SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs767792437 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295784 | AAGTGGTTAGAGCAG[A/G]CATCCTTGTATTCTT | 338692 |
rs767872052 | snp | C/G | 1.66244e-05 | 0.00288304 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67301024 | CTGAGTGAAGAGCAC[C/G]CGCTCTCCCTGGGTG | 338692 |
rs767911749 | snp | C/G | | | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299302 | TCACCCACATCATGG[C/G]CCCCTACCCAGGGTA | 338692 |
rs767964064 | snp | C/T | 1.66479e-05 | 0.00288508 | missense, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292093 | CACTGCTGGCCGCCA[C/T]GCGGCCCAGCGAGGA | 338692 |
rs768150285 | snp | A/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67301085 | CCATCAGCAACGCTC[A/T]CTTTGCCAAGCTGCG | 338692 |
rs768484233 | snp | A/G | 3.40524e-05 | 0.00412614 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301633 | GAGCCTGCTTGAAGC[A/G]GGCACTGAGGCGGAG | 338692 |
rs768576796 | in-del | -/A | 0.000104871 | 0.00724049 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290291 | CCTGGGGTCATCTGG[-/A]GGGCTCCCCTCAGCA | 338692 |
rs768633233 | in-del | -/TTTTTTTTTTTTTTT | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298058 | TTATTGAGGTTTTCT[-/TTTTTTTTTTTTTTT]TTTTTTTTTGAGACG | 338692 |
rs768700070 | snp | G/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67294845 | TGATACAATTATGAA[G/T]CAAATGTTTTTCTTA | 338692 |
rs768811306 | snp | A/G | 1.6654e-05 | 0.00288561 | missense, nc-transcript-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301326 | CGCATCACCTTCAGC[A/G]ACCTGTGTGGCTGTG | 338692 |
rs768831430 | snp | C/G | 1.82988e-05 | 0.00302474 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299804 | ATTGTGACCCCTTAC[C/G]AGCTCCCACCCCTTC | 338692 |
rs768849821 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290621 | GGAAAGAGAGACGGC[C/T]AGGCTCACGTGGGAG | 338692 |
rs768888022 | snp | A/G | | | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288219 | GCGTGGGGTGGCAAA[A/G]TGACCCCAGATGGCA | 338692 |
rs768892992 | snp | A/G | 1.67939e-05 | 0.0028977 | intron-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301407 | GCATCAGGTACCCCA[A/G]CGGGAGGAAGAGGGA | 338692 |
rs768954066 | snp | C/G | 1.68241e-05 | 0.00290031 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301844 | CCCCTCATGGGGCTG[C/G]CTGGGTCCCTGTCCC | 338692 |
rs769206652 | snp | A/C | 1.65897e-05 | 0.00288003 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302163 | CAGAGCCCAGGGGCC[A/C]AGGATCCCCTCCCAG | 338692 |
rs769342217 | snp | A/G | | | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300458 | GTCTGCCTTGGTGGA[A/G]CAGAACAGTTACGCT | 338692 |
rs769379735 | snp | C/G | 1.66613e-05 | 0.00288623 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300158 | TGGGGACTTGCCTCG[C/G]GACAAGGGCTCTTGC | 338692 |
rs769381695 | snp | C/T | 4.8796e-05 | 0.00493919 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301830 | GCTGGAGCGGTGAGC[C/T]CCTCATGGGGCTGGC | 338692 |
rs769566488 | snp | A/G | 0.000116759 | 0.00763976 | missense, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292137 | CGCCTCACCTCTCCT[A/G]TCGTCTCCACCCACC | 338692 |
rs769679150 | snp | C/T | 5.02298e-05 | 0.00501123 | upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67301500 | TAGGGAACCCTTTCC[C/T]GTGCGAGGTGGACCC | 338692 |
rs769767794 | snp | C/T | 3.65484e-05 | 0.00427468 | missense, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67299827 | ACCCCTTCTCCGTAG[C/T]GGGGAAGACTCCATT | 338692 |
rs769820498 | snp | C/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67293058 | ACCCATCGATAGACA[C/T]TTGGGTTATTTGCAT | 338692 |
rs769834509 | snp | C/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296552 | ATCCTTTTATAATGC[C/T]TTTTATTTCTGTTGC | 338692 |
rs769908361 | snp | C/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292431 | TGACTTCTGACCTCA[C/T]ATGTTTTCCCATTAA | 338692 |
rs769999904 | snp | A/G | 1.67601e-05 | 0.00289478 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301394 | CTCTGCTGTTGCCGC[A/G]TCAGGTACCCCAACG | 338692 |
rs770033607 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302427 | AGCTTGGGGCCTGGA[C/G]CCCCAGGAATGAGCA | 338692 |
rs770090006 | snp | A/G | 5.00263e-05 | 0.00500106 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299166 | GGGGGTAGGAGATGA[A/G]GTCCAGGAACTCAGC | 338692 |
rs770175761 | snp | A/C/G | 2.51286e-05 | 0.00354454 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290354 | AGCACTGGAGACCCC[A/C/G]AGATGGTGCAGCTGG | 338692 |
rs770214771 | snp | A/G | | | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67287934 | ATGTGGGGGTCAGGG[A/G]GAGAGAGGAGGCCGT | 338692 |
rs770374398 | snp | A/G | 0.000112076 | 0.00748502 | missense, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290433 | TTCCGGAACTGCTCA[A/G]CAAACTTCGCCAGGT | 338692 |
rs770409852 | snp | C/T | 0.000100964 | 0.00710436 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290317 | CAGCAGCCTGGTGCC[C/T]GCAGTCCTGCAGGAG | 338692 |
rs770424235 | snp | C/G | 1.73884e-05 | 0.00294854 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301663 | GCAGGTGGGACTTGC[C/G]CAGGGGGTGGGCTCT | 338692 |
rs770430593 | snp | A/G | 3.99337e-05 | 0.00446825 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301738 | TGGCTGCAGGTGACC[A/G]TCTGGGAAGCCCTGA | 338692 |
rs770480892 | in-del | -/A | 1.72012e-05 | 0.00293263 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302295 | GGAGGAGGAGGACTT[-/A]ACAGCGGATCCTGCA | 338692 |
rs770526372 | in-del | -/G | 5.3775e-05 | 0.00518504 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299143 | GGAGAGGCTAGGGGT[-/G]GGGGGCTGGGGGTAG | 338692 |
rs770703820 | snp | A/G/T | 3.48938e-05 | 0.00417683 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67300969 | CCGTGCCTCACCCAT[A/G/T]TCCTGTGGTCGGCTG | 338692 |
rs770793899 | snp | A/G | 0.000220132 | 0.0104889 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292046 | GGTGGTGCATGTGGA[A/G]ACACTGGGGCTCACT | 338692 |
rs770814216 | in-del | -/AA | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67293336 | CTCATTTGTTTTTGG[-/AA]TCTAGCCAGCCTAGT | 338692 |
rs770858747 | snp | A/G | 1.85427e-05 | 0.00304483 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299923 | AGACAGGGCTGGCGG[A/G]GGGCCGAGCCTGGGC | 338692 |
rs770877288 | snp | C/T | 1.76235e-05 | 0.0029684 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292202 | CGGGTCCTGGCACAC[C/T]GTGGGTGGGATGGGG | 338692 |
rs770986598 | snp | A/G | 1.68128e-05 | 0.00289933 | intron-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301411 | CAGGTACCCCAACGG[A/G]AGGAAGAGGGAGCCT | 338692 |
rs771048577 | snp | C/G | 4.94988e-05 | 0.00497463 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302185 | CCCTCCCAGGACACC[C/G]CCAGCCCCCGGTCCA | 338692 |
rs771180296 | snp | C/T | 3.39081e-05 | 0.00411739 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302272 | GGAGCGGGAGCGGCG[C/T]GGGCAGCAGGAGGAG | 338692 |
rs771236723 | snp | A/G | 1.72794e-05 | 0.00293928 | intron-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301233 | GCTGCAGGGGCCGGA[A/G]GCACAGGTGGCTCTC | 338692 |
rs771256505 | snp | C/T | 3.31351e-05 | 0.00407019 | missense, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291719 | ACCTGGCAGCGGGGC[C/T]GGAGGAGCTTCATCT | 338692 |
rs771324597 | snp | A/G | 1.67091e-05 | 0.00289038 | missense, nc-transcript-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301312 | ACGTGCTCAATGCCC[A/G]CATCACCTTCAGCAA | 338692 |
rs771332920 | snp | C/T | 0.000208834 | 0.0102163 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67289481 | CGGCCCGGGCCCCAC[C/T]TTCCCGCTGCACCGG | 338692 |
rs771626168 | snp | A/G | | | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301947 | TCTGTCAGCAGCGCT[A/G]TCTGCCACCAAAGGT | 338692 |
rs771659274 | snp | C/T | | | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67287757 | TGGGGCTGAGTGAGG[C/T]GGGAGTCTGGGGAAG | 338692 |
rs771717314 | in-del | -/CCTCGGC | 1.69726e-05 | 0.00291308 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291775 | AAACTCATTGCAGCT[-/CCTCGGC]CCTTGGGTTTCCTGC | 338692 |
rs771792584 | snp | C/T | 5.02744e-05 | 0.00501345 | synonymous-codon, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300013 | CGTGCAGCAGGCAGC[C/T]AGCCCCACCAACCCC | 338692 |
rs771840399 | snp | A/G | 5.56726e-05 | 0.00527572 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301709 | ACGGCAGAAGTGACA[A/G]CTGTGGGCTCTGGTG | 338692 |
rs771860932 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296965 | GTGGTCAACCTAGCT[A/G]AAGGTTTGTCAATTT | 338692 |
rs771884437 | snp | C/T | 1.67052e-05 | 0.00289004 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291754 | GGGCCAGGGTGAGCT[C/T]TGGACAAACTCATTG | 338692 |
rs771884488 | snp | A/C | 1.65239e-05 | 0.00287431 | synonymous-codon, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300097 | GAACATTGGCCGCCC[A/C]ATCGAGATGTCCAGC | 338692 |
rs771926281 | snp | C/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298044 | CTATCCTTTCAATTT[C/T]ATTGAGGTTTTCTTT | 338692 |
rs771970484 | snp | C/T | 1.86708e-05 | 0.00305533 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291972 | TGCGCCCCCTCTGTC[C/T]ACCCCTACCGGCCGG | 338692 |
rs772160747 | in-del | -/TGTA/TGTGTA | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296365 | GTGTGTGTGTGTGTG[-/TGTA/TGTGTA]TATGTGTGTATAGTT | 338692 |
rs772219281 | snp | A/C | 8.4139e-05 | 0.00648555 | upstream-variant-2KB, intron-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67301476 | AGCGTGGCCCCTCTG[A/C]CACCTGCCTAGGGAA | 338692 |
rs772312818 | snp | A/G | 1.65449e-05 | 0.00287614 | missense, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291482 | TTCTCTTAGGCCCCC[A/G]ATTTCTACGTTGAGA | 338692 |
rs772340427 | snp | C/G | | | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290716 | GGAGCAGGGACTTCA[C/G]GTTGACTCGGTGGAT | 338692 |
rs772359362 | snp | A/G | 3.31279e-05 | 0.00406975 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67301100 | ACTTTGCCAAGCTGC[A/G]CGACTTCATCACTCT | 338692 |
rs772381455 | snp | A/C | 4.89896e-05 | 0.00494898 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302174 | GGCCCAGGATCCCCT[A/C]CCAGGACACCCCCAG | 338692 |
rs772440494 | snp | A/G | 3.43979e-05 | 0.00414702 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292178 | TAATGTGGCCTTTGA[A/G]AGGTCGGTCGGGTCC | 338692 |
rs772468383 | snp | C/T | 7.06989e-05 | 0.00594512 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302261 | CGGGAGCAGGAGGAG[C/T]GGGAGCGGCGCGGGC | 338692 |
rs772580704 | snp | C/T | 0.000100925 | 0.00710298 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67301588 | CCTCCGGGACGAGGA[C/T]GATGACCTCCTGCAG | 338692 |
rs772616946 | snp | C/G/T | 3.41561e-05 | 0.00413244 | intron-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301193 | CCTCAGGCATGGCAC[C/G/T]CTCCCTCAGCGCAGT | 338692 |
rs772687637 | snp | C/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67300688 | GGCTGAGGAGGAAAA[C/T]GGGGCTGTGGGCCAG | 338692 |
rs772782674 | snp | A/G | 1.76802e-05 | 0.00297318 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299962 | ACCCTCTGTCACCTT[A/G]ATGGCTGAGTCCGCC | 338692 |
rs772851895 | snp | A/G | 1.64863e-05 | 0.00287104 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301646 | GCGGGCACTGAGGCG[A/G]AGCAGGTGGGACTTG | 338692 |
rs772870483 | snp | A/C | 1.67396e-05 | 0.00289301 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300014 | GTGCAGCAGGCAGCC[A/C]GCCCCACCAACCCCA | 338692 |
rs772874123 | snp | C/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295309 | GTAATCCCAGCTACT[C/G]AGGAGGCTGAGGCAG | 338692 |
rs772951082 | in-del | -/A | 3.32121e-05 | 0.00407492 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299137 | AAGGCAGGAGAGGCT[-/A]GGGGTGGGGGGCTGG | 338692 |
rs772959650 | snp | A/C | 1.68043e-05 | 0.0028986 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291762 | GTGAGCTCTGGACAA[A/C]CTCATTGCAGCTCCT | 338692 |
rs773045418 | snp | A/C | 1.85986e-05 | 0.00304942 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291975 | GCCCCCTCTGTCCAC[A/C]CCTACCGGCCGGCAG | 338692 |
rs773310148 | snp | G/T | 1.66496e-05 | 0.00288522 | missense, nc-transcript-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301339 | GCAACCTGTGTGGCT[G/T]TGATGAGCCCCTGAG | 338692 |
rs773390094 | snp | A/G | 1.72746e-05 | 0.00293888 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290475 | CAGTTATGGAGGTGG[A/G]GTACCATGGCAGGGC | 338692 |
rs773392126 | snp | C/T | 3.65537e-05 | 0.00427499 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299822 | CTCCCACCCCTTCTC[C/T]GTAGCGGGGAAGACT | 338692 |
rs773456687 | snp | C/T | 4.87341e-05 | 0.00493606 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302175 | GCCCAGGATCCCCTC[C/T]CAGGACACCCCCAGC | 338692 |
rs773480001 | snp | A/G | 1.65389e-05 | 0.00287562 | missense, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291489 | AGGCCCCCGATTTCT[A/G]CGTTGAGATGAAGTG | 338692 |
rs773604957 | snp | A/G | 6.60131e-05 | 0.00574476 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299013 | AAGGCTTTGGCCAGC[A/G]TGTGAGGGTGCAGGT | 338692 |
rs773684002 | snp | A/G | 9.88582e-05 | 0.00702989 | missense, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67299564 | TGGAGCTGGTGACAC[A/G]CACACGCACGGAGCA | 338692 |
rs773807360 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290309 | GCTCCCCTCAGCAGC[C/G]TGGTGCCCGCAGTCC | 338692 |
rs773810910 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67300691 | TGAGGAGGAAAACGG[A/G]GCTGTGGGCCAGGCC | 338692 |
rs773964348 | snp | C/T | 1.68909e-05 | 0.00290606 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292157 | CTCCACCCACCTGGA[C/T]ACTCGTAATGTGGCC | 338692 |
rs774009651 | in-del | -/A | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295920 | CCATTCCTCATTGTT[-/A]AGAGTGTTTTTATCA | 338692 |
rs774026750 | snp | C/G | 1.68001e-05 | 0.00289823 | upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67301583 | GAGCCCCTCCGGGAC[C/G]AGGACGATGACCTCC | 338692 |
rs774196086 | snp | C/G | 3.39311e-05 | 0.00411879 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299996 | GGACCCACGCAGGCC[C/G]CCGTGCAGCAGGCAG | 338692 |
rs774213487 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67293266 | GTTTACATTCCCACC[A/G]GCAGCATGTGAGGGT | 338692 |
rs774353990 | snp | C/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67297474 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGGGCC | 338692 |
rs774356353 | snp | C/T | 1.65842e-05 | 0.00287955 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291730 | GGGCCGGAGGAGCTT[C/T]ATCTTCAAGGGCCAG | 338692 |
rs774423203 | snp | A/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67302764 | CCTGCTGGGGACCCG[A/G]TTCGTCCTGCCACCC | 338692 |
rs774449342 | snp | C/T | 7.25189e-05 | 0.00602115 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290460 | AGGTACAGCAGGGCA[C/T]AGTTATGGAGGTGGG | 338692 |
rs774548590 | snp | C/T | 0.000100876 | 0.00710125 | intron-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301408 | CATCAGGTACCCCAA[C/T]GGGAGGAAGAGGGAG | 338692 |
rs774600513 | snp | C/G | | | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288225 | GGTGGCAAAGTGACC[C/G]CAGATGGCACAGGCG | 338692 |
rs774658529 | snp | A/G | 9.76467e-05 | 0.00698669 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302166 | AGCCCAGGGGCCCAG[A/G]ATCCCCTCCCAGGAC | 338692 |
rs774679082 | snp | G/T | 0.000166875 | 0.0091329 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302073 | GCTTCTGCCCCAGCC[G/T]TGGCGCTCACTGGCC | 338692 |
rs774706643 | snp | A/G | | | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290630 | GACGGCCAGGCTCAC[A/G]TGGGAGAGACTGGAC | 338692 |
rs774738435 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67301086 | CATCAGCAACGCTCA[C/T]TTTGCCAAGCTGCGC | 338692 |
rs774768606 | snp | G/T | 1.68783e-05 | 0.00290498 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301846 | CCTCATGGGGCTGGC[G/T]GGGTCCCTGTCCCCC | 338692 |
rs774858371 | snp | A/G | 1.67919e-05 | 0.00289753 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300995 | GGCTGGGCAGGTTCA[A/G]GGCAACACTGTGGCT | 338692 |
rs774937401 | in-del | -/ACCAG | 1.83035e-05 | 0.00302513 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299802 | GCATTGTGACCCCTT[-/ACCAG]CTCCCACCCCTTCTC | 338692 |
rs775121275 | snp | A/G | 1.71199e-05 | 0.00292569 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67300980 | CCATGTCCTGTGGTC[A/G]GCTGGGCAGGTTCAA | 338692 |
rs775132569 | snp | A/G | 1.66815e-05 | 0.00288799 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292076 | TCTGCAGGAGCCCGA[A/G]ACACTGCTGGCCGCC | 338692 |
rs775136797 | snp | A/G | 5.02088e-05 | 0.00501018 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67301501 | AGGGAACCCTTTCCC[A/G]TGCGAGGTGGACCCC | 338692 |
rs775224889 | snp | A/G | 5.4817e-05 | 0.00523503 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67299828 | CCCCTTCTCCGTAGC[A/G]GGGAAGACTCCATTC | 338692 |
rs775367659 | in-del | -/TATATGAATTCTAGAT | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67294276 | CCAGTGTAGGCAGAA[-/TATATGAATTCTAGAT]TCAGCTTGTCAATTT | 338692 |
rs775408495 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291208 | CAAAAAGTACAAAAA[C/T]TAGCTGGGAGTGGTG | 338692 |
rs775419914 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292473 | AGGCTGTGGTTCACG[A/G]CAGCTCTTTGCACCA | 338692 |
rs775433313 | snp | C/T | 1.67705e-05 | 0.00289568 | upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67301577 | CGCAACGAGCCCCTC[C/T]GGGACGAGGACGATG | 338692 |
rs775511462 | snp | C/T | 1.66768e-05 | 0.00288758 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301319 | CAATGCCCGCATCAC[C/T]TTCAGCAACCTGTGT | 338692 |
rs775521094 | snp | C/G | 1.85682e-05 | 0.00304693 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299925 | ACAGGGCTGGCGGGG[C/G]GCCGAGCCTGGGCGG | 338692 |
rs775595634 | snp | G/T | 3.30551e-05 | 0.00406528 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291531 | GCTGGGGTGAGTGGG[G/T]ACCTCTGGGCTCCCA | 338692 |
rs775601317 | snp | A/G | 3.33996e-05 | 0.0040864 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299171 | TAGGAGATGAGGTCC[A/G]GGAACTCAGCTCCTC | 338692 |
rs775895709 | snp | A/G | 1.67211e-05 | 0.00289142 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301835 | AGCGGTGAGCCCCTC[A/G]TGGGGCTGGCTGGGT | 338692 |
rs776084343 | snp | C/T | 2.27079e-05 | 0.00336949 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301762 | GCCCTGACCAACACC[C/T]GGCCCGGTGCCCGCC | 338692 |
rs776133710 | snp | C/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295373 | AGTGAGCCAAAATCA[C/T]GCCACTTCACTCCAG | 338692 |
rs776172414 | snp | A/G | 1.66746e-05 | 0.00288739 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300163 | ACTTGCCTCGGGACA[A/G]GGGCTCTTGCAGACC | 338692 |
rs776262219 | snp | A/C | 1.6768e-05 | 0.00289546 | missense, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292059 | GAGACACTGGGGCTC[A/C]CTCTGCAGGAGCCCG | 338692 |
rs776271108 | in-del | -/AGG | 1.66546e-05 | 0.00288566 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299157 | TGGGGGGCTGGGGGT[-/AGG]AGATGAGGTCCAGGA | 338692 |
rs776281622 | snp | A/G | 0.00023269 | 0.0107838 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300145 | TCTGAGAGCTGGCTG[A/G]GGACTTGCCTCGGGA | 338692 |
rs776351772 | in-del | -/CACTGAG | 0.000114397 | 0.0075621 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302319 | CCTGCAGCTGTCACT[-/CACTGAG]CACTGAGCACTGAGC | 338692 |
rs776363419 | snp | A/G | 1.68128e-05 | 0.00289933 | intron-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301413 | GGTACCCCAACGGGA[A/G]GAAGAGGGAGCCTGC | 338692 |
rs776371000 | snp | A/C | 1.84739e-05 | 0.00303918 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291980 | CTCTGTCCACCCCTA[A/C]CGGCCGGCAGAGGCA | 338692 |
rs776383793 | snp | C/G | | | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291064 | ATAGCAGTGCGTCAA[C/G]ACTTGATGAAGGGCC | 338692 |
rs776618506 | snp | C/G | | | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290647 | GGGAGAGACTGGACC[C/G]TTTGGAAGAGAAGCC | 338692 |
rs776653460 | snp | C/T | 1.68136e-05 | 0.0028994 | upstream-variant-2KB, intron-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67301480 | TGGCCCCTCTGCCAC[C/T]TGCCTAGGGAACCCT | 338692 |
rs776731376 | snp | A/G | 9.79576e-05 | 0.0069978 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299654 | CCGGTCACACCGTGT[A/G]GTGGGGTCACCCTGG | 338692 |
rs776760173 | snp | C/G | 9.93246e-05 | 0.00704645 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302186 | CCTCCCAGGACACCC[C/G]CAGCCCCCGGTCCAC | 338692 |
rs776766945 | snp | C/T | 1.65968e-05 | 0.00288065 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67301117 | GACTTCATCACTCTG[C/T]GCCTTCCACCTGGCT | 338692 |
rs776776678 | snp | G/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292252 | ATTAATGAGGGCAGG[G/T]CGATCCTTGAAGATC | 338692 |
rs777021491 | snp | A/G | 0.000100407 | 0.00708472 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290318 | AGCAGCCTGGTGCCC[A/G]CAGTCCTGCAGGAGG | 338692 |
rs777038046 | in-del | -/C | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295921 | CATTCCTCATTGTTA[-/C]GAGTGTTTTTATCAT | 338692 |
rs777047689 | snp | G/T | 1.66358e-05 | 0.00288402 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299155 | GGTGGGGGGCTGGGG[G/T]TAGGAGATGAGGTCC | 338692 |
rs777051069 | snp | A/C | 0.000127926 | 0.00799667 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302245 | CCTGGAGTTGTCTTC[A/C]CGGGAGCAGGAGGAG | 338692 |
rs777233742 | snp | A/G | 1.66699e-05 | 0.00288698 | missense, nc-transcript-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301386 | GCCCCCAGCTCTGCT[A/G]TTGCCGCATCAGGTA | 338692 |
rs777256067 | in-del | -/CCACCCC | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67302643 | TGTAAAATGAGGAGA[-/CCACCCC]CCACCCTCCGCCCCT | 338692 |
rs777308257 | snp | A/C | | | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301665 | AGGTGGGACTTGCCC[A/C]GGGGGTGGGCTCTGG | 338692 |
rs777311712 | snp | C/T | 3.80445e-05 | 0.00436129 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301719 | TGACAGCTGTGGGCT[C/T]TGGTGGCTGCAGGTG | 338692 |
rs777334984 | in-del | -/TC | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296928 | CCCCCAGCCAAGTCT[-/TC]TCTCTCTTTTTTTGC | 338692 |
rs777412379 | in-del | -/GGAGCG | 6.74059e-05 | 0.00580503 | upstream-variant-2KB, cds-indel, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302256 | TTCACGGGAGCAGGA[-/GGAGCG]GGAGCGGGAGCGGCG | 338692 |
rs777455399 | snp | C/T | | | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67287855 | ATGTCCTGGAGTAAG[C/T]TGAAATGTGGACCTG | 338692 |
rs777513068 | snp | A/G | 1.65247e-05 | 0.00287438 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300098 | AACATTGGCCGCCCC[A/G]TCGAGATGTCCAGCA | 338692 |
rs777531677 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298966 | AGAGTTGGGCACCCC[A/G]GGCAGGCTGGCTGGA | 338692 |
rs777587005 | snp | A/G | 1.65765e-05 | 0.00287888 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67301057 | CAGGTGACCCCCATC[A/G]TCGACCTAATGGCCA | 338692 |
rs777591980 | snp | A/G | 9.51913e-05 | 0.0068983 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301804 | GCCACGGTTTATGAG[A/G]AACAGCTTCAGCTGG | 338692 |
rs777625374 | in-del | -/A | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292696 | CCATTTAAAGCATAC[-/A]GTTCAATGACTTTTA | 338692 |
rs777688960 | snp | C/T | 1.71749e-05 | 0.00293038 | missense, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292036 | ATGACCGGCAGGTGG[C/T]GCATGTGGAGACACT | 338692 |
rs777693372 | snp | A/G | 3.34986e-05 | 0.00409245 | upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67301568 | GGCATGGAGCGCAAC[A/G]AGCCCCTCCGGGACG | 338692 |
rs777725861 | snp | C/T | | | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300180 | GGCTCTTGCAGACCC[C/T]TCTCTGGGCCTGTCA | 338692 |
rs777941281 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67293931 | TAATTTTTGTGTATA[A/G]TGGAAGGTTCTTTTG | 338692 |
rs778090483 | snp | A/G | 7.46687e-05 | 0.00610973 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302268 | AGGAGGAGCGGGAGC[A/G]GCGCGGGCAGCAGGA | 338692 |
rs778178249 | snp | A/G | 0.000750751 | 0.0193601 | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302347 | AGCCATAGCCCCGGG[A/G]GGGCTGGCCAGGCCA | 338692 |
rs778181657 | snp | A/C | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295878 | AGTTTTTGGTAGATA[A/C]CCTTCATCAGGTTAA | 338692 |
rs778230788 | snp | C/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292923 | TAATATGTTGCCTTT[C/T]GTGTCTGGCTTCTTT | 338692 |
rs778247317 | snp | A/G | 1.65611e-05 | 0.00287755 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291715 | CATGACCTGGCAGCG[A/G]GGCCGGAGGAGCTTC | 338692 |
rs778258430 | snp | A/C | 3.82416e-05 | 0.00437257 | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302341 | GCACTGAGCCATAGC[A/C]CCGGGAGGGCTGGCC | 338692 |
rs778264502 | snp | G/T | 1.68001e-05 | 0.00289823 | missense, nc-transcript-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301303 | CCCTTTTCCACGTGC[G/T]CAATGCCCGCATCAC | 338692 |
rs778335339 | snp | A/G | 1.74977e-05 | 0.00295779 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291797 | CCTTGGGTTTCCTGC[A/G]GCTTGGGAGGACGGT | 338692 |
rs778453200 | snp | C/G | 1.70359e-05 | 0.0029185 | intron-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301189 | AGGACCTCAGGCATG[C/G]CACCCTCCCTCAGCG | 338692 |
rs778471417 | snp | C/G | | | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67287671 | AGGGAGACAAACCTC[C/G]GCAGTGGGAGAGGAA | 338692 |
rs778572218 | snp | A/G | 4.32779e-05 | 0.00465157 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301823 | AGCTTCAGCTGGAGC[A/G]GTGAGCCCCTCATGG | 338692 |
rs778619590 | snp | C/G | 1.8251e-05 | 0.00302079 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292226 | GATGGGGACGGATAG[C/G]AAGAGCCACCATTAA | 338692 |
rs778713210 | snp | A/G | 1.66109e-05 | 0.00288187 | | | GRCh38.p7 | 11:67299145 | AGAGGCTAGGGGTGG[A/G]GGGCTGGGGGTAGGA | 338692 |
rs778756837 | in-del | -/C | 0.000157023 | 0.00885928 | | | GRCh38.p7 | 11:67290401 | TACCAGAGGGCCACG[-/C]CAGAGGCTGGCGGGC | 338692 |
rs778832639 | snp | C/G/T | 8.26104e-05 | 0.00642644 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300093 | CACGGAACATTGGCC[C/G/T]CCCCATCGAGATGTC | 338692 |
rs778846686 | in-del | -/G | 1.74528e-05 | 0.00295399 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301666 | GGTGGGACTTGCCCA[-/G]GGGGTGGGCTCTGGC | 338692 |
rs778889226 | snp | C/G/T | 0.00180061 | 0.0299543 | missense, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290412 | CCACGCAGAGGCTGG[C/G/T]GGGCATTCCGGAACT | 338692 |
rs778892060 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298817 | TTTAAACCCAGCCCC[A/G]ACACTATCATACCTC | 338692 |
rs778926569 | snp | C/T | 3.32806e-05 | 0.00407912 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292127 | TGTGGCCAGTCGCCT[C/T]ACCTCTCCTATCGTC | 338692 |
rs778962290 | snp | C/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296743 | TAGGTGATTCTTCAA[C/G]CTCCCAAGTAGCTGG | 338692 |
rs779191140 | snp | C/T | 1.65121e-05 | 0.00287329 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291631 | TAAGATGTGCCCAAG[C/T]GATGTGTACCGCGTG | 338692 |
rs779208652 | snp | C/T | 3.65892e-05 | 0.00427706 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299810 | ACCCCTTACCAGCTC[C/T]CACCCCTTCTCCGTA | 338692 |
rs779419461 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67289704 | CAAGCCCAGGTCACC[A/G]GCCCCTCGCGCCTGA | 338692 |
rs779439638 | snp | C/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292828 | CTTCTTATCCCCTCT[C/T]CCAGTCCTAAGCAAC | 338692 |
rs779467434 | snp | C/T | 1.6543e-05 | 0.00287597 | missense, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291705 | GCTTCGAGCACATGA[C/T]CTGGCAGCGGGGCCG | 338692 |
rs779490434 | snp | C/T | 1.65151e-05 | 0.00287355 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291607 | GCACCCTGCAGTGCC[C/T]CTTGTGTCTAAGATG | 338692 |
rs779492395 | snp | C/T | 5.75192e-05 | 0.00536249 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302222 | TTTGAAGAGCAGCTG[C/T]GCCTGGCCCTGGAGT | 338692 |
rs779499847 | snp | C/T | 3.35999e-05 | 0.00409864 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302246 | CTGGAGTTGTCTTCA[C/T]GGGAGCAGGAGGAGC | 338692 |
rs779590001 | snp | A/G | 5.11627e-05 | 0.00505754 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302158 | GTCCACAGAGCCCAG[A/G]GGCCCAGGATCCCCT | 338692 |
rs779850208 | snp | A/G | 0.000114358 | 0.0075608 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290139 | TGGCCGTGTCTCTGG[A/G]AAACCTGGAGTCTGT | 338692 |
rs779867712 | snp | C/T | 0.000233879 | 0.0108113 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292139 | CCTCACCTCTCCTAT[C/T]GTCTCCACCCACCTG | 338692 |
rs779956748 | snp | C/G | 1.88624e-05 | 0.00307097 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291962 | AGCACTGATTTGCGC[C/G]CCCTCTGTCCACCCC | 338692 |
rs779965146 | in-del | -/A | 3.11182e-05 | 0.00394438 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290251 | CCCCCTGAGGCTGGC[-/A]GGCGGGGGGCAGTGA | 338692 |
rs780065368 | snp | G/T | 1.93924e-05 | 0.00311381 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67300946 | GTCCTCAATGGAAGG[G/T]CCACCAGCCGTGCCT | 338692 |
rs780103882 | snp | C/T | | | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299413 | GCCACCTCCTCCATT[C/T]TGGGGAGCAAGATCT | 338692 |
rs780307865 | snp | G/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67294724 | TTTTGCATTTTTAGA[G/T]AGACAGGATTTCACC | 338692 |
rs780338795 | snp | C/T | 1.83088e-05 | 0.00302557 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299798 | GCGAGCATTGTGACC[C/T]CTTACCAGCTCCCAC | 338692 |
rs780463558 | snp | C/G | | | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290615 | CACGTAGGAAAGAGA[C/G]ACGGCCAGGCTCACG | 338692 |
rs780542122 | snp | C/T | 1.65479e-05 | 0.0028764 | missense, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291477 | CTGGTTTCTCTTAGG[C/T]CCCCGATTTCTACGT | 338692 |
rs780611326 | snp | C/T | 1.82864e-05 | 0.00302372 | synonymous-codon, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299876 | GGCGCAGCAGCATTC[C/T]TCCCACACCGGGGTG | 338692 |
rs780618745 | snp | C/T | 1.65806e-05 | 0.00287924 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291449 | GCAGCAGGCAGGGCG[C/T]TGACAAGCAGCTCTG | 338692 |
rs780644579 | snp | A/G | 9.15776e-05 | 0.00676612 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299789 | AGGGGCGATGCGAGC[A/G]TTGTGACCCCTTACC | 338692 |
rs780713751 | snp | A/G | 5.69849e-05 | 0.00533753 | missense, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290435 | CCGGAACTGCTCAAC[A/G]AACTTCGCCAGGTAC | 338692 |
rs780926886 | snp | C/T | 4.30376e-05 | 0.00463864 | upstream-variant-2KB, missense, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301822 | CAGCTTCAGCTGGAG[C/T]GGTGAGCCCCTCATG | 338692 |
rs780992224 | snp | A/G | | | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300390 | TGAGTACCTGCTGGG[A/G]CCAGCGTGGCACAGT | 338692 |
rs781010010 | snp | A/C | 1.6569e-05 | 0.00287824 | synonymous-codon, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67301065 | CCCCATCATCGACCT[A/C]ATGGCCATCAGCAAC | 338692 |
rs781103774 | snp | C/G | 1.66504e-05 | 0.0028853 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292130 | GGCCAGTCGCCTCAC[C/G]TCTCCTATCGTCTCC | 338692 |
rs781105522 | snp | A/G | 0.000119981 | 0.00774443 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299989 | CGCCCTGGGACCCAC[A/G]CAGGCCCCCGTGCAG | 338692 |
rs781221531 | snp | A/G | 0.000125337 | 0.00791535 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301689 | GCTCTGGCCTCTGCA[A/G]CCACACGGCAGAAGT | 338692 |
rs781606790 | snp | C/T | 0.000100521 | 0.00708875 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301391 | CAGCTCTGCTGTTGC[C/T]GCATCAGGTACCCCA | 338692 |
rs781677045 | snp | A/G | 9.83236e-05 | 0.00701086 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67299574 | GACACGCACACGCAC[A/G]GAGCACCTCTCTGAT | 338692 |
rs796188336 | in-del | -/C | | | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67287513 | TGCAGAATGAAGATA[-/C]AAACGACATGGAGTC | 338692 |
rs796311459 | snp | A/C | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67293101 | GAATAATGCCACTCT[A/C]AGTATTCATGTGCAA | 338692 |
rs796321753 | snp | A/G | | | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288706 | TTCAGGGCCCCGGGG[A/G]CCGCCTCCCCGCATC | 338692 |
rs796635388 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298411 | CTTGAAGAGTGTTCC[A/G]TGTGCGCGTGAGAAG | 338692 |