SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3682238 | snp | C/G | 0.255 | 0.24995 | intron-variant | Eed | Mm_Celera | 7:89958061 | CTTAACTGACCGGCT[C/G]GACGAGCAAAGAAGG | 13626 |
rs3682253 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Eed | GRCm38.p3 | 7:89958074 | CTGGACGAGCAAAGA[A/G]GAGAATCCCCAATCA | 13626 |
rs3682305 | snp | A/G | 0.42 | 0.183303 | intron-variant | Eed | GRCm38.p3 | 7:89958099 | CAATCAAGACAACCC[A/G]ATAGAATATCATCCA | 13626 |
rs6298169 | snp | G/T | 0.5 | 0 | intron-variant | Eed | GRCm38.p3 | 7:89970774 | ATGCCTGTGGAAGTA[G/T]TCTACTGCACTGATG | 13626 |
rs6298240 | snp | C/G | 0.5 | 0 | intron-variant | Eed | Mm_Celera | 7:89970814 | AACAGCCGGAAACAG[C/G]AGTTGAACATGTAGA | 13626 |
rs6298704 | snp | A/G | 0.5 | 0 | intron-variant | Eed | Mm_Celera | 7:89970852 | GTTCTCCAGTAAAAC[A/G]TTATTTATAAAGCTA | 13626 |
rs6298793 | snp | A/G | 0.5 | 0 | intron-variant | Eed | GRCm38.p3 | 7:89970896 | CAGGTTTGCCTTGCT[A/G]CTGACCCTCTGTCCT | 13626 |
rs13465525 | snp | A/G | | | missense, nc-transcript-variant | Eed | Mm_Celera | 7:89976931 | GGAAGTCAAAGAAAT[A/G]CAAATATTCTTTCAA | 13626 |
rs13465526 | snp | A/G | 0.375 | 0.216506 | synonymous-codon, nc-transcript-variant | Eed | GRCm38.p3 | 7:89976999 | AGAACGCCCGGACAC[A/G]CCCACAAATACGCCA | 13626 |
rs13465527 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | Eed | GRCm38.p3 | 7:89980804 | CCTCGGTGCAAAGTG[C/T]CGAGAGGGCGGCGGG | 13626 |
rs30674345 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89976307 | GTGTGTGTAAAGGCC[A/G]GCTTACCAGGCACGT | 13626 |
rs30766626 | snp | A/G | 0.5 | 0 | intron-variant | Eed | GRCm38.p3 | 7:89976568 | ATTTGCTAGGGACCA[A/G]TTAACAGATCACACT | 13626 |
rs30825586 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eed | Mm_Celera | 7:89975791 | CTTCCTGTTATACTG[C/T]ACTCAGTAGGGACAG | 13626 |
rs30971452 | snp | C/T | 0.5 | 0 | intron-variant | Eed | Mm_Celera | 7:89975377 | TCTGTTAGGGAGACC[C/T]CCATCTTAAAAAAAC | 13626 |
rs31039311 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89974499 | GTTTCTAAGACTCCA[C/T]ACACTGACGTCCAGT | 13626 |
rs31055914 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Eed | Mm_Celera | 7:89981664 | AATCAAGGCTATTTA[C/T]TAAAAACCTGTTTGA | 13626 |
rs31099429 | snp | C/G | 0.375 | 0.216506 | intron-variant | Eed | Mm_Celera | 7:89960487 | CAGGATAAAGTTTCA[C/G]TACACATCTATTGGA | 13626 |
rs31111529 | snp | A/G | 0.32 | 0.24 | intron-variant | Eed | GRCm38.p3 | 7:89968337 | CCAGCATCTGTATCG[A/G]GTGGTTCACAATGGT | 13626 |
rs31135477 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Eed | Mm_Celera | 7:89961422 | AAAAAAAATCAAACT[A/C]AGTTCTGCCTAAGAT | 13626 |
rs31145981 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eed | Mm_Celera | 7:89969033 | ATCTTTTAATAATAA[A/G]AGTATGGCTCTTCAC | 13626 |
rs31147231 | snp | C/T | 0.32 | 0.24 | intron-variant | Eed | GRCm38.p3 | 7:89968173 | GGGGTAGGGGTCTGA[C/T]TGAGCAAGAGGACTT | 13626 |
rs31148930 | snp | A/C/G/T | 0.375 | 0.216506 | intron-variant | Eed | GRCm38.p3 | 7:89977151 | TGAGATTGCTCCGCG[A/C/G/T]GTAAGAGCACTGATT | 13626 |
rs31157670 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eed | GRCm38.p3 | 7:89977617 | ACTGGTCTACACCAG[A/G]GACACCAATACAATG | 13626 |
rs31180306 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Eed | GRCm38.p3 | 7:89972438 | GCTCATTCACTACCT[C/T]ATATACTTGGGTGGT | 13626 |
rs31201259 | snp | A/G | 0.32 | 0.24 | intron-variant | Eed | GRCm38.p3 | 7:89964324 | CCTCCTCAGTGCTGG[A/G]ATTAAAGGTGTTCAC | 13626 |
rs31214498 | snp | C/G | 0.32 | 0.24 | intron-variant | Eed | GRCm38.p3 | 7:89968302 | GCAATTGCTGCTCTA[C/G]CAGAGGATGAGTCCA | 13626 |
rs31343201 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89980293 | CGCCTGCGTTCTCCC[A/G]AGCGCGGGTGACACC | 13626 |
rs31381671 | snp | C/G/T | 0.5 | 0 | intron-variant | Eed | GRCm38.p3 | 7:89966917 | AGGCAGGCAGGCAGG[C/G/T]AGGCAAAATGAGTGG | 13626 |
rs31392456 | snp | C/T | 0.5 | 0 | intron-variant | Eed | GRCm38.p3 | 7:89961634 | TGAAACAGCTTCGCA[C/T]GTGCACATCCTCCCA | 13626 |
rs31402209 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89969263 | AACGGAGCTACTAAA[A/C]ACATCTGAAAAACCT | 13626 |
rs31405924 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89972788 | TTACAAGAGGTGCTA[C/T]GGTCATGGTGTCTCT | 13626 |
rs31473440 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89974321 | GCATGGCTGAATCAC[A/G]TGTCTCTCTGTATCT | 13626 |
rs31487939 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Eed | Mm_Celera | 7:89982521 | ACATTTGCTGGGCAC[C/T]CACTTAATAATAAAA | 13626 |
rs31557945 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eed | Mm_Celera | 7:89969029 | CAAAATCTTTTAATA[A/G]TAAGAGTATGGCTCT | 13626 |
rs31598152 | snp | A/G | 0.5 | 0 | intron-variant | Eed | Mm_Celera | 7:89968638 | ACCCAGGACTAACTT[A/G]ACAAGTAACTGTTAA | 13626 |
rs31599277 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Eed | Mm_Celera | 7:89972186 | CATTTTAGCACTCTA[A/G]TTGTAACAATCAGTA | 13626 |
rs31621269 | snp | C/T | 0.5 | 0 | intron-variant | Eed | Mm_Celera | 7:89978052 | CTGCCCAAACAGATA[C/T]AGCTGCAGGAAATAC | 13626 |
rs31640996 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eed | Mm_Celera | 7:89979001 | ACACACACACACACA[C/T]CCTTTGGTGAGGACA | 13626 |
rs31691153 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89974612 | AGAGGCAGAATCTGT[A/G]TTATTTTGATTCCCA | 13626 |
rs31703751 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89956634 | TTAAGTTCAGCTTTG[G/T]ATACGTTCGCATACA | 13626 |
rs31738521 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eed | Mm_Celera | 7:89977174 | CACTGATTGTTCTTC[C/T]GAAGGTCCTGAGTTC | 13626 |
rs31790448 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Eed | Mm_Celera | 7:89981498 | GGCTTAAGTAAGCCT[A/G]TATCTTAAATTACAT | 13626 |
rs31795340 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eed | Mm_Celera | 7:89979810 | AACTTTCAAACTGTT[C/T]CCTCCTTTGCCTTAA | 13626 |
rs31804435 | snp | C/G/T | 0.5 | 0 | intron-variant | Eed | GRCm38.p3 | 7:89957254 | ACGTTGTTCTCTACC[C/G/T]TCTTCAGATTTAAAA | 13626 |
rs31807551 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Eed | Mm_Celera | 7:89966175 | GATGACTCCCATACA[A/G]AGCCTGGTGTAGAAT | 13626 |
rs31834628 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Eed | GRCm38.p3 | 7:89981287 | CGGAGACGACAGGCC[G/T]CCTCCTGGCCCCTCC | 13626 |
rs31836283 | snp | C/T | 0.5 | 0 | intron-variant | Eed | Mm_Celera | 7:89966948 | CCCAGGCTTTATTCT[C/T]ATCACCCAGGAAGCA | 13626 |
rs31860539 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Eed | GRCm38.p3 | 7:89964183 | TACCTACCTACCTAC[A/C]TACCTACCTATCCAC | 13626 |
rs31874271 | snp | A/G | 0.5 | 0 | downstream-variant-500B | Eed | Mm_Celera | 7:89954364 | TTAGAGGCCATAAGA[A/G]GACATTGTGTCCACT | 13626 |
rs31879773 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eed | Mm_Celera | 7:89969045 | TAAGAGTATGGCTCT[C/T]CACTGCAGTGCTTCC | 13626 |
rs31896134 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eed | Mm_Celera | 7:89969103 | GTCCTGGGGTGGCCC[A/G]GCATGTGTGTGGAGG | 13626 |
rs31908984 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eed | Mm_Celera | 7:89969059 | TTCACTGCAGTGCTT[C/T]CTTTATTATTTTGGG | 13626 |
rs31926222 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89974625 | GTATTATTTTGATTC[A/C]CATATCCTTGGTTGC | 13626 |
rs31928756 | snp | G/T | 0.32 | 0.24 | intron-variant | Eed | GRCm38.p3 | 7:89968157 | AAGGGACTATCGGGT[G/T]GGGGTAGGGGTCTGA | 13626 |
rs32018029 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Eed | Mm_Celera | 7:89972341 | ATAAAATATAAACCA[C/T]GAAAGAAAAATTTAA | 13626 |
rs32024598 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Eed | Mm_Celera | 7:89971894 | GCCTTATAAATCCTC[A/G]CACATTTTATGTAAT | 13626 |
rs32058975 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Eed | Mm_Celera | 7:89981356 | ACCGGTTTCTGAAGC[C/T]TCGGGGAGGATTTCA | 13626 |
rs32163733 | snp | C/T | 0.444444 | 0.157135 | utr-variant-5-prime, nc-transcript-variant | Eed | Mm_Celera | 7:89980642 | CGCCACCGCCGCCGC[C/T]CCCCCCACTGTCGCA | 13626 |
rs32165409 | snp | C/T | 0.5 | 0 | intron-variant | Eed | Mm_Celera | 7:89961632 | CCTGAAACAGCTTCG[C/T]ACGTGCACATCCTCC | 13626 |
rs32224874 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eed | GRCm38.p3 | 7:89972754 | AAAATGTCAGCACGT[C/T]CCAACTAAATGCGTT | 13626 |
rs32230014 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Eed | Mm_Celera | 7:89967501 | TATTCTTCCTCTCAT[A/G]GCACTCATCAGAGTC | 13626 |
rs32269857 | snp | A/T | 0.5 | 0 | intron-variant | Eed | Mm_Celera | 7:89977631 | GGGACACCAATACAA[A/T]GCCTCACTCACTCCT | 13626 |
rs32299232 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Eed | Mm_Celera | 7:89960801 | GAGTGTGCTGTAGTT[C/T]CAAACTGGAAAAACA | 13626 |
rs32345220 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Eed | GRCm38.p3 | 7:89982610 | AATGAGACAATTTAG[A/G]TGAAAAAGTTTAAAT | 13626 |
rs32356524 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eed | Mm_Celera | 7:89972200 | AGTTGTAACAATCAG[C/T]ATTGCCAACCTGCCC | 13626 |
rs32389227 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eed | GRCm38.p3 | 7:89957489 | AGGAATGGCCCGCCT[C/T]CTTTAAGGTGGGATC | 13626 |
rs32406317 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89974346 | GTATCTACATTTCTT[C/T]ACTCAGCTGTTGATG | 13626 |
rs32410399 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Eed | Mm_Celera | 7:89961354 | GGAGGGGAAAATGAA[A/G]CCAACAACAGTAAGT | 13626 |
rs32410970 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eed | GRCm38.p3 | 7:89972527 | TTGAAAGGATGAGGA[A/G]GTGTGGCCTTGTTGG | 13626 |
rs32453068 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Eed | GRCm38.p3 | 7:89962545 | ACTTGTAAAACTCCA[C/T]AACATAAACTCTGAC | 13626 |
rs32455016 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eed | Mm_Celera | 7:89980170 | AGGGACGATCTGAGC[A/G]GACCTCGCAGACCCT | 13626 |
rs32455633 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eed | Mm_Celera | 7:89959937 | AGAAAACCAGCTAAA[A/G]ATTCCAAGAAATATT | 13626 |
rs32469633 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Eed | Mm_Celera | 7:89978252 | TAGAGTGAAGCCCAC[G/T]GCTTTTGTGGTCTAA | 13626 |
rs32503923 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Eed | GRCm38.p3 | 7:89981280 | TGGGTTACGGAGACG[A/C]CAGGCCGCCTCCTGG | 13626 |
rs32522989 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89972809 | TGGTGTCTCTTCATA[A/G]CAATAGAACACTAAG | 13626 |
rs45646063 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Eed | Mm_Celera | 7:89971222 | GTTAAGCATTAGAAC[G/T]ATAGTAAAATTGTAA | 13626 |
rs45657463 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eed | Mm_Celera | 7:89969482 | TTCTTTTAATTTAAA[C/T]TATGCATTCTCAGAA | 13626 |
rs45677192 | snp | A/G | | | intron-variant | Eed | GRCm38.p3 | 7:89975584 | CATTGATTTGGGGAA[A/G]GAAAGATGGCTCAGT | 13626 |
rs45724193 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Eed | Mm_Celera | 7:89963549 | TTTTAGTCAAATGCA[C/T]ATTATATTACTAGTT | 13626 |
rs45724642 | snp | A/T | | | intron-variant | Eed | Mm_Celera | 7:89973171 | CTTTTTTTTTTTTTT[A/T]AAAGATTTATTTATT | 13626 |
rs45756058 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Eed | Mm_Celera | 7:89972189 | TTTAGCACTCTAGTT[A/G]TAACAATCAGTATTG | 13626 |
rs45782367 | snp | C/G | 0.32 | 0.24 | intron-variant | Eed | Mm_Celera | 7:89965417 | AGTGCAAAATGGAAG[C/G]TAAGTTACTTGAGCT | 13626 |
rs45877878 | snp | C/T | | | intron-variant | Eed | Mm_Celera | 7:89973571 | GCAGAGCTTAGACTA[C/T]GCAGTCGCCAGCAGT | 13626 |
rs45970587 | snp | A/G | 0.32 | 0.24 | intron-variant | Eed | Mm_Celera | 7:89972126 | TTTCTTACACAAAGA[A/G]TCATACTGTTAACCC | 13626 |
rs46117693 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Eed | GRCm38.p3 | 7:89971323 | AATGCTCCTTCTTCC[A/C/G]TCATCTTACCCTACC | 13626 |
rs46432997 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89969907 | GAAAATGGTACCAGT[C/T]AGCCAAGGCTCAGCT | 13626 |
rs46434256 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eed | GRCm38.p3 | 7:89956988 | CAATCACTCACTTAG[C/T]CAGTGGTCCACACTA | 13626 |
rs46468726 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | Eed | Mm_Celera | 7:89980724 | GAAAAAGGGGCGCGC[A/G]CGCGCGCGCCCTCCC | 13626 |
rs46501726 | snp | A/C | | | intron-variant | Eed | Mm_Celera | 7:89973623 | TTAGGGCTTTATTGC[A/C]ATCTCCTGGTATTCA | 13626 |
rs46622132 | snp | A/C | | | intron-variant | Eed | Mm_Celera | 7:89979015 | ACCCTTTGGTGAGGA[A/C]AGAACCTGTCCCTCC | 13626 |
rs46641819 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Eed | GRCm38.p3 | 7:89969891 | ACAAAATTATAGGAA[A/G]GAAAATGGTACCAGT | 13626 |
rs46646171 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eed | Mm_Celera | 7:89956155 | AGCAAGTCACAGCAT[C/T]GGGACAACCAAGGTG | 13626 |
rs46799472 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Eed | Mm_Celera | 7:89961514 | CATGTTCCATTAACA[A/T]CACCAATCACCCCTC | 13626 |
rs46912410 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eed | Mm_Celera | 7:89957701 | GATTGATAGCCATCA[A/G]ATGACAAATGACAAA | 13626 |
rs46963378 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89969750 | GGGGCAAACCAATAG[C/T]CTAGTACACTCAAGG | 13626 |
rs46998121 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Eed | GRCm38.p3 | 7:89969359 | CAGTAAGAGTCGAGT[A/C/T]GAGGATGACATAATC | 13626 |
rs47107984 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eed | GRCm38.p3 | 7:89972861 | ACTTCTGACATTAAA[A/G]CTATAACACCACCCA | 13626 |
rs47353865 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eed | GRCm38.p3 | 7:89962773 | TAAAGAACGAAGTGC[A/G]GCCACAAAGCTGCCC | 13626 |
rs47395917 | snp | C/T | | | intron-variant | Eed | GRCm38.p3 | 7:89969795 | TCCAGCCCTGCTGCC[C/T]TCTGCCTCCCAACCC | 13626 |
rs47425578 | snp | A/C | | | intron-variant | Eed | Mm_Celera | 7:89965477 | ATCTTCCTTAATTTT[A/C]AATTAAATTTTAATT | 13626 |