SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs64783649 | snp | A/G | 0 | 0 | upstream-variant-2KB | Mylip | Rn_Celera | 17:19705511 | ATTTATATTTTTAAT[A/G]TGAGCAGCTAAATAA | 306825 |
rs66278673 | snp | C/T | 0 | 0 | upstream-variant-2KB | Mylip | Rn_Celera | 17:19705640 | ACATGGACATTTCTC[C/T]AACCCATACCCACTG | 306825 |
rs66331613 | snp | C/T | 0 | 0 | upstream-variant-2KB | Mylip | Rn_Celera | 17:19705528 | GAGCAGCTAAATAAT[C/T]TGTAGAAGCGTAGAA | 306825 |
rs66412906 | snp | A/T | 0 | 0 | upstream-variant-2KB | Mylip | Rn_Celera | 17:19705559 | AATATCAGGTTAAAA[A/T]TTTTTTAGGTTAAGA | 306825 |
rs105193109 | snp | A/G | 0 | 0 | downstream-variant-500B | Mylip | Rn_Celera | 17:19681660 | GTCCCAGACTGTGGA[A/G]TCTGTTTCTGCTATG | 306825 |
rs105661231 | snp | A/G | 0.5 | 0 | intron-variant | Mylip | Rn_Celera | 17:19688305 | TGTGTGTGTGTGTGT[A/G]TATGTGTGTGTGTGT | 306825 |
rs106495659 | snp | A/G | 0 | 0 | intron-variant | Mylip | Rn_Celera | 17:19699684 | ACCCCACCCCATCCC[A/G]CCAGGCCTCTCTACT | 306825 |
rs106537982 | snp | A/G | 0 | 0 | intron-variant | Mylip | Rn_Celera | 17:19688307 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 306825 |
rs106612262 | snp | G/T | 0.266947 | 0.249425 | intron-variant | Mylip | Rn_Celera | 17:19684380 | AACAAGCCTCTAGTG[G/T]TTTTTTGGCTAGCAC | 306825 |
rs107103721 | snp | A/G | 0 | 0 | intron-variant | Mylip | Rn_Celera | 17:19701438 | CGTTTGAAAAAGGAG[A/G]CCACACCCACAGGCT | 306825 |
rs197116484 | snp | A/G | 0 | 0 | intron-variant | Mylip | Rnor_6.0 | 17:19700379 | GAAAAAACCAACGTA[A/G]GAGATTTGATTTAAG | 306825 |
rs197252653 | snp | C/T | 0 | 0 | intron-variant | Mylip | Rn_Celera | 17:19691881 | TACATTCATTCACTA[C/T]AAGGTATGCATGCCA | 306825 |
rs197268106 | snp | A/T | 0 | 0 | intron-variant | Mylip | Rn_Celera | 17:19702405 | CAAGGTTTTAAGGTA[A/T]CAGCAAAGCCAAAAC | 306825 |
rs197313681 | snp | C/T | 0 | 0 | upstream-variant-2KB | Mylip | Rn_Celera | 17:19704807 | CTTTTAGACCTTCCC[C/T]GAGCATTGCTGTGAA | 306825 |
rs197644618 | snp | C/T | 0 | 0 | intron-variant | Mylip | Rn_Celera | 17:19695050 | TTTCCTCTCCTCTCT[C/T]CCCCTCTCTTCCCTC | 306825 |
rs197816064 | snp | C/T | 0 | 0 | intron-variant | Mylip | Rnor_6.0 | 17:19700144 | AGTTCTTAGACTAGA[C/T]TTGGACTCACACTGT | 306825 |
rs198108214 | snp | A/G | 0 | 0 | missense | Mylip | Rn_Celera | 17:19686077 | CTCATGCTGCTGTCA[A/G]AGGACTTCAGAGGCG | 306825 |
rs198142755 | snp | C/T | 0 | 0 | intron-variant | Mylip | Rn_Celera | 17:19702731 | CAGGTCTACAGGTCT[C/T]GAAGGCACAGTGTTT | 306825 |
rs198175710 | snp | C/T | 0 | 0 | upstream-variant-2KB | Mylip | Rn_Celera | 17:19704959 | GATATGTATTTCTGA[C/T]GAGGGGAAAAGTATT | 306825 |
rs198215827 | snp | C/T | 0 | 0 | intron-variant | Mylip | Rn_Celera | 17:19692473 | AAGAGGAAGAAGATG[C/T]GGGTCTAAAATTCTC | 306825 |
rs198349846 | snp | A/G | 0 | 0 | intron-variant | Mylip | Rnor_6.0 | 17:19700878 | ACACATACACAGAAC[A/G]AATGCTGTGTCATGT | 306825 |
rs198788871 | snp | A/T | 0 | 0 | intron-variant | Mylip | Rnor_6.0 | 17:19699890 | CTTAGGCATTTTTTT[A/T]AAAAAGCTTTATATT | 306825 |
rs198953341 | snp | C/T | 0 | 0 | intron-variant | Mylip | Rn_Celera | 17:19695049 | CTTTCCTCTCCTCTC[C/T]CCCCCTCTCTTCCCT | 306825 |
rs199400766 | snp | G/T | 0 | 0 | missense | Mylip | Rn_Celera | 17:19688821 | CAGGTCCGACCCCAA[G/T]GAGGAGTTTCTGTCC | 306825 |