SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4231935 | snp | A/T | 0.32 | 0.24 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155100 | CCCCACCTCCTTTTT[A/T]AAAAAATACACATAG | 17344 |
rs4231936 | snp | A/C | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155125 | ACATAGACCTATGAA[A/C]GGGCTTTCTTGCTTT | 17344 |
rs4231937 | snp | G/T | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155128 | TAGACCTATGAACGG[G/T]CTTTCTTGCTTTACT | 17344 |
rs4231938 | snp | G/T | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155148 | CTTGCTTTACTTAAC[G/T]TTAGGCAGTATAGCT | 17344 |
rs4231939 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155209 | CTTGATATCTGTTCT[A/G]AGACAATTGTAAAGG | 17344 |
rs4231940 | snp | A/C | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155289 | AACATGATCATAGGT[A/C]AGGGATAGTGATTGT | 17344 |
rs4231941 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155294 | GATCATAGGTAAGGG[A/G]TAGTGATTGTAATCC | 17344 |
rs4231942 | snp | C/T | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155298 | ATAGGTAAGGGATAG[C/T]GATTGTAATCCGTTG | 17344 |
rs4231943 | snp | C/T | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155301 | GGTAAGGGATAGTGA[C/T]TGTAATCCGTTGGTC | 17344 |
rs4231944 | snp | C/T | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155312 | GTGATTGTAATCCGT[C/T]GGTCCTAACCTTTTA | 17344 |
rs4231945 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155319 | TAATCCGTTGGTCCT[A/G]ACCTTTTACATCACA | 17344 |
rs4231946 | snp | C/T | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155324 | CGTTGGTCCTAACCT[C/T]TTACATCACACAAGC | 17344 |
rs4231947 | snp | G/T | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155325 | GTTGGTCCTAACCTT[G/T]TACATCACACAAGCT | 17344 |
rs4231948 | snp | A/C | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155327 | TGGTCCTAACCTTTT[A/C]CATCACACAAGCTTC | 17344 |
rs4231949 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155336 | CCTTTTACATCACAC[A/G]AGCTTCCATTAGAGG | 17344 |
rs4231950 | snp | G/T | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155340 | TTACATCACACAAGC[G/T]TCCATTAGAGGAGTA | 17344 |
rs4231951 | snp | A/C | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155355 | TTCCATTAGAGGAGT[A/C]GTAGTGAATTTGAAG | 17344 |
rs4231952 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155358 | CATTAGAGGAGTAGT[A/G]GTGAATTTGAAGGGA | 17344 |
rs4231953 | snp | G/T | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155366 | GAGTAGTAGTGAATT[G/T]GAAGGGAAGGTGTTG | 17344 |
rs4231954 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155405 | CAGTCATGTTGAATG[A/G]AGTTAAGTCAATAGA | 17344 |
rs4231955 | snp | C/T | 0.277778 | 0.248452 | utr-variant-3-prime | Pias2 | Mm_Celera | 18:77155409 | CATGTTGAATGAAGT[C/T]AAGTCAATAGACTTA | 17344 |
rs6210842 | snp | C/T | 0.5 | 0 | intron-variant | Pias2 | GRCm38.p3 | 18:77134447 | agggggtggagtgac[C/T]ttttcacagtggttg | 17344 |
rs6210902 | snp | A/T | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77134483 | agaccattggaaaac[A/T]cagatatgtatattg | 17344 |
rs6228204 | snp | A/C/G/T | 0.44898 | 0.258145 | intron-variant | Pias2 | GRCm38.p3 | 18:77135389 | ACATGCAGCTACTGA[A/C/G/T]ACTGCATACTCAATA | 17344 |
rs6228755 | snp | C/G | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77135484 | AGGCCAGTTGTCTAA[C/G]CCTCATGTTCTGTCT | 17344 |
rs6264387 | snp | A/G | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77072276 | TAGGATAGAGGGAGA[A/G]TGAGAAGTTAANGAG | 17344 |
rs6264404 | snp | C/T | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77072288 | AGANTGAGAAGTTAA[C/T]GAGCTGTTGAAGTTA | 17344 |
rs6372334 | snp | C/T | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77083733 | TATTATCCTTCCCTA[C/T]TCAGGttttcttatt | 17344 |
rs6372852 | snp | A/C/G | 0.44898 | 0.258145 | intron-variant | Pias2 | GRCm38.p3 | 18:77083826 | AGCTTTCTTAGCAGC[A/C/G]CAGTCATCCAGCTAT | 17344 |
rs6373273 | snp | C/T | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77083883 | GTAGTTGAGCAGAGG[C/T]GATCATTTCTCCGAT | 17344 |
rs6393508 | snp | C/T | 0.5 | 0 | intron-variant | Pias2 | GRCm38.p3 | 18:77085289 | cttccttccttcctt[C/T]ctttctttctttctt | 17344 |
rs6393603 | snp | A/T | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77085355 | ttctttctttctttc[A/T]aagatctatttatta | 17344 |
rs6394043 | snp | C/T | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77085381 | tattatatataagta[C/T]actgtagctgtcttc | 17344 |
rs6394136 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77085436 | ATCTCATTACAGATG[A/G]TTGTGAGCTACCATG | 17344 |
rs6408289 | snp | A/G | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77085675 | TAAGTGTCACGAGCA[A/G]ATTTTATTTTATGTT | 17344 |
rs29538941 | snp | G/T | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77083266 | ATCAGATCTCATTAT[G/T]GGTGGTCGTGAGCTG | 17344 |
rs29538962 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias2 | GRCm38.p3 | 18:77126776 | ACAGTATAACAAAAA[C/T]TAGGCAAGATCCTGT | 17344 |
rs29542166 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Pias2 | GRCm38.p3 | 18:77075935 | TTTTATTTATTATGT[G/T]TAAGTACACTGTAGC | 17344 |
rs29553373 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pias2 | GRCm38.p3 | 18:77084833 | AACTTAAATTCTAGC[C/G]CTTTAGTTTCCTGAG | 17344 |
rs29557551 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77127168 | GTAGTCCTGGAGAGA[A/G]CATGCTGGTTAGCAG | 17344 |
rs29557571 | snp | G/T | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77105156 | TTTTTTTTGTTTTTT[G/T]TTTTTTTTTTTTTCG | 17344 |
rs29558251 | snp | A/G | 0.32 | 0.24 | intron-variant | Pias2 | GRCm38.p3 | 18:77109376 | CATCTTACTCGGTTG[A/G]CACAGAATCTTCACT | 17344 |
rs29558703 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Pias2 | Mm_Celera | 18:77109461 | CTGACGTCAACCCTT[A/C]ACTCCCGTGCGGGAG | 17344 |
rs29560603 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pias2 | GRCm38.p3 | 18:77093808 | AGTTTGACTTCATTT[A/T]GCTTTCTAGTTAATG | 17344 |
rs29564607 | snp | A/T | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77141300 | TCAGAATTTTATACC[A/T]TTACTTGAAGGTGAC | 17344 |
rs29573539 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77093103 | TTCTGATGATGGTGA[G/T]TGGTCTTGATTTCTG | 17344 |
rs29574569 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pias2 | Mm_Celera | 18:77141379 | ACATATCTCTCCTGG[G/T]TTTTTTTTTATAATA | 17344 |
rs29575353 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77076880 | ATACAATTTGTTAAA[C/T]GCATGAAACTCAAGA | 17344 |
rs29622150 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pias2 | GRCm38.p3 | 18:77108598 | ACACTTAGTGCTGTT[C/G]TCGCCCTCTGTAACT | 17344 |
rs29623950 | snp | A/C | 0.5 | 0 | intron-variant | Pias2 | GRCm38.p3 | 18:77103303 | TTTAAATTTATATAC[A/C]TAAATTAAACCTTTA | 17344 |
rs29624815 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77120912 | AATGATTATGTGAGA[A/G]GTACATTTGAACAGC | 17344 |
rs29627018 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77137186 | ACAGCAACAACAAAA[A/C/G]CTAAAATAAAGTACC | 17344 |
rs29627639 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pias2 | Mm_Celera | 18:77143291 | AGATGCCCTCATTAC[C/T]ATCCTAGTTCTGCCT | 17344 |
rs29630156 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77132248 | CCTGAGGGAGGTATC[A/G]TTTTTATTTTGCAAA | 17344 |
rs29631118 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, nc-transcript-variant | Pias2, LOC102634716 | GRCm38.p3 | 18:77064532 | CACTTTTCTCCTCAC[C/T]GTACCCACAATTCTT | 17344 |
rs29637619 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pias2 | Mm_Celera | 18:77149173 | TCTTTTCTTTTTTTT[C/T]AGACAGGGTCTCACT | 17344 |
rs29666797 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pias2 | GRCm38.p3 | 18:77150728 | GAAGAACTGACCTGT[A/C]TCATCAGCTTCACCA | 17344 |
rs29673528 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77087070 | GGTTTTAGAGGCGGT[A/G]GGAGACAGATTACTA | 17344 |
rs29677103 | snp | A/G | 0.32 | 0.24 | intron-variant | Pias2 | Mm_Celera | 18:77121770 | TCATTCAGTGCGTAC[A/G]TTATGCGCTTTTTTT | 17344 |
rs29678417 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77117216 | GAAAGCCACTTAATA[A/T]GGTTTCTGGGAGCCA | 17344 |
rs29718824 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias2 | GRCm38.p3 | 18:77123188 | ATAGTATTTTGTGTT[C/T]ACATTTTGGCATGTA | 17344 |
rs29721850 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77132953 | GGATTAAAGGTATGT[A/G]CCACCACCGCCCGGC | 17344 |
rs29736310 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77081501 | CTTAAAGCTCACTCC[C/T]CATGATACATTTCCT | 17344 |
rs29769200 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77131280 | GGGTCAAACTCCCAG[G/T]TAGTGAGTTCCTTAA | 17344 |
rs29769516 | snp | A/C | 0.265928 | 0.249492 | utr-variant-3-prime | Pias2 | GRCm38.p3 | 18:77154729 | TGCCTCTGCTTTTGT[A/C]GTTGTCCTGCATCTG | 17344 |
rs29769842 | snp | A/G | 0.5 | 0 | intron-variant | Pias2 | GRCm38.p3 | 18:77075363 | TCTCTATCTGCTGCA[A/G]TTCCATGCTTACTGA | 17344 |
rs29771232 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77076732 | GAATGAATTTATGAA[A/G]TTCCTAGGCAAATGG | 17344 |
rs29780793 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77132801 | AATTTAGGCTGGAGG[G/T]TTTTTTTTGTTTTTG | 17344 |
rs29782792 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77073583 | AATTTCAGTTTTGTG[C/T]AATTATCATAGGGTG | 17344 |
rs29793985 | snp | C/T | 0.5 | 0 | intron-variant | Pias2 | GRCm38.p3 | 18:77071576 | TAGGTCTATCATTAC[C/T]ACTATGATTTTTCTC | 17344 |
rs29811706 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77140276 | AGGCACTGTGTGTAT[A/G]TTTAACATGCAAGCA | 17344 |
rs29814763 | snp | C/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Pias2, LOC102634716 | Mm_Celera | 18:77066231 | TGTGTGTGTGTGTGT[C/G]TGTCTGTCTGTCTGT | 17344 |
rs29823249 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77142505 | TTCTTCAGTGACACA[C/T]GGCCTGGTCTGCTCT | 17344 |
rs29827307 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pias2 | GRCm38.p3 | 18:77139110 | CGGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 17344 |
rs29828964 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pias2 | GRCm38.p3 | 18:77119522 | GTGTCATTTAACATT[A/T]AAAAAAAAATGTACT | 17344 |
rs29858944 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pias2 | GRCm38.p3 | 18:77127544 | GTTACCTGTACTCAT[A/G]GTGTAATTAAAGACA | 17344 |
rs29869608 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pias2 | Mm_Celera | 18:77149884 | TTTGGTCAAAAAAAA[G/T]GTATTTGGGTTTTAG | 17344 |
rs29871556 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pias2 | GRCm38.p3 | 18:77148068 | TCAACTAGTTAAGAG[C/T]ATTTACGGTTCCTGC | 17344 |
rs29881016 | snp | G/T | 0.5 | 0 | intron-variant | Pias2 | GRCm38.p3 | 18:77072858 | GTGTGCCAATTCGGC[G/T]GGTTTGATGTCTGCT | 17344 |
rs29889939 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77111478 | CTTTCTCCACATCCT[C/T]GCCAGCATCTGCTGT | 17344 |
rs29909097 | snp | A/T | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77093575 | TCTTTTACCATTATT[A/T]TTACTCTTTTGGAGA | 17344 |
rs29909421 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77093896 | TTCTTGAACTATTTT[A/C]TATAAGAACTGTGGT | 17344 |
rs29912840 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77131139 | AGCAGAAACAAAAGA[C/T]TTTTTCCTAACATTC | 17344 |
rs29912844 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77119252 | AAAACATCTCTAAGT[G/T]ATCAGAATGTTCAGT | 17344 |
rs29912956 | snp | A/C | 0.5 | 0 | intron-variant | Pias2 | GRCm38.p3 | 18:77076135 | CAGTTGTATGCCACA[A/C]TTGGCTTTTAAATTT | 17344 |
rs29914218 | snp | A/G | 0.32 | 0.24 | intron-variant | Pias2 | GRCm38.p3 | 18:77133373 | GAGACAGAGTCAAGT[A/G]GATCTCAGTTTAAGA | 17344 |
rs29916505 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pias2 | GRCm38.p3 | 18:77079477 | TTTAAAGAACTTGCT[A/G]AACTTTTCCAGAGTT | 17344 |
rs29918071 | snp | A/T | 0.5 | 0 | intron-variant | Pias2 | Mm_Celera | 18:77082161 | CATGACTTTAAAATT[A/T]TTTTTTTTTTTTTTT | 17344 |
rs29920123 | snp | A/G | 0.32 | 0.24 | intron-variant | Pias2 | GRCm38.p3 | 18:77120450 | CAAGGAAAACAGAAA[A/G]AGGATTCTAACTTTG | 17344 |
rs29923732 | snp | A/G | 0.32 | 0.24 | intron-variant | Pias2 | Mm_Celera | 18:77140617 | AGCAAGAATCACACA[A/G]GCCTTTTAAGTTTTA | 17344 |
rs29957581 | snp | G/T | 0.32 | 0.24 | intron-variant | Pias2 | Mm_Celera | 18:77144264 | CTTTCATTGTGGTTT[G/T]TTTTTTTTTTTTTTT | 17344 |
rs29958697 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77095488 | AATTCGCTCATACCC[C/T]GTTGTTAGAGCAGGT | 17344 |
rs29959396 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77082050 | TGAGCTTCAGCCTCT[A/G]GTACTGACTACAGGC | 17344 |
rs29969021 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pias2 | GRCm38.p3 | 18:77139815 | TGTGACTGTACTTAG[C/T]ATTTTAGCCAGTGCT | 17344 |
rs29998360 | snp | C/T | 0.5 | 0 | intron-variant | Pias2 | GRCm38.p3 | 18:77075344 | TGCACTCCCCCCGCC[C/T]CCTTCTCTATCTGCT | 17344 |
rs30004747 | snp | C/T | 0.5 | 0 | intron-variant | Pias2 | GRCm38.p3 | 18:77128328 | ACCTTTGTGTATTAC[C/T]TAAGTATGGAATTGT | 17344 |
rs30007020 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77095681 | TTAGAGCAGGTTAGC[C/T]TTATGCCCTGTTGTT | 17344 |
rs30020759 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pias2 | Mm_Celera | 18:77080909 | AATTTAGGGGAAGAT[A/G]GTTGAGAAAAAAAAC | 17344 |
rs30027922 | snp | A/T | 0.375 | 0.216506 | intron-variant | Pias2 | Mm_Celera | 18:77132145 | TTTTTTTTTTTTTTT[A/T]AAATTGAGAGAAAGT | 17344 |
rs30066798 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pias2 | Mm_Celera | 18:77095652 | TTAGAGCAGGTTAGC[C/T]TTATGCCCTGTTGTT | 17344 |