SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs261491131 | snp | A/T | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476329 | TCTTTATTATATATT[A/T]CTCTTAACTATAAAT | 23894 |
rs261684277 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474638 | TCGGGCTTGGTGGCA[A/G]GTGCCTTTATGTACT | 23894 |
rs261726366 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470794 | TTTACCTCTACCTTA[C/T]TGTCTTTATAGGGAA | 23894 |
rs261880785 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470324 | TGACAGTGGGAGAAA[C/T]AGCCTTCCCAACAGG | 23894 |
rs261907282 | in-del | -/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100471302 | ACACGAGCTCTGGGG[-/G]TACTGGTTAGTTCAT | 23894 |
rs261913631 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474428 | GTCCTTCTCCTTCTC[-/A]GTCCTACTTCCTCTA | 23894 |
rs261949674 | in-del | -/C | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493639 | ACACCACAAGCCCCT[-/C]CCATTTCCCTTTTCT | 23894 |
rs262027898 | snp | C/T | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100493055 | ATAGCCATAGCCCCA[C/T]CTGCCGCCCCACCCC | 23894 |
rs262131356 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100491613 | GGAAAGGGGATAACA[C/T]TGGAACTGTAAATAA | 23894 |
rs262158927 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100477785 | CTTTTCATCTCTGAC[A/G]TTATATTCTTCATTT | 23894 |
rs262164359 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462872 | CATCTTTTATTTATC[-/T]TTTCCCTACAGCACA | 23894 |
rs262172340 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470374 | AAACCTGAAAATACA[C/T]AGCAATGCACAGAGC | 23894 |
rs262427780 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100475825 | GTGTGAAAAGTGATG[A/C]ATTATTATATATGAA | 23894 |
rs262456098 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474027 | GCCCACCCCCAGGGT[A/G]CACACTGATAGGCCC | 23894 |
rs262470562 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479171 | AAAAAAGTTATCACT[A/G]ACAATTGCTCTTTAC | 23894 |
rs262491456 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473071 | CTATTCCTGGCAGAG[A/G]CAGGCAGATCTCTAA | 23894 |
rs262502771 | in-del | -/GTGTGTGTGTGTGTGTGTGT | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100467829 | TGGTCACTTAACTCC[-/GTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 23894 |
rs262515402 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100469964 | AACCAGAAAAACCAC[G/T]AACTTCATTCTAAAT | 23894 |
rs262612501 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466580 | ACCATCTAACCCCAG[A/G]AGGGCTACCATCAGT | 23894 |
rs262765206 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473658 | GGCACCACATGTGGT[A/G]TTTCTATATAATTAA | 23894 |
rs262782008 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466147 | AACAAGGGCTCAGAC[C/T]TTAGTAGGCCCTGAG | 23894 |
rs262796653 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472647 | CTACAGAAAACTATC[A/T]GAGCTGGGCGGTGGT | 23894 |
rs262811572 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479949 | ACAAGATGGCTCAAC[G/T]GGTAAGAGCACTGAC | 23894 |
rs262849764 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478550 | AACATGTATACATAA[A/T]GTGTATTATATACAT | 23894 |
rs262872879 | in-del | -/TTTG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487962 | TTGTTTGTTTGTTTG[-/TTTG]AATTATTGGAGGATT | 23894 |
rs262886337 | snp | A/C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488290 | CCTTCAGCCAATGAG[A/C/T]TGCCCCTTCCTGGAG | 23894 |
rs262919055 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486587 | AAAACAGCAGTAGCA[G/T]ACGCCACGCCAGTGC | 23894 |
rs262944868 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478421 | CCTTTTATTCTGAGA[A/G]GAGTCTTACTATGTT | 23894 |
rs263006342 | in-del | -/TAT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472430 | CCTATCTGATTACAG[-/TAT]TATTATTATTATTAT | 23894 |
rs263030985 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100487610 | GCTCAGGCTCATTTT[A/G]GACCTCATTTTGTAG | 23894 |
rs263154621 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479470 | AAAAAGCAGAGGAAA[A/T]GGAGGGATGATCTTT | 23894 |
rs263177874 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483666 | AAATGACACAATCCC[A/G]TATTTTTCTTGGGGG | 23894 |
rs263200993 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478073 | CCTCCTTTCTCGTGC[C/G]CAAGTGCTGGCCTGT | 23894 |
rs263265408 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485565 | ACAGCATACATAACA[A/G]AGACAAAAGAAACTG | 23894 |
rs263294549 | in-del | -/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465472 | TAGGAGTCCTGCCCT[-/G]TTCTGAATATAAATG | 23894 |
rs263330523 | in-del | -/G | | | downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100459712 | GAGTTTTGAAGTAAT[-/G]GTTTTTTTTGTTTTG | 23894 |
rs263407565 | snp | A/T | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100459798 | AAGATTTATTTATTT[A/T]TTATATGTGAGTACA | 23894 |
rs263445742 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474204 | AGCTCTAATCTTTCC[A/G]TGAATAGCCTAGACA | 23894 |
rs263476975 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474356 | TCATCTCCACTCACC[A/C]TTGTCCTAAGCTTCC | 23894 |
rs263634187 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490984 | GAGAAACTCTGTCTC[A/G]AAAACCAAAAAAGTA | 23894 |
rs263725553 | in-del | -/T | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460220 | GGATTTGCATCCTTC[-/T]TTTTTTTCTTTCTTC | 23894 |
rs263732330 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482549 | GGCCTGGAGCAATGG[C/G]TCAGCAGCTAAGGGC | 23894 |
rs263801666 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100465845 | ACTGGCTCTGGTAAC[A/T]TTTCAAGAGGAGACA | 23894 |
rs263913810 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460197 | GAAGCACAGGCCAAG[C/T]GAGGTACAGGATTTG | 23894 |
rs263950693 | in-del | -/ACAC | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100460912 | CCACACCCACACTAT[-/ACAC]ACACACACACACACA | 23894 |
rs263991382 | in-del | -/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483203 | TCTCCTTTTCTTTTG[-/C]TTTGGCTCATTTGTC | 23894 |
rs264006176 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466928 | ACCTTACCAGAGAGA[C/T]ATTTCCCACGTTTAC | 23894 |
rs264025695 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100460087 | CCATAGCCAGCTCAG[A/G]AAAGGAAGAGCTCTT | 23894 |
rs264176260 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100488398 | TGAAACACCATGAAC[A/G]AGCAAGCCGTTTCAC | 23894 |
rs264180103 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462660 | TGTCACTACACTGTC[A/G]TAGGACAAAATATGT | 23894 |
rs264305910 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100461107 | CCGACTCATAAATCA[A/G]GTAAATTTGTTTTTA | 23894 |
rs264346260 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | Mm_Celera | 13:100492759 | GTGGGGTGCATTTCT[A/G]TAGACCAAACAGCTA | 23894 |
rs264382002 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100484729 | GCAGTGAAATTATTT[C/T]AAGATGTTTTATATT | 23894 |
rs264419238 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | Gtf2h2 | Mm_Celera | 13:100492386 | TCAGGCGGAAGCTGC[C/T]GCGCTCCCTGCACAC | 23894 |
rs264478063 | in-del | -/TT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473534 | GTTCCTTTTTTTTTC[-/TT]TTGCTTTTTTTTTTT | 23894 |
rs264482790 | snp | A/C | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482175 | TCTGAAAAAATAATA[A/C]TATAAATGGTTATGG | 23894 |
rs264506427 | in-del | -/AC | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464660 | CTTCCCCAAGAAAGT[-/AC]ACACTTAGTGAAAGA | 23894 |
rs264566162 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467973 | GTGCAGGTGAAAGCA[C/G]TGACTAACCAAAAGT | 23894 |
rs264621799 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100492221 | CGCGCATGGCCACTG[C/G]GGAGGCTCTGCCTCG | 23894 |
rs264784645 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485778 | ATAGCCCAATTCAAC[C/T]TTTATACTTTCTGCT | 23894 |
rs264958606 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100470047 | CTCTTTTCAAAAGAT[G/T]GAGACCATTATAGAA | 23894 |
rs264968596 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462276 | CCTTCATGTTTCCTT[C/T]CTTGAAACAGATCTC | 23894 |
rs265041860 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478124 | CAGCTGGCAGCCAGA[C/T]ACTTCTACATCCTGT | 23894 |
rs265128839 | in-del | -/A | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100488138 | TGGGGCTGCTCCCCC[-/A]ACCCCGCCCCGGGGC | 23894 |
rs265164745 | snp | G/T | | | intron-variant, downstream-variant-500B | Gtf2h2 | Mm_Celera | 13:100476452 | TTGTGACATATAAAT[G/T]AATCAAAATTCATAT | 23894 |
rs265201138 | snp | G/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100473242 | CCCCTGAAGTATCTT[G/T]AACATTTTTTTAAAA | 23894 |
rs265258517 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100466813 | TATAAAGCTGAACAG[A/G]TTCCAAAAGAGCCAG | 23894 |
rs265427995 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100478695 | ATTCTATAGCTCAGA[A/G]TGACCTCAAACTCAA | 23894 |
rs265482891 | in-del | -/AATAATAAAATTA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100486553 | ATTAAAAGGCAGCAT[-/AATAATAAAATTA]AAAGGCAAAACAGCA | 23894 |
rs265620091 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100474474 | CATCTCTATTTTGCT[A/G]AGCAATTTTTATAAC | 23894 |
rs265649582 | snp | C/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100481991 | GACAAGGATTACAGG[C/G]AGAAACATTGTTTCA | 23894 |
rs265862684 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100489436 | GGACAGAAAGGCTTC[A/G]AGAACCTCTTTTCCT | 23894 |
rs265896467 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100460477 | GAAGGGGTCCCTCCA[C/T]TGCTGTAGCTGACAC | 23894 |
rs265919328 | in-del | -/AGTCA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482243 | GCTAGAAGAGTCAGG[-/AGTCA]AGTCATCATTGGCTA | 23894 |
rs265926231 | snp | A/G | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100467407 | AAGTGGAGGCAGTAC[A/G]ACATACAGGAAAGAA | 23894 |
rs265969413 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100464477 | AATGGACTAAGTGCT[A/T]TAATTAAAAGATAAA | 23894 |
rs266022153 | in-del | -/ATACACACACACAC | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100460910 | AACCACACCCACACT[-/ATACACACACACAC]ACACACACACACACT | 23894 |
rs266114085 | snp | C/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100485016 | ATCTCTAACCTTTCC[C/T]AAGACTTCTTGGGGG | 23894 |
rs266185302 | in-del | -/A | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100479153 | ATGTACATAACATTT[-/A]AAAAAAAAGTTATCA | 23894 |
rs266237937 | snp | A/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100483144 | TTTTAAAGAACAGAA[A/T]GCCTTCAATTTCTGC | 23894 |
rs266247979 | in-del | -/ATA | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100491913 | GCACACACAGTTCGC[-/ATA]ATATTACTTTTAAGC | 23894 |
rs387003101 | in-del | -/T | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100462554 | GTTTTCTTTTTTTTT[-/T]GAGACAGTCTCTCTA | 23894 |
rs387003135 | in-del | -/AA | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100490418 | AACCCTCTCTCAAAG[-/AA]AAAAAAAAAGTCAGA | 23894 |
rs387367961 | in-del | -/AC | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100460912 | CCACACCCACACTAT[-/AC]ACACACACACACACA | 23894 |
rs387382398 | in-del | -/ATT | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100472466 | ATTATTATTATTATT[-/ATT]GCCTAGTCTGTTGTC | 23894 |
rs387839963 | in-del | -/GAAG | | | intron-variant | Gtf2h2 | Mm_Celera | 13:100482439 | AAGGAAGGAAGGAAG[-/GAAG]AAAAGATGGAAAGAA | 23894 |
rs578297314 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100480240 | GCTACAGTGTACTCA[C/T]ATACATAAAAATAAA | 23894 |
rs578386003 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471346 | CTATAGGGTTGCAGA[C/T]CCTTCAGCTCCTTGG | 23894 |
rs578388746 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100461348 | CCTTAAGTGGTGACC[A/C]ATATCTTCAACAATT | 23894 |
rs578394507 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490377 | TCCAGAGCAAGTTCC[A/G]GGACAGCCAAGGCTA | 23894 |
rs578483869 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100484422 | TTTTTGGAGGAACTC[A/G]CCTTCCTCAATCTCA | 23894 |
rs578497758 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472765 | AGGACAGCCAGGGCT[A/G]CACAGAGAAACCCTG | 23894 |
rs578520466 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470472 | ATAAAGCACTTTACC[A/G]TGCAAACATGAAATT | 23894 |
rs578699398 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100469944 | CTATCTCCAGCACTT[C/T]ACTAAACCAGAAAAA | 23894 |
rs578789602 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100484218 | CTGTGTGCTGGGCAC[A/C]GGGGAAATGCACACT | 23894 |
rs578866645 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470547 | TGTGTAGCCCTGGCT[A/G]TCCCGGAACTCACTC | 23894 |
rs578941822 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473520 | ATGTATCTGTATATA[G/T]TTCCTTTTTTTTTCT | 23894 |
rs579096319 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471670 | ATAGTGTCCACACTT[C/T]GGTCTTTGTTCTTCT | 23894 |
rs579101166 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100480077 | GAAGACGGCTACAGT[G/T]TACTTATATATAATA | 23894 |
rs579109810 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | GRCm38.p3 | 13:100459847 | ACCCCAGAAGAGGAC[A/G]CCAGATCTCATTACG | 23894 |
rs579350812 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471595 | CCTTTCGCCTCAGCT[C/T]CAAACTTTGTCTCTG | 23894 |
rs579465444 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100465459 | TTAGTTGATATACAT[A/G]GGAGTCCTGCCCTTT | 23894 |
rs579469077 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471717 | TGCAAATTGTATCTT[A/G]GGTATTCTAAGTTTC | 23894 |
rs579572038 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100491371 | AACTAACCAGTACCC[A/C]CAGAGCTCCCAGGGA | 23894 |
rs579639221 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473970 | CCCCAGGGTGCCCCC[C/T]CCCCCCGTGTGCCCA | 23894 |
rs579647993 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487362 | GAACAGCAGTTCTCA[A/C]CCTGTGGGACACAAC | 23894 |
rs579701438 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470596 | CGAACTCAGAGATCC[A/G]CCTGCCTCTGCCTCC | 23894 |
rs579796684 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100463920 | TCCACCTCCACACAC[A/G]ACAGACAGACAGACA | 23894 |
rs579849436 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470575 | CTCTGTAGACCTGGC[C/T]GGCCTCGAACTCAGA | 23894 |
rs579884111 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486978 | TGAGGCAAGGAGTCT[A/G]AAGTCAGCTGAGGAA | 23894 |
rs579906384 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100475172 | ATAAAAAAAAGTTCA[A/T]ACCATCTAGTATCAG | 23894 |
rs579959877 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100474013 | CCACCCCCCAGTGTG[C/T]CCACCCCCAGGGTAC | 23894 |
rs580370264 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100482333 | AGGAGAAAGGGAAGA[A/T]GGGGGAATGAGGGGG | 23894 |
rs580376356 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100463918 | CCTCCACCTCCACAC[A/C]CGACAGACAGACAGA | 23894 |
rs580436440 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100462752 | GTTTTGGTTTTTTTG[A/G]CACAAGATCTTACCT | 23894 |
rs580472001 | snp | C/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100482138 | ATGTTGACATACTTT[C/G]AATACAATTTACAGA | 23894 |
rs580508836 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472251 | TTGTTTTGATTTGCA[G/T]TTCCCTGATGATTAA | 23894 |
rs580568749 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100484221 | TGTGCTGGGCACCGG[A/G]GAAATGCACACTACC | 23894 |
rs580741190 | snp | C/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472754 | AAGTGAGTTCCAGGA[C/G]AGCCAGGGCTACACA | 23894 |
rs580837077 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100476633 | ACAAAGGCTAAAAAG[C/T]CAAGAGATATACTTA | 23894 |
rs580846713 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490410 | CACAAAGTAACCCTC[C/T]CTCAAAGAAAAAAAA | 23894 |
rs580854742 | snp | A/C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471529 | AGTGTCAGCGTTTGG[A/C/T]AGCTGATTATGGGAT | 23894 |
rs580891422 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471171 | CTTACCCACCCACTT[C/T]CACTTCTTGGCCCTG | 23894 |
rs581145934 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100478954 | TTCTAACTTAGAGGA[A/G]TAAATTTTAAGTGTT | 23894 |
rs581215649 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471155 | CTCCGCCCCCTGCTC[A/C]CTTACCCACCCACTT | 23894 |
rs581288313 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100488393 | CCCAATGAAACACCA[C/T]GAACAAGCAAGCCGT | 23894 |
rs581390823 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100483246 | AATCTCCTTATATAG[A/C]TCTGGCTGTCCTGGA | 23894 |
rs581430102 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472446 | ATTATTATTATTATT[A/T]TTATTATTATTATTA | 23894 |
rs581444273 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472772 | CCAGGGCTACACAGA[A/G]AAACCCTGTCTCGGA | 23894 |
rs581473466 | snp | C/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100467651 | ACTTGTACAGTCTTT[C/G]GGTCTGTTTTGTTTT | 23894 |
rs581547355 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100483204 | TCTCCTTTTCTTTTG[C/T]TTGGCTCATTTGTCT | 23894 |
rs581610541 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100466831 | CCAAAAGAGCCAGAG[A/G]GACCCTGTCTTAAAA | 23894 |
rs581802647 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100461733 | TGAACCCACAAGAAC[G/T]GTTAAGGCACTAAGA | 23894 |
rs581805710 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470440 | ACGGGTGGTTGGGTG[A/G]ATAACGAGCTCAAAG | 23894 |
rs581852691 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473959 | AGGGTGCCCACCCCC[A/G]GGGTGCCCCCCCCCC | 23894 |
rs581908276 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100480745 | TATAATTTCATAACC[A/G]TTTTAATTATCACTT | 23894 |
rs582057404 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471671 | TAGTGTCCACACTTC[A/G]GTCTTTGTTCTTCTT | 23894 |
rs582180691 | snp | A/G | | | upstream-variant-2KB | Gtf2h2 | GRCm38.p3 | 13:100494384 | AGAACTAGCTCTGTA[A/G]ATTAGACTGGCCTTG | 23894 |
rs582185459 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100480143 | GCAGGTTGACCAGAG[C/T]GGGCAGGGTTGACTG | 23894 |
rs582191489 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | GRCm38.p3 | 13:100460216 | GTACAGGATTTGCAT[C/T]CTTCTTTTTTTCTTT | 23894 |
rs582247874 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100488407 | ATGAACAAGCAAGCC[A/G]TTTCACGGAGCAGCT | 23894 |
rs582473156 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471639 | GGGTGTTTTGTTCCC[A/T]ATTCTAAGAAGGGGC | 23894 |
rs582514784 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473707 | ACAGCATTCACTATT[G/T]AGTTTGTTCCACATA | 23894 |
rs582569972 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486547 | AATAAAATTAAAAGG[A/C]AGCATAATAATAAAA | 23894 |
rs582577461 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470562 | ATCCCGGAACTCACT[C/T]TGTAGACCTGGCTGG | 23894 |
rs582617059 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473971 | CCCAGGGTGCCCCCC[A/C]CCCCCGTGTGCCCAC | 23894 |
rs582730696 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100482141 | TTGACATACTTTCAA[C/T]ACAATTTACAGAAAA | 23894 |
rs582866781 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100484598 | GCTGGCCATAAAAAC[C/T]TGAGGCTATTGAAAA | 23894 |
rs582872692 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470521 | TTTTTCTTTTTGAGA[C/T]AGGGTTTTTCTGTGT | 23894 |
rs582980897 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100465469 | TACATAGGAGTCCTG[C/T]CCTTTCTGAATATAA | 23894 |
rs583088524 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472714 | GGCAGGCGGATTTCT[A/G]AGTTTGAGGCCAGCC | 23894 |
rs583144538 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100483193 | TTAATAAGAAGTCTC[A/C]TTTTCTTTTGTTTGG | 23894 |
rs583166125 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471887 | GTACTCCATTGTGTA[A/G]ATGTACCACATTTTC | 23894 |
rs583287676 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487001 | CTGAGGAAACACAGC[A/G]AGATCTCATCGTGAA | 23894 |
rs583409426 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100482822 | TTCCCAGCAACCACA[G/T]GGTGGCTCACAACCA | 23894 |
rs583417590 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100463919 | CTCCACCTCCACACA[A/C]GACAGACAGACAGAC | 23894 |
rs583478644 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470591 | GGCCTCGAACTCAGA[A/G]ATCCACCTGCCTCTG | 23894 |
rs583524222 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100475191 | ATCTAGTATCAGTAA[A/G]GTTTGGGCAAATAAT | 23894 |
rs583537527 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471157 | CCGCCCCCTGCTCAC[C/T]TACCCACCCACTTCC | 23894 |
rs583821607 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100488399 | GAAACACCATGAACA[A/C]GCAAGCCGTTTCACG | 23894 |
rs583944618 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487864 | GGTTGCCTGGAAGAA[A/C]AACTAGTGAAAGCCA | 23894 |
rs584026543 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471118 | ACATTTCAAATGCTA[A/T]CCTGAAAGTCCCCTA | 23894 |
rs584046120 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472308 | TCTCAGCCATTCGAT[A/G]TTCATCAGTTGAGAA | 23894 |
rs584076409 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470443 | GGTGGTTGGGTGAAT[A/G]ACGAGCTCAAAGGAT | 23894 |
rs584202700 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100484222 | GTGCTGGGCACCGGG[A/G]AAATGCACACTACCT | 23894 |
rs584384212 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472764 | CAGGACAGCCAGGGC[A/T]ACACAGAGAAACCCT | 23894 |
rs584461053 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100488414 | AGCAAGCCGTTTCAC[G/T]GAGCAGCTGCACCAC | 23894 |
rs584500537 | snp | C/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473736 | TAAAATGTTTCAGCT[C/G]TGACAAGTATGTGCA | 23894 |
rs584514820 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100484216 | CACTGTGTGCTGGGC[A/C]CCGGGGAAATGCACA | 23894 |
rs584684748 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471269 | ACTAGACCATCTTCT[A/G]CTACATATGCAGCTA | 23894 |
rs584763674 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100477525 | TTAGTTCCATCCAGT[C/T]TGTTTTTTCTTTTCT | 23894 |
rs584775768 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100480234 | TGTACAGCTACAGTG[G/T]ACTCATATACATAAA | 23894 |
rs584783909 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100461345 | TCTCCTTAAGTGGTG[A/C]CCCATATCTTCAACA | 23894 |
rs584991828 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100479739 | CCAGCCTGGTCTACA[A/T]AGTGAGACCTTGTCT | 23894 |
rs584999017 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gtf2h2 | GRCm38.p3 | 13:100459803 | TTATTTATTTATTAT[A/G]TGTGAGTACACTGTA | 23894 |
rs585017285 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100491242 | TGCCAAATACAGAAG[A/T]GGATGCTCACAGCCA | 23894 |
rs585069916 | snp | C/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100490413 | AAAGTAACCCTCTCT[C/G]AAAGAAAAAAAAAAA | 23894 |
rs585078473 | snp | A/G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471530 | GTGTCAGCGTTTGGA[A/G/T]GCTGATTATGGGATG | 23894 |
rs585088545 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470595 | TCGAACTCAGAGATC[A/C]ACCTGCCTCTGCCTC | 23894 |
rs585274586 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473376 | ATGTCAACACATAGG[G/T]GAAAATAACAAAATC | 23894 |
rs585323744 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100483207 | CCTTTTCTTTTGTTT[G/T]GCTCATTTGTCTTGT | 23894 |
rs585330474 | snp | A/G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100467286 | GCAGAAAAATAGATC[A/G/T]ATCCAGAATGTATAA | 23894 |
rs585345963 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100486909 | TGAGCCGCATCAAAC[A/C]CAGCAGGCACCTGCT | 23894 |
rs585361046 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100487008 | AACACAGCAAGATCT[C/T]ATCGTGAAATTCAAA | 23894 |
rs585507860 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473961 | GGTGCCCACCCCCAG[G/T]GTGCCCCCCCCCCCC | 23894 |
rs585654817 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471640 | GGTGTTTTGTTCCCA[A/G]TTCTAAGAAGGGGCA | 23894 |
rs585660534 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470569 | AACTCACTCTGTAGA[A/C]CTGGCTGGCCTCGAA | 23894 |
rs585858287 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471686 | GGTCTTTGTTCTTCT[C/T]GAGTTTCATGTGTTT | 23894 |
rs585907460 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100481400 | CAGGGGGAGGGTATA[A/G]GGAACTTTCAGAATA | 23894 |
rs586021901 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100482232 | TGGGAAGTAGAGCTA[A/G]AAGAGTCAGGAGTCA | 23894 |
rs586247167 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100462686 | TATGTCTTTGGGGAA[C/T]AAATATGTAAATTTT | 23894 |
rs586370094 | snp | G/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100473993 | TGTGCCCACCCCCAG[G/T]GTGCCCACCCCCCAG | 23894 |
rs586482057 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100484601 | GGCCATAAAAACTTG[A/G]GGCTATTGAAAACAT | 23894 |
rs586484317 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100470529 | TTTGAGATAGGGTTT[C/T]TCTGTGTAGCCCTGG | 23894 |
rs586638352 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100475882 | TTCTAAAATGCTGAT[A/G]CTTTTTGAATAAAAA | 23894 |
rs586820001 | snp | A/C | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472413 | ATATTGGATATTAGT[A/C]CCCTATCTGATTACA | 23894 |
rs586828519 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471170 | ACTTACCCACCCACT[C/T]CCACTTCTTGGCCCT | 23894 |
rs586838011 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100474404 | TAGAGGCAGATCCTC[C/T]GATTCCATGTCCTTC | 23894 |
rs586917078 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100488405 | CCATGAACAAGCAAG[C/T]CGTTTCACGGAGCAG | 23894 |
rs586950367 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100472739 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 23894 |
rs586960786 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100482840 | TGGCTCACAACCATC[C/T]GTAATGAGATCTGAT | 23894 |
rs586994919 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100483197 | TAAGAAGTCTCCTTT[C/T]CTTTTGTTTGGCTCA | 23894 |
rs587326520 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100483231 | GTCTTGTTGATACAG[A/G]ATCTCCTTATATAGC | 23894 |
rs587331669 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100467362 | ATATGCAGAATACAG[C/T]CAATAATATATGTGT | 23894 |
rs587390753 | snp | A/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100465941 | CATATCTTACAAGGA[A/T]AAAAGACAGCAGTTA | 23894 |
rs587469791 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100478231 | GAAGTAACTTAGGTA[C/T]TTACTGATCTATTCA | 23894 |
rs587558096 | snp | A/G | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100488389 | CACCCCCAATGAAAC[A/G]CCATGAACAAGCAAG | 23894 |
rs587563134 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100471143 | CCCCTATACCCTCTC[C/T]GCCCCCTGCTCACTT | 23894 |
rs864301912 | in-del | -/A | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100481455 | TATCTAATAAAAAGG[-/A]AAAAACAGAAAGAAA | 23894 |
rs864315859 | snp | C/T | | | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100463958 | agacagacagacaga[C/T]agactgacTAttttt | 23894 |
rs864319088 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gtf2h2 | GRCm38.p3 | 13:100463958 | AGACAGACAGACAGA[C/T]TGACTGACTATTTTT | 23894 |