SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs706466 | snp | C/T | 0.496937 | 0.0390173 | utr-variant-3-prime, nc-transcript-variant | PRKAA2 | GRCh38.p7 | 1:56715194 | GGAAGAATCTGTAAC[C/T]ATGAAATGCTATGTA | 5563 |
rs706467 | snp | A/G | 0.272241 | 0.249009 | downstream-variant-500B | PRKAA2 | GRCh38.p7 | 1:56715565 | CATATAGAACAATAA[A/G]ATAATTTGTATTTTA | 5563 |
rs706468 | snp | C/T | 0.31014 | 0.242659 | downstream-variant-500B | PRKAA2 | GRCh38.p7 | 1:56715709 | TACAGCACCATGGAA[C/T]GAAATTCTGCCAACA | 5563 |
rs715404 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56676259 | TTGGCCCACCTACAT[A/G]ATCCAGGATAACCTC | 5563 |
rs715405 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56676026 | TGCTCACTGACAAAG[A/G]TCAGCCTAAATATAA | 5563 |
rs721402 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | PRKAA2 | GRCh38.p7 | 1:56713724 | GAGAATTGCATTGTT[A/T]TTTTTTTTCTACTAA | 5563 |
rs857130 | snp | A/C | 0 | 0 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56688043 | TGAAGCATTACAAGA[A/C]ATTCAATCATGAATC | 5563 |
rs857131 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56687294 | TATGTAATATTCTAG[A/T]AGttattttattgag | 5563 |
rs857132 | snp | A/G | 0.499809 | 0.00978247 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56687111 | gaatcacctgaggtc[A/G]agagtctgagaccag | 5563 |
rs857133 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56686971 | cttgaacctgggagg[C/T]ggaggttgcggtaag | 5563 |
rs857147 | snp | C/T | 0.499987 | 0.00259581 | utr-variant-3-prime, nc-transcript-variant | PRKAA2 | GRCh38.p7 | 1:56712116 | ACCTCTCAAAGTTAT[C/T]GTAATAGTAAGTAAA | 5563 |
rs857148 | snp | G/T | 0.499502 | 0.0157669 | utr-variant-3-prime, nc-transcript-variant | PRKAA2 | GRCh38.p7 | 1:56709485 | AAAATTACCTTTTGG[G/T]GCCACAAGATGGCAG | 5563 |
rs857149 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56703131 | ACTTCTGGGCCTTTG[C/T]GCTTGATGTTACTAT | 5563 |
rs857150 | snp | C/T | 0.499451 | 0.0165644 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56702363 | gggcgccgtggctca[C/T]gcctgtaatcccagc | 5563 |
rs857151 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56702329 | ttgggaggccgaggc[A/G]ggcggatcacctgag | 5563 |
rs857152 | snp | A/G | 0.289424 | 0.246872 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56702296 | cgggagttcgagacc[A/G]gcctgaccaacatgg | 5563 |
rs857153 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56701717 | tttttttagtagaga[C/T]ggggtttcaccgtgt | 5563 |
rs857154 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56700139 | ctaaacaaacagaag[C/T]agcagcaacaacata | 5563 |
rs857155 | snp | A/C | 0.499464 | 0.016365 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56698492 | CATTTAATATGTGTT[A/C]GACCTTGTGCATTTT | 5563 |
rs857156 | snp | A/T | 0.49949 | 0.0159663 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56697581 | GAAGTATATATGCTA[A/T]AGAACTATAAACACA | 5563 |
rs857157 | snp | G/T | 0.369929 | 0.220856 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56695166 | TATATCATATATATA[G/T]AGAGAGAGATATTTA | 5563 |
rs857158 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56694253 | TTCCCCCAAAATCTC[A/G]TTTTTCCAAACACAA | 5563 |
rs857159 | snp | A/G | 0.49949 | 0.0159663 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56690353 | acacggtgaaacccc[A/G]tctctactaaaaata | 5563 |
rs932447 | snp | A/G | 0.41275 | 0.189769 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56704556 | AAAGTTGGGCTTAAT[A/G]CTCAACTCAGGAGCT | 5563 |
rs963527 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56675533 | GCATTTGGAATCAGG[C/T]TTGACCTCAACTACC | 5563 |
rs963528 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56675481 | TGTGGCCTTGGATAA[A/G]CTGCTATTACTTTTT | 5563 |
rs997191 | snp | A/G | 0.448452 | 0.152042 | downstream-variant-500B | PRKAA2 | GRCh38.p7 | 1:56715648 | AAAACCAAAGCATTG[A/G]TAGGGCTGGGCTGTG | 5563 |
rs1124900 | snp | G/T | 0.467642 | 0.123012 | intron-variant, upstream-variant-2KB | PRKAA2, LOC101929935 | GRCh38.p7 | 1:56646549 | TTAATTAGTCACATG[G/T]GATTTAATTAACCTG | 5563 |
rs1342382 | snp | A/T | 0.316968 | 0.240864 | utr-variant-3-prime, nc-transcript-variant | PRKAA2 | GRCh38.p7 | 1:56711715 | CAAACATAGGATGTG[A/T]CTTACCAACAGATTG | 5563 |
rs1418442 | snp | A/G | 0.38821 | 0.208322 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56693463 | TTCCCAAACATGAAA[A/G]CATCAAAATATTATT | 5563 |
rs2051040 | snp | A/G | 0.425894 | 0.177655 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56677082 | ACCAAGCTCATGGGT[A/G]GAATTTTAATTCTTA | 5563 |
rs2064421 | snp | C/T | 0.497749 | 0.0334707 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56678075 | AATTCCTTCAGAAAA[C/T]AGCAAATAATTAAAT | 5563 |
rs2064422 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56678003 | GTAAATATAGAAATG[A/G]AGGCAAGAAAACACT | 5563 |
rs2092594 | snp | A/G | 0.499741 | 0.0113788 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56679444 | ctccactctcccacc[A/G]caccctccaaaaaca | 5563 |
rs2092595 | snp | G/T | 0.499741 | 0.0113788 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56679400 | ggaagagagagaaaa[G/T]tttagcttcaggtga | 5563 |
rs2143749 | snp | C/G | 0.455977 | 0.141681 | intron-variant, utr-variant-5-prime | PRKAA2 | GRCh38.p7 | 1:56656794 | CAGAACGTCAGGATG[C/G]CATAACCAAAAACAT | 5563 |
rs2143754 | snp | C/T | 0.499937 | 0.0055907 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56693188 | AGAGAAAGTAGTTTC[C/T]AGGTTTTTAGATTAA | 5563 |
rs2179761 | snp | C/T | 0.323197 | 0.239044 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56691871 | CAAGTTTGTCTTTGT[C/T]GCTAAGCAGAAATAT | 5563 |
rs2206969 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56685271 | CTACTGTCACTGTTT[C/T]AGGTGTAAGTGATAT | 5563 |
rs2206970 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56685014 | AGACTAACTCCTCCA[A/G]TTATGCACTGGATTA | 5563 |
rs2223779 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56686183 | TGTCTTTTGCCCATG[C/T]TTATTGAGTTGACAG | 5563 |
rs2245475 | snp | A/T | 0.467642 | 0.123012 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56657351 | aaacaaactgccagc[A/T]tataattttatgccc | 5563 |
rs2404718 | snp | A/G | 0.437824 | 0.164991 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56648829 | tgaacattgtctcac[A/G]taattactagtcatt | 5563 |
rs2404994 | snp | A/G | 0.467642 | 0.123012 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56657475 | gaggtcaggagtttg[A/G]gaccagcctggccaa | 5563 |
rs2404995 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56657505 | ACATGGTGAAACCCC[A/G]TCTTTACTGAAAATA | 5563 |
rs2746337 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56677116 | AAGTTAAAGAAACAA[A/T]GGATAGGAAAGGTGA | 5563 |
rs2746338 | snp | A/G | 0.497776 | 0.0332724 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56676788 | CATACTCTTGCTGCC[A/G]GTAAGATGCACCACA | 5563 |
rs2746339 | snp | C/T | 0.497722 | 0.0336691 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56673697 | CTCTCAGGAAGTATA[C/T]GCGCACAGTGCTTTG | 5563 |
rs2746340 | snp | C/T | 0.437118 | 0.165792 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56670924 | GGGGGGTGGGGAGAC[C/T]GCAATAAATAAACTG | 5563 |
rs2746341 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56670779 | AATTTATCATGTATA[C/T]ACGTAAATATCCAGA | 5563 |
rs2746342 | snp | A/C | 0.463666 | 0.129795 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56670576 | TACATGGCTACCCAG[A/C]GTACAGCCTGCATCT | 5563 |
rs2746343 | snp | C/T | 0.434109 | 0.169127 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56670141 | ATGAGTTGATGGAAA[C/T]AAATTTTAATTTATA | 5563 |
rs2746344 | snp | C/T | 0.463666 | 0.129795 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56668277 | TGCTATCCCTCCCCC[C/T]TCCCCCCACCCCACA | 5563 |
rs2746345 | snp | C/T | 0.437401 | 0.165472 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56664766 | ATTCTACAAGAGTTC[C/T]TGTAGAAGAGAAAAC | 5563 |
rs2746346 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56661880 | tgtggttgtaacatt[A/G]tattagcaggtacct | 5563 |
rs2746347 | snp | A/G | 0.347253 | 0.230308 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56661246 | TTATTGAGAATTTAC[A/G]TAAAAGATGCCAGTA | 5563 |
rs2746348 | snp | A/G | 0.467439 | 0.123371 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56661036 | ATGCACATATGTTCC[A/G]ACCCCTACCATCCCC | 5563 |
rs2746349 | snp | A/G | 0.46754 | 0.123192 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56660977 | CTTTCACCTCTGCCC[A/G]TGGTGAAACAAAACA | 5563 |
rs2746350 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56658738 | AAAGAAAAAAAAAAG[A/G]AGGCAGGAGGATCAC | 5563 |
rs2746351 | snp | A/C | 0.495213 | 0.048687 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56658576 | GGGGAAGAAAAAAAA[A/C]AACAACAACATTTAC | 5563 |
rs2746352 | snp | C/T | 0.393987 | 0.204372 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56658518 | GAATGTATTAGCATT[C/T]AGTAGACTCTTTAAC | 5563 |
rs2746353 | snp | A/G | 0.435119 | 0.16802 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56657977 | CTACATATATTCTCA[A/G]TCTCGCAAGATATTA | 5563 |
rs2746354 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | PRKAA2 | GRCh38.p7 | 1:56655268 | AAATATATATATATA[G/T]ATATATAAATACATA | 5563 |
rs2746355 | snp | A/T | 0.393987 | 0.204372 | intron-variant, upstream-variant-2KB | PRKAA2 | GRCh38.p7 | 1:56654999 | GAAAAATGATTCTGA[A/T]AAAACAAAGTATATT | 5563 |
rs2796491 | snp | G/T | 0.497473 | 0.0354532 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56675121 | ATTGAAAGATAAATA[G/T]ATTATTTTAAAATTG | 5563 |
rs2796492 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56677098 | ACCCATGAGCTTGGT[A/G]ACTCACCTTTCCTAT | 5563 |
rs2796493 | snp | C/T | 0.497749 | 0.0334707 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56677107 | CTTGGTAACTCACCT[C/T]TCCTATCCATTGTTT | 5563 |
rs2796494 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56677261 | TCTTTCATTATTCCA[A/G]ATGGTTTTCACTTAA | 5563 |
rs2796495 | snp | C/T | 0.497695 | 0.0338674 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56677306 | CTCTGACTTCAACTC[C/T]GTATTATTCATGACT | 5563 |
rs2796496 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56677449 | CTAGAATGAAAGTGG[A/G]GAAGGGAAAGATCTT | 5563 |
rs2796497 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56668189 | TCCCACCTATGAGTG[C/T]ACTCTAAAGAGTCCC | 5563 |
rs2796498 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56678313 | GTTAGTGATTTAAAC[A/G]GAGAGAGCAACCTTA | 5563 |
rs2796499 | snp | A/G | 0.496279 | 0.0429702 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56678765 | cagtagcatgatctc[A/G]gctcactgcaacctc | 5563 |
rs2796502 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56679784 | attggtctacttatg[A/C]ttgggttttatgcca | 5563 |
rs2796503 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56679799 | attgggttttatgcc[A/G]cctttgctatcctga | 5563 |
rs2796504 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56680069 | cttctgctcaacagt[A/G]ggctattagtagtta | 5563 |
rs2796505 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56680258 | ATGTTCACCTTTTCC[A/G]AAGCCCTTAAATTGT | 5563 |
rs2796506 | snp | A/C | 0.499653 | 0.0131743 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56681926 | atggggatggcattg[A/C]atctataattacctt | 5563 |
rs2796507 | snp | C/T | 0.499653 | 0.0131743 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56682877 | cacactagccacatt[C/T]caagtacttaatagc | 5563 |
rs2796508 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56683407 | AAAGAATGAAAGTGT[A/G]AGGAATATGGTGTAT | 5563 |
rs2796509 | snp | C/T | 0.499527 | 0.0153681 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56683663 | tcccttattatatgt[C/T]atatgTTAGACAGtg | 5563 |
rs2796510 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56683715 | tgtagatatctgaag[G/T]gggtgaatgttacac | 5563 |
rs2796511 | snp | A/G | 0.499653 | 0.0131743 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56683720 | atatctgaagtgggt[A/G]aatgttacacataga | 5563 |
rs2796512 | snp | A/G | 0.499653 | 0.0131743 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56683824 | attagagtgagagat[A/G]aggtcagagacataa | 5563 |
rs2796513 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56667491 | TAACTCATAATATAT[A/G]AAATAATGCTATCAT | 5563 |
rs2796514 | snp | A/C | 0.499767 | 0.0107802 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56684806 | ggagatagtaactat[A/C]ggcaGGAGAGGAGAG | 5563 |
rs2796515 | snp | A/G | 0 | 0 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56686448 | cattactataaagga[A/G]tactgaaggctgggt | 5563 |
rs2796516 | snp | A/G | 0.434976 | 0.168179 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56665650 | ttataggttgctgga[A/G]ggaatgtaaattagt | 5563 |
rs2796517 | snp | C/G | 0.437401 | 0.165472 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56665597 | AATTGATGCAAAATG[C/G]GTAACTACTAAAACT | 5563 |
rs2796518 | snp | A/G | 0.293551 | 0.246177 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56665281 | TTTGAGACCAGCATG[A/G]CAAACATGGTGAAAC | 5563 |
rs2796519 | snp | A/G | 0.437401 | 0.165472 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56664915 | GCCTCATACTTAGCA[A/G]GCTGTTTGTATGTAT | 5563 |
rs2796520 | snp | C/T | 0.434687 | 0.168495 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56664904 | AGCAAGCTGTTTGTA[C/T]GTATGTATATATGTG | 5563 |
rs2796521 | snp | A/G | 0.494609 | 0.0516363 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56664893 | TGTATGTATGTATAT[A/G]TGTGTGTGTGTGTGT | 5563 |
rs2796522 | snp | C/T | 0.439224 | 0.163383 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56664830 | TTATGCATACATGTG[C/T]TTCTATGTATATAAA | 5563 |
rs2796523 | snp | C/T | 0.437401 | 0.165472 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56664174 | agtttatgggaacaa[C/T]gactcaaagaaatca | 5563 |
rs2796524 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56663135 | ctgccctccagcctc[A/G]gtgacacaaagacct | 5563 |
rs2796525 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56662947 | aaagttagccaaaac[C/T]ttagcagaaaaactc | 5563 |
rs2796526 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56662450 | atttaattttttttt[A/T]aaatcatctctattt | 5563 |
rs2796527 | snp | C/T | 0.437401 | 0.165472 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56662230 | CTAAATTCAAGTTCT[C/T]ATAAATCTTTCATCT | 5563 |
rs2796528 | snp | C/T | 0.439502 | 0.163061 | intron-variant | PRKAA2 | GRCh38.p7 | 1:56662166 | ctaaattattttgaa[C/T]gacaaatgactatat | 5563 |