SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8174008 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Ldb2 | Rn_Celera | 14:71111360 | TGAGATCCTGAGCAC[A/G]TTTAGACAGCATGGC | 289664 |
rs65183777 | snp | A/G | 0.222901 | 0.248527 | upstream-variant-2KB | Ldb2 | Rn_Celera | 14:70779042 | GCTGGCCTGCCTTGG[A/G]GTCTCCAGACACATG | 289664 |
rs105469008 | snp | A/G | 0.5 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:71020567 | CCCATTTGTGGCTTA[A/G]CAATCCACTTACATT | 289664 |
rs105687690 | snp | A/T | 0 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:71019130 | CTGCCCCTGAAGGAA[A/T]TATAGCACAGATTTT | 289664 |
rs105767366 | snp | G/T | 0.5 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:70976970 | CCTTAAGCTATCTTG[G/T]GCACATATACTTAAC | 289664 |
rs106166832 | snp | A/C | 0 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:70978470 | AGTATGCATATTTAG[A/C]CCTTCATACTGTGTG | 289664 |
rs197724099 | snp | A/C/G/T | 0 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:71044927 | TCTCTCTCTCTCAGA[A/C/G/T]GTTAATTCTTTTAGC | 289664 |
rs198094706 | snp | A/C | 0 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:71044990 | NNTAAGAGAAACAAA[A/C]CATGCTAATTAAATA | 289664 |
rs198244190 | snp | A/G | 0.5 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:71016488 | TTTTCCCAGAGCCAA[A/G]AGGCTCTGTGGAATT | 289664 |
rs198735469 | snp | A/C/G/T | 0 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:71043770 | GGTCTCAGAGATTCT[A/C/G/T]NGATTGCAGTGTGTC | 289664 |
rs198916180 | snp | C/T | 0 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:70819845 | TCTTTATTTCTTCCT[C/T]GACCAGGTTATCATT | 289664 |
rs198942540 | snp | A/C/G/T | 0 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:71043771 | GTCTCAGAGATTCTN[A/C/G/T]GATTGCAGTGTGTCA | 289664 |
rs199154322 | snp | A/C/G/T | 0 | 0 | intron-variant | Ldb2 | Rn_Celera | 14:71028606 | TCTGACCATTTTTTC[A/C/G/T]TAGTGAGATTCTTTT | 289664 |