| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs377727908 | snp | A/G | 3.30857e-05 | 0.00406716 | missense | KCTD3 | GRCh38.p7 | 1:215620247 | GGTAACTTGGGTCCA[A/G]TACAAGCTGAAGTGA | 51133 |
| rs386369625 | in-del | -/CTTC | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591295 | TCCTTCTTTCCTTCC[-/CTTC]TTCCTTCCTTCCTTC | 51133 |
| rs397693523 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598706 | GTCATTGAAAAAAAA[-/A]TTTTTAATTTTATTT | 51133 |
| rs397772450 | in-del | -/T | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589123 | TTAAAATACTTAATT[-/T]CTTTTTCTTCTTTTC | 51133 |
| rs397964441 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569140 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 51133 |
| rs527310739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599395 | ATGATAAGTTTACAG[G/T]TATAGAGATTGTAGT | 51133 |
| rs527376473 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583604 | GGAATGCAGCCCAGC[A/G]GGTCTCAGCCTTATT | 51133 |
| rs527429626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590990 | CTTGTTTCAGTACTT[C/T]GTTAGGAGTAGGTAT | 51133 |
| rs527446887 | snp | C/T | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622162 | AGGAAACTGACTATA[C/T]TAGATTGCATTACAG | 51133 |
| rs527455539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567819 | CCTTGGCGGCCTCCT[C/T]CTTTGGTGTCGACGG | 51133 |
| rs527488937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614086 | CACCCAGGCTGGAGT[A/G]CAGTGGTGTAATATC | 51133 |
| rs527489816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614844 | TTTTGATGAATAAAT[G/T]CTTTGAGATGAATTT | 51133 |
| rs527621597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607559 | GGCAATAAATAGCTG[A/G]TTGCTCAAGATGTTT | 51133 |
| rs527643615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581774 | TTGAGGACATATTTG[G/T]ATTTCCTCACATATA | 51133 |
| rs527697911 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615593 | CCACTGCACTCCAGC[C/G]TGGGCGACAGAGCAG | 51133 |
| rs527703384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589215 | ATCCTAGCTCACTGC[A/G]TCCTCAACCTCCTGG | 51133 |
| rs527760941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575572 | TTGAATTCTAGACTG[C/T]TTCAGATAAAAATGT | 51133 |
| rs527762822 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567043 | GTTTTTCCTTTCCCA[A/C]TCCATGTTGACAAAG | 51133 |
| rs527835365 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618322 | TCCCTCCTTTTTGTC[C/T]GGCCTACTAGGAAGC | 51133 |
| rs527844622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596961 | AGAGACATTTCTTTC[G/T]CTGTGACAGAAGGGT | 51133 |
| rs527880435 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588597 | AATGTCAACACAGAT[A/G]TTCTAGAATAAGCCA | 51133 |
| rs527917285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593071 | ATAGCCCATAATACT[A/G]AATATAGTTGGCTTC | 51133 |
| rs527980278 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614197 | CCACCACGCCTGGCT[A/G]ATTTTTTGCATCTTT | 51133 |
| rs528022236 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597958 | CTTACTTACAGAATT[C/T]ATAGTAAGAAATATG | 51133 |
| rs528033378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588550 | AAGGTACCTGCTGTT[C/T]TTACCAAACGTTGCT | 51133 |
| rs528054790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578689 | TAACACATAATACCT[A/G]TACCATAATTGTAAA | 51133 |
| rs528176748 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570231 | GCTATCGGTAAGGTC[-/T]TTTTTTTTTTTTCCC | 51133 |
| rs528222694 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606233 | TGCATTCTTGTCATT[C/G]TGGTGCCGTTTCAAA | 51133 |
| rs528255498 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566162 | GCTTGCCTTGAAATT[C/T]CTGCCATCCCACTTG | 51133 |
| rs528461954 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576414 | TTGATTAAAAGTTTC[A/C]TCACACTGAAACTGG | 51133 |
| rs528463231 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597267 | TTCAGTTTCTTGTTT[C/T]CTTTTTTTGTTTAAT | 51133 |
| rs528471474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609772 | AGGAAGAAGAACTTA[C/T]TTTGAAAACAAAGAT | 51133 |
| rs528480781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616656 | TCCCAGCTACTCAGG[A/G]GGCTGAGGCAGGAGA | 51133 |
| rs528498829 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581901 | CCTCAAGTTTTTGTA[C/T]CAGTAAGTTACAAAA | 51133 |
| rs528630008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601188 | GTGATCTGCCTGCCT[C/T]GGCAGGTTTCTTTTA | 51133 |
| rs528645407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576400 | TTTTTACTAAGACTT[C/T]GATTAAAAGTTTCCT | 51133 |
| rs528653903 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584286 | ATTTTCCTATTTTCA[G/T]TCTTTCATTTTTACT | 51133 |
| rs528787275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577168 | TATTTGTTCAACAAA[C/T]ATTTATTACATAACT | 51133 |
| rs528799956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569036 | AATGTGTGTTGATTA[C/T]ACTGAAGAGTAGCAG | 51133 |
| rs528938203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570746 | TACCAAGTTAATTTA[A/G]TAGGAGGCAAGTTGC | 51133 |
| rs528941956 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578627 | AAAAAATGTTTGAAA[A/G]TATGGGGAATTTCAG | 51133 |
| rs528953302 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569669 | GGTGCGATCTCGGCT[C/G]ACTGCAAGCTCCGCC | 51133 |
| rs528963774 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616485 | AAACTTCCAGGCCGG[G/T]TGCGGTGGCTCACAC | 51133 |
| rs528996940 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595221 | TTTCTTATTTCTAGT[C/T]CCCAACACGTATAGC | 51133 |
| rs529091158 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601052 | GAGCAATTCTCCTGC[C/T]TCAGCCTCCCGAGCA | 51133 |
| rs529107282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609549 | TTGTGATATATATAA[C/T]TCATCTTTCAAGAGC | 51133 |
| rs529203227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591935 | TTAATTGGACTTACA[A/G]TTCCACATGGCTGGG | 51133 |
| rs529328975 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570494 | CTAGCCATTGAGGAC[G/T]CCTGGACAAAGAGCT | 51133 |
| rs529372830 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608773 | TCCACCCCCGGCCCC[A/C]TTTGAAAGAATCTCA | 51133 |
| rs529597253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576332 | CCTTAGCCTCCCAAA[A/G]TGCAGGGATTACAGG | 51133 |
| rs529654596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619799 | CATTGGTTTCAAGGA[C/T]TTTTCCTCCCATCTT | 51133 |
| rs529662185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575831 | GACTTCATTCCCTAT[G/T]AGTGTTACAGATATT | 51133 |
| rs529662249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583540 | TTGTGACCTTTACCT[C/T]GTGCTGACCTTCCTT | 51133 |
| rs529690054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612727 | TAAAATAAGGTTCAA[C/T]GACTTTGGCAGGATT | 51133 |
| rs529821481 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565506 | CCTTCTCTTGAAGAG[A/T]TGTTCTCCTAATTTT | 51133 |
| rs529871847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579523 | TTTTTTTTTGAGACG[A/G]AGTCTCGCTCTGTCG | 51133 |
| rs529920116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587057 | ACATTCCCAAACTTT[C/T]TGGTTTCAGAACCCC | 51133 |
| rs529989054 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601186 | TGGTGATCTGCCTGC[C/G]TCGGCAGGTTTCTTT | 51133 |
| rs529997506 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618437 | GTTTGCCTATACTGA[C/T]TTTTCTTTTTTAATA | 51133 |
| rs530030594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603573 | AGTGTTTTGAAACTT[A/C]AATAGTATATTTAAT | 51133 |
| rs530045192 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612033 | AGAAACAAATTGTTG[C/G]GACAGAAGTCTGTTA | 51133 |
| rs530062513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572646 | ACGTTTTTGATAATT[C/T]CAGGCTGCTAATTTA | 51133 |
| rs530242742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594798 | AAAAATAAGCTCTGA[A/G]TAAAAGGCCCGAATG | 51133 |
| rs530486048 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606693 | AGGTTTGAAACTTTT[A/G]TAAGTTTGTCAAGAG | 51133 |
| rs530526808 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608385 | TTAAAATGTTAGAGC[A/T]AATTTTTCCTCTTAT | 51133 |
| rs530532025 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566520 | TATCAGTTTGAATTA[C/T]TATGATACAACTATG | 51133 |
| rs530565417 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571661 | TCCGAGACGGAGTCT[C/T]GCTTTGTCGCCCATG | 51133 |
| rs530585007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612227 | TTATAAACAGTTTCT[A/G]TCTTTAAAAAACCTG | 51133 |
| rs530685819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586330 | TTGTGGCTTCATAGG[C/T]AATATAGATCAACAA | 51133 |
| rs530742532 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589059 | CATTTCTAGTTTGAA[A/G]GTCTATACCAAACAA | 51133 |
| rs530745871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593731 | GAAGCAGCCAAAGAT[C/G]TACATAAAACAGTAT | 51133 |
| rs530798904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601722 | GTGTGCACGCGTGCA[C/T]CTAAAGAAAGTTTAT | 51133 |
| rs530802142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579443 | TTTGCCATTGTAGCA[C/T]GAACACATAATGGAC | 51133 |
| rs530803327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611363 | TGTGGTTAACAGAAG[C/G]TTCAACTAATTACAT | 51133 |
| rs530817423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617109 | AGCTGAAAACCTGGA[A/G]GTTCTGAAGGGTGGC | 51133 |
| rs530864892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586955 | GTGGTGGATGTTTTC[A/G]CTGTTTTCTCTCCAC | 51133 |
| rs530935128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592954 | TGACACTTTAAATTT[C/T]GTGAGACCATTCAGA | 51133 |
| rs530986493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616459 | CAAACTTTATATTGG[C/T]GAAATATTAAAAACT | 51133 |
| rs530996505 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580458 | ACAGTTATTGCACAA[A/G]TGGTATAGTTTAATA | 51133 |
| rs531060310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602705 | GTTCTGTAAAGTAGT[A/G]AGAATTTTTGTATTC | 51133 |
| rs531074119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616717 | GTGAGCCGAGATCAC[A/G]CCATTGCACTCCAGC | 51133 |
| rs531196984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607357 | TGTATATTTTCAAAT[A/G]GAGTATCTACTCAGA | 51133 |
| rs531207462 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614634 | TTAATGTTAATTGGT[A/G]TATAGAAATGCTACT | 51133 |
| rs531211614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606764 | TACTCAGTTATGTTA[C/T]TCTGCCACCTGGTGG | 51133 |
| rs531328708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598403 | CTATGAGAACTCCAA[C/T]TTGAGAAACTGATCT | 51133 |
| rs531471059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613963 | TTCATTTGCTTAGGA[C/T]TGCTTTGTCTATTTT | 51133 |
| rs531506497 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215566064 | TTTAATCTGAACTGT[C/T]ACTCATCTTCCCTGT | 51133 |
| rs531518184 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566806 | AATAGGTTGCTGGGC[A/G]TTACACAGTCTAGGG | 51133 |
| rs531572498 | snp | A/G | 1.65201e-05 | 0.00287398 | missense | KCTD3 | GRCh38.p7 | 1:215620194 | ACTTCCAGACTATTA[A/G]TTTGAACAGAAATGT | 51133 |
| rs531621739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596937 | GAAAGGTTTGACCCA[A/G]CAGGGAGTAGAGACA | 51133 |
| rs531740900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580904 | CTGGTAAGTGCTGTT[A/T]ATATCAGTAATCTCA | 51133 |
| rs531758115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615386 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 51133 |
| rs531816297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574288 | ATAATCAGAGAAGAT[C/G]CCTAAGTAGGGAATA | 51133 |
| rs531923096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604539 | TTGGTTTAGCCCAGG[A/G]GTTGAAGACTAGCCT | 51133 |
| rs531942228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612603 | CTATTCAAACTTAAA[G/T]AACATAGTGAATTTG | 51133 |
| rs531979432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613864 | TGGTCTATGTGTTTG[C/T]TTTTGTACCGGTACC | 51133 |
| rs531991320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613291 | GCTGTGGTGTGATCT[C/T]AGCTCACTGCAACCT | 51133 |
| rs531994720 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596959 | GTAGAGACATTTCTT[C/T]CTCTGTGACAGAAGG | 51133 |
| rs532057919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596203 | TAGTTTGACAATCCA[A/G]TAGCTAGTAGTATTT | 51133 |
| rs532074721 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584668 | GTGGCCAGTTTTTCC[C/G]AGGGGCTTTTATCAG | 51133 |
| rs532103564 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598698 | ATTAAAAGGTCATTG[-/A]AAAAAAAATTTTTAA | 51133 |
| rs532160281 | snp | A/T | 4.96824e-05 | 0.00498385 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619081 | TAAGGGTAGGTTCTC[A/T]TACAGAAAGATGTTT | 51133 |
| rs532245315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619968 | CTTTATGTATTTATA[C/T]AGTGTGTTTTATTGG | 51133 |
| rs532283373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597113 | TAAGTATTTGAGTCA[A/G]ATGAACCAGGTTTGT | 51133 |
| rs532301491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573574 | TATGGCGGATAACAA[C/G]TTGTTTATTGTTATT | 51133 |
| rs532310701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574259 | ATTTTATTTCTTGTC[A/G]TATGTAGTTTTTTAT | 51133 |
| rs532313869 | snp | G/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565549 | AATAAAATGAACACG[G/T]TTTCATTTATTTCAG | 51133 |
| rs532392892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594899 | ATTCTAGATAGTTAA[A/G]GCTGCCAAGTCTGTG | 51133 |
| rs532515522 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589613 | GTGTCCAACATAAAC[G/T]GCATTGTTTATGCAG | 51133 |
| rs532516574 | in-del | -/A | 0.00676609 | 0.0577691 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621159 | TATTGAATACCAGAT[-/A]ACCACTATGTAGTAA | 51133 |
| rs532608970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611563 | AATGTGGCACCTTAG[C/G]AAATTTTTTCTTTTA | 51133 |
| rs532616941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580125 | CCCTGCATATTTTAC[C/T]CATGTCTGTATCATC | 51133 |
| rs532718281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583729 | GGAGGAAGATTCATC[C/T]TCTGTAACTTCTGCA | 51133 |
| rs532840672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585180 | TAAGAAAGTAAAAGA[A/G]TAAGAGAATGTCAGC | 51133 |
| rs532960260 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575758 | AGACTACATTCCAAT[C/T]TTAGAAACATTAAAG | 51133 |
| rs532967868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601009 | GTGGCACAATCCCCG[C/T]TCACCGCAACCTCTG | 51133 |
| rs533004364 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617191 | TGGGAATCTATTGTT[C/T]ATCTGTATTCTTTGT | 51133 |
| rs533153879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607864 | CCAGTTTTCTCACTT[C/T]TGTTAAGTAGTCACA | 51133 |
| rs533343778 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622007 | GTAATTATCTTACAC[C/T]CTTCTTCCTCTTTAT | 51133 |
| rs533384198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598310 | ATGGGAAAAGGAGAT[C/G]CAAGAGGAAACCATT | 51133 |
| rs533418440 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589756 | AATTCATCCATGTTG[C/T]TGCATGTATCAGTTG | 51133 |
| rs533465147 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571036 | AGGTTACTAACCTTT[C/T]CCCAAAATGCTGATT | 51133 |
| rs533509539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582330 | TCTCATACAACTTGA[A/G]GTGAAGTATGTTCAT | 51133 |
| rs533526351 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589427 | ATTACAGGCATGAGT[C/T]GCTGTGCCTGGCCAA | 51133 |
| rs533570282 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570075 | AAAACACAGTGTAAC[A/G]TAGTCACTTAAGCCA | 51133 |
| rs533629587 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617071 | AATAATAATAATAAA[C/G]TGAGTTCAGAGCGCT | 51133 |
| rs533645831 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582807 | TCTCAAGTGATTCAC[A/C]CGCCTCAGCCTTCCA | 51133 |
| rs533708735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581954 | GTGAAGACCTGTATG[A/G]TGTTCTCCTAGCTTC | 51133 |
| rs533717929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590158 | TCAGTGATTTTAATT[A/G]TGGCTTTAACTGCAT | 51133 |
| rs533745657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605932 | CCCTCTCTATGGTAC[A/G]TGTTCCACACAGCAG | 51133 |
| rs533853732 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567313 | CTCCTCATTCTAGGC[C/G]GCAGTGGCGGGCGAA | 51133 |
| rs533915729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575109 | ACAGAAAAATTAACC[C/T]GGCATAGTGGCAGGT | 51133 |
| rs533928731 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607044 | GAGAATTTTGTTATA[G/T]AAGAATAGAAAGTAC | 51133 |
| rs533928877 | snp | G/T | 3.29804e-05 | 0.00406068 | missense | KCTD3 | GRCh38.p7 | 1:215620504 | GGCGTCATCACCAAG[G/T]ACTTCCGATGGAGGA | 51133 |
| rs533931342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583062 | TGTGTAATACCCTAA[C/T]TACTATAGAGAAAAA | 51133 |
| rs533943671 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576600 | AAGAAAGTTTGAAGC[-/T]TTTTTTTTTTGAGAC | 51133 |
| rs533947163 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587915 | TGCTGAGTTATGTAG[A/C]TCTACCAAATGTTGA | 51133 |
| rs533985196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606875 | TATTAGCAAAATTGA[C/T]GTAATTGTCCAATTG | 51133 |
| rs534044865 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602476 | GTTAGCTGAAATTTC[-/A]AAAAAAAAAAAAATT | 51133 |
| rs534117771 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600007 | AGCCCTTTCCTTTAG[C/T]GCTAGAACTAAAATG | 51133 |
| rs534185903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613081 | TATGCAGCAAACCAC[A/T]ATGGCACATGTGTAA | 51133 |
| rs534200987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573730 | AAACAAGTTAACTAA[G/T]ACTGAAATTTCAAAT | 51133 |
| rs534266496 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580475 | GGTATAGTTTAATAT[C/G]TAATATGTGAAACTT | 51133 |
| rs534341947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585509 | TTTGCTTTTTGCAGC[A/G]AATGTCAGGTAGTGT | 51133 |
| rs534358013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579741 | CTGACCTCATGATCC[A/G]CCCGCCTCGGCCTCC | 51133 |
| rs534389421 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573911 | TAATGTTTGTCAGTT[A/T]AATTTTTTTTAATAA | 51133 |
| rs534412025 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596326 | CTATGGTTGTTCAAG[C/T]GTAGATGTTAAGTAT | 51133 |
| rs534427984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606236 | ATTCTTGTCATTCTG[A/G]TGCCGTTTCAAAGCC | 51133 |
| rs534469814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576789 | TAGTCATGATGGTCT[C/T]CATCTCCTCACCTCG | 51133 |
| rs534533355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583832 | AAACTGTCAGTATGG[C/T]GAGAACTCTGATTTC | 51133 |
| rs534585490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570109 | TAAGAGAAAAATCCT[G/T]ATATGATTGCCACTG | 51133 |
| rs534652611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616514 | ACCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 51133 |
| rs534751369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571415 | ATCAGATAAATGGGC[A/G]TAGGAACTGCTTATA | 51133 |
| rs534834068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591989 | GGCAAGGAGGAGCAA[A/G]TCACATCTTATGTGG | 51133 |
| rs534874625 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589929 | GTCTTTCTGTGGACA[C/T]TTACTTTCTTAAGGT | 51133 |
| rs534892724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615105 | TTTTATAATTTTTAA[C/G]TTTATGATTCCAAAG | 51133 |
| rs534960147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577472 | TTTAAGTAGATAACA[A/G]AATATTTTTGTTCAC | 51133 |
| rs534981246 | snp | C/T | 3.30344e-05 | 0.004064 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215608090 | CTCTACTCAGCCAGG[C/T]TCTACTCCTTTAGCG | 51133 |
| rs535014994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600396 | CCTTGCCCTACCTAA[C/T]TCATAGTTGACTTCA | 51133 |
| rs535026926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599901 | TTCATTGAAAAAAAA[A/G]AAAAAAAAAGAATGT | 51133 |
| rs535028863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608861 | AGAGAAATATGCAGT[G/T]TTACCAGTTTTAACA | 51133 |
| rs535042749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577361 | GGTTTCCATTCTATC[A/G]TTTGCCTTCTAGACA | 51133 |
| rs535064754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569186 | GAGTGCAGTGGCGCG[A/G]TCTCGGCTCACTGCA | 51133 |
| rs535102805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576711 | TAGCTGGGACTACAG[A/G]CACCCGCCACCACAC | 51133 |
| rs535158399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591515 | GGCACATGCCACCAC[A/G]CCCAGCTAATTTCTG | 51133 |
| rs535195811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568106 | CTCAGATTAGAGTGT[A/T]TTTGAGGACTTTATT | 51133 |
| rs535266221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583404 | AGTGTCTTTTAGCAT[A/G]ATAATGCATTATAAT | 51133 |
| rs535302010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615779 | ACTTTTATATGACAC[A/G]AGAGCCTTCAGAATG | 51133 |
| rs535362657 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594156 | TGAGCCATCATGCCC[A/G]GCCGATTATAACATT | 51133 |
| rs535380184 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614002 | TCTTTTTTGGTTTCA[C/T]AGGAACTTTAGAATA | 51133 |
| rs535416255 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576716 | GGGACTACAGGCACC[C/T]GCCACCACACCCGGC | 51133 |
| rs535478393 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578176 | TCCTTGATTATTGAG[G/T]TTTTTGTCTATAAAT | 51133 |
| rs535607402 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607043 | TGAGAATTTTGTTAT[A/G]TAAGAATAGAAAGTA | 51133 |
| rs535651327 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600316 | GTTTTAGTTATTTCT[A/G]TTTTTAATTAGAATG | 51133 |
| rs535773295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616061 | TATTTTTATGCTTCA[C/T]GGCTAGCTTTGGGGA | 51133 |
| rs535884082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614995 | TATCATATTTACTTA[C/T]TCAATTCTAATATCC | 51133 |
| rs535892999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607050 | TTTGTTATATAAGAA[C/T]AGAAAGTACACAGAT | 51133 |
| rs536014572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575044 | ATTACCTGAGGTCAG[A/G]AGTTCAAGACCAGCA | 51133 |
| rs536018227 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609312 | GCAGAGAAAACAGCA[A/G]GTTAAAAGGGTAGAG | 51133 |
| rs536029832 | snp | A/C | | | upstream-variant-2KB, intron-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567165 | GAAAGGGGCTGGGAT[A/C]GCGTGGGGAGGAGGA | 51133 |
| rs536054358 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572812 | CCTTGTTTAGTTTAA[A/G]TATGAAAGGTAAAAA | 51133 |
| rs536076448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574713 | TCAATAATAAGATCT[C/T]CACAAATCTGTGATG | 51133 |
| rs536099205 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622190 | CAGTACAAGTCAAAT[C/T]GTTTCTTTCTTTTGC | 51133 |
| rs536109210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614147 | ACACTATTCTCCTGC[A/G]TCAGTTCCTGAGTAG | 51133 |
| rs536126899 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618392 | ATTCATGTGGATTGT[A/T]TTTTTTTTTGTCTAT | 51133 |
| rs536132545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568031 | CTGCTGTCCTAGAAT[A/G]CCAACCTTTGCCCCT | 51133 |
| rs536247885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603989 | GAGAAGTCTTAAGAT[C/T]TTTTTTTTTACTGAA | 51133 |
| rs536262303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603315 | TTTTCCTTTGATTCA[A/G]GTATTTTCAGATGAA | 51133 |
| rs536379583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586407 | TTTTTGTTTTTTGTT[A/G]TTGTTTTTTGTTTTT | 51133 |
| rs536384985 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595161 | GGCTTGGAGCAGACT[A/C]TTCCTTGCTTTAGTA | 51133 |
| rs536410550 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571922 | AGGCGTGAGCCACCG[C/T]GCCTAGCCGAGATAA | 51133 |
| rs536472031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571103 | TTGTGATTTTCTAAG[C/T]AGCACATAATTTTAA | 51133 |
| rs536574626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592313 | TGTCTCTCAGGTCCT[C/T]TGCTGCCTGTTGTCC | 51133 |
| rs536622356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602316 | GAGAACTGCAGTGCC[G/T]AAGGATTTCATCTCT | 51133 |
| rs536644027 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585712 | GCTATACATATAATC[A/G/T]CATAGAAAACATTTC | 51133 |
| rs536655713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593024 | AGTAATCGATGTTAG[C/T]TGGTTTTCCTGTTTT | 51133 |
| rs536775483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578390 | TACAACTTTATTTAC[A/C]TAAATAGCATTGATT | 51133 |
| rs536806314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570229 | ATGCTATCGGTAAGG[A/T]CTTTTTTTTTTTTTC | 51133 |
| rs536922512 | in-del | -/TTCTTTTGTG | 0.00058356 | 0.0170716 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607990 | AAAAGTAATTTTGTA[-/TTCTTTTGTG]TTCTCTTTCTCTGCT | 51133 |
| rs537024692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611649 | TTTAAAAATGTTCTA[A/C]TGCAAATTGAAGTAC | 51133 |
| rs537028036 | snp | A/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565900 | CAAATTCATAAACTT[A/T]CTTTCTTTCTTTCTT | 51133 |
| rs537205541 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578334 | CAGCCACTTAACTCC[A/G]CTGTGTATACTACAT | 51133 |
| rs537224348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608976 | CTTGTGTTCTAGATA[C/T]TAGAAATTTTAAAAA | 51133 |
| rs537265014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577508 | GTTTTTATTTACACT[G/T]TTTAATGATTAAGGA | 51133 |
| rs537267006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585531 | AGGTAGTGTGCAAAA[G/T]AACGCTTCTTTTCCT | 51133 |
| rs537310934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609873 | TTCTGTGGTATGAAG[A/G]TATACCTGGTTTCTG | 51133 |
| rs537398363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571004 | ATGAGGGTCTAATTC[C/T]TTTGCCCAGAAATTC | 51133 |
| rs537434494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588796 | TCCAGCCACATCTAT[A/G]TATTCATCTGTTTGC | 51133 |
| rs537443100 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592156 | CCTCTCACAACACCT[A/G]GGAACTACAGGAGCT | 51133 |
| rs537446662 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597202 | AAAATGTTATAAAAG[A/C]GTTGACTCTGATTTG | 51133 |
| rs537455688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601288 | CTATACTTTAAAAAA[A/G]TAAATACAAATGAGA | 51133 |
| rs537578401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584893 | GAGAGAAAGAAATAT[A/G]CTCCAAATTTTGTTT | 51133 |
| rs537627762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604987 | AGTTTAACGAATAGT[A/G]CTTTCTGATTACAAA | 51133 |
| rs537629774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613365 | AGTCATGTTTTACTT[G/T]TTGATTTGAGTTCCT | 51133 |
| rs537715963 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605719 | ACCATCTACTTATCT[A/C]CTCAAGCTGAAAATC | 51133 |
| rs537802227 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607261 | AACATATTTTCTAAA[A/T]TCATAAATGGCAAAA | 51133 |
| rs537808483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580303 | TTCTGAGACTGTAGT[A/G]TATAATGATGTTAGA | 51133 |
| rs537901718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612428 | TCTATTTTAGACCTA[C/T]TTCCATCTACTTTAA | 51133 |
| rs537940359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609672 | ACTAGATGTGGCAGG[C/T]ATGAGAGAGGAAGGA | 51133 |
| rs537983893 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215573445 | AGAGATGAGATGGAA[A/C]CTGAAGGTAATTTTG | 51133 |
| rs537992380 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616346 | AAATACAGGAATAAA[A/T]TCTGATAATTTGTCA | 51133 |
| rs538003961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573634 | ATTGAAAGTAGCAAC[A/G]TTTAAAAATATTAAC | 51133 |
| rs538045886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586858 | AATGATGTTTTAGAA[A/G]AGACATGGGGAACAT | 51133 |
| rs538046509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595041 | ATCCCAGGATCCTTT[C/T]TGTTTTGTTTTGTTT | 51133 |
| rs538110127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596533 | AGACAACCAAGAGCC[A/C]AAGGGACACATTATA | 51133 |
| rs538170201 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587373 | TGATCTTGTGATCCG[C/T]CCACCTCGGCCTCCC | 51133 |
| rs538181795 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587242 | TCAAGCAATTCTCCT[A/G]CCTCAGCCTCCCAAG | 51133 |
| rs538200641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572750 | GCTGGGGTTTGGCCT[A/G]TGTTTCCTGGTGATA | 51133 |
| rs538233763 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590317 | GTAAATGTTTTTTAC[A/G]TATTCTAGATTTGTG | 51133 |
| rs538485716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618522 | TTCAGTTAGCCCTTA[C/T]GTGACTTTGGAACAA | 51133 |
| rs538638763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596394 | AAAGGGTGAGAAATA[C/T]TTGGAGTCCATAATA | 51133 |
| rs538639007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595296 | TGTTTTTAATCCAGG[A/T]TTTGATTAATTCTAA | 51133 |
| rs538734421 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572691 | ATAGATGGATGATAC[A/C]GTGTATACATGCACA | 51133 |
| rs538767073 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586932 | TTGCTTTTCCTGAAT[C/T]CCACTTAGTGGTGGA | 51133 |
| rs538796617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579578 | ATCTTGGCTCACTGC[A/G]AGCTCTGCCTCCTGG | 51133 |
| rs538816906 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615623 | GGCCTCCGTCTCAAG[-/A]AAAAAAAAAAAAAGA | 51133 |
| rs538846464 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593094 | TTGGCTTCACATGTT[C/T]TAAAAAGACATGTTC | 51133 |
| rs538854976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603110 | CTACTTGGCCCCTTA[C/T]GGAAAGTGTACCAAC | 51133 |
| rs538972781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585854 | ATGGAACTGTAGTTC[C/T]ATAGAGTTTTGCATT | 51133 |
| rs538977047 | snp | A/G | 3.35025e-05 | 0.00409269 | missense | KCTD3 | GRCh38.p7 | 1:215579029 | AAAATAAACAACACA[A/G]TCAGATCTGCTGATT | 51133 |
| rs538982642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594034 | CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG | 51133 |
| rs539161617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572118 | CAACACCAGTGTATT[C/G]TGAAAGTGCTCTGTT | 51133 |
| rs539372933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590484 | TCCTCCTTTTGAGCT[C/T]TCTAGATCACTTTAT | 51133 |
| rs539496427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569119 | GTATTTCTTTTCTTT[A/G]ATTTTCTTTTTTTTT | 51133 |
| rs539558282 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576494 | GGCAGGAGGATCCCT[C/T]GAGGCCGGGAGTTTG | 51133 |
| rs539595223 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612385 | CATAATCTTGGCACA[A/G]CTTACAACATAGCAC | 51133 |
| rs539608791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599528 | TATAAGAGAAAAATC[C/T]ACTTCCATTTTATAT | 51133 |
| rs539731896 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603337 | TCAGATGAATCAGTT[A/G]GTAAAACTAGAACAG | 51133 |
| rs539768454 | snp | C/T | 0.000872473 | 0.020868 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581054 | AGTTCAAGATCAGCC[C/T]GACCAACATGGTGAA | 51133 |
| rs539782158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574687 | TGTCCATGTGAAATT[A/G]TAAAAAGTTATCAAT | 51133 |
| rs539876558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619810 | AGGATTTTTCCTCCC[A/G]TCTTTTTTTTAGCTG | 51133 |
| rs539883348 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621321 | GTCTGTGTTTGAAAA[G/T]ATGAAATAAAAATAA | 51133 |
| rs539909561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613819 | TTTAAGTATATGGCT[C/T]TGTTTTCTGGGTTCT | 51133 |
| rs540018583 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215604056 | CTGCCTATTTTATCA[C/T]AGGGAAGCTTTGCGA | 51133 |
| rs540037586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580577 | CCGGTGATTTTTTTT[G/T]TTTTAATTGGGAAAG | 51133 |
| rs540044292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588269 | CCTTGACATAGCCAT[A/G]GTACTTAGTCATACA | 51133 |
| rs540062886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588590 | CAGTGTAAATGTCAA[C/T]ACAGATGTTCTAGAA | 51133 |
| rs540094129 | snp | C/G | 4.95029e-05 | 0.00497484 | missense | KCTD3 | GRCh38.p7 | 1:215620532 | GGAACTGACTCACCT[C/G]GTACTGCGTCCCCAT | 51133 |
| rs540125766 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606888 | GACGTAATTGTCCAA[C/T]TGAATCAACTAAAAA | 51133 |
| rs540162556 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566776 | ACATTAGTTGAGTGC[G/T]TACTATATTCCAGAA | 51133 |
| rs540185496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580760 | ATCACTGTTGAGTTC[C/G]GTTAAGAAAAATAGT | 51133 |
| rs540190934 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565518 | GAGATGTTCTCCTAA[G/T]TTTTAAGTACAGTAT | 51133 |
| rs540238535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581455 | GACTTGTAGACCCTT[G/T]TTTACATATTATGTA | 51133 |
| rs540247962 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574180 | GTGCTTGGTCCTAAC[A/T]TATAGTTACTCTAAG | 51133 |
| rs540302458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595725 | AATGTTCGAAGTTCT[A/G]TGCCTTGAGCATGGT | 51133 |
| rs540318873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612487 | GAGTAGGATTCCTGT[C/G]TTTATGCAGTCTCCT | 51133 |
| rs540371776 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566450 | CCAGAGGCTATTTTT[C/T]ATTTTTTTGGTAAAA | 51133 |
| rs540566709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572975 | GAACAAGTACTATAT[A/T]GCTTTGTTTGCCATA | 51133 |
| rs540591742 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612482 | CGTGAGAGTAGGATT[A/C]CTGTCTTTATGCAGT | 51133 |
| rs540610068 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600936 | AACTATCCTAGCAAA[C/T]ACATTTTTTTTTTTT | 51133 |
| rs540700567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591811 | TAGCCTCAAGTTCTT[C/T]GCCTCCTCAGTTCAG | 51133 |
| rs540722082 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587985 | TGGTATCCCTGCTGA[C/G]TACGTGTGAGGGAGT | 51133 |
| rs540761081 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567463 | GCGAAAGGTGGAGGC[C/T]GGGCCGCCCTTGTGC | 51133 |
| rs540777102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568575 | TCCTATAACTTATGA[G/T]TCACTCCTCTCAGAA | 51133 |
| rs540945462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618073 | AATAAAATGTATATG[C/T]TTCTCTCTTGTCAGT | 51133 |
| rs540965165 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569360 | TCCTGACCTCGTGAT[C/G]CTCCCGCCTCGGCTT | 51133 |
| rs540982866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615481 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGTGCCT | 51133 |
| rs541060204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609383 | CATTAATTGTTGGAT[A/T]ATAGGATATGTGGGT | 51133 |
| rs541195738 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575574 | GAATTCTAGACTGTT[G/T]CAGATAAAAATGTTT | 51133 |
| rs541356335 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591346 | CTTCCTTCCTTCCTT[C/G]TCTCTTTCTCTCTTT | 51133 |
| rs541406499 | snp | A/T | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608495 | CATTTGACATTTGAA[A/T]TTTTTTTTGTTAATC | 51133 |
| rs541434631 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590671 | TTGGACTTTTTAGCT[C/T]TAGTATTACTTTTTG | 51133 |
| rs541448716 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590015 | GAAAAACTGCCAAAC[A/T]GTTTTCCAAAAGTAC | 51133 |
| rs541469739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607453 | AATAAATAAAACTAA[C/T]TGGAGTATGTTTTTT | 51133 |
| rs541496423 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609025 | TACAATGTAGTGAGC[A/C]GTGGGAATTAAAATA | 51133 |
| rs541519565 | snp | A/G | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620996 | TTATGCCTGAGACTT[A/G]TCTTACAATGTTACC | 51133 |
| rs541615814 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570769 | CAAGTTGCATGAAGT[A/G]TAACTGTGGGTATGC | 51133 |
| rs541619130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575506 | ACATTGTAGTTTTAA[G/T]GATTGAACAGTATAA | 51133 |
| rs541624935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597986 | ATGAGATACTTACTT[A/C]GATTTAGACTTTCTA | 51133 |
| rs541630280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582596 | AGACAGAGTCTTGCA[C/T]TGTCACCCAGGCTAG | 51133 |
| rs541658372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614221 | CATCTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 51133 |
| rs541715581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614657 | ATGCTACTGATTTTT[A/G]TACATTGATTTTGTT | 51133 |
| rs541721027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599013 | AAATTATGATAAAAA[A/G]TATTCATAGAATAGT | 51133 |
| rs541754775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576064 | GGTTTTTTTTGTTTG[C/T]TTTTTTTTTTCCTTG | 51133 |
| rs541831173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568443 | GCCCTTGGAGTAAAC[A/G]GACTGAATGCTCTTC | 51133 |
| rs541964086 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610684 | CTGCATAATATACTG[A/G]AGAGCCAGACAGGTT | 51133 |
| rs542229473 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607326 | GTAGTTTTTGCATTA[A/G]TGATACACTTTATGG | 51133 |
| rs542277747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589879 | TCCAATTTGGAGATA[C/T]TATGAATAAAGCTGC | 51133 |
| rs542349981 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588376 | TTACTAAGACCATTA[C/T]ATTCTCTGCCACAGA | 51133 |
| rs542425951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605410 | TGCCCCACTGAGGAG[A/T]TTCTAACTCTTGCTG | 51133 |
| rs542511848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606384 | TCATTTATTTGCTTG[C/T]TTATTATCTCTATCT | 51133 |
| rs542565748 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583275 | GGATTATTCATGAGT[C/G]TTTCAGAAAGGAGCA | 51133 |
| rs542599150 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586232 | CTTTACTAAATTATT[A/C]TTTGGGGAAATATAG | 51133 |
| rs542617511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593416 | CTTTTTGTCATGTAT[C/T]GTCTTCTTGCTAGAT | 51133 |
| rs542641024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594346 | ATAAGGCCAATATGC[C/T]GCACCAAGGTGAGCC | 51133 |
| rs542673431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584952 | AAGCTGCAAAATCTC[A/G]AAAGAAAAGTGTTCT | 51133 |
| rs542819506 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600712 | CTTTTCAAATGAAAG[C/T]CAGGTATAGTATATG | 51133 |
| rs542861201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590921 | TTTCTTTAAAAGTTA[C/T]GAGCTTTGTTCTGGC | 51133 |
| rs542892468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610571 | TTATTCTGAGTTATT[C/T]ATTGTCAATATTTTG | 51133 |
| rs542914844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602458 | GAGCCATATTATTAT[A/G]ATGTTAGCTGAAATT | 51133 |
| rs542930871 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615339 | TAAGAAATCTATCCC[A/G]GCCGGGCGTGGTGGC | 51133 |
| rs542958450 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580824 | TAAAGTTTACAGATA[C/T]AGTTTAAAGAATCCC | 51133 |
| rs542996767 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569461 | TTCACAAGGACATAC[A/T]GTATTATTGTAAAAA | 51133 |
| rs543174486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615898 | AAGTTGTAAGTTAAC[A/G]GAAATAGACTGAGTA | 51133 |
| rs543185650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570344 | ATTCAGAAAGTAGAG[C/T]AGATGAAGTTTCATT | 51133 |
| rs543201010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591710 | GCAGTTAGGCCTTAG[C/G]CAAGGTCTTAGGGAA | 51133 |
| rs543289144 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601292 | ACTTTAAAAAAATAA[A/G]TACAAATGAGACTTT | 51133 |
| rs543307152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601014 | ACAATCCCCGCTCAC[C/T]GCAACCTCTGCCTCC | 51133 |
| rs543334736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584204 | GGATGAGTCCAAATT[A/G]CAGAAAGAACTCAAA | 51133 |
| rs543345435 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618406 | ATTTTTTTTTGTCTA[-/T]TTTTTTTGACCTTGC | 51133 |
| rs543384276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592427 | TGCCATTTATTCTAT[C/T]GTGATCGACAGCTTA | 51133 |
| rs543410226 | snp | A/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568407 | GCTTTTAGGAAGCTC[A/T]GGATATTGGCACGGT | 51133 |
| rs543445578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601588 | CACATGCAAAAAAAG[A/G]GGAGACAACCAATCG | 51133 |
| rs543588602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568783 | TGTAGTGCTTTAATC[C/G]TAAACATTTGATAGC | 51133 |
| rs543606880 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596201 | TCTAGTTTGACAATC[C/T]AGTAGCTAGTAGTAT | 51133 |
| rs543628132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569370 | GTGATGCTCCCGCCT[C/T]GGCTTCCCAAAGTGC | 51133 |
| rs543699087 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599161 | ATACACAGCAAAACT[A/G]TCATTCAAACCTGAA | 51133 |
| rs543756698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616572 | TCAAGATCAGCCTGA[C/G]CAACATGGAGAAACC | 51133 |
| rs543837127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584013 | TAAGAAGGCTTTTCA[C/T]GAACTGGGAAATTGT | 51133 |
| rs543913315 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591590 | TCGATCTCTTGACCT[C/T]GTAATCCGCCCGCCT | 51133 |
| rs543933247 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619643 | ACAATATTTATCTGT[G/T]GTTCTATTATGTTGT | 51133 |
| rs543973563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599956 | GCCTTATCTGTCCCC[A/G]TTTTCCTGCCATGAA | 51133 |
| rs543984656 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575584 | CTGTTTCAGATAAAA[A/G]TGTTTCCTCAGGTGT | 51133 |
| rs544094857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590834 | ATTTTCCTGTTTCAC[A/T]TGTCTAGAGAGTTTT | 51133 |
| rs544222801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580741 | ATACATAAACTATTT[A/G]TTTATCACTGTTGAG | 51133 |
| rs544233096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579814 | TTAACAAAACTATTA[A/G]CCAAAACAGGCAGAA | 51133 |
| rs544245525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611423 | TAAGATTTTGTGTGT[G/T]GTCTTCTAAAAAGTA | 51133 |
| rs544253977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603462 | TTTTTGAAAAAAAGA[A/C]AACAAAAGACACAGC | 51133 |
| rs544308064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617837 | TTAAATATATATTAC[A/G]TATATTTAGTATATA | 51133 |
| rs544339394 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614183 | ATTACAAATGCATGC[C/T]ACCACGCCTGGCTAA | 51133 |
| rs544399947 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215611740 | TAAGAAATTCTTTTC[A/T]TATATTAATATTAAT | 51133 |
| rs544402349 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587004 | CCTGAATGTGGGGTA[A/C]GTCACTTTCTTGCTC | 51133 |
| rs544554068 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589493 | AGTGAACCTACAACC[A/G]ATAGATACTATGCAA | 51133 |
| rs544685017 | snp | G/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568087 | ACAGCCTTCCTTACC[G/T]CATCTCAGATTAGAG | 51133 |
| rs544801672 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579750 | TGATCCGCCCGCCTC[A/G/T]GCCTCCCAAAGTGCT | 51133 |
| rs544915572 | snp | G/T | 6.82058e-05 | 0.00583937 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611947 | ATTGTAAAAATATTT[G/T]TATTCAGAAGCCACC | 51133 |
| rs544922072 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571560 | TACTGTCTTTCCTTC[A/C]GTTAGCCAATGAAAG | 51133 |
| rs544987742 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579357 | GGGTTGCCAAAATTT[A/T]TCTGGTAAGAGCCAG | 51133 |
| rs545022157 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587380 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 51133 |
| rs545033267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586917 | TGCTCTATGAAAATA[C/T]TGCTTTTCCTGAATC | 51133 |
| rs545209699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592378 | CATTTTTTTTTTTGT[C/T]GTTACTGCTGTTTTA | 51133 |
| rs545272354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584344 | TTGCAAAATAAGCTT[C/T]AGTCTTATTATACTT | 51133 |
| rs545283661 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613937 | TGGGTAGTGTGACGT[C/G]TCTGGCTTTGTTCAT | 51133 |
| rs545295754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585092 | TCATCCAGACCCCCA[A/G]AAAAGAGTTCTTGGA | 51133 |
| rs545295834 | snp | C/G | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620650 | ATAGTTGTTTCGTTA[C/G]ATTTAGATGAAAGTT | 51133 |
| rs545320989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590302 | TCCTGTTACTTATTT[A/G]TAAATGTTTTTTACA | 51133 |
| rs545420065 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621593 | ACAATTTTTTTTCAT[G/T]TAATTGGAATGATCT | 51133 |
| rs545433733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570438 | TGATTAATTCTGTTA[C/T]GGGCAAGTGTGATTT | 51133 |
| rs545536704 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607296 | TATATTTTTTATTAA[A/T]GCATGCCAAAAAAAG | 51133 |
| rs545602949 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580857 | ATGTATTTTTTTTTT[A/T]AAAATCTGAATTTAT | 51133 |
| rs545690673 | snp | A/C | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565652 | TCTTGGATTCAAAGG[A/C]TGTTAGCAACTATTC | 51133 |
| rs545690727 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607840 | ATATTTTGCAGCAAG[C/G]TAAAACATCCAGTTT | 51133 |
| rs545744888 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567482 | CCGCCCTTGTGCACC[C/G]CAGGATTGACCCGGG | 51133 |
| rs545808182 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575356 | TTTAAAAAAAAAAAA[A/T]TGTCATTACCTTTCC | 51133 |
| rs545865186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588406 | ACTTTCGGGAACATA[A/G]AAGGCCAAATCTTTA | 51133 |
| rs546095316 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573227 | GCTTAAAAAGAGATA[A/T]TACAGGATTGGATAT | 51133 |
| rs546320795 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577199 | ATTTTATACAAGCAC[A/T]ATGCTAGGCACTGTG | 51133 |
| rs546356250 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599728 | CTTTCTCTGTTTTCC[C/T]GTATGGAGGGGTAGA | 51133 |
| rs546372939 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593431 | CGTCTTCTTGCTAGA[G/T]GCCTTGCTTTTACAA | 51133 |
| rs546481083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579525 | TTTTTTTGAGACGGA[G/T]TCTCGCTCTGTCGCT | 51133 |
| rs546533712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612531 | TGAATGCTGCACTTA[C/T]GCTTCCATTATATGG | 51133 |
| rs546568943 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618826 | GTCTTTTTAGTTTCA[C/T]AGCTTCTTTTTAAAT | 51133 |
| rs546635803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603605 | CTTGATTATTTGAGA[A/G]TGATTTAGTATTGTA | 51133 |
| rs546637718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594010 | GATTACAGGCGTGTG[C/G]TACCATACCCAGCTA | 51133 |
| rs546668772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596327 | TATGGTTGTTCAAGT[A/G]TAGATGTTAAGTATA | 51133 |
| rs546698260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613246 | TATTTATGAATGAGA[C/T]GGAGTCTTGCTCTTT | 51133 |
| rs546805126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572665 | GCTGCTAATTTAGGT[A/G]ATGGCAGACAATAGA | 51133 |
| rs546851722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602943 | AGTAGGACTTAAATT[A/G]TATTGCTCTAGAAAT | 51133 |
| rs546901567 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594780 | CTGGAACACATGGGG[C/T]TTAAAAATAAGCTCT | 51133 |
| rs546946801 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582593 | TTGAGACAGAGTCTT[G/T]CACTGTCACCCAGGC | 51133 |
| rs546948902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586432 | GTTTTTGGTGCATTG[A/G]TGTGTATTCCGTTTG | 51133 |
| rs547000412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611519 | CCAAAGATAGTAAAT[A/G]TCTTAACAGGTCTCC | 51133 |
| rs547063874 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583187 | ATGGCTACTCCATAG[C/T]CAGAGCAGCCCTGAG | 51133 |
| rs547202405 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567840 | GTGTCGACGGGGACC[C/G]AGAGTCGCAGGAACG | 51133 |
| rs547206910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610800 | ATGGAGATGGTAAAT[A/G]ATAGTACCTCCCTTA | 51133 |
| rs547239276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599456 | ATAGACTGGTATTTT[A/G]AAACTGTAAATTTAA | 51133 |
| rs547255873 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609049 | TAAAATAAAACAGTT[G/T]CATTTTGCAACTTTG | 51133 |
| rs547337908 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572650 | TTTTGATAATTCCAG[A/G]CTGCTAATTTAGGTA | 51133 |
| rs547355736 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215592398 | CTGCTGTTTTAAAGT[G/T]GAGAATAATCGGGTG | 51133 |
| rs547444346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583613 | CCCAGCAGGTCTCAG[C/T]CTTATTTTACTCAGT | 51133 |
| rs547468504 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580846 | AGAATCCCAGATGTA[-/T]TTTTTTTTTTAAAAA | 51133 |
| rs547489419 | snp | A/G | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622176 | ACTAGATTGCATTAC[A/G]GTACAAGTCAAATCG | 51133 |
| rs547505391 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586244 | ATTCTTTGGGGAAAT[A/G]TAGAACTGTAGTCTC | 51133 |
| rs547562846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614114 | ATCAGCTTACTGCAA[G/T]CTCTGCCTCCCGGGT | 51133 |
| rs547568492 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618323 | CCCTCCTTTTTGTCC[A/G]GCCTACTAGGAAGCT | 51133 |
| rs547663547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588560 | CTGTTTTTACCAAAC[A/G]TTGCTTTGCATCATC | 51133 |
| rs547737189 | snp | A/G | 0.00012667 | 0.00795734 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580981 | TTTAAGAGTGTTTTG[A/G]CTGGGCACGGTGGGT | 51133 |
| rs547757389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574957 | AAATTTCCATAAAAA[G/T]TTATCAATTATGGGC | 51133 |
| rs547851109 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610410 | CCAAGGAAAGGAGCC[A/T]GTTTGGGAAGGGAAA | 51133 |
| rs547861387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589513 | ATACTATGCAAAAAT[C/G]TTTTGCTACATAAAG | 51133 |
| rs547903459 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215621956 | ATCAATGAAAGAAAA[C/T]ATTAGGCAAAGCATA | 51133 |
| rs548020300 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569844 | TGGTTTGAACAGTTT[A/G]CAAGACATGAAATTG | 51133 |
| rs548067510 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618443 | CTATACTGATTTTTC[C/T]TTTTTAATAAACTCC | 51133 |
| rs548084549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589337 | CACTGTATAGATAGG[G/T]TCTCACTATGTTGCC | 51133 |
| rs548098679 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215566109 | ATGAGGTACAATGCA[C/G]TGGTAAGGATGGTGA | 51133 |
| rs548168121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573666 | GTAATAAATATATTG[A/G]TACAGCTATAACTAT | 51133 |
| rs548171986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580908 | TAAGTGCTGTTTATA[C/T]CAGTAATCTCAGGTT | 51133 |
| rs548305418 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574360 | AGGATATGAGCTTAC[A/G]TTGGCATTAGAAGAA | 51133 |
| rs548569951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588464 | CTTTTATGTTCTTGA[A/G]AGTCTATGGCAGAGA | 51133 |
| rs548704710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585462 | TATTTTTATTTAGGC[C/T]CTTAGGTGACCATCA | 51133 |
| rs548809737 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595125 | AGCTTCAGGATAAGG[G/T]GTTATACAGCAGTAT | 51133 |
| rs548978218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592636 | TAATGTGATAGGTAG[C/T]TATGTTATGAGCTGG | 51133 |
| rs549212574 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609455 | TCGTGGAAGGCATCT[A/G]TACATCAAACTAAGA | 51133 |
| rs549302583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583578 | TGTGACTAAGAATGC[C/T]TAACCTCCTGGGAAT | 51133 |
| rs549321655 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618482 | TTTTGAAGTAGGCTG[C/G]GATAACTAATTCAGT | 51133 |
| rs549348828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584524 | CAAATACCTGTATGA[A/G]TTGGGTAAGTTTCTT | 51133 |
| rs549351462 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572853 | GATTTCATATAATGC[C/T]AGAAAATAAATGTGG | 51133 |
| rs549409827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583755 | CTGCAGTCTGAATAG[A/G]GATGATGGTATTTCT | 51133 |
| rs549410644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615010 | TTCAATTCTAATATC[C/T]CCTCTTCTGTTATTT | 51133 |
| rs549414428 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568924 | AGTCTTATGGAGATT[G/T]ATGTCTCCTAATGTA | 51133 |
| rs549434385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577267 | CAGGGAATTTATAGT[A/G]TAATTGGGGAGATTA | 51133 |
| rs549459968 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609659 | ATGGTGGTCATTGAC[A/T]AGATGTGGCAGGCAT | 51133 |
| rs549558607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582944 | AATTTTTTAAAAAAC[A/C]GGTAAATTCACATAT | 51133 |
| rs549590573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575839 | TCCCTATTAGTGTTA[C/T]AGATATTAAAGTTAA | 51133 |
| rs549603793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598455 | TACAGATATGACACC[A/G]GTTAGAACACTTTCT | 51133 |
| rs549631966 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576274 | GGGTTTCACTGTGTT[G/T]CCCAGGCTGATTGCA | 51133 |
| rs549726898 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576366 | GAGCCACTACGCCCA[G/T]CCAGAAAAGGTTTTT | 51133 |
| rs549915544 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567196 | ACGAAATGGAATCCC[C/G]CGTGGGCAGGCGGCT | 51133 |
| rs549985058 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589173 | CAGGGTCTTGCTCTG[C/T]CACACAGGCTGGAGT | 51133 |
| rs550005103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591338 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCTCTCTTT | 51133 |
| rs550030450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608733 | GTGTGCATACACATA[C/T]ACAGTCTTCATAGAG | 51133 |
| rs550143960 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568008 | ACCAGGCCCATGTGG[C/G]AGAGTAGCTGCTGTC | 51133 |
| rs550156511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575744 | CATGAAATGCACACA[A/G]ACTACATTCCAATTT | 51133 |
| rs550183111 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622102 | CAGGAATAAAAGGCC[A/C]TTAAAAAGAAGATAG | 51133 |
| rs550204553 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621360 | GGCAAAGCTTTGAGT[A/G]CCCAGAAGGGAAAGC | 51133 |
| rs550234356 | snp | A/G | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621202 | GATTTTAATTTAGTC[A/G]TGCGTCATTTTCTGA | 51133 |
| rs550336888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618364 | TCATATTCTATTCCT[C/G]TATGCTTCTCAAATT | 51133 |
| rs550343104 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566526 | TTTGAATTATTATGA[C/T]ACAACTATGACAAAA | 51133 |
| rs550438554 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589434 | GCATGAGTCGCTGTG[A/C]CTGGCCAATTTCTTT | 51133 |
| rs550440804 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616675 | TGAGGCAGGAGAATC[G/T]CTTGAACCCAGGAGG | 51133 |
| rs550452247 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605112 | TTGCTTTCTAGAGGA[A/G]TCTTACATTAACTCC | 51133 |
| rs550467823 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582834 | TCCAAAGTGCTGGGA[G/T]TCCAGGCGTGAGCCA | 51133 |
| rs550523890 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596273 | GGTGGGTAGGGTGAA[G/T]AATTATTAGATTGAT | 51133 |
| rs550529354 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215611051 | AGCTACTAAGTGTAA[G/T]GGGAAAAGAGAATTA | 51133 |
| rs550652611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612605 | ATTCAAACTTAAAGA[A/G]CATAGTGAATTTGCT | 51133 |
| rs550681892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602810 | ATTCAGTAATACTAA[C/T]AGGTTTGGATGTGCT | 51133 |
| rs550766903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593739 | CAAAGATCTACATAA[A/T]ACAGTATTGTAGAGG | 51133 |
| rs550776890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578896 | TGGAAGATGTATTTC[A/G]GCTTTAATGAAATTC | 51133 |
| rs550789714 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583431 | TAATTAGCGTATAAT[A/G]AGCAGTGAGGACGAC | 51133 |
| rs550801292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586365 | TTATTTGTAATAGGA[A/G]GGTGGATGGGTAACT | 51133 |
| rs550820859 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610725 | CCACTTCCATCATAT[A/C]GGACCTATGAGAACT | 51133 |
| rs550864182 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579460 | AACACATAATGGACA[A/G]TATGTAACAAGTAAG | 51133 |
| rs550883845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616720 | AGCCGAGATCACGCC[A/G]TTGCACTCCAGCCTG | 51133 |
| rs550989802 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570900 | CAAATGATTATGCTC[A/T]TCATGTGTAATTTTA | 51133 |
| rs550997434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601767 | TAAAATTGGATATTG[A/G]TTGCCTCTTTACCAG | 51133 |
| rs551002289 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580084 | TAGATTGAAAAGCTA[-/T]TTTTTTTTTAGTCAT | 51133 |
| rs551062541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585628 | TGAGTTTAAAAATAG[A/G]TACTTCATAGTTCAA | 51133 |
| rs551087800 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571725 | CAGCTCCACCTCCTG[A/G]GTTCACGCCATTGTC | 51133 |
| rs551163082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569818 | AAGATACAAAATAGT[A/G]CATATATTACTGGTT | 51133 |
| rs551320495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606753 | TATTTTGTGTATACT[C/T]AGTTATGTTATTCTG | 51133 |
| rs551400318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617733 | GGGGCTGCAGTGGAC[C/T]TGAGTGAATATGCTT | 51133 |
| rs551446808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613142 | GAACTTAAAAGTTAC[A/G]GGGAAAAAGTTTTTT | 51133 |
| rs551483949 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615488 | AGCCAGGCGTGGTGG[C/T]GGGTGCCTGTAGTCC | 51133 |
| rs551483992 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576360 | AGGAATGAGCCACTA[C/T]GCCCAGCCAGAAAAG | 51133 |
| rs551522567 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580073 | ATTTTATATTTTTAG[A/G]TTGAAAAGCTATTTT | 51133 |
| rs551524564 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571776 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 51133 |
| rs551630459 | snp | A/G | | | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215618988 | ACCAAGGCGCTACTT[A/G]TTCACAGGCCATACA | 51133 |
| rs551645500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616417 | GGAAATTTTAAAATC[C/T]GATAATGCCCATGAA | 51133 |
| rs551663292 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615781 | TTTTATATGACACGA[C/G]AGCCTTCAGAATGAA | 51133 |
| rs551675062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586297 | TGTATGCAAGTATAC[A/T]ATACCCCAAGGATAA | 51133 |
| rs551691332 | in-del | -/TAAG | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215621824 | GCGTTTTCAGTTATT[-/TAAG]TAACAGTTCTGTTTA | 51133 |
| rs551722757 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589619 | AACATAAACTGCATT[A/G]TTTATGCAGTTAGGC | 51133 |
| rs551778877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609775 | AAGAAGAACTTATTT[C/T]GAAAACAAAGATGAA | 51133 |
| rs551816281 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570082 | AGTGTAACATAGTCA[C/T]TTAAGCCACTGTAAG | 51133 |
| rs551851490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592125 | TCCCCATGATTCAGT[C/T]ATTTCCCATGGGGTT | 51133 |
| rs551867347 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601207 | AGGTTTCTTTTAGCA[A/C/T]AAATATGGGAAGGTA | 51133 |
| rs551875755 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602262 | TATTCATTAGTTTAT[C/T]ATGTGACTAGGTCAA | 51133 |
| rs551913842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605619 | TGGATCTCTGGTTGT[A/C]TGTTTAATAGGCATC | 51133 |
| rs552001243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569063 | GCAGTATAATCATTT[A/G]CAATCCCTACACTGG | 51133 |
| rs552003860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597120 | TTGAGTCAAATGAAC[C/T]AGGTTTGTATGTAAT | 51133 |
| rs552137215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587740 | TCTTTTCAGAAAATT[G/T]TGCATAGTCTTCTTT | 51133 |
| rs552200265 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587217 | TCACTGCAACCTCTG[C/T]CTCCTGGGCTCAAGC | 51133 |
| rs552256669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588604 | ACACAGATGTTCTAG[A/G]ATAAGCCATGAAATT | 51133 |
| rs552565254 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215592353 | AAACAGTTGTTTCAT[A/G]TATTTTGTCCATTTT | 51133 |
| rs552581878 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595894 | TACCTGATTCTTAAA[G/T]GAAAGAGGAAAAAAT | 51133 |
| rs552612490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603751 | TATGTTGAGTACCTG[C/T]GGTGTCTCAGGCACT | 51133 |
| rs552765642 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603159 | TGTGGATTTTTTTTT[A/T]AAATCTAGTTAAAAG | 51133 |
| rs552854866 | snp | A/G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574967 | AAAAAGTTATCAATT[A/G/T]TGGGCTGGGTGGGGT | 51133 |
| rs552883784 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585582 | AGGTAAGCCAAAAGA[G/T]AAATTTTATAGTTAT | 51133 |
| rs552998835 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613741 | AGTAATCCCAGCACC[A/G]TTTATTGAATAGGGA | 51133 |
| rs553030123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604069 | CATAGGGAAGCTTTG[C/T]GAGGGTAGCTTTTTT | 51133 |
| rs553030240 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594347 | TAAGGCCAATATGCC[A/G]CACCAAGGTGAGCCT | 51133 |
| rs553068561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578409 | ATAGCATTGATTGGG[C/T]TGGATTTTCCATGGC | 51133 |
| rs553176517 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601474 | CTTGCTTACTGTGTA[A/C]CTTTGGACAGGTCAT | 51133 |
| rs553407003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617067 | ATAAAATAATAATAA[C/T]AAACTGAGTTCAGAG | 51133 |
| rs553420920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571523 | AGTTTACATTTAAAT[A/G]TCTTTAATAAATGAA | 51133 |
| rs553427734 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622222 | TACAGGAGATTGAAC[A/C]TTGATGCAGTGGTTT | 51133 |
| rs553442573 | snp | A/T | 0.000148332 | 0.0086107 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577746 | ATGTGCTCTTTTAAT[A/T]TTTGGTGTTTATGAT | 51133 |
| rs553468968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571133 | ATTATTTGGAATACA[A/G]TTGGTGAATAAGTGG | 51133 |
| rs553489264 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621570 | TAAGAGCAAAAGAAC[A/G]TTTTTGTACAATTTT | 51133 |
| rs553561436 | snp | A/G | 1.90188e-05 | 0.00308367 | synonymous-codon, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215575957 | AAATTTTCTTCGGAC[A/G]AAAGAACTAGACTTA | 51133 |
| rs553592872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584964 | CTCGAAAGAAAAGTG[C/T]TCTTGACTCCAAAGT | 51133 |
| rs553601609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589754 | GAAATTCATCCATGT[C/T]GTTGCATGTATCAGT | 51133 |
| rs553665314 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588993 | ATTGGGTATACTTCT[C/T]TAGCCACTGTGATGT | 51133 |
| rs553665422 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598695 | GAAAATTAAAAGGTC[A/G]TTGAAAAAAAATTTT | 51133 |
| rs553716835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575284 | AAAAGTTACCAATTA[C/T]GTATTTTACATTTTT | 51133 |
| rs553740899 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566206 | TTTGAGCAAGTTTTT[C/T]TGATCATTTTCATTC | 51133 |
| rs553778238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582334 | ATACAACTTGAGGTG[A/G]AGTATGTTCATAATA | 51133 |
| rs553792184 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576648 | CCCAGACTCACTGCA[A/G]TCTCCACCTCCCGGG | 51133 |
| rs553796571 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582930 | GTACCTTCTTTGTAA[-/T]TTTTTTAAAAAACAG | 51133 |
| rs553875033 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567423 | CACGGAGAAGAGGCC[C/T]GGGCGGCCCGGCGGC | 51133 |
| rs553931159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573138 | TTGAATGAATGAAGT[C/G]AGCAGTTGCAGATAG | 51133 |
| rs553976460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605226 | AGAAGATAATGCATC[G/T]TTTGTGAAAGATGTA | 51133 |
| rs554008942 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215621814 | TTATGTCAATGCGTT[C/T]TCAGTTATTTAAGTA | 51133 |
| rs554018270 | snp | C/T | 1.65866e-05 | 0.00287976 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573845 | TTTTTTCCAGGTATG[C/T]CTTATAATTCTTTAG | 51133 |
| rs554120262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579744 | ACCTCATGATCCGCC[C/T]GCCTCGGCCTCCCAA | 51133 |
| rs554378234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605031 | GAAGAAATTCATTGT[A/G]TATGGAAGATGATTT | 51133 |
| rs554395110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588132 | TACTTTGTTTATTTT[C/T]TGAGGATAGTTCTGC | 51133 |
| rs554520567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588236 | GCTCTTTGCTCCAGC[A/G]TTTGTGAAGGTGCTT | 51133 |
| rs554590403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596566 | ATGGAGAAATGACAT[C/T]AATTTTGGCAGTAGA | 51133 |
| rs554639030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618581 | CTGATCCGTCAATGT[A/G]GATAAAAATTGTTCT | 51133 |
| rs554653977 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612441 | TATTTCCATCTACTT[G/T]AACATGGAGAGAAAT | 51133 |
| rs554809675 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572325 | GAAAAAACAACATCT[A/G]CTTTTTTAATACAAA | 51133 |
| rs554906470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586872 | AAAGACATGGGGAAC[A/G]TCTTTTCACCACTTT | 51133 |
| rs554932163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570008 | TTTGAATCCTACACT[C/T]GTGCAGCATTTTAGA | 51133 |
| rs554942549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569255 | GCATCCCGAGTAGCT[C/G]GGTCACAGGCGCGCG | 51133 |
| rs555031969 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600732 | TATAGTATATGAAAA[C/G]TAAAAGTCCCTTAAC | 51133 |
| rs555118616 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576067 | TTTTTTTGTTTGTTT[G/T]TTTTTTTCCTTGAGT | 51133 |
| rs555123898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587266 | TCCCAAGTAGCTGGG[A/G]CTACAGGCACATGCC | 51133 |
| rs555159924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610040 | AATTAATTATAAAAC[C/T]CAGTAAGATAAAGGG | 51133 |
| rs555174128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616505 | GTGGCTCACACCTGT[A/G]ATCCCAGCACTTTGG | 51133 |
| rs555246640 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599012 | TAAATTATGATAAAA[A/T]GTATTCATAGAATAG | 51133 |
| rs555248058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583788 | CTATTAGGGTCTTCT[C/G]CATTCAGAGTAGAGG | 51133 |
| rs555282755 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607262 | ACATATTTTCTAAAA[A/T]CATAAATGGCAAAAT | 51133 |
| rs555363665 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215573401 | AGAAGTTTTGTCCTA[C/T]TAGAGGGGAAAACCA | 51133 |
| rs555376294 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581604 | CCACCACATTATTAC[A/G]CAAAATTTAACTCAC | 51133 |
| rs555575155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583405 | GTGTCTTTTAGCATG[A/T]TAATGCATTATAATT | 51133 |
| rs555599484 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577042 | AGTTCTGAATCTTCC[A/G]TTTTTTAAAAATTTT | 51133 |
| rs555626560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614137 | TCCCGGGTTCACACT[A/G]TTCTCCTGCGTCAGT | 51133 |
| rs555792175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590616 | TTCTACAGTATTCAA[C/T]CTGCAGTTAAGTTCA | 51133 |
| rs555832662 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607999 | TTTGTATTCTTTTGT[A/G]TTCTCTTTCTCTGCT | 51133 |
| rs555834449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598991 | TAAATGTGCTATAAT[A/G]AAAGATAAATTATGA | 51133 |
| rs555836023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615877 | GTAGAACTGTGACTG[A/G]ACAAAAAGTTGTAAG | 51133 |
| rs555878372 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589049 | TTAGATTTTTCATTT[C/T]TAGTTTGAAGGTCTA | 51133 |
| rs555921302 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567244 | CCTAGCCTCCCTACG[C/T]GCCAGCCCCGCGGCG | 51133 |
| rs555922273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599830 | ATCCTCCCAGAGAAT[A/G]AATGGTAAAAATGTT | 51133 |
| rs555949507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590846 | CACATGTCTAGAGAG[C/T]TTTGATTATGTGCTG | 51133 |
| rs555957678 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569154 | TTGAGACGGAGTCTT[G/T]CTCTGTCGCCTGGCT | 51133 |
| rs555985104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589842 | TTTATCCATTCACCC[A/G]TTGATAGACATTTGG | 51133 |
| rs556000390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575046 | TACCTGAGGTCAGAA[G/T]TTCAAGACCAGCATG | 51133 |
| rs556058163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590533 | GAGCCCTGATTTTTT[A/G]TTTCATTTTTTTCTC | 51133 |
| rs556107917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568325 | TTCAGAATTTCTTGG[C/T]GCATGGGCTTGAAGG | 51133 |
| rs556169235 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576059 | TAAAAGGTTTTTTTT[G/T]TTTGTTTTTTTTTTT | 51133 |
| rs556173488 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588396 | TCTGCCACAGACTTT[C/T]GGGAACATAAAAGGC | 51133 |
| rs556498943 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611999 | GCATAATTTGACATA[C/T]TGACCAAAGAGTGCT | 51133 |
| rs556526845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573923 | GTTAAATTTTTTTTA[A/T]TAAAAAAGGTTAACT | 51133 |
| rs556628408 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614139 | CCGGGTTCACACTAT[A/T]CTCCTGCGTCAGTTC | 51133 |
| rs556635133 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587199 | CAATGGCATGATCTC[A/G]GCTCACTGCAACCTC | 51133 |
| rs556671952 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590721 | TTCTTCTGCTAAGAT[G/T]TCTTGTCTTTTTGTT | 51133 |
| rs556694187 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578333 | ACAGCCACTTAACTC[C/T]GCTGTGTATACTACA | 51133 |
| rs556701426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574701 | TATAAAAAGTTATCA[A/G]TAATAAGATCTCCAC | 51133 |
| rs556891811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613603 | GGTTGATATTTCCTA[A/G]GTTTCCTTCTAGGGT | 51133 |
| rs556906311 | snp | C/G | 1.65111e-05 | 0.0028732 | missense | KCTD3 | GRCh38.p7 | 1:215620542 | CACCTGGTACTGCGT[C/G]CCCATCTCCTACAAA | 51133 |
| rs556986542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616991 | AAGGGGAGAGGAGCC[A/G]AAGGCTAAGTTGATC | 51133 |
| rs557028302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611702 | TGATGTTGAGCTGAA[A/G]TGTGATACCATATTG | 51133 |
| rs557032196 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602360 | TTTGTATTCAGTTTT[A/G]TACTGAAGTCAAACA | 51133 |
| rs557123118 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570243 | GTCTTTTTTTTTTTT[C/T]CCCTCAGGAGAATAG | 51133 |
| rs557164651 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608992 | TAGAAATTTTAAAAA[G/T]TGCGGTGAACATCAA | 51133 |
| rs557292018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611020 | CTTTTTATGAATTGT[A/G]AGTTGATATTATTTT | 51133 |
| rs557373548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584908 | GCTCCAAATTTTGTT[C/T]ATAAGAGTATACTTT | 51133 |
| rs557459241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577512 | TTATTTACACTTTTT[A/G]ATGATTAAGGATAAT | 51133 |
| rs557501769 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596792 | TTATTTTTCCTCTAG[A/G]TTAGGACAGGCTTGA | 51133 |
| rs557516706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569361 | CCTGACCTCGTGATG[C/T]TCCCGCCTCGGCTTC | 51133 |
| rs557559511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602272 | TTTATTATGTGACTA[A/G]GTCAAATTAAACTGG | 51133 |
| rs557590815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591649 | GTGAGCCACCGCGCC[C/T]GGCCAGCAGCCTTTC | 51133 |
| rs557636514 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599098 | ACCAGAAGACGACAA[C/T]GGGCATTCTCCAAAT | 51133 |
| rs557653748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577482 | TAACAGAATATTTTT[A/G]TTCACATGCAGTTTT | 51133 |
| rs557656397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600548 | CACACTATAATTGTC[C/T]GTTATTTTTCTTTCT | 51133 |
| rs557675008 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602998 | TAGCCAAGCTGGCTC[G/T]TTTTGATACCACTGT | 51133 |
| rs557742282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570110 | AAGAGAAAAATCCTG[A/T]TATGATTGCCACTGA | 51133 |
| rs557753054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616869 | AAAGTCTTCCAAATG[A/T]TAAGTGTCTTTTTGT | 51133 |
| rs557766455 | in-del | -/CTTTCTTTCTTTCTTTCTTTCTTTCTTT | 0.00716266 | 0.059414 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565896 | ACACAAATTCATAAA[-/CTTTCTTTCTTTCTTTCTTTCTTTCTTT]CTTTCTTTCTTTCTT | 51133 |
| rs557785001 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572512 | GGTAGTCACAGTCAC[C/T]CTGGCCTGCAATCCA | 51133 |
| rs557839868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601578 | ATCTAGTGATCACAT[A/G]CAAAAAAAGAGGAGA | 51133 |
| rs557857214 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614235 | ACGGGGTTTCACTGT[A/G]TTAGCCAGGATGGTC | 51133 |
| rs557913578 | snp | C/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569017 | CCCTAAAGAGGAGGC[C/T]TGCAATGTGTGTTGA | 51133 |
| rs557965298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582437 | CGTAACTCTATTCTT[C/T]GCATAGCTGTCTTAA | 51133 |
| rs557981067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576798 | TGGTCTCCATCTCCT[C/T]ACCTCGTAATCCACC | 51133 |
| rs558029467 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582333 | CATACAACTTGAGGT[C/G]AAGTATGTTCATAAT | 51133 |
| rs558031363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584835 | TATTGCTGTAAGTTA[A/G]GAATACTCACAAATA | 51133 |
| rs558063918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616535 | GGAGGCTGAGGTGGG[C/T]GGATCACCTGAGGTC | 51133 |
| rs558068400 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587660 | TGTGATACATTGTTT[G/T]GATTGAAGTATATGA | 51133 |
| rs558125329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606001 | CCTGATGGCTTCTAA[C/T]TGTATTTAGAATAAA | 51133 |
| rs558159339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608880 | CCAGTTTTAACAGTT[A/G]TTATATAATCCCAGT | 51133 |
| rs558211407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590763 | GCTGTTTAATTTGTT[A/G]AAGTATTTGTCTGCT | 51133 |
| rs558299168 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591549 | TTTTAGTAGAGACAG[G/T]TTTCACCATCTTGAC | 51133 |
| rs558553111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596409 | TTTGGAGTCCATAAT[A/G]TTTATGTGATAAAAA | 51133 |
| rs558567007 | snp | C/T | 4.98915e-05 | 0.00499432 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215595387 | TGTTCCTGTAGATGC[C/T]CTCTTCTTTATTGGT | 51133 |
| rs558580208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604118 | ATCACCTGTCAACTC[C/T]TGACTTTATATAGGT | 51133 |
| rs558604409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618534 | TTACGTGACTTTGGA[A/G]CAATCATTTGCTGAT | 51133 |
| rs558622456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611979 | TTTGTCTTACAAAAC[A/G]TATGGCATAATTTGA | 51133 |
| rs558634959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617763 | TACCTTCCACTAGTT[A/T]TACATTGTCCCACTA | 51133 |
| rs558831201 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591066 | AGGCTGTAGTTCTTA[C/T]TTTTAAGATGTTGCT | 51133 |
| rs558982654 | in-del | -/TAATT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605259 | GAAAGTTTCTCAATC[-/TAATT]AAACACCATGTGGAG | 51133 |
| rs558986041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571670 | GAGTCTCGCTTTGTC[A/G]CCCATGCTGGAGTGC | 51133 |
| rs559120059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586269 | AGTCTCTTTCAAGTC[A/G]TTATATGTGCTATGT | 51133 |
| rs559150004 | snp | C/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215566068 | ATCTGAACTGTTACT[C/T]ATCTTCCCTGTCTAA | 51133 |
| rs559189553 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569934 | AAATAAGTAGTAATG[A/G]TATGGCCCGTAGAAA | 51133 |
| rs559361571 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579304 | ATTTTTATTTAAAAT[A/G]TTGTGTAATCTTCTA | 51133 |
| rs559491635 | in-del | -/GTCTGGATCTCTGG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605601 | CCCTGTATATCCAGT[-/GTCTGGATCTCTGG]TTGTATGTTTAATAG | 51133 |
| rs559553972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601644 | TGGGAAATACAATTT[A/T]AAAAAAATATTTTGA | 51133 |
| rs559595273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585504 | CTAAGTTTGCTTTTT[A/G]CAGCGAATGTCAGGT | 51133 |
| rs559655268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616275 | GAACATTTTAAATCA[A/G]TTTACAGATATTATT | 51133 |
| rs559670876 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620843 | TTAACAGATCATTTA[C/T]AAAGCAGGAGTCCAT | 51133 |
| rs559688500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592704 | ATTTGTTGTTAACAA[A/G]TATTCTTCAGAACAT | 51133 |
| rs559721949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591791 | TGTACTGTATCTACT[A/G]ACTCTAGCCTCAAGT | 51133 |
| rs559732052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619959 | TATAATACACTTTAT[A/G]TATTTATATAGTGTG | 51133 |
| rs559760620 | snp | A/G | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570371 | CATTTAGAATTGTTA[A/G]TATTCGTTATTTACA | 51133 |
| rs559833721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569486 | TAAAAATTAAGCAGT[A/G]TTGTTATTTACTATG | 51133 |
| rs559884584 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615016 | TCTAATATCCCCTCT[C/T]CTGTTATTTCTGATA | 51133 |
| rs559932878 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583586 | AGAATGCCTAACCTC[A/C]TGGGAATGCAGCCCA | 51133 |
| rs559939945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574834 | ATAGTAGGAAGAGTT[G/T]TATTACTGGCTGCCA | 51133 |
| rs559949772 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588313 | TATAGTTGAAATTAA[A/G]TTTTTATCAGTACAA | 51133 |
| rs560031106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605507 | TCTTTATCTGCACTT[C/T]CCTAGTTATTTGAAT | 51133 |
| rs560049007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577145 | TAGTCTTTTTTTTTT[G/T]TCTATTTTATTTGTT | 51133 |
| rs560082874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594892 | TAGACACATTCTAGA[C/T]AGTTAAGGCTGCCAA | 51133 |
| rs560122805 | snp | A/G | 1.66067e-05 | 0.00288151 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580034 | GCTTTGCTTTTACAG[A/G]TGGCAGTTTGAAAAT | 51133 |
| rs560180992 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576114 | TGCCCAGGCTGGAGT[G/T]CAGGAGTGCAGTGGC | 51133 |
| rs560198486 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610450 | GGAGGTGGGGGAAGC[A/G]AGGGCAAAGAAGGTA | 51133 |
| rs560203207 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596747 | AGCTTAAGGATCAAG[G/T]CTGGTTTGAAAAAAA | 51133 |
| rs560209440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587686 | TATGAAGAAAACTTG[A/G]TCTTACACAGATATG | 51133 |
| rs560216791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595763 | GCAAATTTTATTTCC[A/G]GAATAGGAGCACAGA | 51133 |
| rs560235029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613846 | TTCTGCATCCTGTTG[C/T]TTTGGTCTATGTGTT | 51133 |
| rs560295543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592596 | AAGTGAAAGAAATTT[C/T]ATTACTTGCTTGGTG | 51133 |
| rs560356912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574232 | TAATAATCACTGAAT[A/G]AAAGTGGCATAATTT | 51133 |
| rs560420175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580810 | TCTAAAATGTCTTCT[A/G]AAGTTTACAGATATA | 51133 |
| rs560457729 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614023 | CTTTAGAATAGTTTT[G/T]TTTTTTTTTTTTTTT | 51133 |
| rs560505476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604383 | AAACGCAGTGTTTAT[C/G]TGAGAAAAATATACT | 51133 |
| rs560664769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612118 | ATTTAAGAGTTTCAC[C/T]GATGCTGTGGACAGT | 51133 |
| rs560754887 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617222 | AATTAACTCGTAAAT[A/C/G]CGAGCTTTCCTTTGA | 51133 |
| rs560810505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618663 | CTTTTTTTGAAGTTG[A/G]GTATTATCCTAATGA | 51133 |
| rs560844200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573985 | TAGATAACTTACTTT[C/T]AGTGGTCTTTAACAT | 51133 |
| rs560904058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573317 | CTTGAATTATTGGAC[A/G]TGAAGAGAGTGATCT | 51133 |
| rs560920874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602848 | TAAGTCATCATTTCA[C/T]TTAAGTTATTAAAAG | 51133 |
| rs560952069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587022 | CACTTTCTTGCTCCT[C/T]ATTGTTGCTTCTAGA | 51133 |
| rs560974936 | in-del | -/TG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597548 | AGAATCAGATAACTC[-/TG]TGTGTATTCTGAGAA | 51133 |
| rs561058135 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603528 | AAGTATGATGTAAGC[A/G]ATGTAATGGGTATGT | 51133 |
| rs561079956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619710 | AAAGTTCCATAATGT[C/T]TTTTTAGTTATCATA | 51133 |
| rs561179281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579520 | TTTTTTTTTTTTGAG[A/G]CGGAGTCTCGCTCTG | 51133 |
| rs561198212 | snp | A/G | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621054 | GAACTTGGTCTCCCA[A/G]CACTTATTGTGATTG | 51133 |
| rs561231871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611488 | TCTTTTAAGTTATAA[A/G]AATCTAAGCACATCC | 51133 |
| rs561249840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587425 | TGAGCCACCATGCCC[A/G]GCCTTTCTGTAGGTT | 51133 |
| rs561345951 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616483 | AAAAACTTCCAGGCC[A/G]GGTGCGGTGGCTCAC | 51133 |
| rs561346516 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618372 | TATTCCTGTATGCTT[C/G]TCAAATTCATGTGGA | 51133 |
| rs561448348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600121 | ACTGAAAAGTACTCA[A/G]TGTTTTCCTGGTATA | 51133 |
| rs561558098 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591349 | CCTTCCTTCCTTCTC[A/T]CTTTCTCTCTTTCTT | 51133 |
| rs561564643 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606454 | TCTCAGCACTTAGCA[A/T]AATTCTGACACGTAA | 51133 |
| rs561586826 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567016 | CATCAACTTTTACTA[C/T]CTCTAGGATTAGTTT | 51133 |
| rs561611140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617885 | ATATATAATATATAT[A/G]TATATCTTCTAGTGA | 51133 |
| rs561760564 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575403 | TTGAGATTAGTAAAA[G/T]TATTATGAGAATAGT | 51133 |
| rs561790843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568650 | AGGCTTGGTAAGGAG[A/G]TAAACAAGGAAATGC | 51133 |
| rs561798283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574949 | GTTGGTATAAATTTC[A/C]ATAAAAAGTTATCAA | 51133 |
| rs561811750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615405 | GCGGGCAGATCACAA[G/T]GTCAGGAGATTGAGA | 51133 |
| rs561919637 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567606 | CCCTGCAGCCGTCGC[C/G]GCTGCCTCGGGCTAC | 51133 |
| rs561991817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582630 | GCAGTGGCGTGATCT[C/T]GGGTCACTGCAACAC | 51133 |
| rs562103003 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600539 | AGTGCCTGTCACACT[A/G]TAATTGTCTGTTATT | 51133 |
| rs562224994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581760 | ACGAAGGAAGACAAT[C/T]GAGGACATATTTGGA | 51133 |
| rs562232870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588511 | TAGTAAAGTTTAGTG[C/T]CACTGTCCTGGTTTG | 51133 |
| rs562348854 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567596 | GCCCCGCTGGCCCTG[C/T]AGCCGTCGCCGCTGC | 51133 |
| rs562370307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606396 | TTGTTTATTATCTCT[A/C]TCTCTTCTAGAAAAT | 51133 |
| rs562386392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581711 | GCTTTCACCAAGTGT[C/T]TGACATTTCAGAGCA | 51133 |
| rs562581983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574267 | TCTTGTCATATGTAG[C/T]TTTTTATAATCAGAG | 51133 |
| rs562597173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580891 | AGGTTTGGCATGTCT[A/G]GTAAGTGCTGTTTAT | 51133 |
| rs562600881 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599246 | CCTTTTGAGAAGAAC[A/G]TTATATTTGAAGGGG | 51133 |
| rs562621767 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621665 | AGCATTTATTGGTGA[A/G]TAATGTATATATCCC | 51133 |
| rs562659916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588449 | AATCTTTGATTTGGC[C/T]TTTTATGTTCTTGAA | 51133 |
| rs562767570 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566773 | CTAACATTAGTTGAG[C/T]GCTTACTATATTCCA | 51133 |
| rs562846382 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620926 | AGGATGGTGCCCATA[C/T]AGGTGAGCATCCCTT | 51133 |
| rs562934541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596925 | ACAGCACAGCTAGAA[A/G]GGTTTGACCCAACAG | 51133 |
| rs562994290 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593054 | TCATTTCTGCCTTTC[A/G]CATAGCCCATAATAC | 51133 |
| rs562996927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586177 | GAAAGATAAAACTAT[C/T]TTTTTTTAAAGTTTC | 51133 |
| rs563042170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612602 | TCTATTCAAACTTAA[A/G]GAACATAGTGAATTT | 51133 |
| rs563050537 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583398 | GGTGAGAGTGTCTTT[C/T]AGCATGATAATGCAT | 51133 |
| rs563059145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585417 | GTTGTATTACTTGGC[A/G]TACATATTTAAGGGA | 51133 |
| rs563151165 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571020 | TTTGCCCAGAAATTC[C/T]AGGTTACTAACCTTT | 51133 |
| rs563169493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579747 | TCATGATCCGCCCGC[C/T]TCGGCCTCCCAAAGT | 51133 |
| rs563172151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592496 | TAAAAAATTTTGAAA[A/T]TATAATACACTGGTA | 51133 |
| rs563183127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613113 | AGACCTGCACATCCC[A/G]CACATGTACCCCAGA | 51133 |
| rs563499312 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580336 | GGATTATTAATGTGA[A/G]CTCCCTGATGGTCTA | 51133 |
| rs563587431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610469 | GCAAAGAAGGTATGA[A/C]GAATAGGTTATGGGT | 51133 |
| rs563600561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569378 | CCCGCCTCGGCTTCC[C/T]AAAGTGCTGGAATTA | 51133 |
| rs563736732 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589416 | AAAGTGCTGGGATTA[C/T]AGGCATGAGTCGCTG | 51133 |
| rs563761928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600015 | CCTTTAGTGCTAGAA[C/T]TAAAATGATTTAGCT | 51133 |
| rs563820626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615680 | AAATTATGTTTGTTT[C/T]GTGGAAGCAGAAGGG | 51133 |
| rs563848487 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575596 | AAAATGTTTCCTCAG[G/T]TGTCACTTTTACCAA | 51133 |
| rs563893661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600965 | TTTTTGGATACCAAG[C/T]CTCACTCTGTTGCCC | 51133 |
| rs563941118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590222 | CCTGTACTTAATGAC[C/T]GTTTGTATATTTTCT | 51133 |
| rs563959943 | in-del | -/T | 0.233235 | 0.249437 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571630 | GAAGTGGAGATAAAC[-/T]TTTTTTTTTTTTTTT | 51133 |
| rs563984053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568578 | TATAACTTATGAGTC[A/C]CTCCTCTCAGAAAAG | 51133 |
| rs564103139 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612201 | AACATAAATACTTAT[A/T]AATTTTGTTATTATA | 51133 |
| rs564141842 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575620 | TTACCAAAGGTATCA[A/G]TACAAGTGATTTTAT | 51133 |
| rs564198004 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567891 | AGCCTGGAGGGGAAC[A/G]TGGGGGCCTCCAGGC | 51133 |
| rs564205585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609431 | CTGAGTGAATAGGCC[A/G]GTGCCGGATCGTGGA | 51133 |
| rs564413894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616067 | TATGCTTCATGGCTA[A/G]CTTTGGGGAAAGAGC | 51133 |
| rs564445363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583426 | CATTATAATTAGCGT[A/G]TAATGAGCAGTGAGG | 51133 |
| rs564618159 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622006 | TGTAATTATCTTACA[C/T]CCTTCTTCCTCTTTA | 51133 |
| rs564638662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598172 | ATGATTTCATGGGAC[A/G]GTAGAAATTGAGCCT | 51133 |
| rs564706052 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572537 | AATCCAGTGCTATTT[A/C]ATAGCCCACTTAGAA | 51133 |
| rs564774958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589352 | GTCTCACTATGTTGC[C/T]CAGGTCTTGAATTCC | 51133 |
| rs564906834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617089 | AGTTCAGAGCGCTTC[C/T]AGATAGCTGAAAACC | 51133 |
| rs564953194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573261 | GAAAAACTATTACAG[A/G]GAAGGTAAAACCTGA | 51133 |
| rs564956223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618702 | ATATGGGCCATCTCC[A/G]TAGAGCTGTATATTT | 51133 |
| rs564974362 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608542 | TGAAGCTAGAAAAAC[A/G]TTGGTCCCTATAAAT | 51133 |
| rs564992356 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579751 | GATCCGCCCGCCTCG[A/G]CCTCCCAAAGTGCTG | 51133 |
| rs565120600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603434 | ATCTAAATTTGCAAT[G/T]GGGTCTGGGCACTTT | 51133 |
| rs565132774 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586947 | CCCACTTAGTGGTGG[A/T]TGTTTTCACTGTTTT | 51133 |
| rs565195691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586327 | ATATTGTGGCTTCAT[A/G]GGCAATATAGATCAA | 51133 |
| rs565204315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594604 | CCATAGATACTATTA[C/T]ACCCTGTGCATCCTT | 51133 |
| rs565221452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616711 | GTTGCAGTGAGCCGA[A/G]ATCACGCCATTGCAC | 51133 |
| rs565252747 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610717 | TTTGAATTCCACTTC[A/C]ATCATATAGGACCTA | 51133 |
| rs565255123 | in-del | -/TG | 0.00119737 | 0.0244387 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621123 | GTGAAAAACATATCA[-/TG]TAATTCAAAAACACT | 51133 |
| rs565321708 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588140 | TTATTTTTTGAGGAT[A/G]GTTCTGCCAAACACC | 51133 |
| rs565351921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598738 | ATGGTTAAATAGAAG[C/T]GCAGCTAAAAGAAAA | 51133 |
| rs565357398 | in-del | -/AA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574454 | TTTATATTAGAATAT[-/AA]GAGGTTAAATTAGTA | 51133 |
| rs565458829 | snp | A/G/T | 8.25367e-05 | 0.00642358 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577773 | TGATTTGACTCATGT[A/G/T]TGAAAGTTGCCCTAA | 51133 |
| rs565461477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570858 | ATGGGTATGGGATAA[A/G]AAACAAATCAAAACA | 51133 |
| rs565506837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577206 | ACAAGCACTATGCTA[A/G]GCACTGTGAGGTATA | 51133 |
| rs565517079 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620870 | CCATTTTAACACTTA[A/C/G]CGACTTTTTTTGGTT | 51133 |
| rs565592917 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602415 | AGGTGGAAAATTGGA[A/G]CTCCCCTTACGCTGA | 51133 |
| rs565660775 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616510 | TCACACCTGTAATCC[C/G]AGCACTTTGGGAGGC | 51133 |
| rs565705517 | snp | A/G | 1.67167e-05 | 0.00289103 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578129 | TCCTTGTATCATTAA[A/G]CAAGTACAAGCATAT | 51133 |
| rs565781616 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572048 | CTGCTGTTACTGACA[C/G]TGAGACTGATACTGC | 51133 |
| rs565832615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577384 | TCTAGACAATTTATT[G/T]GTACTAGCCTGATAG | 51133 |
| rs565839451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583828 | TTAGAAACTGTCAGT[A/G]TGGTGAGAACTCTGA | 51133 |
| rs565845115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584809 | GAAAACAGATTCTTA[C/T]TGTAGTTACATATTG | 51133 |
| rs565845846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591982 | GGCAGAAGGCAAGGA[A/G]GAGCAAGTCACATCT | 51133 |
| rs565891168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608852 | TTTTTAGAAAGAGAA[A/G]TATGCAGTGTTACCA | 51133 |
| rs565914233 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577471 | TTTTAAGTAGATAAC[-/AG]AATATTTTTGTTCAC | 51133 |
| rs566097583 | snp | A/G | 1.65531e-05 | 0.00287686 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215608051 | TGTCCGGACGTGGAC[A/G]GTAACACGATTCAGA | 51133 |
| rs566156998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601095 | GGCATGCGCCACTAC[A/G]CCCAGCTAATTTTGT | 51133 |
| rs566288847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618494 | CTGGGATAACTAATT[C/T]AGTCAAGTACAATTC | 51133 |
| rs566311632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575844 | ATTAGTGTTACAGAT[A/G]TTAAAGTTAAAAGAT | 51133 |
| rs566401304 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568085 | ACACAGCCTTCCTTA[C/G]CTCATCTCAGATTAG | 51133 |
| rs566614959 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596333 | TGTTCAAGTGTAGAT[G/T]TTAAGTATATAGTTG | 51133 |
| rs566659291 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215592365 | CATATATTTTGTCCA[-/T]TTTTTTTTTTGTTGT | 51133 |
| rs566670227 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606679 | CAGATATTTCATGTA[C/G]GTTTGAAACTTTTGT | 51133 |
| rs566722663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586442 | CATTGATGTGTATTC[C/T]GTTTGCTTCATTGCT | 51133 |
| rs566732397 | snp | C/T | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622138 | ATTATGTAATAGAAT[C/T]GCATAAAAAGGAAAC | 51133 |
| rs566745332 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573208 | TACAGTGAAATTACT[A/G]TGAGCTTAAAAAGAG | 51133 |
| rs566795980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613955 | TGGCTTTGTTCATTT[A/G]CTTAGGATTGCTTTG | 51133 |
| rs566861222 | snp | A/G | 5.08195e-05 | 0.00504055 | missense | KCTD3 | GRCh38.p7 | 1:215579012 | TAGGTATTCCTAGTC[A/G]TAAAATAAACAACAC | 51133 |
| rs566964833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572052 | TGTTACTGACACTGA[A/G]ACTGATACTGCTAAA | 51133 |
| rs566967501 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609250 | ACTGATACATGAAGG[A/G]TAGACATTTGTTGGG | 51133 |
| rs567084429 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599676 | GGGAGAGAAGAACTC[A/T]GCAGTTGTAACTCAC | 51133 |
| rs567123408 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572764 | TGTGTTTCCTGGTGA[G/T]AGTGCATGGTAACTA | 51133 |
| rs567222482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612251 | AAACCTGGAACTTAA[A/G]TATTTTCCATCCCAT | 51133 |
| rs567227681 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595130 | CAGGATAAGGTGTTA[C/T]ACAGCAGTATGAGAT | 51133 |
| rs567268038 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618391 | AATTCATGTGGATTG[G/T]ATTTTTTTTTGTCTA | 51133 |
| rs567344871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604719 | TTTATTATGACCCTG[A/C]TAAGAGGAATTTTTA | 51133 |
| rs567408477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603973 | GATTTTAAGATGACC[A/G]GAGAAGTCTTAAGAT | 51133 |
| rs567424942 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571295 | TGGACCAAGTCAGTT[C/T]TCTGTGACTGGGGTA | 51133 |
| rs567494803 | snp | A/G | 1.84766e-05 | 0.0030394 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578971 | AAGGTGAACTTAGGA[A/G]TGTATTTGTTTTCTT | 51133 |
| rs567515661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592985 | GTGTCTTTGTTGATT[C/T]CCTAGAACCTCATCC | 51133 |
| rs567527999 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616024 | TAGCTGTTCACAGAA[A/C]GATAGGGACATGTTA | 51133 |
| rs567564139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581222 | TTGTACTCCAACCTG[C/T]GCAACAGAGCAAGAC | 51133 |
| rs567594901 | snp | C/T | 0.000167282 | 0.009144 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601823 | ACCAGAAAATAGAAA[C/T]TATAATTACTATCTA | 51133 |
| rs567657406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601435 | GGAAATCAGTTGCTT[G/T]GTTTACTAGTTCTGA | 51133 |
| rs567702709 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586342 | AGGCAATATAGATCA[A/C]CAAAATTTTATTTGT | 51133 |
| rs567736005 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586388 | GGGTAACTGTTTAGT[G/T]TTTTTTTTGTTTTTT | 51133 |
| rs567760438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593748 | ACATAAAACAGTATT[A/G]TAGAGGTGAGACTTA | 51133 |
| rs567951649 | snp | A/G | 0.00159669 | 0.0282099 | missense | KCTD3 | GRCh38.p7 | 1:215578034 | GTGAAGAATTGGAGC[A/G]TTCCTCTTGTGGCAG | 51133 |
| rs567990822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598562 | ATGGAAACAAATAAC[A/G]AAAAGTCATTAAACA | 51133 |
| rs568013701 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589606 | AAAGAAGGTGTCCAA[C/T]ATAAACTGCATTGTT | 51133 |
| rs568047329 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602695 | TAACAGACTAGTTCT[A/G]TAAAGTAGTAAGAAT | 51133 |
| rs568052907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606815 | ACATTGTTTTCCCTA[C/T]AGTGCATTTTAATCC | 51133 |
| rs568060773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582991 | TTCTGTAGTTGTTAT[A/G]GTTATTTTTAAATAT | 51133 |
| rs568064799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590386 | TGAAAATGTCTAGAG[A/G]CATTTTTGGTTGACA | 51133 |
| rs568098570 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594648 | ATCAAATTATAATTG[G/T]TTGCAGTTTTTTCTC | 51133 |
| rs568112112 | snp | G/T | 0.0577344 | 0.159793 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614036 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTAAG | 51133 |
| rs568150806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573712 | TCATTAGCCAGTGTA[G/T]TAAAACAAGTTAACT | 51133 |
| rs568152669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580915 | TGTTTATATCAGTAA[C/T]CTCAGGTTTATATTT | 51133 |
| rs568157400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582325 | TCTATTCTCATACAA[C/T]TTGAGGTGAAGTATG | 51133 |
| rs568237770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574387 | AGAAATTTTTTTAGA[A/T]CAATAATTGAAACTT | 51133 |
| rs568500957 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566178 | CTGCCATCCCACTTG[C/T]TACCTATGTAATTTT | 51133 |
| rs568534504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587271 | AGTAGCTGGGACTAC[A/G]GGCACATGCCACCAC | 51133 |
| rs568746740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587866 | TTATCATACATGCTT[C/T]TATAAGATGTTGGGC | 51133 |
| rs568791760 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601015 | CAATCCCCGCTCACC[A/G]CAACCTCTGCCTCCC | 51133 |
| rs568807779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597130 | TGAACCAGGTTTGTA[C/T]GTAATCTTAAAAGTT | 51133 |
| rs568861939 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616808 | ATTGTGAAATACATA[C/T]TTGGTCTTTGTCTCT | 51133 |
| rs568862280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613324 | AGACATGTGTCTGTT[C/T]GTGTCGTTTGCCCAC | 51133 |
| rs568871526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598380 | AAGCACAAAGACTTG[C/T]CTTTGTTCTATGAGA | 51133 |
| rs568916830 | snp | A/G | 0.000434615 | 0.014735 | missense | KCTD3 | GRCh38.p7 | 1:215620103 | GAAGCAGCTACTTAC[A/G]GTTCCATGAGGCCTT | 51133 |
| rs568939368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579643 | AGCTGGGACTACAGG[C/T]GGCCGCCACCATGCC | 51133 |
| rs568969833 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609591 | CTTGACAGTGAAGAC[A/G]TGAGAGAGTGAAGCA | 51133 |
| rs568983825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588760 | TAGCTAATACCAGCT[A/G]GATACAAGTAAAATA | 51133 |
| rs569025207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580196 | GGTAAATGTTTCTGA[C/T]AGCCTTTATCTGTTG | 51133 |
| rs569092698 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616324 | ACTAAATTATGATCA[A/T]CTTGATAAATACAGG | 51133 |
| rs569106331 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612703 | ATTTCCCTTATCCCA[A/G]TTTCTTTATAAAATA | 51133 |
| rs569324481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594154 | CATGAGCCATCATGC[C/G]CGGCCGATTATAACA | 51133 |
| rs569404101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603872 | GTGTGTTATAATTAC[C/T]GTGATAGAACCTAAT | 51133 |
| rs569428143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577295 | TTAAGATAGATATGT[A/G]TAGAAATAATTGCGA | 51133 |
| rs569510573 | in-del | -/TT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598466 | CACCAGTTAGAACAC[-/TT]TCTCAGAAGAGAGCA | 51133 |
| rs569520724 | in-del | -/AAT | 0.00795532 | 0.062565 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215621896 | CCATAATTTAAAAAA[-/AAT]AATGGGGGGAGGGAG | 51133 |
| rs569527105 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580568 | AGTGTAGACCGGTGA[-/T]TTTTTTTTTTTTTAA | 51133 |
| rs569541886 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594921 | AAGTCTGTGTGTTCA[C/G]ATCACTAGTTCTTAA | 51133 |
| rs569747202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569184 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 51133 |
| rs569806561 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590550 | TTCATTTTTTTCTCC[A/T]TTCTTCAGTTTAGAT | 51133 |
| rs569863910 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591347 | TTCCTTCCTTCCTTC[C/T]CTCTTTCTCTCTTTC | 51133 |
| rs569913099 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583689 | CCCTTTTACAAGGGT[A/T]CTCTTAATCCTAAGG | 51133 |
| rs569947319 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587276 | CTGGGACTACAGGCA[C/T]ATGCCACCACGTCCA | 51133 |
| rs569972055 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622155 | CATAAAAAGGAAACT[A/G]ACTATACTAGATTGC | 51133 |
| rs569999455 | snp | G/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565270 | TAATATATACATATA[G/T]GATCAGATATTATAT | 51133 |
| rs570026220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614924 | TTCTCTGCATAGTGA[A/G]GAAACTGCCAAATGT | 51133 |
| rs570144729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583198 | ATAGCCAGAGCAGCC[C/T]TGAGGGCTGCTTGAC | 51133 |
| rs570259233 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574062 | AACTTTAGATTATTA[A/T]TGACTTCCAGTTTGC | 51133 |
| rs570281143 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567231 | AGGAGCACATTCCCC[A/T]AGCCTCCCTACGCGC | 51133 |
| rs570289841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582117 | TCTTTAATCCTTGTG[A/G]AGTTTACTTTTTTGT | 51133 |
| rs570318645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575829 | AAGACTTCATTCCCT[A/G]TTAGTGTTACAGATA | 51133 |
| rs570343322 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575032 | CGAGGCAAGTGGATT[A/G]CCTGAGGTCAGAAGT | 51133 |
| rs570409079 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590483 | TTCCTCCTTTTGAGC[A/T]TTCTAGATCACTTTA | 51133 |
| rs570449150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576443 | GGATGTGGTGGTACA[C/T]GCCTATAATCCCAGC | 51133 |
| rs570457012 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566754 | GTGTGTTTTCTGCGT[A/G]TGTCTAACATTAGTT | 51133 |
| rs570493557 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571911 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 51133 |
| rs570525838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607822 | GTTTACTTAATGTAC[C/T]TTATATTTTGCAGCA | 51133 |
| rs570545531 | snp | A/G | 4.43459e-05 | 0.00470861 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575998 | TGCACTCTTTTTAAA[A/G]TAAATTCTTACTGAT | 51133 |
| rs570633071 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567114 | CTCAATCTGCGAATC[A/G]GCTTCCTCGTTTTAG | 51133 |
| rs570662844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599488 | TTTACATGTAGAAAT[C/T]AGTGGTAATCACTGT | 51133 |
| rs570714784 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613590 | GGGCTGATGTCCAGG[G/T]TGATATTTCCTAGGT | 51133 |
| rs570909371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606903 | TTGAATCAACTAAAA[A/G]TATTTAAATTATTTT | 51133 |
| rs570940875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614857 | ATTCTTTGAGATGAA[C/T]TTTTTACATCAAAGT | 51133 |
| rs571004046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614125 | GCAAGCTCTGCCTCC[C/T]GGGTTCACACTATTC | 51133 |
| rs571051620 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581925 | TACAAAACCTTTAAA[A/C]AAAGAGTAGTACAGT | 51133 |
| rs571065616 | snp | C/T | | | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215611890 | CCCATCACCAACAAA[C/T]TATTTGTAAGACTCT | 51133 |
| rs571074701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603047 | CACAATGACAGAATT[A/G]AGAGGTTGTGACAGA | 51133 |
| rs571119844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574614 | GCAACAAAGTGACCA[A/G]TGGTATTTATTTGCT | 51133 |
| rs571131543 | snp | A/C | 0.000280269 | 0.0118345 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581002 | CACGGTGGGTCACGC[A/C]TGTAATCCCAGCACT | 51133 |
| rs571239395 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603160 | GTGGATTTTTTTTTT[A/T]AATCTAGTTAAAAGG | 51133 |
| rs571262680 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571863 | GTCTCCATCTGCTGA[C/T]CTCGTGATCTGCCCG | 51133 |
| rs571266966 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590179 | TTAACTGCATTTTTC[C/T]GATGATTAATAATAT | 51133 |
| rs571287994 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610023 | TTATAAACAGCCCTG[G/T]AAATTAATTATAAAA | 51133 |
| rs571347811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612186 | TTTTTTTCATGGCCA[A/G]ACATAAATACTTATT | 51133 |
| rs571350565 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215619075 | GAAGATAAGGGTAGG[-/T]TTCTCATACAGAAAG | 51133 |
| rs571363253 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615566 | TGGAGCTTGCAGTGA[C/G]CTGAGATCGCGCCAC | 51133 |
| rs571468862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578204 | AATCTATTAGAAATG[A/G]TAAGAACTTTTGATT | 51133 |
| rs571476042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578779 | GTAAACAGTATGACA[A/G]TACCAGAAATCTGTT | 51133 |
| rs571497534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585522 | GCGAATGTCAGGTAG[C/T]GTGCAAAAGAACGCT | 51133 |
| rs571500338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580382 | TGTTTTGTATTCTAT[A/G]GCAAGGGAGAGTACA | 51133 |
| rs571520921 | in-del | -/TAGAATTTCATGAG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589667 | TAGGTTTCCTTTATC[-/TAGAATTTCATGAG]TAGAATTATATAGTA | 51133 |
| rs571521992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601258 | ATTTTCCTGGAAAAA[C/G]TAATTTTTTTATTCC | 51133 |
| rs571723889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601716 | ATATGTGTGTGCACG[C/T]GTGCACCTAAAGAAA | 51133 |
| rs571763683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592918 | TCACTGGTGCTCAGG[A/G]TTGTTTAGCCTAAGC | 51133 |
| rs571853126 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600921 | GTAAAATAGTATTGC[A/C]ACTATCCTAGCAAAC | 51133 |
| rs571881399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576154 | GCTCACTGCAACCTC[C/T]GCCTTTCAGGTTCAA | 51133 |
| rs571929446 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569719 | TCCTGTCTCAGCCTG[G/T]CACTGTGACATTTTA | 51133 |
| rs571952270 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608958 | ACAAATATTTATCGA[A/G]TACTTGTGTTCTAGA | 51133 |
| rs572016685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568552 | AAAAATCGTAGTTTT[C/T]GTGGATTTCCTATAA | 51133 |
| rs572017046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576766 | GTAGAGATGGGGTTT[C/T]ACCGTTTTAGTCATG | 51133 |
| rs572135335 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610046 | TTATAAAACCCAGTA[A/C]GATAAAGGGGACAGG | 51133 |
| rs572337060 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615444 | GCTAACACGGTGAAA[A/C]CCTGTCTCTACTAAA | 51133 |
| rs572360039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589916 | CATTCAAGTAGAAGT[A/C]TTTCTGTGGACATTT | 51133 |
| rs572423739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599875 | GGGAAGCGCTAGGCT[C/T]CTGCTGCTCTTTCAT | 51133 |
| rs572445534 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591169 | ACTCCATCTACCCAC[A/G]TATGACCTCTGATAT | 51133 |
| rs572489074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590631 | TCTGCAGTTAAGTTC[A/G]TCTAGTGAATTTTCA | 51133 |
| rs572491952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599003 | AATAAAAGATAAATT[A/G]TGATAAAAAGTATTC | 51133 |
| rs572509426 | snp | C/T | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620902 | GGAAACATATTACCA[C/T]GTCTTAATAGGATGG | 51133 |
| rs572546407 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582686 | CCCACCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 51133 |
| rs572554952 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621517 | GGTTAAAGGTTTTGG[C/G]TGCTGTAAGAATGTG | 51133 |
| rs572604499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613739 | CCAGTAATCCCAGCA[C/T]CATTTATTGAATAGG | 51133 |
| rs572669256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606418 | CTAGAAAATTCTCCA[A/G]TAGCAGAAACTTTGT | 51133 |
| rs572721620 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617730 | CTGGGGGCTGCAGTG[G/T]ACCTGAGTGAATATG | 51133 |
| rs572846138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595230 | TCTAGTCCCCAACAC[A/G]TATAGCACATAGTTT | 51133 |
| rs572951735 | snp | A/G | 0.000318202 | 0.0126095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611925 | GACTGGAAAAAGGTA[A/G]CACTTTATTGTAAAA | 51133 |
| rs572977254 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610645 | AATAAAATTAGAGAT[C/G]AGAAGGTTCCAGTAA | 51133 |
| rs573033456 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602511 | ACATTTGTCTTCCTA[C/T]TAAAATAACTAATTT | 51133 |
| rs573056403 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592376 | TCCATTTTTTTTTTT[G/T]TTGTTACTGCTGTTT | 51133 |
| rs573109025 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582841 | TGCTGGGATTCCAGG[C/T]GTGAGCCACTGTGCC | 51133 |
| rs573119020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601510 | CTCTTGTATGAGAAA[C/G]GGAAAAGAGAGGGAC | 51133 |
| rs573135951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603339 | AGATGAATCAGTTAG[C/T]AAAACTAGAACAGCC | 51133 |
| rs573157095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594565 | AAGATATATTTTCAA[C/T]CCCCTTTCCATACCC | 51133 |
| rs573294579 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603813 | ATTCAGTCTTTGTCA[A/G]TAAGGAATAGAAGTA | 51133 |
| rs573349637 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566593 | ACCTCTGAAACATAA[C/G]GCACTATCTTTGTTA | 51133 |
| rs573501928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584991 | AAGTCAGCTAATTGG[C/T]GCTGCAGTCTATTTC | 51133 |
| rs573509766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593372 | GAAGATACTTCTAAC[A/G]ATACTTAGCAGGTTT | 51133 |
| rs573578075 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582936 | TCTTTGTAATTTTTT[-/A]AAAAAACAGGTAAAT | 51133 |
| rs573631769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603303 | ATGACATGCTTTTTT[C/T]CCTTTGATTCAAGTA | 51133 |
| rs573693199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602375 | ATACTGAAGTCAAAC[A/G]TGACCAGTAAACAAA | 51133 |
| rs573701661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586222 | ATTTGGAGGACTTTA[C/T]TAAATTATTCTTTGG | 51133 |
| rs573721046 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594218 | CTTAGACCCTATTTC[A/G]TAGTTGAGATAAGAA | 51133 |
| rs573760315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616632 | AGGCCTGGTGGCACA[C/T]GCCTGTAATCCCAGC | 51133 |
| rs573763343 | snp | C/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215566110 | TGAGGTACAATGCAG[C/T]GGTAAGGATGGTGAA | 51133 |
| rs573917283 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571100 | CCTTTGTGATTTTCT[A/G]AGTAGCACATAATTT | 51133 |
| rs573951724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584945 | TTGTTAAAAGCTGCA[A/G]AATCTCGAAAGAAAA | 51133 |
| rs574010251 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611057 | TAAGTGTAATGGGAA[A/T]AGAGAATTATTAAAA | 51133 |
| rs574044088 | snp | A/C/G | 0.00280392 | 0.0373376 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608686 | ATACACCATACATAC[A/C/G]TGTGCACATGGGCAC | 51133 |
| rs574053993 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589148 | CTTTTCTTTCCTTTT[C/T]TTTCTGAGACAGGGT | 51133 |
| rs574102992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600576 | TCTCACAAGTTACCA[G/T]CTCCTAGAGAGCAAG | 51133 |
| rs574192266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600112 | ACTGATATCACTGAA[A/G]AGTACTCAATGTTTT | 51133 |
| rs574246835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596652 | GAAATGAGGAAGTAA[A/G]AGATCAGAGAAGAGA | 51133 |
| rs574291710 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591673 | GCCTTTCTTTCCTTG[A/C]GGATTCTTGCCCTGC | 51133 |
| rs574374530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584203 | AGGATGAGTCCAAAT[A/T]GCAGAAAGAACTCAA | 51133 |
| rs574439952 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620701 | ACATTAGTTTTTACA[C/T]TAAAACTTTACAAGA | 51133 |
| rs574623066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588837 | TACAATTCTACAGAC[A/C]AGAGATTGACTCTCT | 51133 |
| rs574769647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612456 | TAACATGGAGAGAAA[C/T]TGTCTGTCTCCGTGA | 51133 |
| rs574789130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572917 | TAACATTGTAGTTCA[A/G]GGTGATATCTTAAAA | 51133 |
| rs574865783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613067 | GTGATGGGTTGATCT[A/G]TGCAGCAAACCACTA | 51133 |
| rs574918833 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591444 | CTGACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 51133 |
| rs574999119 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594941 | CTAGTTCTTAAATAT[C/T]GGGTCCATGAGCAAG | 51133 |
| rs574999965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617957 | CCTGTCATTTGTTCT[A/G]CAGTTTATCATTCTT | 51133 |
| rs575224920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617785 | GTCCCACTATATATA[C/T]ATATAATGTATATAT | 51133 |
| rs575274415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579795 | GAGCCACTGTGCCCG[G/T]CTCTTAACAAAACTA | 51133 |
| rs575288422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573930 | TTTTTTTAATAAAAA[A/G]GGTTAACTCTTAAAA | 51133 |
| rs575361692 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611984 | CTTACAAAACATATG[G/T]CATAATTTGACATAT | 51133 |
| rs575377344 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575546 | ATTTATTCATGTTTT[C/G]GAAGTATTAATTGAA | 51133 |
| rs575410719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580618 | CTTAGTTCAAAATCA[C/G]TGTACTCATTGAGAA | 51133 |
| rs575463216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579219 | TAATTACTTTTAAAG[A/G]TTTTTGCCTCATCTC | 51133 |
| rs575473194 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618392 | TTCATGTGGATTGTA[-/T]TTTTTTTTTGTCTAT | 51133 |
| rs575535712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578553 | AGAGCCTGATTTTAC[C/G]TGTGTTATAATGGAC | 51133 |
| rs575544454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595604 | TAAATGTAGTGGTAA[A/T]TTTTTTTGCTAGATG | 51133 |
| rs575571853 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607246 | TTCATTGCTAATAAT[A/G]ACATATTTTCTAAAA | 51133 |
| rs575757522 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608433 | AAGAATGTCATCTTC[A/T]CATGTTAACTACTTT | 51133 |
| rs575807041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582565 | TTTTTTGTTTTGTTT[G/T]GTTTTTGAGATTTTG | 51133 |
| rs575836564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571548 | AATGAATTGTTTTAC[G/T]GTCTTTCCTTCAGTT | 51133 |
| rs575919110 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576063 | AGGTTTTTTTTGTTT[G/T]TTTTTTTTTTTCCTT | 51133 |
| rs575933147 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575493 | GCATTATTAAAGTAC[A/C]TTGTAGTTTTAATGA | 51133 |
| rs575974762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568354 | GGATCTGTTCAACTT[C/T]TAGGACAGTGTGTCC | 51133 |
| rs576255132 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621680 | ATAATGTATATATCC[C/T]CATTCCAAGAAATAT | 51133 |
| rs576337025 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597674 | GAACAAGAATTCAAA[A/G]TGAATTTCTGTGGTC | 51133 |
| rs576424905 | snp | A/G | 0.00120846 | 0.0245514 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621581 | GAACGTTTTTGTACA[A/G]TTTTTTTTCATTTAA | 51133 |
| rs576435316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589851 | TCACCCGTTGATAGA[C/G]ATTTGGCTTATTTCC | 51133 |
| rs576438421 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620864 | AGGAGTCCATTTTAA[C/T]ACTTACCGACTTTTT | 51133 |
| rs576565470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614387 | AGTTTGATAAGAATA[A/G]CATTGATGTAATTAC | 51133 |
| rs576588367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574712 | ATCAATAATAAGATC[C/T]CCACAAATCTGTGAT | 51133 |
| rs576630868 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605469 | TGTTGGATTGCCCTT[A/G]AGCTCTTTCCTGGAC | 51133 |
| rs576677815 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566283 | GAAAGATGACAAAAT[A/G]TCTAAACCACCGGGT | 51133 |
| rs576794809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575352 | TTAGTTTAAAAAAAA[A/T]AAATTGTCATTACCT | 51133 |
| rs576905262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588317 | GTTGAAATTAAGTTT[C/T]TATCAGTACAAATTT | 51133 |
| rs576911224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597457 | GAAACATAGGTTATA[C/T]ATGTTTCATTCTCAT | 51133 |
| rs576970212 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596875 | AATGGAGATTATTTC[A/C]GGTCCCATAAAAGTC | 51133 |
| rs577126412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605279 | AAACACCATGTGGAG[A/C]TGAAATTCAGTCCAT | 51133 |
| rs577310953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606109 | TGTCACTTTTCTCAT[C/T]GCTGATAACACTCTA | 51133 |
| rs577456545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596956 | GGAGTAGAGACATTT[C/T]TTTCTCTGTGACAGA | 51133 |
| rs577493835 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599592 | CAGTATGGTTTCTTG[A/G]ATTCTTGCCATGAAG | 51133 |
| rs577514067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618673 | AGTTGAGTATTATCC[C/T]AATGATGGATACAAT | 51133 |
| rs577527783 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601586 | ATCACATGCAAAAAA[A/C]GAGGAGACAACCAAT | 51133 |
| rs577593095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569429 | TGGCCGATAGTTAAT[A/G]TATTTCTATTCAGAC | 51133 |
| rs577637607 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579855 | GGCCTGGTGGCTGTA[A/C]TTTGCCAACCCCCGG | 51133 |
| rs577648369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619349 | TTGGGGAAATTGACT[A/G]AAATATTGTAATCAC | 51133 |
| rs577649201 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613269 | TGCTCTTTTGCCAGG[C/G]TAGAGTGCTGTGGTG | 51133 |
| rs577674537 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610909 | TTAGCTAATAATAAA[C/G]ATGACATTGGTTCAT | 51133 |
| rs577714728 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602291 | AAATTAAACTGGTTT[A/G]TTTCTTTTTGAGAAC | 51133 |
| rs577715370 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614284 | GATCCGCTCACCTCC[A/G]CCTCCCAAAGTGCTG | 51133 |
| rs577735695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610317 | AAAAGGCCAAGAAGC[A/G]ATCAAAGGTCATTTT | 51133 |
| rs577770912 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614019 | GGAACTTTAGAATAG[-/T]TTTTTTTTTTTTTTT | 51133 |
| rs577791396 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569362 | CTGACCTCGTGATGC[G/T]CCCGCCTCGGCTTCC | 51133 |
| rs577797653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577493 | TTTTGTTCACATGCA[C/G]TTTTTATTTACACTT | 51133 |
| rs577903792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609537 | ATGATACTAGATTTG[C/T]GATATATATAATTCA | 51133 |
| rs577908925 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616082 | GCTTTGGGGAAAGAG[C/T]GTTCTGGTTTCTGTG | 51133 |
| rs578025850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616536 | GAGGCTGAGGTGGGC[A/G]GATCACCTGAGGTCG | 51133 |
| rs578027056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576985 | ATTTTTAAAATAAGG[A/G]CAAATTACAACTGAA | 51133 |
| rs578045154 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583465 | AGGTCACTTTTGTTG[A/C]CATCTTGGTTTCAGT | 51133 |
| rs578049739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591597 | CTTGACCTCGTAATC[C/T]GCCCGCCTCAGCCTC | 51133 |
| rs578050703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576292 | CAGGCTGATTGCAAA[C/T]GCCTGAGCTCAGGCA | 51133 |
| rs578093423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599092 | GTAGACACCAGAAGA[C/T]GACAACGGGCATTCT | 51133 |
| rs578147513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583953 | ACAGCAGTATATTCT[A/C]CAATAACAAGGCAAA | 51133 |
| rs578221763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599952 | CATGGCCTTATCTGT[C/G]CCCATTTTCCTGCCA | 51133 |
| rs730882243 | in-del | -/CCCTTGCGAATGAAAGATAATGATCTTCTTGTAACTGA | | | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215602099 | GATATGCAGAAGTTC[lengthTooLong]ACTGTATCATGATCC | 51133 |
| rs745321455 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608331 | TTTTCTGATTAAATT[A/C]TATAAATTCACAAAA | 51133 |
| rs745324096 | snp | A/G | 1.69784e-05 | 0.00291357 | missense | KCTD3 | GRCh38.p7 | 1:215620602 | GTGATTCTTCAGGTC[A/G]GGAGTACAGCTTGTG | 51133 |
| rs745348598 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566973 | AAATCTCCAAATGTT[A/C]CCTGCATTTGCACTG | 51133 |
| rs745436625 | snp | C/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565349 | ATTTGTTTTTGTTAA[C/T]GGTGTTCCAATTTAT | 51133 |
| rs745471321 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577677 | CTTTGTAGGGGAGTG[A/G]GTATTAATGTTCTCA | 51133 |
| rs745515630 | snp | C/T | 1.65081e-05 | 0.00287293 | missense | KCTD3 | GRCh38.p7 | 1:215620539 | ACTCACCTGGTACTG[C/T]GTCCCCATCTCCTAC | 51133 |
| rs745549946 | snp | C/G | 1.7999e-05 | 0.00299987 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595522 | TCTGAAATGTATGCT[C/G]ATTATGTATTTTTTT | 51133 |
| rs745558827 | snp | A/C | 4.94474e-05 | 0.00497205 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604196 | AGTACGAGTGATTGT[A/C]CAACACCCAGAGACA | 51133 |
| rs745593367 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617262 | GCCACTCTAGCAAAT[C/T]AGTTGAACCTAAGGA | 51133 |
| rs745615303 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577565 | AAAATAATTTTTAAA[A/G]CCTTATGACTATATA | 51133 |
| rs745774862 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215621811 | TGATTATGTCAATGC[A/G]TTTTCAGTTATTTAA | 51133 |
| rs745780087 | snp | A/G | 4.94458e-05 | 0.00497197 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215579991 | TGCCCATTTTGCTGT[A/G]TGTTACAGGTAGTGT | 51133 |
| rs745792990 | snp | C/T | 1.65699e-05 | 0.00287831 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215611844 | TTTTGGAGAGCGAGA[C/T]GATCAACAGGTGTTT | 51133 |
| rs745800209 | snp | G/T | 1.69015e-05 | 0.00290696 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608188 | GTGGGTTAGGTTATT[G/T]TAGGGCATTTTTAGG | 51133 |
| rs745817437 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600503 | TCCCCTCTCTCCTGT[A/G]ATTGTATTGTAGTCT | 51133 |
| rs745899183 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586379 | AAGGTGGATGGGTAA[C/T]TGTTTAGTTTTTTTT | 51133 |
| rs745951177 | in-del | -/TG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599461 | CTGGTATTTTAAAAC[-/TG]TAAATTTAAATTTAC | 51133 |
| rs745988824 | in-del | -/T | 0.00013269 | 0.00814416 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618872 | CAGGGCTCTTTCTGC[-/T]TTTTCTTTTGCAGAA | 51133 |
| rs745995048 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588506 | GTCACTAGTAAAGTT[C/T]AGTGCCACTGTCCTG | 51133 |
| rs745997249 | snp | A/G | 1.72594e-05 | 0.00293758 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604091 | AGCTTTTTTATTATC[A/G]TTCCATAATGTATCA | 51133 |
| rs746045454 | snp | C/T | 1.65343e-05 | 0.00287521 | missense | KCTD3 | GRCh38.p7 | 1:215620223 | GTAGAAAGAGCTGTC[C/T]CTGAAAATGGTAACT | 51133 |
| rs746118968 | snp | A/C/T | 1.65877e-05 | 0.00287986 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573759 | ATCATGTTCTCACTT[A/C/T]TAATACCAGATGATT | 51133 |
| rs746123864 | snp | C/T | 0.000535699 | 0.0163573 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620102 | TGAAGCAGCTACTTA[C/T]GGTTCCATGAGGCCT | 51133 |
| rs746164285 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607687 | TAAACTAGGAAACTG[-/T]TTACTATGTAGTTTG | 51133 |
| rs746168341 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598261 | CCCAGTAATCTTGGA[A/G]CAAGAAAGTTTGATG | 51133 |
| rs746191461 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581988 | AATTTTCTACATGGT[C/T]AGGTTTTATGTTTAT | 51133 |
| rs746316704 | snp | C/G | 1.67677e-05 | 0.00289544 | missense | KCTD3 | GRCh38.p7 | 1:215579027 | GTAAAATAAACAACA[C/G]AGTCAGATCTGCTGA | 51133 |
| rs746338190 | in-del | -/ATTA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588371 | TTAGTTACTAAGACC[-/ATTA]ATTACATTCTCTGCC | 51133 |
| rs746365881 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583561 | GACCTTCCTTGTTAC[G/T]CTGTGACTAAGAATG | 51133 |
| rs746371029 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610448 | TGGGAGGTGGGGGAA[A/G]CGAGGGCAAAGAAGG | 51133 |
| rs746406363 | snp | G/T | 1.88906e-05 | 0.00307326 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578954 | ATATTTTTAATTTTT[G/T]AAAGGTGAACTTAGG | 51133 |
| rs746571322 | snp | A/G | 2.02423e-05 | 0.00318131 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215575974 | AAGAACTAGACTTAA[A/G]GTAAGAAATGCACTC | 51133 |
| rs746661393 | snp | C/T | 1.79149e-05 | 0.00299285 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595306 | CCAGGTTTTGATTAA[C/T]TCTAAAAATGGTGAC | 51133 |
| rs746689813 | snp | C/T | 1.65921e-05 | 0.00288024 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619111 | TGTCACAAGGTTAAG[C/T]TTTTCACTTAAGTGA | 51133 |
| rs746718675 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593529 | AGAGAATACCTAGCA[C/T]CAGTATAAGATTCAA | 51133 |
| rs746741770 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602652 | TTTTATAACTTTCAG[C/T]GCATTTTAGAGGCCA | 51133 |
| rs746745892 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600046 | AACTTGAGTAAGAAA[A/G]TTGGTTAGTGGTGTG | 51133 |
| rs746751650 | snp | G/T | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620671 | GATGAAAGTTAAACT[G/T]TACTGAATTTCAGTA | 51133 |
| rs746804560 | in-del | -/TAA | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622286 | GCCCCCATTATGCCT[-/TAA]TAATTTTTTCATTAT | 51133 |
| rs746847148 | snp | A/G | 3.49272e-05 | 0.0041788 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579165 | TACAGAAATAGAAAA[A/G]GAAAAATACGTATGT | 51133 |
| rs746859457 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579700 | AGATGAGGTTTCACC[A/G]TGTTAGCCAGTATGG | 51133 |
| rs746870087 | snp | C/G | 1.66355e-05 | 0.002884 | missense | KCTD3 | GRCh38.p7 | 1:215608161 | GTAGCTATTCCTCTG[C/G]AAATGACATAGGTGG | 51133 |
| rs746942540 | snp | C/T | 1.64982e-05 | 0.00287208 | missense | KCTD3 | GRCh38.p7 | 1:215620527 | ATGGAGGAACTGACT[C/T]ACCTGGTACTGCGTC | 51133 |
| rs746942755 | snp | C/T | 1.64874e-05 | 0.00287113 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577639 | ACAGGTTTCCAGTGT[C/T]AGAGAATTTACATCA | 51133 |
| rs747035565 | snp | A/G | 0.000119471 | 0.00772796 | missense | KCTD3 | GRCh38.p7 | 1:215620082 | CAGCACCATGATACC[A/G]CCCATGAAGCAGCTA | 51133 |
| rs747056267 | snp | C/T | 1.66106e-05 | 0.00288184 | missense | KCTD3 | GRCh38.p7 | 1:215620115 | TACGGTTCCATGAGG[C/T]CTTACAGAGAAAGTC | 51133 |
| rs747110522 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614234 | GACGGGGTTTCACTG[C/T]GTTAGCCAGGATGGT | 51133 |
| rs747229417 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598653 | AAGGAATAGGACAAA[G/T]CAGAAAATGGAGGGA | 51133 |
| rs747229842 | snp | C/G | 6.60982e-05 | 0.00574846 | missense | KCTD3 | GRCh38.p7 | 1:215619275 | CAGCATAGCCACTTA[C/G]GAGAATCAAATTCTA | 51133 |
| rs747264194 | snp | G/T | 1.648e-05 | 0.0028705 | missense | KCTD3 | GRCh38.p7 | 1:215579936 | ATCCACGAAAGGTGC[G/T]AATAGTAGCTGGCCA | 51133 |
| rs747282972 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585556 | TTTCCTTCATCTTCT[A/G]TATTCTCTTTAGGTA | 51133 |
| rs747298143 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585220 | TGTTTATTAGGTAAG[G/T]ATTTAAGTATTTTCA | 51133 |
| rs747371933 | snp | C/T | 1.66571e-05 | 0.00288587 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578126 | AATTCCTTGTATCAT[C/T]AAGCAAGTACAAGCA | 51133 |
| rs747427567 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600244 | CTGCATGACATTGAG[A/G]GGGTACAGAAATTAG | 51133 |
| rs747457535 | snp | A/G | 1.73072e-05 | 0.00294165 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604085 | GAGGGTAGCTTTTTT[A/G]TTATCGTTCCATAAT | 51133 |
| rs747467855 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608622 | TGTCTCCTTTGATAT[C/T]CTCTGATTTCAGCAA | 51133 |
| rs747506971 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605493 | CCTGGACTCTGTATT[C/T]TTTATCTGCACTTTC | 51133 |
| rs747536577 | snp | A/G | 1.64974e-05 | 0.00287201 | intron-variant, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577950 | TAAAAATGGAGTACT[A/G]TTTTTCTGTTTGCAT | 51133 |
| rs747562074 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566820 | CATTACACAGTCTAG[A/G]GGTTTTTGTCCTTTG | 51133 |
| rs747562455 | in-del | -/AAATA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607441 | TTCTATTCACAAAAT[-/AAATA]AAACTAATTGGAGTA | 51133 |
| rs747699390 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571426 | GGGCGTAGGAACTGC[G/T]TATAAACACCTAGAC | 51133 |
| rs747704075 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215586597 | GGTTGGAGGGCCACA[C/T]GGAGACAAAGACAAA | 51133 |
| rs747707980 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595072 | ATTTTAAATCTATCA[A/G]TCAGGTTATTTTGAT | 51133 |
| rs747749660 | snp | G/T | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620790 | ATAATCATATCTCTT[G/T]TGACATTTTGGAAAT | 51133 |
| rs747807604 | snp | G/T | 1.65083e-05 | 0.00287296 | missense | KCTD3 | GRCh38.p7 | 1:215618901 | AATATGTGAGATCCA[G/T]GCTGTTGACTGTACT | 51133 |
| rs748019319 | snp | C/T | 5.39345e-05 | 0.00519272 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575888 | GAAAATAAAACTGTT[C/T]TCTTTTTTACAGATA | 51133 |
| rs748096891 | snp | A/C | 1.66045e-05 | 0.00288132 | missense | KCTD3 | GRCh38.p7 | 1:215620402 | GAAAAGGTCATCAGA[A/C]GATGAAAATGAAAAT | 51133 |
| rs748115170 | snp | C/T | 5.00313e-05 | 0.00500131 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574052 | TTTAAAAACTAACTT[C/T]AGATTATTAATGACT | 51133 |
| rs748122942 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589644 | TTAGGCTTTTTGTCA[C/T]CATAGATTAGGTTTC | 51133 |
| rs748130168 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600441 | CTTCCTCTGTGAACC[C/T]TCCTTGATCTTTGCT | 51133 |
| rs748222158 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617223 | ATTAACTCGTAAATG[C/T]GAGCTTTCCTTTGAA | 51133 |
| rs748298903 | snp | C/T | 3.29804e-05 | 0.00406068 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215579916 | ATCAACAGGATTTCC[C/T]GTGGATCCACGAAAG | 51133 |
| rs748301679 | snp | A/G | 1.71434e-05 | 0.0029277 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579148 | GCTAGGTAAGCAAAG[A/G]TTACAGAAATAGAAA | 51133 |
| rs748358448 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615574 | GCAGTGAGCTGAGAT[C/T]GCGCCACTGCACTCC | 51133 |
| rs748383926 | snp | A/G | 9.02014e-05 | 0.0067151 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607978 | AAATGAGTTTTTAAA[A/G]GTAATTTTGTATTCT | 51133 |
| rs748390133 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585429 | GGCATACATATTTAA[C/G]GGAAAATGAAGTTGA | 51133 |
| rs748411649 | snp | A/C | 3.31301e-05 | 0.00406989 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619089 | GGTTCTCATACAGAA[A/C]GATGTTTGTCACAAG | 51133 |
| rs748411887 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576814 | ACCTCGTAATCCACC[C/T]GCCTTGGCCTCCCAA | 51133 |
| rs748413007 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601723 | TGTGCACGCGTGCAC[C/G]TAAAGAAAGTTTATT | 51133 |
| rs748466885 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580812 | TAAAATGTCTTCTAA[A/T]GTTTACAGATATAGT | 51133 |
| rs748508071 | snp | A/G | 1.73631e-05 | 0.00294639 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602036 | TACCTTTCAGTTTTA[A/G]ATAGATATGCTATTT | 51133 |
| rs748508115 | in-del | -/CGGCAGCTTCCCCGCGGCGGCGGC | 8.84721e-05 | 0.00665043 | cds-indel, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567703 | GGCGGGAGGGCACTG[-/CGGCAGCTTCCCCGCGGCGGCGGC]CGGCAGCGGCGAGAT | 51133 |
| rs748537780 | in-del | -/T | 1.6967e-05 | 0.00291259 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602242 | TCTTGACTTTTTATC[-/T]TTTTTATTCATTAGT | 51133 |
| rs748575571 | snp | C/T | 5.31948e-05 | 0.00515699 | missense | KCTD3 | GRCh38.p7 | 1:215620059 | AACTGTATTTCAGCC[C/T]TCAGCTTCAGCACCA | 51133 |
| rs748586243 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586900 | TTTAAGTGAAACCTG[A/G]CTGCTCTATGAAAAT | 51133 |
| rs748638779 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612352 | TAAAATAAAAATGAT[A/G]TTAATAACACTAATT | 51133 |
| rs748680936 | snp | A/G | 1.85475e-05 | 0.00304523 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601828 | AAAATAGAAATTATA[A/G]TTACTATCTAACATC | 51133 |
| rs748715752 | snp | A/G | 1.64961e-05 | 0.00287189 | missense | KCTD3 | GRCh38.p7 | 1:215619257 | CCAGCAACTTCCGTA[A/G]TTCAGCATAGCCACT | 51133 |
| rs748754848 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583423 | ATGCATTATAATTAG[C/T]GTATAATGAGCAGTG | 51133 |
| rs748827870 | snp | C/T | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621044 | ATTGTCTTTGGAACT[C/T]GGTCTCCCAACACTT | 51133 |
| rs748842916 | snp | A/C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581750 | ATGTAAAGTGACGAA[A/C/G]GAAGACAATTGAGGA | 51133 |
| rs748850999 | snp | A/G | 3.31148e-05 | 0.00406894 | missense | KCTD3 | GRCh38.p7 | 1:215611885 | TTGTTCCCATCACCA[A/G]CAAACTATTTGTAAG | 51133 |
| rs748904464 | snp | A/G | 1.70945e-05 | 0.00292351 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608208 | GCATTTTTAGGTACT[A/G]TATTAACTGTTCAGA | 51133 |
| rs748931956 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606759 | GTGTATACTCAGTTA[C/T]GTTATTCTGCCACCT | 51133 |
| rs748957425 | snp | A/C | 5.23985e-05 | 0.00511825 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620626 | GCTTGTGAAAACTCA[A/C]CAAAATGAATAGTTG | 51133 |
| rs749050996 | snp | G/T | 3.30732e-05 | 0.00406638 | missense | KCTD3 | GRCh38.p7 | 1:215620233 | CTGTCCCTGAAAATG[G/T]TAACTTGGGTCCAAT | 51133 |
| rs749117455 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215611079 | TATTAAAATTTTATG[-/T]TTTAAGTTTTAAACA | 51133 |
| rs749124593 | snp | A/G | 3.31686e-05 | 0.00407225 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573762 | ATGTTCTCACTTATA[A/G]TACCAGATGATTTTT | 51133 |
| rs749145771 | snp | A/T | 1.67973e-05 | 0.00289799 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574025 | AATTAGCACATTTGT[A/T]TATACTCAGATTTTA | 51133 |
| rs749205838 | snp | A/G | 4.94344e-05 | 0.00497139 | missense | KCTD3 | GRCh38.p7 | 1:215586556 | TTGGATTGGACTATC[A/G]AACGAGTAGCTTTAA | 51133 |
| rs749241788 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615832 | AGTGTCCATTTTTAT[A/G]CTTAGGTTAGAAGAA | 51133 |
| rs749258811 | snp | C/T | 1.66045e-05 | 0.00288132 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618867 | TCCCATCAGGGCTCT[C/T]TCTGCTTTTCTTTTG | 51133 |
| rs749264060 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576208 | CGAGTAGCTGGGACT[A/G]TAGGCACATGCCACC | 51133 |
| rs749274688 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587092 | TCCTCTTAAAAAGTT[A/G]CTCAGGACCTGAAAG | 51133 |
| rs749277581 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589068 | TTTGAAGGTCTATAC[C/T]AAACAATTTCTGGAT | 51133 |
| rs749335442 | in-del | -/AAA | 2.19113e-05 | 0.00330986 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575994 | AAATGCACTCTTTTT[-/AAA]AAAGTAAATTCTTAC | 51133 |
| rs749411888 | snp | A/C | 3.34236e-05 | 0.00408787 | missense | KCTD3 | GRCh38.p7 | 1:215579036 | ACAACACAGTCAGAT[A/C]TGCTGATTCTAGGAA | 51133 |
| rs749461860 | snp | A/G | 1.64827e-05 | 0.00287073 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604247 | TTTTCAGACTTTCAC[A/G]GTTCACCGAAGTCCC | 51133 |
| rs749498716 | snp | C/G | 1.66134e-05 | 0.00288208 | missense | KCTD3 | GRCh38.p7 | 1:215620387 | TTTTTCAGAATCCAA[C/G]AAAAGGTCATCAGAA | 51133 |
| rs749502652 | in-del | -/TTCTT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215611732 | GGTACGTATAAGAAA[-/TTCTT]TTCTTATATTAATAT | 51133 |
| rs749553653 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572970 | GGACTGAACAAGTAC[G/T]ATATTGCTTTGTTTG | 51133 |
| rs749572148 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613677 | CTGTTGATTTTTGTA[C/T]GTAGTAAGAGGAAGG | 51133 |
| rs749722819 | snp | C/T | 6.96027e-05 | 0.00589886 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595330 | TGGTGACTGATTAAC[C/T]TTTTTATTTTTTATT | 51133 |
| rs749780037 | snp | G/T | 1.65666e-05 | 0.00287802 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619124 | AGCTTTTCACTTAAG[G/T]GATTTTAATGACTAT | 51133 |
| rs749793655 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576523 | TGAGGCTGCAGTGAG[C/T]TATGATCATGCCTCT | 51133 |
| rs749802239 | snp | A/G | 1.77087e-05 | 0.00297557 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579869 | AATTTGCCAACCCCC[A/G]GTTTAGAATGTAAAA | 51133 |
| rs749804216 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596743 | TGATAGCTTAAGGAT[C/G]AAGGCTGGTTTGAAA | 51133 |
| rs749823364 | snp | A/G | 1.66172e-05 | 0.00288242 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215579115 | TGTTCTCTCTGGAAC[A/G]GGAGAAGAAACTGTT | 51133 |
| rs749827838 | in-del | -/AAAAT | 0.000120162 | 0.00775026 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611777 | TTTGTAAAATGAGAA[-/AAAAT]AAAATTTTAATTAAT | 51133 |
| rs749869382 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586340 | ATAGGCAATATAGAT[C/T]AACAAAATTTTATTT | 51133 |
| rs749911276 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585025 | TGGGTTGGGGGTCTC[C/T]CCACTATCTCATTTC | 51133 |
| rs749950219 | in-del | -/AAT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616770 | CGTCTAATGAAAAAA[-/AAT]AATAATTTCCTTTGT | 51133 |
| rs750005490 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585058 | GGTTTCCCAGGAAGA[G/T]GTTACTGGAAAGGGG | 51133 |
| rs750025083 | snp | A/G | 1.65176e-05 | 0.00287376 | missense | KCTD3 | GRCh38.p7 | 1:215620161 | CAAGAAGGACTGAGA[A/G]CTTTCACAGTTATAG | 51133 |
| rs750033259 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609842 | ATACTATTCTGTGGT[A/C]TGAAGATATACCTGG | 51133 |
| rs750043610 | snp | C/T | 1.66788e-05 | 0.00288775 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601971 | TAAGTGTTCAGTCAC[C/T]TAAAATGCTCCTGCT | 51133 |
| rs750100558 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569059 | AGTAGCAGTATAATC[A/G]TTTACAATCCCTACA | 51133 |
| rs750100873 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215620046 | TGTCATTTTTAAAAA[C/T]TGTATTTCAGCCTTC | 51133 |
| rs750167999 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607184 | TATGTATGTGTGTAT[A/G]TAAGAAATTTTAGAT | 51133 |
| rs750201441 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594760 | ATTAAATGGAGATTG[A/C]AGTGCTGGAACACAT | 51133 |
| rs750220939 | snp | C/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215566045 | GATTCCTAGTTGCTG[C/T]TGCTTTAATCTGAAC | 51133 |
| rs750249179 | snp | A/G | 0.000121825 | 0.00780369 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618175 | CTTTCACTTTCCTTA[A/G]AGTTGATTGTTGCAT | 51133 |
| rs750315564 | snp | C/T | 5.26542e-05 | 0.00513072 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578993 | TGTTTTCTTCTTCTC[C/T]TTATAGGTATTCCTA | 51133 |
| rs750340992 | in-del | -/CAATATATTA | 1.65548e-05 | 0.002877 | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215601940 | GATGTAACAATGGAT[-/CAATATATTA]CATAGGTAAGTGTTC | 51133 |
| rs750393753 | snp | A/T | 4.97294e-05 | 0.0049862 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578104 | CACTTTATTAAATCT[A/T]TTAAAAAATTCCTTG | 51133 |
| rs750399397 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579462 | CACATAATGGACAAT[A/G]TGTAACAAGTAAGCA | 51133 |
| rs750462173 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589410 | CTTTCCAAAGTGCTG[G/T]GATTACAGGCATGAG | 51133 |
| rs750541734 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606021 | TTTAGAATAAATTTA[A/T]ATTTCTACCATAGCC | 51133 |
| rs750572725 | snp | A/T | 1.66142e-05 | 0.00288216 | missense | KCTD3 | GRCh38.p7 | 1:215620381 | TGAAGGTTTTTCAGA[A/T]TCCAAGAAAAGGTCA | 51133 |
| rs750591543 | snp | A/G | 1.66963e-05 | 0.00288927 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574165 | AAATTAATGCTTATA[A/G]TGCTTGGTCCTAACA | 51133 |
| rs750609950 | snp | A/G | 5.05514e-05 | 0.00502724 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573864 | ATAATTCTTTAGTGT[A/G]TATTTTAATACATTT | 51133 |
| rs750657689 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590556 | TTTTTCTCCATTCTT[C/T]AGTTTAGATATCTTT | 51133 |
| rs750666446 | snp | C/G | 1.65258e-05 | 0.00287448 | missense | KCTD3 | GRCh38.p7 | 1:215619048 | CACTGCTATGGATAT[C/G]GTTAACAAAAGTGAA | 51133 |
| rs750711909 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597287 | TTTTGTTTAATTCCA[C/T]CCCCTCGCCCACACA | 51133 |
| rs750778675 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576918 | ATAACCAGTTTCACA[A/G]ATAAAAACAATTTAA | 51133 |
| rs750879840 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618193 | TTGATTGTTGCATGA[G/T]AGTACAGGAAAAATA | 51133 |
| rs750888151 | in-del | -/GT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215592289 | ATGTGGGGCTTGTCA[-/GT]GTGTTTCTGTCTCTC | 51133 |
| rs750930223 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614440 | ACAATATTAATTCTT[G/T]CTATCCATGGTCATG | 51133 |
| rs750944047 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600158 | TTTGGCATTGGCTTT[A/C]ATTAAAAGCCTGACC | 51133 |
| rs751016033 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571480 | TAGTAGTCAACTTCT[A/G]TGTGTTCCCTAAAGT | 51133 |
| rs751072146 | snp | A/G | 1.72627e-05 | 0.00293786 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595512 | TGAAAATATTTCTGA[A/G]ATGTATGCTGATTAT | 51133 |
| rs751078644 | in-del | -/CCATCTCCTACAAAGACTACT | 4.95405e-05 | 0.00497673 | cds-indel | KCTD3 | GRCh38.p7 | 1:215620543 | CCTGGTACTGCGTCC[-/CCATCTCCTACAAAGACTACT]CCATCTCCTACAAAG | 51133 |
| rs751184890 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588058 | ATTTTCACTTGAAAC[A/G]TTGAATTTTTATCAT | 51133 |
| rs751207267 | in-del | -/AATTTTTTAAATGA | 1.68142e-05 | 0.00289945 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601993 | GCTCCTGCTTAATGT[-/AATTTTTTAAATGA]GAACAAGAAAACATT | 51133 |
| rs751237140 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613201 | TTCCTGTTAATAGTC[C/T]ATTAGGAAGGTTATT | 51133 |
| rs751359094 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600940 | ATCCTAGCAAACACA[-/T]TTTTTTTTTTTTTTG | 51133 |
| rs751366498 | snp | A/T | 1.84446e-05 | 0.00303677 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620655 | TGTTTCGTTACATTT[A/T]GATGAAAGTTAAACT | 51133 |
| rs751372529 | snp | C/T | 3.30868e-05 | 0.00406723 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578094 | CAGGTATTTTCACTT[C/T]ATTAAATCTTTTAAA | 51133 |
| rs751429261 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596454 | CCATTGAGTGGGTAT[A/C]TAGAAAGAAACAAAA | 51133 |
| rs751541355 | snp | A/G | 1.65353e-05 | 0.00287531 | missense | KCTD3 | GRCh38.p7 | 1:215601895 | TTCCTATAACTAGTT[A/G]TGACACTGCTGGATC | 51133 |
| rs751543265 | in-del | -/AACT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607010 | CCCTTTTCACCAGAA[-/AACT]GACAGTCTAATAATT | 51133 |
| rs751552497 | snp | A/G | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565537 | TAAGTACAGTATAAT[A/G]AAATGAACACGGTTT | 51133 |
| rs751556344 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576060 | AAAAGGTTTTTTTTG[C/T]TTGTTTTTTTTTTTC | 51133 |
| rs751629994 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215592744 | ATCCAAAGAAAATTG[G/T]TAGGGCTGGTATATC | 51133 |
| rs751650648 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591021 | CCTCTTCTAGCTTTA[A/T]TTGTAATTTTAGGGC | 51133 |
| rs751668804 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568564 | TTTTGTGGATTTCCT[A/G]TAACTTATGAGTCAC | 51133 |
| rs751725763 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609245 | TTTGAACTGATACAT[A/G]AAGGATAGACATTTG | 51133 |
| rs751734594 | snp | C/T | 1.66333e-05 | 0.00288381 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215611829 | TTCTGATCAAGGACC[C/T]TTTGGAGAGCGAGAC | 51133 |
| rs751753216 | in-del | -/TGA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591873 | CCGTTTTCACACTGC[-/TGA]TGATAAAGACATACT | 51133 |
| rs751754686 | snp | A/G | 1.72374e-05 | 0.00293571 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611960 | TTGTATTCAGAAGCC[A/G]CCTTTTGTCTTACAA | 51133 |
| rs751757662 | snp | A/G | 1.67902e-05 | 0.00289738 | missense | KCTD3 | GRCh38.p7 | 1:215586496 | TTCTTCCTTAACAGA[A/G]TCAAAGAATCTTCAG | 51133 |
| rs751987275 | snp | G/T | 1.65378e-05 | 0.00287552 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620465 | AGGGGGAGGATTCCT[G/T]GGAAGAAAGAAAGTT | 51133 |
| rs752038729 | snp | A/G | 1.66117e-05 | 0.00288194 | missense | KCTD3 | GRCh38.p7 | 1:215620350 | TGGATAGTGGATTGG[A/G]AGTGCATAAAATAGC | 51133 |
| rs752076250 | snp | A/G | 1.66153e-05 | 0.00288225 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574142 | AATAATAATTGATAC[A/G]TATTCCTAAATTAAT | 51133 |
| rs752091917 | snp | A/G | 1.65247e-05 | 0.00287438 | missense | KCTD3 | GRCh38.p7 | 1:215620211 | TTGAACAGAAATGTA[A/G]AAAGAGCTGTCCCTG | 51133 |
| rs752122384 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615772 | TTATTATACTTTTAT[A/G]TGACACGAGAGCCTT | 51133 |
| rs752165452 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596610 | TATATATTAGTTAGG[C/T]GTTGGTGGAAGAAAG | 51133 |
| rs752225604 | snp | C/T | 3.31818e-05 | 0.00407306 | missense | KCTD3 | GRCh38.p7 | 1:215579080 | ACAGAAGGTGAAGCC[C/T]GGGGAAATGGTACAC | 51133 |
| rs752241128 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613493 | TGTGGTGCAAGTGCT[C/T]TTTACTTTAATAAGG | 51133 |
| rs752299545 | in-del | -/ACCAAAA | 1.74005e-05 | 0.00294957 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620625 | AGCTTGTGAAAACTC[-/ACCAAAA]TGAATAGTTGTTTCG | 51133 |
| rs752369885 | snp | C/T | 1.68156e-05 | 0.00289957 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604317 | GGTAAAATGATTTCA[C/T]TATACTGGTAAGGAA | 51133 |
| rs752399695 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584669 | TGGCCAGTTTTTCCC[A/G]GGGGCTTTTATCAGC | 51133 |
| rs752444006 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616393 | AAAACCCTAGCAACT[-/A]AAAAAAAGGGAAATT | 51133 |
| rs752499134 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578150 | ACAAGCATATGAATA[G/T]GAAAAACTGCTCCTT | 51133 |
| rs752572246 | snp | C/T | 1.66474e-05 | 0.00288503 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215595456 | AGTGTGGAATGCTGT[C/T]ACTCAGCACTGGCAG | 51133 |
| rs752606632 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583315 | CAGAACTGAATGTTC[C/T]TCCCCTTTTTAGACC | 51133 |
| rs752778140 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618328 | CTTTTTGTCCGGCCT[A/G]CTAGGAAGCTCATCT | 51133 |
| rs752814681 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612144 | CAGTTAGGAGGGACT[-/A]AGTGATAGAATAAGA | 51133 |
| rs752873551 | snp | C/T | 3.63981e-05 | 0.00426588 | intron-variant | KCTD3 | GRCh38.p7 | 1:215620047 | GTCATTTTTAAAAAC[C/T]GTATTTCAGCCTTCA | 51133 |
| rs752876423 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594548 | CAGATGGCTTCTTTT[C/G]TAAGATATATTTTCA | 51133 |
| rs752893439 | snp | G/T | 1.68795e-05 | 0.00290507 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611815 | TTGACATTTTTGTTT[G/T]CTGATCAAGGACCTT | 51133 |
| rs753008152 | in-del | -/TCCTTCCTTCCTTCCTTCTCTCTTTCTC | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591329 | CCTTCCTTCCTTCCT[-/TCCTTCCTTCCTTCCTTCTCTCTTTCTC]TCTTTCTTCTCTTTC | 51133 |
| rs753060421 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605703 | CTTAGTATACAGTAT[C/T]ACCATCTACTTATCT | 51133 |
| rs753065934 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603913 | AGGAGGTGAATAGTT[A/T]CGTCTTGGAGTGAGG | 51133 |
| rs753068948 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585319 | AGGAAAAATTGATAC[A/G]TTTTTCTCTATTGCT | 51133 |
| rs753077953 | snp | C/G | 0.000113727 | 0.00753993 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567775 | GGGGACCAGGTGAGT[C/G]GGCGGGTAGCGGGCT | 51133 |
| rs753166538 | snp | C/T | 1.65195e-05 | 0.00287393 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620183 | CAGTTATAGGGACTT[C/T]CAGACTATTAATTTG | 51133 |
| rs753245490 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599618 | TGAAGTTGTTAGGAC[A/G]AAGAAGAGGAGGCCA | 51133 |
| rs753331599 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616403 | GCAACTAAAAAAAGG[A/G]AAATTTTAAAATCTG | 51133 |
| rs753372548 | snp | A/G | 0.000115493 | 0.00759825 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604169 | GATCGCCTATGGTAC[A/G]AGCTCTGGAGCAGTA | 51133 |
| rs753392254 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597871 | GGAATCCTAGGCCCA[C/T]ATTTTGTTGGGGAGA | 51133 |
| rs753439799 | snp | A/G | 1.66037e-05 | 0.00288125 | missense | KCTD3 | GRCh38.p7 | 1:215620323 | GAGTAGAAATAAAAA[A/G]TTTGAGAGAATTGGA | 51133 |
| rs753465450 | snp | A/G | 1.72785e-05 | 0.00293921 | missense | KCTD3 | GRCh38.p7 | 1:215579000 | TTCTTCTCTTTATAG[A/G]TATTCCTAGTCGTAA | 51133 |
| rs753479757 | snp | G/T | 0.00028224 | 0.011876 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578114 | AATCTTTTAAAAAAT[G/T]CCTTGTATCATTAAG | 51133 |
| rs753482899 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608973 | GTACTTGTGTTCTAG[A/G]TATTAGAAATTTTAA | 51133 |
| rs753540307 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570754 | TAATTTAGTAGGAGG[A/C]AAGTTGCATGAAGTA | 51133 |
| rs753555990 | snp | A/T | 1.70679e-05 | 0.00292124 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602250 | TTTTTATCTTTTTAT[A/T]CATTAGTTTATTATG | 51133 |
| rs753671676 | snp | C/G | 1.68278e-05 | 0.00290062 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586710 | ATCTTGTTTATGTTG[C/G]AATTTGATGATATTA | 51133 |
| rs753698423 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585921 | CACCCTATCCTTTTT[C/T]ATATAATAGTGCTAA | 51133 |
| rs753719617 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593002 | CTAGAACCTCATCCT[C/T]CTCTGGAGTAATCGA | 51133 |
| rs753757515 | snp | A/G | 9.92934e-05 | 0.00704534 | missense | KCTD3 | GRCh38.p7 | 1:215619065 | TTAACAAAAGTGAAG[A/G]TAAGGGTAGGTTCTC | 51133 |
| rs753844942 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610940 | TTAATAAGTACATGT[A/G]TGATTCATGTAACAT | 51133 |
| rs753972359 | in-del | -/TCTT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597742 | TTGATTTAGCTTCTC[-/TCTT]TCCTGTTGTGAGGCA | 51133 |
| rs753994499 | snp | A/T | 7.259e-05 | 0.0060241 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607966 | TGAAAAAAGTTAAAA[A/T]GAGTTTTTAAAAGTA | 51133 |
| rs754024958 | snp | A/C | 1.64931e-05 | 0.00287163 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577619 | CTTTCATGTCAGATG[A/C]TAATACAGGTTTCCA | 51133 |
| rs754025549 | snp | A/G | 3.61919e-05 | 0.00425378 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575855 | AGATATTAAAGTTAA[A/G]AGATTAATTTGTAAT | 51133 |
| rs754034054 | snp | C/G/T | 3.32382e-05 | 0.00407654 | missense | KCTD3 | GRCh38.p7 | 1:215620572 | AGACTACTCCATCTC[C/G/T]TCGGCATAAAAAAAG | 51133 |
| rs754075467 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605954 | ACACAGCAGCCAGAA[A/G]CATCTTTTAGAAACA | 51133 |
| rs754079827 | snp | A/G | 4.98442e-05 | 0.00499196 | missense | KCTD3 | GRCh38.p7 | 1:215595415 | GGTAACCAGTTGGTG[A/G]CCACGAGTCATACAG | 51133 |
| rs754104380 | in-del | -/TAT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602449 | GCATTTGTTGAGCCA[-/TAT]TATTATAATGTTAGC | 51133 |
| rs754121485 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574316 | ATACTATATATGGCA[A/G]TTTAAGTATTCATGA | 51133 |
| rs754175683 | snp | G/T | 0.0010543 | 0.0229355 | missense, utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567716 | TGCGGCAGCTTCCCC[G/T]CGGCGGCGGCCGGCA | 51133 |
| rs754210465 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569593 | TCTTGGCACTGTAAC[-/T]TTTTTTTTTTTTTTT | 51133 |
| rs754253518 | in-del | -/AGTTG | 1.77376e-05 | 0.002978 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620637 | CTCACCAAAATGAAT[-/AGTTG]TTTCGTTACATTTAG | 51133 |
| rs754295216 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618024 | TTCTTTGGACCTCAC[G/T]CTCTTGTGAAGATTC | 51133 |
| rs754329940 | snp | A/C | 3.30191e-05 | 0.00406306 | missense | KCTD3 | GRCh38.p7 | 1:215608118 | GCGTCATTCAAGATA[A/C]TATCCCTGGAGGAGA | 51133 |
| rs754390900 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575491 | GTGCATTATTAAAGT[A/G]CATTGTAGTTTTAAT | 51133 |
| rs754439281 | snp | G/T | 0.000165843 | 0.00910461 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618873 | CAGGGCTCTTTCTGC[G/T]TTTCTTTTGCAGAAT | 51133 |
| rs754451976 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582623 | TAGAGTGCAGTGGCG[-/T]TGATCTCGGGTCACT | 51133 |
| rs754466811 | in-del | -/AGC | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593379 | CTTCTAACAATACTT[-/AGC]AGGTTTTTTGTTTTG | 51133 |
| rs754488602 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612255 | CTGGAACTTAAATAT[G/T]TTCCATCCCATATAA | 51133 |
| rs754560060 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571583 | AATGAAAGAATACTT[C/T]TCCTTACAAATTGTA | 51133 |
| rs754565308 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596496 | AACTCTGGGGGAACA[C/T]TAGCATTTAAGGGGA | 51133 |
| rs754600318 | in-del | -/A | 6.66644e-05 | 0.00577302 | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215620580 | CCATCTCCTCGGCAT[-/A]AAAAAAGTGATTCTT | 51133 |
| rs754625647 | snp | C/T | 1.70586e-05 | 0.00292045 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215579007 | CTTTATAGGTATTCC[C/T]AGTCGTAAAATAAAC | 51133 |
| rs754631611 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609040 | AGTGGGAATTAAAAT[A/G]AAACAGTTGCATTTT | 51133 |
| rs754651620 | in-del | -/TA | 1.70612e-05 | 0.00292067 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602075 | GCTGTTTAAAATTTT[-/TA]TGTTTTAGATATGCA | 51133 |
| rs754663429 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575213 | GCCCAGATCGTGCCA[C/T]TGCACTCCAGCCTAG | 51133 |
| rs754717304 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604172 | CGCCTATGGTACGAG[C/T]TCTGGAGCAGTACGA | 51133 |
| rs754726066 | snp | C/T | 0.000166132 | 0.00911255 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215595417 | TAACCAGTTGGTGGC[C/T]ACGAGTCATACAGGG | 51133 |
| rs754727606 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595033 | TGGCATGGATCCCAG[C/G]ATCCTTTTTGTTTTG | 51133 |
| rs754735094 | snp | A/G/T | 3.32891e-05 | 0.00407966 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578124 | AAAATTCCTTGTATC[A/G/T]TTAAGCAAGTACAAG | 51133 |
| rs754745010 | snp | A/G | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620772 | TTGGAATAATGAGAT[A/G]CAATAATCATATCTC | 51133 |
| rs754758333 | snp | A/G | 3.59512e-05 | 0.00423961 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575858 | TATTAAAGTTAAAAG[A/G]TTAATTTGTAATTTG | 51133 |
| rs754761370 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581223 | TGTACTCCAACCTGC[A/G]CAACAGAGCAAGACT | 51133 |
| rs754885361 | snp | A/T | 1.68207e-05 | 0.00290001 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586711 | TCTTGTTTATGTTGC[A/T]ATTTGATGATATTAA | 51133 |
| rs754920722 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606066 | TGTTCTAGATTCTAC[C/G]TACCTTTAAAATTTC | 51133 |
| rs754944208 | snp | C/G | 1.68352e-05 | 0.00290126 | missense | KCTD3 | GRCh38.p7 | 1:215579137 | GAAACTGTTAGGCTA[C/G]GTAAGCAAAGATTAC | 51133 |
| rs754951802 | snp | G/T | 1.65515e-05 | 0.00287671 | missense | KCTD3 | GRCh38.p7 | 1:215619066 | TAACAAAAGTGAAGA[G/T]AAGGGTAGGTTCTCA | 51133 |
| rs754972599 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215586588 | TGCAAAGGTGGTTGG[A/G]GGGCCACATGGAGAC | 51133 |
| rs755010877 | snp | A/G | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622139 | TTATGTAATAGAATC[A/G]CATAAAAAGGAAACT | 51133 |
| rs755015004 | snp | A/G | 4.95266e-05 | 0.00497603 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215608120 | GTCATTCAAGATACT[A/G]TCCCTGGAGGAGACA | 51133 |
| rs755042210 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577763 | TTGGTGTTTATGATT[G/T]GACTCATGTATGAAA | 51133 |
| rs755048502 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215592874 | CCCCTTAAGACAGGA[A/G]CTGGTCATTACTTCT | 51133 |
| rs755084873 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576155 | CTCACTGCAACCTCC[A/G]CCTTTCAGGTTCAAA | 51133 |
| rs755128005 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607774 | CTTTACTACATTTAT[-/A]AACCTACAAGCTATT | 51133 |
| rs755168952 | snp | C/T | 3.29837e-05 | 0.00406088 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577625 | TGTCAGATGATAATA[C/T]AGGTTTCCAGTGTTA | 51133 |
| rs755175770 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598561 | CATGGAAACAAATAA[C/T]GAAAAGTCATTAAAC | 51133 |
| rs755220959 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600268 | AAATTAGGATTATAT[A/G]CAGGAAGAGCTTAGA | 51133 |
| rs755286981 | snp | C/T | 0.000839278 | 0.0204679 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567736 | GGCGGCCGGCAGCGG[C/T]GAGATCGTCCAACTG | 51133 |
| rs755290507 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609012 | TGAACATCAACTTAC[-/A]AATGTAGTGAGCAGT | 51133 |
| rs755322754 | snp | C/G/T | 3.29817e-05 | 0.00406078 | missense | KCTD3 | GRCh38.p7 | 1:215620506 | CGTCATCACCAAGTA[C/G/T]TTCCGATGGAGGAAC | 51133 |
| rs755395359 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618520 | AATTCAGTTAGCCCT[C/T]ACGTGACTTTGGAAC | 51133 |
| rs755423090 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601654 | AATTTAAAAAAAATA[C/T]TTTGAAGGAAGTATA | 51133 |
| rs755430942 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569479 | ATTATTGTAAAAATT[A/C]AGCAGTATTGTTATT | 51133 |
| rs755463496 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585028 | GTTGGGGGTCTCTCC[A/G]CTATCTCATTTCATG | 51133 |
| rs755558603 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597662 | TATTGGTTCTGGGAA[C/T]AAGAATTCAAAGTGA | 51133 |
| rs755563441 | snp | C/T | 6.71062e-05 | 0.00579212 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579891 | AATGTAAAATATTTC[C/T]TTTTCCAAAATCAAC | 51133 |
| rs755587926 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581652 | GAGGATGATGCTATT[A/G]CATTTTCCAGTCTTT | 51133 |
| rs755643626 | snp | A/G | 1.65897e-05 | 0.00288003 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578109 | TATTAAATCTTTTAA[A/G]AAATTCCTTGTATCA | 51133 |
| rs755646471 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596685 | CAGCAAATTCAAATA[C/T]CTTTCAAGAAGTTTG | 51133 |
| rs755688219 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215604658 | ATTTAGGAGATGTGA[-/T]TTTTTTTTTTTTTTT | 51133 |
| rs755803112 | snp | C/G | 1.6967e-05 | 0.00291259 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602242 | TTCTTGACTTTTTAT[C/G]TTTTTATTCATTAGT | 51133 |
| rs755835011 | snp | C/T | 1.65157e-05 | 0.0028736 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620168 | GACTGAGAGCTTTCA[C/T]AGTTATAGGGACTTC | 51133 |
| rs755856016 | in-del | -/TTCC | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571553 | ATTGTTTTACTGTCT[-/TTCC]TTCAGTTAGCCAATG | 51133 |
| rs755878992 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566531 | ATTATTATGATACAA[C/T]TATGACAAAACAATT | 51133 |
| rs755901570 | snp | A/T | 1.64825e-05 | 0.00287071 | missense | KCTD3 | GRCh38.p7 | 1:215586546 | GAGCCCATATTTGGA[A/T]TGGACTATCGAACGA | 51133 |
| rs755947685 | in-del | -/AACA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579801 | CTGTGCCCGGCTCTT[-/AACA]AAACTATTAACCAAA | 51133 |
| rs755967718 | snp | A/G | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215566047 | TTCCTAGTTGCTGCT[A/G]CTTTAATCTGAACTG | 51133 |
| rs756026995 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569933 | AAAATAAGTAGTAAT[A/G]GTATGGCCCGTAGAA | 51133 |
| rs756029041 | snp | A/C | 1.67736e-05 | 0.00289595 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618847 | CTTTTTAAATAATTG[A/C]TCATTCCCATCAGGG | 51133 |
| rs756081513 | snp | C/G | 1.65474e-05 | 0.00287636 | missense | KCTD3 | GRCh38.p7 | 1:215611875 | ATCCAGAAAGTTGTT[C/G]CCATCACCAACAAAC | 51133 |
| rs756159197 | snp | C/T | 1.66164e-05 | 0.00288235 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620384 | AGGTTTTTCAGAATC[C/T]AAGAAAAGGTCATCA | 51133 |
| rs756243309 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584007 | ACTAAATAAGAAGGC[-/T]TTTCATGAACTGGGA | 51133 |
| rs756257395 | snp | C/T | 1.67061e-05 | 0.00289011 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574166 | AATTAATGCTTATAG[C/T]GCTTGGTCCTAACAT | 51133 |
| rs756345486 | snp | A/T | 1.67668e-05 | 0.00289537 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586705 | GAAGAATCTTGTTTA[A/T]GTTGCAATTTGATGA | 51133 |
| rs756364021 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588999 | TATACTTCTCTAGCC[A/G]CTGTGATGTCGTAAC | 51133 |
| rs756375567 | snp | G/T | 1.70513e-05 | 0.00291982 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573867 | ATTCTTTAGTGTATA[G/T]TTTAATACATTTATT | 51133 |
| rs756398946 | snp | A/G | 0.000132133 | 0.00812706 | missense | KCTD3 | GRCh38.p7 | 1:215620173 | AGAGCTTTCACAGTT[A/G]TAGGGACTTCCAGAC | 51133 |
| rs756425451 | snp | C/T | 7.09685e-05 | 0.00595644 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579868 | TAATTTGCCAACCCC[C/T]GGTTTAGAATGTAAA | 51133 |
| rs756463628 | in-del | -/A/GA | 0.000176298 | 0.00938713 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620633 | AAACTCACCAAAATG[-/A/GA]AATAGTTGTTTCGTT | 51133 |
| rs756477419 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572040 | CACGGCTTCTGCTGT[C/T]ACTGACACTGAGACT | 51133 |
| rs756585074 | snp | C/G | 3.32011e-05 | 0.00407424 | missense | KCTD3 | GRCh38.p7 | 1:215579108 | CACAGCCTGTTCTCT[C/G]TGGAACGGGAGAAGA | 51133 |
| rs756600456 | in-del | -/TTCACCTCTG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614529 | TTGTCTTAAAGATCT[-/TTCACCTCTG]TGGTTTGCTGTATTT | 51133 |
| rs756673299 | snp | A/G | | | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215574102 | GAATTTCAACACTTC[A/G]AGATGAAACTGGTGC | 51133 |
| rs756684322 | snp | A/G | 8.27137e-05 | 0.0064304 | missense | KCTD3 | GRCh38.p7 | 1:215601931 | TTCTGCTTGGATGTA[A/G]CAATGGATCAATATA | 51133 |
| rs756689198 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584892 | AGAGAGAAAGAAATA[C/T]GCTCCAAATTTTGTT | 51133 |
| rs756689216 | snp | A/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565301 | ATTTTCAATCATTTG[A/T]TATATGTTGCAAATA | 51133 |
| rs756702176 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576229 | ACATGCCACCATGCC[C/T]GGCTGATTTTTTGTA | 51133 |
| rs756705332 | snp | A/C | 3.43513e-05 | 0.00414421 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604349 | TTGGCTCTGTGTGTT[A/C]TTTTCATTAAAAGAA | 51133 |
| rs756750863 | snp | G/T | 1.64803e-05 | 0.00287052 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577660 | ATTTACATCATTTGT[G/T]TCTTTGTAGGGGAGT | 51133 |
| rs756812022 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599695 | GTTGTAACTCACTGT[A/G]ACTCTGCTTATCCTC | 51133 |
| rs756885224 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566885 | CAAAACAAAAAAACT[G/T]CTTGGGAGATTGGGG | 51133 |
| rs756890346 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578974 | GTGAACTTAGGAATG[C/T]ATTTGTTTTCTTCTT | 51133 |
| rs756914057 | snp | A/G | 1.74595e-05 | 0.00295456 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595515 | AAATATTTCTGAAAT[A/G]TATGCTGATTATGTA | 51133 |
| rs756953535 | snp | A/G | 1.88895e-05 | 0.00307317 | intron-variant | KCTD3 | GRCh38.p7 | 1:215620028 | ACAGAGTGAAATCTG[A/G]ACTGTCATTTTTAAA | 51133 |
| rs757008653 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619226 | CACATCTCGCTGTGC[C/T]ACTCCTAACATCAGT | 51133 |
| rs757035025 | snp | C/T | 1.66203e-05 | 0.00288268 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215611832 | TGATCAAGGACCTTT[C/T]GGAGAGCGAGACGAT | 51133 |
| rs757081154 | snp | C/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568945 | TCCTAATGTAAGAAA[C/T]GGAGTTTTTCCTAAA | 51133 |
| rs757088465 | snp | C/G | 1.8492e-05 | 0.00304067 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620656 | GTTTCGTTACATTTA[C/G]ATGAAAGTTAAACTT | 51133 |
| rs757126826 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609361 | GTTTAGAAAATGTCA[A/G]GAAGGTCATTAATTG | 51133 |
| rs757154836 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607042 | TTGAGAATTTTGTTA[C/T]ATAAGAATAGAAAGT | 51133 |
| rs757158523 | snp | G/T | 6.5937e-05 | 0.00574144 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577751 | CTCTTTTAATATTTG[G/T]TGTTTATGATTTGAC | 51133 |
| rs757237505 | snp | A/G | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565806 | GCAAAGGCAGTTAAC[A/G]TTGTTTAAAGCAAGC | 51133 |
| rs757326625 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593056 | ATTTCTGCCTTTCAC[A/C]TAGCCCATAATACTG | 51133 |
| rs757334367 | snp | G/T | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621576 | CAAAAGAACGTTTTT[G/T]TACAATTTTTTTTCA | 51133 |
| rs757336248 | snp | C/T | 0.000117656 | 0.00766904 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604315 | CAGGTAAAATGATTT[C/T]ATTATACTGGTAAGG | 51133 |
| rs757367543 | snp | A/C | 1.66078e-05 | 0.00288161 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573852 | CAGGTATGTCTTATA[A/C]TTCTTTAGTGTATAT | 51133 |
| rs757431192 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588414 | GAACATAAAAGGCCA[A/T]ATCTTTAATTTAATC | 51133 |
| rs757468025 | snp | C/T | 1.74397e-05 | 0.00295289 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611968 | AGAAGCCACCTTTTG[C/T]CTTACAAAACATATG | 51133 |
| rs757476915 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589226 | CTGCATCCTCAACCT[C/T]CTGGGCCCAGGCACT | 51133 |
| rs757484446 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588346 | TTTTACTGCTTCATC[A/G]AGGACATTCTTTAGT | 51133 |
| rs757504936 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575698 | ATTCAGAGGAAGAAA[A/G]AGACACCATCTCAAG | 51133 |
| rs757523086 | snp | C/T | 4.98128e-05 | 0.00499038 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573739 | AACTAATACTGAAAT[C/T]TCAAATCATGTTCTC | 51133 |
| rs757525261 | snp | A/G | 5.01341e-05 | 0.00500645 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215586501 | CCTTAACAGAATCAA[A/G]GAATCTTCAGGATGG | 51133 |
| rs757534992 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605974 | TTTTAGAAACACAAA[C/T]GAAGTTTGATTCCTG | 51133 |
| rs757657355 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613701 | AGGAAGGGGTTGAGT[C/T]TGAATCTTCTGCAAA | 51133 |
| rs757671061 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597884 | CACATTTTGTTGGGG[A/C]GAGAGGGGATTGACT | 51133 |
| rs757671413 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574361 | GGATATGAGCTTACA[C/T]TGGCATTAGAAGAAA | 51133 |
| rs757731294 | in-del | -/GTT | 1.77491e-05 | 0.00297896 | utr-variant-3-prime, cds-indel | KCTD3 | GRCh38.p7 | 1:215620638 | TCACCAAAATGAATA[-/GTT]GTTTCGTTACATTTA | 51133 |
| rs757741262 | snp | A/C | 3.29609e-05 | 0.00405948 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604211 | ACAACACCCAGAGAC[A/C]GTTGGGTCAGGTCCT | 51133 |
| rs757796855 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574266 | TCTTGTCATATGTAG[-/T]TTTTTTATAATCAGA | 51133 |
| rs757800901 | snp | G/T | 1.66161e-05 | 0.00288232 | missense | KCTD3 | GRCh38.p7 | 1:215620353 | ATAGTGGATTGGAAG[G/T]GCATAAAATAGCTGA | 51133 |
| rs757805980 | snp | A/G | 1.64879e-05 | 0.00287118 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619199 | CAAATTACTCGATCA[A/G]TGTGATTTGAGCACA | 51133 |
| rs757827427 | snp | A/C/G | 3.45819e-05 | 0.00415812 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604090 | TAGCTTTTTTATTAT[A/C/G]GTTCCATAATGTATC | 51133 |
| rs757856277 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610068 | GGGGACAGGGAGGCT[C/T]TTCATTCCTCTTTAT | 51133 |
| rs757857647 | snp | G/T | 3.39345e-05 | 0.00411899 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586724 | GCAATTTGATGATAT[G/T]AATATTTTGAAGTTT | 51133 |
| rs757869556 | snp | C/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569231 | GTTTCAAGCGATTCT[C/T]CTGCCTCAGCATCCC | 51133 |
| rs757915508 | in-del | -/GTAA | 1.66062e-05 | 0.00288146 | splice-donor-variant | KCTD3 | GRCh38.p7 | 1:215601954 | CAATATATTACATAG[-/GTAA]GTAAGTGTTCAGTCA | 51133 |
| rs757941126 | snp | A/T | 1.65688e-05 | 0.00287821 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619091 | TTCTCATACAGAAAG[A/T]TGTTTGTCACAAGGT | 51133 |
| rs757965414 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215611748 | TCTTTTCTTATATTA[A/T]TATTAATGTTCCTTT | 51133 |
| rs758050675 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571825 | TTTAGTAGAGACGGG[C/G]TTTCACCGTGTTAGC | 51133 |
| rs758084276 | snp | A/G | 9.95338e-05 | 0.00705387 | missense | KCTD3 | GRCh38.p7 | 1:215579081 | CAGAAGGTGAAGCCC[A/G]GGGAAATGGTACACA | 51133 |
| rs758091433 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575523 | ATTGAACAGTATAAG[A/G]AAGTATTATTTATTC | 51133 |
| rs758137688 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609889 | TATACCTGGTTTCTG[A/G]AGAAAGAACTTAACT | 51133 |
| rs758141880 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577738 | CATTAGGTATGTGCT[C/T]TTTTAATATTTGGTG | 51133 |
| rs758198060 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579623 | CCTGCCTCAGCCTCC[A/G]GAGTAGCTGGGACTA | 51133 |
| rs758289854 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594761 | TTAAATGGAGATTGC[A/C]GTGCTGGAACACATG | 51133 |
| rs758303436 | snp | A/C | 1.64882e-05 | 0.00287121 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577634 | ATAATACAGGTTTCC[A/C]GTGTTAGAGAATTTA | 51133 |
| rs758326957 | snp | G/T | 5.01895e-05 | 0.00500921 | splice-donor-variant | KCTD3 | GRCh38.p7 | 1:215595473 | CTCAGCACTGGCAGG[G/T]TAGTTTAAAGCATAT | 51133 |
| rs758385541 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603104 | TGTTTACTACTTGGC[C/T]CCTTACGGAAAGTGT | 51133 |
| rs758394764 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581055 | GTTCAAGATCAGCCC[A/G]ACCAACATGGTGAAA | 51133 |
| rs758438036 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607328 | AGTTTTTGCATTAGT[A/G]ATACACTTTATGGTG | 51133 |
| rs758511278 | snp | A/C | 0.000123327 | 0.00785165 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580972 | CTTTTATGTTTTAAG[A/C]GTGTTTTGGCTGGGC | 51133 |
| rs758580953 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215619812 | GATTTTTCCTCCCAT[C/G]TTTTTTTTAGCTGTT | 51133 |
| rs758621435 | snp | A/G | 1.71267e-05 | 0.00292627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602252 | TTTATCTTTTTATTC[A/G]TTAGTTTATTATGTG | 51133 |
| rs758646916 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615359 | GGCGTGGTGGCTCAC[A/G]GCTGTAGTCCCAGCA | 51133 |
| rs758671530 | snp | A/G | 1.64898e-05 | 0.00287135 | missense | KCTD3 | GRCh38.p7 | 1:215579917 | TCAACAGGATTTCCT[A/G]TGGATCCACGAAAGG | 51133 |
| rs758679958 | snp | C/T | 1.68476e-05 | 0.00290233 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611816 | TGACATTTTTGTTTT[C/T]TGATCAAGGACCTTT | 51133 |
| rs758759313 | snp | C/T | 0.000132111 | 0.00812639 | missense | KCTD3 | GRCh38.p7 | 1:215608134 | TATCCCTGGAGGAGA[C/T]AGAAAGTCATGGTAG | 51133 |
| rs758831128 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585326 | ATTGATACATTTTTC[C/T]CTATTGCTTTGAAGT | 51133 |
| rs758883526 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588107 | GTGGTTTTCCTTTAG[A/T]TAACAGGCTTACTTT | 51133 |
| rs758922915 | snp | A/G | 6.63636e-05 | 0.00575998 | missense | KCTD3 | GRCh38.p7 | 1:215579074 | AATTCTACAGAAGGT[A/G]AAGCCCGGGGAAATG | 51133 |
| rs758924755 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215573623 | CTTAACTCTGAATTG[A/G]AAGTAGCAACGTTTA | 51133 |
| rs759014699 | snp | A/G | 1.72314e-05 | 0.0029352 | missense | KCTD3 | GRCh38.p7 | 1:215620074 | TTCAGCTTCAGCACC[A/G]TGATACCACCCATGA | 51133 |
| rs759039238 | snp | A/G | 1.65594e-05 | 0.0028774 | stop-gained | KCTD3 | GRCh38.p7 | 1:215608048 | TCATGTCCGGACGTG[A/G]ACAGTAACACGATTC | 51133 |
| rs759079025 | snp | G/T | 1.67798e-05 | 0.00289648 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604312 | TATCAGGTAAAATGA[G/T]TTCATTATACTGGTA | 51133 |
| rs759155222 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614418 | TTTGTGTAGCATGGC[C/T]ATTTTAACAATATTA | 51133 |
| rs759187293 | snp | C/T | 0.000134406 | 0.00819665 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619312 | TTAAAGAGTTGGGTA[C/T]TATAAACAAAATTTA | 51133 |
| rs759197746 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599276 | GAAGAAATGGAATGC[A/C]TTAAGCAGTGATTAG | 51133 |
| rs759341724 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616145 | TGGCTTGCCTTGCAG[A/G]TCAGAGAGAAACTTT | 51133 |
| rs759389924 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584253 | TCTAATAAAAAGCAT[A/G]CCATAGTTTTTGAAA | 51133 |
| rs759420601 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582464 | TTAACCAGAGGGTTG[C/G]TTCACTAGGCAGCAG | 51133 |
| rs759457885 | snp | A/G | 1.64985e-05 | 0.0028721 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619178 | TCCAACCGAAGAAGA[A/G]CTACTCAAATTACTC | 51133 |
| rs759506092 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577858 | TTTTTGTGGATTTTC[A/G]TAGTAAAAAGATGTT | 51133 |
| rs759652537 | snp | A/C/T | 3.6143e-05 | 0.00425093 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620645 | AATGAATAGTTGTTT[A/C/T]GTTACATTTAGATGA | 51133 |
| rs759659958 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595642 | GAGCATATTTTCAAG[A/G]GTTTAAGTTACTTTG | 51133 |
| rs759710390 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570113 | AGAAAAATCCTGATA[C/T]GATTGCCACTGAAGT | 51133 |
| rs759766848 | snp | A/G | 1.66078e-05 | 0.00288161 | missense | KCTD3 | GRCh38.p7 | 1:215601874 | TACATCAGGTTCAAG[A/G]TGTTGTTCCTATAAC | 51133 |
| rs759779046 | in-del | -/G | 1.80501e-05 | 0.00300411 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579179 | AAGAAAAATACGTAT[-/G]TTTTTAGTGCTGGGT | 51133 |
| rs759845713 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215619842 | TCAAAAATTCAGCAT[A/G]TCTGTGAATATATGA | 51133 |
| rs759855963 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580089 | TTGAAAAGCTATTTT[G/T]TTTTAGTCATCAAGT | 51133 |
| rs759871824 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605889 | CATCCTTTCTCCCCT[A/C]GATGACTGTAGTAAC | 51133 |
| rs759885449 | snp | C/G | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621225 | TTTTCTGATTCTCAT[C/G]ATTGGGAGATCTTAA | 51133 |
| rs759893852 | snp | A/G | 1.71549e-05 | 0.00292868 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586467 | ATTGCTGCTGAGTCT[A/G]CCTTATGTGCCTGTT | 51133 |
| rs759919025 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603531 | TATGATGTAAGCAAT[G/T]TAATGGGTATGTTTA | 51133 |
| rs759927749 | snp | A/G | 3.32563e-05 | 0.00407763 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580039 | GCTTTTACAGGTGGC[A/G]GTTTGAAAATTAATT | 51133 |
| rs760085722 | snp | C/T | 3.36661e-05 | 0.00410267 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611931 | AAAAAGGTAACACTT[C/T]ATTGTAAAAATATTT | 51133 |
| rs760112893 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605574 | ACCTGTGACCATCCA[A/G]AGAGTTCCAAACCCT | 51133 |
| rs760117391 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567418 | CGGAGCACGGAGAAG[A/G]GGCCCGGGCGGCCCG | 51133 |
| rs760203281 | in-del | -/GTT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582057 | TATTAACGAAGAGTA[-/GTT]GTGTGAATTGCTGCC | 51133 |
| rs760297198 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575332 | CTTATGTATTCTGTG[A/G]TGCTTTAGTTTAAAA | 51133 |
| rs760305977 | snp | A/G | 3.31203e-05 | 0.00406928 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215574083 | TCCAGTTTGCTGAGT[A/G]GGAGAATTTCAACAC | 51133 |
| rs760324422 | snp | A/T | 1.65523e-05 | 0.00287678 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215573824 | TTATGTGGATTCCAG[A/T]TTCTTTTTTTTCCAG | 51133 |
| rs760347795 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617448 | TAGAGGACACTTAGC[G/T]GGTGTCTGCTGCAGA | 51133 |
| rs760400337 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585810 | TTAGGTATTAAAGAA[C/T]ACATTAGCTTTTACA | 51133 |
| rs760426861 | snp | A/T | 1.65427e-05 | 0.00287595 | missense | KCTD3 | GRCh38.p7 | 1:215619060 | TATGGTTAACAAAAG[A/T]GAAGATAAGGGTAGG | 51133 |
| rs760488202 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600652 | GGATAATATGTGGTA[C/T]ATAAAAAGTACTTAA | 51133 |
| rs760492026 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584672 | CCAGTTTTTCCCAGG[A/G]GCTTTTATCAGCTCT | 51133 |
| rs760524530 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568361 | TTCAACTTCTAGGAC[A/G]GTGTGTCCAGAAACT | 51133 |
| rs760639726 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613035 | AATAGCTAATGGATG[A/C]TGGGTTTAATACCTA | 51133 |
| rs760689889 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577184 | ATTTATTACATAACT[A/T]TTTTATACAAGCACT | 51133 |
| rs760700186 | snp | A/G | 3.30611e-05 | 0.00406565 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604280 | AACAAAAATCATGCT[A/G]TCAGAGAAGCATCTT | 51133 |
| rs760755487 | snp | G/T | 4.79099e-05 | 0.00489415 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576011 | AAGTAAATTCTTACT[G/T]ATAAATATGTGTTTT | 51133 |
| rs760777568 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597150 | TCTTAAAAGTTTTTT[C/G]CAAAATCATCAGGAC | 51133 |
| rs760801324 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582210 | TTTATTACGTAAATC[A/T]TTCTTTGTCAGTGAA | 51133 |
| rs760866516 | snp | C/T | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621464 | ATTAAATTAAAACAC[C/T]AGTTTGTTCACTTGT | 51133 |
| rs760867146 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596022 | TTTACTACAGCAATC[C/T]AGCAATCAAGAAGCA | 51133 |
| rs760939774 | snp | C/T | 0.000115688 | 0.00760465 | intron-variant, synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619154 | TTTGTTCTCCTAAGA[C/T]GTAGGTGGTCCAACC | 51133 |
| rs761055803 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602387 | AACATGACCAGTAAA[C/T]AAACATAATTTGAGG | 51133 |
| rs761059574 | snp | A/G | 1.65127e-05 | 0.00287334 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215608105 | TTCTACTCCTTTAGC[A/G]TCATTCAAGATACTA | 51133 |
| rs761131149 | snp | G/T | 1.65754e-05 | 0.00287879 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620564 | TCCTACAAAGACTAC[G/T]CCATCTCCTCGGCAT | 51133 |
| rs761234540 | snp | C/T | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620632 | GAAAACTCACCAAAA[C/T]GAATAGTTGTTTCGT | 51133 |
| rs761259978 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617545 | CCAAGGAGTGAAGGA[A/C]ATTCTGCCCCAAAAT | 51133 |
| rs761279951 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578254 | ATTATATATTGGAGC[A/T]GGGGTTTGGCAAACT | 51133 |
| rs761335988 | snp | A/C/G | 4.95572e-05 | 0.0049776 | synonymous-codon, missense | KCTD3 | GRCh38.p7 | 1:215620151 | TTAGCAAGGGCAAGA[A/C/G]GGACTGAGAGCTTTC | 51133 |
| rs761358724 | snp | C/T | 1.65581e-05 | 0.00287728 | synonymous-codon, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215573792 | TAATTGCAGATTTAG[C/T]ACCTCAAGACAAACT | 51133 |
| rs761440039 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586268 | TAGTCTCTTTCAAGT[C/T]GTTATATGTGCTATG | 51133 |
| rs761448206 | snp | G/T | 1.72033e-05 | 0.0029328 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586457 | CGTTTGCTTCATTGC[G/T]GCTGAGTCTACCTTA | 51133 |
| rs761448532 | snp | C/T | 9.16632e-05 | 0.00676928 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567709 | AGGGCACTGCGGCAG[C/T]TTCCCCGCGGCGGCG | 51133 |
| rs761464024 | snp | A/G | 1.82058e-05 | 0.00301705 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578979 | CTTAGGAATGTATTT[A/G]TTTTCTTCTTCTCTT | 51133 |
| rs761464544 | snp | C/T | 1.65658e-05 | 0.00287795 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580025 | ATTAATAATGCTTTG[C/T]TTTTACAGGTGGCAG | 51133 |
| rs761502594 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584385 | TTTGTATAAAGTGCA[A/G]CAAGAATAATTAGTT | 51133 |
| rs761513372 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588585 | ATCATCAGTGTAAAT[-/G]TCAACACAGATGTTC | 51133 |
| rs761612767 | in-del | -/CA | 1.91642e-05 | 0.00309544 | intron-variant | KCTD3 | GRCh38.p7 | 1:215620012 | ATGTTCCTGAGAAAT[-/CA]CAGAGTGAAATCTGA | 51133 |
| rs761635028 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587821 | TTAAATTAAAATCCA[C/T]CAGACTATTTTGTAC | 51133 |
| rs761667920 | in-del | -/TTTCA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585231 | TAAGTATTTAAGTAT[-/TTTCA]TTTGTTTATCTTAAC | 51133 |
| rs761729781 | snp | C/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568848 | CGTTCTTAGGGTTTT[C/T]CCTCTTCCCCCAAAT | 51133 |
| rs761745143 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572766 | TGTTTCCTGGTGATA[A/G]TGCATGGTAACTAGT | 51133 |
| rs761761442 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608252 | CTAATAAAACCACAA[A/C]AATGAGTTTTAAATA | 51133 |
| rs761807245 | snp | G/T | 1.65625e-05 | 0.00287766 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578097 | GTATTTTCACTTTAT[G/T]AAATCTTTTAAAAAA | 51133 |
| rs761807792 | snp | G/T | 1.68932e-05 | 0.00290625 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604119 | TCACCTGTCAACTCT[G/T]GACTTTATATAGGTG | 51133 |
| rs761812300 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612997 | GGGTGAGCGGGGCCG[A/G]GGAGAGAGAGAGCAT | 51133 |
| rs761859136 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602220 | AGTACATGGCCAATT[A/G]TATACATTCTTGACT | 51133 |
| rs761861112 | snp | A/G | 1.65567e-05 | 0.00287716 | missense | KCTD3 | GRCh38.p7 | 1:215620271 | GAAGTGAAAGGGGCA[A/G]CAGGGGAATGTAATA | 51133 |
| rs761936598 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583898 | TCGATTTAAGAAAGC[A/G]CTGAGTAAGCTTATC | 51133 |
| rs761995052 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598993 | AATGTGCTATAATAA[A/G]AGATAAATTATGATA | 51133 |
| rs762006908 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574125 | ACTGGTGCTGTGAGT[A/G]TAATAATAATTGATA | 51133 |
| rs762026561 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582508 | AGGTGAAATAACAGA[A/G]CATATTCTTGTTTTA | 51133 |
| rs762086679 | snp | G/T | 1.65121e-05 | 0.00287329 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619039 | GGATCTGACCACTGC[G/T]ATGGATATGGTTAAC | 51133 |
| rs762116028 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590442 | TCCCTTCCTCTTTTC[C/T]CCATCTCTCCCTTGC | 51133 |
| rs762200669 | in-del | -/CTC | 4.96372e-05 | 0.00498158 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619145 | TAATGACTATTTGTT[-/CTC]CTAAGATGTAGGTGG | 51133 |
| rs762234731 | snp | A/T | 1.67083e-05 | 0.00289031 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215595357 | TATTGTCATTTAAGG[A/T]GTGTTCAGCCTGGGT | 51133 |
| rs762293357 | snp | A/G | 1.65302e-05 | 0.00287486 | missense | KCTD3 | GRCh38.p7 | 1:215620470 | GAGGATTCCTTGGAA[A/G]AAAGAAAGTTCCCTA | 51133 |
| rs762362576 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616460 | AAACTTTATATTGGC[A/G]AAATATTAAAAACTT | 51133 |
| rs762378956 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576796 | GATGGTCTCCATCTC[C/T]TCACCTCGTAATCCA | 51133 |
| rs762411741 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601712 | GTGTATATGTGTGTG[C/T]ACGCGTGCACCTAAA | 51133 |
| rs762418960 | snp | A/T | 1.66175e-05 | 0.00288244 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574145 | AATAATTGATACATA[A/T]TCCTAAATTAATGCT | 51133 |
| rs762484391 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605446 | TCATCTTTTGCCCAG[C/T]TGCTGAGTGTTGGAT | 51133 |
| rs762508782 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571081 | TAATATGATTTTAAG[C/T]AGACCTTTGTGATTT | 51133 |
| rs762512569 | snp | C/T | 3.60601e-05 | 0.00424603 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579860 | GGTGGCTGTAATTTG[C/T]CAACCCCCGGTTTAG | 51133 |
| rs762573826 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603111 | TACTTGGCCCCTTAC[A/G]GAAAGTGTACCAACC | 51133 |
| rs762575198 | snp | A/G | 1.64953e-05 | 0.00287182 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580010 | TACAGGTAGTGTATA[A/G]TTAATAATGCTTTGC | 51133 |
| rs762583056 | in-del | -/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215566013 | AGGAAAGCCAAAAGA[-/T]TGGACACCCTGGTTT | 51133 |
| rs762608483 | snp | G/T | 1.65157e-05 | 0.0028736 | missense | KCTD3 | GRCh38.p7 | 1:215602147 | ACTGAACTGTATCAT[G/T]ATCCTTCAAATGATG | 51133 |
| rs762609457 | snp | C/T | 3.30846e-05 | 0.00406709 | stop-gained | KCTD3 | GRCh38.p7 | 1:215608058 | ACGTGGACAGTAACA[C/T]GATTCAGAGGAATGA | 51133 |
| rs762647340 | in-del | -/TC | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608622 | TGTCTCCTTTGATAT[-/TC]TCTGATTTCAGCAAA | 51133 |
| rs762649466 | in-del | -/AGAG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584877 | CTGGAGAAATCAGAT[-/AGAG]AGAAAGAAATATGCT | 51133 |
| rs762664738 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588728 | ATACCAGATGGGTAC[A/G]AGTAAAACACCAGGT | 51133 |
| rs762714834 | in-del | -/AAC | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622118 | TAAAAAGAAGATAGT[-/AAC]AACTATTATGTAATA | 51133 |
| rs762765961 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583661 | TTGAACACCTCTGAC[A/G]TGTTTTCCCCTTCCC | 51133 |
| rs762770005 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596449 | ATTTTCCATTGAGTG[G/T]GTATATAGAAAGAAA | 51133 |
| rs762786354 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597313 | ACACACACAGAATTA[C/T]GTTACAAAAGAATAT | 51133 |
| rs762794206 | snp | A/G | 1.65803e-05 | 0.00287922 | missense | KCTD3 | GRCh38.p7 | 1:215620119 | GTTCCATGAGGCCTT[A/G]CAGAGAAAGTCCTTT | 51133 |
| rs762821763 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574179 | AGTGCTTGGTCCTAA[A/C]ATATAGTTACTCTAA | 51133 |
| rs762980329 | snp | A/G | 0.00013217 | 0.0081282 | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567660 | CTGGGGAAGGAGGGC[A/G]GCGAGCGCGTCCGGA | 51133 |
| rs762996470 | snp | C/G | 1.91896e-05 | 0.00309749 | intron-variant | KCTD3 | GRCh38.p7 | 1:215620014 | GTTCCTGAGAAATCA[C/G]AGAGTGAAATCTGAA | 51133 |
| rs763005526 | in-del | -/ATGAAA | 1.66056e-05 | 0.00288141 | cds-indel | KCTD3 | GRCh38.p7 | 1:215620404 | AAAGGTCATCAGAAG[-/ATGAAA]ATGAAAATAAAATAG | 51133 |
| rs763029398 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608914 | CTGCATGATTCTAGG[C/T]ACTGGAAGTTTATAT | 51133 |
| rs763060290 | snp | A/G | 3.40994e-05 | 0.00412899 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611949 | TGTAAAAATATTTGT[A/G]TTCAGAAGCCACCTT | 51133 |
| rs763089131 | snp | A/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568118 | TGTATTTGAGGACTT[A/T]ATTTAGTAGAAACCT | 51133 |
| rs763152182 | snp | A/G | 1.86444e-05 | 0.00305317 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578963 | ATTTTTGAAAGGTGA[A/G]CTTAGGAATGTATTT | 51133 |
| rs763175136 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566369 | TACTTATCTTACATC[C/G]ATATGTACTATTAAC | 51133 |
| rs763208559 | snp | A/T | | | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215608060 | GTGGACAGTAACACG[A/T]TTCAGAGGAATGATC | 51133 |
| rs763259313 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578493 | CAAAATTTAAGGAAT[G/T]CTGCAGAGATAAGTC | 51133 |
| rs763263618 | snp | C/G | 6.64341e-05 | 0.00576304 | missense | KCTD3 | GRCh38.p7 | 1:215620341 | TGAGAGAATTGGATA[C/G]TGGATTGGAAGTGCA | 51133 |
| rs763266488 | snp | C/G | 0.000594001 | 0.0172235 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567797 | TAGCGGGCTTGCAGC[C/G]GGGATGCCTTGGCGG | 51133 |
| rs763348658 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576982 | AATATTTTTAAAATA[A/T]GGACAAATTACAACT | 51133 |
| rs763350671 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594125 | CTGGCCTCCCAAAGT[A/G]CTGGGATTGCAGGCA | 51133 |
| rs763424866 | snp | C/T | 1.65883e-05 | 0.00287991 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574126 | CTGGTGCTGTGAGTA[C/T]AATAATAATTGATAC | 51133 |
| rs763447871 | snp | C/G | 0.000130463 | 0.00807555 | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567662 | GGGGAAGGAGGGCGG[C/G]GAGCGCGTCCGGAGC | 51133 |
| rs763480374 | snp | A/G | 1.9158e-05 | 0.00309494 | intron-variant | KCTD3 | GRCh38.p7 | 1:215620015 | TTCCTGAGAAATCAC[A/G]GAGTGAAATCTGAAC | 51133 |
| rs763522580 | snp | A/T | 3.32298e-05 | 0.004076 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619289 | ACGAGAATCAAATTC[A/T]AGGTAGGTTAAAGAG | 51133 |
| rs763551206 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215586646 | GAGAGTAGCATCATC[C/T]TGTGGAGTGTTCAGG | 51133 |
| rs763569339 | snp | C/G | 3.40541e-05 | 0.00412625 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586480 | CTACCTTATGTGCCT[C/G]TTCTTCCTTAACAGA | 51133 |
| rs763575633 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215618943 | ATTTACAGTGAGGGA[A/G]TGTGAGGGATCCAGT | 51133 |
| rs763611735 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617977 | TTATCATTCTTTGTC[C/T]GAATTGTATAAAAGC | 51133 |
| rs763659987 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616317 | GTAATTCACTAAATT[A/G]TGATCATCTTGATAA | 51133 |
| rs763699127 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600720 | ATGAAAGCCAGGTAT[A/C]GTATATGAAAAGTAA | 51133 |
| rs763781534 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578663 | AAGCAGTTAAATTAT[C/T]ACATAGTACCTAACA | 51133 |
| rs763895825 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215578074 | TCATGGTTACTTGCC[C/T]CCACCAGGTATTTTC | 51133 |
| rs763944875 | snp | A/T | 1.82194e-05 | 0.00301817 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620649 | AATAGTTGTTTCGTT[A/T]CATTTAGATGAAAGT | 51133 |
| rs763976246 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584270 | CATAGTTTTTGAAAC[-/A]ATTTTCCTATTTTCA | 51133 |
| rs763983761 | snp | C/T | 1.65677e-05 | 0.00287812 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215602188 | TCTGAGTGTTTACCT[C/T]ACACCCAAAACAAGT | 51133 |
| rs764059999 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610893 | AAGTACAGTGTAAGT[A/G]TTAGCTAATAATAAA | 51133 |
| rs764085143 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580587 | TTTTTTTTTTAATTG[A/G]GAAAGTGATAGGACT | 51133 |
| rs764130996 | snp | A/G | 3.30557e-05 | 0.00406531 | missense | KCTD3 | GRCh38.p7 | 1:215620214 | AACAGAAATGTAGAA[A/G]GAGCTGTCCCTGAAA | 51133 |
| rs764150434 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568362 | TCAACTTCTAGGACA[A/G]TGTGTCCAGAAACTG | 51133 |
| rs764182521 | snp | C/G | 3.30524e-05 | 0.00406511 | missense | KCTD3 | GRCh38.p7 | 1:215620146 | CTTTATTAGCAAGGG[C/G]AAGAAGGACTGAGAG | 51133 |
| rs764258287 | snp | A/C | 8.49712e-05 | 0.00651754 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586483 | CCTTATGTGCCTGTT[A/C]TTCCTTAACAGAATC | 51133 |
| rs764299346 | snp | A/T | 1.70985e-05 | 0.00292386 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611953 | AAAATATTTGTATTC[A/T]GAAGCCACCTTTTGT | 51133 |
| rs764313873 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605781 | CACCTCCCACATAGT[A/G]CAATTCATCAGTAAG | 51133 |
| rs764354231 | snp | C/G | 3.33333e-05 | 0.00408235 | missense | KCTD3 | GRCh38.p7 | 1:215611825 | TGTTTTCTGATCAAG[C/G]ACCTTTTGGAGAGCG | 51133 |
| rs764361600 | snp | C/T | 1.64874e-05 | 0.00287113 | stop-gained | KCTD3 | GRCh38.p7 | 1:215604185 | AGCTCTGGAGCAGTA[C/T]GAGTGATTGTACAAC | 51133 |
| rs764453648 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615055 | TCTGTTATTTCTAAC[A/C]GTAACACTGTGCAAT | 51133 |
| rs764466122 | snp | G/T | 1.66134e-05 | 0.00288208 | missense | KCTD3 | GRCh38.p7 | 1:215620348 | ATTGGATAGTGGATT[G/T]GAAGTGCATAAAATA | 51133 |
| rs764512232 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589064 | CTAGTTTGAAGGTCT[A/T]TACCAAACAATTTCT | 51133 |
| rs764513153 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570244 | TCTTTTTTTTTTTTT[-/C]CCTCAGGAGAATAGA | 51133 |
| rs764523659 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590223 | CTGTACTTAATGACC[A/G]TTTGTATATTTTCTT | 51133 |
| rs764557545 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590247 | TTTTCTTTTGAGAAG[G/T]GTCTCTGTAAATCAT | 51133 |
| rs764594531 | snp | A/T | 1.78449e-05 | 0.00298699 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579176 | AAAAAGAAAAATACG[A/T]ATGTTTTTAGTGCTG | 51133 |
| rs764703288 | snp | C/T | 1.65954e-05 | 0.00288053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573850 | TCCAGGTATGTCTTA[C/T]AATTCTTTAGTGTAT | 51133 |
| rs764738821 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215586663 | GTGGAGTGTTCAGGA[C/T]GGGGGAAGTGGAAGT | 51133 |
| rs764757546 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587839 | GACTATTTTGTACTT[C/T]GAGTGGATCTTTTAT | 51133 |
| rs764826261 | snp | C/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569046 | GATTATACTGAAGAG[C/T]AGCAGTATAATCATT | 51133 |
| rs764835860 | snp | C/T | 1.65916e-05 | 0.00288019 | missense | KCTD3 | GRCh38.p7 | 1:215579078 | CTACAGAAGGTGAAG[C/T]CCGGGGAAATGGTAC | 51133 |
| rs764891620 | in-del | -/GACA | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622252 | ATGTCTGTCTACTCT[-/GACA]GACACTAATTTCTCA | 51133 |
| rs764928504 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614075 | TCTCACTCTGTCACC[A/C]AGGCTGGAGTGCAGT | 51133 |
| rs764943756 | in-del | -/TG | 3.64894e-05 | 0.00427122 | intron-variant | KCTD3 | GRCh38.p7 | 1:215620047 | GTCATTTTTAAAAAC[-/TG]TATTTCAGCCTTCAG | 51133 |
| rs765002707 | snp | A/G | 3.29826e-05 | 0.00406082 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577626 | GTCAGATGATAATAC[A/G]GGTTTCCAGTGTTAG | 51133 |
| rs765021044 | snp | A/G | 1.66161e-05 | 0.00288232 | missense | KCTD3 | GRCh38.p7 | 1:215595418 | AACCAGTTGGTGGCC[A/G]CGAGTCATACAGGGA | 51133 |
| rs765031541 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570880 | ATCAAAACAGAAAAG[C/G]CTTTCAAATGATTAT | 51133 |
| rs765077564 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575223 | TGCCACTGCACTCCA[G/T]CCTAGATGAGAGAGC | 51133 |
| rs765108371 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616251 | CAGGACTCTGAGGAG[G/T]GAGTTGTTGAACATT | 51133 |
| rs765112176 | snp | A/C | 1.69166e-05 | 0.00290827 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619327 | TTATAAACAAAATTT[A/C]TTTCTTTTGGGGAAA | 51133 |
| rs765208259 | in-del | -/AA | 1.67919e-05 | 0.00289753 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586708 | AATCTTGTTTATGTT[-/AA]GCAATTTGATGATAT | 51133 |
| rs765216671 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596249 | CATAGGAAGAGAAGC[A/G]GAGAGGCTGGTGGGT | 51133 |
| rs765304641 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594702 | ATGTCTTGTCTTCTC[A/G]TGTTTTTTAATCCTA | 51133 |
| rs765316986 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613082 | ATGCAGCAAACCACT[A/G]TGGCACATGTGTAAC | 51133 |
| rs765378411 | snp | C/T | 3.38284e-05 | 0.00411255 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611814 | TTTGACATTTTTGTT[C/T]TCTGATCAAGGACCT | 51133 |
| rs765402492 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602789 | AGTTCTAAGAAACAA[-/T]TTTGTATTCAGTAAT | 51133 |
| rs765460316 | snp | C/T | 1.65545e-05 | 0.00287697 | synonymous-codon, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215573834 | TCCAGATTCTTTTTT[C/T]TCCAGGTATGTCTTA | 51133 |
| rs765485594 | snp | C/G/T | 3.29632e-05 | 0.00405964 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577736 | TCCATTAGGTATGTG[C/G/T]TCTTTTAATATTTGG | 51133 |
| rs765491489 | snp | A/C/T | 9.97932e-05 | 0.00706317 | synonymous-codon, missense | KCTD3 | GRCh38.p7 | 1:215620574 | ACTACTCCATCTCCT[A/C/T]GGCATAAAAAAAGTG | 51133 |
| rs765551961 | snp | C/T | 1.71094e-05 | 0.00292479 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586473 | GCTGAGTCTACCTTA[C/T]GTGCCTGTTCTTCCT | 51133 |
| rs765590153 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215592273 | CAGCAAGCCAGGGGG[A/C]ATGTGGGGCTTGTCA | 51133 |
| rs765603382 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599732 | CTCTGTTTTCCCGTA[G/T]GGAGGGGTAGACATG | 51133 |
| rs765637782 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575741 | TCTCATGAAATGCAC[A/G]CAGACTACATTCCAA | 51133 |
| rs765664552 | snp | C/T | 5.01668e-05 | 0.00500808 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567766 | GAACGTAGGGGGGAC[C/T]AGGTGAGTCGGCGGG | 51133 |
| rs765774490 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617612 | ACATTAGAGAAATTG[G/T]CATTTCAGAAGGGGA | 51133 |
| rs765820011 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580046 | CAGGTGGCAGTTTGA[A/G]AATTAATTGTGATTT | 51133 |
| rs765869759 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616496 | CCGGGTGCGGTGGCT[C/T]ACACCTGTAATCCCA | 51133 |
| rs765872755 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587914 | TTGCTGAGTTATGTA[G/T]ATCTACCAAATGTTG | 51133 |
| rs765879722 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613160 | GAAAAAGTTTTTTGC[A/G]TGTCAAACAAATGAA | 51133 |
| rs765902886 | snp | A/G | 1.70032e-05 | 0.0029157 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611943 | CTTTATTGTAAAAAT[A/G]TTTGTATTCAGAAGC | 51133 |
| rs765920144 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215573391 | GGGGATATGAAGAAG[C/T]TTTGTCCTATTAGAG | 51133 |
| rs765925681 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589767 | GTTGTTGCATGTATC[A/C]GTTGTCTGTTCCTTT | 51133 |
| rs766000351 | snp | C/G | 1.66026e-05 | 0.00288115 | missense | KCTD3 | GRCh38.p7 | 1:215620308 | AGAGAAAGTCTCCTG[C/G]AGTAGAAATAAAAAG | 51133 |
| rs766016193 | in-del | -/T | 1.67866e-05 | 0.00289707 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601990 | AATGCTCCTGCTTAA[-/T]GTAATTTTTTAAATG | 51133 |
| rs766077458 | snp | C/T | 1.69945e-05 | 0.00291496 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602245 | TTGACTTTTTATCTT[C/T]TTATTCATTAGTTTA | 51133 |
| rs766083928 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596453 | TCCATTGAGTGGGTA[C/T]ATAGAAAGAAACAAA | 51133 |
| rs766113356 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571241 | ATGTATGAATCCTTG[C/G]ATCCTTCAATTTACC | 51133 |
| rs766128891 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613433 | GTTTGCAGATATTTT[C/T]TCCTATCCTGTAGGT | 51133 |
| rs766181213 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614349 | AAATAGTTTTTTCTA[A/T]TTCTGTGAAAAATGT | 51133 |
| rs766187565 | snp | A/G | 1.67635e-05 | 0.00289507 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586706 | AAGAATCTTGTTTAT[A/G]TTGCAATTTGATGAT | 51133 |
| rs766187841 | snp | G/T | 1.65474e-05 | 0.00287636 | missense | KCTD3 | GRCh38.p7 | 1:215619064 | GTTAACAAAAGTGAA[G/T]ATAAGGGTAGGTTCT | 51133 |
| rs766316534 | in-del | -/AAG | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622108 | TAAAAGGCCATTAAA[-/AAG]AAGATAGTAACTATT | 51133 |
| rs766379053 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582731 | CACACCTGGCCAATT[C/T]TTGTATTTTTAGTAG | 51133 |
| rs766380685 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568252 | AATTAGGGGATTTGT[A/G]ATTTGAAAGATTTCT | 51133 |
| rs766389693 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597324 | ATTACGTTACAAAAG[A/G]ATATTAATAAGGAAT | 51133 |
| rs766396691 | snp | C/T | 7.66587e-05 | 0.0061906 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576019 | TCTTACTGATAAATA[C/T]GTGTTTTTAATATGT | 51133 |
| rs766424324 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577713 | GAAGCAGAATTTTAC[A/G]GGATCACTCCATTAG | 51133 |
| rs766458856 | snp | G/T | 1.65935e-05 | 0.00288036 | missense | KCTD3 | GRCh38.p7 | 1:215579071 | CTAAATTCTACAGAA[G/T]GTGAAGCCCGGGGAA | 51133 |
| rs766464911 | in-del | -/A | 1.65023e-05 | 0.00287244 | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215620534 | ACTGACTCACCTGGT[-/A]ACTGCGTCCCCATCT | 51133 |
| rs766469105 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581139 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51133 |
| rs766479624 | snp | C/G | 1.65765e-05 | 0.00287888 | missense | KCTD3 | GRCh38.p7 | 1:215620565 | CCTACAAAGACTACT[C/G]CATCTCCTCGGCATA | 51133 |
| rs766550326 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594281 | GCCAGGATCCCAACC[C/G]TGGTTCTCCTGACTC | 51133 |
| rs766554950 | snp | A/G | 1.66147e-05 | 0.0028822 | missense | KCTD3 | GRCh38.p7 | 1:215595403 | CTCTTCTTTATTGGT[A/G]ACCAGTTGGTGGCCA | 51133 |
| rs766713796 | snp | G/T | 1.65952e-05 | 0.00288051 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580033 | TGCTTTGCTTTTACA[G/T]GTGGCAGTTTGAAAA | 51133 |
| rs766740712 | snp | A/C | 7.07076e-05 | 0.00594549 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620635 | AACTCACCAAAATGA[A/C]TAGTTGTTTCGTTAC | 51133 |
| rs766746318 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578837 | TTTTCATTTTCATTT[A/T]ATTTTTTAATTGTAA | 51133 |
| rs766843182 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618089 | TTCTCTCTTGTCAGT[C/T]TGTGTGGTGTCAGTT | 51133 |
| rs766847008 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602490 | CAAAAAAAAAAAAAA[-/T]TCTGCACATTTGTCT | 51133 |
| rs766855908 | snp | A/G | 1.65102e-05 | 0.00287312 | missense | KCTD3 | GRCh38.p7 | 1:215608115 | TTAGCGTCATTCAAG[A/G]TACTATCCCTGGAGG | 51133 |
| rs767031844 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597519 | AGAAAGGCATTATGT[A/C]CTTTACTTCCTAAAG | 51133 |
| rs767036571 | snp | C/T | 1.65504e-05 | 0.00287662 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215573806 | GTACCTCAAGACAAA[C/T]TCTTATGTGGATTCC | 51133 |
| rs767041205 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601535 | AGGGACCTGGTCAGA[C/T]TCGGCCTTCCAGTTC | 51133 |
| rs767126902 | snp | C/T | 1.69355e-05 | 0.00290989 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602234 | TATATACATTCTTGA[C/T]TTTTTATCTTTTTAT | 51133 |
| rs767137449 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215573669 | ATAAATATATTGGTA[C/T]AGCTATAACTATAAA | 51133 |
| rs767150134 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587351 | AGCCAGGATGGTCTC[A/G]ATCTCCTGATCTTGT | 51133 |
| rs767182703 | in-del | -/CAC | 1.73688e-05 | 0.00294688 | utr-variant-3-prime, cds-indel | KCTD3 | GRCh38.p7 | 1:215620624 | CAGCTTGTGAAAACT[-/CAC]CAAAATGAATAGTTG | 51133 |
| rs767204117 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614726 | GCCTTTGGCAGAGAC[A/T]GTGGGGTTTTCTAGG | 51133 |
| rs767225949 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583200 | AGCCAGAGCAGCCCT[G/T]AGGGCTGCTTGACTG | 51133 |
| rs767308364 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599308 | AAAGATGTTGGTAAA[C/T]ACGATGGTAAATTTA | 51133 |
| rs767309598 | snp | G/T | 0.000121588 | 0.0077961 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618161 | CATTTGGAGGTAAAC[G/T]TTCACTTTCCTTAGA | 51133 |
| rs767374688 | snp | C/G | 1.76893e-05 | 0.00297394 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578990 | ATTTGTTTTCTTCTT[C/G]TCTTTATAGGTATTC | 51133 |
| rs767382243 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608301 | TTTGAAATTCTAAAC[A/G]GAATTTTAGTGTGTT | 51133 |
| rs767528806 | snp | A/G | 1.65002e-05 | 0.00287225 | missense | KCTD3 | GRCh38.p7 | 1:215586667 | AGTGTTCAGGATGGG[A/G]GAAGTGGAAGTGAAA | 51133 |
| rs767552468 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584612 | TTTACTTACCCCAGA[C/T]AGGTCAGAAACCTTG | 51133 |
| rs767578129 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569655 | GGCTGGAGTGCAGTG[C/G]TGCGATCTCGGCTCA | 51133 |
| rs767618101 | snp | C/G | 1.67022e-05 | 0.00288978 | missense | KCTD3 | GRCh38.p7 | 1:215595358 | ATTGTCATTTAAGGA[C/G]TGTTCAGCCTGGGTG | 51133 |
| rs767650351 | snp | C/T | 1.66263e-05 | 0.00288321 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574147 | TAATTGATACATATT[C/T]CTAAATTAATGCTTA | 51133 |
| rs767686189 | snp | A/G | 3.30469e-05 | 0.00406477 | missense | KCTD3 | GRCh38.p7 | 1:215619046 | ACCACTGCTATGGAT[A/G]TGGTTAACAAAAGTG | 51133 |
| rs767734660 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580257 | ATGTAACTGAGATAT[C/T]CTGATGTATTATTTA | 51133 |
| rs767757526 | snp | A/G | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621303 | TTTCAAGTTGGAGCA[A/G]TTGTCTGTGTTTGAA | 51133 |
| rs767759649 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590991 | TTGTTTCAGTACTTT[A/G]TTAGGAGTAGGTATC | 51133 |
| rs767776750 | in-del | -/A | 1.64838e-05 | 0.00287083 | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215579998 | TTTGCTGTGTGTTAC[-/A]GGTAGTGTATAATTA | 51133 |
| rs767800739 | snp | C/T | 0.000115617 | 0.00760233 | missense | KCTD3 | GRCh38.p7 | 1:215620548 | GTACTGCGTCCCCAT[C/T]TCCTACAAAGACTAC | 51133 |
| rs767826671 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595732 | GAAGTTCTATGCCTT[A/G]AGCATGGTAGTCCAG | 51133 |
| rs767858599 | snp | C/T | 1.65373e-05 | 0.00287548 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215608063 | GACAGTAACACGATT[C/T]AGAGGAATGATCTCT | 51133 |
| rs767858716 | snp | C/G | 1.65762e-05 | 0.00287886 | missense | KCTD3 | GRCh38.p7 | 1:215579090 | AAGCCCGGGGAAATG[C/G]TACACAGCCTGTTCT | 51133 |
| rs767906899 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603709 | CAGTAGTGTTCTTGG[C/T]ATGGCAGATTTATGA | 51133 |
| rs768009034 | snp | A/C | 3.30109e-05 | 0.00406256 | missense | KCTD3 | GRCh38.p7 | 1:215620491 | AAGTTCCCTATCTGG[A/C]GTCATCACCAAGTAC | 51133 |
| rs768084321 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588865 | TCTGCCAAATCTTTA[C/G]ATTGAAGAGTTACTG | 51133 |
| rs768093736 | snp | C/T | 1.7219e-05 | 0.00293414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586453 | ATTCCGTTTGCTTCA[C/T]TGCTGCTGAGTCTAC | 51133 |
| rs768141908 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590308 | TACTTATTTGTAAAT[-/G]TTTTTTACATATTCT | 51133 |
| rs768163370 | snp | A/C | 1.65608e-05 | 0.00287752 | missense | KCTD3 | GRCh38.p7 | 1:215611887 | GTTCCCATCACCAAC[A/C]AACTATTTGTAAGAC | 51133 |
| rs768176131 | snp | A/T | 7.04929e-05 | 0.00593645 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576007 | TTTAAAGTAAATTCT[A/T]ACTGATAAATATGTG | 51133 |
| rs768258816 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577833 | TTTGATGGACTTGTT[C/G]AGTGCTTAGTTTTTG | 51133 |
| rs768277980 | in-del | -/AA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616854 | CCTTCAAAAATTCTT[-/AA]AGTCTTCCAAATGAT | 51133 |
| rs768281448 | snp | A/T | 5.13474e-05 | 0.00506666 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604106 | GTTCCATAATGTATC[A/T]CCTGTCAACTCTTGA | 51133 |
| rs768315514 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215619109 | TTTGTCACAAGGTTA[A/G]GCTTTTCACTTAAGT | 51133 |
| rs768334146 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579710 | TCACCGTGTTAGCCA[G/T]TATGGTCTCGATCCC | 51133 |
| rs768359754 | snp | C/T | 1.71243e-05 | 0.00292607 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608211 | TTTTTAGGTACTATA[C/T]TAACTGTTCAGAAGA | 51133 |
| rs768446798 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570533 | AGGTATATGTTTCCA[A/G]TTCCCAGGCTTTATC | 51133 |
| rs768452920 | snp | G/T | 6.70916e-05 | 0.00579148 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574034 | ATTTGTTTATACTCA[G/T]ATTTTAAAAACTAAC | 51133 |
| rs768518911 | snp | C/T | 3.32226e-05 | 0.00407556 | missense | KCTD3 | GRCh38.p7 | 1:215620395 | AATCCAAGAAAAGGT[C/T]ATCAGAAGATGAAAA | 51133 |
| rs768549999 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588512 | AGTAAAGTTTAGTGC[C/T]ACTGTCCTGGTTTGT | 51133 |
| rs768619362 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586746 | TTGAAGTTTATAAAA[A/G]AGATTGACACTGAAT | 51133 |
| rs768672402 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589135 | AATTCTTTTTCTTCT[A/T]TTCTTTCCTTTTTTT | 51133 |
| rs768702197 | snp | A/G | 6.62745e-05 | 0.00575612 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573778 | TACCAGATGATTTTT[A/G]ATTGCAGATTTAGTA | 51133 |
| rs768831982 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | KCTD3 | GRCh38.p7 | 1:215618980 | GGCTCAAGACCAAGG[C/T]GCTACTTGTTCACAG | 51133 |
| rs768904217 | snp | G/T | 5.00363e-05 | 0.00500156 | missense | KCTD3 | GRCh38.p7 | 1:215579041 | ACAGTCAGATCTGCT[G/T]ATTCTAGGAATGGTC | 51133 |
| rs768994178 | snp | C/T | 1.64857e-05 | 0.00287099 | stop-gained | KCTD3 | GRCh38.p7 | 1:215604254 | ACTTTCACAGTTCAC[C/T]GAAGTCCCGTAACAA | 51133 |
| rs769079043 | snp | A/G | 2.271e-05 | 0.00336964 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576002 | CTCTTTTTAAAGTAA[A/G]TTCTTACTGATAAAT | 51133 |
| rs769107319 | snp | A/G | 1.65518e-05 | 0.00287674 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619138 | GTGATTTTAATGACT[A/G]TTTGTTCTCCTAAGA | 51133 |
| rs769129915 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584414 | TTCCTATATAGGCTC[-/T]TTTTAAATTGACTTT | 51133 |
| rs769167120 | snp | A/T | 1.7208e-05 | 0.00293321 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595336 | CTGATTAACCTTTTT[A/T]TTTTTTATTGTCATT | 51133 |
| rs769285993 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595811 | AATCTGTTCAGAGAT[G/T]ATAGCATGCTAAATA | 51133 |
| rs769292520 | in-del | -/TT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593859 | AATTGGAATACAACT[-/TT]TTTTTTTTTTTTTTT | 51133 |
| rs769292591 | snp | G/T | 1.7042e-05 | 0.00291903 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608203 | TTAGGGCATTTTTAG[G/T]TACTATATTAACTGT | 51133 |
| rs769298034 | snp | C/T | 3.42337e-05 | 0.00413711 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620609 | TTCAGGTCAGGAGTA[C/T]AGCTTGTGAAAACTC | 51133 |
| rs769324492 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581943 | GAGTAGTACAGTGAA[-/G]GACCTGTATGATGTT | 51133 |
| rs769343047 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600698 | TGTTTAGATTTTAAC[-/T]TTTCAAATGAAAGCC | 51133 |
| rs769372657 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602940 | CATAGTAGGACTTAA[A/G]TTGTATTGCTCTAGA | 51133 |
| rs769492315 | snp | A/G | 4.95323e-05 | 0.00497631 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620540 | CTCACCTGGTACTGC[A/G]TCCCCATCTCCTACA | 51133 |
| rs769579701 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614252 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCA | 51133 |
| rs769598401 | snp | A/G | 0.000329544 | 0.0128321 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581062 | ATCAGCCCGACCAAC[A/G]TGGTGAAACCCCATC | 51133 |
| rs769618795 | snp | A/G | | | missense | KCTD3 | GRCh38.p7 | 1:215586602 | GAGGGCCACATGGAG[A/G]CAAAGACAAAATGGT | 51133 |
| rs769631513 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577683 | AGGGGAGTGAGTATT[A/G]ATGTTCTCAGGCATG | 51133 |
| rs769644407 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588594 | GTAAATGTCAACACA[C/G]ATGTTCTAGAATAAG | 51133 |
| rs769747048 | snp | A/T | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215621830 | TCAGTTATTTAAGTA[A/T]CAGTTCTGTTTAAAG | 51133 |
| rs769791287 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215573254 | ATATTTAGAAAAACT[A/G]TTACAGGGAAGGTAA | 51133 |
| rs769799591 | snp | A/C | 1.87756e-05 | 0.0030639 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578957 | TTTTTAATTTTTGAA[A/C]GGTGAACTTAGGAAT | 51133 |
| rs770010722 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584195 | GGATAAGCAGGATGA[G/T]TCCAAATTGCAGAAA | 51133 |
| rs770100579 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215611419 | ATTTTAAGATTTTGT[A/G]TGTTGTCTTCTAAAA | 51133 |
| rs770119890 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568041 | AGAATGCCAACCTTT[A/G]CCCCTCCCAACAGGC | 51133 |
| rs770139728 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | KCTD3 | GRCh38.p7 | 1:215586631 | GTTGCTGTTGCCTCA[A/G]AGAGTAGCATCATCT | 51133 |
| rs770155251 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610343 | ATTTTTTTTTATTCC[G/T]CCAACTTTCTCCCTC | 51133 |
| rs770186991 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607767 | TTTTTAACCTTTACT[A/G]CATTTATAACCTACA | 51133 |
| rs770234318 | snp | A/C | 4.97319e-05 | 0.00498633 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619117 | AAGGTTAAGCTTTTC[A/C]CTTAAGTGATTTTAA | 51133 |
| rs770287520 | snp | A/T | 1.64814e-05 | 0.00287061 | missense | KCTD3 | GRCh38.p7 | 1:215618929 | ACTACAATATCCTCA[A/T]TTACAGTGAGGGAAT | 51133 |
| rs770299439 | in-del | -/ATA | 3.31664e-05 | 0.00407211 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574125 | ACTGGTGCTGTGAGT[-/ATA]ATAATAATTGATACA | 51133 |
| rs770330290 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567442 | CGGCCCGGCGGCCTG[C/G]AGGCCGCGAAAGGTG | 51133 |
| rs770333349 | snp | C/T | 1.65416e-05 | 0.00287586 | missense | KCTD3 | GRCh38.p7 | 1:215604282 | CAAAAATCATGCTAT[C/T]AGAGAAGCATCTTGT | 51133 |
| rs770345244 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593730 | TGAAGCAGCCAAAGA[C/T]CTACATAAAACAGTA | 51133 |
| rs770358302 | snp | A/C | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622269 | ACACTAATTTCTCAG[A/C]TTGCCCCCATTATGC | 51133 |
| rs770382387 | snp | A/G/T | 3.31045e-05 | 0.00406834 | missense | KCTD3 | GRCh38.p7 | 1:215620455 | GAGGATTTGAAGGGG[A/G/T]AGGATTCCTTGGAAG | 51133 |
| rs770383686 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572294 | AATGCTTTTAGGTGG[A/T]CCTCTCTGGCTTTAA | 51133 |
| rs770452831 | snp | C/T | 1.65002e-05 | 0.00287225 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620531 | AGGAACTGACTCACC[C/T]GGTACTGCGTCCCCA | 51133 |
| rs770468530 | snp | G/T | 0.000125849 | 0.00793151 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575983 | ACTTAAGGTAAGAAA[G/T]GCACTCTTTTTAAAG | 51133 |
| rs770470316 | snp | A/G | 0.000115619 | 0.00760239 | missense | KCTD3 | GRCh38.p7 | 1:215619162 | CCTAAGATGTAGGTG[A/G]TCCAACCGAAGAAGA | 51133 |
| rs770533493 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594112 | TGATCCACCCGCCCT[A/G]GCCTCCCAAAGTGCT | 51133 |
| rs770556443 | snp | C/T | 7.17103e-05 | 0.00598749 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595309 | GGTTTTGATTAATTC[C/T]AAAAATGGTGACTGA | 51133 |
| rs770591421 | snp | A/C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589818 | ATTGAAATAATACGG[A/C/T]AGAATTTGTTTATCC | 51133 |
| rs770647639 | in-del | -/TTT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593858 | GAATTGGAATACAAC[-/TTT]TTTTTTTTTTTTTTT | 51133 |
| rs770654552 | snp | A/G | 1.67562e-05 | 0.00289444 | missense | KCTD3 | GRCh38.p7 | 1:215608172 | TCTGGAAATGACATA[A/G]GTGGGTTAGGTTATT | 51133 |
| rs770685676 | snp | A/T | 3.31082e-05 | 0.00406854 | synonymous-codon, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215574094 | GAGTGGGAGAATTTC[A/T]ACACTTCGAGATGAA | 51133 |
| rs770712596 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602902 | AAATATTCAAGAGTA[-/T]TACCTATGAATTTGA | 51133 |
| rs770784409 | snp | A/T | 3.29565e-05 | 0.00405921 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215579964 | CCATCACAACTGGAT[A/T]GTAGCTGCATATGCC | 51133 |
| rs770785753 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574871 | TTTCTAATTGATTTA[C/T]ATAAGCTTTAAAAGA | 51133 |
| rs770786917 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577878 | AAAAAGATGTTGTCA[A/G]CTCTGACTTAATTAA | 51133 |
| rs770838275 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576209 | GAGTAGCTGGGACTG[A/T]AGGCACATGCCACCA | 51133 |
| rs770939970 | snp | G/T | 1.73794e-05 | 0.00294778 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602047 | TTTAAATAGATATGC[G/T]ATTTATTTTAATGCT | 51133 |
| rs770941129 | snp | C/T | 1.71132e-05 | 0.00292511 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608003 | TATTCTTTTGTGTTC[C/T]CTTTCTCTGCTAGTC | 51133 |
| rs770952641 | in-del | -/A | 4.28032e-05 | 0.00462599 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611794 | AATAAAATTTTAATT[-/A]ATTTTTTGACATTTT | 51133 |
| rs770977380 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581560 | GTTTTGTTACTGTAC[A/G]CAATACTAAAGATTG | 51133 |
| rs771003517 | snp | A/G | 1.69789e-05 | 0.00291362 | missense | KCTD3 | GRCh38.p7 | 1:215620086 | ACCATGATACCACCC[A/G]TGAAGCAGCTACTTA | 51133 |
| rs771006182 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612627 | GAATTTGCTGGCAGA[C/T]GGCTGAACTAATTCT | 51133 |
| rs771007497 | in-del | -/A | 0.000281861 | 0.0118681 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578106 | TTTATTAAATCTTTT[-/A]AAAAAATTCCTTGTA | 51133 |
| rs771032529 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572453 | GATGGACTTGCAAAG[C/T]TGAGAGATCTGTGAG | 51133 |
| rs771053787 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587218 | CACTGCAACCTCTGC[C/T]TCCTGGGCTCAAGCA | 51133 |
| rs771201972 | snp | A/G | 4.95774e-05 | 0.00497858 | missense | KCTD3 | GRCh38.p7 | 1:215619276 | AGCATAGCCACTTAC[A/G]AGAATCAAATTCTAG | 51133 |
| rs771247825 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570101 | AGCCACTGTAAGAGA[A/C]AAATCCTGATATGAT | 51133 |
| rs771406569 | snp | G/T | 1.64928e-05 | 0.00287161 | intron-variant, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577953 | AAATGGAGTACTGTT[G/T]TTCTGTTTGCATGTA | 51133 |
| rs771475217 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605503 | GTATTCTTTATCTGC[A/G]CTTTCCTAGTTATTT | 51133 |
| rs771498003 | snp | C/T | | | missense | KCTD3 | GRCh38.p7 | 1:215579918 | CAACAGGATTTCCTG[C/T]GGATCCACGAAAGGT | 51133 |
| rs771502343 | snp | G/T | 1.66319e-05 | 0.00288369 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574060 | CTAACTTTAGATTAT[G/T]AATGACTTCCAGTTT | 51133 |
| rs771502821 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | KCTD3 | GRCh38.p7 | 1:215586622 | GACAAAATGGTTGCT[C/G]TTGCCTCAGAGAGTA | 51133 |
| rs771522270 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587101 | AAAGTTACTCAGGAC[C/T]TGAAAGAATGTAGGT | 51133 |
| rs771523504 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596765 | GGTTTGAAAAAAAAG[A/C]TAATTGGTGCTTTAT | 51133 |
| rs771627622 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589305 | GGCACCACCACGCCT[A/G]GCTATTATTTTTTAA | 51133 |
| rs771681462 | snp | A/G | 3.31505e-05 | 0.00407113 | missense | KCTD3 | GRCh38.p7 | 1:215620286 | ACAGGGGAATGTAAT[A/G]TATCTGAGAGAAAGT | 51133 |
| rs771690664 | snp | C/T | 1.64898e-05 | 0.00287135 | missense | KCTD3 | GRCh38.p7 | 1:215618915 | AGGCTGTTGACTGTA[C/T]TACAATATCCTCATT | 51133 |
| rs771708402 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590084 | GTTCTCCACATCCTA[A/G]TCAACACTTTGTATT | 51133 |
| rs771720213 | snp | C/T | 9.9633e-05 | 0.00705738 | missense | KCTD3 | GRCh38.p7 | 1:215579066 | ATGGTCTAAATTCTA[C/T]AGAAGGTGAAGCCCG | 51133 |
| rs771749430 | snp | C/T | 1.7192e-05 | 0.00293185 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586460 | TTGCTTCATTGCTGC[C/T]GAGTCTACCTTATGT | 51133 |
| rs771843763 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617296 | GGCTGTGGGAACCCT[A/G]ATTTACAGTCAGTCA | 51133 |
| rs771906182 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591727 | AAGGTCTTAGGGAAA[C/T]GCTTATGCAACTTTT | 51133 |
| rs771933071 | snp | A/G | 1.77893e-05 | 0.00298234 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607987 | TTTAAAAGTAATTTT[A/G]TATTCTTTTGTGTTC | 51133 |
| rs771986654 | in-del | -/TTAAG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215611477 | ATGTATACGTCTCTT[-/TTAAG]TTATAAGAATCTAAG | 51133 |
| rs772005151 | in-del | -/CAGT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617302 | GGGAACCCTGATTTA[-/CAGT]CAGTCAGTTAGAAGC | 51133 |
| rs772020911 | snp | A/G | 3.29837e-05 | 0.00406088 | missense | KCTD3 | GRCh38.p7 | 1:215604263 | GTTCACCGAAGTCCC[A/G]TAACAAAAATCATGC | 51133 |
| rs772196597 | snp | C/T | 1.66059e-05 | 0.00288144 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620405 | AAGGTCATCAGAAGA[C/T]GAAAATGAAAATAAA | 51133 |
| rs772214540 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572729 | AAACATCCCTTAGCC[A/G]TTTTGGCTGGGGTTT | 51133 |
| rs772336622 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582048 | TGTTACTTCTATTAA[C/T]GAAGAGTAGTTGTGT | 51133 |
| rs772404490 | snp | A/G | 3.45799e-05 | 0.00415798 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579154 | TAAGCAAAGATTACA[A/G]AAATAGAAAAAGAAA | 51133 |
| rs772407776 | in-del | -/A | | | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215602167 | TCAAATGATGCTATT[-/A]ACTGCTCTGAGTGTT | 51133 |
| rs772457778 | snp | C/G | 1.74964e-05 | 0.00295769 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620627 | CTTGTGAAAACTCAC[C/G]AAAATGAATAGTTGT | 51133 |
| rs772491252 | snp | A/G | 6.93301e-05 | 0.0058873 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601846 | ACTATCTAACATCTG[A/G]TAATACTCTCACTAC | 51133 |
| rs772495411 | snp | A/G | 3.30126e-05 | 0.00406266 | intron-variant, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577942 | AGAGAAAATAAAAAT[A/G]GAGTACTGTTTTTCT | 51133 |
| rs772543420 | snp | A/G | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565797 | TGTGTTAGGGCAAAG[A/G]CAGTTAACATTGTTT | 51133 |
| rs772546146 | in-del | -/CCTGCAAATA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584505 | ATGGGTTTATCATTG[-/CCTGCAAATA]CCTGTATGAGTTGGG | 51133 |
| rs772585334 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577693 | GTATTAATGTTCTCA[A/G]GCATGAAGCAGAATT | 51133 |
| rs772611689 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587540 | CTTAAGTAACATTTT[A/T]AATGAGAACCTCATT | 51133 |
| rs772675082 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588595 | TAAATGTCAACACAG[A/G]TGTTCTAGAATAAGC | 51133 |
| rs772721307 | snp | C/T | 1.6582e-05 | 0.00287936 | synonymous-codon, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215574073 | ATTAATGACTTCCAG[C/T]TTGCTGAGTGGGAGA | 51133 |
| rs772755824 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603078 | GACAGTGTGGCATGC[A/G]GAGTTTAAAATGTTT | 51133 |
| rs772811324 | snp | A/C | 4.96504e-05 | 0.00498224 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215573811 | TCAAGACAAACTCTT[A/C]TGTGGATTCCAGATT | 51133 |
| rs772820453 | in-del | -/CA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597297 | TTCCACCCCCTCGCC[-/CA]CACACACAGAATTAC | 51133 |
| rs772849762 | snp | C/G | 4.97352e-05 | 0.00498649 | missense | KCTD3 | GRCh38.p7 | 1:215620290 | GGGAATGTAATATAT[C/G]TGAGAGAAAGTCTCC | 51133 |
| rs772880495 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215586624 | CAAAATGGTTGCTGT[C/T]GCCTCAGAGAGTAGC | 51133 |
| rs772923100 | snp | C/T | | | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619238 | TGCTACTCCTAACAT[C/T]AGTCCAGCAACTTCC | 51133 |
| rs772940568 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587859 | GGATCTTTTATCATA[C/T]ATGCTTTTATAAGAT | 51133 |
| rs772987937 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589472 | AACTCTTGGGTATTC[A/G]GTCTCAGTGAACCTA | 51133 |
| rs773029286 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590592 | ATCTACCTTTAATGT[-/C]TTTTATACTTCTACA | 51133 |
| rs773040338 | snp | C/T | 1.65996e-05 | 0.00288089 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620417 | AGATGAAAATGAAAA[C/T]AAAATAGAGTTTAGG | 51133 |
| rs773109529 | snp | A/C | 1.74318e-05 | 0.00295222 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579163 | ATTACAGAAATAGAA[A/C]AAGAAAAATACGTAT | 51133 |
| rs773161410 | in-del | -/T | 1.68346e-05 | 0.00290121 | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215620096 | CACCCATGAAGCAGC[-/T]ACTTACGGTTCCATG | 51133 |
| rs773178275 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574840 | GGAAGAGTTTTATTA[C/T]TGGCTGCCATTTCCC | 51133 |
| rs773195286 | snp | A/T | 1.66048e-05 | 0.00288134 | missense | KCTD3 | GRCh38.p7 | 1:215579065 | AATGGTCTAAATTCT[A/T]CAGAAGGTGAAGCCC | 51133 |
| rs773215363 | snp | A/G | 1.65143e-05 | 0.00287348 | missense | KCTD3 | GRCh38.p7 | 1:215604275 | CCCGTAACAAAAATC[A/G]TGCTATCAGAGAAGC | 51133 |
| rs773228160 | snp | A/G | 1.6656e-05 | 0.00288578 | missense | KCTD3 | GRCh38.p7 | 1:215595373 | GTGTTCAGCCTGGGT[A/G]TTCCTGTAGATGCTC | 51133 |
| rs773247939 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574917 | GCCAGATCTTTTGTA[A/G]ATGATTCAAAATAGG | 51133 |
| rs773301861 | snp | C/T | 1.67371e-05 | 0.0028928 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604129 | ACTCTTGACTTTATA[C/T]AGGTGTCAGTGGTAA | 51133 |
| rs773311207 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615892 | GACAAAAAGTTGTAA[A/G]TTAACAGAAATAGAC | 51133 |
| rs773317291 | snp | C/T | 5.12422e-05 | 0.00506147 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601852 | TAACATCTGATAATA[C/T]TCTCACTACATCAGG | 51133 |
| rs773323864 | snp | C/G | 1.65143e-05 | 0.00287348 | missense | KCTD3 | GRCh38.p7 | 1:215619271 | AGTTCAGCATAGCCA[C/G]TTACGAGAATCAAAT | 51133 |
| rs773377223 | snp | A/G | 1.65293e-05 | 0.00287479 | intron-variant, splice-acceptor-variant | KCTD3 | GRCh38.p7 | 1:215619152 | TATTTGTTCTCCTAA[A/G]ATGTAGGTGGTCCAA | 51133 |
| rs773400266 | snp | C/T | 2.38666e-05 | 0.00345438 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576010 | AAAGTAAATTCTTAC[C/T]GATAAATATGTGTTT | 51133 |
| rs773414138 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566337 | TTATTAAGCTTATCA[A/T]CAACTGGGAGAAATA | 51133 |
| rs773426084 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608907 | CAGTTCTCTGCATGA[A/T]TCTAGGCACTGGAAG | 51133 |
| rs773461881 | snp | C/T | 6.60077e-05 | 0.00574452 | intron-variant, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577948 | AATAAAAATGGAGTA[C/T]TGTTTTTCTGTTTGC | 51133 |
| rs773486401 | snp | A/G | 0.000140442 | 0.00837862 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620631 | TGAAAACTCACCAAA[A/G]TGAATAGTTGTTTCG | 51133 |
| rs773544876 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593813 | ATAAAGTGTTTTTCA[A/G]ATGATTAAGATAATG | 51133 |
| rs773642109 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602210 | AAAACAAGTTAGTAC[A/G]TGGCCAATTATATAC | 51133 |
| rs773655251 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579793 | GTGAGCCACTGTGCC[C/T]GGCTCTTAACAAAAC | 51133 |
| rs773655923 | in-del | -/T | 2.61141e-05 | 0.00361336 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575890 | AATAAAACTGTTCTC[-/T]TTTTTTACAGATATT | 51133 |
| rs773699233 | snp | A/T | 1.65619e-05 | 0.00287762 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215573786 | GATTTTTAATTGCAG[A/T]TTTAGTACCTCAAGA | 51133 |
| rs773715867 | snp | A/C | 1.65307e-05 | 0.0028749 | missense | KCTD3 | GRCh38.p7 | 1:215620554 | CGTCCCCATCTCCTA[A/C]AAAGACTACTCCATC | 51133 |
| rs773725900 | snp | G/T | 1.64776e-05 | 0.00287028 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577707 | AGGCATGAAGCAGAA[G/T]TTTACGGGATCACTC | 51133 |
| rs773735971 | in-del | -/TTATGTC | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622236 | CCTTGATGCAGTGGT[-/TTATGTC]TGTCTACTCTGACAC | 51133 |
| rs773742961 | snp | C/G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595229 | TTCTAGTCCCCAACA[C/G/T]GTATAGCACATAGTT | 51133 |
| rs773904451 | snp | A/G | 1.72166e-05 | 0.00293394 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586455 | TCCGTTTGCTTCATT[A/G]CTGCTGAGTCTACCT | 51133 |
| rs773955766 | snp | A/G | 1.65814e-05 | 0.00287931 | missense | KCTD3 | GRCh38.p7 | 1:215611899 | AACAAACTATTTGTA[A/G]GACTCTCATCGACTG | 51133 |
| rs773967382 | snp | A/C | 9.14202e-05 | 0.00676031 | missense, utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567690 | AGCCGCCGGAGATGG[A/C]GGGAGGGCACTGCGG | 51133 |
| rs773991238 | snp | A/G | 1.64871e-05 | 0.00287111 | missense | KCTD3 | GRCh38.p7 | 1:215604258 | TCACAGTTCACCGAA[A/G]TCCCGTAACAAAAAT | 51133 |
| rs774010213 | snp | A/G | 1.72656e-05 | 0.00293812 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608223 | ATATTAACTGTTCAG[A/G]AGAAGCATATCAACT | 51133 |
| rs774091695 | snp | C/T | 1.66696e-05 | 0.00288696 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602207 | CCCAAAACAAGTTAG[C/T]ACATGGCCAATTATA | 51133 |
| rs774196444 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614390 | TTGATAAGAATAGCA[G/T]TGATGTAATTACTTT | 51133 |
| rs774254657 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586751 | GTTTATAAAAGAGAT[C/T]GACACTGAATATGAA | 51133 |
| rs774311698 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589141 | TTTTCTTCTTTTCTT[A/T]CCTTTTTTTTCTGAG | 51133 |
| rs774332620 | snp | A/C | 1.64792e-05 | 0.00287042 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619003 | GTTCACAGGCCATAC[A/C]AATGGCAGTATTCAA | 51133 |
| rs774393776 | snp | A/C | 1.66754e-05 | 0.00288746 | missense | KCTD3 | GRCh38.p7 | 1:215579042 | CAGTCAGATCTGCTG[A/C]TTCTAGGAATGGTCT | 51133 |
| rs774396351 | in-del | -/G | 1.73673e-05 | 0.00294675 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611967 | CAGAAGCCACCTTTT[-/G]TCTTACAAAACATAT | 51133 |
| rs774425298 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612096 | GACTTTATGCTTACT[C/T]TCTGGGATTTAAGAG | 51133 |
| rs774440678 | snp | A/G | 3.30453e-05 | 0.00406467 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620147 | TTTATTAGCAAGGGC[A/G]AGAAGGACTGAGAGC | 51133 |
| rs774518771 | in-del | -/AAC | 1.75114e-05 | 0.00295896 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579168 | GAAATAGAAAAAGAA[-/AAC]AAATACGTATGTTTT | 51133 |
| rs774533421 | in-del | -/CATACCCTTTTT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594574 | TTTCAACCCCCTTTC[-/CATACCCTTTTT]ACCCCATAGATACTA | 51133 |
| rs774553049 | snp | C/G | 1.64914e-05 | 0.00287149 | missense | KCTD3 | GRCh38.p7 | 1:215586664 | TGGAGTGTTCAGGAT[C/G]GGGGAAGTGGAAGTG | 51133 |
| rs774748365 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582865 | CTGTGCCTGGCCTTG[-/T]TCTACATATTTTAAA | 51133 |
| rs774836275 | snp | A/T | 1.64933e-05 | 0.00287165 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580009 | TTACAGGTAGTGTAT[A/T]ATTAATAATGCTTTG | 51133 |
| rs774841953 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595628 | CTAGATGCATATTTG[A/C]GCATATTTTCAAGAG | 51133 |
| rs774855223 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577686 | GGAGTGAGTATTAAT[A/G]TTCTCAGGCATGAAG | 51133 |
| rs774866116 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581969 | ATGTTCTCCTAGCTT[A/C]ACTAATTTTCTACAT | 51133 |
| rs774922342 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593860 | ATTGGAATACAACTT[-/T]TTTTTTTTTTTTTTT | 51133 |
| rs774963598 | snp | A/T | 1.69545e-05 | 0.00291152 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595343 | ACCTTTTTATTTTTT[A/T]TTGTCATTTAAGGAG | 51133 |
| rs775041920 | snp | C/T | 1.71021e-05 | 0.00292416 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608206 | GGGCATTTTTAGGTA[C/T]TATATTAACTGTTCA | 51133 |
| rs775058413 | snp | A/T | 1.65468e-05 | 0.00287631 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215608054 | CCGGACGTGGACAGT[A/T]ACACGATTCAGAGGA | 51133 |
| rs775124341 | snp | A/C | 1.88163e-05 | 0.00306721 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579189 | CGTATGTTTTTAGTG[A/C]TGGGTGATATTGAGT | 51133 |
| rs775135835 | snp | C/T | 3.3024e-05 | 0.00406336 | missense | KCTD3 | GRCh38.p7 | 1:215620541 | TCACCTGGTACTGCG[C/T]CCCCATCTCCTACAA | 51133 |
| rs775241373 | snp | A/C | 1.69847e-05 | 0.00291411 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619331 | AAACAAAATTTATTT[A/C]TTTTGGGGAAATTGA | 51133 |
| rs775243140 | snp | C/G | 0.000150989 | 0.00868744 | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567642 | CGGGCTCGGCGGTCC[C/G]GGCTGGGGAAGGAGG | 51133 |
| rs775335139 | snp | C/T | 1.65201e-05 | 0.00287398 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215602138 | CTTCTTGTAACTGAA[C/T]TGTATCATGATCCTT | 51133 |
| rs775363636 | snp | A/G | 1.65853e-05 | 0.00287964 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573761 | CATGTTCTCACTTAT[A/G]ATACCAGATGATTTT | 51133 |
| rs775434552 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583502 | TGGCTTCTTTACTCC[A/G]TCCTGTTTTGTCAGC | 51133 |
| rs775440800 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602623 | TTAAAAATTTAAGCT[A/G]TAGAAAAAAGGCATT | 51133 |
| rs775517262 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585778 | ATTAAAAACTGACAG[G/T]ATATTTATTAGAGAA | 51133 |
| rs775563850 | snp | G/T | 1.87619e-05 | 0.00306278 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578959 | TTTAATTTTTGAAAG[G/T]TGAACTTAGGAATGT | 51133 |
| rs775593441 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580353 | TCCCTGATGGTCTAT[A/C]TCTAATGATTCAGTG | 51133 |
| rs775610952 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617393 | AGACCGAGTCTTCTA[-/C]CCGTGTGATATGACA | 51133 |
| rs775634223 | in-del | -/TAG | 0.00111037 | 0.0235361 | cds-indel | KCTD3 | GRCh38.p7 | 1:215619288 | ACGAGAATCAAATTC[-/TAG]TAGGTAGGTTAAAGA | 51133 |
| rs775687420 | snp | A/T | 1.65715e-05 | 0.00287845 | synonymous-codon, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215574118 | AGATGAAACTGGTGC[A/T]GTGAGTATAATAATA | 51133 |
| rs775690119 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614188 | AAATGCATGCCACCA[C/T]GCCTGGCTAATTTTT | 51133 |
| rs775869097 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606994 | CCTAGAACAAAATGT[C/T]CCCTTTTCACCAGAA | 51133 |
| rs775875921 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597015 | GTTGAAGAATATTAT[C/T]AAATACTGCAGAGAT | 51133 |
| rs775966801 | snp | A/G | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621437 | TTTTCAGTGTTAACA[A/G]CAATCATGATAATTA | 51133 |
| rs775967712 | snp | A/G | 1.78312e-05 | 0.00298585 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595317 | TTAATTCTAAAAATG[A/G]TGACTGATTAACCTT | 51133 |
| rs775981877 | snp | G/T | 1.70116e-05 | 0.00291642 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608007 | CTTTTGTGTTCTCTT[G/T]CTCTGCTAGTCTGTG | 51133 |
| rs776077434 | in-del | -/AG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574956 | TAAATTTCCATAAAA[-/AG]TTATCAATTATGGGC | 51133 |
| rs776098921 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | KCTD3 | GRCh38.p7 | 1:215618939 | CCTCATTTACAGTGA[C/G]GGAATGTGAGGGATC | 51133 |
| rs776129807 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594485 | GAGCTTGCCCATATT[C/T]AGTCTCCCAATTTGA | 51133 |
| rs776153201 | snp | A/G | | | intron-variant, missense | KCTD3 | GRCh38.p7 | 1:215619153 | ATTTGTTCTCCTAAG[A/G]TGTAGGTGGTCCAAC | 51133 |
| rs776158988 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617539 | TTTTTGCCAAGGAGT[A/G]AAGGACATTCTGCCC | 51133 |
| rs776298076 | snp | C/T | 2.12859e-05 | 0.00326228 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575987 | AAGGTAAGAAATGCA[C/T]TCTTTTTAAAGTAAA | 51133 |
| rs776348973 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602874 | AAAAGAAACCATAAT[C/T]TTTAGTATGAAAGAA | 51133 |
| rs776352669 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601037 | CTGCCTCCCAGGTTC[A/G]AGCAATTCTCCTGCC | 51133 |
| rs776388694 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587760 | TAGTCTTCTTTGATT[A/C]TTTATCAAAACTCTA | 51133 |
| rs776458283 | in-del | -/AATT | 0.000435004 | 0.0147415 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580047 | AGGTGGCAGTTTGAA[-/AATT]AATTGTGATTTTATA | 51133 |
| rs776501093 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577787 | TATGAAAGTTGCCCT[A/G]AATGAAATGTGTTTA | 51133 |
| rs776579248 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570546 | CAATTCCCAGGCTTT[A/C]TCTCTAACTAGCCTA | 51133 |
| rs776580908 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588519 | TTTAGTGCCACTGTC[C/G]TGGTTTGTGCTAAGT | 51133 |
| rs776632640 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615831 | AAGTGTCCATTTTTA[C/T]GCTTAGGTTAGAAGA | 51133 |
| rs776672427 | snp | C/T | 3.55537e-05 | 0.00421611 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579174 | AGAAAAAGAAAAATA[C/T]GTATGTTTTTAGTGC | 51133 |
| rs776739978 | snp | C/T | 1.64857e-05 | 0.00287099 | intron-variant, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577965 | GTTTTTCTGTTTGCA[C/T]GTACTCTTGACAAGT | 51133 |
| rs776748909 | snp | A/T | 5.15814e-05 | 0.00507819 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602067 | ATTTTAATGCTGTTT[A/T]AAATTTTTATGTTTT | 51133 |
| rs776752299 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582169 | TTTATTTTCTTCTCA[A/G]TGGGTAGGTAATTAT | 51133 |
| rs776765173 | snp | G/T | 1.66868e-05 | 0.00288845 | missense | KCTD3 | GRCh38.p7 | 1:215601867 | CTCTCACTACATCAG[G/T]TTCAAGATGTTGTTC | 51133 |
| rs776795540 | snp | C/G | 1.68439e-05 | 0.00290201 | missense | KCTD3 | GRCh38.p7 | 1:215620094 | ACCACCCATGAAGCA[C/G]CTACTTACGGTTCCA | 51133 |
| rs776807781 | in-del | -/TATT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574618 | CAAAGTGACCAATGG[-/TATT]TATTTGCTGTGGTGA | 51133 |
| rs776831426 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582496 | AAGATGATGGAGAGG[G/T]GAAATAACAGAGCAT | 51133 |
| rs776858944 | snp | A/C | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215566069 | TCTGAACTGTTACTC[A/C]TCTTCCCTGTCTAAA | 51133 |
| rs776917826 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597307 | TCGCCCACACACACA[C/G]AATTACGTTACAAAA | 51133 |
| rs777025652 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215592152 | GGTTCCTCTCACAAC[A/G]CCTGGGAACTACAGG | 51133 |
| rs777026322 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583801 | CTGCATTCAGAGTAG[A/G]GGAGAGCTCAGTTAG | 51133 |
| rs777109753 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605699 | CCATCTTAGTATACA[A/G]TATCACCATCTACTT | 51133 |
| rs777128971 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593496 | CTGGTCTTGAGTATA[C/G]TACAGTTCTGAACAA | 51133 |
| rs777149420 | snp | A/G | 4.11717e-05 | 0.00453698 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611795 | ATAAAATTTTAATTA[A/G]TTTTTTGACATTTTT | 51133 |
| rs777160625 | snp | A/C | 1.79207e-05 | 0.00299333 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595305 | TCCAGGTTTTGATTA[A/C]TTCTAAAAATGGTGA | 51133 |
| rs777160897 | in-del | -/ATAGTTGAGTAGC | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607626 | TTCTGATCTAGGTTA[-/ATAGTTGAGTAGC]ATAAGCAGAAACAGT | 51133 |
| rs777212365 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567346 | GTGAGCGCTGCGGTA[A/T]TTTGTCCCGAACGGT | 51133 |
| rs777224114 | snp | A/G | 6.63086e-05 | 0.0057576 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619102 | AAAGATGTTTGTCAC[A/G]AGGTTAAGCTTTTCA | 51133 |
| rs777247780 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597691 | GAATTTCTGTGGTCT[C/G]ATGGGCTAGGCTGGA | 51133 |
| rs777264179 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581685 | GTTTGCATTGATCAC[A/G]ATCTTTCTGTGCTTT | 51133 |
| rs777285795 | snp | G/T | 1.79014e-05 | 0.00299172 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620641 | CCAAAATGAATAGTT[G/T]TTTCGTTACATTTAG | 51133 |
| rs777333161 | snp | C/T | 1.68496e-05 | 0.0029025 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595484 | CAGGTTAGTTTAAAG[C/T]ATATTACAGAAGTGA | 51133 |
| rs777363630 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | KCTD3 | GRCh38.p7 | 1:215619218 | GATTTGAGCACATCT[C/T]GCTGTGCTACTCCTA | 51133 |
| rs777392751 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614378 | GTCATTGGTAGTTTG[A/G]TAAGAATAGCATTGA | 51133 |
| rs777398423 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571930 | GCCACCGCGCCTAGC[C/T]GAGATAAACTTTTAA | 51133 |
| rs777439589 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583362 | AGACATTAGATGTCA[C/T]TTGTAAACTATCATG | 51133 |
| rs777614174 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589728 | GGCTTTTTATTAAGC[A/G]TAATGCTTTTGAAAT | 51133 |
| rs777657224 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599721 | TCCTCTGCTTTCTCT[G/T]TTTTCCCGTATGGAG | 51133 |
| rs777680046 | snp | A/G | 1.65833e-05 | 0.00287948 | missense | KCTD3 | GRCh38.p7 | 1:215608152 | AAAGTCATGGTAGCT[A/G]TTCCTCTGGAAATGA | 51133 |
| rs777767972 | snp | G/T | 1.73733e-05 | 0.00294726 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607996 | AATTTTGTATTCTTT[G/T]GTGTTCTCTTTCTCT | 51133 |
| rs777787194 | in-del | -/ATA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215573759 | ATCATGTTCTCACTT[-/ATA]ATACCAGATGATTTT | 51133 |
| rs777795720 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588308 | AGATATATAGTTGAA[A/G]TTAAGTTTTTATCAG | 51133 |
| rs777798476 | in-del | -/ATC | | | utr-variant-3-prime, cds-indel | KCTD3 | GRCh38.p7 | 1:215621119 | GTTTGTGAAAAACAT[-/ATC]ATGTAATTCAAAAAC | 51133 |
| rs777819516 | snp | A/G | 1.71953e-05 | 0.00293212 | missense | KCTD3 | GRCh38.p7 | 1:215620076 | CAGCTTCAGCACCAT[A/G]ATACCACCCATGAAG | 51133 |
| rs777899618 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602289 | TCAAATTAAACTGGT[G/T]TATTTCTTTTTGAGA | 51133 |
| rs777905897 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581217 | CACCATTGTACTCCA[A/G]CCTGCGCAACAGAGC | 51133 |
| rs778005324 | snp | C/T | 0.000124758 | 0.00789706 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580977 | ATGTTTTAAGAGTGT[C/T]TTGGCTGGGCACGGT | 51133 |
| rs778050878 | in-del | -/AATG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586832 | GAGGAATGATCTGAT[-/AATG]AAGGAAAAATGATGT | 51133 |
| rs778081696 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569720 | CCTGTCTCAGCCTGG[C/T]ACTGTGACATTTTAT | 51133 |
| rs778198792 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596731 | AGAGAATCCAAGTGA[C/T]AGCTTAAGGATCAAG | 51133 |
| rs778212018 | snp | C/T | 1.72835e-05 | 0.00293964 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604084 | CGAGGGTAGCTTTTT[C/T]ATTATCGTTCCATAA | 51133 |
| rs778222839 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582935 | CTTCTTTGTAATTTT[G/T]TAAAAAACAGGTAAA | 51133 |
| rs778279718 | in-del | -/TC | 1.70287e-05 | 0.00291788 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608007 | CTTTTGTGTTCTCTT[-/TC]TCTGCTAGTCTGTGC | 51133 |
| rs778338391 | snp | C/T | 1.65457e-05 | 0.00287621 | missense | KCTD3 | GRCh38.p7 | 1:215618888 | TTTTCTTTTGCAGAA[C/T]ATGTGAGATCCAGGC | 51133 |
| rs778357951 | in-del | -/AG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608301 | TTTGAAATTCTAAAC[-/AG]AATTTTAGTGTGTTT | 51133 |
| rs778360428 | snp | A/T | 3.29468e-05 | 0.00405861 | missense | KCTD3 | GRCh38.p7 | 1:215586596 | TGGTTGGAGGGCCAC[A/T]TGGAGACAAAGACAA | 51133 |
| rs778390804 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585034 | GGTCTCTCCACTATC[G/T]CATTTCATGGTTTCC | 51133 |
| rs778390831 | snp | C/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565317 | TATATGTTGCAAATA[C/T]CTTTTCTCATTCTGC | 51133 |
| rs778447955 | in-del | -/TAA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610899 | AGTGTAAGTATTAGC[-/TAA]TAATAAAGATGACAT | 51133 |
| rs778474888 | in-del | -/TT | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620788 | CAATAATCATATCTC[-/TT]TTGACATTTTGGAAA | 51133 |
| rs778477465 | snp | A/C | 1.7031e-05 | 0.00291808 | missense | KCTD3 | GRCh38.p7 | 1:215579008 | TTTATAGGTATTCCT[A/C]GTCGTAAAATAAACA | 51133 |
| rs778581330 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566918 | TAAATTGAAGAGGGT[A/C]AAGTAAGCAGTTTTC | 51133 |
| rs778637749 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591483 | CTGCCTCAGCCTCTC[A/G]AGTAGCTGGGACTAC | 51133 |
| rs778683334 | snp | C/T | 3.13229e-05 | 0.00395733 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575878 | TTTGTAATTTGAAAA[C/T]AAAACTGTTCTCTTT | 51133 |
| rs778761094 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618441 | GCCTATACTGATTTT[A/T]CTTTTTTAATAAACT | 51133 |
| rs778769269 | snp | A/C | 1.67239e-05 | 0.00289166 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574044 | ACTCAGATTTTAAAA[A/C]CTAACTTTAGATTAT | 51133 |
| rs778771433 | snp | A/T | 1.68519e-05 | 0.0029027 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586712 | CTTGTTTATGTTGCA[A/T]TTTGATGATATTAAT | 51133 |
| rs778848862 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617246 | CCTTTGAATTCTGTG[A/T]GCCACTCTAGCAAAT | 51133 |
| rs778851331 | snp | A/G | 1.65222e-05 | 0.00287417 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579905 | CTTTTTCCAAAATCA[A/G]CAGGATTTCCTGTGG | 51133 |
| rs778860191 | snp | C/G/T | 1.66131e-05 | 0.00288206 | missense | KCTD3 | GRCh38.p7 | 1:215579114 | CTGTTCTCTCTGGAA[C/G/T]GGGAGAAGAAACTGT | 51133 |
| rs778895356 | snp | C/T | 1.66109e-05 | 0.00288187 | missense | KCTD3 | GRCh38.p7 | 1:215620397 | TCCAAGAAAAGGTCA[C/T]CAGAAGATGAAAATG | 51133 |
| rs778912204 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585996 | GTCCATCTGAAGTAC[-/A]AAAAGCAAGAGATTC | 51133 |
| rs778951815 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574364 | TATGAGCTTACATTG[G/T]CATTAGAAGAAATTT | 51133 |
| rs778961123 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606005 | ATGGCTTCTAATTGT[A/G]TTTAGAATAAATTTA | 51133 |
| rs779058565 | snp | G/T | 1.70848e-05 | 0.00292269 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579147 | GGCTAGGTAAGCAAA[G/T]ATTACAGAAATAGAA | 51133 |
| rs779121407 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596943 | TTTGACCCAACAGGG[A/T]GTAGAGACATTTCTT | 51133 |
| rs779145837 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589263 | GTCCCCCCACCTCAG[C/T]CTCCTTAGTAGCTAG | 51133 |
| rs779207627 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613877 | TGTTTTTGTACCGGT[A/G]CCATGCTGTTTTGGT | 51133 |
| rs779235253 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572455 | TGGACTTGCAAAGTT[G/T]AGAGATCTGTGAGAC | 51133 |
| rs779386048 | snp | C/T | 1.67421e-05 | 0.00289323 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601979 | CAGTCACTTAAAATG[C/T]TCCTGCTTAATGTAA | 51133 |
| rs779386580 | snp | C/T | 1.79816e-05 | 0.00299841 | intron-variant | KCTD3 | GRCh38.p7 | 1:215620054 | TTAAAAACTGTATTT[C/T]AGCCTTCAGCTTCAG | 51133 |
| rs779418227 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585320 | GGAAAAATTGATACA[-/T]TTTTCTCTATTGCTT | 51133 |
| rs779435168 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569373 | ATGCTCCCGCCTCGG[C/T]TTCCCAAAGTGCTGG | 51133 |
| rs779437869 | snp | A/G | 1.85596e-05 | 0.00304622 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601825 | CAGAAAATAGAAATT[A/G]TAATTACTATCTAAC | 51133 |
| rs779503839 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598230 | CTCAGTCCCTGAGAA[G/T]ACTGGGAAAAGTTTG | 51133 |
| rs779531597 | snp | A/G | 1.65578e-05 | 0.00287726 | missense | KCTD3 | GRCh38.p7 | 1:215611884 | GTTGTTCCCATCACC[A/G]ACAAACTATTTGTAA | 51133 |
| rs779602644 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593249 | CTTAGCTTTGTGTGT[C/G]TGTGTTGTACTTTAT | 51133 |
| rs779699158 | snp | G/T | 1.65343e-05 | 0.00287521 | missense | KCTD3 | GRCh38.p7 | 1:215620231 | AGCTGTCCCTGAAAA[G/T]GGTAACTTGGGTCCA | 51133 |
| rs779707326 | snp | G/T | 1.90896e-05 | 0.00308941 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573891 | ATTTATTTACCAAAA[G/T]ATAATAATGTTTGTC | 51133 |
| rs779710590 | snp | A/T | 1.65919e-05 | 0.00288022 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578110 | ATTAAATCTTTTAAA[A/T]AATTCCTTGTATCAT | 51133 |
| rs779723592 | snp | A/T | 1.64811e-05 | 0.00287059 | missense | KCTD3 | GRCh38.p7 | 1:215586550 | CCATATTTGGATTGG[A/T]CTATCGAACGAGTAG | 51133 |
| rs779800518 | snp | A/C/G | 3.30361e-05 | 0.00406413 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577775 | ATTTGACTCATGTAT[A/C/G]AAAGTTGCCCTAAAT | 51133 |
| rs779904120 | snp | A/G | 1.66502e-05 | 0.00288527 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618859 | TTGCTCATTCCCATC[A/G]GGGCTCTTTCTGCTT | 51133 |
| rs779997073 | snp | C/G | 0.000863185 | 0.0207569 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581091 | TCTCTACTGAAGATA[C/G]AAAAATTAGCCAGGT | 51133 |
| rs779997610 | snp | G/T | 3.43997e-05 | 0.00414713 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604352 | GCTCTGTGTGTTATT[G/T]TCATTAAAAGAATGA | 51133 |
| rs780105796 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591006 | GTTAGGAGTAGGTAT[A/C]CTCTTCTAGCTTTAT | 51133 |
| rs780107844 | snp | C/G | 1.67391e-05 | 0.00289297 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215579031 | AATAAACAACACAGT[C/G]AGATCTGCTGATTCT | 51133 |
| rs780129344 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574005 | GTCTTTAACATTTGG[G/T]AAAGAATTAGCACAT | 51133 |
| rs780198515 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604244 | GCTTTTTCAGACTTT[C/T]ACAGTTCACCGAAGT | 51133 |
| rs780253532 | snp | A/C | 1.66142e-05 | 0.00288216 | missense | KCTD3 | GRCh38.p7 | 1:215620385 | GGTTTTTCAGAATCC[A/C]AGAAAAGGTCATCAG | 51133 |
| rs780267273 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583681 | TTCCCCTTCCCTTTT[A/G]CAAGGGTACTCTTAA | 51133 |
| rs780303348 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576086 | TTTTCCTTGAGTTGC[A/T]GTCTTGCTCTGTTGC | 51133 |
| rs780355090 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576315 | CTCAGGCAGTCTCCC[C/T]GCCTTAGCCTCCCAA | 51133 |
| rs780356706 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598611 | CCAAATTGGAAATAA[C/T]GGAACAATTAGAAAG | 51133 |
| rs780369998 | snp | A/T | 3.64027e-05 | 0.00426615 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575852 | TACAGATATTAAAGT[A/T]AAAAGATTAATTTGT | 51133 |
| rs780431483 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215611555 | GTACTGTTAATGTGG[C/T]ACCTTAGGAAATTTT | 51133 |
| rs780454913 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615722 | ACCCCTTTAACAAAA[G/T]ATAGGCTAGCAAGAG | 51133 |
| rs780541756 | in-del | -/GA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618023 | TTCTTTGGACCTCAC[-/GA]TCTCTTGTGAAGATT | 51133 |
| rs780559180 | snp | A/G | 1.64841e-05 | 0.00287085 | missense | KCTD3 | GRCh38.p7 | 1:215619233 | CGCTGTGCTACTCCT[A/G]ACATCAGTCCAGCAA | 51133 |
| rs780586384 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579219 | AATTACTTTTAAAGA[-/T]TTTTTGCCTCATCTC | 51133 |
| rs780652200 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585149 | AGTCCTTAGAGTAAA[C/G]TGAAAGCAAGTTCAT | 51133 |
| rs780745691 | in-del | -/A | 1.68088e-05 | 0.00289899 | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215602086 | TTTTATGTTTTAGAT[-/A]ATGCAGAAGTTCCCC | 51133 |
| rs780817271 | snp | A/C | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622175 | TACTAGATTGCATTA[A/C]AGTACAAGTCAAATC | 51133 |
| rs780828089 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579499 | GTTCTAACAAAACTA[-/T]TTTTTTTTTTTTTTT | 51133 |
| rs780845957 | snp | C/T | 0.000185546 | 0.00963009 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581027 | AGCACTTTGGGAGGC[C/T]GAGATGGGTGGAGTT | 51133 |
| rs780857722 | snp | A/C | 1.66738e-05 | 0.00288732 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601969 | GGTAAGTGTTCAGTC[A/C]CTTAAAATGCTCCTG | 51133 |
| rs780870230 | snp | A/G | 1.65792e-05 | 0.00287912 | missense | KCTD3 | GRCh38.p7 | 1:215611840 | GACCTTTTGGAGAGC[A/G]AGACGATCAACAGGT | 51133 |
| rs780947319 | snp | C/T | 1.79486e-05 | 0.00299566 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595521 | TTCTGAAATGTATGC[C/T]GATTATGTATTTTTT | 51133 |
| rs780968071 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570443 | AATTCTGTTATGGGC[-/A]AGTGTGATTTTGGGC | 51133 |
| rs781009870 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215604973 | AATACTAATTTTCAA[C/G]TTTAACGAATAGTAC | 51133 |
| rs781040944 | snp | G/T | 0.000132316 | 0.00813269 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620665 | CATTTAGATGAAAGT[G/T]AAACTTTACTGAATT | 51133 |
| rs781045402 | snp | C/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565940 | CAGCTCATCAGTTAT[C/T]GTTAGTGTTAGTGTA | 51133 |
| rs781049450 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589520 | GCAAAAATGTTTTGC[C/T]ACATAAAGCACAATA | 51133 |
| rs781144946 | snp | C/T | 1.68505e-05 | 0.00290258 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608184 | ATAGGTGGGTTAGGT[C/T]ATTTTAGGGCATTTT | 51133 |
| rs781147924 | snp | A/G | 3.2956e-05 | 0.00405918 | missense | KCTD3 | GRCh38.p7 | 1:215579975 | GGATTGTAGCTGCAT[A/G]TGCCCATTTTGCTGT | 51133 |
| rs781243677 | snp | A/G | 1.66194e-05 | 0.00288261 | missense | KCTD3 | GRCh38.p7 | 1:215620356 | GTGGATTGGAAGTGC[A/G]TAAAATAGCTGAAGG | 51133 |
| rs781296290 | snp | A/G | 1.65315e-05 | 0.00287498 | missense | KCTD3 | GRCh38.p7 | 1:215620220 | AATGTAGAAAGAGCT[A/G]TCCCTGAAAATGGTA | 51133 |
| rs781456628 | snp | A/G | 1.6777e-05 | 0.00289624 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573862 | TTATAATTCTTTAGT[A/G]TATATTTTAATACAT | 51133 |
| rs781505014 | snp | A/G | 1.67231e-05 | 0.00289159 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578133 | TGTATCATTAAGCAA[A/G]TACAAGCATATGAAT | 51133 |
| rs781597719 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600391 | TTTCCCCTTGCCCTA[C/T]CTAACTCATAGTTGA | 51133 |
| rs781608243 | snp | A/G | 1.64846e-05 | 0.0028709 | missense | KCTD3 | GRCh38.p7 | 1:215618920 | GTTGACTGTACTACA[A/G]TATCCTCATTTACAG | 51133 |
| rs781614010 | snp | C/T | 3.31939e-05 | 0.0040738 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573752 | ATTTCAAATCATGTT[C/T]TCACTTATAATACCA | 51133 |
| rs781686457 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215610189 | GGTGAAATCTACATT[A/G]TAATGGGTAATGGGG | 51133 |
| rs781749247 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569517 | TGGATGGCTTAATAC[C/T]GAGTGAACTCTTATT | 51133 |
| rs781751946 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571816 | TTTCGTAGTTTTAGT[A/G]GAGACGGGGTTTCAC | 51133 |
| rs796145475 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597230 | TTGGGTAAGAAAAGT[-/A]AAAAAAAAAAAAAAG | 51133 |
| rs796171902 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603650 | GATGGTAATTCTAGG[C/T]TAGACATAATAAGGA | 51133 |
| rs796224873 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566363 | AAATAATACTTATCT[G/T]ACATCCATATGTACT | 51133 |
| rs796360385 | in-del | -/GA | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620633 | AAAACTCACCAAAAT[-/GA]ATAGTTGTTTCGTTA | 51133 |
| rs796364818 | multinucleotide-polymorphism | AAAACTCAAGCCCTTTGCT/GATCTGCCTGCCTCGGCAG | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601175 | TCCTGACCTCTGGTG[lengthTooLong]TTTCTTTTAGCACAA | 51133 |
| rs796428692 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598044 | AATATTGAAACAATG[C/T]ATATTGTTTATACTA | 51133 |
| rs796432189 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583056 | CTTTATTGTGTAATA[-/C]CCTAATTACTATAGA | 51133 |
| rs796457711 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584027 | ATGAACTGGGAAATT[A/G]TTGTAACCAAGCTGA | 51133 |
| rs796605624 | in-del | -/ACT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608441 | CATCTTCACATGTTA[-/ACT]ACTTTTATTTATTAT | 51133 |
| rs796612367 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575045 | TTACCTGAGGTCAGA[A/G]GTTCAAGACCAGCAT | 51133 |
| rs796711873 | multinucleotide-polymorphism | CG/TA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607050 | TTGTTATATAAGAAT[CG/TA]AAAGTACACAGATGT | 51133 |
| rs796747211 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606678 | CAGATATTTCATGTA[-/G]GGTTTGAAACTTTTG | 51133 |
| rs796839419 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579589 | CTGCAAGCTCTGCCT[C/T]CTGGGTTTACGCCAT | 51133 |
| rs796839685 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615218 | GAACCAAAGATTTTG[-/T]TTAAGGACAGTTCAG | 51133 |
| rs796974016 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616866 | CTTAAAGTCTTCCAA[A/G]TGATAAGTGTCTTTT | 51133 |
| rs796982797 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603149 | AGAATGAGCTGTGGA[-/T]TTTTTTTTTTAAATC | 51133 |