SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13453495 | snp | C/T | 0.337162 | 0.234314 | utr-variant-3-prime | Chfr | Rn_Celera | 12:52563287 | AGCTGTCAGATATGT[C/T]AGAAACATTCTCCGG | 288734 |
rs13453496 | snp | A/G | 0 | 0 | utr-variant-3-prime | Chfr | Rn_Celera | 12:52562980 | TGTCTTGAGTATCCA[A/G]GTCCTTGACACAGGG | 288734 |
rs104899849 | snp | A/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52570576 | TCACACTAAGCCCAC[A/G]CTCCCTTCTTGCCCT | 288734 |
rs105128230 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52571368 | TCTCAAAAAATTCCA[C/T]AAAGGCTTTCAAAGC | 288734 |
rs105143473 | snp | G/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52568677 | AACTAAATGCCAAAT[G/T]CGAAGCCCAGGGGCA | 288734 |
rs105153366 | snp | A/C | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52576770 | TTTGGGTAACAGATA[A/C]AGAATGATCATTTTG | 288734 |
rs105191168 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52575060 | CAGCCATTGTATAAA[C/T]GAATAGCTCCATGAG | 288734 |
rs105259775 | snp | A/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52566435 | CAATTAGGCTAAGCT[A/G]CCTGGCCAAACTAGG | 288734 |
rs105407120 | snp | A/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52565418 | GAAGTGAGTCTTCTC[A/T]TAGCAGCCTTCAGAT | 288734 |
rs105677882 | snp | A/C | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52587413 | TTTCCAGCCTCAGCT[A/C]GAGGGCTTCTTGGTG | 288734 |
rs105771603 | snp | A/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52571042 | TCTTCTTAGGAAGGG[A/T]CAGAGTCAAAGACAA | 288734 |
rs105800735 | snp | A/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52566984 | CACCAGCACAGCAAG[A/T]CCTTTACTAAGCTCT | 288734 |
rs105862425 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rnor_6.0 | 12:52590523 | ACTGAGCCATCTCTC[C/T]AGCCCTAGATGACTG | 288734 |
rs105887026 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52584342 | AGCTCTTCTATCACC[C/T]GATTCCCACAGCCAG | 288734 |
rs106224042 | snp | C/T | 0 | 0 | downstream-variant-500B | Chfr | Rn_Celera | 12:52562577 | GTGGACCCTCACATA[C/T]GAAAACAACACAAGA | 288734 |
rs106297885 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Chfr | Rn_Celera | 12:52597810 | AGCGTGGGTCTCCCC[A/G]CTCCGGGGGTCTTTC | 288734 |
rs106369036 | snp | G/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52576060 | TACATAATGCATGCA[G/T]GCATACACACACATA | 288734 |
rs106474230 | snp | A/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52568272 | TTCTTGTGCTGTCAT[A/G]TCTCTGGCACTCTAT | 288734 |
rs106475703 | snp | G/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52570042 | CACACGCTCACGCGC[G/T]CTCTCTCTCTCTCTC | 288734 |
rs106628561 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52576542 | CATCTTTTCTGTTTT[C/T]CTTTTAAGTTGGAGT | 288734 |
rs106657986 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52565448 | TGAAGATGTAGAACT[C/T]TCAGCTCTCCCTGCA | 288734 |
rs106667227 | snp | A/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52574639 | TCGGATATAAAGTGA[A/G]GTATTTTCAGGACTC | 288734 |
rs106766032 | snp | C/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52579711 | GGGCTAAGGCCAAGA[C/G]AACAGGGCCCAGAGG | 288734 |
rs106917541 | snp | A/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52571858 | CCACCATGTGGTTGC[A/T]AGGAATTGAACTCAG | 288734 |
rs107023832 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52569936 | CGCTTCCTAGGTAAG[C/T]GCTCTACCACTGAGC | 288734 |
rs107066335 | snp | A/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52584037 | GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG | 288734 |
rs107134343 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52577767 | AGTGAGGACAGCACC[C/T]ACCACACGACAGCTG | 288734 |
rs107187939 | snp | C/T | 0 | 0 | upstream-variant-2KB | Chfr | Rn_Celera | 12:52596936 | AAGTAGCAGTGGCTG[C/T]CTCTAGGGAGATGGA | 288734 |
rs107351084 | snp | C/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52573929 | AAGACAGCTTGGTCT[C/G]TGACCCTAGCCCCAA | 288734 |
rs107530723 | snp | A/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52577874 | CTACTCAGTGCACAC[A/G]GACTCAGACTCCAAG | 288734 |
rs197019432 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52564237 | ACTTCCCCCTCTCCA[C/T]AGACCAGGGCAACAT | 288734 |
rs197036842 | snp | A/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52571613 | CCTTGAAAAGGGACA[A/G]TCTCCAATGTCTGCT | 288734 |
rs197077152 | snp | G/T | 0 | 0 | upstream-variant-2KB | Chfr | Rn_Celera | 12:52597138 | CAAGTAGGATTAGGT[G/T]ATCTCTAATGTGATT | 288734 |
rs197093490 | snp | G/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52594242 | CTCTTGGAAGGCGGA[G/T]GCAGAGGCAGAGACA | 288734 |
rs197474105 | snp | A/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52565118 | TGGGCAACAGCTCCA[A/G]TGCCTTAATCTGAAC | 288734 |
rs197773098 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52578856 | TAAGTCCAGGGCAGC[C/T]AGGGCTACATACAGA | 288734 |
rs198186537 | snp | A/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52569100 | AGCAAGTCTGAGCCT[A/T]GTCAGGGACATAACC | 288734 |
rs198307406 | snp | A/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52595237 | TAAATCGCCCTCTGA[A/G]CATATTCTTTGTTCT | 288734 |
rs198424302 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52570070 | CTCTCTCTCTCTCTC[C/T]CCGTTCCTTCCTCCC | 288734 |
rs199221696 | snp | A/G | 0 | 0 | intron-variant, missense | Chfr | Rn_Celera | 12:52575644 | TATAAAAAAAAAAAA[A/G]AAAGAAAACCAAGCC | 288734 |
rs199225378 | snp | A/G | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52564271 | AGATCCTTGCAGAAA[A/G]TGGCATTGTCTTTGC | 288734 |
rs199352131 | snp | C/T | 0 | 0 | intron-variant | Chfr | Rn_Celera | 12:52581549 | GCAACCACATGGTGG[C/T]TCACACCCATCTGTG | 288734 |