NR1I2 rs80320762G>A | Previously reported, Intron 2 | A | 3 (0.048) |
NR1I2 rs12721616C>T | Previously reported, Intron 2 | T | 14 (0.219) |
NR1I2 rs112813596G>A | Previously reported, Intron 3 | A | 1 (0.016) |
NR1I3 rs35205211C>G | Previously reported, Exon 4, Ala86Ala | G | 2 (0.032) |
NR1I3 rs34161743C>T | Previously reported, Exon 4, Arg97Trp | T | 1 (0.016) |
NR1I2 36726T>C | Novel, Intron 1 | C | 5 (0.078) |
NR1I2 36857G>A* | Novel, Exon 2 | A | 1 (0.016) |
NR1I2 36905C>T | Novel, Exon 2 | T | 2 (0.031) |