Table 1 SNPs with high frequencies of nonzero estimated effects
From: Genome-wide case-control study in GAW17 using coalesced rare variants
SNP | Gene | Chromosome | Frequency (%) |
|---|---|---|---|
C13S523* | FLT1 | 13 | 41 |
C12S707 | PRR4 | 12 | 6.5 |
C12S708 | PRR4 | 12 | 6 |
C12S706 | PRR4 | 12 | 5.5 |
C12S709 | TAS2R48 | 12 | 5.5 |
C8S890* | PTK2B | 8 | 3.5 |
C12S705 | TAS2R48 | 12 | 3.5 |
C16S3298 | CCDC135 | 16 | 3.5 |
C6S5380* | VNN1 | 6 | 3 |
C19S2864 | ZNF91 | 19 | 3 |