SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs231582 | snp | C/G | 0.379746 | 0.213696 | upstream-variant-2KB | PARD6B | GRCh38.p7 | 20:50730747 | GGGCTCTCTTGGCTT[C/G]ATTTTGTCCGAAGAG | 84612 |
rs231583 | snp | C/T | 0.412917 | 0.189626 | upstream-variant-2KB | PARD6B | GRCh38.p7 | 20:50730344 | TCTCCCTGTGGGACC[C/T]GGGAATCCAAGAGCT | 84612 |
rs1054185 | snp | A/G | 0.366473 | 0.221211 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50752469 | ATTTATTACTTTCCA[A/G]TGCATCCACTTAGAA | 84612 |
rs1136848 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | PARD6B | GRCh38.p7 | 20:50744144 | TCTGAGAAGCAGTCT[C/T]GCTCTTGTTGCCCAG | 84612 |
rs1136849 | snp | A/G | | | intron-variant | PARD6B | GRCh38.p7 | 20:50744244 | ctcatcctcccgagt[A/G]ggtgggattacaggc | 84612 |
rs1136850 | snp | C/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50744405 | aagtgtgacccactg[C/T]acTGCGCTGGCTGCA | 84612 |
rs2064278 | snp | G/T | 0.344147 | 0.231595 | intron-variant | PARD6B | GRCh38.p7 | 20:50746645 | TGATTAGCTAGATGG[G/T]AGAACAAAGGTGGCT | 84612 |
rs2179467 | snp | A/C | | | intron-variant | PARD6B | GRCh38.p7 | 20:50737454 | GGGGGAGGACACTTA[A/C]ATGCTTTCCTTTGGT | 84612 |
rs2294592 | snp | A/C | 0.406986 | 0.194565 | intron-variant | PARD6B | GRCh38.p7 | 20:50748197 | cgccactatgcccag[A/C]taatttttgtatttt | 84612 |
rs2294593 | snp | A/G | 0.344592 | 0.231414 | intron-variant | PARD6B | GRCh38.p7 | 20:50747873 | CCTCATTTAGATGGC[A/G]TAGCTGCTTCTCAGT | 84612 |
rs2294594 | snp | C/T | 0.366885 | 0.220993 | intron-variant | PARD6B | GRCh38.p7 | 20:50738739 | TCAGTGTTTACATCC[C/T]TCCACAATAGTAACT | 84612 |
rs3810537 | snp | A/G | 0.000148369 | 0.00861177 | missense | PARD6B | GRCh38.p7 | 20:50750178 | CCGGTCAGTCTACTG[A/G]TAACAGCCTTCTTGG | 84612 |
rs4809811 | snp | C/T | 0.471483 | 0.115954 | intron-variant | PARD6B | GRCh38.p7 | 20:50735203 | ACATTATTATCTTCA[C/T]ACGTGGAAGGGAAAA | 84612 |
rs5841809 | in-del | -/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50746079 | AGTTTTTTTTTTTTT[-/T]CTAGATTTGCTTTTT | 84612 |
rs5841810 | in-del | -/A | 0.409721 | 0.192325 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50752332 | TGCACTTTTTATGCC[-/A]AAAAAAAAAAAAATT | 84612 |
rs5841811 | in-del | -/C | 0.402982 | 0.197728 | downstream-variant-500B | PARD6B | GRCh38.p7 | 20:50754059 | TCTGAAATTCAAATT[-/C]CACTTAGTTATACTT | 84612 |
rs6013006 | snp | A/G | 0.36606 | 0.221428 | intron-variant | PARD6B | GRCh38.p7 | 20:50739239 | ATCATCTGAGGTCAG[A/G]AGTTCATGACTAGCA | 84612 |
rs6013007 | snp | C/T | 0.478768 | 0.100824 | intron-variant | PARD6B | GRCh38.p7 | 20:50749079 | ccaggtgcggtggct[C/T]acgcctataattcca | 84612 |
rs6013008 | snp | C/G | 0.494272 | 0.053207 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50751515 | cgcctgccaccatgc[C/G]tggctaatttttagt | 84612 |
rs6020714 | snp | A/G | | | upstream-variant-2KB | PARD6B | GRCh38.p7 | 20:50730720 | ACCTGACGGACTTAA[A/G]GCGTGCAGAGTCTCT | 84612 |
rs6020717 | snp | C/T | 0.46875 | 0.121031 | intron-variant | PARD6B | GRCh38.p7 | 20:50735943 | AAAATGGAGGAGAAA[C/T]TGTGACTTTTGATAA | 84612 |
rs6020718 | snp | C/T | 0.168135 | 0.236216 | intron-variant | PARD6B | GRCh38.p7 | 20:50738978 | TTAATCTCGTAGCCT[C/T]TGTGTGTGTATGTAT | 84612 |
rs6020721 | snp | G/T | 0.47365 | 0.111716 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50750539 | ATGAGGACTTGTACA[G/T]TTGGCTAGTTTAAAA | 84612 |
rs6091205 | snp | C/T | 0.081446 | 0.184634 | intron-variant | PARD6B | GRCh38.p7 | 20:50749267 | agaattgcttgaacc[C/T]gggaggcggaggttg | 84612 |
rs6091207 | snp | C/T | 0 | 0 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50750920 | TTGGGGACCTCAGCT[C/T]TTAAAGGTCTCATGT | 84612 |
rs6091208 | snp | C/T | 0 | 0 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50750929 | TCAGCTCTTAAAGGT[C/T]TCATGTTCCCAATAt | 84612 |
rs6096071 | snp | C/T | 0.173643 | 0.238054 | upstream-variant-2KB | PARD6B | GRCh38.p7 | 20:50729640 | tacacataaacaaag[C/T]actttggggtcctcc | 84612 |
rs6096073 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | PARD6B | GRCh38.p7 | 20:50736663 | AAATCCTGTTTATCA[C/T]GGACTAGATGAAGCC | 84612 |
rs6096074 | snp | A/G | 0.365024 | 0.221967 | intron-variant | PARD6B | GRCh38.p7 | 20:50741108 | tgagactacaggtgc[A/G]tgccaccatgcctgg | 84612 |
rs6096077 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | PARD6B | GRCh38.p7 | 20:50747722 | TATCTTCCTTCAGCC[A/G]TATAATTTAACCATA | 84612 |
rs6096079 | snp | A/T | 0.0154538 | 0.0865337 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50751183 | ccatgttgcccaagt[A/T]ggtcttgaactcctg | 84612 |
rs6096083 | snp | A/G | 0.402454 | 0.198136 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50752910 | TTCTTCCATTTATAT[A/G]CTATTTTTAATGGCA | 84612 |
rs6096084 | snp | C/T | 0 | 0 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50753077 | ACACTACCTCTCTCT[C/T]TTTTTTTTTAAAGTT | 84612 |
rs6122969 | snp | A/T | 0.118584 | 0.212673 | intron-variant | PARD6B | GRCh38.p7 | 20:50743374 | GAACACTAGAAAGGC[A/T]TTGCTTTAAACTTTG | 84612 |
rs6122970 | snp | C/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50747381 | TGAGATTGGTGTTTT[C/T]TGTGGCAGCAGCTGA | 84612 |
rs6122971 | snp | C/T | 0.103438 | 0.202533 | downstream-variant-500B | PARD6B | GRCh38.p7 | 20:50754226 | GGCGGATCATGAGGT[C/T]AGGAGTTGGAGACCA | 84612 |
rs6126085 | snp | A/T | 0.115438 | 0.210697 | intron-variant | PARD6B | GRCh38.p7 | 20:50737751 | CAATCTTTCCTTAAT[A/T]AAAAATACTTGCTCT | 84612 |
rs6126086 | snp | A/G | 0.310386 | 0.242597 | intron-variant | PARD6B | GRCh38.p7 | 20:50743530 | ATTTTTATGAATCAG[A/G]GTTTAAAGTTGTCTA | 84612 |
rs6126087 | snp | A/G | 0.311614 | 0.242289 | intron-variant | PARD6B | GRCh38.p7 | 20:50745727 | acccaggctggtctt[A/G]aactactaagctgaa | 84612 |
rs6126088 | snp | C/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50747489 | TTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 84612 |
rs6126089 | snp | C/T | 0.396727 | 0.202413 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50752954 | ATTCTGTGAGTCTTA[C/T]AAATTTGACTCTTGA | 84612 |
rs6512670 | snp | C/T | 0.489259 | 0.0724914 | intron-variant | PARD6B | GRCh38.p7 | 20:50748675 | gggactccaggcaga[C/T]gctacctaccacacc | 84612 |
rs7260805 | snp | A/G | 0.0376037 | 0.131863 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50751716 | CCATGTTATAAAGCT[A/G]AGGAAGCtttttttt | 84612 |
rs7262779 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PARD6B | GRCh38.p7 | 20:50743598 | TTTTAACAAAAGATA[C/T]GGCCCAGAAATGAAA | 84612 |
rs7265589 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | PARD6B | GRCh38.p7 | 20:50741884 | TGAGCAGATGCTTAA[C/T]TAGAAATCTGATTTT | 84612 |
rs7268617 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50751989 | gcaggcatgagcGCC[C/T]AGCCAGGAAGCTATC | 84612 |
rs7268691 | snp | G/T | 0.067446 | 0.170804 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50752073 | CCTATAGCTTTCATA[G/T]TTTCAAATTAATTCT | 84612 |
rs7269716 | snp | A/G | 0.472052 | 0.11486 | intron-variant | PARD6B | GRCh38.p7 | 20:50743784 | GTCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 84612 |
rs7272158 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PARD6B | GRCh38.p7 | 20:50745450 | GATCTATCTCATTTA[A/G]CCATTTTATATTAGA | 84612 |
rs7272925 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PARD6B | GRCh38.p7 | 20:50733294 | ccggccgtggtggca[C/T]atgcctgtaatccca | 84612 |
rs7273801 | snp | A/G | 0.467234 | 0.12373 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50751486 | tcagcctcccaagta[A/G]ctgggactacaggcg | 84612 |
rs8121734 | snp | A/C | | | intron-variant | PARD6B | GRCh38.p7 | 20:50743788 | cagctactcggaagg[A/C]tgaggcaggagaatg | 84612 |
rs8121741 | snp | C/G | | | intron-variant | PARD6B | GRCh38.p7 | 20:50743825 | acccaggaggcggag[C/G]ttgcagtgagcctag | 84612 |
rs8121745 | snp | C/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50743850 | gcctagatcgcgcca[C/T]tgcactccagcctgg | 84612 |
rs8121846 | snp | A/G | | | intron-variant | PARD6B | GRCh38.p7 | 20:50743769 | tggtgggcgcctgta[A/G]tcccagctactcgga | 84612 |
rs8121848 | snp | C/G | | | intron-variant | PARD6B | GRCh38.p7 | 20:50743775 | gcgcctgtagtccca[C/G]ctactcggaaggctg | 84612 |
rs8126455 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50751592 | acctcctgatccgcc[C/T]gcctcggcctcccaa | 84612 |
rs8184449 | snp | A/G | | | intron-variant | PARD6B | GRCh38.p7 | 20:50739590 | CTTTCCTGGGTTTGG[A/G]GGAACTAAAGTCCAC | 84612 |
rs8184464 | snp | G/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50736518 | TGCTGGTCTCCGCAG[G/T]GATTCCCAAGAGCAT | 84612 |
rs9941734 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | PARD6B | GRCh38.p7 | 20:50743750 | aaaaattagccgggc[A/C/T]tggtggtgggcgcct | 84612 |
rs9941758 | snp | A/G | | | intron-variant | PARD6B | GRCh38.p7 | 20:50743844 | cagtgagcctagatc[A/G]cgccactgcactcca | 84612 |
rs10427451 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PARD6B | GRCh38.p7 | 20:50743209 | cctgataatcagcca[A/G]gtggaggatcTGTTG | 84612 |
rs10626068 | in-del | -/TTTC | 0.366266 | 0.221319 | intron-variant | PARD6B | GRCh38.p7 | 20:50747414 | TAGGATTTTCAACTA[-/TTTC]TTTTGTGGAGGAGGA | 84612 |
rs11086315 | snp | A/G | 0.310632 | 0.242536 | intron-variant | PARD6B | GRCh38.p7 | 20:50734782 | cacctaggcctccca[A/G]agtgtttggattata | 84612 |
rs11086316 | in-del | -/A | 0.395453 | 0.203331 | intron-variant | PARD6B | GRCh38.p7 | 20:50749343 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAATA | 84612 |
rs11387842 | in-del | -/A | 0 | 0 | intron-variant | PARD6B | GRCh38.p7 | 20:50732907 | TTTCAAAAAAAAAAA[-/A]GTAATGGAGCATCAT | 84612 |
rs11467364 | in-del | -/T | | | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50751373 | TTTTTTTTTTTTTTT[-/T]TGAGATGGAGTCTCG | 84612 |
rs11469337 | in-del | -/TG | 0 | 0 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50752541 | TTTTATTGTACAGTG[-/TG]CACAAGCACAATGGT | 84612 |
rs11469346 | in-del | -/CT | | | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50753069 | ATTTTTACACACTAC[-/CT]CTCTCTTTTTTTTTT | 84612 |
rs11469424 | in-del | -/GT | 0.34146 | 0.23267 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50752538 | TGATTTTATTGTACA[-/GT]GTGCACAAGCACAAT | 84612 |
rs11481771 | in-del | -/A | 0.486725 | 0.0803809 | upstream-variant-2KB | PARD6B | GRCh38.p7 | 20:50730604 | AGAAAAAAAAAAAAA[-/A]GCCCTGAAAGACTGG | 84612 |
rs11484143 | in-del | -/A | | | intron-variant | PARD6B | GRCh38.p7 | 20:50745427 | AAAAAAAAAAAAAAA[-/A]GTTGCCAGATCTATC | 84612 |
rs11697683 | snp | C/T | 0.469148 | 0.120308 | intron-variant | PARD6B | GRCh38.p7 | 20:50742122 | CAGGGGCGTGACCTC[C/T]ACTCACTGCAACCTC | 84612 |
rs11698397 | snp | A/C | 0 | 0 | intron-variant | PARD6B | GRCh38.p7 | 20:50743543 | AGGGTTTAAAGTTGT[A/C]TAAGGAATATACATT | 84612 |
rs11700356 | snp | C/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50749557 | GCTAGTTTGTTTATA[C/T]ACCAAATATATTTTG | 84612 |
rs12624657 | snp | C/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50743980 | GTCACCTTTGACACA[C/T]ACCTATTTTTTAGTC | 84612 |
rs12624665 | snp | C/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50744099 | CCAAATTTACTGAAG[C/T]AGCttcttttttttt | 84612 |
rs12625496 | snp | C/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50744063 | CCATTTCCATGTCCT[C/T]TGCTCCAGGCCAGGT | 84612 |
rs12625745 | snp | A/T | 0.470327 | 0.118136 | intron-variant | PARD6B | GRCh38.p7 | 20:50745174 | GTGGCTCACGCCTGT[A/T]ATCCCAGCACTTTGG | 84612 |
rs13040463 | snp | C/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50747490 | ttttttctttctttc[C/T]ttttttttttttttt | 84612 |
rs13041875 | snp | A/G | | | intron-variant | PARD6B | GRCh38.p7 | 20:50744134 | tttttttttttctga[A/G]aagcagtctcgctct | 84612 |
rs13042106 | snp | A/T | | | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50750949 | GTTCCCAATATTTTA[A/T]TTTGATTTttttttt | 84612 |
rs33962686 | in-del | -/TTTC | | | intron-variant | PARD6B | GRCh38.p7 | 20:50747415 | AGGATTTTCAACTAT[-/TTTC]TTTGTGGAGGAGGAG | 84612 |
rs34049117 | in-del | -/CT/CTT | 0 | 0 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50753076 | ACACTACCTCTCTCT[-/CT/CTT]TTTTTTTTTTAAAGT | 84612 |
rs34129043 | snp | C/G | | | intron-variant | PARD6B | GRCh38.p7 | 20:50733986 | TTACTTCTGTCTAAA[C/G]TACATGTTGTATATT | 84612 |
rs34138084 | in-del | -/C | | | intron-variant | PARD6B | GRCh38.p7 | 20:50746851 | TTATATAGGCTTTCC[-/C]TTATTGATTGTTTTA | 84612 |
rs34186531 | in-del | -/C | | | intron-variant | PARD6B | GRCh38.p7 | 20:50735034 | TATGCCTGTAATCCC[-/C]AGCTACTCCGGAGGC | 84612 |
rs34538740 | in-del | -/A | 0.379354 | 0.213933 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50751280 | GATTTTTGTTTTTTT[-/A]ATGTTCCTTTCTAAT | 84612 |
rs35130685 | in-del | -/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50733711 | GTTATAAGTTTAGTT[-/T]GGATTTGTGGGAGTT | 84612 |
rs35206987 | in-del | -/TA | | | intron-variant | PARD6B | GRCh38.p7 | 20:50733594 | GTGACTTGCTTGAGC[-/TA]TATAGCGTTAAGATG | 84612 |
rs35225833 | in-del | -/T | | | intron-variant | PARD6B | GRCh38.p7 | 20:50745857 | CAAGAGTGATTATAT[-/T]AGCCTGTAATACCTA | 84612 |
rs35346940 | in-del | -/G | | | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50752144 | ACTTTGGAAATATGG[-/G]AAGTCTCTCCTTTAA | 84612 |
rs35582500 | snp | A/G | 0.47023 | 0.118317 | intron-variant | PARD6B | GRCh38.p7 | 20:50733468 | CGGCTTGGCACTTAC[A/G]TGAGGATTGGCACTA | 84612 |
rs35818153 | in-del | -/A | | | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50752345 | CCAAAAAAAAAAAAA[-/A]TTGGGTTTTCCTTCA | 84612 |
rs36193479 | in-del | -/A | | | intron-variant | PARD6B | GRCh38.p7 | 20:50739879 | GGAAGGGTGGGGGGA[-/A]GGGGAGAAGGCAGTG | 84612 |
rs41283604 | snp | G/T | 0.0226793 | 0.104049 | missense | PARD6B | GRCh38.p7 | 20:50750206 | TGGCTACCCACAGCA[G/T]ATTGAACCAAGCTTT | 84612 |
rs41283606 | snp | C/T | 0.014056 | 0.0826465 | synonymous-codon | PARD6B | GRCh38.p7 | 20:50750342 | TTAACACAGATAGAG[C/T]TAAGCTTTGAGTCTG | 84612 |
rs41283608 | snp | A/G/T | 0.000505455 | 0.0158896 | missense | PARD6B | GRCh38.p7 | 20:50750466 | AACTCTTAGAAGAAG[A/G/T]TGGAACAATCATAAC | 84612 |
rs45601831 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | PARD6B | GRCh38.p7 | 20:50749204 | AAAAGTTAGCCAGGC[C/T]TGGTGGCACACACCT | 84612 |
rs45624032 | snp | G/T | 0.0718919 | 0.175435 | utr-variant-3-prime | PARD6B | GRCh38.p7 | 20:50752325 | AAACTTGTGCACTTT[G/T]TATGCCAAAAAAAAA | 84612 |