SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs538009197 | snp | C/T | 0.000317681 | 0.0125992 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062998 | GCAGCCTCAGCCTCT[C/T]CCCCATCTCCAACTT | 23510 |
rs538478904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055868 | AGAAACCCTGTCTAC[C/T]AAAAATACGAAAATT | 23510 |
rs538508661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061443 | TGAGTCCTGGAGTTC[A/G]GAGACCAGCCTGGGC | 23510 |
rs538517326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055454 | GGTATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 23510 |
rs538594541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058692 | TAATCCCAGCTATTC[A/G]GGAGGCTGAGGCGGG | 23510 |
rs538599643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052490 | ACTTTGGGAGGCCAA[A/G]GCAGATGGATCACCT | 23510 |
rs538633552 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064283 | CGAGCATGTGGGTCT[C/T]GCTGAGCAGTCATGG | 23510 |
rs538697225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057916 | TACAGCATTGTCGGC[C/T]GGACACAGTGGCTCA | 23510 |
rs538723412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057082 | GCCTCAGCTTCCCGA[A/G]TAGCTAGATTACAGG | 23510 |
rs538808872 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047901 | TCTCTGCCCCTGACA[A/T]CCCACTGAGATCTGC | 23510 |
rs538844795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040779 | TAGTCCCAGCTACAT[A/G]GGAGGCTGAGGCAAG | 23510 |
rs538877949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053334 | ATTGTCGCTGCTTAC[C/T]AGATGGCGGGAGGAG | 23510 |
rs538915173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052891 | AGAGTAAGACTCCGT[C/T]TCAAAAAATAAGTAA | 23510 |
rs539001263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050011 | GAAAGCTTGTAATGG[C/T]TGTACTAGTTAATGA | 23510 |
rs539140866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054788 | CCACTCCAGCCTGGG[C/T]GACAGAGGGAGACTC | 23510 |
rs539221670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034885 | TCAATCTTATGATCT[C/G]ACGTCAGACGCCTCA | 23510 |
rs539237559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033044 | AGGTCCCAAGAGAAG[C/T]ACAATGGTAACCGAC | 23510 |
rs539268299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040362 | ATATTAGACTGGGAA[C/T]AGGAGCTCAAGGGTC | 23510 |
rs539295010 | snp | A/T | 0.336017 | 0.234736 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044404 | TAGAGACGGGGTTTC[A/T]CCTTGTTAGCCAGGA | 23510 |
rs539301620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037821 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACAAGGT | 23510 |
rs539328890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046520 | CTGAACGCTCTATAC[A/G]TTCGAATCCTGGAAG | 23510 |
rs539356489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043913 | CAGCAACTTGCTCCA[C/G]AGTTTTACAAACTTA | 23510 |
rs539414071 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058623 | GCCAACATGGTGAAT[-/C]CCCCTTCTCTACTAA | 23510 |
rs539500175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060730 | CACCCTGGGATCAAC[C/T]GCCTGAGTAAATATG | 23510 |
rs539611891 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060513 | ACAACAGCGCGACAG[C/G]CAAGACCAGCTGCTC | 23510 |
rs539878084 | in-del | -/A | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041354 | GTGAGACTCCAACTC[-/A]AAAAAAAAAAAAAAA | 23510 |
rs539895168 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040830 | GGCGGAGATTGCAGT[A/G]AGCTGAGATGGCCCC | 23510 |
rs539941994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055904 | AGTGTGGTAGCGGGC[A/G]CCTATAATCCCAGCT | 23510 |
rs539949148 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048351 | ACTTTACGTATTCAC[A/C]TTTAAGTTCTCAACT | 23510 |
rs539992751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045191 | GGGAGTTTCAAAAGG[C/G]GAGGGAGTATACGAA | 23510 |
rs540027903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060017 | AATCCACCGTGAAGA[A/G]CTTGGTGAACAGCTG | 23510 |
rs540134202 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065309 | TAAGATTTCTGGGAG[C/T]GTTGTTCACCCACCC | 23510 |
rs540147730 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065257 | CTGCAACCCAATGAC[A/G]CCTGTATTGTTCCAG | 23510 |
rs540148829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036925 | CCTCCGCTGCCTTTC[A/G]TCTTCAACCCGGCCT | 23510 |
rs540192201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056216 | TTGATGTTCAAAGGT[A/G]GCTTTGTAGTTGGTT | 23510 |
rs540253515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061960 | GATGAAGAACAGGCC[A/C]ATTTCTCCCCGGGGG | 23510 |
rs540364821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055100 | TCCTCTGTCACCCAG[A/G]CAGGAGTGCAGTGGC | 23510 |
rs540455756 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035960 | ACACGGCACCCACCA[C/G]CCCACTACTCTGTGC | 23510 |
rs540518206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056713 | GTTGTATGTGGCTCT[A/G]AGATGAAGTTGGCTG | 23510 |
rs540627868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055556 | CCCTGTCTACTGGCC[A/G]GGCGTGGTGGCTCAT | 23510 |
rs540679336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052963 | CCTCTCCTTGGTGTT[C/T]TTCTGGCAAACCCTC | 23510 |
rs540762870 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064408 | CCTTCTATGAAAGCC[G/T]CCTCGAGCCAGGTGC | 23510 |
rs540819698 | in-del | -/C | 0.00234577 | 0.034167 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063055 | GGATGTAAACTAAGA[-/C]CCCGAAAACTCCAGA | 23510 |
rs540835930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035496 | CGGGTTATGTTTCAG[C/T]CTATCGTTATGAAGT | 23510 |
rs540859421 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044582 | CCAGACCTCAGGTGA[G/T]CCACCCACCTCAGCC | 23510 |
rs540871779 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034400 | TGGCTGCCGGCACCA[A/T]AAGAAACCTTGCGAG | 23510 |
rs540922382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044298 | GCAAACTCCGCTTCC[C/T]GGGTTCACGCCATTC | 23510 |
rs540979970 | snp | A/G/T | 0.000150758 | 0.00868098 | upstream-variant-2KB, synonymous-codon, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047565 | CCTCTGCTGCCAGGA[A/G/T]GACCCGGAGCTGGAC | 23510 |
rs541057177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039925 | TGGCTTCTTTCACTC[C/T]GCATAATTATTTTGA | 23510 |
rs541120167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046006 | CCACGTTCTTCTGCC[A/G]TGGTTTCAGCCGGTC | 23510 |
rs541156129 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058283 | AGTGAGCTGAGATGG[C/T]GCCATTGCACTCCAG | 23510 |
rs541250483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035179 | GGTTCGAGTCCCTTC[A/G]TGGTCGGAACGTTTT | 23510 |
rs541255786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041810 | GTTCTGGGCTGTAGC[A/G]CGTTATGCCGATCGG | 23510 |
rs541382411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034459 | ACTCGAACCCACAAT[C/T]CCTGGCTTAGGAGGC | 23510 |
rs541402066 | snp | A/C | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044184 | CACCCACCACCACAC[A/C]CAGCTAATTTTTGTA | 23510 |
rs541451531 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037339 | ACAAAGCAAGATTCC[A/G]TATCAGAAAAAAAAA | 23510 |
rs541514852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043468 | AAATACAAAAATTAG[C/G]CGGGCGTGATGGCAT | 23510 |
rs541556703 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036747 | GTCTGCATCCTCAGA[G/T]CCTCAGCGGGATGGC | 23510 |
rs541745643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061823 | TCTGTCTTCCCTTGC[C/T]GTGCTCGACGGGGCG | 23510 |
rs541810983 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034512 | CTGGGGCGCGGTAAG[A/G]CGCTAAACCCACGTG | 23510 |
rs541878455 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057416 | GATCTTTTGTGATAC[C/T]CTGAATTTTGTACTT | 23510 |
rs541962984 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031170 | TCCTTTAAAGTAAAG[A/G]CGTGGTCCCTGTCCT | 23510 |
rs542069107 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048897 | CTTAATAACAAACAC[A/G]CTACAGAAGAATGTT | 23510 |
rs542091493 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058057 | GGCTGGGCACAGTGG[C/T]TCATGCCTGTAATCC | 23510 |
rs542113121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033066 | GTAACCGACGCTGCC[C/T]TTGGCTGAACTTCTT | 23510 |
rs542118944 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053831 | CAGTCTCATGGGGTA[C/T]GCTTCAGCAGCTGCT | 23510 |
rs542155838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054435 | TCGTCATATGTTTGT[C/T]GTGTGTTTGAATGGC | 23510 |
rs542159624 | snp | C/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030612 | AACAGTAAGTTGGAA[C/G]TGGAAGGAGATTTTT | 23510 |
rs542381976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049493 | TGTCTGAGGGAGTCA[C/T]GATTAAGGAAGCCTC | 23510 |
rs542420665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054834 | AAAAAGAAGCTTGAA[A/G]TATAGCCAGGAAAAT | 23510 |
rs542518448 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043331 | AGCCCAGCTCTCTTG[A/G]CCGGGCGCAGTGGCT | 23510 |
rs542645113 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056775 | TTTTTCTTTATTTTT[G/T]TGTGTGTGGATTTTC | 23510 |
rs542647058 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063317 | TCTTTACAACAGCAG[C/T]TGGGCTGGGTTCCCA | 23510 |
rs542749820 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055580 | GGCTCATGCCTGTAA[A/T]CCCAGCACTTTGGGA | 23510 |
rs542754894 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050407 | GCTGGGATTACAGGC[A/G]TGCACCACCATGCTT | 23510 |
rs542844571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046151 | GTAGTGGCGTGGTCT[C/T]GGCTCACTGCAACCT | 23510 |
rs542883130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052066 | CAAAAATATCAAGTT[C/G]AGGAGGTGTCCAACA | 23510 |
rs542941123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045034 | GATAGTCACATAGGT[C/T]CTTTTCTATTTTCCT | 23510 |
rs542959123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044632 | CAGGCATGAGCCACC[A/G]CGCCCGGCCTGCATT | 23510 |
rs543020039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050898 | GCCCAGGCTGGTCTC[A/G]AATGTCTGGCCTCAC | 23510 |
rs543025066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041823 | GCGCGTTATGCCGAT[C/T]GGGTGTCTTCACCAA | 23510 |
rs543089440 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053471 | TATGAGATGGAGTCT[C/T]GCCCTGTCGCCCAGG | 23510 |
rs543161948 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052564 | CTGTCTCTACTAAAA[A/G]TACAAAAAATTAGCC | 23510 |
rs543206341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033935 | ATGGATAAGGCACTG[A/G]CCTCCTAAGCCAGGG | 23510 |
rs543238455 | in-del | -/ATA | 0.00328227 | 0.0403777 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059118 | TAAATAAATAAAATT[-/ATA]ATAATAATAAATAAT | 23510 |
rs543331096 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038765 | ACAAACCTGTCGAGG[C/T]TCACCTTTCCATTTA | 23510 |
rs543376950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035110 | GAGGTAGCTGCAGCC[A/G]GAGACCGCGTGGCCT | 23510 |
rs543438416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035051 | CGAGCAGTGAAGCTG[A/C]GGCACGCCGGAGCGT | 23510 |
rs543449378 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053212 | CTGGAGGTGTGTGTG[G/T]AACACCGTTTGCAGT | 23510 |
rs543502234 | snp | A/T | 0.00162611 | 0.0284677 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047636 | CTTCGAACCCCCTGG[A/T]TTCTCGTAGATCGGT | 23510 |
rs543575001 | snp | A/C | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053050 | TTTACAACATCGCGT[A/C]CCTTGTGCGGCTGGT | 23510 |
rs543627244 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031740 | ACCTTAGTTTCCCCA[C/T]CTATAAACTAGGGGG | 23510 |
rs543711750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042470 | ATGTAATTCCTTAAT[A/G]CTGTTTTGTTTCTAG | 23510 |
rs543750752 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035732 | CTACTCAGGAGGCGG[A/C]GGCAGCAGGAGAATC | 23510 |
rs543790036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033685 | CCAAGCGGACCCTCG[A/G]GGCTCCATGGGGCGT | 23510 |
rs543970460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056597 | TTGTTCTAGGAATGT[C/T]AAGACCTTTTTGATG | 23510 |
rs544006226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056138 | CAGCAGTTTGCAAAA[A/G]TGAAGAGAAGGGCTT | 23510 |
rs544143317 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038344 | GATGGGGTTTCACCA[C/T]CTTGGCCAGGCTGGT | 23510 |
rs544344926 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063367 | CTGGGGGATGAGGGC[A/G]GAAGGCCTAGCTCCT | 23510 |
rs544372782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037494 | GTTATCTCATTTAAT[G/T]CTCATTACAATCCTG | 23510 |
rs544410125 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065606 | GAATCTGGCCTTTTT[C/T]CATGGCAATGAGGTG | 23510 |
rs544488718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061911 | AGTGGAGCTCATACT[C/T]TTCCTCCTGGGGAGG | 23510 |
rs544503108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059923 | GTAGAATGAGTCCCT[A/C]AAGGAGACTGGGATT | 23510 |
rs544513066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043545 | TTGAACCTGGGCGGC[A/G]GAGGTTGCAGTGAGC | 23510 |
rs544595236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060638 | GGCTGGGCGCGTGGC[A/G]AGTGGGCCCGGCCAG | 23510 |
rs544622073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054527 | AAGCTTGAAGTCGGC[C/T]GGGCGCGGTGGCTCA | 23510 |
rs544684612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058202 | GGTGGTGGGCGGCTG[G/T]AATCCCAGCTATTCA | 23510 |
rs544765254 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044224 | TTTTTTTTGAGACGG[A/G]GTCTCGCTCTGTCGC | 23510 |
rs544848887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041179 | GTCTGGGCAACATGG[C/T]GAAACCCCGTCTCTA | 23510 |
rs545076631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051363 | TATCACAGCTCACTG[C/T]GACATCCACCTCCCG | 23510 |
rs545080110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057597 | CAGAGTCTTACTCTG[C/T]CGCCCAGGCTGGAGT | 23510 |
rs545117542 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063407 | CCTGTACTTTAAGGA[C/T]GCTGGAGCCAAGAGG | 23510 |
rs545158057 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035068 | GCACGCCGGAGCGTT[A/T]AATGGCCATCAAATT | 23510 |
rs545257272 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047266 | ATGGCGGAACTGCAG[C/G]TGGACCCGGCGATGG | 23510 |
rs545357023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039380 | TCCTATTGCTCTATG[A/G]AGAAACTGTGGTTAC | 23510 |
rs545387889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039832 | TCTCAACCATCCCCA[G/T]GCAGCCACTGTAGAC | 23510 |
rs545453471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036604 | TCCCCCTAATGCTGG[A/G]GTTGCCCCCTTCACA | 23510 |
rs545455410 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054853 | AGCCAGGAAAATAGA[C/T]CCTCTCTTTCATGCG | 23510 |
rs545491480 | in-del | -/GTTT | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041665 | GTAGAAAAAAAGTCA[-/GTTT]GTTCCAAAGGGAGAC | 23510 |
rs545514326 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042592 | TTTTGGTTCTGGGGT[A/G]TGATCTCTGCAAAAG | 23510 |
rs545590127 | snp | A/G | | | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75032663 | AGTGAGGTTAGAGCT[A/G]TAAGATCCAAGACCC | 23510 |
rs545613127 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066336 | AGGCGCCTGCCTGCG[C/T]GCCTGGCTAATTTTT | 23510 |
rs545746562 | in-del | -/T | 0.494651 | 0.0514399 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044373 | ACCGCGCCCGGCTAA[-/T]TTTTTGTATTTTTAG | 23510 |
rs545774468 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031107 | GAGACTCCGTCTCAA[A/C]AATAAAATAAAATAA | 23510 |
rs545838319 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030650 | TCTCAGGCTAGCATT[G/T]CAGTAGTAGATTGCT | 23510 |
rs545839871 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057633 | GGCGCGATCTCAGCT[C/T]GCTGCAACTTCTGCC | 23510 |
rs545988532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035154 | TCTGACTTCGGATCA[A/G]AAGATTGAGGGTTCG | 23510 |
rs546024569 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032404 | AGTCAGGGACACGTT[C/T]TGGAACTAGGGCGGC | 23510 |
rs546085553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037271 | ATGGTGTGAACCCGG[A/G]AGGCAAAGGTTGCAA | 23510 |
rs546127583 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031757 | TATAAACTAGGGGGG[G/T]TTTTTTGTTTTGTTT | 23510 |
rs546175167 | snp | C/T | 3.42753e-05 | 0.00413962 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059498 | TTCTCAGTCTGCGCC[C/T]GGTCATTGCAGGGCC | 23510 |
rs546200289 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064523 | ATGACTGCAGACTGT[G/T]CCAAATGTCTTTTGA | 23510 |
rs546213293 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064949 | TTGTGCCCAGTCTCG[C/T]TGAGGCGCTTGTCCC | 23510 |
rs546222322 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051685 | TTATTTCTGAACTAT[C/T]TGAGAATAGATTGCA | 23510 |
rs546308021 | in-del | -/TTTTTTTTC | 0.00440086 | 0.0467018 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033123 | ACTTTTATTTAATAA[-/TTTTTTTTC]TTTTTTTTCTTTTTT | 23510 |
rs546338070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055361 | TGCCTGGCATAAGTT[C/T]ACTTTTAAAAGTAAA | 23510 |
rs546406394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044770 | TCAGGGTCAGATATT[A/G]AAAGACTGCAAAGTC | 23510 |
rs546467758 | snp | A/T | 0.336017 | 0.234736 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044407 | AGACGGGGTTTCACC[A/T]TGTTAGCCAGGATGG | 23510 |
rs546508363 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058958 | AAAAAATTAGCCGGG[C/T]GTGGTGGCGGGTGCC | 23510 |
rs546575109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051000 | TTTTTTTGAGACGGA[A/G]TCTTGCTCTGTTGCC | 23510 |
rs546598257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055672 | AACCCTGTCTCTACT[A/G]AAAATACAAAAGTAG | 23510 |
rs546630648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036970 | AGGAGCCATGCACCC[A/T]GGCTCTCCTCTGCTT | 23510 |
rs546970934 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043604 | GACACAGAGTGAGAC[G/T]CTGTCTCAAAAAAAA | 23510 |
rs546971572 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032086 | GGTTATGTTATTAGC[A/G]CCTTCCTCATAGGGT | 23510 |
rs547077735 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047949 | CCTCTTCAGTCCCCC[A/C]ACTGCCGGTGCCAGA | 23510 |
rs547105287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054620 | ACCATCCTGGCTAAC[A/G]CGGTGAAACCCCGTC | 23510 |
rs547106034 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037795 | TGGCCCACGCCTGTA[A/G]TCCCAGCACTTTGGG | 23510 |
rs547111769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049131 | AATTGTTGTCTTGGG[A/G]CGCTGACAAAGATGG | 23510 |
rs547320680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034657 | TCCCCACCGGGCTAC[A/C]CAAGAGCTCCATGCG | 23510 |
rs547363835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035090 | CATCAAATTGGCCTC[C/T]CTAGGAGGTAGCTGC | 23510 |
rs547405767 | in-del | -/AA | 0.00358779 | 0.0422022 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052243 | TTTACCGAAAATAGC[-/AA]AGAGATATTTCCTAG | 23510 |
rs547431178 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046762 | CTGAGGAAGGGATCG[C/G]GGGGCGAGGAGCGGC | 23510 |
rs547431296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040258 | GGAGCTCAAAGGGCT[A/G]GAAGCTACGAATCCT | 23510 |
rs547476825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039424 | GCTCACTCTGACAGG[A/C]AAACCACAGCTTTTC | 23510 |
rs547492176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046408 | AATTCTTAAAAATCT[A/G]TTGCTTAATCCCCAG | 23510 |
rs547537779 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030678 | GCTCTGGCATGTATA[A/C]ATTTCTTAAACTGTT | 23510 |
rs547553451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045636 | TGGCTCTGTTCTGCC[C/T]GGCTCACCGGCGGTC | 23510 |
rs547647255 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063435 | AGGATTGTTCCCGTG[C/T]CGTGCCATGGTTTCA | 23510 |
rs547731996 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062899 | TGCGGCTGCACCCCT[G/T]CTTGCTTCCTGGGAT | 23510 |
rs547832790 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065241 | CAAGTTTCCCTCCTC[A/G]CTGCAACCCAATGAC | 23510 |
rs547861964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033859 | TTCTCTAGGAAAAGG[A/G]GACACTCGCTTATGA | 23510 |
rs548042479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042060 | GGCCTTTGGCCATAC[A/G]CATCCTTCCTAAGCT | 23510 |
rs548099105 | snp | C/G/T | 0.00319106 | 0.0398404 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066041 | CTGAAACCACCAAAG[C/G/T]GGGTGTTGGGCCTTC | 23510 |
rs548174925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054699 | GTAGTCCCAGCTGCT[C/T]GGGAGGCTGAAGCAG | 23510 |
rs548237613 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75032784 | CTAGAGGGCGGCAGC[A/G]GGAAAGCAGAGAAGG | 23510 |
rs548317227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053239 | CAGTGCAGGGAATGC[A/G]CACTCAGCCAAACTG | 23510 |
rs548327664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035896 | AGGGCAGTGGGGGTG[C/T]TGCCCAACTCTGTGG | 23510 |
rs548348812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046651 | GAAGTCTGCCGCGCT[C/G]GGAGCGGACTGCACG | 23510 |
rs548360541 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052854 | AGCCAAGATCGCACC[-/A]CTGAACTCCAGCCTG | 23510 |
rs548366500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055124 | CAGTGGCATGATCTC[A/G]GCTTACTGCAACCTC | 23510 |
rs548400976 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050793 | TCCCTATATCCCAGA[C/T]TAACCAATTTTCAAT | 23510 |
rs548405076 | snp | C/T | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060097 | TACTTCTCTCCGCCT[C/T]GTGCTTACGACTGAG | 23510 |
rs548496200 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031450 | AGAAAGGTCTCAGTA[C/G]ATTGCTGGAGGCAGA | 23510 |
rs548664503 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059056 | TGAGCCAAGATTGCA[C/T]CATTGCACTCCAGCC | 23510 |
rs548666135 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051531 | CCTCGTGATCCACCC[A/G]CCTTGGCCTCCCGAA | 23510 |
rs548710285 | in-del | -/TC | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064944 | CGGCCTTGTGCCCAG[-/TC]TCGTTGAGGCGCTTG | 23510 |
rs548726955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058553 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGACCAGG | 23510 |
rs548740243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034235 | GGGTTCCCAGGACAC[C/T]CCAGCTCCACCTGGC | 23510 |
rs548802615 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039558 | ACAGGGCTCAGCCAC[A/T]GAATGGTCAGGACAC | 23510 |
rs548865959 | snp | A/G | 8.2411e-05 | 0.00641862 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039106 | AATGTAAACAGAGAC[A/G]GAAAGCAGAATATCC | 23510 |
rs548899897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053689 | CTCAGGTGATCTGCC[C/T]GCCTCAGCCTCCCAA | 23510 |
rs548924539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044796 | AAGTCAAAAATCTCT[A/G]TAAGCTTGGAGTGGA | 23510 |
rs548965266 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051200 | GGATGGTCTCATCTC[A/C/G]ATCTCCTGACCTTGT | 23510 |
rs548981252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058095 | TTGGGGGCCCAAGGC[A/G]GGCGGATCACCTGAG | 23510 |
rs549122421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044358 | CTACAGGCGCCCGCC[A/T]CCGCGCCCGGCTAAT | 23510 |
rs549348670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038049 | GTGAGACTCCATCTT[A/C]AAAAATAATAATAAA | 23510 |
rs549435293 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037665 | CTCTATGATCTACTA[A/C]CTTGCTTTAAACCAT | 23510 |
rs549608415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040712 | CCAACATGGTGAAAC[A/C]CCGTCTCTACTAAAA | 23510 |
rs549640445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033223 | ATCCCCCCACCTCAC[C/T]CTCCCAAAGTGCTGG | 23510 |
rs549764098 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064678 | TCTACACACCTATGC[A/G]CCACATTTTACAGCT | 23510 |
rs549874123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034484 | GGAGGCCAGTGCCTT[A/T]TCCATTAGGCCACTG | 23510 |
rs549966015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052763 | GCCGGGTGTGGTGGT[A/G]TGTGCCTGTAGTCCC | 23510 |
rs549967202 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065140 | GCCGCCATGAAAAGA[C/G]TGCTCTTGAGCCCCA | 23510 |
rs550016425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059158 | TTACCTTATTTTTGA[C/T]TTGGGGAAATGGATT | 23510 |
rs550051611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052403 | CCAGCCTGGCCAACA[C/T]GGCAAAACCCCGTCT | 23510 |
rs550109857 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030845 | GCTCATGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 23510 |
rs550176668 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055618 | GCAGGTGGATCACCT[C/G]AGGTCAGGAGTTCAA | 23510 |
rs550203491 | snp | C/G | 3.34997e-05 | 0.00409252 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062979 | CATCTCTGTCTTTCC[C/G]TCAGCAGCCTCAGCC | 23510 |
rs550272338 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032457 | TACTGGATGCTGGAG[G/T]ATTATGAGGACAGAA | 23510 |
rs550359261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060506 | TAACCAGACAACAGC[A/G]CGACAGCCAAGACCA | 23510 |
rs550366253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050504 | CTAACCTCAAGTGAT[C/G]CACCTGCCTCAGCCT | 23510 |
rs550454180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055624 | GGATCACCTGAGGTC[A/G]GGAGTTCAAGACGAG | 23510 |
rs550493385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055299 | GCCTCAAGTGATCCA[C/T]TTGCCTCAGCCTCCC | 23510 |
rs550566751 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060712 | TCGGTCGCCGCCACT[C/G/T]GCCACCCTGGGATCA | 23510 |
rs550720013 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048301 | GACAAGACACTTAAA[C/G]CATTTCCAGTTTGAA | 23510 |
rs550736778 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031983 | GCCAAGCTGGTCTCA[A/G]ACTCCTGACCTCAAG | 23510 |
rs550789120 | in-del | -/ACAA | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036245 | TTTTGTCTGCAGCAG[-/ACAA]ACAAGCTGGGGCTAC | 23510 |
rs550798208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036795 | ACTGCAGTCTCGCAG[C/G]GGAAGGGTGTGGTAC | 23510 |
rs550808301 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030962 | TACAATTAGCCAGGC[A/G]TGGTGGTGGGCGCCT | 23510 |
rs550857448 | snp | A/C | 0.00133626 | 0.0258136 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036068 | TTTCTTTTTCTTCTT[A/C]CCTGAGACGGAGTCT | 23510 |
rs551014273 | snp | C/T | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060519 | GCGCGACAGCCAAGA[C/T]CAGCTGCTCTTGATG | 23510 |
rs551135025 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037257 | GCTGAGGCAGGAGAA[C/T]GGTGTGAACCCGGGA | 23510 |
rs551218471 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056861 | CCAAGCCCAAGATGT[A/G]GGCCTCAACCCTACC | 23510 |
rs551252056 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042814 | TGAACCCAGGAGGTG[A/G]AGGTTGCAGTGAGTC | 23510 |
rs551258375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034312 | ACAGAGGGTCCTGCA[A/G]GAGAAGGCGAGGGGC | 23510 |
rs551301672 | in-del | -/GTCAGA | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045649 | CCCGGCTCACCGGCG[-/GTCAGA]GTTTAAGGTTCTCTC | 23510 |
rs551460044 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039415 | AGTGGGGGCGCTCAC[C/T]CTGACAGGCAAACCA | 23510 |
rs551495513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051574 | CAGGCGTGAGCCACC[A/G]TGCCCGACCTTTTTT | 23510 |
rs551532655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051230 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTACT | 23510 |
rs551607991 | in-del | -/CCTGTAAT | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054545 | GCGCGGTGGCTCACG[-/CCTGTAAT]CCCAGCACTTTGGGA | 23510 |
rs551741681 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064722 | TGAACTGCCGTCCTC[A/G]GTAAAAGCAGCCACC | 23510 |
rs551769692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033828 | CCCACTCCATGGATC[A/G]CGCCTCTGTCAGGCC | 23510 |
rs551977246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035221 | CTATAATCTTCCCTC[A/C]CTTGTTTTAGACCCA | 23510 |
rs552098076 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065195 | ATAGACAGGAGTGGT[A/G]TTTCCGCCCTCTCGG | 23510 |
rs552108091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053922 | CCCAGGCTGGCCTCC[C/T]AAAGTGCTAGGATTA | 23510 |
rs552146492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059698 | CCAATTAATAACCAC[A/G]GGAGACGGCTACGGC | 23510 |
rs552174649 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031289 | AGTGAATGCCAGGCA[C/T]TCACAGCGTGGGGTG | 23510 |
rs552184652 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052693 | ATGCCATTGCACTCC[A/T]ACCTGGGCAACAAGA | 23510 |
rs552185618 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051038 | GAGTGCAGTGGCGCA[A/G]TCTCGGCTCACTGCA | 23510 |
rs552230189 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030939 | CATCTCTACTAACAA[C/T]ACAAAAATACAATTA | 23510 |
rs552308077 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058419 | TGAGGCAGGAGAATC[C/G]CTTGAACCAGGGAGG | 23510 |
rs552348833 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064119 | ATGTATGTATGTGCT[A/G]GGCAGTCTGGGGACC | 23510 |
rs552368789 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060251 | TTTTTTTTTTGGAAA[A/G]TCAAATCCCTTTCTT | 23510 |
rs552372029 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047689 | CCTCACAGGCAGCCC[C/T]CTCAGGCCGGGACCC | 23510 |
rs552433448 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047006 | TTCCTCAGCCAACCC[C/T]AAAGCCAAGGGGGTG | 23510 |
rs552483165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052816 | AGAGAATCATTTGAA[C/T]GCAGGAGGCGGAGGT | 23510 |
rs552531606 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045303 | ACCACAGGACCAGAG[C/T]GAAATTAAAATTGCT | 23510 |
rs552552250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043172 | GTTGTAATGAGCTGA[C/G]ATGGCATCAGTGCAC | 23510 |
rs552572731 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050057 | ACTCTGTTTCAGCTA[A/G]TAGAAAGAGGAATTG | 23510 |
rs552728914 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035099 | GGCCTCTCTAGGAGG[A/C/G/T]AGCTGCAGCCGGAGA | 23510 |
rs552793842 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053477 | ATGGAGTCTCGCCCT[A/G]TCGCCCAGGCCGGAG | 23510 |
rs552843669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033509 | CAATATTCATGATTA[A/C]TACTTGTCTGTTCTC | 23510 |
rs552888230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044014 | AGCAGCACCAGCACA[C/T]GTTGTGCACTTTTTT | 23510 |
rs552967766 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031113 | CCGTCTCAAAAATAA[A/G]ATAAAATAAAATTGG | 23510 |
rs553081789 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054803 | CGACAGAGGGAGACT[C/G]CATCTCAAAAAAAAA | 23510 |
rs553182886 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033591 | CTGTAGAGGCGGACA[C/G]CAAGGCTCAGGGCGG | 23510 |
rs553483525 | snp | C/T | 1.65072e-05 | 0.00287286 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042246 | AGTAAGCCCAGTCGA[C/T]AGCTGGTGGATTCTC | 23510 |
rs553517018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060567 | TTGTCCTGGTTGAAG[C/T]TGGCAAAGAGCAGCT | 23510 |
rs553546615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041784 | GGCACGTGGATTGCT[C/T]GAGCCCAAGAGTTCT | 23510 |
rs553584770 | in-del | -/C | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038466 | CCTTTTCTAATACCA[-/C]TTTTGTGCTCAAAAG | 23510 |
rs553676399 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066060 | TGTTGGGCCTTCTCC[C/G]TCCTCCCTTTCATTT | 23510 |
rs553697719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058038 | CTAAAAATCCAAAAA[A/T]ATTGGCTGGGCACAG | 23510 |
rs553713549 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065396 | GGCTGATCACATCAG[A/G]GAGGTCTGCGTGGCA | 23510 |
rs553822752 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061784 | TGTGACTGAGGCAAA[C/T]GTCCATTTTGTTGGC | 23510 |
rs553887765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75061062 | AAGCAAAGGATTTTT[G/T]TAATGTATTCTTTGT | 23510 |
rs553946644 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039204 | CGGCTACCCATCATC[C/T]TTACCTCTTTCTCAT | 23510 |
rs553983652 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057270 | CCTATTTCTTAGAAT[A/G]GTATTTTTTGTAGGT | 23510 |
rs554025488 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037787 | GGATGCAGTGGCCCA[C/T]GCCTGTAATCCCAGC | 23510 |
rs554060434 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063584 | TTAGGTAAAGCATAG[A/T]GTTGCCAGAGTACCC | 23510 |
rs554148374 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063215 | ACTCCCTCCCCACCT[G/T]CAGGACTCCGAAGAC | 23510 |
rs554196358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059298 | ACAGTATGCTGGCTT[C/G]TGGTCACTTAAAAAG | 23510 |
rs554282153 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064799 | AAAAAAGTTAGATGT[A/G]GCCAAGGAAAGTAGT | 23510 |
rs554284151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058753 | CAGTGAGCTGAGATC[A/G]CGCCACTGTACTCCA | 23510 |
rs554407936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045004 | CAAACATCAGTGTAT[C/T]GGGGAACTTGCCCCG | 23510 |
rs554499405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050848 | TGGGGAGATCTTTTT[C/G]TTGTTTTTTTAAGAG | 23510 |
rs554566500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040459 | ATCTGAAAAGGACAG[C/G]TGGACTTGATGACCA | 23510 |
rs554719440 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064409 | CTTCTATGAAAGCCT[A/C]CTCGAGCCAGGTGCT | 23510 |
rs554767967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042992 | TTTGGGAGGCCAAGA[C/T]GGTTGGATCACCTGA | 23510 |
rs554790322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052567 | TCTCTACTAAAAATA[C/T]AAAAAATTAGCCAGG | 23510 |
rs554827656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042435 | CTTTATATGTTGTCA[C/T]AAGGGCATCAAGAAT | 23510 |
rs554834691 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048534 | TAACTTTAAAGAGAT[C/T]TCAAAACCCTTGCTT | 23510 |
rs554881177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040887 | CAAGACTCCGTCTCA[A/G]AAAAAAAAAAAAAAG | 23510 |
rs554888774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041814 | TGGGCTGTAGCGCGT[C/T]ATGCCGATCGGGTGT | 23510 |
rs554909752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034958 | ACTAGTCCAGGTGCC[A/G]CTCCGCTCGGGGGTG | 23510 |
rs554948236 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047116 | CCCGCGCGGGTCCCC[A/G]GGCGCTGGTTGGGGG | 23510 |
rs554966687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037881 | GGTGAAACCCCGTCT[C/T]TACTAAAAATAAAAC | 23510 |
rs555035331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052846 | TTGCCGTGAGCCAAG[A/G]TCGCACCACTGAACT | 23510 |
rs555079216 | in-del | -/AATAAC | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048885 | TTTTCTCCCTTTCTT[-/AATAAC]AAACACGCTACAGAA | 23510 |
rs555092550 | snp | A/T | 0.336245 | 0.234652 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044434 | ATGGTCTCGATCTCC[A/T]GACCTCATGATCCAC | 23510 |
rs555159883 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050641 | CCCCTCAAGCATTTA[G/T]CCTTTGTGATACAAA | 23510 |
rs555243147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033634 | TCCTCCAAACCTCAG[C/T]CTTCATACCCCATGG | 23510 |
rs555296996 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035224 | TAATCTTCCCTCCCT[C/T]GTTTTAGACCCAGAA | 23510 |
rs555466733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050142 | AGAAGTAATGGGAAT[A/G]GTACATACAGTGAAT | 23510 |
rs555498324 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037865 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 23510 |
rs555664327 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037626 | TTTCTACCACCATAC[-/T]TTTTTCTTTAAATAC | 23510 |
rs555865746 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063707 | CTCCCGGCTGCCACC[A/G]CATGCAGCTTTGCCT | 23510 |
rs555896115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036993 | CTCTGCTTATGTTAA[C/G]ACTACGCTGATTTCT | 23510 |
rs556010509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055409 | TTCTATGTTAGATTT[C/T]ATATATCAAAGTTTT | 23510 |
rs556034157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046017 | TGCCATGGTTTCAGC[C/T]GGTCTCTCTGTTTGG | 23510 |
rs556047371 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060990 | CATGGGTTGTAAAAC[A/G]TCGCCAAGAGTTTAA | 23510 |
rs556051085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054868 | CCCTCTCTTTCATGC[A/G]ATTAGACTGTTTTAA | 23510 |
rs556137080 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052887 | CGACAGAGTAAGACT[-/C]CGTCTCAAAAAATAA | 23510 |
rs556193177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056544 | TTAGTCTTCTAGATT[C/T]TGAAGGCTTGTGGAT | 23510 |
rs556291970 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034776 | TGGGAGGAATAGGGA[C/T]GGACGAGGGCGGAGG | 23510 |
rs556411850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052865 | CACCACTGAACTCCA[G/T]CCTGGGCGACAGAGT | 23510 |
rs556462150 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064263 | TTGTGTCCACACTTT[C/G]TCTCCGAGCATGTGG | 23510 |
rs556540744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058152 | AACATGGTGAGACTT[C/G]GTCTCTACTAAAAAT | 23510 |
rs556544571 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048611 | GAAGCCAGTTTCTTC[G/T]TGTTCCTTTTACTGT | 23510 |
rs556563636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045779 | AACACAATTATTACA[A/G]GGTCCTGGAACGATA | 23510 |
rs556595559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054318 | GCACCTGGCCTTGAT[C/T]TTGATATTAACTCAG | 23510 |
rs556747028 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056344 | AGACATTTTGGTAAT[C/T]TAGCCTTATCCTCAG | 23510 |
rs556755023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040310 | TTCTGTGTCCCAAGC[A/G]GAAACGAATACGCAT | 23510 |
rs556816290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039722 | TCTAACAGCTTTGTT[A/G]AGGTATATCTGAAAT | 23510 |
rs556868260 | snp | A/G | 1.65048e-05 | 0.00287265 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049287 | TCCTCAACTACCTCC[A/G]CCACGGGAAACTCAT | 23510 |
rs556893098 | snp | A/T | 0.000399281 | 0.0141238 | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75035317 | CAATCAGGCTTTGCA[A/T]CCCGGGACGCTTCCG | 23510 |
rs557017001 | snp | A/C/G/T | 4.95261e-05 | 0.00497604 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042508 | GGCAAGTATGGGGTT[A/C/G/T]CCTCTCAGAAACATA | 23510 |
rs557064077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | KCTD2 | GRCh38.p7 | 17:75059980 | CCAGGGTCAGAACTT[C/T]TTGGTTCTGAATGTC | 23510 |
rs557115457 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059337 | TTTTTAAAGAGAAGG[A/G]AAAAAAAGAAACGCC | 23510 |
rs557157483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041053 | GAGAAATTACAGCTA[A/T]AAGGGACAGTTAAAA | 23510 |
rs557203025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043092 | CCAGCCGTGGTGGCC[C/T]GCGCCATAATCCCAG | 23510 |
rs557218992 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047240 | AGCAGCGGTGGCGGC[G/T]GCGGTCCAAGATGGC | 23510 |
rs557226264 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031067 | GATCGCACCACCACA[C/G]TCCAGCCAGCCTGGG | 23510 |
rs557285010 | in-del | -/T | 0.185155 | 0.241444 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051584 | CCACCATGCCCGACC[-/T]TTTTTTTTTTTAAAT | 23510 |
rs557285359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033892 | GGAAGGGATGGCACG[A/G]CCACGTGCCCCAAGC | 23510 |
rs557346779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033698 | CGGGGCTCCATGGGG[C/T]GTCCCAGTGCCGGGG | 23510 |
rs557409734 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047871 | GAGAACGCACTCCAC[A/G]CCCCTTCTCCATATT | 23510 |
rs557486463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039145 | TTCCTGCCACCAGGT[A/G]AAAGATGTGTGGTCA | 23510 |
rs557490748 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064868 | GGACTTTGGAAGAGG[C/T]GCTCCTTGGCCAGGT | 23510 |
rs557651506 | snp | A/G | 1.67928e-05 | 0.0028976 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063038 | TCAGGAGAGAGGATC[A/G]CGGATGTAAACTAAG | 23510 |
rs557815165 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038660 | ACAGTGAAATACACT[A/G]CCATAGCCCCTAGTG | 23510 |
rs557831541 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042464 | ATTCATATGTAATTC[C/T]TTAATACTGTTTTGT | 23510 |
rs557876643 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044567 | GGATGGGCTGAAACT[C/G]CAGACCTCAGGTGAT | 23510 |
rs557902933 | snp | G/T | | | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038603 | TTTGAAACCAAAGAG[G/T]AAGTTGAAGAGAATC | 23510 |
rs558114524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75061001 | AAACGTCGCCAAGAG[C/T]TTAATGCCCTCCACT | 23510 |
rs558167195 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035380 | GGGCCCCATTTCTTG[C/T]TGTCTCTCTTGAGCT | 23510 |
rs558253101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058714 | TGAGGCGGGAGAATC[G/T]CTTGAACCGGGGAGG | 23510 |
rs558278949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75032840 | AGAGTGCTGGATCCC[A/T]GCAACGGACAAGTTA | 23510 |
rs558290656 | in-del | -/TTT | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034003 | GTTCCTTTTACGGAA[-/TTT]TTTATTTCTTTTCTC | 23510 |
rs558354187 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057148 | TAGTAGAGACAGGGT[A/T]TCCCCATGTTGGCCA | 23510 |
rs558392329 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031867 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 23510 |
rs558403064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050675 | TCAATTACCCTCTTT[C/T]AGTTAAGTATCTTTT | 23510 |
rs558532217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045995 | ATCTTCACAATCCAC[A/G]TTCTTCTGCCATGGT | 23510 |
rs558550341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052519 | CTGAGGTCAGGAGTT[C/G]AAGACCAGCCTGACC | 23510 |
rs558586270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051829 | ACAGCTTATATTGCA[C/G]TTTTGTCAGTTGTCC | 23510 |
rs558672046 | in-del | -/A | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048525 | TCCTGCCCTAACTTT[-/A]AAAGAGATTTCAAAA | 23510 |
rs558787776 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047902 | CTCTGCCCCTGACAT[C/G]CCACTGAGATCTGCA | 23510 |
rs558831398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057114 | GTGCACCACCACGCC[C/T]GGCTAATTTTTGTAT | 23510 |
rs558857000 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047337 | GGGTGGCCCAGTCCG[C/T]GGGCCCCCCAGCCCA | 23510 |
rs558859888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059210 | GTTGCTCAAGCATTC[A/C]TCCCTCTGAAGTTCA | 23510 |
rs558864436 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046555 | CGAAGGGGAAGGGCG[C/T]AGCCCCGCAGCCAGC | 23510 |
rs558903303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034901 | ACGTCAGACGCCTCA[C/T]CCCTTAGGCCACGCG | 23510 |
rs558939854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052899 | ACTCCGTCTCAAAAA[A/G]TAAGTAAATAAATAA | 23510 |
rs558965430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040405 | TCACTAACTCGGAAC[C/G]CTGGACAATTCTTTA | 23510 |
rs558986152 | snp | C/T | 0.00016472 | 0.00907375 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042593 | TTTGGTTCTGGGGTA[C/T]GATCTCTGCAAAAGC | 23510 |
rs559048302 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048841 | GAATGTCCATCTCAA[A/G]CAAAGATTTCAGTTA | 23510 |
rs559061759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035100 | GCCTCTCTAGGAGGT[A/G]GCTGCAGCCGGAGAC | 23510 |
rs559099035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060687 | GGCGGGTCAGGCTGC[A/G]CTCAGGGTCTCGGTC | 23510 |
rs559139257 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052688 | AGATCATGCCATTGC[A/G]CTCCAACCTGGGCAA | 23510 |
rs559149251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035857 | AACAAACAAACAAAC[A/G]AAAAACTCCAGTCCC | 23510 |
rs559243791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039851 | GCCACTGTAGACAAA[A/C]TACATTTTCTAGAGT | 23510 |
rs559347438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060339 | CCACAAGCTGTGGTG[C/T]CCACTGGAAAAATGT | 23510 |
rs559362382 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032410 | GGACACGTTCTGGAA[C/G]TAGGGCGGCGGCAGC | 23510 |
rs559442785 | in-del | -/T | | | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75032663 | GTGAGGTTAGAGCTG[-/T]TAAGATCCAAGACCC | 23510 |
rs559458460 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053662 | TGGTCAGGCTGGTCT[C/T]GAACTCCCGACCTCA | 23510 |
rs559464280 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058963 | ATTAGCCGGGCGTGG[G/T]GGCGGGTGCCTGTAG | 23510 |
rs559532346 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057293 | TTGTAGGTGATTGAT[A/C]CTGGTGCATTTGAGA | 23510 |
rs559638989 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031781 | TTTGTTTGTTTGTTT[G/T]TTTGAGACAGAGTCT | 23510 |
rs559679578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042097 | GGGATCTGGCTGTCA[C/T]GCTGTGTATGTAATT | 23510 |
rs559703370 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047899 | ATTCTCTGCCCCTGA[C/T]ATCCCACTGAGATCT | 23510 |
rs559781106 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064955 | CCAGTCTCGTTGAGG[C/T]GCTTGTCCCTGTCTG | 23510 |
rs559836167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035161 | TCGGATCAGAAGATT[A/G]AGGGTTCGAGTCCCT | 23510 |
rs559902147 | snp | C/T | | | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066196 | TTTTTTTTTTTTTTT[C/T]CCCCGAGATGGAGTC | 23510 |
rs559926956 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045201 | AAAGGGGAGGGAGTA[C/T]ACGAATAGGTGTGGG | 23510 |
rs559971531 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053590 | GGACTACAGGTGTGT[A/G]CCACCACGCCTGACT | 23510 |
rs560028964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033777 | ACCGCGGTATCTTCC[C/T]GCCCGCTCACCAAAA | 23510 |
rs560033321 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050348 | CTCACTGCAACCTCA[A/G]CCTCCTGGGTTCAAG | 23510 |
rs560120280 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033209 | CTGGGCTCAAGCAAT[-/C]CCCCCCACCTCACCC | 23510 |
rs560178840 | snp | A/G | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060330 | ACTAACTTCCCACAA[A/G]CTGTGGTGTCCACTG | 23510 |
rs560227685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056742 | TGTGTGTGGATTTTC[G/T]TTTTGTTTCATTTTG | 23510 |
rs560253578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062023 | TTAAACCTTTGATAA[C/G]TTAAAAGTTCAGTCG | 23510 |
rs560299989 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036941 | TCTTCAACCCGGCCT[C/T]ACTCCTACCAATCAG | 23510 |
rs560336005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055567 | GGCCGGGCGTGGTGG[C/T]TCATGCCTGTAATCC | 23510 |
rs560436833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051190 | ATATTAGCCAGGATG[A/G]TCTCATCTCGATCTC | 23510 |
rs560493197 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043609 | AGAGTGAGACTCTGT[A/C]TCAAAAAAAAAAAAA | 23510 |
rs560673698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055105 | TGTCACCCAGGCAGG[A/G]GTGCAGTGGCATGAT | 23510 |
rs560753903 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038013 | GAGATCGTCCCACTG[C/T]ACTCCAGCCTGGGCG | 23510 |
rs560794148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046771 | GGATCGCGGGGCGAG[A/G]AGCGGCAGCTACACA | 23510 |
rs561055248 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064622 | TATCTGTAGCATAGC[A/G]TAGAACCCGGTATAC | 23510 |
rs561094053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039474 | CCATATGGAAAACCA[C/G]CTTAGGATGGCAGCA | 23510 |
rs561125201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058287 | AGCTGAGATGGTGCC[A/G]TTGCACTCCAGCCTG | 23510 |
rs561148855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034464 | AACCCACAATCCCTG[C/G]CTTAGGAGGCCAGTG | 23510 |
rs561213243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057664 | TCCGGGGTTCAAGCA[C/G]TTCTCCCGCCTCAGC | 23510 |
rs561420469 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75034061 | GACCTTGGTCTCTAG[C/T]TCGACTCCCGTGCAA | 23510 |
rs561526384 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055581 | GCTCATGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 23510 |
rs561610259 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031914 | GGAACTCAGGTGCCC[A/G]CCACACCCAGCTAAT | 23510 |
rs561613974 | snp | C/T | | | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066136 | GGACGGATGGGCTGC[C/T]CACCAGAGAGCTGGA | 23510 |
rs561615612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75061128 | TCTTATTACTGTCCC[A/G]TGGGAAGACGGAGGG | 23510 |
rs561678413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043541 | TCACTTGAACCTGGG[C/T]GGCGGAGGTTGCAGT | 23510 |
rs561742996 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032419 | CTGGAACTAGGGCGG[C/T]GGCAGCAGGGATGGG | 23510 |
rs561913594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053730 | TTACAGGCGTGAGGC[A/G]CTGCGCCCAGCTTGG | 23510 |
rs561954059 | snp | C/G | 5.01073e-05 | 0.00500511 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042687 | TCAAATAAAAACAAG[C/G]CTTTTTTATGAGGTG | 23510 |
rs561965614 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052343 | TGTAATCCCAACACT[A/T]GGAAGGCCAAGGTGG | 23510 |
rs562011294 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055314 | CTTGCCTCAGCCTCC[A/C]AAAGTGCTGGGATTA | 23510 |
rs562043678 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060100 | TTCTCTCCGCCTCGT[A/G]CTTACGACTGAGCTA | 23510 |
rs562132305 | snp | C/T | 0.00107715 | 0.0231822 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059631 | TAACAGAGCAGCAAT[C/T]CCAGGCCCCGTTCAA | 23510 |
rs562167100 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065127 | AGATTCCATAGTTGC[C/T]GCCATGAAAAGACTG | 23510 |
rs562360738 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75048982 | CGCCTAAATGAGTAT[A/C/G]ACTGTCTGTAACACC | 23510 |
rs562365858 | snp | A/C | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041459 | TACCAAAAAAAAAAA[A/C]AAAACAAAACGAAAA | 23510 |
rs562451165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062658 | CTTAAGTTCCTGGAA[A/G]ACTGTTTCTTTTCCC | 23510 |
rs562549086 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040117 | TCTTCGGCATCCACC[C/T]GGGCAGTATATTTAT | 23510 |
rs562609514 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046207 | CCTGCCTCAGCCTCC[C/T]GAGCAGCTGGGATTA | 23510 |
rs562685897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056116 | ACTCTTTTATCCACT[C/T]TATCTCCAGCAGTTT | 23510 |
rs562710420 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046673 | GACTGCACGAGACAC[A/G]GCTTGTGGCAGCGCC | 23510 |
rs562889133 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063861 | TCTTCTTACTCCCCA[G/T]TGACCCTGTCTTCCT | 23510 |
rs562971050 | snp | A/G | 0.336245 | 0.234652 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044361 | CAGGCGCCCGCCACC[A/G]CGCCCGGCTAATTTT | 23510 |
rs563020870 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030973 | AGGCGTGGTGGTGGG[C/T]GCCTGTAGTCCCAGC | 23510 |
rs563041713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050423 | TGCACCACCATGCTT[A/G]ACTAATTTTTTGTAT | 23510 |
rs563094773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033936 | TGGATAAGGCACTGG[C/T]CTCCTAAGCCAGGGA | 23510 |
rs563205778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041260 | CTCGGGGGGATGAGG[C/T]GGGAGGAAGGCTTGA | 23510 |
rs563219492 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038848 | TCAACCACAGAGAAG[A/C]AGCACACCCAGAACT | 23510 |
rs563298064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037146 | TCAGGAGATCGAGAC[C/T]GTCCTGCCTAACACG | 23510 |
rs563373453 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065168 | CCAAGGCACAGGCAC[A/G]TGCTCTGGGAAATAG | 23510 |
rs563437333 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052596 | GGCGTGGTGGCAAGC[A/G]CCTGTAATCCCAGCT | 23510 |
rs563486723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034498 | TATCCATTAGGCCAC[C/T]GGGGCGCGGTAAGAC | 23510 |
rs563492504 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065614 | CCTTTTTCCATGGCA[A/G]TGAGGTGGGGCCCAG | 23510 |
rs563494177 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031755 | CCTATAAACTAGGGG[G/T]GTTTTTTTGTTTTGT | 23510 |
rs563522324 | snp | G/T | 0.00289497 | 0.0379355 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053065 | CCCTTGTGCGGCTGG[G/T]TAAGGAAAGGATACG | 23510 |
rs563552800 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031248 | TACAAAATTTCCTAG[A/T]TCATTCAGTAATTCA | 23510 |
rs563554644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036473 | CGCAAAAATGCTGAA[C/T]AATCCAAGAGGGCAT | 23510 |
rs563556023 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049790 | TTCCCTGTAAATGTT[G/T]GCAGCTGACCTAATT | 23510 |
rs563607657 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058868 | TTTGGGAGGCCGAGG[A/C]GGGTGGATCACGAGG | 23510 |
rs563616116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035776 | AGGCCGAGGTTGCAG[A/T]GAGCCGTGATCGCGC | 23510 |
rs563648146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058384 | TGGCACATGCCTGTA[A/G]TCCCAGCTACTCGGG | 23510 |
rs564016118 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064486 | TGCTTGCCAAGGTAC[A/G]TCTGGGTAGTAGTTT | 23510 |
rs564053950 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059291 | AAAAGCCACAGTATG[C/G]TGGCTTGTGGTCACT | 23510 |
rs564095060 | in-del | -/A/AA/AAAAAA | 0.454302 | 0.144085 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041447 | AAACCTGTCTCTACC[-/A/AA/AAAAAA]AAAAAAAAAAAAAAA | 23510 |
rs564109529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061168 | TGCCTCCCTTCTGGA[A/T]GAGGAAGTTTGTTTC | 23510 |
rs564203559 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036574 | TTATTTAGCACAGGG[A/T]ATCTCCCAAAGGGCT | 23510 |
rs564234947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061918 | CTCATACTCTTCCTC[C/T]TGGGGAGGCCTCACC | 23510 |
rs564263475 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059940 | AGGAGACTGGGATTC[A/G]ACAACAATCCTTCCA | 23510 |
rs564362736 | snp | A/C | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032441 | AGGGATGGGGAGGAA[A/C]TACTGGATGCTGGAG | 23510 |
rs564530332 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044227 | TTTTTGAGACGGAGT[C/T]TCGCTCTGTCGCCCA | 23510 |
rs564840117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057623 | GGAGTGCAATGGCGC[A/G]ATCTCAGCTCGCTGC | 23510 |
rs564859013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052665 | CAGGCGGAGTTTGCA[G/T]TGAGCCAAGATCATG | 23510 |
rs564863011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046272 | TATTTTTAGTAGAGG[A/C]GGGGTTTCACTACGT | 23510 |
rs564932907 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035081 | TTTAATGGCCATCAA[A/T]TTGGCCTCTCTAGGA | 23510 |
rs564948226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052234 | GGTCATGGGTTTACC[A/G]AAAATAGCAAAGAGA | 23510 |
rs564965245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058241 | CTGAAGCAGGAGAAT[C/T]GCTTGAACTCGGGAG | 23510 |
rs565067096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044696 | AAAAATACAGAAAAC[A/G]ACTACAGCCACTTAA | 23510 |
rs565092130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041180 | TCTGGGCAACATGGC[A/G]AAACCCCGTCTCTAC | 23510 |
rs565139532 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039396 | AGAAACTGTGGTTAC[C/G]CTGAGTGGGGGCGCT | 23510 |
rs565205644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046736 | CCCCTGACCCCGCGC[A/G]CCAAGGAGGGCTGAG | 23510 |
rs565281208 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065836 | TTTGAATAGTCTGAA[A/T]TGCTGTGACTTTTTT | 23510 |
rs565325506 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065204 | AGTGGTATTTCCGCC[C/T]TCTCGGAGGGCTGGT | 23510 |
rs565344358 | snp | C/T | 3.30437e-05 | 0.00406457 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038946 | TTTATAAATTCTCAA[C/T]TGGTTGGTGAGGCCA | 23510 |
rs565404599 | snp | G/T | 3.34504e-05 | 0.00408951 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040035 | TTAACTTAGCTATAA[G/T]AGAGAGCTGTCAAGA | 23510 |
rs565483275 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033996 | GGTGAAAGTTCCTTT[C/T]ACGGAATTTTTTATT | 23510 |
rs565510813 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062875 | CACCAGAAGCACTGC[A/G]GGTGAGGCTGCGGCT | 23510 |
rs565527938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059224 | CATCCCTCTGAAGTT[C/G]AGAATTATTTTACCT | 23510 |
rs565548039 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039493 | AGGATGGCAGCACCC[A/G]GCTGCTTCTGCAAGT | 23510 |
rs565553456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034447 | ACCCCAGGTGGGACT[C/G]GAACCCACAATCCCT | 23510 |
rs565799306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052521 | GAGGTCAGGAGTTCA[A/G]GACCAGCCTGACCAA | 23510 |
rs565816750 | snp | A/T | 0.000399281 | 0.0141238 | splice-acceptor-variant | KCTD2 | GRCh38.p7 | 17:75035230 | TCCCTCCCTTGTTTT[A/T]GACCCAGAAACGCCT | 23510 |
rs565879335 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048448 | CAGAGCTGGAGTTGC[A/G]TAAACATTTGTTGTT | 23510 |
rs566006185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040881 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 23510 |
rs566008011 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047732 | CCCTCCCACACTACT[C/T]GCAGGGGCCTCAGAG | 23510 |
rs566041708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052818 | AGAATCATTTGAACG[C/T]AGGAGGCGGAGGTTG | 23510 |
rs566181240 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064133 | TAGGCAGTCTGGGGA[A/C]CCCCTGTGTCTCTGA | 23510 |
rs566322713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050554 | AGGCCTGAGCCTCCG[C/T]GCCCGACCTGAGATG | 23510 |
rs566339336 | snp | A/C | 1.64817e-05 | 0.00287064 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039078 | TCTGGAAAGAGGGGG[A/C]ATGTGTTTAGTTAAT | 23510 |
rs566464032 | snp | A/G | 0.336017 | 0.234736 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044412 | GGGTTTCACCTTGTT[A/G]GCCAGGATGGTCTCG | 23510 |
rs566542553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062337 | TGCTCCTCACTTCTT[C/G]CCTGGCCTTCTAGAG | 23510 |
rs566566205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055379 | TTTTAAAAGTAAAAA[A/G]TAATGCCTTGGTCTT | 23510 |
rs566670853 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057841 | GCTGGGATTATAGGC[A/G]TGAGTCACTGCACCC | 23510 |
rs566826511 | in-del | -/A | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056372 | AGTTTCCCACATTCT[-/A]AAAAAAATGATTGCT | 23510 |
rs566835390 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035115 | AGCTGCAGCCGGAGA[C/G]CGCGTGGCCTAATGG | 23510 |
rs566870325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036982 | CCCAGGCTCTCCTCT[C/G]CTTATGTTAAGACTA | 23510 |
rs567039238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75032739 | GGCAAGGCTGAGCCC[C/G]GGGCGGGCGGGTTGG | 23510 |
rs567066024 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048022 | GCTTTCTCAGACTCC[C/T]TCTCGGACCCCTCTG | 23510 |
rs567101402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037531 | GTAAATGAGAAAATT[A/T]AATTCTCAAGACAGT | 23510 |
rs567188217 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066131 | AGGTGGGACGGATGG[A/G]CTGCCCACCAGAGAG | 23510 |
rs567200934 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032108 | TCATAGGGTTATTGT[A/G]GGATTTCAGTGAATA | 23510 |
rs567277890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034687 | GGTGACGACGCGCGG[A/G]GACCAGGAGCCCGCG | 23510 |
rs567340610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040266 | AAGGGCTGGAAGCTA[C/T]GAATCCTTAAAGGTC | 23510 |
rs567351443 | snp | C/G/T | 5.04599e-05 | 0.00502273 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062297 | TGCTTGTTCGCACCC[C/G/T]CTCCGTGGGCTTTTC | 23510 |
rs567461317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058565 | AGCACTTTGGGAGAC[C/T]AGGGCAGGTGGATCA | 23510 |
rs567498541 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064229 | GGCAGCACCCTCTTT[C/T]GGGCTGCATCCACAG | 23510 |
rs567587449 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063648 | GAGGATGGGGTGTCC[G/T]TTGTTGTGGTTGGAG | 23510 |
rs567612776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035094 | AAATTGGCCTCTCTA[A/G]GAGGTAGCTGCAGCC | 23510 |
rs567644801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056498 | TGGAGAGCATTATAA[A/G]ATTTCTGTTTGATGA | 23510 |
rs567703692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033862 | TCTAGGAAAAGGGGA[C/T]ACTCGCTTATGAGGG | 23510 |
rs567714565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060448 | AAAAAGTCCTCTAAC[A/G]TAAGCCTTCCAAGGT | 23510 |
rs567855819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045644 | TTCTGCCCGGCTCAC[C/T]GGCGGTCAGAGTTTA | 23510 |
rs567944651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041870 | GTGACCTCCCAGGAG[C/T]GGGGGACCACCAGGT | 23510 |
rs568021517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054700 | TAGTCCCAGCTGCTC[A/G]GGAGGCTGAAGCAGG | 23510 |
rs568142271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049867 | GTGGTTTGTAGGGCA[C/T]TGGGACTATAAGTGG | 23510 |
rs568239931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043019 | CTGAGGTCAGGAGTT[C/G]GAGACCAGCATGGCC | 23510 |
rs568322468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035904 | GGGGGTGCTGCCCAA[C/T]TCTGTGGCCTCAGTC | 23510 |
rs568387068 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75035284 | CCCGGGATCCGAAGC[C/T]GGGGAGCTGCTTCTG | 23510 |
rs568418535 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047191 | GGCCCGGCTCTCCCT[G/T]CCGAGAAATGGGCCG | 23510 |
rs568446539 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041637 | GTCTCAAAAGAAAAA[A/G]GACAGGAAAAGAGTA | 23510 |
rs568467517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052848 | GCCGTGAGCCAAGAT[C/T]GCACCACTGAACTCC | 23510 |
rs568508913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053298 | AAACAGAATAGGCCT[A/G]TGTCCCAATAGAATG | 23510 |
rs568546902 | snp | C/T | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060105 | TCCGCCTCGTGCTTA[C/T]GACTGAGCTATCAAA | 23510 |
rs568568805 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031030 | GGTGTGAACCCAGGA[A/G]GCAGAGCTTGCAGTG | 23510 |
rs568573403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059084 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 23510 |
rs568829023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051220 | CCTGACCTTGTGATC[C/T]GCCTGCCTCAGCCTC | 23510 |
rs568905672 | snp | A/G | | | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066335 | CAGGCGCCTGCCTGC[A/G]CGCCTGGCTAATTTT | 23510 |
rs568981342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056283 | AGTCTCTTTGCTATC[C/T]TACCTTTACGTGGTA | 23510 |
rs569084466 | in-del | -/A | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041064 | CTATAAGGGACAGTT[-/A]AAAAAAAGCAGAGGC | 23510 |
rs569245227 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061186 | GGAAGTTTGTTTCAG[A/G]CAGGCGGAGGCGCCC | 23510 |
rs569280725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038055 | CTCCATCTTAAAAAA[A/T]AATAATAAAATAAAA | 23510 |
rs569282558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75032777 | TGCCTAGCTAGAGGG[C/T]GGCAGCAGGAAAGCA | 23510 |
rs569423387 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058185 | AAAACTTAGCCAAGC[A/G]TGGTGGTGGGCGGCT | 23510 |
rs569470111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055819 | CCTGGGCAACAGGAG[C/T]GAAACTCCCATCTAA | 23510 |
rs569511318 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064274 | CTTTCTCTCCGAGCA[C/T]GTGGGTCTCGCTGAG | 23510 |
rs569554169 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051035 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 23510 |
rs569591657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060992 | TGGGTTGTAAAACGT[C/T]GCCAAGAGTTTAATG | 23510 |
rs569672467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035217 | GCAACTATAATCTTC[C/T]CTCCCTTGTTTTAGA | 23510 |
rs569750758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057079 | CCTGCCTCAGCTTCC[C/T]GAGTAGCTAGATTAC | 23510 |
rs569761291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040737 | CTAAAAATACAAAAA[C/T]TAGCTGTGCAAGGTG | 23510 |
rs569864586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053332 | AGATTGTCGCTGCTT[A/G]CCAGATGGCGGGAGG | 23510 |
rs569867603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059171 | GACTTGGGGAAATGG[A/T]TTAAATCTAAGTTTG | 23510 |
rs569900130 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75038197 | ACGATCTTGGCTCAC[C/T]GCAACCTCTGCCTCC | 23510 |
rs569949370 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031001 | AGCTACTTGGGAGGC[C/T]GAGGTGGGAGAATGG | 23510 |
rs570022754 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052460 | GTGCGGTGGCTTTAC[G/T]CCTGTAATCCCAGAA | 23510 |
rs570043548 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048262 | GGGCAGGATGCATGG[C/T]TGCTAACCAAAGGGT | 23510 |
rs570064491 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063488 | GTTAGCAGCTGCTTC[A/G]GAACACCGTCCCTCC | 23510 |
rs570075297 | snp | G/T | 0.000100423 | 0.00708531 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062980 | ATCTCTGTCTTTCCC[G/T]CAGCAGCCTCAGCCT | 23510 |
rs570113281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055345 | CAGGCATGAGGCACC[A/G]TGCCTGGCATAAGTT | 23510 |
rs570141651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040321 | AAGCGGAAACGAATA[C/T]GCATCTCAATACTGG | 23510 |
rs570150526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054747 | AGGAGGCGGAGCTTG[C/T]AGTGAGCCAAGATCG | 23510 |
rs570223652 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75046948 | ACCCTGGCTGCCCAC[A/G]GTCCTCCGCAGCAAG | 23510 |
rs570386390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050505 | TAACCTCAAGTGATC[C/T]ACCTGCCTCAGCCTC | 23510 |
rs570387047 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060713 | CGGTCGCCGCCACTC[A/G]CCACCCTGGGATCAA | 23510 |
rs570425522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049986 | ATCTGGGAGCTTTGG[C/T]TCTGAGTAAGAAAGC | 23510 |
rs570443364 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052734 | GTTTCGGGCGGGGGG[A/G]AAAAATAGAAACAGC | 23510 |
rs570544122 | snp | A/G | 0.336017 | 0.234736 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044396 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCTTGTT | 23510 |
rs570549825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060507 | AACCAGACAACAGCG[C/T]GACAGCCAAGACCAG | 23510 |
rs570660154 | in-del | -/AGA | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034719 | TGCCCTGTAACCCCG[-/AGA]AGAAGTGCTCGGCGA | 23510 |
rs570717381 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032029 | AACCTCACAAAGTGC[G/T]GGGATTACAGGTGTG | 23510 |
rs570764045 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034747 | GGCGAGCGCAGAGGC[C/T]GGTGGAGCATAGCTG | 23510 |
rs570814184 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042111 | ATGCTGTGTATGTAA[G/T]TATCCCTGTTCCTGC | 23510 |
rs570912000 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048342 | TTCTTTTTAACTTTA[C/T]GTATTCACCTTTAAG | 23510 |
rs570973220 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047897 | ATATTCTCTGCCCCT[C/G]ACATCCCACTGAGAT | 23510 |
rs571087228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042830 | AGGTTGCAGTGAGTC[A/G]AGACTGCATCACTGC | 23510 |
rs571289329 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045338 | AAGTTTTGGGCACCA[C/T]TGTCATTGATAACAT | 23510 |
rs571455358 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063557 | CTAGCTGCAGTTTGT[C/T]GAATTGAGGTTTTAG | 23510 |
rs571478887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034315 | GAGGGTCCTGCAAGA[A/G]AAGGCGAGGGGCGCA | 23510 |
rs571605547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061562 | GGCTGACGTGGGAGG[A/T]TCACTTGAGACCAGG | 23510 |
rs571676784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038152 | TAGAGGCAAAGTCTC[A/G]CTCTGTCACTCAGGC | 23510 |
rs571811354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056869 | AAGATGTGGGCCTCA[A/G]CCCTACCTTCGGTTT | 23510 |
rs571825430 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064316 | TGCGGTAGAGCCAGG[A/G]GACCCTGTCTGCCCC | 23510 |
rs571877089 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062098 | TGCCACATGAATGTT[C/T]ACTGTATTCTTGGTT | 23510 |
rs572036008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058731 | TTGAACCGGGGAGGC[A/G]GAGTTGCAGTGAGCT | 23510 |
rs572062987 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058251 | AGAATCGCTTGAACT[C/G]GGGAGGCGGAGATTG | 23510 |
rs572156254 | snp | A/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048675 | AGTCCTGGCAGTACC[A/G]AGCTTCCTCTGGGCA | 23510 |
rs572209882 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051863 | TAATGGCCTTTATAG[A/C]AAATTTATTCCTATA | 23510 |
rs572261784 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063953 | GTGGGGAAGGCTGTT[G/T]CTTTGAAAGTTGCCA | 23510 |
rs572268249 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041803 | CCCAAGAGTTCTGGG[C/G]TGTAGCGCGTTATGC | 23510 |
rs572327287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041192 | GGCGAAACCCCGTCT[C/G]TACCAAAAATACAAA | 23510 |
rs572347822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039908 | ACTCTTCTTTTTCTT[G/T]TTGGCTTCTTTCACT | 23510 |
rs572502642 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044015 | GCAGCACCAGCACAC[G/T]TTGTGCACTTTTTTT | 23510 |
rs572562092 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043334 | CCAGCTCTCTTGGCC[A/G]GGCGCAGTGGCTCAT | 23510 |
rs572834531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037835 | CGGGCGGATCACAAG[G/T]TCAGGAGATCGAGAC | 23510 |
rs572855986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049480 | AAACTACCAGTCTTG[C/T]CTGAGGGAGTCATGA | 23510 |
rs572944121 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036214 | GTGAGCCACTGGGCC[C/T]GGCCAGGGAATGGAG | 23510 |
rs573024490 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033059 | CACAATGGTAACCGA[A/C]GCTGCCCTTGGCTGA | 23510 |
rs573168018 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031689 | GGGTCAGCTCCCATC[C/T]GTCCACCTCCCCCAG | 23510 |
rs573171699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053782 | CTTTAGCATGTGATC[A/G]AGTCACATGCAGCTC | 23510 |
rs573231503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036313 | TTTTTAGTATAGACG[A/G]GGTTTCACCGTGTTA | 23510 |
rs573316479 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065013 | GGGCTGGAGCTCCTA[C/G]ACCAACCCCAGCTTT | 23510 |
rs573323929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035433 | TCCAAACATTCGCCT[C/T]GTAAACGTGCTCTAC | 23510 |
rs573508362 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060586 | CAAAGAGCAGCTGGC[C/T]GGCGCCGGCCTCCCC | 23510 |
rs573573317 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043194 | TCAGTGCACCCTAGC[C/T]TGGGCAACACAGCAA | 23510 |
rs573634475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041249 | GGTCCCAGTTACTCG[A/G]GGGGATGAGGTGGGA | 23510 |
rs573649573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034404 | TGCCGGCACCAAAAG[A/G]AACCTTGCGAGCACA | 23510 |
rs573655743 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051627 | GTCCTTCATTCTCTA[-/T]TTCCCCCTCCCTACC | 23510 |
rs573689219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033924 | CCAGTGGCCTAATGG[A/C]TAAGGCACTGGCCTC | 23510 |
rs573723630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062593 | AACTGTGCTTTTTTC[A/G]CTGCCTCAGGAGAAA | 23510 |
rs573736225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046045 | TGGGGTCCCTGATTT[C/T]CCGCAACATCAGTGG | 23510 |
rs573774227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052583 | AAAAAATTAGCCAGG[C/T]GTGGTGGCAAGCGCC | 23510 |
rs573913461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058048 | AAAAAAATTGGCTGG[G/T]CACAGTGGCTCATGC | 23510 |
rs573944559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050879 | TCAGAGTCTATCTTA[C/T]CTTGCCCAGGCTGGT | 23510 |
rs574004029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057279 | TAGAATAGTATTTTT[G/T]GTAGGTGATTGATCC | 23510 |
rs574114590 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049928 | GGTCCCACTGAAGGC[A/G]TTCAGTTGTAAAGGG | 23510 |
rs574129314 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053431 | AGAGGTCTTGGTTGC[A/G]CCCGTTGGCCGCTCT | 23510 |
rs574214326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059314 | TGGTCACTTAAAAAG[A/G]AAAACATTTTTTAAA | 23510 |
rs574227442 | in-del | -/AAAC | 0.00359137 | 0.0422231 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035840 | CGTCTCAAAACAAAC[-/AAAC]AAACAAACAAACAAA | 23510 |
rs574278619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039206 | GCTACCCATCATCCT[C/T]ACCTCTTTCTCATAT | 23510 |
rs574280169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051269 | AGACATGAGCCACCG[C/T]GCCCGACCTTTTTTT | 23510 |
rs574290942 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037812 | CCCAGCACTTTGGGA[A/G]GCTGAGGCGGGCGGA | 23510 |
rs574341865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045005 | AAACATCAGTGTATC[A/G]GGGAACTTGCCCCGA | 23510 |
rs574341868 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038733 | GCGCCTACACAGCCC[A/G]TCAGACAACCAGCCC | 23510 |
rs574405676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044602 | CCACCTCAGCCTTGC[A/G]AAGTGCTGGAATTAC | 23510 |
rs574484496 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035033 | CAACAGGCGGCCAGG[C/G/T]TGCGAGCAGTGAAGC | 23510 |
rs574498540 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054079 | TTGGAGTGCAGTGGC[A/G]TGATCACAGCTCACT | 23510 |
rs574510297 | snp | A/G | | | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75035352 | TGGCGTCATTATGCA[A/G]CCAGGGTAAGTAGGG | 23510 |
rs574600761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042440 | TATGTTGTCATAAGG[A/G]CATCAAGAATTCATA | 23510 |
rs574650354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058820 | AATAATAAATAGGCC[A/G]GGCGCGGTGGCTCAT | 23510 |
rs574661451 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048572 | AATTATTTTTATCTA[C/T]TCTATATCCTCCTTG | 23510 |
rs574676992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036436 | CAATTACCTTTTTAA[G/T]GTAAAATTAATGCAT | 23510 |
rs574737269 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064441 | CTGGGCACCTTCAGA[A/G]GTGATGTCCTGTGTG | 23510 |
rs574738178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035716 | GCGCCTGTAAACCCA[C/G]CTACTCAGGAGGCGG | 23510 |
rs574802918 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041820 | GTAGCGCGTTATGCC[G/T]ATCGGGTGTCTTCAC | 23510 |
rs574827273 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035109 | GGAGGTAGCTGCAGC[A/C/T]GGAGACCGCGTGGCC | 23510 |
rs574884688 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038530 | ACCTAGCCATTTGGA[C/T]CAGCTGTTCTTGTGA | 23510 |
rs574892366 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064870 | ACTTTGGAAGAGGCG[C/T]TCCTTGGCCAGGTCC | 23510 |
rs574895250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046670 | GCGGACTGCACGAGA[C/T]ACGGCTTGTGGCAGC | 23510 |
rs574948377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037905 | ATAAAACAAATTAGC[C/T]GGGCGTGATGGCGGG | 23510 |
rs575056145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056117 | CTCTTTTATCCACTT[C/T]ATCTCCAGCAGTTTG | 23510 |
rs575090034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037528 | TTTGTAAATGAGAAA[A/C]TTAAATTCTCAAGAC | 23510 |
rs575167162 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062689 | TCCACTGTGCACCCC[C/G]CTCACCCCCAACACA | 23510 |
rs575214392 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056671 | AAATGGATTTGATGT[C/T]ATTCAAAGACACCCT | 23510 |
rs575261109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044222 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 23510 |
rs575439543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037918 | GCCGGGCGTGATGGC[A/G]GGCACCTGTAGTCCG | 23510 |
rs575598607 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066269 | CTCACTGCAACCTCT[G/T]CCTCCCATGTTCAAG | 23510 |
rs575671413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060633 | TTCATGGCTGGGCGC[A/G]TGGCGAGTGGGCCCG | 23510 |
rs575680843 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065532 | ATGCCAGCCAGGCCC[A/G]GGAGTGCCCAGCATC | 23510 |
rs575756679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060151 | TTGGAGCTTCACTGT[C/T]CTCCTCCATTAGATG | 23510 |
rs575829023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049546 | GGGTGAGAAGGAAGA[C/T]AGGTAGCTCCGCTTT | 23510 |
rs575836243 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031735 | TCTGAACCTTAGTTT[A/C]CCCACCTATAAACTA | 23510 |
rs575928197 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056784 | ATTTTTTTGTGTGTG[A/G]ATTTTCAAACATGTT | 23510 |
rs576041284 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063391 | AGCTCCTTGGAAATG[A/G]CCTGTACTTTAAGGA | 23510 |
rs576068890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058153 | ACATGGTGAGACTTC[A/G]TCTCTACTAAAAATA | 23510 |
rs576137176 | in-del | -/AAACAAAC | 0.0019984 | 0.0315469 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035833 | GCGAAAGCCGTCTCA[-/AAACAAAC]AAACAAACAAACAAA | 23510 |
rs576235180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034828 | TGCTGGGATTCGGGC[A/G]AGGGCTGCTCGCTCC | 23510 |
rs576283437 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046020 | CATGGTTTCAGCCGG[-/TC]TCTCTGTTTGGGGTC | 23510 |
rs576340440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052888 | GACAGAGTAAGACTC[C/T]GTCTCAAAAAATAAG | 23510 |
rs576428446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052622 | CAGCTACTTGGAAGG[C/G]TGAGGCAGCAGAATC | 23510 |
rs576467415 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048716 | GTGTGTGAGATTACA[A/G]CTGGCAGTGCAAACT | 23510 |
rs576554935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054337 | ATATTAACTCAGATA[C/T]AGTAACAAGAGCGAA | 23510 |
rs576642755 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033410 | ATCTAGTATATATAT[A/T]TTTCTACTATTACAA | 23510 |
rs576689077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045961 | GTATTAATTTGGGGA[A/G]CTAATAAATGTCCAT | 23510 |
rs576817490 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057151 | TAGAGACAGGGTATC[C/G]CCATGTTGGCCACAC | 23510 |
rs577102070 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032363 | GTAGGAAAGTGTGCA[C/T]GGCTGGCAACTGACC | 23510 |
rs577142908 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031095 | GGGTGACACAGTGAG[A/G]CTCCGTCTCAAAAAT | 23510 |
rs577156282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035368 | CCAGGGTAAGTAGGG[A/C]CCCATTTCTTGTTGT | 23510 |
rs577162164 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051604 | TTTTTTTAAATCATA[C/T]TTGCATTGTCCTTCA | 23510 |
rs577220566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041747 | AAAGCCCCCTGGGGC[A/G]TGGTGGCGCATGCCT | 23510 |
rs577327377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | KCTD2 | GRCh38.p7 | 17:75059982 | AGGGTCAGAACTTTT[C/T]GGTTCTGAATGTCTT | 23510 |
rs577405012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051403 | GATTTTCCTGCCTCA[A/G]CCTCCTGAGTACCTG | 23510 |
rs577461554 | in-del | -/GGAAATTTAATACTGATGCTTTTATCT | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051787 | CAGTTATCAAACTCA[-/GGAAATTTAATACTGATGCTTTTATCT]ACAGCTTATATTGCA | 23510 |
rs577469631 | in-del | -/AGAC | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065182 | CGTGCTCTGGGAAAT[-/AGAC]AGGAGTGGTATTTCC | 23510 |
rs577480511 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064948 | CTTGTGCCCAGTCTC[A/G]TTGAGGCGCTTGTCC | 23510 |
rs577555771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033893 | GAAGGGATGGCACGG[C/T]CACGTGCCCCAAGCC | 23510 |
rs577557918 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040793 | TGGGAGGCTGAGGCA[A/G]GAGAACTGCTTGAAC | 23510 |
rs577650238 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059686 | CAGTGTGGATGGCCA[A/G]TTAATAACCACGGGA | 23510 |
rs577701642 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038699 | TGCCATTTCAGCAGT[C/G]CTGGGGCCTCAGTAA | 23510 |
rs577788994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056642 | ATCTGTCCTTTTTAT[G/T]TAGTGAAACTGAAAA | 23510 |
rs577793689 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063101 | TCAGCAGAGCCCCTC[C/T]GTGAAGTGAAACCTC | 23510 |
rs577815218 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75038028 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 23510 |
rs577874357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062427 | TACGGAGCACTGACA[A/G]GTGTTTTTAGTTAGA | 23510 |
rs577946088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055477 | TCCCAGCACTCTGGG[A/G]GGCTGAGGAGGGCAG | 23510 |
rs578058598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060669 | GGAGGGCGCGCGTGC[A/G]AGGGCGGGTCAGGCT | 23510 |
rs578217661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044573 | GCTGAAACTCCAGAC[C/T]TCAGGTGATCCACCC | 23510 |
rs578240196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044291 | GCTCACTGCAAACTC[C/T]GCTTCCCGGGTTCAC | 23510 |
rs578240658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050718 | ATTAAAAAAACTTTA[C/T]TTTGAAGTAATTTAA | 23510 |
rs745437240 | snp | C/T | 3.44127e-05 | 0.00414791 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049354 | TGTTTGCATTGGGGA[C/T]TTTCAAAATGCAAGT | 23510 |
rs745452010 | snp | A/C/G | 3.29491e-05 | 0.00405877 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039248 | GGCCTTTGAGAGAGA[A/C/G]ACCCACTCAGCACAA | 23510 |
rs745464284 | snp | C/G | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060535 | CAGCTGCTCTTGATG[C/G]CCTTTTCACTTCTGT | 23510 |
rs745578066 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052655 | TTGAACCCAGCAGGC[A/G]GAGTTTGCAGTGAGC | 23510 |
rs745611418 | snp | C/T | 1.6507e-05 | 0.00287284 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042226 | CTTGGCCACATTGGC[C/T]TTGTAGTAAGCCCAG | 23510 |
rs745653532 | in-del | -/T | 1.64762e-05 | 0.00287016 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040084 | AGCAGGAGCCTCAAC[-/T]TACTTACATCTTCTT | 23510 |
rs745666457 | snp | A/C | 1.65056e-05 | 0.00287272 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042510 | CAAGTATGGGGTTCC[A/C]TCTCAGAAACATACT | 23510 |
rs745874398 | in-del | -/C | 1.67315e-05 | 0.00289231 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062987 | TCTTTCCCTCAGCAG[-/C]CTCAGCCTCTCCCCC | 23510 |
rs745900066 | snp | A/C | 6.10321e-05 | 0.00552379 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047473 | GCGGCCCGCTGGGTC[A/C]GGCTGAACGTGGGAG | 23510 |
rs745946222 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055411 | CTATGTTAGATTTCA[C/T]ATATCAAAGTTTTCT | 23510 |
rs745954094 | snp | G/T | 3.2993e-05 | 0.00406145 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038972 | GGCCAATAGGGATAC[G/T]TTTTCTTGTCTAATT | 23510 |
rs746164124 | snp | A/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048769 | TCAGGAGCATTGCCA[A/G]CTACACAGAGGTTTT | 23510 |
rs746181312 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035181 | TTCGAGTCCCTTCGT[A/G]GTCGGAACGTTTTAA | 23510 |
rs746420911 | snp | C/T | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060073 | GAAGTGTGGTGCGGC[C/T]GTTTCCCCTACTTCT | 23510 |
rs746443842 | snp | C/G | | | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038729 | AGTGGCGCCTACACA[C/G]CCCGTCAGACAACCA | 23510 |
rs746476235 | snp | A/G | 1.77256e-05 | 0.00297699 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039991 | TTCCTTTATATGGCT[A/G]TTAACTCTTCCATTT | 23510 |
rs746529154 | snp | C/T | 4.94303e-05 | 0.00497119 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040081 | AATAAGCAGGAGCCT[C/T]AACTACTTACATCTT | 23510 |
rs746635593 | snp | G/T | 0.000201707 | 0.0100406 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049376 | AATGCAAGTAGAATC[G/T]TTAAAGTTGTTTTAC | 23510 |
rs746706267 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042816 | AACCCAGGAGGTGGA[A/G]GTTGCAGTGAGTCGA | 23510 |
rs746707929 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050638 | CATCCCCTCAAGCAT[G/T]TATCCTTTGTGATAC | 23510 |
rs746722852 | in-del | -/CTT | 1.65999e-05 | 0.00288091 | cds-indel, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042181 | GGTGTGAAGTCTCAC[-/CTT]CTTCTCAAAGTCATC | 23510 |
rs746742064 | in-del | -/C | 3.39772e-05 | 0.00412158 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063066 | AAGACCCCGAAAACT[-/C]CAGACCTTCAGGAGA | 23510 |
rs746743881 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034026 | TTCTTTTCTCTTCCC[C/T]TCTCAGGGATGCTGG | 23510 |
rs746947469 | snp | C/T | 1.64882e-05 | 0.00287121 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042524 | CCTCTCAGAAACATA[C/T]TGACCTGGAGGTGAG | 23510 |
rs746986507 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042403 | CTCCTAAGATCATCA[C/T]GAAAATGCAAGGATT | 23510 |
rs747024163 | snp | C/G | 1.64827e-05 | 0.00287073 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039101 | TAGTTAATGTAAACA[C/G]AGACGGAAAGCAGAA | 23510 |
rs747050476 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037850 | GTCAGGAGATCGAGA[C/T]CATCCTGGCTAACAT | 23510 |
rs747099083 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064996 | GCATGCCTGATCAGC[A/G]TGGGCTGGAGCTCCT | 23510 |
rs747106362 | snp | A/C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035169 | GAAGATTGAGGGTTC[A/C/G]AGTCCCTTCGTGGTC | 23510 |
rs747232473 | snp | A/T | 6.59718e-05 | 0.00574296 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038987 | TTTTTCTTGTCTAAT[A/T]TGGTTTCTGGGAAAG | 23510 |
rs747232585 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048035 | CCCTCTCGGACCCCT[C/T]TGCCAAGTTGGGCTT | 23510 |
rs747233566 | snp | A/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048405 | ACCATCTTATATCCC[A/G]TATAGCACTCAGCTG | 23510 |
rs747320911 | snp | A/C | | | intron-variant, missense | KCTD2 | GRCh38.p7 | 17:75060006 | ATGTCTTATGTAATC[A/C]ACCGTGAAGAGCTTG | 23510 |
rs747385741 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046517 | GCCCTGAACGCTCTA[C/T]ACGTTCGAATCCTGG | 23510 |
rs747475094 | snp | C/T | 1.85475e-05 | 0.00304523 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047492 | TGAACGTGGGAGGCA[C/T]CTACTTCGTGACCAC | 23510 |
rs747492021 | in-del | -/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057574 | TTTTTTTTTTTTTTT[-/C]CTCGAGGCAGAGTCT | 23510 |
rs747532368 | snp | A/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031084 | CCAGCCAGCCTGGGT[A/G]ACACAGTGAGACTCC | 23510 |
rs747614206 | snp | A/G | 0.000117573 | 0.00766633 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040031 | TAACTTAACTTAGCT[A/G]TAATAGAGAGCTGTC | 23510 |
rs747640765 | snp | A/C | 1.64779e-05 | 0.00287031 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040158 | GGGAACCTTCAGCGC[A/C]TTAAACTACAAACAC | 23510 |
rs747727755 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049089 | CAAAATTTGCCATCA[C/G]TAAAGTCTTTTTTAG | 23510 |
rs747765218 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040106 | CATCTTCTTTTTCTT[C/T]GGCATCCACCTGGGC | 23510 |
rs747782619 | snp | C/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045099 | GAAATTTTAAAGCTG[C/G]GCGTCCGGGGGAGAC | 23510 |
rs747801741 | snp | A/G | 1.77379e-05 | 0.00297802 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053142 | AGGAGGGTTGTTTCA[A/G]GTGGGCTTCTGTCGG | 23510 |
rs747857577 | snp | A/G | 4.97228e-05 | 0.00498587 | utr-variant-3-prime, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038928 | CTTCCTCCTGGACTC[A/G]ATTTTATAAATTCTC | 23510 |
rs747885588 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061698 | GTAGCTGATCAGTGA[C/T]TGGCTCGGTGCTTTC | 23510 |
rs747948016 | snp | C/G | 1.65045e-05 | 0.00287263 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053079 | GTTAAGGAAAGGATA[C/G]GGGACAATGAGAACA | 23510 |
rs747954394 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75032989 | CAGAAAAGAATGTCC[C/T]CAAGTCTCCTTTGCC | 23510 |
rs747966137 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041757 | GGGGCGTGGTGGCGC[A/G]TGCCTGGCTGAGGCA | 23510 |
rs748092199 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034478 | GGCTTAGGAGGCCAG[C/T]GCCTTATCCATTAGG | 23510 |
rs748107403 | snp | C/T | 1.65061e-05 | 0.00287277 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059571 | AGCTCACGCAGATGG[C/T]GTCCACGATGTCCGA | 23510 |
rs748129589 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053997 | CATAATATCAAGCTG[C/T]TCTTTATGATGGTGT | 23510 |
rs748192529 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034652 | CGGCGTCCCCACCGG[A/G]CTACACAAGAGCTCC | 23510 |
rs748223396 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064097 | CCTCTGTACTGTCCC[C/T]AGTGGTATGTATGTA | 23510 |
rs748293657 | snp | A/T | 1.64749e-05 | 0.00287005 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039199 | GGCAACGGCTACCCA[A/T]CATCCTTACCTCTTT | 23510 |
rs748354097 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051080 | CCAGGTTCACGTCAT[A/T]CTCCTGCCTCAGCCT | 23510 |
rs748566338 | snp | A/G | | | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038601 | GGTTTGAAACCAAAG[A/G]GGAAGTTGAAGAGAA | 23510 |
rs748586465 | snp | G/T | 3.65758e-05 | 0.00427628 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047633 | GGCCTTCGAACCCCC[G/T]GGTTTCTCGTAGATC | 23510 |
rs748688534 | in-del | -/TCATT | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037485 | ACTTCCCAGGTTATC[-/TCATT]TAATTCTCATTACAA | 23510 |
rs748693634 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037599 | CAGGTCCTCTGACTT[C/T]AAGGACAATTCTTTC | 23510 |
rs748735120 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061467 | CCTGGGCAACATAGC[A/G]AGACCCCCCTTCTCT | 23510 |
rs748836239 | snp | A/C | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060189 | TGTTAAATTCTGTTG[A/C]CTTCAAAACATAGGA | 23510 |
rs748883449 | snp | C/G | 2.27918e-05 | 0.0033757 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047597 | CAGACAAGGTGTGCC[C/G]CGCCCTCGGGCGCGC | 23510 |
rs748925886 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032480 | GGACAGAAAATTGGC[C/T]TGGGTAGTGTGGGAG | 23510 |
rs749032087 | snp | C/T | 1.79654e-05 | 0.00299706 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059472 | TGCAAACTGTGGTGT[C/T]CTTGGTGCTGTTCTC | 23510 |
rs749057036 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053652 | TTCACCATGTTGGTC[A/T]GGCTGGTCTCGAACT | 23510 |
rs749104132 | snp | A/G | 3.29495e-05 | 0.00405877 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040177 | AACTACAAACACAAG[A/G]GCACGGGAACCTTCA | 23510 |
rs749305952 | snp | C/T | 0.00016472 | 0.00907375 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042578 | AACTAGCAATGGCCT[C/T]TTGGTTCTGGGGTAT | 23510 |
rs749338930 | in-del | -/CTACCCATCATCCTTACCTCTTT | 0.000181206 | 0.00951683 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039192 | TATTATAGGCAACGG[-/CTACCCATCATCCTTACCTCTTT]CTCATATTCTACAAT | 23510 |
rs749434067 | snp | G/T | 1.67142e-05 | 0.00289081 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042690 | AATAAAAACAAGGCT[G/T]TTTTATGAGGTGAAT | 23510 |
rs749449907 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053112 | ACTTCACAAGTAATG[C/T]ATTTGGAACTGTTAA | 23510 |
rs749501271 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053905 | AGAGTCTCACTCTCT[C/T]CCCCAGGCTGGCCTC | 23510 |
rs749620539 | snp | C/T | 3.29495e-05 | 0.00405877 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039217 | TCCTTACCTCTTTCT[C/T]ATATTCTACAATCCT | 23510 |
rs749673678 | snp | C/T | 3.30289e-05 | 0.00406366 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039312 | TCTGAAACCAGGCTG[C/T]ATTCTACCCCAGCAG | 23510 |
rs749677365 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036380 | CTCACCTCGGCCTCC[C/T]GAAGTGTTGTGATTA | 23510 |
rs749723660 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042370 | TTCCTATGGCCTGGA[A/G]GGTCACCACACTTTC | 23510 |
rs749725456 | snp | G/T | 8.28192e-05 | 0.00643449 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047640 | GAACCCCCTGGTTTC[G/T]CGTAGATCGGTCCCC | 23510 |
rs749835626 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048896 | TCTTAATAACAAACA[C/T]GCTACAGAAGAATGT | 23510 |
rs749874986 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051989 | TCCTATTAAGTTTGG[C/T]CCACATAAATTTGTA | 23510 |
rs749886691 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055018 | AATCTATTGCAGCAC[A/G]GAATTTTCCTGCCAT | 23510 |
rs749890262 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041541 | CTAAGACAGAAGGAT[A/G]GCTTGAGCTTGGGAG | 23510 |
rs750071882 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053370 | CAGGGCACTTTAGGT[C/G]TAAAACCTGTTCTCT | 23510 |
rs750143990 | snp | G/T | 1.9368e-05 | 0.00311185 | upstream-variant-2KB, synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047412 | CGCCGTCGCGCAGCC[G/T]CTGGAGCCGGGTCCC | 23510 |
rs750146973 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048365 | CCTTTAAGTTCTCAA[C/T]TTAAAGGCACTGACC | 23510 |
rs750174734 | snp | G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039502 | GCACCCGGCTGCTTC[G/T]GCAAGTTCCTCATCC | 23510 |
rs750193573 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035108 | AGGAGGTAGCTGCAG[C/T]CGGAGACCGCGTGGC | 23510 |
rs750242757 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062206 | AGAACTAAATAATTC[C/T]ACCAATGGCATCGTC | 23510 |
rs750312438 | snp | A/G | 1.6486e-05 | 0.00287102 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039285 | ACCTTTAAGAAGAAA[A/G]AGAAATTCAGTTCTG | 23510 |
rs750456662 | snp | C/T | 4.9561e-05 | 0.00497775 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059587 | GTCCACGATGTCCGA[C/T]GGCTGGAAATTCGAA | 23510 |
rs750695898 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037394 | GTCACAAGTCTCCCC[G/T]GCGTAGACCATGCAG | 23510 |
rs750712497 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063401 | AAATGGCCTGTACTT[C/T]AAGGACGCTGGAGCC | 23510 |
rs750714779 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049838 | TCAGGTGTATCATTA[C/T]TTGCCTCATCTTTGT | 23510 |
rs750760328 | snp | C/G | 1.65285e-05 | 0.00287471 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040052 | GAGAGCTGTCAAGAT[C/G]AAGAGAATTTTAGAA | 23510 |
rs750770837 | snp | C/G | 1.64765e-05 | 0.00287019 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040149 | CTCTGGCACGGGAAC[C/G]TTCAGCGCATTAAAC | 23510 |
rs750908946 | snp | C/T | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053058 | ATCGCGTCCCTTGTG[C/T]GGCTGGTTAAGGAAA | 23510 |
rs751014824 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034423 | CTTGCGAGCACAGCC[C/T]CTCTCGACACCCCAG | 23510 |
rs751078885 | snp | A/G | 1.72068e-05 | 0.00293311 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053130 | TTGGAACTGTTAAGG[A/G]GGGTTGTTTCAAGTG | 23510 |
rs751144005 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064496 | GGTACGTCTGGGTAG[C/T]AGTTTCTGGAAATGA | 23510 |
rs751211993 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035153 | GTCTGACTTCGGATC[A/G]GAAGATTGAGGGTTC | 23510 |
rs751275161 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034520 | CGGTAAGACGCTAAA[C/T]CCACGTGCTCCTTGA | 23510 |
rs751291608 | snp | G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045043 | ATAGGTTCTTTTCTA[G/T]TTTCCTAAGCGTCGA | 23510 |
rs751332842 | snp | C/G | 3.35306e-05 | 0.00409441 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062294 | GCTTGCTTGTTCGCA[C/G]CCCCTCCGTGGGCTT | 23510 |
rs751371804 | snp | A/G | 0.00019757 | 0.0099371 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047428 | CTGGAGCCGGGTCCC[A/G]GACCACCCGAGCGGG | 23510 |
rs751394200 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057704 | AGCTGGGATTACAGG[C/T]ACGTGCCACCTCACC | 23510 |
rs751433744 | snp | A/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062223 | CCAATGGCATCGTCA[A/T]AGAGCCGAGCGAAAA | 23510 |
rs751484690 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053671 | TGGTCTCGAACTCCC[A/G]ACCTCAGGTGATCTG | 23510 |
rs751508407 | in-del | -/A | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033481 | ATAAGCAAGATTTTC[-/A]GTGTTTATGTTTCAA | 23510 |
rs751591600 | snp | C/G | 1.65083e-05 | 0.00287296 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049294 | CTACCTCCGCCACGG[C/G]AAACTCATCATCACT | 23510 |
rs751612036 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062038 | CTTAAAAGTTCAGTC[A/G]GAAGAGGGGTGATTT | 23510 |
rs751621842 | snp | A/C | 3.34275e-05 | 0.00408811 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047628 | CCCCGGGCCTTCGAA[A/C]CCCCTGGTTTCTCGT | 23510 |
rs751675154 | snp | A/C | 4.94575e-05 | 0.00497259 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039195 | TATAGGCAACGGCTA[A/C]CCATCATCCTTACCT | 23510 |
rs751678915 | snp | C/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048661 | GCTGCTCAGAGCCAA[C/G]TCCTGGCAGTACCGA | 23510 |
rs751823957 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033106 | CCTTCGGATGTGAGT[A/C]GACTTTTATTTAATA | 23510 |
rs751846836 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061307 | CCTGCGTGTGTATTT[C/T]CTCTTTAGAATTAAA | 23510 |
rs751878822 | snp | A/G | 0.000304095 | 0.012327 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042150 | CACAGGCATGTTACA[A/G]GCTCAGTGCTTTAGA | 23510 |
rs751916277 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041906 | AAGAAGGGGTGAACC[A/G]GCCCAGGTCAGAAAC | 23510 |
rs751976224 | in-del | -/CTC | | | cds-indel, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064391 | GGGCTCTGGGGACTT[-/CTC]CTTCTATGAAAGCCT | 23510 |
rs752034912 | snp | C/T | 1.65935e-05 | 0.00288036 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059526 | GCCCCGTGAAGCACG[C/T]GTACAGAGTCCTGCA | 23510 |
rs752111254 | snp | A/C | 1.6546e-05 | 0.00287624 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059536 | GCACGTGTACAGAGT[A/C]CTGCAGTGTCAGGAA | 23510 |
rs752152162 | snp | G/T | 1.67837e-05 | 0.00289682 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042162 | ACAAGCTCAGTGCTT[G/T]AGAGGTGTGAAGTCT | 23510 |
rs752207938 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034516 | GGCGCGGTAAGACGC[C/T]AAACCCACGTGCTCC | 23510 |
rs752237528 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063646 | GGGAGGATGGGGTGT[C/T]CTTTGTTGTGGTTGG | 23510 |
rs752265375 | snp | C/T | 0.000100078 | 0.00707313 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059615 | GAACAGGTACATCTC[C/T]TAACAGAGCAGCAAT | 23510 |
rs752289142 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039181 | GAGAGAACCCATATT[A/G]TAGGCAACGGCTACC | 23510 |
rs752321048 | snp | A/C | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044968 | AGTTACCAGGGAACC[A/C]AGCACCCTTACAGAC | 23510 |
rs752429600 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75046932 | CCACTCACCTTCACC[G/T]ACCCTGGCTGCCCAC | 23510 |
rs752431187 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056494 | TTCCTGGAGAGCATT[A/G]TAAGATTTCTGTTTG | 23510 |
rs752449544 | snp | A/G | 1.81207e-05 | 0.00300999 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047534 | TAGGCCGGGAGCCCA[A/G]GTCATTTCTCTGCCG | 23510 |
rs752596248 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053817 | GAGCCACTTGAAACC[A/G]GTCTCATGGGGTACG | 23510 |
rs752599745 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035184 | GAGTCCCTTCGTGGT[C/G]GGAACGTTTTAATCC | 23510 |
rs752600867 | snp | A/G | 3.429e-05 | 0.00414051 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063081 | CCAGACCTTCAGGAG[A/G]GCAGTCAGCAGAGCC | 23510 |
rs752606879 | snp | C/T | 3.25759e-05 | 0.0040357 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047454 | GCGGGCAGGGGGCGG[C/T]GGCGCGGCCCGCTGG | 23510 |
rs752657197 | snp | A/G | | | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060699 | TGCACTCAGGGTCTC[A/G]GTCGCCGCCACTCGC | 23510 |
rs752764856 | snp | G/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047858 | CACCTGCACCCACGA[G/T]AACGCACTCCACACC | 23510 |
rs752783118 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053032 | TGCTGGAGGAAGCGG[A/G]GTTTTACAACATCGC | 23510 |
rs752836537 | snp | A/G | 8.44131e-05 | 0.00649611 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040028 | CTCTAACTTAACTTA[A/G]CTATAATAGAGAGCT | 23510 |
rs752888890 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031849 | GGGTCACTGCAACCT[C/T]CGCCTCCTGGGTTCA | 23510 |
rs752935269 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031999 | ACTCCTGACCTCAAG[C/T]GATCAGTCTGCCTCA | 23510 |
rs752936968 | snp | G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039782 | CATTTGATAAGTTTT[G/T]ATATAGGTATCCACC | 23510 |
rs752942777 | snp | A/G | 1.65814e-05 | 0.00287931 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049318 | CATCACTAAGGAGTT[A/G]GCAGAAGAAGGTAAG | 23510 |
rs752969906 | in-del | -/ACCT | 1.64811e-05 | 0.00287059 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052980 | CTGGCAAACCCTCGC[-/ACCT]ACCTATCTGACTGCA | 23510 |
rs752977010 | snp | C/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030810 | GCATGCATACTAAAA[C/G]TGGAATGCCAGGCAC | 23510 |
rs752992424 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065661 | TTTGTTTCTGCACAG[G/T]TGTAACTGCTCTTGG | 23510 |
rs753033450 | in-del | -/T | 0.00712204 | 0.0592478 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036046 | GAGAATAAATGCTAA[-/T]TTTTTTTTTCTTTTT | 23510 |
rs753294042 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064442 | TGGGCACCTTCAGAA[A/G]TGATGTCCTGTGTGC | 23510 |
rs753309178 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042062 | CCTTTGGCCATACGC[A/G]TCCTTCCTAAGCTTC | 23510 |
rs753332473 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033293 | GTAGCCTTTAATAAT[A/G]GATTTTAAATGTGTG | 23510 |
rs753403665 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042630 | GTCAATGGTTTTTAG[A/G]GCAAGTTTTCGCCCA | 23510 |
rs753470778 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055243 | TATTTTTAGTAGAGA[C/T]GGTGTTTCGCCATAT | 23510 |
rs753625031 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058863 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 23510 |
rs753649163 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036530 | CCACGTGCCTTTAGC[C/T]GAGCCTGTTCCCAGT | 23510 |
rs753707325 | snp | C/T | 0.000121899 | 0.00780607 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047621 | GGCGCGCCCCCGGGC[C/T]TTCGAACCCCCTGGT | 23510 |
rs753763650 | snp | A/T | 1.64814e-05 | 0.00287061 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039080 | TGGAAAGAGGGGGAA[A/T]GTGTTTAGTTAATGT | 23510 |
rs753789149 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035775 | GAGGCCGAGGTTGCA[A/G]TGAGCCGTGATCGCG | 23510 |
rs753822175 | snp | A/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030596 | GGATTTTAGAGGCAC[A/G]AACAGTAAGTTGGAA | 23510 |
rs753892254 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048508 | CAGATTGATGGAAAC[C/T]TATCCTGCCCTAACT | 23510 |
rs753976531 | in-del | -/GCTC | 1.6513e-05 | 0.00287336 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062249 | AAAAGGCGAAGGTAA[-/GCTC]GGAGCCCCTTCCCTG | 23510 |
rs753978768 | snp | C/T | 3.35295e-05 | 0.00409434 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062969 | CATCCCCCGACATCT[C/T]TGTCTTTCCCTCAGC | 23510 |
rs754036751 | snp | A/C | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039646 | GCCTTCAGTGCTTTC[A/C]AGCAAATAATTAGGT | 23510 |
rs754101499 | snp | A/G | 1.6638e-05 | 0.00288422 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040041 | TAGCTATAATAGAGA[A/G]CTGTCAAGATCAAGA | 23510 |
rs754182203 | snp | A/T | 3.36627e-05 | 0.00410246 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049337 | GAAGAAGGTAAGCGC[A/T]CTGTTTGCATTGGGG | 23510 |
rs754248954 | in-del | -/AT | | | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066176 | GGGGAGGAGTGTGAG[-/AT]TTTTTTTTTTTTTTT | 23510 |
rs754426332 | snp | G/T | 9.94893e-05 | 0.00705229 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062282 | CAGTTGCCTCTGGCT[G/T]GCTTGTTCGCACCCC | 23510 |
rs754440386 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033914 | GCCCCAAGCCCCAGT[A/G]GCCTAATGGATAAGG | 23510 |
rs754453242 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033909 | CACGTGCCCCAAGCC[A/C]CAGTGGCCTAATGGA | 23510 |
rs754519788 | snp | A/G | 4.94328e-05 | 0.00497131 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040156 | ACGGGAACCTTCAGC[A/G]CATTAAACTACAAAC | 23510 |
rs754617252 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042107 | TGTCATGCTGTGTAT[A/G]TAATTATCCCTGTTC | 23510 |
rs754718742 | in-del | -/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050160 | CATACAGTGAATTCC[-/T]TTGCATCCACTATCC | 23510 |
rs754722394 | snp | C/T | 0.000106028 | 0.00728029 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047435 | CGGGTCCCGGACCAC[C/T]CGAGCGGGCAGGGGG | 23510 |
rs754742506 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055251 | GTAGAGATGGTGTTT[C/T]GCCATATTGACCAGG | 23510 |
rs754864922 | snp | A/C | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062229 | GCATCGTCATAGAGC[A/C]GAGCGAAAAGGCGAA | 23510 |
rs754879076 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053718 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGGCACTG | 23510 |
rs755055591 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046118 | GACGGAGTCTCGCAC[C/T]GTCGCCTGGGCTGGA | 23510 |
rs755133151 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039287 | CTTTAAGAAGAAAGA[A/G]AAATTCAGTTCTGAA | 23510 |
rs755181489 | snp | C/G | 3.42542e-05 | 0.00413835 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047629 | CCCGGGCCTTCGAAC[C/G]CCCTGGTTTCTCGTA | 23510 |
rs755212224 | in-del | -/A | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061316 | GTATTTCCTCTTTAG[-/A]ATTAAATTCTGAATT | 23510 |
rs755303689 | snp | C/G | | | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038411 | GCCTCCCAAAATGCT[C/G]GGATTACAGGCGTGA | 23510 |
rs755438661 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050301 | CTTTTTTTTTTCTTC[A/G]CTCAGGCTGGAGTGC | 23510 |
rs755474534 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063530 | CAAGACGTGCAGCAG[A/G]TGCAAAGGGTTCTAG | 23510 |
rs755493665 | snp | C/G | 1.68929e-05 | 0.00290623 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042152 | CAGGCATGTTACAAG[C/G]TCAGTGCTTTAGAGG | 23510 |
rs755560156 | in-del | -/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044199 | CAGCTAATTTTTGTA[-/T]TTTTTTTTTTTTTTT | 23510 |
rs755628833 | snp | G/T | 1.65343e-05 | 0.00287521 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042488 | GTTTTGTTTCTAGAT[G/T]CAGTGGCAAGTATGG | 23510 |
rs755682846 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042036 | TATTTACAGTTCAAT[C/T]GACCACAAGGCCTTT | 23510 |
rs755797949 | snp | C/T | 1.65427e-05 | 0.00287595 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059537 | CACGTGTACAGAGTC[C/T]TGCAGTGTCAGGAAG | 23510 |
rs755800646 | snp | A/C | 1.64819e-05 | 0.00287066 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039072 | TCTCCATCTGGAAAG[A/C]GGGGGAATGTGTTTA | 23510 |
rs755919136 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065538 | GCCAGGCCCAGGAGT[A/G]CCCAGCATCCCCCAA | 23510 |
rs756031659 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034575 | ACACGGCCCTGCTGT[A/G]GGTCACCGCGCTCCA | 23510 |
rs756039865 | in-del | -/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035198 | TCGGAACGTTTTAAT[-/C]CCTGCAACTATAATC | 23510 |
rs756097781 | snp | A/G | 1.65236e-05 | 0.00287429 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038945 | TTTTATAAATTCTCA[A/G]TTGGTTGGTGAGGCC | 23510 |
rs756197972 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056871 | GATGTGGGCCTCAAC[A/C]CTACCTTCGGTTTCA | 23510 |
rs756329376 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052941 | TTAGCAAGCATGTAA[C/T]CTTCATCCTCTCCTT | 23510 |
rs756550281 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040614 | GTGTTAGCCGGGTGC[A/G]GTGGCTCATGCCTGT | 23510 |
rs756581780 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039202 | AACGGCTACCCATCA[C/T]CCTTACCTCTTTCTC | 23510 |
rs756585463 | snp | A/G | 1.6617e-05 | 0.00288239 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049324 | TAAGGAGTTGGCAGA[A/G]GAAGGTAAGCGCACT | 23510 |
rs756880381 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063910 | GGACCAAAGATGAAG[G/T]CACTTATGGACCCTT | 23510 |
rs757019710 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045056 | TATTTTCCTAAGCGT[C/T]GACTGGCTTGACAGA | 23510 |
rs757114306 | snp | C/G | 1.65165e-05 | 0.00287367 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059546 | AGAGTCCTGCAGTGT[C/G]AGGAAGAAGAGCTCA | 23510 |
rs757180655 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043338 | CTCTCTTGGCCGGGC[A/G]CAGTGGCTCATTTCT | 23510 |
rs757278265 | in-del | -/C | 1.65138e-05 | 0.00287343 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039316 | AAACCAGGCTGCATT[-/C]TACCCCAGCAGCTGC | 23510 |
rs757325882 | snp | C/T | 1.67525e-05 | 0.00289413 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062978 | ACATCTCTGTCTTTC[C/T]CTCAGCAGCCTCAGC | 23510 |
rs757338851 | in-del | -/C | 1.66884e-05 | 0.00288858 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062291 | TGGCTTGCTTGTTCG[-/C]CACCCCCTCCGTGGG | 23510 |
rs757358043 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036978 | TGCACCCAGGCTCTC[C/T]TCTGCTTATGTTAAG | 23510 |
rs757366994 | snp | C/G | 2.25096e-05 | 0.00335474 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047466 | CGGCGGCGCGGCCCG[C/G]TGGGTCAGGCTGAAC | 23510 |
rs757378166 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048673 | CAAGTCCTGGCAGTA[C/T]CGAGCTTCCTCTGGG | 23510 |
rs757422682 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035974 | ACCCCACTACTCTGT[A/G]CTTGGAGGAAGAGGG | 23510 |
rs757474225 | snp | C/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044368 | CCGCCACCGCGCCCG[C/G]CTAATTTTTTGTATT | 23510 |
rs757538052 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061334 | TAAATTCTGAATTCT[A/G]TTATCCAAAAAGGTT | 23510 |
rs757632761 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064627 | TAGCATAGCATAGAA[-/C]CCCGGTATACAGGGG | 23510 |
rs757652491 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031110 | ACTCCGTCTCAAAAA[C/T]AAAATAAAATAAAAT | 23510 |
rs757660850 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044728 | AAAAAAGTCAGAATA[C/T]AGGAAAATAGTCCTC | 23510 |
rs757685789 | snp | C/G | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042529 | CAGAAACATACTGAC[C/G]TGGAGGTGAGGGTCT | 23510 |
rs757690780 | snp | A/G | 0.000160704 | 0.00896249 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039971 | TTGCATTTATTGACA[A/G]GTCATTCCTTTATAT | 23510 |
rs757691854 | snp | A/C | 1.66283e-05 | 0.00288338 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040042 | AGCTATAATAGAGAG[A/C]TGTCAAGATCAAGAG | 23510 |
rs757706235 | snp | A/G | | | intron-variant, synonymous-codon | KCTD2 | GRCh38.p7 | 17:75060010 | CTTATGTAATCCACC[A/G]TGAAGAGCTTGGTGA | 23510 |
rs757718075 | snp | C/T | 1.69415e-05 | 0.00291041 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049342 | AGGTAAGCGCACTGT[C/T]TGCATTGGGGATTTT | 23510 |
rs757881759 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032338 | CTGCCCACGACAGAA[C/T]GAGGAGACTGTAGGA | 23510 |
rs758044712 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063697 | GGATTTGGGGCTCCC[A/G]GCTGCCACCACATGC | 23510 |
rs758154364 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043178 | ATGAGCTGAGATGGC[A/G]TCAGTGCACCCTAGC | 23510 |
rs758264870 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055386 | AGTAAAAAATAATGC[C/T]TTGGTCTTTCTATGT | 23510 |
rs758322292 | snp | C/G | 1.65614e-05 | 0.00287757 | utr-variant-5-prime, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042656 | GCCCAGCCATTTTGG[C/G]ATCCTGAAAAATAAG | 23510 |
rs758358261 | snp | C/T | 1.72148e-05 | 0.00293379 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059655 | CGTTCAAGGGGTCTG[C/T]AGCTCTTCAAACAAT | 23510 |
rs758522700 | snp | A/C | 4.94425e-05 | 0.0049718 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039087 | AGGGGGAATGTGTTT[A/C]GTTAATGTAAACAGA | 23510 |
rs758557061 | snp | A/C/T | 6.31517e-05 | 0.00561895 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047624 | GCGCCCCCGGGCCTT[A/C/T]GAACCCCCTGGTTTC | 23510 |
rs758760900 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030893 | ACGTGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 23510 |
rs758800791 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039827 | TCCCCTCTCAACCAT[C/T]CCCAGGCAGCCACTG | 23510 |
rs758820951 | in-del | -/C | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044992 | ACAGACTTTCCCAAA[-/C]CATCAGTGTATCGGG | 23510 |
rs758837010 | in-del | -/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052350 | CCAACACTTGGAAGG[-/C]CAAGGTGGGCGGATC | 23510 |
rs758854590 | snp | A/G | 8.243e-05 | 0.00641936 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040067 | CAAGAGAATTTTAGA[A/G]TAAGCAGGAGCCTCA | 23510 |
rs758879814 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042381 | TGGAGGGTCACCACA[C/T]TTTCCTCTCCTAAGA | 23510 |
rs758884290 | snp | A/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046704 | TACATCAGCGGCGCC[A/T]GGGACACAGCCGGGC | 23510 |
rs758893541 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052412 | CCAACATGGCAAAAC[C/G]CCGTCTCTGCGAAAA | 23510 |
rs758910833 | snp | C/T | 1.64757e-05 | 0.00287012 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039177 | GAAAGAGAGAACCCA[C/T]ATTATAGGCAACGGC | 23510 |
rs759078271 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044914 | GCCTGTTTCCTGTTG[C/T]GGAGGGGAGGTGTTA | 23510 |
rs759090280 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035174 | TTGAGGGTTCGAGTC[C/T]CTTCGTGGTCGGAAC | 23510 |
rs759142093 | snp | C/T | 1.67449e-05 | 0.00289347 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047601 | CAAGGTGTGCCCCGC[C/T]CTCGGGCGCGCCCCC | 23510 |
rs759145164 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056305 | TACGTGGTATCTTTC[A/G]CTATTGTAGATATTT | 23510 |
rs759264615 | snp | A/T | 1.64811e-05 | 0.00287059 | stop-gained, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039044 | TGATCAAATGGAATT[A/T]AGTTCTTCATCTTCT | 23510 |
rs759315013 | snp | C/T | 5.07962e-05 | 0.0050394 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063058 | TGTAAACTAAGACCC[C/T]GAAAACTCCAGACCT | 23510 |
rs759407287 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036831 | TTACGCACATTAAAG[A/G]CCTTGCACAGCTACC | 23510 |
rs759424042 | snp | A/G | 1.80654e-05 | 0.00300539 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047529 | GACCTTAGGCCGGGA[A/G]CCCAAGTCATTTCTC | 23510 |
rs759467100 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062874 | GCACCAGAAGCACTG[C/T]GGGTGAGGCTGCGGC | 23510 |
rs759517568 | snp | A/C | 4.94254e-05 | 0.00497094 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040187 | ACAAGGGCACGGGAA[A/C]CTTCAGCGCATTAAA | 23510 |
rs759594962 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041809 | AGTTCTGGGCTGTAG[C/T]GCGTTATGCCGATCG | 23510 |
rs759681150 | snp | A/G | 3.31219e-05 | 0.00406938 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049315 | CATCATCACTAAGGA[A/G]TTGGCAGAAGAAGGT | 23510 |
rs759820505 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043868 | TGCTTGCCCCAGAGG[A/G]CTGCTAAAAGTGTCA | 23510 |
rs759872606 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064281 | TCCGAGCATGTGGGT[C/G]TCGCTGAGCAGTCAT | 23510 |
rs759910183 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065137 | GTTGCCGCCATGAAA[A/T]GACTGCTCTTGAGCC | 23510 |
rs759950428 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042594 | TTGGTTCTGGGGTAT[A/G]ATCTCTGCAAAAGCT | 23510 |
rs759958305 | in-del | -/T | 1.68052e-05 | 0.00289867 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049208 | AATGATACCCTTGTG[-/T]TTGGTTGGCAGGATG | 23510 |
rs760048047 | in-del | -/TCA | | | cds-indel, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049299 | TCCGCCACGGGAAAC[-/TCA]TCATCACTAAGGAGT | 23510 |
rs760072331 | snp | A/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031924 | TGCCCGCCACACCCA[A/G]CTAATTTTTGTATTT | 23510 |
rs760122800 | snp | A/C/T | 3.3298e-05 | 0.00408021 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059610 | AATTCGAACAGGTAC[A/C/T]TCTCTTAACAGAGCA | 23510 |
rs760135285 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034509 | CCACTGGGGCGCGGT[A/G]AGACGCTAAACCCAC | 23510 |
rs760272077 | snp | A/G | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062129 | CATCAGCTCATCAGC[A/G]TCGGATCTTCCTATA | 23510 |
rs760291646 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036650 | GGGGCTCAGCGGTGC[C/T]CTCCTTGAACAGCGC | 23510 |
rs760365779 | in-del | -/CC | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044503 | AGCCACCGCGCCCGG[-/CC]CTAATTTTTGTATTT | 23510 |
rs760396294 | snp | C/T | 2.75782e-05 | 0.00371327 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047615 | CCCTCGGGCGCGCCC[C/T]CGGGCCTTCGAACCC | 23510 |
rs760513418 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035499 | GTTATGTTTCAGTCT[A/G]TCGTTATGAAGTTAA | 23510 |
rs760522887 | snp | C/T | 1.68863e-05 | 0.00290566 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049203 | TCCACAATGATACCC[C/T]TGTGTTTGGTTGGCA | 23510 |
rs760542171 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049187 | AAATACTCCTCAAAG[A/G]TCCACAATGATACCC | 23510 |
rs760553279 | snp | A/C | | | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040142 | ATTTATCCTCTGGCA[A/C]GGGAACCTTCAGCGC | 23510 |
rs760556467 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061838 | TGTGCTCGACGGGGC[A/G]TGGGCATGTTAATCC | 23510 |
rs760558450 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048399 | ACTCACACCATCTTA[C/T]ATCCCATATAGCACT | 23510 |
rs760652840 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058690 | TGTAATCCCAGCTAT[G/T]CGGGAGGCTGAGGCG | 23510 |
rs760698134 | snp | A/G | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060602 | GGCGCCGGCCTCCCC[A/G]CTCTGGCTCGCCAGG | 23510 |
rs760749877 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052072 | TATCAAGTTCAGGAG[A/G]TGTCCAACATGACTA | 23510 |
rs760769344 | snp | C/G | 6.62899e-05 | 0.00575678 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053093 | ACGGGACAATGAGAA[C/G]AGAACTTCACAAGTA | 23510 |
rs760839517 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051085 | TTCACGTCATTCTCC[G/T]GCCTCAGCCTCCCGA | 23510 |
rs760839886 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064165 | CACCCCCCTGACCCC[C/T]GCCATTACTTTCTTT | 23510 |
rs760937375 | in-del | -/CC | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041445 | AAAAACCTGTCTCTA[-/CC]CCAAAAAAAAAAAAA | 23510 |
rs761012190 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033897 | GGATGGCACGGCCAC[A/G]TGCCCCAAGCCCCAG | 23510 |
rs761035012 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057233 | TGCTGGGATTACAGG[C/T]GTGAGCAACCATACC | 23510 |
rs761040863 | in-del | -/AC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062702 | CCCCTCACCCCCAAC[-/AC]ACACACACACACACA | 23510 |
rs761107023 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034427 | CGAGCACAGCCCCTC[G/T]CGACACCCCAGGTGG | 23510 |
rs761152163 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033896 | GGGATGGCACGGCCA[C/T]GTGCCCCAAGCCCCA | 23510 |
rs761167354 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054604 | AGGTCAGGAGATCGA[C/G]ACCATCCTGGCTAAC | 23510 |
rs761264837 | in-del | -/CGGGCGCGCCCC | 2.3988e-05 | 0.00346315 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047604 | GGTGTGCCCCGCCCT[-/CGGGCGCGCCCC]CGGGCCTTCGAACCC | 23510 |
rs761277428 | snp | A/G | 3.29549e-05 | 0.00405911 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042618 | AAAAGCTACCCAGTC[A/G]ATGGTTTTTAGAGCA | 23510 |
rs761290171 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065446 | CCAGTGACCCACACT[A/C]TCTGCTGCCCAGTAC | 23510 |
rs761315254 | snp | C/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042866 | AGCCTGGGAGACACA[C/G]CAAGACTCCAACTCA | 23510 |
rs761346256 | snp | C/T | 0.000232149 | 0.0107713 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062280 | GGCAGTTGCCTCTGG[C/T]TTGCTTGTTCGCACC | 23510 |
rs761356262 | in-del | -/AAAC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035833 | GCGAAAGCCGTCTCA[-/AAAC]AAACAAACAAACAAA | 23510 |
rs761357305 | snp | C/G | | | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066386 | TATTTTGCTGTGTTG[C/G]CCAGGCTGGTCTCGA | 23510 |
rs761421326 | snp | C/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048270 | TGCATGGCTGCTAAC[C/G]AAAGGGTTGAGAGGT | 23510 |
rs761424258 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065051 | GGTTCAGCAAGGAGG[-/C]CTGGGGGTCAGACAC | 23510 |
rs761469308 | snp | A/G | 2.26493e-05 | 0.00336513 | upstream-variant-2KB, synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047406 | GGCTGCCGCCGTCGC[A/G]CAGCCGCTGGAGCCG | 23510 |
rs761540914 | snp | A/G | 1.64811e-05 | 0.00287059 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039277 | AAGATTTCACCTTTA[A/G]GAAGAAAGAGAAATT | 23510 |
rs761665654 | snp | C/T | 1.73685e-05 | 0.00294685 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040009 | AACTCTTCCATTTAA[C/T]TCACTCTAACTTAAC | 23510 |
rs761682347 | snp | C/T | 1.73996e-05 | 0.00294949 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059494 | GCTGTTCTCAGTCTG[C/T]GCCTGGTCATTGCAG | 23510 |
rs761691109 | snp | C/T | 1.65051e-05 | 0.00287267 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049286 | ATCCTCAACTACCTC[C/T]GCCACGGGAAACTCA | 23510 |
rs761793547 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039409 | ACCCTGAGTGGGGGC[A/G]CTCACTCTGACAGGC | 23510 |
rs761821991 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034415 | AAAGAAACCTTGCGA[A/G]CACAGCCCCTCTCGA | 23510 |
rs761862946 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049159 | TGGTGAAATCCTGCC[C/G]TGCCTTTGTTTAAAA | 23510 |
rs761898764 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040211 | CATTAAACTACAAAC[A/G]CAAGGACAGTGAGTC | 23510 |
rs761930990 | snp | A/C | 1.71935e-05 | 0.00293197 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063084 | GACCTTCAGGAGAGC[A/C]GTCAGCAGAGCCCCT | 23510 |
rs761973103 | snp | A/G | 4.94254e-05 | 0.00497094 | intron-variant, synonymous-codon | ATP5H, KCTD2 | GRCh38.p7 | 17:75040143 | TTTATCCTCTGGCAC[A/G]GGAACCTTCAGCGCA | 23510 |
rs761984402 | snp | C/T | 3.29484e-05 | 0.00405871 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062074 | GCACTTTCGAAAGTA[C/T]GTTAAGATTGCCACA | 23510 |
rs762038335 | snp | C/G | 0.000247327 | 0.0111177 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039010 | TGGGAAAGCTTCATT[C/G]AAGTCCTCAATGGTC | 23510 |
rs762102722 | snp | G/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031297 | CCAGGCACTCACAGC[G/T]TGGGGTGGGGAGGAG | 23510 |
rs762129274 | snp | G/T | 6.91659e-05 | 0.00588032 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059495 | CTGTTCTCAGTCTGC[G/T]CCTGGTCATTGCAGG | 23510 |
rs762134651 | snp | C/T | 1.67925e-05 | 0.00289758 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053110 | GAACTTCACAAGTAA[C/T]GTATTTGGAACTGTT | 23510 |
rs762255709 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042792 | GCAAGTCTTCACAAG[A/G]ATCACTTGAACCCAG | 23510 |
rs762277910 | snp | C/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041917 | AACCGGCCCAGGTCA[C/G]AAACAGAGCAGGTCA | 23510 |
rs762278012 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055876 | TGTCTACTAAAAATA[C/T]GAAAATTGTCTGAGT | 23510 |
rs762298308 | snp | C/G/T | 3.60876e-05 | 0.00424767 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047517 | GACCACCAGACAGAC[C/G/T]TTAGGCCGGGAGCCC | 23510 |
rs762361932 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054929 | AGGCAGAGTCGTGCT[C/G]CACCATGACTACCTG | 23510 |
rs762382591 | snp | A/C/G | 3.61149e-05 | 0.00424928 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047513 | TCGTGACCACCAGAC[A/C/G]GACCTTAGGCCGGGA | 23510 |
rs762457263 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046855 | GTGACAAGGGTCGGC[C/G]TGAGGTTTGGAGAGG | 23510 |
rs762547652 | snp | A/G | 1.67767e-05 | 0.00289622 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063031 | AGATTCTTCAGGAGA[A/G]AGGATCGCGGATGTA | 23510 |
rs762596851 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035144 | GGATAAGGCGTCTGA[C/T]TTCGGATCAGAAGAT | 23510 |
rs762606856 | snp | G/T | 3.2969e-05 | 0.00405998 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039032 | TCAATGGTCATCTGA[G/T]CAAATGGAATTAAGT | 23510 |
rs762703331 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057635 | CGCGATCTCAGCTCG[C/T]TGCAACTTCTGCCTC | 23510 |
rs762713145 | snp | A/G | 0.000357846 | 0.0133714 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047423 | AGCCGCTGGAGCCGG[A/G]TCCCGGACCACCCGA | 23510 |
rs762723242 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063847 | CTGCACCTGCAGCCT[C/G]TTCTTACTCCCCATT | 23510 |
rs762751308 | in-del | -/CT | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043688 | TTACTAAAAATAACA[-/CT]CTTATTGCATAAAAG | 23510 |
rs762825474 | snp | A/C | 1.71296e-05 | 0.00292652 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040018 | ATTTAATTCACTCTA[A/C]CTTAACTTAGCTATA | 23510 |
rs762911086 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061940 | GGCCTCACCAATGAT[A/G]CCCTGATGAAGAACA | 23510 |
rs763000682 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051711 | TTGCAGATTTCACCC[C/T]TTAATATTTGTATAT | 23510 |
rs763238119 | snp | C/G/T | 1.70603e-05 | 0.0029206 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053122 | TAATGTATTTGGAAC[C/G/T]GTTAAGGAGGGTTGT | 23510 |
rs763240856 | snp | A/G | 5.01593e-05 | 0.00500771 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059516 | TCATTGCAGGGCCCC[A/G]TGAAGCACGTGTACA | 23510 |
rs763264238 | snp | A/C | 1.65138e-05 | 0.00287343 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042259 | GATAGCTGGTGGATT[A/C]TCAGGTAAAGCAGCC | 23510 |
rs763287590 | snp | G/T | 1.69166e-05 | 0.00290827 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042146 | TACCCACAGGCATGT[G/T]ACAAGCTCAGTGCTT | 23510 |
rs763352643 | snp | A/G | 1.65228e-05 | 0.00287422 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059588 | TCCACGATGTCCGAC[A/G]GCTGGAAATTCGAAC | 23510 |
rs763516205 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049936 | TGAAGGCATTCAGTT[A/G]TAAAGGGGACTGTCC | 23510 |
rs763518477 | snp | A/C | 1.64762e-05 | 0.00287016 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039167 | GTGTGGTCATGAAAG[A/C]GAGAACCCATATTAT | 23510 |
rs763648692 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064495 | AGGTACGTCTGGGTA[A/G]TAGTTTCTGGAAATG | 23510 |
rs763675074 | snp | C/T | 0.000131785 | 0.00811635 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062143 | CATCGGATCTTCCTA[C/T]AACTACGGCAATGAG | 23510 |
rs763699483 | snp | A/T | 1.64773e-05 | 0.00287026 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039267 | CACTCAGCACAAGAT[A/T]TCACCTTTAAGAAGA | 23510 |
rs763840671 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059446 | CATTTGAAGAGCCTC[C/T]TTGGGGCAGCTGCAA | 23510 |
rs763872558 | snp | C/G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039492 | TAGGATGGCAGCACC[C/G/T]GGCTGCTTCTGCAAG | 23510 |
rs763950578 | in-del | -/TT | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033333 | AAAATGTGCTTATTC[-/TT]TGTTAGAATTAGGGT | 23510 |
rs763962942 | snp | C/G | 1.8283e-05 | 0.00302344 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047548 | AAGTCATTTCTCTGC[C/G]GCCTCTGCTGCCAGG | 23510 |
rs763987074 | in-del | -/A | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053126 | GTATTTGGAACTGTT[-/A]AGGAGGGTTGTTTCA | 23510 |
rs764087405 | snp | C/T | 5.66701e-05 | 0.00532276 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047616 | CCTCGGGCGCGCCCC[C/T]GGGCCTTCGAACCCC | 23510 |
rs764117725 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75038232 | TTCAATCAAGCCTCA[A/C]GCTGAGGCCAAGATG | 23510 |
rs764159225 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033074 | CGCTGCCCTTGGCTG[A/G]ACTTCTTCTGTTAAA | 23510 |
rs764248233 | snp | A/G | 1.64749e-05 | 0.00287005 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040139 | TATATTTATCCTCTG[A/G]CACGGGAACCTTCAG | 23510 |
rs764281363 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061970 | AGGCCCATTTCTCCC[C/T]GGGGGCTTTGGTAGT | 23510 |
rs764289937 | snp | C/G | 1.6574e-05 | 0.00287867 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053095 | GGGACAATGAGAACA[C/G]AACTTCACAAGTAAT | 23510 |
rs764313640 | snp | C/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048583 | TCTACTCTATATCCT[C/G]CTTGTGGTAATAGAA | 23510 |
rs764358483 | in-del | -/T | 1.79651e-05 | 0.00299704 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059474 | CAAACTGTGGTGTCC[-/T]TGGTGCTGTTCTCAG | 23510 |
rs764403834 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032003 | CTGACCTCAAGTGAT[C/T]AGTCTGCCTCAACCT | 23510 |
rs764459721 | snp | A/G | 3.29658e-05 | 0.00405978 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042629 | AGTCAATGGTTTTTA[A/G]AGCAAGTTTTCGCCC | 23510 |
rs764483746 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033941 | AAGGCACTGGCCTCC[G/T]AAGCCAGGGATTGTG | 23510 |
rs764547110 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064246 | GCTGCATCCACAGAG[-/T]TTTGTGTCCACACTT | 23510 |
rs764595481 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054854 | GCCAGGAAAATAGAC[C/G]CTCTCTTTCATGCGA | 23510 |
rs764701655 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065361 | TTCTTGCTTGAAAGC[A/G]TTGTGCCCTCTGAGT | 23510 |
rs764727292 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051770 | TGTAACCACAGACAG[A/T]ACAGTTATCAAACTC | 23510 |
rs764822377 | snp | A/T | 2.09295e-05 | 0.00323486 | upstream-variant-2KB, missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047408 | CTGCCGCCGTCGCGC[A/T]GCCGCTGGAGCCGGG | 23510 |
rs764870739 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056397 | ATTGCTTACTATAGA[C/T]TTTAAAGTACCATGA | 23510 |
rs764914296 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062205 | GAGAACTAAATAATT[C/G]TACCAATGGCATCGT | 23510 |
rs764915092 | snp | C/T | 1.72725e-05 | 0.0029387 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040013 | CTTCCATTTAATTCA[C/T]TCTAACTTAACTTAG | 23510 |
rs764916246 | in-del | -/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062854 | CCCAGCAAGAGAGTG[-/T]TTTCGCACCAGAAGC | 23510 |
rs765023851 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050798 | ATATCCCAGATTAAC[C/G]AATTTTCAATGTTAT | 23510 |
rs765051597 | snp | A/G | 1.65037e-05 | 0.00287256 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042646 | GCAAGTTTTCGCCCA[A/G]CCATTTTGGGATCCT | 23510 |
rs765204583 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036933 | GCCTTTCATCTTCAA[C/T]CCGGCCTTACTCCTA | 23510 |
rs765228578 | snp | A/G | 1.64855e-05 | 0.00287097 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039284 | CACCTTTAAGAAGAA[A/G]GAGAAATTCAGTTCT | 23510 |
rs765248933 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049440 | GCATGTGCAGGTATA[C/G]TTTCAGGTTTATGAA | 23510 |
rs765254692 | snp | A/G | 3.46326e-05 | 0.00416114 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063091 | AGGAGAGCAGTCAGC[A/G]GAGCCCCTCTGTGAA | 23510 |
rs765274829 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75032810 | GAAGGCATCCCTGCA[A/G]GTTGGCCCTGGGGCA | 23510 |
rs765385788 | snp | C/G | 1.70006e-05 | 0.00291548 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042137 | CCTGCTCCCTACCCA[C/G]AGGCATGTTACAAGC | 23510 |
rs765606418 | snp | A/G | 1.68105e-05 | 0.00289914 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053111 | AACTTCACAAGTAAT[A/G]TATTTGGAACTGTTA | 23510 |
rs765647522 | snp | A/C | | | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066113 | AGAATGCAGAGAAAC[A/C]GAAGGTGGGACGGAT | 23510 |
rs765681666 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034514 | GGGGCGCGGTAAGAC[A/G]CTAAACCCACGTGCT | 23510 |
rs765851627 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053435 | GTCTTGGTTGCACCC[A/G]TTGGCCGCTCTTTTT | 23510 |
rs765885772 | snp | A/T | 0.00100418 | 0.0223849 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047424 | GCCGCTGGAGCCGGG[A/T]CCCGGACCACCCGAG | 23510 |
rs765903080 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034408 | GGCACCAAAAGAAAC[C/G]TTGCGAGCACAGCCC | 23510 |
rs765937015 | in-del | -/AG | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049458 | TCAGGTTTATGAAAC[-/AG]AGCAGAAACTACCAG | 23510 |
rs765961993 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039038 | GTCATCTGATCAAAT[A/G]GAATTAAGTTCTTCA | 23510 |
rs766081000 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035150 | GGCGTCTGACTTCGG[A/G]TCAGAAGATTGAGGG | 23510 |
rs766112848 | snp | A/G | 1.66884e-05 | 0.00288858 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062291 | CTGGCTTGCTTGTTC[A/G]CACCCCCTCCGTGGG | 23510 |
rs766127013 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035505 | TTTCAGTCTATCGTT[A/T]TGAAGTTAAACAGCA | 23510 |
rs766287396 | snp | C/T | 1.71091e-05 | 0.00292476 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040019 | TTTAATTCACTCTAA[C/T]TTAACTTAGCTATAA | 23510 |
rs766317464 | snp | C/T | | | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049291 | CAACTACCTCCGCCA[C/T]GGGAAACTCATCATC | 23510 |
rs766377900 | in-del | -/A | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059308 | GGCTTGTGGTCACTT[-/A]AAAAGAAAAACATTT | 23510 |
rs766402093 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062209 | ACTAAATAATTCTAC[C/T]AATGGCATCGTCATA | 23510 |
rs766405284 | snp | C/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048467 | ACATTTGTTGTTTTC[C/G]TTTATTCCTCTTCTC | 23510 |
rs766421770 | snp | G/T | | | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060693 | TCAGGCTGCACTCAG[G/T]GTCTCGGTCGCCGCC | 23510 |
rs766459415 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030580 | TGCTGCATTAGGCAG[C/T]GGATTTTAGAGGCAC | 23510 |
rs766531599 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75038308 | CCACCACGCCTGGCT[A/C]ATTTCTGCATTTTTA | 23510 |
rs766825444 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042878 | ACAGCAAGACTCCAA[C/T]TCAAAAAAAAAGAAA | 23510 |
rs766855123 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050300 | TCTTTTTTTTTTCTT[C/T]GCTCAGGCTGGAGTG | 23510 |
rs766889223 | in-del | -/C | 2.63134e-05 | 0.00362712 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047611 | CCGCCCTCGGGCGCG[-/C]CCCCCGGGCCTTCGA | 23510 |
rs766917509 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058527 | TAATAAGGCTGGGTG[C/T]GGTGGCTCATGCCTG | 23510 |
rs766925974 | snp | C/T | 3.32231e-05 | 0.00407559 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059524 | GGGCCCCGTGAAGCA[C/T]GTGTACAGAGTCCTG | 23510 |
rs766995787 | in-del | -/AAAGG | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043228 | TCCGTCTCAAAAAGA[-/AAAGG]AAAGGACAGTGTAGC | 23510 |
rs767027713 | snp | G/T | 1.64819e-05 | 0.00287066 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039067 | CATCTTCTCCATCTG[G/T]AAAGAGGGGGAATGT | 23510 |
rs767031557 | in-del | -/GTCGGAAC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035182 | TCGAGTCCCTTCGTG[-/GTCGGAAC]GTTTTAATCCCTGCA | 23510 |
rs767055399 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051341 | CCAGGCTGGAGTGCA[A/G]TGGCACTATCACAGC | 23510 |
rs767082680 | snp | G/T | 1.65496e-05 | 0.00287655 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059535 | AGCACGTGTACAGAG[G/T]CCTGCAGTGTCAGGA | 23510 |
rs767108074 | snp | C/G | 7.54878e-05 | 0.00614314 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047608 | TGCCCCGCCCTCGGG[C/G]GCGCCCCCGGGCCTT | 23510 |
rs767131774 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035434 | CCAAACATTCGCCTC[G/T]TAAACGTGCTCTACA | 23510 |
rs767183455 | snp | C/T | 1.66985e-05 | 0.00288946 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047530 | ACCTTAGGCCGGGAG[C/T]CCAAGTCATTTCTCT | 23510 |
rs767188491 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053159 | TGGGCTTCTGTCGGT[A/C]GGTCTGTGATTTGAA | 23510 |
rs767194942 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065450 | TGACCCACACTCTCT[G/T]CTGCCCAGTACTGCC | 23510 |
rs767223618 | snp | A/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048272 | CATGGCTGCTAACCA[A/G]AGGGTTGAGAGGTGA | 23510 |
rs767256698 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047655 | TCGTAGATCGGTCCC[C/T]AGAGTCCTGAGACAC | 23510 |
rs767291731 | snp | A/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031715 | CCCAGCTGCTATCTA[A/G]CCTCTCTGAACCTTA | 23510 |
rs767424339 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046676 | TGCACGAGACACGGC[-/T]TGTGGCAGCGCCTAC | 23510 |
rs767461056 | snp | A/C | 1.64963e-05 | 0.00287192 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039298 | AAGAGAAATTCAGTT[A/C]TGAAACCAGGCTGCA | 23510 |
rs767510951 | snp | C/T | 3.4013e-05 | 0.00412376 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063067 | AGACCCCGAAAACTC[C/T]AGACCTTCAGGAGAG | 23510 |
rs767670890 | snp | A/G | 3.29582e-05 | 0.00405931 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053030 | TGTGCTGGAGGAAGC[A/G]GAGTTTTACAACATC | 23510 |
rs767846385 | snp | C/T | 0.000131781 | 0.00811621 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042596 | GGTTCTGGGGTATGA[C/T]CTCTGCAAAAGCTAC | 23510 |
rs767906344 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049316 | ATCATCACTAAGGAG[C/T]TGGCAGAAGAAGGTA | 23510 |
rs767950776 | snp | C/T | 1.68343e-05 | 0.00290118 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042157 | ATGTTACAAGCTCAG[C/T]GCTTTAGAGGTGTGA | 23510 |
rs767986448 | in-del | -/GGGTGGGCGA | 1.7433e-05 | 0.00295232 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049364 | GGGATTTTCAAAATG[-/GGGTGGGCGA]CAAGTAGAATCTTTA | 23510 |
rs768026916 | snp | A/C | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031960 | AGAGATGGGGTTTCA[A/C]TATGTTGGCCAAGCT | 23510 |
rs768080143 | snp | G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042016 | AGAGCCTAAATTCCT[G/T]CACCTATTTACAGTT | 23510 |
rs768134773 | snp | C/T | | | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75035325 | CTTTGCATCCCGGGA[C/T]GCTTCCGGTTATGGC | 23510 |
rs768136189 | snp | A/G | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060356 | CACTGGAAAAATGTA[A/G]TCCTTGATATTTCTA | 23510 |
rs768144554 | snp | C/T | | | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75032603 | CTTCGAGGAGGGGTG[C/T]CCAGTGGTGATGCCC | 23510 |
rs768153184 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040086 | GCAGGAGCCTCAACT[A/G]CTTACATCTTCTTTT | 23510 |
rs768226494 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048194 | GTTACTGTTTGCCGC[C/T]GCAAATCTAGGCTAA | 23510 |
rs768261210 | snp | A/C | 1.64852e-05 | 0.00287094 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052970 | TTGGTGTTTTTCTGG[A/C]AAACCCTCGCACCTA | 23510 |
rs768267752 | in-del | -/AA | 1.66371e-05 | 0.00288414 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042296 | CCCACAAGGAAAGGC[-/AA]AAGTTAGGATTGTTC | 23510 |
rs768282823 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061554 | ACTCAGGAGGCTGAC[A/G]TGGGAGGATCACTTG | 23510 |
rs768314636 | snp | G/T | 3.54478e-05 | 0.00420983 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039992 | TCCTTTATATGGCTG[G/T]TAACTCTTCCATTTA | 23510 |
rs768314674 | snp | A/G | 1.64977e-05 | 0.00287203 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053075 | GCTGGTTAAGGAAAG[A/G]ATACGGGACAATGAG | 23510 |
rs768434668 | snp | A/G | 1.64863e-05 | 0.00287104 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042526 | TCTCAGAAACATACT[A/G]ACCTGGAGGTGAGGG | 23510 |
rs768589940 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034229 | CCCAAAGGGTTCCCA[G/T]GACACCCCAGCTCCA | 23510 |
rs768677766 | snp | A/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043515 | GTACTCAAGAGGCTT[A/T]GACAGGACAATCACT | 23510 |
rs768702395 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048674 | AAGTCCTGGCAGTAC[C/T]GAGCTTCCTCTGGGC | 23510 |
rs768759393 | snp | C/T | 1.75026e-05 | 0.0029582 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059491 | GGTGCTGTTCTCAGT[C/T]TGCGCCTGGTCATTG | 23510 |
rs768841052 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033867 | GAAAAGGGGACACTC[A/G]CTTATGAGGGGAAGG | 23510 |
rs768861153 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042725 | AGTTGGGAAAAATGA[C/T]AAATAACAAAATAAG | 23510 |
rs768892576 | snp | C/T | 1.8504e-05 | 0.00304165 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047493 | GAACGTGGGAGGCAC[C/T]TACTTCGTGACCACC | 23510 |
rs768933724 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057085 | TCAGCTTCCCGAGTA[C/G]CTAGATTACAGGTGT | 23510 |
rs768947436 | snp | C/G | 1.64814e-05 | 0.00287061 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039103 | GTTAATGTAAACAGA[C/G]ACGGAAAGCAGAATA | 23510 |
rs769139162 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036090 | ACGGAGTCTCGCTCT[A/G]TCACCCAGGGTGGAG | 23510 |
rs769151913 | snp | C/G | 1.671e-05 | 0.00289045 | intron-variant | KCTD2 | GRCh38.p7 | 17:75063007 | GCCTCTCCCCCATCT[C/G]CAACTTTCAGATTCT | 23510 |
rs769172054 | in-del | -/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031757 | TATAAACTAGGGGGG[-/T]TTTTTTGTTTTGTTT | 23510 |
rs769212698 | snp | G/T | 0.000320564 | 0.0126562 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047262 | CAAGATGGCGGAACT[G/T]CAGCTGGACCCGGCG | 23510 |
rs769244650 | snp | C/T | 4.96907e-05 | 0.00498426 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062277 | CTGGGCAGTTGCCTC[C/T]GGCTTGCTTGTTCGC | 23510 |
rs769297666 | snp | A/C/G/T | 0.000100257 | 0.00707961 | intron-variant | KCTD2 | GRCh38.p7 | 17:75063002 | CCTCAGCCTCTCCCC[A/C/G/T]ATCTCCAACTTTCAG | 23510 |
rs769438997 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031421 | GCAGGACCTGAAGCA[C/T]GATGAATGACATAAG | 23510 |
rs769443824 | snp | A/G | 3.29462e-05 | 0.00405857 | intron-variant, synonymous-codon | ATP5H, KCTD2 | GRCh38.p7 | 17:75040107 | ATCTTCTTTTTCTTC[A/G]GCATCCACCTGGGCA | 23510 |
rs769534718 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040251 | ACACCCAGGAGCTCA[A/G]AGGGCTGGAAGCTAC | 23510 |
rs769605595 | snp | A/G | 3.30158e-05 | 0.00406286 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053080 | TTAAGGAAAGGATAC[A/G]GGACAATGAGAACAG | 23510 |
rs769678134 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065131 | TCCATAGTTGCCGCC[-/A]TGAAAAGACTGCTCT | 23510 |
rs769694753 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039344 | TGCTAAGGTAGGAGT[C/T]GTCCCAGCCCACTCC | 23510 |
rs769829788 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055453 | AGGTATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23510 |
rs769999055 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054668 | AAAAATTAGCCAGGC[A/G]TGGTGATGGGTGCCT | 23510 |
rs770024565 | snp | C/T | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060147 | ACAGTTGGAGCTTCA[C/T]TGTTCTCCTCCATTA | 23510 |
rs770063406 | in-del | -/TG | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058790 | GCGACAGAGTGAGAC[-/TG]TGTCTTAAAAAATAA | 23510 |
rs770118940 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035186 | GTCCCTTCGTGGTCG[G/T]AACGTTTTAATCCCT | 23510 |
rs770166543 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036091 | CGGAGTCTCGCTCTG[G/T]CACCCAGGGTGGAGT | 23510 |
rs770167290 | in-del | -/AATAA | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75038059 | ATCTTAAAAAATAAT[-/AATAA]AATAAAATAATTTTC | 23510 |
rs770222616 | snp | A/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048158 | GTCCATATTTAGATC[A/G]AATGCGTTTTTTGGA | 23510 |
rs770310383 | snp | A/G | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060074 | AAGTGTGGTGCGGCC[A/G]TTTCCCCTACTTCTC | 23510 |
rs770323445 | snp | A/G | 2.37425e-05 | 0.00344539 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047599 | GACAAGGTGTGCCCC[A/G]CCCTCGGGCGCGCCC | 23510 |
rs770424610 | snp | A/G | 2.01258e-05 | 0.00317214 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047583 | CCCGGAGCTGGACTC[A/G]GACAAGGTGTGCCCC | 23510 |
rs770528340 | snp | C/T | | | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038792 | TTTAAACAAAAACCC[C/T]GCTGCCAGTGAGGCC | 23510 |
rs770720014 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045583 | AGAAAAAGAATTCAG[C/T]GATATTTCTCCCATT | 23510 |
rs770729701 | snp | A/G | | | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75034086 | GTGCAACGTGTTGAG[A/G]AGGAGCCACCTCCTC | 23510 |
rs770777319 | snp | A/C | 9.88338e-05 | 0.00702902 | intron-variant, synonymous-codon | ATP5H, KCTD2 | GRCh38.p7 | 17:75040122 | GGCATCCACCTGGGC[A/C]GTATATTTATCCTCT | 23510 |
rs770941747 | snp | C/T | 1.65261e-05 | 0.0028745 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053087 | AAGGATACGGGACAA[C/T]GAGAACAGAACTTCA | 23510 |
rs770954721 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065730 | CTGAGAGAGGAGGCC[C/T]GAGAGGACACCCCAC | 23510 |
rs770983210 | snp | A/C | 1.67508e-05 | 0.00289398 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042695 | AAACAAGGCTTTTTT[A/C]TGAGGTGAATTTTCA | 23510 |
rs770996693 | snp | C/T | 8.93631e-05 | 0.00668383 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059478 | CTGTGGTGTCCTTGG[C/T]GCTGTTCTCAGTCTG | 23510 |
rs771038084 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052873 | AACTCCAGCCTGGGC[A/G]ACAGAGTAAGACTCC | 23510 |
rs771103888 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062091 | TTAAGATTGCCACAT[A/G]AATGTTCACTGTATT | 23510 |
rs771160351 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053911 | TCACTCTCTCCCCCA[A/G]GCTGGCCTCCCAAAG | 23510 |
rs771168168 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065076 | AGACACCAATGTTGA[A/G]CACCTCCTGAGGGCG | 23510 |
rs771267119 | snp | G/T | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059598 | CCGACGGCTGGAAAT[G/T]CGAACAGGTACATCT | 23510 |
rs771300802 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048069 | CAGCTGCAGGAAGCG[C/T]TCCTTGTGATATCAC | 23510 |
rs771397498 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035084 | AATGGCCATCAAATT[A/G]GCCTCTCTAGGAGGT | 23510 |
rs771427575 | snp | A/T | 3.44281e-05 | 0.00414884 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049191 | ACTCCTCAAAGGTCC[A/T]CAATGATACCCTTGT | 23510 |
rs771523215 | in-del | -/AAAC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035836 | AAGCCGTCTCAAAAC[-/AAAC]AAACAAACAAACAAA | 23510 |
rs771524275 | snp | C/G | 3.29522e-05 | 0.00405894 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039168 | TGTGGTCATGAAAGA[C/G]AGAACCCATATTATA | 23510 |
rs771577492 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039225 | TCTTTCTCATATTCT[A/G]CAATCCTGGCCTTTG | 23510 |
rs771588978 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037659 | GCATTACTCTATGAT[C/G]TACTACCTTGCTTTA | 23510 |
rs771597496 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031101 | CACAGTGAGACTCCG[C/T]CTCAAAAATAAAATA | 23510 |
rs771648255 | snp | A/T | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060565 | TGTTGTCCTGGTTGA[A/T]GTTGGCAAAGAGCAG | 23510 |
rs771652548 | snp | C/T | 1.77979e-05 | 0.00298306 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039984 | CAAGTCATTCCTTTA[C/T]ATGGCTGTTAACTCT | 23510 |
rs771699699 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75038335 | TTTAGTAGAGATGGG[A/G]TTTCACCATCTTGGC | 23510 |
rs771716951 | snp | A/C | 1.69913e-05 | 0.00291468 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049199 | AAGGTCCACAATGAT[A/C]CCCTTGTGTTTGGTT | 23510 |
rs771727363 | in-del | -/ATT | | | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066176 | GGGGAGGAGTGTGAG[-/ATT]TTTTTTTTTTTTTTT | 23510 |
rs771729863 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033635 | CCTCCAAACCTCAGT[C/T]TTCATACCCCATGGT | 23510 |
rs771789902 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062386 | CTCGTTTTGTTATTT[C/T]TGACTGTTGTAATTT | 23510 |
rs771820944 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046357 | AAAATTCTGGGATTA[C/G]AGGCGTGAGCCACCG | 23510 |
rs771875933 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061722 | TGCTTTCCAGAGCCT[C/T]CTGTCCCCAGTCTAG | 23510 |
rs771917957 | in-del | -/CA | | | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060833 | TTCTAAAAGAAAACT[-/CA]CACTTTGCATTAATG | 23510 |
rs771929492 | snp | G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041758 | GGGCGTGGTGGCGCA[G/T]GCCTGGCTGAGGCAC | 23510 |
rs771969311 | in-del | -/TCT | 9.88403e-05 | 0.00702925 | intron-variant, cds-indel | ATP5H, KCTD2 | GRCh38.p7 | 17:75040093 | CCTCAACTACTTACA[-/TCT]TCTTTTTCTTCGGCA | 23510 |
rs772019277 | snp | A/C | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040522 | GAAATTCTGATTTCT[A/C]TTCTGCATGGAACCC | 23510 |
rs772094660 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040195 | ACGGGAACCTTCAGC[A/G]CATTAAACTACAAAC | 23510 |
rs772144503 | snp | G/T | 0.00032175 | 0.0126796 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047231 | CGCGCGGGCAGCAGC[G/T]GTGGCGGCGGCGGTC | 23510 |
rs772149859 | snp | C/G | 3.30115e-05 | 0.00406259 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042241 | CTTGTAGTAAGCCCA[C/G]TCGATAGCTGGTGGA | 23510 |
rs772274092 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035061 | AGCTGCGGCACGCCG[C/G]AGCGTTTAATGGCCA | 23510 |
rs772335746 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034661 | CACCGGGCTACACAA[A/G]AGCTCCATGCGGTGA | 23510 |
rs772352175 | snp | G/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046428 | TTAATCCCCAGCGCC[G/T]AGAACAGATCATGCG | 23510 |
rs772353365 | snp | C/G | 3.7914e-05 | 0.0043538 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047484 | GGTCAGGCTGAACGT[C/G]GGAGGCACCTACTTC | 23510 |
rs772379208 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034422 | CCTTGCGAGCACAGC[A/C]CCTCTCGACACCCCA | 23510 |
rs772528651 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065868 | GTGTGAATAAAGATA[C/T]GAAACTTCTGAATCT | 23510 |
rs772569477 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054201 | TTTTTGTATTTTGGG[C/T]AGAAACGAGCCTTGT | 23510 |
rs772594043 | in-del | -/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051277 | CCACCGCGCCCGACC[-/T]TTTTTTTTTTTTTTT | 23510 |
rs772694426 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062112 | TCACTGTATTCTTGG[C/T]TCATCAGCTCATCAG | 23510 |
rs772707748 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050559 | TGAGCCTCCGCGCCC[A/G]ACCTGAGATGTTTGG | 23510 |
rs772732144 | snp | C/T | 3.32121e-05 | 0.00407492 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062284 | GTTGCCTCTGGCTTG[C/T]TTGTTCGCACCCCCT | 23510 |
rs772733244 | snp | G/T | 3.34292e-05 | 0.00408821 | intron-variant | KCTD2 | GRCh38.p7 | 17:75063014 | CCCCATCTCCAACTT[G/T]CAGATTCTTCAGGAG | 23510 |
rs772815865 | in-del | -/CT | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063803 | AGGCGGCATCCTGCA[-/CT]GAGTCAGACAAGTGG | 23510 |
rs772859273 | snp | C/T | 5.41423e-05 | 0.00520271 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047516 | TGACCACCAGACAGA[C/T]CTTAGGCCGGGAGCC | 23510 |
rs772901767 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant, synonymous-codon | ATP5H, KCTD2 | GRCh38.p7 | 17:75040113 | TTTTTCTTCGGCATC[C/T]ACCTGGGCAGTATAT | 23510 |
rs772913499 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059614 | CGAACAGGTACATCT[C/G]TTAACAGAGCAGCAA | 23510 |
rs772973630 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049153 | CAAAGATGGTGAAAT[C/T]CTGCCCTGCCTTTGT | 23510 |
rs772976827 | in-del | -/TG | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061819 | CGTTCTGTCTTCCCT[-/TG]TGCTGTGCTCGACGG | 23510 |
rs773021785 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75032743 | AGGCTGAGCCCCGGG[C/T]GGGCGGGTTGGGGGA | 23510 |
rs773060821 | snp | A/G/T | 3.3022e-05 | 0.00406326 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053082 | AAGGAAAGGATACGG[A/G/T]ACAATGAGAACAGAA | 23510 |
rs773072576 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061750 | TAGGGCTTCTGCTGA[C/T]AGAGGAGCCAGCTGT | 23510 |
rs773183990 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053011 | GTTTTGTCCTTGTTC[C/T]AGGTGTGCTGGAGGA | 23510 |
rs773196407 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065227 | GGGCTGGTGTTCACC[A/G]AGTTTCCCTCCTCGC | 23510 |
rs773214034 | in-del | -/C | | | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038595 | ACCAGGGGTTTGAAA[-/C]CAAAGAGGAAGTTGA | 23510 |
rs773216574 | snp | C/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031726 | TCTAACCTCTCTGAA[C/G]CTTAGTTTCCCCACC | 23510 |
rs773239074 | snp | C/T | 1.71861e-05 | 0.00293134 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040016 | CCATTTAATTCACTC[C/T]AACTTAACTTAGCTA | 23510 |
rs773239403 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064956 | CAGTCTCGTTGAGGC[A/G]CTTGTCCCTGTCTGC | 23510 |
rs773251505 | in-del | -/CCA | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043580 | TAGCGCCATTGCACT[-/CCA]CCAGCCTGGACACAG | 23510 |
rs773359299 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051274 | TGAGCCACCGCGCCC[A/G]ACCTTTTTTTTTTTT | 23510 |
rs773744503 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057198 | ATCTTAGGCGAGCCA[C/T]CAACCTCAGCCTCCC | 23510 |
rs773754416 | snp | A/C | 0.000120336 | 0.00775587 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049192 | CTCCTCAAAGGTCCA[A/C]AATGATACCCTTGTG | 23510 |
rs773804238 | snp | C/G | | | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75035357 | TCATTATGCAGCCAG[C/G]GTAAGTAGGGCCCCA | 23510 |
rs773825426 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042841 | AGTCGAGACTGCATC[A/G]CTGCACTCCAGCCTG | 23510 |
rs773849536 | snp | G/T | 2.14167e-05 | 0.00327229 | upstream-variant-2KB, splice-donor-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047591 | TGGACTCAGACAAGG[G/T]GTGCCCCGCCCTCGG | 23510 |
rs773858586 | snp | C/T | 1.80361e-05 | 0.00300295 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047524 | AGACAGACCTTAGGC[C/T]GGGAGCCCAAGTCAT | 23510 |
rs773900989 | snp | A/C | 1.64781e-05 | 0.00287033 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039159 | TGAAAGATGTGTGGT[A/C]ATGAAAGAGAGAACC | 23510 |
rs773934350 | snp | A/G | 1.6476e-05 | 0.00287014 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039171 | GGTCATGAAAGAGAG[A/G]ACCCATATTATAGGC | 23510 |
rs773952295 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059455 | AGCCTCCTTGGGGCA[A/G]CTGCAAACTGTGGTG | 23510 |
rs774025355 | snp | A/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048264 | GCAGGATGCATGGCT[A/G]CTAACCAAAGGGTTG | 23510 |
rs774090922 | snp | C/T | 4.73765e-05 | 0.00486683 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047600 | ACAAGGTGTGCCCCG[C/T]CCTCGGGCGCGCCCC | 23510 |
rs774115424 | snp | A/G | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060461 | ACATAAGCCTTCCAA[A/G]GTGATACTTTCAGAA | 23510 |
rs774131038 | in-del | -/AG | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060300 | CATGGCATTTAAAAC[-/AG]ACATTGCTACATCAC | 23510 |
rs774148960 | snp | C/T | 1.68556e-05 | 0.00290302 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063049 | GATCGCGGATGTAAA[C/T]TAAGACCCCGAAAAC | 23510 |
rs774335851 | snp | A/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045872 | TATTGACTGGGGAAG[A/T]GATAAGTGTCCATGA | 23510 |
rs774360491 | snp | C/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039535 | AGACCTACAGAATGC[C/G]TGTTTTCACAGGGCT | 23510 |
rs774423670 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063178 | CCCCCTGTGAAGAAG[C/T]GTTCTGGTCAAAACT | 23510 |
rs774424117 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040123 | GCATCCACCTGGGCA[A/G]TATATTTATCCTCTG | 23510 |
rs774426167 | snp | C/G/T | 0.000107149 | 0.00731877 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059480 | GTGGTGTCCTTGGTG[C/G/T]TGTTCTCAGTCTGCG | 23510 |
rs774534523 | in-del | -/CAG | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033589 | TTCTGTAGAGGCGGA[-/CAG]CAAGGCTCAGGGCGG | 23510 |
rs774585349 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034563 | CATAGTGCCCAAACA[A/C]GGCCCTGCTGTGGGT | 23510 |
rs774651758 | snp | C/T | 1.65723e-05 | 0.00287852 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059599 | CGACGGCTGGAAATT[C/T]GAACAGGTACATCTC | 23510 |
rs774652694 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039231 | TCATATTCTACAATC[C/T]TGGCCTTTGAGAGAG | 23510 |
rs774708814 | snp | C/T | 1.65745e-05 | 0.00287871 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042282 | AAGCAGCCAACCTGC[C/T]CACAAGGAAAGGCAA | 23510 |
rs774784900 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062097 | TTGCCACATGAATGT[C/T]CACTGTATTCTTGGT | 23510 |
rs774858538 | in-del | -/C | 3.30497e-05 | 0.00406494 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047627 | CCCCGGGCCTTCGAA[-/C]CCCCCTGGTTTCTCG | 23510 |
rs774895538 | snp | A/G | 3.55448e-05 | 0.00421558 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039988 | TCATTCCTTTATATG[A/G]CTGTTAACTCTTCCA | 23510 |
rs774937785 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046852 | GGCGTGACAAGGGTC[A/G]GCGTGAGGTTTGGAG | 23510 |
rs774941904 | snp | A/G | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060185 | GACTTGTTAAATTCT[A/G]TTGCCTTCAAAACAT | 23510 |
rs774978025 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054865 | AGACCCTCTCTTTCA[C/T]GCGATTAGACTGTTT | 23510 |
rs775119730 | snp | C/T | 1.69746e-05 | 0.00291325 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049200 | AGGTCCACAATGATA[C/T]CCTTGTGTTTGGTTG | 23510 |
rs775132837 | in-del | -/GGCACGGGAACCTTCAGCGCATTAAACTACAAACACAAG | 0.000461171 | 0.015178 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040138 | GTATATTTATCCTCT[lengthTooLong]GGCACGGGAACCTTC | 23510 |
rs775229599 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063813 | CTGCACTGAGTCAGA[C/T]AAGTGGGAGCTGTAG | 23510 |
rs775244895 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041302 | AGAGGTTGCAGTGAG[C/T]TGAGATGGCGCCACT | 23510 |
rs775257261 | snp | A/G | 3.29495e-05 | 0.00405877 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039249 | GCCTTTGAGAGAGAC[A/G]CCCACTCAGCACAAG | 23510 |
rs775262708 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051694 | AACTATTTGAGAATA[A/G]ATTGCAGATTTCACC | 23510 |
rs775277581 | snp | A/C | 5.5209e-05 | 0.00525371 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047614 | GCCCTCGGGCGCGCC[A/C]CCGGGCCTTCGAACC | 23510 |
rs775347970 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064071 | GTTTCTAACCTTGGC[A/G]GACCTGCTCCCCTCT | 23510 |
rs775540863 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75038118 | AGTTAACTGTGCAAC[A/G]TAAGTTTCCCTTTTT | 23510 |
rs775630337 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054702 | GTCCCAGCTGCTCGG[A/G]AGGCTGAAGCAGGAG | 23510 |
rs775724598 | snp | G/T | 1.65318e-05 | 0.002875 | stop-gained, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053088 | AGGATACGGGACAAT[G/T]AGAACAGAACTTCAC | 23510 |
rs775735277 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046359 | AATTCTGGGATTACA[A/G]GCGTGAGCCACCGCG | 23510 |
rs775752272 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055456 | TATGGTGGCTCACGC[A/C]TGTAATCCCAGCACT | 23510 |
rs775844571 | in-del | -/AT | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054425 | ATCCTGCCATTCGTC[-/AT]ATGTTTGTCGTGTGT | 23510 |
rs775852601 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052947 | AGCATGTAACCTTCA[A/T]CCTCTCCTTGGTGTT | 23510 |
rs775901694 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042609 | GATCTCTGCAAAAGC[C/T]ACCCAGTCAATGGTT | 23510 |
rs775901861 | in-del | -/TTTAA | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035065 | CGGCACGCCGGAGCG[-/TTTAA]TTTAATGGCCATCAA | 23510 |
rs775929264 | snp | C/G | | | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066080 | CCCTTTCATTTTACT[C/G]AATCTGAAAAGACCC | 23510 |
rs775992831 | snp | C/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048178 | CGTTTTTTGGAAAGA[C/G]GTTACTGTTTGCCGC | 23510 |
rs776018965 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065261 | AACCCAATGACACCT[A/G]TATTGTTCCAGCGCT | 23510 |
rs776113976 | snp | C/T | 1.6517e-05 | 0.00287372 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062254 | GGCGAAGGTAAGGAG[C/T]CCCTTCCCTGGGCAG | 23510 |
rs776152275 | in-del | -/TTCACATGGTAATT | 1.68067e-05 | 0.00289881 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042328 | ATAAGCAGTAGAAAA[-/TTCACATGGTAATT]TTCCTATCCCTTCTT | 23510 |
rs776202294 | snp | C/T | 8.82153e-05 | 0.00664077 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039996 | TTATATGGCTGTTAA[C/T]TCTTCCATTTAATTC | 23510 |
rs776283310 | snp | C/G | 1.65666e-05 | 0.00287802 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062279 | GGGCAGTTGCCTCTG[C/G]CTTGCTTGTTCGCAC | 23510 |
rs776293251 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043158 | CCCAGGAGGCAGAGG[C/T]TGTAATGAGCTGAGA | 23510 |
rs776315590 | snp | A/C | 1.64817e-05 | 0.00287064 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052971 | TGGTGTTTTTCTGGC[A/C]AACCCTCGCACCTAT | 23510 |
rs776330242 | in-del | -/ACAC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062700 | CCCCCCTCACCCCCA[-/ACAC]ACACACACACACACA | 23510 |
rs776410269 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062809 | GGCAAAGCTTTGGTC[C/T]AACAGCATATAAGCT | 23510 |
rs776415161 | snp | A/C | | | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038813 | CAGTGAGGCCAGCTC[A/C]GAAGAGAGGCTTAAT | 23510 |
rs776436658 | snp | C/T | 1.64795e-05 | 0.00287045 | splice-acceptor-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039272 | AGCACAAGATTTCAC[C/T]TTTAAGAAGAAAGAG | 23510 |
rs776523382 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050716 | TAATTAAAAAAACTT[C/T]ATTTTGAAGTAATTT | 23510 |
rs776558493 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033778 | CCGCGGTATCTTCCC[G/T]CCCGCTCACCAAAAG | 23510 |
rs776650424 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040568 | TGGAAGGAGCACTGC[A/G]TAATGAATGGTCTCC | 23510 |
rs776665404 | in-del | -/CTGGGG | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045863 | TCAGAAGAGTATTGA[-/CTGGGG]AAGTGATAAGTGTCC | 23510 |
rs776673962 | snp | A/G | 1.65031e-05 | 0.00287251 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049278 | TTGGTCCTATCCTCA[A/G]CTACCTCCGCCACGG | 23510 |
rs776684087 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049340 | GAAGGTAAGCGCACT[C/G]TTTGCATTGGGGATT | 23510 |
rs776697079 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061871 | CCGCTGACGGGGGGG[G/T]ACTTCAGAGCTTGGG | 23510 |
rs776757246 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051043 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAAGCTC | 23510 |
rs776782132 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065090 | AGCACCTCCTGAGGG[C/T]GCCGTTTCCTTCATT | 23510 |
rs776810180 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052875 | CTCCAGCCTGGGCGA[C/G]AGAGTAAGACTCCGT | 23510 |
rs776874628 | snp | A/G | 3.29516e-05 | 0.00405891 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040207 | AGCGCATTAAACTAC[A/G]AACACAAGGACAGTG | 23510 |
rs776992875 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036154 | CACCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 23510 |
rs776993783 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064268 | TCCACACTTTCTCTC[C/T]GAGCATGTGGGTCTC | 23510 |
rs777062224 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044882 | CCTGTCCTGTCCTTC[C/T]TTTCTTTCTCAGGAC | 23510 |
rs777088196 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039003 | TGGTTTCTGGGAAAG[C/T]TTCATTCAAGTCCTC | 23510 |
rs777109257 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045412 | ATTTATTAGGTGGGA[A/G]TTTCCTTTTCCTAAT | 23510 |
rs777180410 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058777 | TACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTGT | 23510 |
rs777244758 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034481 | TTAGGAGGCCAGTGC[C/T]TTATCCATTAGGCCA | 23510 |
rs777275749 | snp | A/G | 0.00034089 | 0.013051 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047269 | GCGGAACTGCAGCTG[A/G]ACCCGGCGATGGCGG | 23510 |
rs777328890 | snp | A/G | 1.80677e-05 | 0.00300558 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047511 | CTTCGTGACCACCAG[A/G]CAGACCTTAGGCCGG | 23510 |
rs777346570 | snp | A/G | 3.30437e-05 | 0.00406457 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042205 | AAAGTCATCCACCAA[A/G]CCAGCCTTGGCCACA | 23510 |
rs777365742 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051474 | ATTTTTGGTAGAGAC[A/G]GGGGTTTCACCATGT | 23510 |
rs777417383 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040176 | AAACTACAAACACAA[A/G]GGCACGGGAACCTTC | 23510 |
rs777510631 | snp | C/T | 1.65353e-05 | 0.00287531 | stop-gained, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059540 | GTGTACAGAGTCCTG[C/T]AGTGTCAGGAAGAAG | 23510 |
rs777577285 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034515 | GGGCGCGGTAAGACG[C/G]TAAACCCACGTGCTC | 23510 |
rs777678768 | snp | G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042329 | TAAGCAGTAGAAAAT[G/T]CACATGGTAATTTTC | 23510 |
rs777731264 | snp | A/C | 1.80549e-05 | 0.00300452 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059460 | CCTTGGGGCAGCTGC[A/C]AACTGTGGTGTCCTT | 23510 |
rs777761234 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056685 | TTATTCAAAGACACC[C/G]TCTTTTATACTTGTT | 23510 |
rs777864720 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062230 | CATCGTCATAGAGCC[A/G]AGCGAAAAGGCGAAG | 23510 |
rs778022887 | snp | A/G/T | 8.23697e-05 | 0.00641711 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062089 | TGTTAAGATTGCCAC[A/G/T]TGAATGTTCACTGTA | 23510 |
rs778036872 | in-del | -/TG | 1.64811e-05 | 0.00287059 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039093 | AATGTGTTTAGTTAA[-/TG]TAAACAGAGACGGAA | 23510 |
rs778065097 | snp | C/T | | | intron-variant, missense | KCTD2 | GRCh38.p7 | 17:75059985 | GTCAGAACTTTTTGG[C/T]TCTGAATGTCTTATG | 23510 |
rs778083795 | snp | A/G | 4.95045e-05 | 0.00497492 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039308 | CAGTTCTGAAACCAG[A/G]CTGCATTCTACCCCA | 23510 |
rs778128903 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052966 | CTCCTTGGTGTTTTT[C/T]TGGCAAACCCTCGCA | 23510 |
rs778317230 | snp | A/G | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042266 | GGTGGATTCTCAGGT[A/G]AAGCAGCCAACCTGC | 23510 |
rs778403583 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061636 | GCTTGGGTGACAGAG[C/T]TAGACCCTGTCTGGA | 23510 |
rs778434521 | snp | A/G | 1.69324e-05 | 0.00290962 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042142 | TCCCTACCCACAGGC[A/G]TGTTACAAGCTCAGT | 23510 |
rs778470297 | snp | C/G | 4.04916e-05 | 0.00449935 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047639 | CGAACCCCCTGGTTT[C/G]TCGTAGATCGGTCCC | 23510 |
rs778522908 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033957 | AAGCCAGGGATTGTG[G/T]GTTCGAGTCCCACCT | 23510 |
rs778627892 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055290 | GAACTTCAGGCCTCA[A/G]GTGATCCACTTGCCT | 23510 |
rs778759356 | snp | A/G | | | | | GRCh38.p7 | 17:75047915 | ATCCCACTGAGATCT[A/G]CATGAGTTTTCCCTG | 23510 |
rs778775268 | in-del | -/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053601 | GTGTGCCACCACGCC[-/T]GACTAATTTTTGTAT | 23510 |
rs778872662 | snp | A/G | 3.3961e-05 | 0.0041206 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059645 | TCCCAGGCCCCGTTC[A/G]AGGGGTCTGCAGCTC | 23510 |
rs778932369 | in-del | -/TAACT | 3.44347e-05 | 0.00414923 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040016 | CCATTTAATTCACTC[-/TAACT]TAACTTAGCTATAAT | 23510 |
rs778990649 | snp | A/C | 8.24735e-05 | 0.00642106 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062241 | AGCCGAGCGAAAAGG[A/C]GAAGGTAAGGAGCCC | 23510 |
rs778994163 | snp | C/T | 2.05717e-05 | 0.00320709 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047472 | CGCGGCCCGCTGGGT[C/T]AGGCTGAACGTGGGA | 23510 |
rs779022349 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035860 | AAACAAACAAACAAA[A/C]AACTCCAGTCCCTAG | 23510 |
rs779130110 | in-del | -/CCTCAG | 1.6759e-05 | 0.00289469 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062978 | ACATCTCTGTCTTTC[-/CCTCAG]CAGCCTCAGCCTCTC | 23510 |
rs779153820 | snp | A/C | 0.000326424 | 0.0127713 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047159 | TCTCCCCTCTGCCCC[A/C]CCCCCGCCGATGGGC | 23510 |
rs779185589 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046142 | GGCTGGAGTGTAGTG[C/G]CGTGGTCTCGGCTCA | 23510 |
rs779281430 | snp | A/C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051377 | GCGACATCCACCTCC[A/C/T]GGGTTCAAGCGATTT | 23510 |
rs779299031 | snp | A/G | | | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038584 | ACTCCCTTGGAACCA[A/G]GGGTTTGAAACCAAA | 23510 |
rs779339534 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044807 | CTCTATAAGCTTGGA[A/G]TGGAATGCAAGGGAG | 23510 |
rs779406577 | in-del | -/GGT | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052139 | TGCAGCTAATGGGCA[-/GGT]GCCAGGTAGGGAAAG | 23510 |
rs779410958 | snp | C/T | 5.1209e-05 | 0.00505983 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049347 | AGCGCACTGTTTGCA[C/T]TGGGGATTTTCAAAA | 23510 |
rs779532718 | snp | A/G | 1.78328e-05 | 0.00298598 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039975 | ATTTATTGACAAGTC[A/G]TTCCTTTATATGGCT | 23510 |
rs779561722 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041621 | GACAGAGCAAAACTC[C/T]GTCTCAAAAGAAAAA | 23510 |
rs779574256 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053069 | TGTGCGGCTGGTTAA[A/G]GAAAGGATACGGGAC | 23510 |
rs779732528 | snp | C/T | 1.79877e-05 | 0.00299892 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049374 | AAAATGCAAGTAGAA[C/T]CTTTAAAGTTGTTTT | 23510 |
rs779749366 | snp | A/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032456 | ATACTGGATGCTGGA[A/G]GATTATGAGGACAGA | 23510 |
rs779779159 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065646 | CTCCTCTAAAGTGAC[G/T]TTGTTTCTGCACAGT | 23510 |
rs779836729 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050948 | CTCCTGAGTAGCTGC[A/G]ATTATAGGCATGAGC | 23510 |
rs779854064 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052705 | TCCAACCTGGGCAAC[A/G]AGAATGAAACTCTGT | 23510 |
rs779857793 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040292 | AGGTCATACTGAAAG[A/G]CATTCTGTGTCCCAA | 23510 |
rs779870587 | snp | A/G | 1.66319e-05 | 0.00288369 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042671 | GATCCTGAAAAATAA[A/G]TCAAATAAAAACAAG | 23510 |
rs779889082 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034578 | CGGCCCTGCTGTGGG[C/T]CACCGCGCTCCAAGC | 23510 |
rs779917999 | snp | C/T | 1.64931e-05 | 0.00287163 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042520 | GTTCCCTCTCAGAAA[C/T]ATACTGACCTGGAGG | 23510 |
rs779936789 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064749 | CACCCCTTCAAGAGT[C/T]ACAGGCATCCATCCA | 23510 |
rs779941658 | in-del | -/A | 3.39121e-05 | 0.00411763 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063060 | TAAACTAAGACCCCG[-/A]AAACTCCAGACCTTC | 23510 |
rs779948552 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059430 | CTTTTCAGTGTTTAT[G/T]CATTTGAAGAGCCTC | 23510 |
rs779950482 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056880 | CTCAACCCTACCTTC[A/G]GTTTCATGACCTCTT | 23510 |
rs780027714 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035122 | GCCGGAGACCGCGTG[A/G]CCTAATGGATAAGGC | 23510 |
rs780032917 | in-del | -/CAT | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052181 | ATGGAGTGAGCAGAA[-/CAT]CATACCCTGGCGTTT | 23510 |
rs780075309 | snp | C/G | 1.86517e-05 | 0.00305377 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047490 | GCTGAACGTGGGAGG[C/G]ACCTACTTCGTGACC | 23510 |
rs780081233 | snp | A/C | 1.64825e-05 | 0.00287071 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039099 | TTTAGTTAATGTAAA[A/C]AGAGACGGAAAGCAG | 23510 |
rs780129045 | in-del | -/AAAC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035832 | GCGAAAGCCGTCTCA[-/AAAC]AAACAAACAAACAAA | 23510 |
rs780142442 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047846 | CCACACTGCGCCCAC[C/T]TGCACCCACGAGAAC | 23510 |
rs780446191 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75049880 | CATTGGGACTATAAG[C/T]GGGTCTAGTCCACTT | 23510 |
rs780728997 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033273 | TGAGCCACCGCACCC[G/T]GTCTGTAGCCTTTAA | 23510 |
rs780753732 | snp | C/G | 8.8691e-05 | 0.00665865 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053140 | TAAGGAGGGTTGTTT[C/G]AAGTGGGCTTCTGTC | 23510 |
rs780808672 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065009 | GCGTGGGCTGGAGCT[A/C]CTAGACCAACCCCAG | 23510 |
rs780869210 | snp | A/T | 3.29484e-05 | 0.00405871 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040095 | TCAACTACTTACATC[A/T]TCTTTTTCTTCGGCA | 23510 |
rs780889216 | snp | A/T | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053077 | TGGTTAAGGAAAGGA[A/T]ACGGGACAATGAGAA | 23510 |
rs780902615 | snp | C/T | 0.000280082 | 0.0118306 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040157 | CGGGAACCTTCAGCG[C/T]ATTAAACTACAAACA | 23510 |
rs780990418 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052647 | AGAATCTCTTGAACC[C/G]AGCAGGCGGAGTTTG | 23510 |
rs780999530 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063967 | TTCTTTGAAAGTTGC[C/G]AAATGTGTTATGTTG | 23510 |
rs781001037 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043370 | TAATCCCAGCACTTT[A/G]GGAGGCTGAGGTGGG | 23510 |
rs781008234 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034541 | TGCTCCTTGATAGGT[A/G]TTCAACCATAGTGCC | 23510 |
rs781098093 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034126 | AAAGCCGGTAAGCTC[G/T]GGTCTTGCCAAGCCC | 23510 |
rs781200853 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040418 | ACCCTGGACAATTCT[C/T]TATGATGATAAGCTT | 23510 |
rs781247341 | snp | A/G | 8.28123e-05 | 0.00643423 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047448 | ACCCGAGCGGGCAGG[A/G]GGCGGCGGCGCGGCC | 23510 |
rs781369227 | in-del | -/CA | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056133 | ATCTCCAGCAGTTTG[-/CA]AAAGTGAAGAGAAGG | 23510 |
rs781467181 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036021 | TGTGCAAGTGTACTT[A/G]GACATAGGGGAGAAT | 23510 |
rs781479259 | snp | C/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048693 | CTTCCTCTGGGCACA[C/G]AGCTGGGGTGTGTGA | 23510 |
rs781532412 | snp | A/C | 1.64754e-05 | 0.00287009 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039197 | TAGGCAACGGCTACC[A/C]ATCATCCTTACCTCT | 23510 |
rs781695464 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062019 | AGAGTTAAACCTTTG[A/G]TAACTTAAAAGTTCA | 23510 |
rs796084534 | in-del | -/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036331 | TTTCACCGTGTTAGC[-/C]AGGATGGTCTCAATT | 23510 |
rs796272152 | in-del | -/A | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040885 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 23510 |
rs796434185 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043629 | AAAAAAAAAAAAAAA[C/T]AAACCCCAGCTCTCT | 23510 |
rs796593176 | in-del | -/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053445 | ACCCGTTGGCCGCTC[-/T]TTTTTTTTTTTATGA | 23510 |
rs796603439 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044127 | CCTCCCAGGCTCAAG[C/T]GATTCTCCTGCCTCA | 23510 |
rs796749655 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064963 | GTTGAGGCGCTTGTC[C/T]CTGTCTGCTTTCCTG | 23510 |
rs796767817 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036797 | TGCAGTCTCGCAGGG[A/G]AAGGGTGTGGTACTT | 23510 |
rs796808133 | in-del | -/C | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043626 | AAAAAAAAAAAAAAA[-/C]AACAAACCCCAGCTC | 23510 |
rs796831549 | in-del | -/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061260 | CCTCGCCTGCTCACT[-/G]GGATGCCCTCACCCT | 23510 |