| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs8143481 | snp | C/G/T | | | utr-variant-3-prime | Nosip | Rn_Celera | 1:101072487 | AGGGCCACACATCCA[C/G/T]CCTGTTCACGTCCAA | 292894 |
| rs8145601 | snp | G/T | | | utr-variant-3-prime | Nosip | Rn_Celera | 1:101072476 | ACCTAATAAACTTGG[G/T]CGTGAACAGGCTGGA | 292894 |
| rs8148425 | snp | A/G | | | missense | Nosip | Rn_Celera | 1:101071791 | CCCACTCGGTCCACA[A/G]AGTCGTCCAGCTGTG | 292894 |
| rs8149626 | snp | A/G | | | synonymous-codon | Nosip | Rn_Celera | 1:101072062 | CCGCTGCAGCACGAT[A/G]ATGTCCCGCTCCGTC | 292894 |
| rs105760098 | snp | C/G | 0 | 0 | intron-variant | Nosip | Rn_Celera | 1:101065606 | CCGGTTGGTTTTTTT[C/G]CCAGAGCTGGGGNCC | 292894 |
| rs106003700 | snp | G/T | 0 | 0 | intron-variant | Nosip | Rn_Celera | 1:101065631 | GGGNCCGANCCCAGG[G/T]TCTTGCGCTTCCTAG | 292894 |
| rs197750648 | snp | C/G | 0 | 0 | intron-variant | Nosip | Rn_Celera | 1:101060093 | TGCCTCTGTAGCTGG[C/G]CAGNCTGTCTTTGTT | 292894 |
| rs198463575 | snp | A/T | 0 | 0 | intron-variant | Nosip | Rn_Celera | 1:101065694 | ACCCCGTAAAGAATT[A/T]TTTATGAGTGTTTTG | 292894 |
| rs199267918 | snp | A/T | 0 | 0 | intron-variant | Nosip | Rn_Celera | 1:101065693 | AACCCCGTAAAGAAT[A/T]ATTTATGAGTGTTTT | 292894 |