SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3089912 | snp | C/T | 0.492564 | 0.0605205 | intron-variant | Ahi1 | GRCm38.p3 | 10:20996320 | CAGTGACAAAGTATG[C/T]TTCAAAATATTAAGA | 52906 |
rs4228153 | snp | A/T | 0.21875 | 0.248039 | downstream-variant-500B | Ahi1 | Mm_Celera | 10:21080598 | AGTGAGCTCTGGGTA[A/T]GCCAAGAGACCCAGC | 52906 |
rs4228154 | snp | C/T | 0.21875 | 0.248039 | downstream-variant-500B | Ahi1 | GRCm38.p3 | 10:21080563 | AATGAAATGGAAGAA[C/T]GACTGAGGAAGATGG | 52906 |
rs4228155 | snp | A/G | 0.261853 | 0.249719 | downstream-variant-500B | Ahi1 | GRCm38.p3 | 10:21080494 | Gcacaccacgcaaac[A/G]ctcgtgcatgcacac | 52906 |
rs4228156 | snp | G/T | 0.21875 | 0.248039 | utr-variant-3-prime, nc-transcript-variant | Ahi1 | GRCm38.p3 | 10:21080346 | CAAGTTCAGAGTGAC[G/T]GAGCTGCCTGCCCAA | 52906 |
rs4228157 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime, nc-transcript-variant | Ahi1 | GRCm38.p3 | 10:21080280 | GCCGCTGGTACTGGC[C/T]GCTGAGCCTTCGGGG | 52906 |
rs4228158 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime, nc-transcript-variant | Ahi1 | GRCm38.p3 | 10:21080277 | GCTGGTACTGGCCGC[C/T]GAGCCTTCGGGGCTG | 52906 |
rs4228159 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime, nc-transcript-variant | Ahi1 | GRCm38.p3 | 10:21080257 | CTTCGGGGCTGAGGG[C/T]TGTGGGCTTCAGCAG | 52906 |
rs6171262 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Ahi1 | Mm_Celera | 10:20996261 | TTACTCCACTTAGAA[C/T]ATTTTAATTCACAAT | 52906 |
rs6171745 | snp | C/T | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:20996313 | AAATATATCTTAATA[C/T]TTTGAAACATACTTT | 52906 |
rs6172265 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:20996386 | AAGAGAAAACATAAT[A/G]CATATTTAATGTATT | 52906 |
rs6195595 | snp | A/T | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21030761 | cccataaaagcatca[A/T]atctgaaccataata | 52906 |
rs6196119 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21030842 | aataaagtatctcca[A/G]aatcccactgagtnc | 52906 |
rs6196139 | snp | C/T | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21030856 | anaatcccactgagt[C/T]ctgtgttggccatct | 52906 |
rs6209633 | snp | C/G | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21031027 | tcgcagcactggggc[C/G]catctagcttgaacc | 52906 |
rs6210151 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21031124 | gatactgtctcctca[A/G]cattccnctctggtt | 52906 |
rs6210164 | snp | C/G/T | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21031131 | tctcctcancattcc[C/G/T]ctctggttctgagtc | 52906 |
rs6210701 | snp | C/T | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21031224 | ccaaacctctcactg[C/T]gcactgcccagccat | 52906 |
rs6221936 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Ahi1 | Mm_Celera | 10:21076369 | GGGAGGTTGATGGTT[A/T]AGCCCACCTGCGCAG | 52906 |
rs6221949 | snp | G/T | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21005350 | attaataatttttat[G/T]naagataatttatat | 52906 |
rs6221950 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21005351 | ttaataatttttatn[A/G]aagataatttatatC | 52906 |
rs6223038 | snp | C/T | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21076551 | cccaaaagtccccca[C/T]accctccccccacca | 52906 |
rs6223120 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21005578 | CTTTTTTCATGTTAT[A/G]TATGATCCATTTTTC | 52906 |
rs6365782 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Ahi1 | GRCm38.p3 | 10:21025573 | TGAAACATTCCGCAA[A/T]GCATGACAGCATCCC | 52906 |
rs6398316 | snp | A/T | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:20994647 | ccctttatagtgtgc[A/T]gtnctaccttgctgt | 52906 |
rs6398321 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:20994650 | tttatagtgtgcngt[A/G]ctaccttgctgtggc | 52906 |
rs13467889 | snp | A/G | 0.231111 | 0.249285 | missense, nc-transcript-variant | Ahi1 | Mm_Celera | 10:21074451 | AAGAAAAGCGAGCCG[A/G]TGGTCCGCAAAGTCA | 52906 |
rs29311643 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahi1 | GRCm38.p3 | 10:21013972 | GAAAGGAGCTGAGGC[A/G]CTGCAGTCTGTGTTG | 52906 |
rs29314232 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahi1 | Mm_Celera | 10:21054685 | TGGTTTTTTTTTTTT[C/T]TTGGTTTTTTTTTTT | 52906 |
rs29314829 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Ahi1 | GRCm38.p3 | 10:21020717 | CCTGAGCTGGGAAAT[C/T]CCATTCTTCTGTGGA | 52906 |
rs29314862 | snp | A/T | 0.495 | 0.0497494 | intron-variant | Ahi1 | GRCm38.p3 | 10:20981818 | CCTGTTTCCTGCATA[A/T]TCTCTTCAATCTAGT | 52906 |
rs29315295 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21046889 | AAGTCTGAAGAAACC[A/G]TGCAAGAGAGTCAGG | 52906 |
rs29315682 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahi1 | Mm_Celera | 10:20973851 | ATATGCATCTAGAGT[C/T]AAGAGCTCCGGGGTA | 52906 |
rs29316106 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahi1 | Mm_Celera | 10:20975556 | AAAGGCTGGAAAACA[A/G]TTTTCCAAGCAAATG | 52906 |
rs29316342 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahi1 | Mm_Celera | 10:20988303 | CCGTTTCCATCAGAA[C/T]ACTTCCTATGTACTT | 52906 |
rs29316365 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ahi1 | Mm_Celera | 10:21009535 | TCCCTGAGTAGCCTA[A/G]GTTGGCCTCAAACTC | 52906 |
rs29316828 | snp | C/T | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:20975503 | GCTGCTTACAGGAAA[C/T]CCATATCAGGGAAAA | 52906 |
rs29317169 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahi1 | Mm_Celera | 10:21020135 | TGTCTTTAAAAAGAA[C/T]TATTGATCTCTGTGT | 52906 |
rs29318431 | snp | A/C | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:20998179 | CCCTTATGTAAATTC[A/C]TATAATTGAAAGGTC | 52906 |
rs29319486 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21046847 | GTGTGAGTGTGAGGC[A/G]ACTGCAGTTTACAGC | 52906 |
rs29319673 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ahi1, Gm20149 | GRCm38.p3 | 10:21048673 | ACTGGAGAAGGGTCG[A/C]GAAGACTTGGAGCAT | 52906 |
rs29319714 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:21006405 | TTGGGTACCCGTCAG[A/G]AGCAACCAGTCTAAC | 52906 |
rs29320473 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ahi1 | GRCm38.p3 | 10:21004079 | TGTGGTTAATAACTA[C/T]GGAAATGGGCATAAA | 52906 |
rs29320741 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahi1 | GRCm38.p3 | 10:21004718 | TGCACTGGGCCTGCC[A/G]TGCTCCCTGCTCCTC | 52906 |
rs29320903 | snp | A/G | 0.49827 | 0.0293608 | intron-variant, nc-transcript-variant | Ahi1, Gm20149 | Mm_Celera | 10:21044359 | AGCTGTGCCCAATAT[A/G]TACATGCTTCTCACT | 52906 |
rs29321482 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ahi1 | GRCm38.p3 | 10:21057658 | TTGCGTCATATCCCC[G/T]AAGATCATCGGAAAA | 52906 |
rs29321618 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahi1 | Mm_Celera | 10:20983251 | ATTGCTTTCCCAGTG[C/T]GCCCCCTGTAGTCCA | 52906 |
rs29321863 | snp | G/T | 0.5 | 0 | intron-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21042644 | GGCCTTCATGCTGCA[G/T]TTGGCCTTGGCACTT | 52906 |
rs29322283 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ahi1 | GRCm38.p3 | 10:21032108 | AGCACAGTAACAGAG[C/G]GGGCGGTGGGCAGGA | 52906 |
rs29322679 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ahi1 | Mm_Celera | 10:20971175 | AATATGTTTAAAGGC[C/T]TTTGTAGAGAAGCAG | 52906 |
rs29323486 | snp | A/G | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21047096 | GGCATGAAACAAGCA[A/G]CTACTGCTTTGACTT | 52906 |
rs29323856 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21036973 | TTCCTGAGCTGACAG[A/G]GTCCTGTTCAGAAAA | 52906 |
rs29324619 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ahi1 | GRCm38.p3 | 10:21029981 | GCCAATGTCTCACAA[A/G]TCCTGGGTGCCTCCA | 52906 |
rs29324674 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:20989053 | AAACCTAGTGTAAAC[A/G]CCTACTACCTAGGCT | 52906 |
rs29324694 | snp | A/T | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:21071509 | AGCAGTCGTCTTAAA[A/T]CTCCTTATAAGTACT | 52906 |
rs29325386 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Ahi1 | GRCm38.p3 | 10:21057921 | CTAAGGTAAGTGTCC[C/G]TGTGACAGCACAGTA | 52906 |
rs29325540 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahi1 | Mm_Celera | 10:20981230 | AATATACACACACAC[A/G]CGCGCGTGTGTGTGT | 52906 |
rs29325686 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahi1 | Mm_Celera | 10:20969347 | TTTTAAAGTAGACTT[C/T]ATTGTTTAAAAAACC | 52906 |
rs29326738 | snp | A/G | 0.489796 | 0.070696 | intron-variant, nc-transcript-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21047025 | TGTGCGGTCTCTGTG[A/G]AATTGGCACGTGTCA | 52906 |
rs29327323 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Ahi1 | GRCm38.p3 | 10:20982583 | ATGATGAGCTGTTGA[C/T]GGCGTGTTCTGACCT | 52906 |
rs29327598 | snp | C/T | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:21050507 | GCACAGCAGCAACAG[C/T]GTTCGTCCCGTGTGA | 52906 |
rs29327856 | snp | A/G | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21045598 | CATTGTCACTTTGCT[A/G]ACATTTATGGTTTTA | 52906 |
rs29328216 | snp | C/T | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:20992472 | CTGGCTATCTTGGAA[C/T]TCACTCCATAGGTCA | 52906 |
rs29328736 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21042580 | GATAGGCCCAGCTAC[C/T]CTGATGCTCCTCTGC | 52906 |
rs29329150 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ahi1 | GRCm38.p3 | 10:20990957 | ATCCTTTCATCAAGA[A/G]CTCCAAGGAATGAGC | 52906 |
rs29329237 | snp | A/C | 0.49827 | 0.0293608 | upstream-variant-2KB, intron-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21040628 | TATTTATCACACACA[A/C]AAAAAATGCAGTAAC | 52906 |
rs29329333 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21042433 | TGTCTTAGGACTCTT[C/T]CCCTGGATGGTCACG | 52906 |
rs29329363 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:21075461 | AAGTGGTGCAGGCAA[A/G]ATGGCTCAGCAGTTA | 52906 |
rs29329820 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Ahi1 | Mm_Celera | 10:21020781 | ACACAAGCGCCTAAG[C/T]GTTTCCTATGTATCT | 52906 |
rs29330479 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Ahi1 | GRCm38.p3 | 10:20988316 | AACACTTCCTATGTA[C/G]TTTGTTCCACAAAAC | 52906 |
rs29331953 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:20998578 | GTCATTATCGTGGTC[A/G]TTGTTGGCTGCTTTT | 52906 |
rs29332486 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahi1 | Mm_Celera | 10:20983008 | AGACACACCAGAAGA[A/G]GGCATCAGATCTCAT | 52906 |
rs29332549 | snp | A/T | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21030656 | CAAACAGGCCAATTT[A/T]AAAAAAAAGAATTAT | 52906 |
rs29332596 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahi1 | GRCm38.p3 | 10:21013451 | CATACTTGCCCACAT[A/G]AATGTGTACATACAG | 52906 |
rs29332714 | snp | C/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Ahi1, Gm20149 | Mm_Celera | 10:21044396 | GGCTTTATTCTTAAT[C/G]TCCTCAATATAATAA | 52906 |
rs29332875 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:21068164 | GAGGAAGGGACTAGA[A/G]ATAGGGTACACTCTT | 52906 |
rs29333552 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21045771 | AAAATGACATAGTAA[A/G]CACTGTTCAGATACC | 52906 |
rs29333710 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21042374 | TACTCATGGTGATGG[C/T]AATCCGACCATGGCC | 52906 |
rs29334546 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ahi1 | Mm_Celera | 10:20998624 | CGAGTTGTACACGCA[A/T]TGTGCTCAGGCGTGT | 52906 |
rs29334876 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahi1 | GRCm38.p3 | 10:20981235 | ACACACACACACGCG[C/T]GTGTGTGTGTGTGTG | 52906 |
rs29335419 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ahi1 | GRCm38.p3 | 10:21029638 | ATGGAGGGGGCTGTT[C/T]TATGGAGAGGCTCAG | 52906 |
rs29335811 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahi1 | GRCm38.p3 | 10:20989081 | GCTCACAGTGGAAAC[A/G]GGAGTGTCAGAAGTT | 52906 |
rs29336147 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | Mm_Celera | 10:21013152 | GGTAGGGGAGTGGGG[A/G]GAAGGGGTATGGGGA | 52906 |
rs29336854 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Ahi1 | GRCm38.p3 | 10:20979224 | AGATAATCCAATGCC[A/T]TCTCACGCGATCATC | 52906 |
rs29337110 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:20982101 | CTTGCCCGCTGCTGC[A/G]GGGCTCAGCCAGCCT | 52906 |
rs29337151 | snp | C/T | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:20979642 | CTCAAACCAAGAGTA[C/T]TTACCTGAAAAATTG | 52906 |
rs29337436 | snp | A/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21044376 | ACATGCTTCTCACTG[A/T]TTGGGGCTTTATTCT | 52906 |
rs29337735 | snp | A/G | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:21011190 | AAGAGTAGGCTGTGC[A/G]TGCTTTTTAAAGAAT | 52906 |
rs29337895 | snp | A/T | 0.5 | 0 | intron-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21042645 | GCCTTCATGCTGCAT[A/T]TGGCCTTGGCACTTC | 52906 |
rs29337908 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Ahi1 | GRCm38.p3 | 10:20979765 | AGATCTGACAGTGGG[A/C]GTGCTCTGTTAACTG | 52906 |
rs29337930 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ahi1 | Mm_Celera | 10:20973743 | ATTCCCATTTTTTTG[G/T]CCCTGGCATTCCCCT | 52906 |
rs29341427 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahi1 | GRCm38.p3 | 10:21006730 | TCTGGTACTTCTGTA[C/T]GTGCTTTTCATGCTT | 52906 |
rs29342289 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahi1 | GRCm38.p3 | 10:21013929 | AGCTGTTCATTCTAG[C/T]GTCATGTGGAGAGAG | 52906 |
rs29342587 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Ahi1, Gm20149 | GRCm38.p3 | 10:21034583 | TTTCATCGTGGTTTC[A/G]TTCAGGCAAAACTTG | 52906 |
rs29342961 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahi1 | GRCm38.p3 | 10:20981231 | ATATACACACACACA[C/T]GCGCGTGTGTGTGTG | 52906 |
rs29342972 | snp | A/C | 0.5 | 0 | intron-variant | Ahi1 | GRCm38.p3 | 10:21050501 | TATAAAGCACAGCAG[A/C]AACAGCGTTCGTCCC | 52906 |
rs29343304 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Ahi1 | GRCm38.p3 | 10:20991197 | CCCGGATGCCATACC[G/T]GGCCAACTGTATTGC | 52906 |
rs29345141 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahi1 | Mm_Celera | 10:21061446 | TGTGTAGCCCTGGCT[A/G]TCCTGGAACTCACTT | 52906 |
rs29345856 | snp | A/G | 0.455 | 0.143091 | intron-variant | Ahi1 | GRCm38.p3 | 10:21057572 | GATGCACCTTCCTCC[A/G]TTCAGGACTTCAATC | 52906 |
rs29346537 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Ahi1 | GRCm38.p3 | 10:20995913 | GAACCTAAAAGTAAC[G/T]TGGTAACCTGCAGAT | 52906 |