SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3669254 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44733518 | TGCTTCCCAGTTCAG[C/T]CCTGGGCTGGACAAT | 16826 |
rs3680791 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Ldb2 | Mm_Celera | 5:44766195 | CAGCTGGAGGCACAC[A/G]AATTACTCAAAGTCT | 16826 |
rs3680838 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ldb2 | Mm_Celera | 5:44766222 | GTCTAAGTGAAGCAA[C/T]ATTTGTTGAGAACCT | 16826 |
rs3682080 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ldb2 | Mm_Celera | 5:44766405 | CAACTTCCTGACAAG[A/T]TCTTATCTCATTGGA | 16826 |
rs3682082 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ldb2 | Mm_Celera | 5:44766406 | AACTTCCTGACAAGT[A/T]CTTATCTCATTGGAC | 16826 |
rs3682106 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ldb2 | Mm_Celera | 5:44766418 | AGTTCTTATCTCATT[A/G]GACAGAGAATTCTTC | 16826 |
rs3682488 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44775871 | CTTCTGGCATTTGAG[A/T]ACTATAGCCCATGTC | 16826 |
rs3682554 | snp | A/C/G | 0.5 | 0 | intron-variant | Ldb2 | GRCm38.p3 | 5:44775900 | TCAGAATAAACAGTA[A/C/G]CCCTTGTCGTTGATG | 16826 |
rs3682557 | snp | C/T | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44775902 | AGAATAAACAGTAAC[C/T]CTTGTCGTTGATGAA | 16826 |
rs3683866 | snp | A/C | 0.32 | 0.24 | intron-variant | Ldb2 | GRCm38.p3 | 5:44776145 | ACTGTGCATTTTCTT[A/C]TTTTTTCCTAAGCTA | 16826 |
rs3683881 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44776160 | CTTTTTTCCTAAGCT[A/G]TAAAATGCATCTTTC | 16826 |
rs3686770 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44753930 | ACTATATACTGTTAA[C/T]AGTAGTGCTAATGGT | 16826 |
rs3686881 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44753988 | CTGTAGTTCCAGCAT[A/T]GAGCTGGATGGTTCA | 16826 |
rs3688016 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44754153 | GACAAGGTATGCTGC[A/G]CGCTCACTCAGTCTT | 16826 |
rs3689331 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44754389 | TAGTTGTGTTTTCCC[C/T]TACTGGCAATGGGTC | 16826 |
rs3696875 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ldb2 | Mm_Celera | 5:44766511 | CCAACGTTAGAATGA[A/G]CCGAATGTAGTTGTC | 16826 |
rs3697444 | snp | C/G | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44766616 | AAGAACTCTCCCATC[C/G]TCTGTGAGGACATTT | 16826 |
rs3697461 | snp | A/C | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44766628 | ATCGTCTGTGAGGAC[A/C]TTTCCTGCTACACTT | 16826 |
rs3701707 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ldb2 | Mm_Celera | 5:44767349 | GAGTCTTTACACAAG[A/G]AGGCCTTTGAACAAA | 16826 |
rs3706190 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ldb2 | Mm_Celera | 5:44770945 | AAATGCTAGACGGTC[A/G]GTCGTGAAAGCCAAT | 16826 |
rs3715555 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44728471 | TGTCTATGCAGAGCC[A/G]AGCTTCTGAGTCCTG | 16826 |
rs6156365 | snp | A/G | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44782237 | GGCCTGTTTGCATAG[A/G]CAACATTTGGTTCCC | 16826 |
rs6156833 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44782276 | TGTTTAAACATAAGA[A/G]CATTCTTCTCTTCTG | 16826 |
rs6157430 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ldb2 | Mm_Celera | 5:44782438 | CTAGCCATGGATTCT[A/G]TGTTAATGACACAGA | 16826 |
rs6164095 | snp | A/G | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44794488 | CCTTCAGAAAGCCAT[A/G]GAGAGTCCACTTTTT | 16826 |
rs6168331 | snp | C/T | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44716888 | TGGGTTCATTTTCCC[C/T]CTTCAGTCTGCAAAC | 16826 |
rs6193807 | snp | C/T | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44536974 | CCCCAAACCATTCTC[C/T]CAAACACATCTCGAN | 16826 |
rs6193834 | snp | A/G | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44536989 | NCAAACACATCTCGA[A/G]CACTGGAATTAATTT | 16826 |
rs6208062 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ldb2 | Mm_Celera | 5:44757962 | TTAAAGCCTTGTATC[A/T]TTCTGAGTTTGCTCT | 16826 |
rs6208670 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ldb2 | Mm_Celera | 5:44758084 | AACTCTAAACCCCTG[A/G]ATCCATAATCCCCAG | 16826 |
rs6257971 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Ldb2 | Mm_Celera | 5:44728094 | ATCTAAGGAAAACGG[C/T]GAGCAAAGCGCTCAA | 16826 |
rs6258462 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ldb2 | Mm_Celera | 5:44728181 | AACACGGAGCTGGGA[C/T]GTGTGTTCGCTCACA | 16826 |
rs6258951 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ldb2 | Mm_Celera | 5:44728265 | GTCTCTCTGCCCAGC[A/C]TGTCACTTGCCTGTT | 16826 |
rs6261576 | snp | C/G | 0.5 | 0 | intron-variant | Ldb2 | GRCm38.p3 | 5:44695573 | tctctctctctctct[C/G]tctctctctctcNNN | 16826 |
rs6345262 | snp | A/G | 0.32 | 0.24 | intron-variant | Ldb2 | Mm_Celera | 5:44771510 | TTGTGATGAAGAACA[A/G]AGCCCAAAGAAGAGT | 16826 |
rs6379676 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ldb2 | Mm_Celera | 5:44708120 | TTGGGTTGGACACAC[A/G]TTATTATTTCTTATT | 16826 |
rs6379718 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ldb2 | Mm_Celera | 5:44708141 | ATTTCTTATTGACTC[A/G]GTAATCACTAACCCT | 16826 |
rs6380212 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ldb2 | Mm_Celera | 5:44708208 | TTTTCAGCTTGAAAT[C/T]CCCAAGACCTGTATA | 16826 |
rs6380279 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ldb2 | Mm_Celera | 5:44708243 | GCTTTTGACTCAAAT[C/T]ACCCANTTCATCAGC | 16826 |
rs6380296 | snp | A/G | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44708249 | GACTCAAATNACCCA[A/G]TTCATCAGCTAGTTA | 16826 |
rs6380764 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44708304 | GGGTGGGGGTACTGA[C/G]TTTCTAGGATAGCTG | 16826 |
rs6382366 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Ldb2 | Mm_Celera | 5:44708638 | GGAATAATTATTTTG[A/T]ATCAGAGAATGAAAC | 16826 |
rs6382759 | snp | C/T | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44708661 | AATGAAACAAGAAAC[C/T]AAAATACAAAGGAGG | 16826 |
rs6384595 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44702431 | ACTTTATTTTTGAGG[A/C]AGGGTCTCTATCTGA | 16826 |
rs6385177 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44702527 | ACTGGGATTACAGAT[A/G]TGTGTCACTGCATCT | 16826 |
rs6385218 | snp | A/G | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44702555 | tctgacattatacat[A/G]ggttttagggagcat | 16826 |
rs6385639 | snp | G/T | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44702582 | gcattgcatgtgtat[G/T]ctcatgcttggatac | 16826 |
rs6385670 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44702601 | ATGCTTGGATACAAA[C/T]ACCATACTAATAGAC | 16826 |
rs6385768 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ldb2 | Mm_Celera | 5:44702657 | GAACTTTCTGTAAGT[C/T]CTTTGTCTACAATGT | 16826 |
rs6386815 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Ldb2 | Mm_Celera | 5:44702847 | TGAAAGGGATGGGAA[G/T]TCCAACATGTAAGAG | 16826 |
rs13478219 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44647501 | AAATACTAAAAAAAT[G/T]CATACATTTTTTCAC | 16826 |
rs13478220 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ldb2 | Mm_Celera | 5:44700573 | TTCTTGTCCCCCACC[C/T]TTTCCCAACATCTCT | 16826 |
rs13478221 | snp | C/T | 0.428062 | 0.175482 | intron-variant | Ldb2 | Mm_Celera | 5:44750337 | CATAAAGTCTTGGAA[C/T]CCAAAGCCTTTCCCT | 16826 |
rs29501053 | snp | A/G | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44483901 | TCTTATAATAACTGT[A/G]AGCCAGACCTCAATG | 16826 |
rs29505407 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44757915 | AGGACTCTGTTGGGG[A/G]TAGCATGTCACTGGG | 16826 |
rs29505800 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44750747 | AAAAGAGTAAGAGGA[A/G]AAAGAGCAAGGTCAA | 16826 |
rs29506288 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44791713 | TACCTGTGGTTATGC[A/G]CGTGAGAAGGCATAA | 16826 |
rs29507808 | snp | C/G | 0.32 | 0.24 | intron-variant | Ldb2 | Mm_Celera | 5:44714890 | ACTCGATGCCCCACA[C/G]CTACATGGGCTTTCA | 16826 |
rs29508129 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44705753 | CCTGTGTTCCATCTC[G/T]AGTACTCTAGTAACA | 16826 |
rs29509073 | snp | A/G | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44686918 | GCCTTTCTCTGCACC[A/G]TCTAGCTGAAGTGGC | 16826 |
rs29509376 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44767698 | TTACATTCTGTCTGA[C/T]GTTTATCAGCATCTC | 16826 |
rs29510251 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44799009 | CAACACAGACGCAAA[C/T]ATCCACAAAATCTCT | 16826 |
rs29514427 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44482187 | TTTCTTCCTTGGCCC[A/T]TGGGAATCCAACATT | 16826 |
rs29519363 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44739086 | CACCTTGGTGAGCTT[A/C]AAGCTTAGCAATGAA | 16826 |
rs29521461 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44782973 | CAGACCCAAGAATTC[C/T]CAGTATTTTCCTTTG | 16826 |
rs29522712 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44771011 | CCTTGAGCAAACTGG[C/T]TTGATAAAACCACCT | 16826 |
rs29523046 | snp | A/G | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44493113 | GCCCAATCCTTTTAA[A/G]TGGTAAGAACAGAGC | 16826 |
rs29523620 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Ldb2 | Mm_Celera | 5:44692821 | ATTCAAGAAGAACTT[A/C]AAAAACAGTCTATGA | 16826 |
rs29526092 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44772090 | TTAATCTGACAGTTT[C/T]AGGAACAATCTGCTG | 16826 |
rs29526525 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44499835 | TAGATTTTTGCGATA[C/T]ATCTCAAAGGATCTT | 16826 |
rs29526820 | snp | C/T | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44781995 | TTTACTGGCTTGCTT[C/T]CCCTGGCTTGCTCAG | 16826 |
rs29526961 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44764739 | CCATAATAGCCAATC[A/C]GATATGCATAACATC | 16826 |
rs29527407 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44782481 | ACTCAAGAAATACAC[A/G]GGTATGGCCCTCACA | 16826 |
rs29527457 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ldb2 | GRCm38.p3 | 5:44496718 | TAGGACGAGAACACA[C/G]AGGCTTAATAACATT | 16826 |
rs29527978 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44731846 | AAAAGATGGCCTAGT[C/T]GGCCATCACTGGAAA | 16826 |
rs29528505 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | GRCm38.p3 | 5:44698576 | GTCTGTGATGGAATC[A/G/T]GCCAGAGTGGTGAAG | 16826 |
rs29530666 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44758245 | TAATACAAGCCTAAA[A/G]TAGAAACCTAGAGAT | 16826 |
rs29531343 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44479668 | GCCAAGGTTTGCCAA[A/T]GCCGTGGTTAACATT | 16826 |
rs29532787 | snp | A/G | 0.32 | 0.24 | intron-variant | Ldb2 | Mm_Celera | 5:44497993 | TACACTGTTTTGTCT[A/G]CTGGCCTTCCTGGCA | 16826 |
rs29533529 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44590899 | ATGGAGAAATTATTG[C/T]AGCAGGATATAGTTT | 16826 |
rs29533650 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44661858 | GAGAGAGAGAGAGAG[C/T]AAGAGAGGTGGTGGT | 16826 |
rs29534695 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44574691 | GAAACCCCTCAAAAC[A/C]TGTCAGTCAGGTGAG | 16826 |
rs29539435 | snp | C/T | 0.32 | 0.24 | intron-variant | Ldb2 | Mm_Celera | 5:44673061 | CCTGTGGGTTAGGAA[C/T]AGGACCCATAACCCA | 16826 |
rs29543403 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Ldb2 | Mm_Celera | 5:44657121 | GCATTGTCCTTCCTC[A/G]TTGCTCTTGCTACTG | 16826 |
rs29544103 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44779248 | AGTAAACGAATGTTC[C/T]GTCCATTGTACCAGC | 16826 |
rs29544918 | snp | G/T | 0.32 | 0.24 | intron-variant | Ldb2 | Mm_Celera | 5:44712541 | CTTTGGAAGGGTTTG[G/T]TATGGCAAGAGTATT | 16826 |
rs29545365 | snp | A/G | 0.32 | 0.24 | intron-variant | Ldb2 | Mm_Celera | 5:44481694 | AGATGCATTTAAGGA[A/G]TAGTGCTTATAAGAC | 16826 |
rs29545601 | snp | C/T | 0.32 | 0.24 | intron-variant | Ldb2 | Mm_Celera | 5:44759274 | AAAAGACATAGTGTA[C/T]CCTGCCCCCCAAACA | 16826 |
rs29545783 | snp | A/T | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44687297 | ATGTAAAAAATAAAA[A/T]TACTATCAGCAGGAA | 16826 |
rs29545846 | snp | G/T | 0.32 | 0.24 | intron-variant | Ldb2 | Mm_Celera | 5:44696619 | ATCGCTCCAGCAGCA[G/T]CAGCAGCAGCAGCAG | 16826 |
rs29546679 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44551743 | CCTCTCTCTCTCTCT[A/C]TATATATATATATAT | 16826 |
rs29547357 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ldb2 | Mm_Celera | 5:44742551 | CATTTTCTTCTCACC[A/G]GCAGTATCACTGAGA | 16826 |
rs29547594 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44715547 | ATAGAGGGAATGCTA[G/T]CCTAGAAAGAGGTGA | 16826 |
rs29548223 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Ldb2 | Mm_Celera | 5:44655183 | AAACTGTCAGGCAGC[A/T]TGTGGACATAAGCCA | 16826 |
rs29550313 | snp | C/T | 0.5 | 0 | intron-variant | Ldb2 | Mm_Celera | 5:44763742 | CTTTTGTTTACTGTG[C/T]CAGCCTGTCATGGTA | 16826 |
rs29558783 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Ldb2 | Mm_Celera | 5:44694287 | TTCACTGATGTTAAC[G/T]CTAGCTGACTTGAGT | 16826 |
rs29559575 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Ldb2 | Mm_Celera | 5:44663457 | GGCACTCGTTTTGTT[A/T]AATTGTTTGTTTTAT | 16826 |
rs29561129 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44499526 | CTCTATTATAATAGC[A/G]CTCCATGAGACAGAA | 16826 |
rs29561167 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ldb2 | Mm_Celera | 5:44764637 | GGCCTGCTACTATTA[A/T]AAGTGGCTATTGAGT | 16826 |
rs29562049 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ldb2 | Mm_Celera | 5:44626434 | AGAGGAACAATGATC[A/T]GGGAAAAGAACAGAG | 16826 |