PPARA
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs14842snpA/T0.08509190.187897utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variantPPARA, CDPF1GRCh38.p722:46243560GATTTTTTTTTAAAA[A/T]TAAGGTTATTTTATA5465
rs14843snpA/T0.08509190.187897utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variantPPARA, CDPF1GRCh38.p722:46243565CCCAAGATTTTTTTT[A/T]AAAATTAAGGTTATT5465
rs129600snpC/T0.3868840.209196intron-variant, nc-transcript-variantPPARA, LOC105373074GRCh38.p722:46161262GGGCACACATCCTTC[C/T]GAAATTCCTTCTAGA5465
rs135536snpC/G0.2118190.247067intron-variant, upstream-variant-2KBPPARA, LOC105373074GRCh38.p722:46172421GGCTGGTCTCCAACT[C/G]CTGACTTCAGGTGAT5465
rs135537snpA/G0.002791620.0372561intron-variant, nc-transcript-variantPPARA, LOC105373074GRCh38.p722:46172172CAGGTTCCTCACCTG[A/G]AGGAGAACCCTGATC5465
rs135538snpC/G0.4976130.0344622intron-variantPPARA, LOC105373074GRCh38.p722:46168728gtgatatctttctac[C/G]aagagagatgtctat5465
rs135539snpG/T0.4970910.0380279intron-variantPPARA, LOC105373074GRCh38.p722:46163368TATGATTAGAGTTAA[G/T]AATCACCTAGGATTT5465
rs135540snpA/T0.3641930.222396intron-variant, downstream-variant-500BPPARA, LOC105373074GRCh38.p722:46160713CTCAGGAGGCTGAGG[A/T]GGGAGGATTGCTTGA5465
rs135541snpA/C0.4311770.172264intron-variantPPARAGRCh38.p722:46160467CTACTAAAAATACAA[A/C]AATTTAGCCAGGCAT5465
rs135542snpA/G0.3106320.242536intron-variantPPARAGRCh38.p722:46160138CCAGCTGCCACCCTT[A/G]GCTGGGAATGGGAGC5465
rs135543snpA/G0.3448150.231323intron-variantPPARAGRCh38.p722:46159422CAGTTGTCAAAGTGG[A/G]GGGAAAAAAACGACA5465
rs135545snpA/G0.4289370.17459intron-variantPPARAGRCh38.p722:46158146GCTGGGATTACAGGT[A/G]TGAGCCTCCACGCCT5465
rs135547snpC/G0.4421130.159977intron-variantPPARAGRCh38.p722:46157755TTAATGTGACAGTCA[C/G]AGCAGGAGAAGGACC5465
rs135548snpC/T0.2836840.24772intron-variantPPARAGRCh38.p722:46157608TATTTAAATAGATCC[C/T]CAGGTCATCTTATAA5465
rs135549snpA/G0.4913680.0651254intron-variantPPARAGRCh38.p722:46157413GTCTAGGTGTGGGGG[A/G]AGCTGCAGAGGTCTG5465
rs135550snpA/G0.4167080.186302intron-variantPPARAGRCh38.p722:46157339GGTGCCGCTGTCTGC[A/G]CTCCTGTTTAGGTGC5465
rs135551snpC/T0.411410.19091intron-variantPPARAGRCh38.p722:46157126AGGAGTTAGACTCAG[C/T]GAGGACAGTCAGACT5465
rs135552snpA/G0.3257990.238232intron-variantPPARAGRCh38.p722:46156920CCTGAGGTCACAATC[A/G]CCTTCAAAACACACA5465
rs135553snpA/G0.4986520.0259235intron-variantPPARAGRCh38.p722:46156848TTGGGAGGCTGAAGC[A/G]GGTGGATCACCTGAG5465
rs135554snpA/T0.3004210.244863intron-variantPPARAGRCh38.p722:46156824ACCTGAGGTCAGAAG[A/T]TCAAAACCAGCCTGG5465
rs135555snpC/G0.3019320.244547intron-variantPPARAGRCh38.p722:46154412CAGGCTGGTCTTGAA[C/G]CCCTGGGCTCAAGCA5465
rs761543snpA/G0.003985640.0444627intron-variantPPARAGRCh38.p722:46188492GGTTGCAAAGGCAGC[A/G]TGATGAGGGCTGTTA5465
rs881740snpA/G0.3108780.242475intron-variant, utr-variant-5-primePPARA, LOC105373074GRCh38.p722:46171489AGGAGCAAGCCCAGG[A/G]CAGGTGAGTGGGTCA5465
rs1042311snpC/T0.007801360.0619663missense, nc-transcript-variantPPARAGRCh38.p722:46231883TCCAGAACAAGGAGG[C/T]GGAGGTCCGCATCTT5465
rs1055657snpA/G0.1998730.244923utr-variant-3-prime, nc-transcript-variantPPARAGRCh38.p722:46242220ACCGGGCGTGGGGGG[A/G]CATGCCGCAGCCCTG5465
rs1055658snpC/G0.003587790.0422022utr-variant-3-prime, nc-transcript-variantPPARAGRCh38.p722:46242260CGGGCACCTTCCCCG[C/G]ACCCCCAGGCCTTGG5465
rs1055659snpC/T0.2963640.245663utr-variant-3-prime, nc-transcript-variantPPARAGRCh38.p722:46242401CAGTCAGTTCCTTTT[C/T]TCATGTACCTCACAA5465
rs1134224snpA/T0.3979940.201489utr-variant-3-prime, nc-transcript-variantPPARAGRCh38.p722:46237474ggggtggcacacatc[A/T]gtagtcccagctact5465
rs1555208snpA/C0.08872190.191022intron-variantPPARAGRCh38.p722:46181313GGTCAATCACACACT[A/C]GCCTCAGAGCACACA5465
rs1800204snpA/G4.94898e-050.00497418missense, utr-variant-5-prime, nc-transcript-variantPPARAGRCh38.p722:46218273CACAGGGCTTCTTTC[A/G]GCGAACGATTCGACT5465
rs1800206snpC/G0.08131330.184512 PPARA22 allele_origin=G(germline)/C(germline)22:46218377CGATTTCACAAGTGC[C/G]TTTCTGTCGGGATGT5465
rs1800234snpC/T0.01905690.0957368missense, intron-variant, nc-transcript-variantPPARAGRCh38.p722:46219983AGGTCAAAGCCCGGG[C/T]CATCCTCTCAGGAAA5465
rs1800235snpC/T0.005908960.054033synonymous-codon, intron-variant, nc-transcript-variantPPARAGRCh38.p722:46220008AGGAAAGGCCAGTAA[C/T]AATCCAGTAGGTGTT5465
rs1800236snpC/G1.67122e-050.00289064synonymous-codon, nc-transcript-variantPPARAGRCh38.p722:46231842GGCTGAGAAGACGCT[C/G]GTGGCCAAGCTGGTG5465
rs1800242snpA/G/T4.94208e-050.00497075missense, nc-transcript-variantPPARAGRCh38.p722:46231990AACTTGGACCTGAAC[A/G/T]ATCAAGTGACATTGC5465
rs1800243snpC/G00missense, nc-transcript-variant, downstream-variant-500BPPARAGRCh38.p722:46235199TTGTACATGTGCTCA[C/G]ACTCCACCTGCAGAG5465
rs1800244snpC/T0.0002049620.0101212utr-variant-3-prime, nc-transcript-variant, downstream-variant-500BPPARAGRCh38.p722:46235408CAGCCACACCTTTTC[C/T]AGGAGTTCTGAAGCT5465
rs1800245snpA/C/T0.04867410.148216intron-variantPPARAGRCh38.p722:46219745CCTGGGGGAGCCCCT[A/C/T]GTCCAGCCCTGTCCG5465
rs1800246snpA/G0.1255280.21681intron-variantPPARAGRCh38.p722:46219728CATTCCTGGTTTAAA[A/G]TCCTGGGGGAGCCCC5465
rs1973929snpA/G00intron-variantPPARAGRCh38.p722:46211716cctgggtgacagagc[A/G]agacAAGAAGGCGAG5465
rs2229245snpC/G4.94287e-050.00497111missense, nc-transcript-variantPPARAGRCh38.p722:46235156GGCCTTCTAAACGTA[C/G]GACACATTGAAAAAA5465
rs2238833snpA/G0.001596170.0282053intron-variantPPARAGRCh38.p722:46158704GGGATATTTAAGTGG[A/G]ATGAATTTTTTGAAG5465
rs2283673snpA/G0.03645090.129988intron-variantPPARAGRCh38.p722:46231501TCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC5465
rs2336904snpC/T0.04601420.144533intron-variantPPARAGRCh38.p722:46225846CTCCACCCCCACACA[C/T]GCACACACACACATG5465
rs2336905snpC/T0.01111960.0737302intron-variantPPARAGRCh38.p722:46229443ttgtaatcccagcta[C/T]tcgggaggctgaggc5465
rs3747246snpA/G0.05208250.152737utr-variant-3-prime, nc-transcript-variantPPARAGRCh38.p722:46241930AAAAAAAAAAAAAAA[A/G]AGAGAGAAAAAATAA5465
rs3840962in-del-/CA/CACACAutr-variant-3-prime, nc-transcript-variantPPARAGRCh38.p722:46242761ACACACACACACACA[-/CA/CACACA]GCTCTTCATTTCTCC5465
rs3892755snpC/T0.1681350.236216utr-variant-3-prime, nc-transcript-variantPPARAGRCh38.p722:46239702AGGAAGTGGCTTCCT[C/T]GTGGCCAGCAGGAAG5465
rs4253616snpA/G0.005575420.0525036intron-variantPPARAGRCh38.p722:46152423CAGACGTGAGCCACC[A/G]TGCCTGGCCTAGGAT5465
rs4253617snpA/G0.1265640.217402intron-variantPPARAGRCh38.p722:46152697GGATAGGCTGAAGAA[A/G]CGGGCCAGATGATAC5465
rs4253618snpA/G0.004383320.0466095intron-variantPPARAGRCh38.p722:46152814TGGCAAGTTGGGTGC[A/G]GTGGCTCACTCCTGT5465
rs4253619snpC/T0.07041250.17392intron-variantPPARAGRCh38.p722:46152887gccaggagttcgaga[C/T]cagcctggccaacat5465
rs4253620snpC/T0.1282880.218372intron-variantPPARAGRCh38.p722:46152960gcatggtggcggaca[C/T]ctgtaatcccagcta5465
rs4253621snpA/G0.02289470.104514intron-variantPPARAGRCh38.p722:46153451TGAGGTTACAGGTGC[A/G]AGCCACCGCGCCGGG5465
rs4253622snpC/G0.07704980.180522intron-variantPPARAGRCh38.p722:46153488TCCGACATCTTAAAC[C/G]TAAAGTAGGAGACGT5465
rs4253623snpA/G0.1967710.244268intron-variantPPARAGRCh38.p722:46154203AAAAGAAACTTAAAG[A/G]TAATCCTCATCATGG5465
rs4253624snpC/T0.01190910.0762411intron-variantPPARAGRCh38.p722:46155064TTTGCTTATTATAAA[C/T]ATATTTGAAACATGC5465
rs4253625in-del-/CTGT0.006766090.0577691intron-variantPPARAGRCh38.p722:46155234GTTAGAGGTTGTGGC[-/CTGT]CTAATTTCTGCTTTT5465
rs4253626snpA/T0.004780850.0486577intron-variantPPARAGRCh38.p722:46155284TCTGTTTTTATTTGT[A/T]TTTGGTAGCCTGGCA5465
rs4253627snpC/G0.0003992810.0141238intron-variantPPARAGRCh38.p722:46155306AGCCTGGCATAGAGT[C/G]CATTTTTCTTTTCTT5465
rs4253628snpA/G0.01032950.0711199intron-variantPPARAGRCh38.p722:46155376CTGGCGTGCAGTGGC[A/G]CAATCTCAGCTCACT5465
rs4253629snpA/G0.07704980.180522intron-variantPPARAGRCh38.p722:46155512TAGAGACGGGGTTTT[A/G]CCATGTTGGCCAGGC5465
rs4253630snpA/G0.006766090.0577691intron-variantPPARAGRCh38.p722:46156123GGTTTTGAGGCTCAC[A/G]TATGGTAAAAGTGGT5465
rs4253632snpC/T0.01032950.0711199intron-variantPPARAGRCh38.p722:46159398CGTATTTTGCTTGAG[C/T]TGTACGATTGTCGTT5465
rs4253633snpA/G0.005178220.0506191intron-variantPPARAGRCh38.p722:46159771AGGCTTTGGAAAATG[A/G]GAGGCATGAAGGGGA5465
rs4253634snpG/T0.01190910.0762411intron-variantPPARAGRCh38.p722:46159872ACTTGCGTGACAAGT[G/T]ATGACTAATGACACT5465
rs4253635snpA/G0.01151440.0749975intron-variantPPARAGRCh38.p722:46160087AGGGCTGGGAAGTGC[A/G]GATCCAGGGCTGGTG5465
rs4253636snpC/T0.01387990.0821421intron-variantPPARAGRCh38.p722:46160112CTGGTGCACTGAACC[C/T]AGAGGAGCAGGCTCC5465
rs4253637snpC/T0.01741750.0916809intron-variantPPARA, LOC105373074GRCh38.p722:46166912GGAAATGCAAGGAAC[C/T]CAGAGTTGCTAAAAT5465
rs4253638snpA/G0.01663250.0896639intron-variantPPARA, LOC105373074GRCh38.p722:46167060ATGGAACAGAATAGC[A/G]AGTCCAGAAATAGAT5465
rs4253639snpA/G0.01741750.0916809intron-variantPPARA, LOC105373074GRCh38.p722:46167234CTCATAATTATTATC[A/G]TTATATTATACTATT5465
rs4253640snpC/G0.06148240.164198intron-variantPPARA, LOC105373074GRCh38.p722:46167439GTGGATCACTTGGCC[C/G]CAGGAGTTACAAGAC5465
rs4253641in-del-/A0.1063280.204593intron-variantPPARA, LOC105373074GRCh38.p722:46167495GTCTCTACAAAAAAA[-/A]TGAAAAAATTAGTTG5465
rs4253642snpA/G0.01741750.0916809intron-variantPPARA, LOC105373074GRCh38.p722:46167520TAGTTGAGCATGATG[A/G]CACTCACCTGTAGTC5465
rs4253643snpC/T0.06148240.164198intron-variantPPARA, LOC105373074GRCh38.p722:46167945AGTCCTAGCTACTCA[C/T]GAAGCTGAGGCAGGA5465
rs4253644snpA/G0.01741750.0916809intron-variantPPARA, LOC105373074GRCh38.p722:46167946GTCCTAGCTACTCAC[A/G]AAGCTGAGGCAGGAG5465
rs4253645snpA/G0.01663250.0896639intron-variantPPARA, LOC105373074GRCh38.p722:46168213AAAAATTAGCCGGAC[A/G]TGGTGGTAGGCGCCT5465
rs4253646snpA/G0.06148240.164198intron-variantPPARA, LOC105373074GRCh38.p722:46168284GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC5465
rs4253647snpA/G0.02562150.110247intron-variantPPARA, LOC105373074GRCh38.p722:46168328CTGCACTCCAGCCTG[A/G]ACAACAGAGCGAGAC5465
rs4253648snpA/G0.3561690.226336intron-variantPPARA, LOC105373074GRCh38.p722:46168331cactccagcctggac[A/G]acagagcgagactcc5465
rs4253650snpA/G0.08509190.187897intron-variantPPARA, LOC105373074GRCh38.p722:46168786aagcagtctgaccaa[A/G]tatgcgtaagaatgt5465
rs4253651snpC/T0.1013010.200969intron-variantPPARA, LOC105373074GRCh38.p722:46168791gtctgaccaagtatg[C/T]gtaagaatgtggaat5465
rs4253652snpC/T0.05208250.152737intron-variant, upstream-variant-2KBPPARA, LOC105373074GRCh38.p722:46172942AAACCCTTACTAGAT[C/T]TCCTGTTCTGTCTTA5465
rs4253653snpG/T0.06148240.164198intron-variant, upstream-variant-2KBPPARA, LOC105373074GRCh38.p722:46173005ATTCCATTTTTACCC[G/T]TAAATGGCTTGCTTC5465
rs4253654snpA/G0.002791620.0372561intron-variant, upstream-variant-2KBPPARA, LOC105373074GRCh38.p722:46173247ACAGTTATGTTTTTA[A/G]TTTTCTTTTATTTGT5465
rs4253655snpA/G0.1069870.205054intron-variant, upstream-variant-2KBPPARA, LOC105373074GRCh38.p722:46173274TTGTTGTGTTGAATA[A/G]GAATGTAGCTCTGGG5465
rs4253656in-del-/A0.020160.0983543intron-variant, upstream-variant-2KBPPARA, LOC105373074GRCh38.p722:46173594TCATAAAAGACAAAG[-/A]AAAGCTGCGGAAATG5465
rs4253657snpC/T0.0213330.101051intron-variant, utr-variant-5-prime, upstream-variant-2KBPPARAGRCh38.p722:46176044CTTGGAAGGCTGAGG[C/T]AGGAGGACTGCTTGA5465
rs4253658snpA/C0.0781510.181571intron-variant, utr-variant-5-prime, upstream-variant-2KBPPARAGRCh38.p722:46176087GAGGTTGCAAGGAGC[A/C]GAAATTGTGNCACTG5465
rs4253659snpA/C0.09449670.195752intron-variant, utr-variant-5-prime, upstream-variant-2KBPPARAGRCh38.p722:46176097GGAGCNGAAATTGTG[A/C]CACTGTACTCCAGCC5465
rs4253660snpA/G0.07851770.181917intron-variantPPARAGRCh38.p722:46176261GAGGCGAAGGCGGGC[A/G]GATCACCAGAGGTCA5465
rs4253661snpA/G0.09233590.194016intron-variantPPARAGRCh38.p722:46176284AGAGGTCAGCAGTTT[A/G]AGACCAGCCTGGCCA5465
rs4253662snpA/G0.0467750.145601intron-variantPPARAGRCh38.p722:46176847AAGAGGTACATACAC[A/G]TTTAGGAGCATCGTG5465
rs4253663snpA/G0.07373760.17729intron-variantPPARAGRCh38.p722:46176986ggggccaaggcgggc[A/G]gatcacgaggttagg5465
rs4253664snpC/T0.1178860.21224intron-variantPPARAGRCh38.p722:46176998GGCAGATCACGAGGT[C/T]AGGAGATTGAGACCA5465
rs4253665snpA/C/G/T0.05713140.159743intron-variantPPARAGRCh38.p722:46177006acgaggttaggagat[A/C/G/T]gagaccatcctggct5465
rs4253666snpC/T0.01466720.084371intron-variantPPARAGRCh38.p722:46177017agattgagaccatcc[C/T]ggctaacacagtgaa5465
rs4253667snpA/G0.01820190.0936463intron-variantPPARAGRCh38.p722:46177027CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC5465
rs4253668snpC/T0.0306650.119967intron-variantPPARAGRCh38.p722:46177037AACACAGTGAAACCC[C/T]GTCTCTACTACAAAT5465
rs4253669snpA/C0.240190.249807intron-variantPPARAGRCh38.p722:46177048accctgtctctacta[A/C]aaatacaaaaaaatt5465
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