SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3693019 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr70 | GRCm38.p3 | 15:8093533 | TTCGGAAGGAACCAG[A/C]AATTACAATTCTCTC | 545085 |
rs3694333 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Wdr70 | GRCm38.p3 | 15:8093777 | AGAGCAGAGCAAAGA[A/G]CACTGTGAGCACTGA | 545085 |
rs3694826 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Wdr70 | GRCm38.p3 | 15:8093796 | TGTGAGCACTGAGCT[G/T]GCCCTGAGCTGGCCA | 545085 |
rs3705269 | snp | C/G | 0.46875 | 0.121031 | intron-variant | Wdr70 | Mm_Celera | 15:8097007 | GGTTATCTTTTAATT[C/G]GTCTATTAATGAGCT | 545085 |
rs3706410 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Wdr70 | GRCm38.p3 | 15:8097199 | TAACCAGGTGCATAC[C/T]ACACGGTAAAATCCC | 545085 |
rs3706458 | snp | A/C | 0.5 | 0 | intron-variant | Wdr70 | GRCm38.p3 | 15:8097235 | CAAGGAGCTAAGAGG[A/C]AAAAGGGTCAGAAGC | 545085 |
rs3706499 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | GRCm38.p3 | 15:8097251 | AAAAGGGTCAGAAGC[A/G]CACGGTCATCCTCAG | 545085 |
rs3721416 | snp | A/C | 0.5 | 0 | intron-variant | Wdr70 | GRCm38.p3 | 15:8097287 | ATACAAAGTCTAAGG[A/C]AAGCCTGAGCTGTGT | 545085 |
rs4136308 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:8096966 | gaaaccctgtctcaa[A/G]caaaacaaaaCAAAC | 545085 |
rs6152764 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr70 | Mm_Celera | 15:8019390 | TGGAATTTACAAAAT[C/T]NCTCATTTCCATAGC | 545085 |
rs6152765 | snp | C/T | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:8019391 | GGAATTTACAAAATN[C/T]CTCATTTCCATAGCA | 545085 |
rs6165420 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:8098388 | gaataggaagaagag[A/G]aaaagaggaggtgga | 545085 |
rs6165974 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Wdr70 | GRCm38.p3 | 15:8098481 | ACCCTTTTATCGACT[A/C]ATTACCTAGAAGAAG | 545085 |
rs6166066 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Wdr70 | GRCm38.p3 | 15:8098547 | AGAACTAGGTACATC[A/T]GAGAGACATTTGTTC | 545085 |
rs6189517 | snp | C/G | 0.5 | 0 | intron-variant | Wdr70 | GRCm38.p3 | 15:8093909 | TAAACAGTAAATATA[C/G]AAATTCACTATTACC | 545085 |
rs6202319 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Wdr70 | Mm_Celera | 15:8100655 | GTGACAAATTACCCT[A/G]AACTTCAACCAGTAA | 545085 |
rs6202838 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Wdr70 | GRCm38.p3 | 15:8100710 | AAATATGTTATTATT[A/G]GTGCTAATATTTCTT | 545085 |
rs6202925 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | Wdr70 | Mm_Celera | 15:8100767 | GATACTGGAGTAGAA[C/G]TTTATGAATGATATT | 545085 |
rs6203405 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Wdr70 | Mm_Celera | 15:8100815 | AAGCTCATAAGTAAT[A/G]GTTTCAGNTCCTCAA | 545085 |
rs6203426 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Wdr70 | Mm_Celera | 15:8100823 | AAGTAATNGTTTCAG[C/T]TCCTCAANTGTCAAG | 545085 |
rs6203448 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Wdr70 | Mm_Celera | 15:8100831 | GTTTCAGNTCCTCAA[C/T]TGTCAAGGAGAAGAA | 545085 |
rs6204010 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Wdr70 | Mm_Celera | 15:8100943 | ATTAGAATTGGTATT[C/T]ATCACNATAAACATC | 545085 |
rs6204027 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | Wdr70 | Mm_Celera | 15:8100949 | ATTGGTATTNATCAC[C/G]ATAAACATCATTTTA | 545085 |
rs6204074 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Wdr70 | Mm_Celera | 15:8100972 | TCATTTTAAAAAGAC[A/G]CTCTGCTATCAATCA | 545085 |
rs6204587 | snp | C/T | 0.359862 | 0.224567 | upstream-variant-2KB | Wdr70 | Mm_Celera | 15:8101037 | TTTCTGTTGAGTATG[C/T]GTGAAACAACTTCAT | 545085 |
rs6223450 | snp | C/T | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7996437 | CTATTGACAGCCTCT[C/T]CTTACCTCTACCACT | 545085 |
rs6225042 | snp | G/T | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7996666 | AGGAAAAAAAGCAAT[G/T]AGAAAAATATCATCC | 545085 |
rs6225185 | snp | A/C/G | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7996755 | ggagggatgtagctc[A/C/G]gtttcacagtacttg | 545085 |
rs6226179 | snp | C/T | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7996888 | gagaaattcaagtca[C/T]tcttggctacagtag | 545085 |
rs6227830 | snp | A/C | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7990630 | GTAAAAATGTTATAA[A/C]GGCATAGAAAAAGCT | 545085 |
rs6228943 | snp | C/T | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7990829 | ATGtgtatatgtaca[C/T]gtgcaggcctgtgca | 545085 |
rs6230623 | snp | G/T | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7984528 | TACATCACCATTACA[G/T]CTCACCATTATGAGG | 545085 |
rs6231224 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7984642 | TATCTGTGATTGGTC[A/G]TATTTgttgattgac | 545085 |
rs6231725 | snp | C/T | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7984685 | tcaagcagccttagc[C/T]ccgcctccgcctcct | 545085 |
rs6231783 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7984720 | actgggatcacaggt[A/G]tgcagcaacatgcta | 545085 |
rs6232257 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7984795 | gaagcaagcactctg[A/G]gttatgttctcagcc | 545085 |
rs6232838 | snp | C/T | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7984925 | ATCCTGCTAAGTGAA[C/T]AGGACATTCTTGAGG | 545085 |
rs6399227 | snp | C/T | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:8019036 | AAGGGCCCAGAAAGG[C/T]GGAGCCTCAGNNCAG | 545085 |
rs6399244 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:8019047 | AAGGNGGAGCCTCAG[A/G]NCAGAGTGTAATGGT | 545085 |
rs6399265 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:8019048 | AGGNGGAGCCTCAGN[A/G]CAGAGTGTAATGGTC | 545085 |
rs6412113 | snp | C/T | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:8098067 | tgacctcttctggcc[C/T]ccataggtactgcag | 545085 |
rs6412525 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:8019135 | AATTGCAATTGATGT[A/G]AATTTATTACTGACA | 545085 |
rs6413092 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Wdr70 | Mm_Celera | 15:8052895 | GCTCGACAACAAAAG[A/G]ATGATCAGAAGGAAT | 545085 |
rs6413181 | snp | C/T | 0.5 | 0 | intron-variant | Wdr70 | GRCm38.p3 | 15:8098194 | agctcaagcctttaa[C/T]ccaggcaaccgggag | 545085 |
rs6413253 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | GRCm38.p3 | 15:8098233 | aagcagatctttacg[A/G]gttcgatgccagcct | 545085 |
rs29314726 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr70 | Mm_Celera | 15:7937058 | AAATGCTGTCTTTTT[C/T]CCACTGGATGGTTTT | 545085 |
rs30752441 | snp | A/G | 0.5 | 0 | intron-variant | Wdr70 | Mm_Celera | 15:7937069 | CCATTTGTTGAAAAT[A/G]CTGTCTTTTTTTCTA | 545085 |
rs31697822 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr70 | Mm_Celera | 15:8054189 | AAAGATGAGGAGGAC[A/G]AGGAGGGCGAGGATG | 545085 |
rs31994245 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr70 | Mm_Celera | 15:7924772 | TGGGTGGTGGTGGTG[A/G]TAGCAATGGTGAGGA | 545085 |
rs32402510 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr70 | Mm_Celera | 15:8067795 | TCCTAGTGCAGTCTG[C/T]AGTGTCCTAGTGCAG | 545085 |
rs32682534 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Wdr70 | GRCm38.p3 | 15:8095207 | CACACTGGTGACTAT[G/T]TCTACTTCACTATCC | 545085 |
rs32682535 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr70 | GRCm38.p3 | 15:8095091 | TGGAACCCAGAGCCT[C/T]ACTTATGCTTACTAG | 545085 |
rs32682536 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr70 | GRCm38.p3 | 15:8095019 | TACATGAGCTGATAA[C/G]GTACAGAACTCCCAG | 545085 |
rs32682537 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Wdr70 | GRCm38.p3 | 15:8094906 | GTTCATAGAACCAGC[A/G]CTCTCACTCTAAACA | 545085 |
rs32682538 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Wdr70 | GRCm38.p3 | 15:8094876 | ATGCTACAGTCTACT[A/G]CCAAGAACTGTGTTG | 545085 |
rs32682539 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Wdr70 | GRCm38.p3 | 15:8094633 | ACAGCATTGCTCTGT[G/T]GGGGAAAGACTCTTA | 545085 |
rs32682540 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Wdr70 | GRCm38.p3 | 15:8094422 | CATACAAATTTCAGA[A/G/T]TCTTAGAAGTAAGAT | 545085 |
rs32682541 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr70 | Mm_Celera | 15:8093844 | AGCTTCACCGATGGA[G/T]CAATAACCAGGCCAT | 545085 |
rs32682542 | snp | A/G | 0.42 | 0.183303 | intron-variant | Wdr70 | Mm_Celera | 15:8093768 | TTCTTCCCTAGAGCA[A/G]AGCAAAGAACACTGT | 545085 |
rs32682543 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr70 | Mm_Celera | 15:8093434 | CCACACTTTTACAGG[A/G]TTCTGGTGTATAGAC | 545085 |
rs32683544 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wdr70 | GRCm38.p3 | 15:8093186 | ATATTAAAGAAACTG[C/T]TATTCTGCTTCGCTT | 545085 |
rs32683547 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Wdr70 | Mm_Celera | 15:8092241 | ATTTTAACTTTTGAA[C/T]ATTTTATTTATTACT | 545085 |
rs32683548 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr70 | Mm_Celera | 15:8092122 | ACGTACATATGACTA[C/T]ATACACATCGACATC | 545085 |
rs32683549 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr70 | Mm_Celera | 15:8091494 | GCCTGCCTAACAAGA[A/C]TTCCAACTGTCTTTA | 545085 |
rs32683550 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr70 | Mm_Celera | 15:8091465 | TGCTAAAGTAAGATG[A/G]TTGAGAGTTTGAGGC | 545085 |
rs32683551 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Wdr70 | GRCm38.p3 | 15:8091440 | TGTTACAGCCACATG[A/G]CCTCAAATTTGCTAA | 545085 |
rs32683552 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr70 | GRCm38.p3 | 15:8091389 | ACCGCATCTCGCCTT[A/C]CATGTGGACAGATAC | 545085 |
rs32683553 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr70 | Mm_Celera | 15:8091360 | TCTAAGAGCACTGCG[A/G]TTGGATGCATGCTAC | 545085 |
rs32684224 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr70 | Mm_Celera | 15:8091150 | GTAGGGAAAGCAGTT[C/T]CACTTATCCTTTCAG | 545085 |
rs32684225 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr70 | Mm_Celera | 15:8090994 | CTGTGATTAGCATGG[G/T]AAGTTGAGGAATCCT | 545085 |
rs32684226 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Wdr70 | GRCm38.p3 | 15:8090903 | CCTGGCTGCTCACCT[A/G]GACTCTTTAGACTCT | 545085 |
rs32684227 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Wdr70 | GRCm38.p3 | 15:8090889 | ACTGAATCACTTCAC[C/G]TGGCTGCTCACCTAG | 545085 |
rs32684228 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr70 | Mm_Celera | 15:8090867 | AAAGGCGGCACACCT[C/G]GAACCCACTGAATCA | 545085 |
rs32684229 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Wdr70 | GRCm38.p3 | 15:8090812 | GGAATAGACTCATTG[A/T]TGAATCTAAACCTGC | 545085 |
rs32684230 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr70 | Mm_Celera | 15:8090703 | TCCTTATGATTTCCT[C/G]AGTGACAGGAACTGT | 545085 |
rs32684231 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr70 | Mm_Celera | 15:8090654 | ACTGGAGTACATACA[A/G]TGTTACAAGCATTTT | 545085 |
rs32684232 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr70 | Mm_Celera | 15:8090406 | ATAGATCCACGGATT[A/T]TAGTTCTAAATTCAA | 545085 |
rs32684233 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr70 | Mm_Celera | 15:8090227 | AGTATTTGGGTTACA[G/T]AGACCCAACGTAAAA | 545085 |
rs32684474 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr70 | Mm_Celera | 15:8000027 | GATGTCATTTAATAA[C/T]GGCACTTCTATTCCT | 545085 |
rs32684475 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr70 | Mm_Celera | 15:7999940 | GAGATACAGAGAAGC[C/T]AGAACAGTTAACCAT | 545085 |
rs32684476 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Wdr70 | Mm_Celera | 15:7999246 | TCATAATGTGAACCA[A/T]AATGAAAACGGTTCT | 545085 |
rs32684477 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Wdr70 | Mm_Celera | 15:7997291 | AACCTCTCACCATGA[C/G]ATTAGCCGGTGAGAC | 545085 |
rs32684478 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Wdr70 | Mm_Celera | 15:7997177 | TTACACATCAAAGCC[A/G]TTAGTTGATACATAG | 545085 |
rs32684479 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Wdr70 | Mm_Celera | 15:7996409 | ACATGTCAAGTTCTC[A/C]AAAAACAGCACTCTA | 545085 |
rs32684480 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr70 | Mm_Celera | 15:7996320 | AGACTCTGAAGTATC[A/G]TGTATCCTGAGAAAC | 545085 |
rs32684481 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Wdr70 | Mm_Celera | 15:7995926 | GAAGATTTTGACATC[A/T]TGATGGATCCACTTA | 545085 |
rs32684482 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Wdr70 | Mm_Celera | 15:7994939 | CACGGTGCTTCTAAC[A/G]GTTCTTTCTTCCTTA | 545085 |
rs32684483 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr70 | Mm_Celera | 15:7994728 | CTGCTATCACCACTA[A/C]CAAGGCAGCAGAAAC | 545085 |
rs32684494 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr70 | Mm_Celera | 15:8025438 | TTGGGTTCATTTCCA[C/T]TCAGGTAAAACACAC | 545085 |
rs32684495 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Wdr70 | Mm_Celera | 15:8024176 | ATTTTGATGACCATC[A/G]TAACATATAACCTGA | 545085 |
rs32684496 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Wdr70 | Mm_Celera | 15:8021985 | ACATGAATGAAAACA[A/C]ATGAACCTTGCTGTG | 545085 |
rs32684497 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Wdr70 | Mm_Celera | 15:8021882 | TCTACAATAACGTGA[G/T]ATTCTTCATTCACTG | 545085 |
rs32684498 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr70 | Mm_Celera | 15:8021601 | TTCACTGAGTTCCTT[C/T]CTGCCCAACATGCAC | 545085 |
rs32684499 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr70 | Mm_Celera | 15:8021495 | ATACAGTTCCAATGC[A/G]CACTCCTCGTCTCTA | 545085 |
rs32684500 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr70 | Mm_Celera | 15:8021412 | AACAGTTCTGTAGTA[C/G]CTGATGCAGAGACTC | 545085 |
rs32684501 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr70 | Mm_Celera | 15:8021385 | CCATACAGCAATGAA[G/T]ACCATTTAAAGAACA | 545085 |
rs32684502 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr70 | Mm_Celera | 15:8020870 | CATTTCAAACACATA[C/T]GTCCAATAAGGAAAT | 545085 |
rs32684503 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr70 | Mm_Celera | 15:8020852 | AATTGACATACCTAC[A/G]TGCATTTCAAACACA | 545085 |
rs32684514 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Wdr70 | Mm_Celera | 15:8074155 | TCAGAAGCAGTCGCT[A/G]CTTCAGAAAATTTGG | 545085 |
rs32684515 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdr70 | Mm_Celera | 15:8074109 | TGTAAGGCGGAAGCT[C/G]ACAGCACAGGCTCAG | 545085 |