SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs946022 | snp | G/T | 0.499897 | 0.00718776 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78962416 | AAATTATTTAAGGTA[G/T]TATTTATAAGGCTAT | 55023 |
rs1044309 | snp | C/T | 0.499396 | 0.0173617 | utr-variant-3-prime, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78936858 | AAAATTAATATTACA[C/T]TTACTAAGAAACTAT | 55023 |
rs1044313 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78935903 | AGTAACTACAAACTT[A/T]TTTTTAAATAAATAG | 55023 |
rs1056958 | snp | C/T | 0 | 0 | missense, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78946787 | TCTGCTCTTCGTTTT[C/T]ATAAAAGAAATACCA | 55023 |
rs1056959 | snp | A/G | 0 | 0 | missense, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78946759 | CCATAACCAAAAGGA[A/G]GAAGAAAAGAAACAG | 55023 |
rs1056960 | snp | C/T | 1.64893e-05 | 0.0028713 | missense, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78946061 | GAGCAACCATCTACT[C/T]CTTCAGCTGCAAAGA | 55023 |
rs1135076 | snp | A/G | | | synonymous-codon, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78946017 | AGCTAATGCATCTGC[A/G]ATACCAGGGAAAACA | 55023 |
rs1283320 | snp | C/G | 0.189576 | 0.242588 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78948398 | CAATAAAAACACACA[C/G]GTGAAACAGGAAGAG | 55023 |
rs1338023 | snp | G/T | 0.338069 | 0.233974 | intron-variant | PHIP | GRCh38.p7 | 6:79018611 | AAACACAAATCTGAA[G/T]TGGAATCTTAGCACT | 55023 |
rs1413967 | snp | A/C | 0.105569 | 0.204058 | upstream-variant-2KB | PHIP | GRCh38.p7 | 6:79079295 | TCTTTCAATATCCTT[A/C]GGCAGGTTATCGATC | 55023 |
rs1415861 | snp | C/T | 0.107341 | 0.205301 | intron-variant | PHIP | GRCh38.p7 | 6:79038611 | ACTCTTCTTTTTTTT[C/T]CCCTAGCCTCTCAGG | 55023 |
rs1415862 | snp | A/G | 0.148996 | 0.228688 | intron-variant | PHIP | GRCh38.p7 | 6:78990321 | ACACTCAGGAAGTAC[A/G]TATCTCTCTCAATTA | 55023 |
rs1415863 | snp | A/G | 0.126219 | 0.217206 | intron-variant | PHIP | GRCh38.p7 | 6:78990442 | CTACCTCTCTTAATG[A/G]AGAAAATGAGAAATA | 55023 |
rs1538233 | snp | G/T | 0.49655 | 0.04139 | intron-variant | PHIP | GRCh38.p7 | 6:79034018 | gccataagggtgcag[G/T]tcatggcaccctaaa | 55023 |
rs1538234 | snp | C/T | 0.131038 | 0.219882 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78966862 | TAGCATAGGCTAGAG[C/T]CTGAAAGACTTGGGT | 55023 |
rs1538235 | snp | C/T | 0.499218 | 0.0197529 | intron-variant, downstream-variant-500B | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78979733 | CTTTTGTGAATCACA[C/T]GTAAAACATTAAAAA | 55023 |
rs1547731 | snp | A/G | 0.499816 | 0.0095829 | intron-variant | PHIP | GRCh38.p7 | 6:79066387 | TTCTATAAAAAAATT[A/G]TAGAATTTATTTAAA | 55023 |
rs1572584 | snp | A/G | 0.499087 | 0.0213463 | intron-variant | PHIP | GRCh38.p7 | 6:78980573 | tacagcgggtttgag[A/G]aaaaagcttggtaaa | 55023 |
rs1572585 | snp | C/T | 0.499928 | 0.00598999 | intron-variant | PHIP | GRCh38.p7 | 6:78980859 | TCATAATTCTAGCCT[C/T]AATATGGACTATTAA | 55023 |
rs1572586 | snp | C/T | | | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78966624 | CTATTCTTTTTAAAA[C/T]AGAGGACACTCCTTG | 55023 |
rs1832396 | snp | C/G | | | intron-variant | PHIP | GRCh38.p7 | 6:79021125 | TTTATTAAATTTATT[C/G]GTTAATCAAAATAAT | 55023 |
rs1876387 | snp | A/G | 0.016154 | 0.0884085 | missense, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78940874 | CTCATGGGGGGTTCA[A/G]AGCCTTTGAGTTCTT | 55023 |
rs1876388 | snp | G/T | 0.00388348 | 0.0438937 | missense, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78940934 | TCTATCTTTTTTCGG[G/T]TACTTCTCCTTAACA | 55023 |
rs1890229 | snp | C/T | 0.499794 | 0.0101529 | | | GRCh38.p7 | 6:78985312 | ACACCTTTCTAAAGA[C/T]TTTATATAACATTTG | 55023 |
rs1890230 | snp | A/G | 0.125874 | 0.217008 | | | GRCh38.p7 | 6:78985607 | ACACTTTGAGAGGTC[A/G]AGGTGGGCAGATCAC | 55023 |
rs1933238 | snp | A/C | 0.186737 | 0.241863 | intron-variant | PHIP | GRCh38.p7 | 6:79011692 | CAAGAAAAATAAACC[A/C]CTCAGTTTCTCTGGA | 55023 |
rs1984195 | snp | C/T | 0.49991 | 0.00671008 | synonymous-codon, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78947674 | GTTATGTAAAGATGT[C/T]AGACTTATTTTCAGT | 55023 |
rs2050659 | snp | A/C | 0.499396 | 0.0173617 | intron-variant | PHIP | GRCh38.p7 | 6:79024652 | TACTAAAAATACAAA[A/C]AACTTATACGGGAGT | 55023 |
rs2050660 | snp | C/T | 0.499368 | 0.0177603 | intron-variant | PHIP | GRCh38.p7 | 6:79025009 | ATTAATATGGGCGAC[C/T]GCACAAATGCAAAAT | 55023 |
rs2050661 | snp | A/G | 0.499502 | 0.0157669 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78951408 | TTTTGAGTTTAATCA[A/G]ATATTCAAAGCAAGA | 55023 |
rs2050662 | snp | C/G | 0.499515 | 0.0155675 | intron-variant | PHIP | GRCh38.p7 | 6:79043356 | ATTTCCTTAAAAGCT[C/G]TCTATGAAATAGTTT | 55023 |
rs2050663 | snp | C/T | 0.498927 | 0.0231381 | intron-variant | PHIP | GRCh38.p7 | 6:79043677 | CCAAAGCTTGATACA[C/T]TGACTCCAGCTGAAA | 55023 |
rs2063123 | snp | C/T | 0.474813 | 0.109357 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78948818 | TCAACAGTCCCTCAG[C/T]ATGCGACTATATTTT | 55023 |
rs2065986 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | PHIP | GRCh38.p7 | 6:79003448 | CATCTCCAGTTTATA[C/T]ACCCCAAGTTAAGAA | 55023 |
rs2095724 | snp | C/T | 0.499918 | 0.00638925 | intron-variant | PHIP | GRCh38.p7 | 6:79032384 | ttacccacagtagaa[C/T]ttatttcaaaattgg | 55023 |
rs2105143 | snp | A/G | 0.474723 | 0.109542 | intron-variant | PHIP | GRCh38.p7 | 6:79033230 | aaaaaatggtaaatg[A/G]acactggtttcaact | 55023 |
rs2152951 | snp | A/G | 0.499928 | 0.00598999 | intron-variant | PHIP | GRCh38.p7 | 6:79052455 | GTGCTTTCTAAGCTA[A/G]GTTAGGTATTTTGGA | 55023 |
rs2174739 | snp | A/G | 0.499053 | 0.0217445 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78949453 | tttaaatcatctcag[A/G]gctgggaccagacaa | 55023 |
rs2275290 | snp | C/T | 0.437858 | 0.164953 | synonymous-codon, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78946853 | AGCATGAGTTTGCGC[C/T]TGTCTGCTTTCTTTG | 55023 |
rs2275291 | snp | A/T | 0.40444 | 0.196605 | synonymous-codon, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78946845 | TTTGCGCCTGTCTGC[A/T]TTCTTTGAAGAACAC | 55023 |
rs2485701 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78940828 | GTCATCCTCATTATA[A/G]AAAGCTGTCCTTCGA | 55023 |
rs3763160 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78965558 | ATCTCCCCTACTTCA[A/G]GGTGTACAATAATAA | 55023 |
rs3805746 | snp | C/T | 0.402277 | 0.198272 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78962721 | TGTGTGTATATTAAG[C/T]TGGGGGAGACCAGTA | 55023 |
rs3805747 | snp | A/G | 0.49949 | 0.0159663 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78962805 | ATCATGTCAGCCTGA[A/G]TATGTCAAGTGTTTT | 55023 |
rs3812161 | snp | G/T | 0.187685 | 0.242109 | intron-variant | PHIP | GRCh38.p7 | 6:79076928 | CAAGACATTATTTTT[G/T]CCCCCTCTGTCGTTT | 55023 |
rs3818839 | snp | C/G | 0.383824 | 0.211166 | intron-variant | PHIP | GRCh38.p7 | 6:78990608 | CTAAAGAAAGTTCTT[C/G]ATGAGGCTTCAGTGT | 55023 |
rs3834844 | in-del | -/CTT | 0.00636936 | 0.0560724 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78965553 | gctgaatctccccta[-/CTT]caaggtgtacaataa | 55023 |
rs3834845 | in-del | -/C | | | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78967330 | AAGCATTCTTGACAC[-/C]ACCACTACCTCACAC | 55023 |
rs3841155 | in-del | -/TCT | 0.00636936 | 0.0560724 | intron-variant | PHIP | GRCh38.p7 | 6:78991560 | ATAAAATTATCTTCT[-/TCT]CATGAGTTCATTTTT | 55023 |
rs3841156 | in-del | -/AGA | | | intron-variant | PHIP | GRCh38.p7 | 6:78991348 | TCTATATGGAACAGA[-/AGA]TTATCAAAGCATAGG | 55023 |
rs3902856 | snp | C/T | 0.474363 | 0.110278 | intron-variant | PHIP | GRCh38.p7 | 6:78990120 | GCTGGTGAAGAAGGC[C/T]AGTTATTTATTTTTC | 55023 |
rs3929865 | snp | C/T | 0.131038 | 0.219882 | intron-variant | PHIP | GRCh38.p7 | 6:79029291 | GATTTTCCAACAGAA[C/T]TGCAAGCATTCTTAA | 55023 |
rs3929866 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PHIP | GRCh38.p7 | 6:79029388 | AGATAATCTGAGCAT[A/G]AATTCAATGAAACTC | 55023 |
rs3929867 | snp | A/G | 0.335788 | 0.23482 | intron-variant | PHIP | GRCh38.p7 | 6:79029633 | ctcccaggttcaagt[A/G]gttctcatgcctcag | 55023 |
rs4144107 | snp | A/C | | | intron-variant | PHIP | GRCh38.p7 | 6:78989101 | AAAAAACACAAAAAA[A/C]ttaataaagctatct | 55023 |
rs4406190 | snp | A/G | 0.499879 | 0.0077866 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78971934 | gtcaaactgcaaggc[A/G]gcagcgaggctgggg | 55023 |
rs4565265 | snp | A/G | 0.499918 | 0.00638925 | intron-variant | PHIP | GRCh38.p7 | 6:79032241 | ggctgatcagggtgg[A/G]gttgctgaaggttgg | 55023 |
rs4594915 | snp | A/C | 0 | 0 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78977147 | tccaacaatgataga[A/C]tggattaagaaaatg | 55023 |
rs4706080 | snp | C/T | 0.499923 | 0.00618962 | intron-variant | PHIP | GRCh38.p7 | 6:79051280 | GGACAAATAAATCAC[C/T]GTAATAGTAACTATA | 55023 |
rs4706745 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78948811 | CAGCTTTTCAACAGT[C/T]CCTCAGTATGCGACT | 55023 |
rs4706746 | snp | A/G | 0.474544 | 0.10991 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78964459 | TTTTTGTTTTTTAAA[A/G]ATCTTATTTATTTTT | 55023 |
rs4706747 | snp | A/G | 0.499477 | 0.0161657 | intron-variant | PHIP | GRCh38.p7 | 6:79012922 | TCAAAAGATCCACTC[A/G]GATTTATTACCATTA | 55023 |
rs4706748 | snp | A/G | 0.126219 | 0.217206 | intron-variant | PHIP | GRCh38.p7 | 6:79012955 | AAAACATTTCTTCAT[A/G]GACATATCACTAACT | 55023 |
rs4706749 | snp | C/T | 0.131038 | 0.219882 | intron-variant | PHIP | GRCh38.p7 | 6:79038336 | ctttacatggctccc[C/T]tgagcctcttttgta | 55023 |
rs5877635 | in-del | -/T | | | utr-variant-3-prime, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78937691 | AAGGCCAATCTTTAG[-/T]TTATAATACATGCAG | 55023 |
rs5877636 | in-del | -/A | 0.474723 | 0.109542 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78944968 | TAAAAGTCAGTCTAG[-/A]AAAAATAAGTAGTTT | 55023 |
rs5877639 | in-del | -/TTT | 0.131038 | 0.219882 | intron-variant | PHIP | GRCh38.p7 | 6:79038667 | TCTTCTTTTGTCTGC[-/TTT]TTTAAAAGCTGAAGT | 55023 |
rs6454090 | snp | A/T | 0.481932 | 0.0933148 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78943989 | AGATCCTGTCTTTTT[A/T]TAAAAAAAAAAAAAA | 55023 |
rs6454091 | snp | A/T | 0.481932 | 0.0933148 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78943990 | GATCCTGTCTTTTTT[A/T]AAAAAAAAAAAAAAA | 55023 |
rs6454092 | snp | A/G | 0.499866 | 0.0081858 | intron-variant | PHIP | GRCh38.p7 | 6:78992255 | ggtgtgagccaccgc[A/G]ccggcccaaaatggt | 55023 |
rs6454094 | snp | C/T | 0.105214 | 0.203807 | intron-variant | PHIP | GRCh38.p7 | 6:79040092 | ATCTATAAGTAGCAG[C/T]AGGAAAAACCTAATG | 55023 |
rs6454095 | snp | C/T | 0.154618 | 0.231089 | intron-variant | PHIP | GRCh38.p7 | 6:79056657 | ACATCCAACAATGCA[C/T]AGGAAAGCTGCCTAC | 55023 |
rs6900790 | snp | C/T | 0 | 0 | utr-variant-3-prime, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78940645 | GTTCTACTTATTCCT[C/T]AACTGTACCTGCTTT | 55023 |
rs6904138 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHIP | GRCh38.p7 | 6:78997297 | TGAATAGTTTATACT[A/G]CCCTTCCAGAAAAAT | 55023 |
rs6907674 | snp | A/T | 0.030665 | 0.119967 | intron-variant | PHIP | GRCh38.p7 | 6:79007047 | TCCCTTATTTGAAAA[A/T]TCTCATACTGACTAA | 55023 |
rs6915558 | snp | A/T | 0.499866 | 0.0081858 | intron-variant | PHIP | GRCh38.p7 | 6:79059339 | AATTTTTAAAAAATT[A/T]ACATCAAGACATATC | 55023 |
rs6917206 | snp | C/G | 0.046775 | 0.145601 | intron-variant | PHIP | GRCh38.p7 | 6:79059997 | GCTGTATTAATCCGG[C/G]TAAGGCAAGGGCCTG | 55023 |
rs6918296 | snp | C/T | 0.127599 | 0.217986 | intron-variant | PHIP | GRCh38.p7 | 6:79031203 | TCTGCCTCAGCCTCC[C/T]AAAGTGCTGGGATTA | 55023 |
rs6925447 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PHIP | GRCh38.p7 | 6:79062834 | GCTGGCAATCTTGTC[C/T]TACCTGCTCACCTCT | 55023 |
rs6928507 | snp | A/C | | | intron-variant | PHIP | GRCh38.p7 | 6:79054534 | ATGGAAAGAAAAAAC[A/C]CTGAATATAGCATAT | 55023 |
rs6928518 | snp | A/G | | | intron-variant | PHIP | GRCh38.p7 | 6:79054548 | CACTGAATATAGCAT[A/G]TTAGAAAAAGATAAG | 55023 |
rs6929315 | snp | C/T | 0.107341 | 0.205301 | intron-variant | PHIP | GRCh38.p7 | 6:79054898 | TTTATTCAAACTAGT[C/T]TTCTCAGAGAATCAC | 55023 |
rs6940635 | snp | C/T | 0.103794 | 0.20279 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78961256 | ATGATAAGCTGAATA[C/T]AGGCAAAATAAGAAC | 55023 |
rs6940637 | snp | C/T | 0.499928 | 0.00598999 | intron-variant | PHIP | GRCh38.p7 | 6:78996128 | TGACTCATTCCTCTC[C/T]AGAGGAGGAGTAAAT | 55023 |
rs7454519 | snp | C/G | 0 | 0 | intron-variant | PHIP | GRCh38.p7 | 6:79061145 | CTTTTGGAACAACTT[C/G]AAAATACTGCTTAAT | 55023 |
rs7739298 | snp | A/G | 0.126219 | 0.217206 | intron-variant | PHIP | GRCh38.p7 | 6:79044643 | GATAGTATTACCAAG[A/G]TGTACTTTAATTCCC | 55023 |
rs7740307 | snp | A/T | 0.401747 | 0.198678 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78944437 | GCAGGAAGACCAGTT[A/T]GGAAACTAGGAAAAT | 55023 |
rs7741282 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PHIP | GRCh38.p7 | 6:79032661 | ttaacttcctccact[A/G]aagtcttgaacccct | 55023 |
rs7741943 | snp | A/G | 0.499464 | 0.016365 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78972850 | aataaaaagaaatga[A/G]caaagcctccaagaa | 55023 |
rs7742034 | snp | A/G | 0.499853 | 0.008585 | intron-variant | PHIP | GRCh38.p7 | 6:79027389 | TGGTCAACTATCCAT[A/G]TTGTTGTCTAGTATT | 55023 |
rs7742431 | snp | A/G | 0.497912 | 0.032244 | synonymous-codon, utr-variant-3-prime, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78969860 | TCGCCTGTATTTTGC[A/G]TCATCAAATTGTTGT | 55023 |
rs7742746 | snp | A/G/T | 0.00622081 | 0.0554375 | intron-variant, downstream-variant-500B | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78969810 | ACCACATCAAACATC[A/G/T]ATAGCTTCTAAATAA | 55023 |
rs7742874 | snp | A/G | 0 | 0 | synonymous-codon, utr-variant-3-prime, intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78969851 | TATATTCCATCGCCT[A/G]TATTTTGCATCATCA | 55023 |
rs7744876 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PHIP | GRCh38.p7 | 6:79073320 | CATATAACCCTTCAC[A/G]CCTAACATATTTTAT | 55023 |
rs7746653 | snp | C/G | | | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78973595 | ggcaaattggataaa[C/G]agtcaagacccatca | 55023 |
rs7747479 | snp | A/C | 0.101372 | 0.201025 | missense | PHIP | GRCh38.p7 | 6:78998283 | CTGGTATTACTGATA[A/C]CTGCTTCACCAGAAC | 55023 |
rs7749615 | snp | G/T | 0.336474 | 0.234568 | intron-variant | PHIP | GRCh38.p7 | 6:78992058 | gctctgccccccggg[G/T]ttcacaccattctcc | 55023 |
rs7750810 | snp | A/T | 0 | 0 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78977847 | GAATCACTCTAGCAT[A/T]AAAAAGTTTTTGTTT | 55023 |
rs7751287 | snp | A/G | 0.499872 | 0.0079862 | intron-variant | PHIP, IRAK1BP1 | GRCh38.p7 | 6:78974174 | aaattataacaaact[A/G]tctctcagaccacag | 55023 |
rs7751422 | snp | C/T | 0.170408 | 0.236992 | intron-variant | PHIP | GRCh38.p7 | 6:79034363 | CACAGGTCTTTATGA[C/T]GTGGCTTTCTACTGT | 55023 |