| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs782557076 | snp | A/G/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48821602 | CTATCTCCCAGGCTC[A/G/T]AGCAAGCAATTCTCA | 10013 |
| rs782557397 | snp | C/T | 2.35474e-05 | 0.0034312 | synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48820210 | TGCCCACCTCACCCA[C/T]CTGCTGATGGGCCTT | 10013 |
| rs782558009 | snp | A/G | 6.47983e-05 | 0.00569166 | intron-variant | HDAC6 | GRCh38.p7 | X:48816434 | CAGACCCTCCTCACT[A/G]TCCTGCGGGTGCTCC | 10013 |
| rs782558307 | in-del | -/GAC | 3.2078e-05 | 0.00400474 | intron-variant | HDAC6 | GRCh38.p7 | X:48802848 | CATGCCCTGGACTCT[-/GAC]GACCCTTCTCTCTGA | 10013 |
| rs782558876 | snp | C/T | 0.000137091 | 0.00827809 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48816170 | TACCCCAGCGCATCT[C/T]GCGGATCATGTGCCG | 10013 |
| rs782560252 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48800709 | GTCTGATGCAGAACC[C/T]CCGGACTGCTTATCT | 10013 |
| rs782560444 | snp | C/T | 0.000617093 | 0.0175547 | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823486 | CTCGAGCACAGACCA[C/T]CAGACCCCCCCAACC | 10013 |
| rs782560801 | snp | A/G | 2.6729e-05 | 0.00365565 | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823513 | AACCTCACCTGTGCA[A/G]GGAACTACACCCCAG | 10013 |
| rs782563201 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48817720 | ATTTCTGGCCTATAG[A/C]AGCTGCCTCGACAGA | 10013 |
| rs782563575 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48813003 | ACCTCCGCCTCCTGG[C/G]TTCAAGCAATTCTCC | 10013 |
| rs782564776 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48802021 | GGGACTGGCTGAAGA[C/G]GGTTAGCGAAACGTT | 10013 |
| rs782565463 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | HDAC6 | GRCh38.p7 | X:48810614 | TTTATTTATTTATTT[A/T]TTTATTTTTTTTGAG | 10013 |
| rs782568572 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48802367 | GTTGGAAAGGGCAGG[C/G]CCTAAGACGGACTGT | 10013 |
| rs782570244 | snp | A/G | | | intron-variant | HDAC6 | GRCh38.p7 | X:48807577 | GAGTGCAGTGATGCA[A/G]TCTTGGCTCACTGCA | 10013 |
| rs782570777 | snp | G/T | 0.000110969 | 0.00744798 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48822871 | CAGAGGCAGGAAGGG[G/T]GACAGTACCCACACT | 10013 |
| rs782571093 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | HDAC6 | GRCh38.p7 | X:48803366 | TGAAAGGGTTCTTTT[A/G]TGTAGCTAACAAACA | 10013 |
| rs782571413 | snp | G/T | 2.53158e-05 | 0.00355771 | intron-variant | HDAC6 | GRCh38.p7 | X:48822578 | TCCAAATTCCCCAAT[G/T]AACCCCCACCATACC | 10013 |
| rs782571832 | snp | A/T | | | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48820498 | TTGGCAAAGCAGCCT[A/T]ATGAGGTAGGGTAAG | 10013 |
| rs782575092 | snp | A/G | 2.28967e-05 | 0.00338346 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48816040 | TGATGAATCACTGCA[A/G]CTTGTGGGACAGGTA | 10013 |
| rs782575558 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48804390 | AACCCCTTTCCCAGA[G/T]ATTCTTTTCGGTCTT | 10013 |
| rs782577537 | snp | A/G | 8.56238e-05 | 0.00654252 | intron-variant | HDAC6 | GRCh38.p7 | X:48819980 | AGGTTCTGTGTCTCC[A/G]TCTCTCTGACTTGCA | 10013 |
| rs782578358 | snp | A/G | 3.06819e-05 | 0.00391663 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48820292 | TTCCCACAGTGGGAG[A/G]GTAGTTTGGAAATGT | 10013 |
| rs782580533 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48800728 | GACTGCTTATCTCTC[C/T]GGTCCCAGCTTATAG | 10013 |
| rs782582853 | snp | C/T | 7.85608e-05 | 0.00626691 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48815427 | AAGGCGTCAGTGCTT[C/T]GCTCCACACCCTTCT | 10013 |
| rs782583391 | snp | A/C | | | intron-variant | HDAC6 | GRCh38.p7 | X:48817494 | CCCCCAAATCCTGAT[A/C]CTTGTGGGGACCTGG | 10013 |
| rs782584427 | snp | G/T | 4.95225e-05 | 0.00497582 | missense, intron-variant, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48818356 | AACGGGCCCCGCATG[G/T]GTGATGCTGACTACC | 10013 |
| rs782585905 | in-del | -/T | 2.61797e-05 | 0.0036179 | splice-donor-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48823786 | GCCTCACTGATCAGG[-/T]TGAGCTCAGGGAGAG | 10013 |
| rs782586433 | snp | A/G | | | intron-variant | HDAC6 | GRCh38.p7 | X:48811944 | TTTTCCTTCAAAGCT[A/G]ATCCCAGATACCATA | 10013 |
| rs782586456 | snp | C/G | 7.15909e-05 | 0.0059825 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48808066 | CCAGCACAGTCTTAT[C/G]GATGGCTATTGCATG | 10013 |
| rs782586891 | snp | A/G | 2.6448e-05 | 0.00363639 | intron-variant | HDAC6 | GRCh38.p7 | X:48814632 | CTGTCAGCGGCTCGG[A/G]ACAGGTGGCTGAACA | 10013 |
| rs782588392 | snp | C/G | | | intron-variant | HDAC6 | GRCh38.p7 | X:48804681 | AACAAAAGCCTGTGT[C/G]TTCAGGGTAAAGGGG | 10013 |
| rs782590029 | snp | A/G | 3.35593e-05 | 0.00409616 | intron-variant | HDAC6 | GRCh38.p7 | X:48816421 | ACCAGGGAGGGGACA[A/G]ACCCTCCTCACTGTC | 10013 |
| rs782595236 | snp | C/T | | | upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48800420 | TCAGAAACCTCTCTT[C/T]TGATCCAACAGAAAA | 10013 |
| rs782596608 | snp | C/T | 2.64431e-05 | 0.00363605 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48822902 | CAAGGATCTCCCTCC[C/T]TGGTTCCAGAGGTAG | 10013 |
| rs782599847 | snp | A/C | 0.00063997 | 0.0178767 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48824139 | GGGATGCTGACCCCC[A/C]CCTGACACTCACACC | 10013 |
| rs782600692 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48811654 | GAGGCCTCTTCTTTG[A/G]GGTAACATCTCTTTT | 10013 |
| rs782600755 | snp | C/T | | | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48807098 | GGTACATCTTATCAT[C/T]ATTGGCATCCCAGAA | 10013 |
| rs782602970 | snp | C/T | 4.69384e-05 | 0.00484428 | intron-variant | HDAC6 | GRCh38.p7 | X:48814418 | TCTCCAACTCTCTTA[C/T]CTCTTTTTCTTCTGC | 10013 |
| rs782606485 | snp | A/C | 3.30038e-05 | 0.00406212 | intron-variant | HDAC6 | GRCh38.p7 | X:48823630 | GCAAGAAGGGGCAAG[A/C]ATCGGGCTTCTCTGA | 10013 |
| rs782606810 | snp | A/G | 2.59541e-05 | 0.00360228 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48823807 | TCAGGGAGAGGCTGG[A/G]ACTGTGGCTTCCTTC | 10013 |
| rs782607617 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48804111 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCATTGC | 10013 |
| rs782608619 | snp | A/G | 3.03283e-05 | 0.003894 | intron-variant | HDAC6 | GRCh38.p7 | X:48818422 | TACGAGGTACAGCTC[A/G]GGATAGATCGCAGGA | 10013 |
| rs782609857 | snp | A/G | 2.8335e-05 | 0.00376387 | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823429 | CCAGACTACGTCAGA[A/G]GAGGCTCCAGGGGGC | 10013 |
| rs782610388 | snp | C/T | 5.20711e-05 | 0.00510224 | intron-variant | HDAC6 | GRCh38.p7 | X:48819963 | TGTGTCTCCTAGTCT[C/T]CAGGTTCTGTGTCTC | 10013 |
| rs782611978 | snp | A/G | 2.94092e-05 | 0.00383454 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48805445 | CTCCCCAGCTTCCCG[A/G]AAGGCCCTGAGCGGC | 10013 |
| rs782614872 | snp | A/T | 4.36272e-05 | 0.0046703 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48816482 | CTGAGTACGTGGGTC[A/T]TCTCCGGGCCACAGA | 10013 |
| rs782615111 | snp | A/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48813125 | TGTTGGCCATGCTGG[A/T]CTCGAACTTCTGGCC | 10013 |
| rs782615649 | snp | A/G | | | intron-variant | HDAC6 | GRCh38.p7 | X:48804400 | CCAGAGATTCTTTTC[A/G]GTCTTCTACTCTTCC | 10013 |
| rs782615746 | snp | C/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48821152 | CCCTGGTTACTGTTA[C/T]GCGTTGTTCAGATAT | 10013 |
| rs782618071 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | HDAC6 | GRCh38.p7 | X:48818937 | GTATGTCTCTGACTG[A/G]GAGGTAGCTGCCTTC | 10013 |
| rs782618133 | snp | A/G | 1.6701e-05 | 0.00288968 | missense, intron-variant, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48818246 | TGTCCCTGCACCGCT[A/G]TGATCATGGCACCTT | 10013 |
| rs782620270 | snp | A/G | 2.29022e-05 | 0.00338387 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48816029 | TGACCAAAATATGAT[A/G]AATCACTGCAACTTG | 10013 |
| rs782621164 | snp | A/G | 6.1601e-05 | 0.00554948 | synonymous-codon, nc-transcript-variant, missense | HDAC6 | GRCh38.p7 | X:48818053 | CAGGATCCTGATTGT[A/G]GATTGGGATGTCCAC | 10013 |
| rs782621991 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | HDAC6 | GRCh38.p7 | X:48819117 | CCTTCTGTGTGTGTA[C/T]AACTGTATGTGCAAA | 10013 |
| rs782623802 | snp | C/T | 3.32541e-05 | 0.00407749 | missense, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48823182 | CCATTTCTGAGGCAG[C/T]CATTGGGGGAGCCAT | 10013 |
| rs782624104 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48808288 | TTGGGATGTGCACCA[C/T]GGTCAAGGAACACAG | 10013 |
| rs782624163 | snp | C/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48813680 | TTTTCAGTATCTGTT[C/T]TGCGTGTCGGTCATA | 10013 |
| rs782625936 | snp | A/G | 3.13642e-05 | 0.00395994 | intron-variant | HDAC6 | GRCh38.p7 | X:48823664 | ATCTCTTACTTCTGC[A/G]TGTCCAGGGGGCCTC | 10013 |
| rs782626352 | snp | A/G | | | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48820563 | CTGAGGCACAAAGAG[A/G]TGTGATGACTAGCCT | 10013 |
| rs782627904 | snp | C/T | | | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48815196 | ACTTCTTTGTGCCTC[C/T]GCTTTCCTTCTATAA | 10013 |
| rs782629350 | snp | C/T | 7.18176e-05 | 0.00599196 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48815311 | GTATGCACTCTCTTA[C/T]TATCATCATTATTAT | 10013 |
| rs782629816 | snp | C/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48804993 | GAACCAGGGAAGAGA[C/T]CAGTGTAGGTGAAGC | 10013 |
| rs782630218 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48802549 | TGTGGAGAATCAGAT[C/T]GCGTAAGGAATGGAA | 10013 |
| rs782632210 | snp | G/T | 4.13685e-05 | 0.0045478 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48808049 | CCTCCTGGACATCAC[G/T]CCCAGCACAGTCTTA | 10013 |
| rs782634209 | snp | G/T | 0.000294507 | 0.0121312 | utr-variant-5-prime, upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48801886 | CAGGTCGCCAGAAAC[G/T]TGGTGGAGCGAGCCA | 10013 |
| rs782635907 | snp | A/C | 2.34786e-05 | 0.00342618 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48824117 | TGGCCCGGGAGCAAA[A/C]TGCAGGGGGATGCTG | 10013 |
| rs782637538 | snp | C/T | 2.42172e-05 | 0.00347966 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48814917 | GGCTCCCTGGGGCGG[C/T]AGGTGGGTTGCATGG | 10013 |
| rs782638402 | snp | G/T | 2.291e-05 | 0.00338445 | intron-variant | HDAC6 | GRCh38.p7 | X:48815654 | TCAAGTAGGAAGTGG[G/T]GTGTGGGCCTGGTGT | 10013 |
| rs782638509 | snp | C/T | 2.60892e-05 | 0.00361164 | intron-variant | HDAC6 | GRCh38.p7 | X:48814624 | CCGCCCTTCTGTCAG[C/T]GGCTCGGGACAGGTG | 10013 |
| rs782641355 | snp | C/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48819786 | ACCTCATGATCTGCC[C/T]GCCTCGGCCTCCCAA | 10013 |
| rs782641404 | snp | A/G | 2.6274e-05 | 0.0036244 | intron-variant | HDAC6 | GRCh38.p7 | X:48816673 | AGGAGGACCTGGGGG[A/G]AATGGAAAAAGAGAG | 10013 |
| rs782641811 | snp | C/G | 7.21839e-05 | 0.00600722 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48823048 | CATGGGGAAAGTCAC[C/G]TCGGCATCATTTGGG | 10013 |
| rs782642083 | snp | C/G | 2.95644e-05 | 0.00384465 | intron-variant | HDAC6 | GRCh38.p7 | X:48817298 | GTGAGGGCAGGCTGT[C/G]CGATCTTAGCACCCT | 10013 |
| rs782645601 | snp | C/T | 2.67946e-05 | 0.00366013 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48822885 | GTGACAGTACCCACA[C/T]TCAAGGATCTCCCTC | 10013 |
| rs782647002 | snp | A/G | 2.90457e-05 | 0.00381078 | intron-variant | HDAC6 | GRCh38.p7 | X:48805528 | GTCCTTTCAGGTAAG[A/G]CCCCCAAGCCAACAC | 10013 |
| rs782647121 | snp | G/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48812605 | TCTACTTTCTAGAAA[G/T]TCATTGAAGTCTCTT | 10013 |
| rs782651797 | snp | A/G | 6.59185e-05 | 0.00574064 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48802914 | CCCGCTCTATCCCCA[A/G]TCTAGCGGAGGTAAA | 10013 |
| rs782653053 | snp | A/G | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48803209 | TTCCATTGCCTCTGG[A/G]ATGACAGGTGAGGCT | 10013 |
| rs782653288 | snp | A/G | 4.15515e-05 | 0.00455785 | intron-variant | HDAC6 | GRCh38.p7 | X:48820009 | CATCTCCATGTCTTC[A/G]TTTGTCCTTTTCTCC | 10013 |
| rs782654216 | snp | A/G/T | 5.40362e-05 | 0.00519766 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823529 | GGAACTACACCCCAG[A/G/T]TATCTCCCAGTACAC | 10013 |
| rs782655746 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48821571 | GCAATGGCGCTATCT[C/G]GGCTCACTGCAGCCT | 10013 |
| rs782658962 | snp | C/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48810537 | TCTTTCTAGGACTTC[C/T]GTTAGTCAGATGTTA | 10013 |
| rs782660849 | snp | C/T | 5.38177e-05 | 0.00518709 | intron-variant | HDAC6 | GRCh38.p7 | X:48814653 | TGGCTGAACATCCCC[C/T]ATCACACTCCTGTGT | 10013 |
| rs782664245 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | HDAC6, ERAS | GRCh38.p7 | X:48824786 | TTAAGAGAACTGCGA[C/T]GATTAATTGTGGATC | 10013 |
| rs782664775 | snp | A/G | 3.09717e-05 | 0.00393509 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823394 | ACCTCGGAGGCAGCC[A/G]TGGAGGGAGCCACAC | 10013 |
| rs782665404 | snp | A/G | 4.63494e-05 | 0.00481379 | missense, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48822711 | TGCTGACCCTGCCAC[A/G]GCCCCCACTATCAGG | 10013 |
| rs782666265 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | HDAC6 | GRCh38.p7 | X:48811707 | TATCTGTTGTACTTA[C/T]CTTTTCCAGTGTAGC | 10013 |
| rs782666554 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48814328 | AATGAGAGAATGAAC[A/G]AGTGGTTGAATGGGG | 10013 |
| rs782666966 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48813200 | AGGTGTGAACCACTG[C/T]GCCCAGCCCTCTGGT | 10013 |
| rs782667241 | snp | C/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48821595 | GCAGCCTCTATCTCC[C/T]AGGCTCGAGCAAGCA | 10013 |
| rs782668755 | snp | A/G | 2.7541e-05 | 0.00371076 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823448 | GCTCCAGGGGGCACC[A/G]AGCTGATCCAAACTC | 10013 |
| rs782668806 | snp | A/G | | | upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48800136 | CACACACCTCACACA[A/G]AAGGAATACCTCTCC | 10013 |
| rs782673692 | snp | G/T | 4.50552e-05 | 0.00474611 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48815415 | GCGCCCTGGCTGAAG[G/T]CGTCAGTGCTTCGCT | 10013 |
| rs782674246 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | HDAC6 | GRCh38.p7 | X:48817025 | GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCAGG | 10013 |
| rs782674799 | snp | C/T | 4.67957e-05 | 0.0048369 | missense, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48824178 | CAGGTCTACTGTGGT[C/T]GTTACATCAATGGCC | 10013 |
| rs782675259 | snp | C/T | 4.57028e-05 | 0.0047801 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48816172 | CCCCAGCGCATCTTG[C/T]GGATCATGTGCCGTC | 10013 |
| rs782676547 | snp | C/T | 3.09607e-05 | 0.00393439 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48815469 | GCCCCATGCTGGAGT[C/T]ACCTGGTGCCCCCTG | 10013 |
| rs782677829 | snp | A/C/G | 6.73826e-05 | 0.0058041 | missense, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48823188 | CTGAGGCAGCCATTG[A/C/G]GGGAGCCATGCTGGG | 10013 |
| rs782679240 | snp | A/G | 0.000253743 | 0.0112609 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48815257 | TGTCCAGTGAATTCA[A/G]TGAGGCACCCTTCTA | 10013 |
| rs782681446 | snp | A/G | 3.23091e-05 | 0.00401914 | intron-variant | HDAC6 | GRCh38.p7 | X:48808250 | TCCCCTCTCTCTGCT[A/G]CTCCTAGGGTCCTTA | 10013 |
| rs782681765 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48804242 | CAAATTTTTCATCCT[A/G]GCCTCAAAGGTTCCA | 10013 |
| rs782682354 | snp | A/G | 2.33212e-05 | 0.00341468 | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48815987 | CCTGACATGGCCAGT[A/G]CTACAGTCTCGCACA | 10013 |
| rs782683092 | snp | C/T | 7.69093e-05 | 0.0062007 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48823822 | GACTGTGGCTTCCTT[C/T]TCTTGCCAATTTGTG | 10013 |
| rs782685934 | snp | A/G | 9.6396e-05 | 0.00694181 | intron-variant | HDAC6 | GRCh38.p7 | X:48814611 | GTGAGGCCCAGCCCC[A/G]CCCTTCTGTCAGCGG | 10013 |
| rs782686779 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48810297 | GCCCAGACTGGTCTC[A/G]AACTCCTGACCTCAA | 10013 |
| rs782686853 | snp | A/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48809880 | CTCAACCTGTAGTAG[A/T]TTTATCTAGCCTTCT | 10013 |
| rs782687727 | snp | A/G | 8.26697e-05 | 0.00642869 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48805475 | CTCCATGCCATCAAG[A/G]AGCAACTGATCCAGG | 10013 |
| rs782688640 | snp | A/G | 2.58625e-05 | 0.00359591 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | HDAC6, ERAS | GRCh38.p7 | X:48824626 | AAGCCCCAGAATACG[A/G]TCCCTCTTCACCTTC | 10013 |
| rs782690281 | snp | A/T | 0.000521349 | 0.016137 | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823366 | TGTAGGAGGAGCTAC[A/T]CTGGCCCAGACCACC | 10013 |
| rs782691674 | snp | C/G | | | intron-variant, utr-variant-3-prime | HDAC6 | GRCh38.p7 | X:48806580 | GTTCTCTCCCTTACT[C/G]CCTTTCTGGCTCCCC | 10013 |
| rs782692797 | snp | C/T | 6.32841e-05 | 0.00562477 | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48808285 | AGATTGGGATGTGCA[C/T]CACGGTCAAGGAACA | 10013 |
| rs782693366 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48803858 | TGTATGAGTTGATGT[A/C]TTTGTTAAAATACTT | 10013 |
| rs782693640 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48800545 | TTTCTTTGGTGAGTG[G/T]AGGGGTTTAAAGGTC | 10013 |
| rs782694100 | snp | A/G | 4.74383e-05 | 0.00487 | intron-variant | HDAC6 | GRCh38.p7 | X:48808363 | GGTGCTAGACTCCCA[A/G]CCACCTCCCACCCTT | 10013 |
| rs782696759 | snp | C/T | 8.34411e-05 | 0.00645861 | intron-variant | HDAC6 | GRCh38.p7 | X:48807998 | GAGGAGGACCCCTCA[C/T]ATACTCCAAGCTGTT | 10013 |
| rs782698415 | snp | C/T | 2.86156e-05 | 0.00378246 | missense, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48823127 | CTCACTCAGGACCAG[C/T]CCTCAGAGGCAGCCA | 10013 |
| rs782701334 | snp | A/G | 3.64837e-05 | 0.00427089 | missense, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48815013 | CTAACCCACCTGCTC[A/G]TGGGTCTGGCAGGAG | 10013 |
| rs782703824 | snp | A/G | 4.90587e-05 | 0.00495247 | missense, upstream-variant-2KB, nc-transcript-variant | HDAC6, ERAS | GRCh38.p7 | X:48824568 | GATGTGAAGAACATC[A/G]CCCACCAGAACAAGT | 10013 |
| rs782704923 | snp | C/T | | | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48816561 | CATCTATATCTGCCC[C/T]AGTACCTTCGCCTGT | 10013 |
| rs782707910 | snp | C/G | 0.000324412 | 0.0127319 | intron-variant | HDAC6 | GRCh38.p7 | X:48819880 | CATGTCTCTAAGTCT[C/G]CATCTATTTCTTCTA | 10013 |
| rs782708608 | snp | G/T | 1.86478e-05 | 0.00305345 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48805665 | AAGAGCTGATGTTGG[G/T]TCACAGGTGAAGGCT | 10013 |
| rs782710702 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | HDAC6 | GRCh38.p7 | X:48822185 | AGTCGTCTTGTGCAG[A/G]TCAGGTCAGTGGTTA | 10013 |
| rs782712121 | snp | A/T | 0.000276243 | 0.0117493 | intron-variant | HDAC6 | GRCh38.p7 | X:48818172 | GCACCTCAGGGGTAC[A/T]GGAGCCCCTAACCAG | 10013 |
| rs782714342 | snp | C/T | 3.42448e-05 | 0.00413778 | intron-variant | HDAC6 | GRCh38.p7 | X:48805426 | TCTGTGACTGTGACT[C/T]CATCTCCCCAGCTTC | 10013 |
| rs782714737 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48814030 | TTGTCATAGGGGCAG[C/G]TAGTGGGCGGACATG | 10013 |
| rs782715705 | snp | C/T | 2.53434e-05 | 0.00355964 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48822947 | CCCTCCAGTTCTAAG[C/T]TGGTCACCAAGAAGG | 10013 |
| rs782716021 | snp | A/G | 3.78e-05 | 0.00434725 | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823324 | TGTTGGGGGAGCCAC[A/G]CTGGGCCAGACTACC | 10013 |
| rs782718298 | snp | G/T | 0.00087939 | 0.0209505 | missense, nc-transcript-variant, intron-variant | HDAC6 | GRCh38.p7 | X:48817452 | ACTATCAGTGGGCAT[G/T]CCCTACGGTAAGGAC | 10013 |
| rs782719563 | snp | C/T | | | missense, nc-transcript-variant, intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48820212 | CCCACCTCACCCACC[C/T]GCTGATGGGCCTTGC | 10013 |
| rs782720394 | snp | A/G | 9.6446e-05 | 0.00694361 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48815081 | TTCGTCCCTCAGCCT[A/G]TGGATCCTGGAGGGC | 10013 |
| rs782720709 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48809788 | GCCTGGGTGATAGAC[G/T]GAGACCCCATCTAAA | 10013 |
| rs782720948 | snp | C/T | 2.93015e-05 | 0.00382751 | intron-variant | HDAC6 | GRCh38.p7 | X:48823595 | GAATCTCAGGTAAGG[C/T]TCACCACACCCAGGT | 10013 |
| rs782721379 | snp | C/T | 8.56568e-05 | 0.00654378 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48815075 | CTCACCTTCGTCCCT[C/T]AGCCTGTGGATCCTG | 10013 |
| rs782725207 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48817246 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 10013 |
| rs782729099 | snp | C/G | 9.47104e-05 | 0.00688086 | intron-variant | HDAC6 | GRCh38.p7 | X:48819878 | TCCATGTCTCTAAGT[C/G]TGCATCTATTTCTTC | 10013 |
| rs782734047 | snp | C/G | 4.9637e-05 | 0.00498157 | missense, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48823076 | GGGGAAGAGTCCACT[C/G]CAGGCCAGACTAACT | 10013 |
| rs782734600 | snp | C/T | 2.29098e-05 | 0.00338443 | missense, nc-transcript-variant, intron-variant | HDAC6 | GRCh38.p7 | X:48820151 | GGCTTTGATGCTGCA[C/T]GGGGGGATCCGCTGG | 10013 |
| rs782735601 | snp | C/T | 0.000159585 | 0.00893124 | intron-variant | HDAC6 | GRCh38.p7 | X:48815381 | CACAACTCCTTGCCC[C/T]AGGGTGGCTACAACC | 10013 |
| rs782735977 | snp | C/T | 2.34797e-05 | 0.00342627 | intron-variant, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48814811 | GAGGGTAGGTAGCCT[C/T]ATGGAGTCTGTTCCC | 10013 |
| rs782736253 | snp | A/G | 7.895e-05 | 0.00628242 | synonymous-codon, intron-variant, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48818310 | GATCGGCCGGGCTGC[A/G]GGCACAGGCTTCACC | 10013 |
| rs782737021 | snp | C/T | 2.36857e-05 | 0.00344127 | intron-variant | HDAC6 | GRCh38.p7 | X:48815551 | CCACATTCCTTGACA[C/T]CATATTTTCTCCCTG | 10013 |
| rs782737408 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48807971 | GAGAGCAGGGGACAG[C/T]CTGTCTCTGCAGAGG | 10013 |
| rs782741101 | snp | C/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48803966 | TCAGGAGTTCGAGAC[C/T]GGTCTGACCAACGCG | 10013 |
| rs782744379 | snp | C/T | 5.04058e-05 | 0.00501999 | intron-variant | HDAC6 | GRCh38.p7 | X:48803120 | CTCCTTTTTTTTTTC[C/T]TCTGCAGGATCTGAA | 10013 |
| rs782744492 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48821131 | GCATGAGCCACCGCA[C/T]CTGGCCCCTGGTTAC | 10013 |
| rs782744833 | snp | C/T | 3.30006e-05 | 0.00406192 | intron-variant | HDAC6 | GRCh38.p7 | X:48808221 | CAGATTCACCTTGAT[C/T]TCCTTGCACAGAGTC | 10013 |
| rs782745280 | snp | A/C | 2.39518e-05 | 0.00346054 | intron-variant | HDAC6 | GRCh38.p7 | X:48814605 | CCCAAAGTGAGGCCC[A/C]GCCCCGCCCTTCTGT | 10013 |
| rs782747542 | snp | A/G | 8.37696e-05 | 0.00647131 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48805635 | TCTCTCCCCAGGCCC[A/G]GTTTGCTGAAAAGGA | 10013 |
| rs782748566 | snp | C/G | 5.10165e-05 | 0.00505031 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | HDAC6, ERAS | GRCh38.p7 | X:48824619 | CCACACTAAGCCCCA[C/G]AATACGGTCCCTCTT | 10013 |
| rs782749355 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48805191 | ATGCACAGAAAGGAC[C/T]GTTGAGGTGGCGAGG | 10013 |
| rs782749418 | snp | A/G | 1.65179e-05 | 0.00287379 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48822822 | GGGGGTGATGGGGGG[A/G]ACCCAGGGAAGGAGG | 10013 |
| rs782750634 | snp | A/G | | | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823384 | GGCCCAGACCACCTC[A/G]GAGGCAGCCATGGAG | 10013 |
| rs782750767 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48814209 | ATGGATAAATAAAGA[A/T]AAGAATGAAAAAATG | 10013 |
| rs782751243 | snp | A/G | 2.38334e-05 | 0.00345197 | intron-variant, utr-variant-3-prime | HDAC6 | GRCh38.p7 | X:48806509 | TGGTGGCAATCTTGG[A/G]GTCCCCATCCCTATG | 10013 |
| rs782751538 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48811102 | TGAGGCCAGGAGTTC[A/G]AGACCAGTCTGGCCA | 10013 |
| rs782756117 | snp | C/G | 2.30513e-05 | 0.00339487 | intron-variant | HDAC6 | GRCh38.p7 | X:48820086 | CTCATGCTTATACAT[C/G]TCTTCTCTCCCTGCC | 10013 |
| rs782756521 | snp | A/C | 0.000116268 | 0.00762369 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | HDAC6 | GRCh38.p7 | X:48822688 | CCTCCTTGGAGACCC[A/C]CCACCCCTGCTGACC | 10013 |
| rs782756884 | snp | A/G | 7.02354e-05 | 0.0059256 | missense, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48824283 | TACTGTCAGGCCTAT[A/G]TCCACCACCAGGTGG | 10013 |
| rs782757455 | snp | C/T | 3.02663e-05 | 0.00389002 | synonymous-codon, intron-variant, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48818349 | GGCATGGAACGGGCC[C/T]CGCATGGGTGATGCT | 10013 |
| rs782757474 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | HDAC6 | GRCh38.p7 | X:48811394 | TTTCTTGGTCCTTCT[C/G]TTTTATGCTGATGGT | 10013 |
| rs782759897 | snp | A/C | 2.86098e-05 | 0.00378208 | missense, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48823128 | TCACTCAGGACCAGC[A/C]CTCAGAGGCAGCCAC | 10013 |
| rs782760207 | snp | G/T | 4.95841e-05 | 0.00497892 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48814927 | GGCGGCAGGTGGGTT[G/T]CATGGAGCCAGGCTG | 10013 |
| rs782761225 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48801586 | AAGAAAAAGCTTGCA[C/T]CGCAGCCCTGTCGGG | 10013 |
| rs782763955 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48803932 | TTTGGGGGGGCCAAG[G/T]CAGGTGGATCACTTG | 10013 |
| rs782767431 | snp | A/G | 3.11949e-05 | 0.00394924 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48802890 | GAAATATTAAAAAGG[A/G]AGCCGTTCCCCGCTC | 10013 |
| rs782771772 | snp | A/G | 7.96591e-05 | 0.00631056 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48823108 | AGAGACAGCTGTGGT[A/G]GCCCTCACTCAGGAC | 10013 |
| rs782772892 | snp | G/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48819907 | TCTACCTCTGAGTCT[G/T]TATTTCTTTTCTTCC | 10013 |
| rs782775597 | snp | C/T | 1.71e-05 | 0.00292399 | intron-variant, upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48802654 | CCACGCTCCTCCCCC[C/T]ACCCCCAGAACCGCG | 10013 |
| rs782776085 | snp | C/T | 5.04732e-05 | 0.00502335 | intron-variant | HDAC6 | GRCh38.p7 | X:48808372 | CTCCCAGCCACCTCC[C/T]ACCCTTACAGGCCCA | 10013 |
| rs782776738 | snp | A/G | | | intron-variant | HDAC6 | GRCh38.p7 | X:48808852 | TTGACAGTTTAGGTT[A/G]TATCCTTACAGATTT | 10013 |
| rs782777663 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48809689 | CACCTGTATTTCCAG[C/T]TACTCAGGAGGCTGA | 10013 |
| rs782778504 | snp | G/T | 2.31669e-05 | 0.00340337 | missense, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48824256 | TACATCGACCTGTCA[G/T]CCTGGTGTTACTACT | 10013 |
| rs782780151 | snp | A/C | 4.90527e-05 | 0.00495216 | missense, upstream-variant-2KB, nc-transcript-variant | HDAC6, ERAS | GRCh38.p7 | X:48824590 | AGAACAAGTTTGGGG[A/C]GGATATGCCCCACCC | 10013 |
| rs782781030 | snp | C/G | 5.28081e-05 | 0.00513821 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823770 | GATGCAGGGATCTAG[C/G]GGCCTCACTGATCAG | 10013 |
| rs782782779 | snp | C/T | 4.77247e-05 | 0.00488468 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48806669 | CTGGTGGATGCGGTC[C/T]TGGGGGCTGAGATCC | 10013 |
| rs782784005 | snp | A/G | 4.17859e-05 | 0.00457069 | intron-variant | HDAC6 | GRCh38.p7 | X:48816296 | GTGCCTGGGGTGGGT[A/G]GATTCCCAGGACTGT | 10013 |
| rs782784600 | snp | A/G | | | intron-variant, upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48801492 | AGACACCGCCGACCC[A/G]AAGGGCTCCTAAGTG | 10013 |
| rs782785894 | snp | G/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48806166 | TGAAAGTAGGATTTG[G/T]TGTGGCTACTGCAGG | 10013 |
| rs782786675 | snp | A/G | 2.28266e-05 | 0.00337828 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48824011 | CCTAGACGTGACCCA[A/G]CCTTGTGGGGACTGT | 10013 |
| rs782790098 | snp | G/T | 3.91397e-05 | 0.00442361 | missense, nc-transcript-variant, intron-variant | HDAC6 | GRCh38.p7 | X:48802705 | ACTATGACCTCAACC[G/T]GCCAGGATTCCACCA | 10013 |
| rs782790420 | snp | A/G | | | intron-variant | HDAC6 | GRCh38.p7 | X:48804016 | AAAAATACAAAAATT[A/G]GTTGGGCGTGGTGGC | 10013 |
| rs782791803 | snp | A/G | | | intron-variant, upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48801588 | GAAAAAGCTTGCACC[A/G]CAGCCCTGTCGGGAA | 10013 |
| rs782792078 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | HDAC6 | GRCh38.p7 | X:48812238 | TGCATTCTTCCTTAT[G/T]AACAAACGTGTGTAA | 10013 |
| rs782792208 | snp | A/G | 3.16301e-05 | 0.00397669 | intron-variant | HDAC6 | GRCh38.p7 | X:48823611 | TCACCACACCCAGGT[A/G]GGGGCAAGAAGGGGC | 10013 |
| rs782792317 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | HDAC6 | GRCh38.p7 | X:48804078 | TGAGGCAGGAGAATC[A/G]CTTGATCTGGGAGGC | 10013 |
| rs782794339 | snp | A/G | 4.74586e-05 | 0.00487104 | intron-variant | HDAC6 | GRCh38.p7 | X:48814594 | CCACCTCTGCCCCCA[A/G]AGTGAGGCCCAGCCC | 10013 |
| rs782795837 | snp | A/G | 4.50796e-05 | 0.00474739 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48815033 | TCTGGCAGGAGGCAA[A/G]CTGATCCTGTCTCTG | 10013 |
| rs782796374 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48817183 | CGGGAACCTGGCAGG[A/C]GGCGCTTGCAGTGAG | 10013 |
| rs782796954 | snp | A/G | 7.27687e-05 | 0.00603151 | synonymous-codon, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48816612 | TGCCTGCCGCCTGGT[A/G]GAGGCTGTGCTCTCA | 10013 |
| rs782797482 | snp | A/G | 3.29337e-05 | 0.00405781 | intron-variant | HDAC6 | GRCh38.p7 | X:48817504 | CTGATCCTTGTGGGG[A/G]CCTGGATGCTCCCCC | 10013 |
| rs782798063 | snp | A/G | 2.37801e-05 | 0.00344811 | intron-variant, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48814794 | CTTGAAGGTTAGGCT[A/G]TGAGGGTAGGTAGCC | 10013 |
| rs782799645 | snp | A/G | 2.37431e-05 | 0.00344543 | synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48820216 | CCTCACCCACCTGCT[A/G]ATGGGCCTTGCCAGT | 10013 |
| rs782800530 | snp | C/T | 4.68198e-05 | 0.00483815 | intron-variant, utr-variant-3-prime | HDAC6 | GRCh38.p7 | X:48806483 | TGGATGAGAACTCTG[C/T]GGGCAGGGAATGGTG | 10013 |
| rs782800939 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | HDAC6 | GRCh38.p7 | X:48801528 | ACAGGGACGGAGGGG[C/T]GGCGGCTATGGCATC | 10013 |
| rs782802842 | snp | A/G | 2.52902e-05 | 0.00355591 | intron-variant, downstream-variant-500B | HDAC6 | GRCh38.p7 | X:48822813 | AGTGGATTTGGGGGT[A/G]ATGGGGGGAACCCAG | 10013 |
| rs782803339 | snp | A/C | 3.22914e-05 | 0.00401804 | intron-variant | HDAC6 | GRCh38.p7 | X:48805433 | CTGTGACTCCATCTC[A/C]CCAGCTTCCCGGAAG | 10013 |
| rs782804500 | snp | G/T | 3.79809e-05 | 0.00435764 | intron-variant | HDAC6 | GRCh38.p7 | X:48816289 | GACCCCGGTGCCTGG[G/T]GTGGGTGGATTCCCA | 10013 |
| rs782807715 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48821230 | TTTTTTTTTTTGAGA[C/T]GTTGTCTTGCTCTGT | 10013 |
| rs782810859 | snp | A/G | 2.63744e-05 | 0.00363133 | intron-variant | HDAC6 | GRCh38.p7 | X:48803093 | GACTCAGGGCCTAAA[A/G]TGGATCTGTGTCTCC | 10013 |
| rs782811110 | snp | C/T | 2.3677e-05 | 0.00344063 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | HDAC6 | GRCh38.p7 | X:48822652 | ATCCATCTCAGAGTC[C/T]ATGGCTGCCTGCACT | 10013 |
| rs782812700 | snp | C/T | | | intron-variant | HDAC6 | GRCh38.p7 | X:48814335 | GAATGAACGAGTGGT[C/T]GAATGGGGAAATGAG | 10013 |
| rs782814101 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | HDAC6 | GRCh38.p7 | X:48812976 | GCAGTGGCCCGATCT[C/T]GGCTCACTGCAACCT | 10013 |
| rs782815444 | snp | C/G | | | intron-variant, utr-variant-3-prime | HDAC6 | GRCh38.p7 | X:48806881 | CCTGCCTCCTCTCAT[C/G]GGAGGTAGTCATTGG | 10013 |
| rs782816419 | snp | C/T | 0.000112501 | 0.00749918 | missense, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48823311 | CCTCAGAGGATGCTG[C/T]TGGGGGAGCCACGCT | 10013 |
| rs782819209 | snp | C/T | 6.92145e-05 | 0.00588239 | intron-variant | HDAC6 | GRCh38.p7 | X:48815572 | TTTCTCCCTGCCCTG[C/T]AGTGCCCAGGCTTCA | 10013 |
| rs782820336 | snp | A/G | 3.10169e-05 | 0.00393795 | missense, intron-variant, nc-transcript-variant | HDAC6 | GRCh38.p7 | X:48818342 | TCAACGTGGCATGGA[A/G]CGGGCCCCGCATGGG | 10013 |