SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1574103 | snp | A/G | 0.00844059 | 0.0644131 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290128 | GTTTCCCAGAGACAC[A/G]GCCAGCTCCAGTGGG | 338692 |
rs2004225 | snp | A/T | 0.209693 | 0.246729 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291228 | CTGGGACCACAGGTG[A/T]GTGCCACCACTCCCA | 338692 |
rs2051458 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291116 | taatcccagcgcttt[C/T]tgaggccaaagtggg | 338692 |
rs2298815 | snp | A/G | 0.108213 | 0.205904 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301388 | GGTACCTGATGCGGC[A/G]ACAGCAGAGCTGGGG | 338692 |
rs3802744 | snp | A/G | 0.0209421 | 0.100162 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299401 | GGTTCAGACCCTGCC[A/G]CCTCCTCCATTTTGG | 338692 |
rs3802745 | snp | G/T | 0.177182 | 0.23916 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299407 | GACCCTGCCACCTCC[G/T]CCATTTTGGGGAGCA | 338692 |
rs4244821 | snp | C/T | 0.188631 | 0.242351 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67297666 | GAGTAGCTGGGACTA[C/T]AGGCGCCTGCCACCA | 338692 |
rs4930192 | snp | C/T | 0.32885 | 0.23724 | upstream-variant-2KB, intron-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67302546 | CCGCCATCCACAGTG[C/T]CTCTCCACAGCGCCC | 338692 |
rs5792410 | in-del | -/G | | | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290066 | TGCTGGGGGAGACGG[-/G]ACACTCACAAAGGGC | 338692 |
rs7104898 | snp | A/G | 0 | 0 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67287707 | GAAAAGAGGCCAGAC[A/G]GGAAGAACGTGGTCC | 338692 |
rs10896166 | snp | C/T | 0.180064 | 0.240019 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292980 | ATCCAAGTTGTAGCA[C/T]GTAACTATTTCTTTC | 338692 |
rs10896167 | snp | C/T | 0.454182 | 0.144256 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298418 | AGTGTTCCGTGTGCG[C/T]GTGAGAAGCGTGTGT | 338692 |
rs11227758 | snp | C/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67289633 | GGAGCCCCCCCCCCC[C/G]CCCCGCCCGCTCAGC | 338692 |
rs11227759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291809 | TGCGGCTTGGGAGGA[C/T]GGTGCTGCCTTTTCT | 338692 |
rs11227760 | snp | A/G | 0.01739 | 0.091611 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298387 | TTTCTTAATGGCCTA[A/G]TGTATGGCCTTGAAG | 338692 |
rs11227761 | snp | A/T | 0.0569829 | 0.158885 | upstream-variant-2KB, intron-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67302952 | TTTGCGCAAGTCACT[A/T]CCGCCTGCGTAGCTG | 338692 |
rs11601700 | snp | A/C | 0.454182 | 0.144256 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67297031 | ttaattttctctatt[A/C]tttttctattctcta | 338692 |
rs11826864 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67302667 | ACCCTCCGCCCCTCA[A/G]GGCTGAAAGGAGCTG | 338692 |
rs12285051 | snp | C/T | 0.139564 | 0.224285 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295213 | acgaggtcaggagat[C/T]gagaccatcctggct | 338692 |
rs12285097 | snp | C/T | 0.243061 | 0.249904 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295289 | aggcttggtggcggg[C/T]gcctgtaatcccagc | 338692 |
rs12291831 | snp | C/T | 0.084364 | 0.187256 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67294908 | taaaattacaattga[C/T]ttctgtatgttgacc | 338692 |
rs34404014 | snp | A/G | 0.000486168 | 0.0155836 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67299604 | TCAGGACAAGTCGAG[A/G]AGCAAAGGTAAACCC | 338692 |
rs34979469 | in-del | -/T | 0 | 0 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67297527 | TCATAAGTTTTTTGG[-/T]TTTTTTTTTTTTTTC | 338692 |
rs35159418 | in-del | -/AC | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298807 | AAGGATGTTTTTAAA[-/AC]CCCAGCCCCGACACT | 338692 |
rs35285998 | in-del | -/C | | | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67287327 | GCAATGGCCTTTGAG[-/C]CCAGGCCTCCAGCAT | 338692 |
rs35600142 | in-del | -/G | | | frameshift-variant, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290421 | GCTGGCGGGCATTCC[-/G]GGAACTGCTCAACAA | 338692 |
rs35676170 | in-del | -/C | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295734 | AGCAAGACTCCATCT[-/C]AAAACAGTAAATAAA | 338692 |
rs35848734 | in-del | -/GT/GTGT | 0.433236 | 0.170072 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296338 | GCCATTTGGGCCTGA[-/GT/GTGT]GTGTGTGTGTGTGTG | 338692 |
rs35965170 | snp | G/T | 0.0515216 | 0.152008 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292028 | AGTGGACCATGACCG[G/T]CAGGTGGTGCATGTG | 338692 |
rs35992096 | in-del | -/C | | | frameshift-variant, nc-transcript-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290373 | GGTGCAGCTGGTGCT[-/C]CCAGTATCGGGACTA | 338692 |
rs55733135 | snp | A/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67293830 | TCCCTTCACCCATTT[A/T]AAAAATTGGGTCATC | 338692 |
rs56309751 | in-del | -/GT/GTGT | 0.5 | 0 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296366 | TGTGTGTGTGTGTGT[-/GT/GTGT]ATGTGTGTATAGTTT | 338692 |
rs57589444 | snp | G/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67294636 | ACCTCCACCTCCTGG[G/T]TTCAAGCAGTTCTCC | 338692 |
rs58530946 | snp | C/T | 0.148661 | 0.22854 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288011 | GAGCTGTGTTCAAGA[C/T]GGCAGAAATCAGGAG | 338692 |
rs60229295 | snp | C/T | 0.177182 | 0.23916 | intron-variant, missense | ANKRD13D | GRCh38.p7 | 11:67300885 | GCAGGGCACTCCAGG[C/T]CAGGCAGAAGGTGGG | 338692 |
rs61180657 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298222 | GTCCACCACCGTGCC[C/T]GGCTAATTTTTTGTA | 338692 |
rs61300057 | snp | A/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67294381 | TAGTACCATGTTAAC[A/T]ATGTTAAGTCTTCTA | 338692 |
rs61740832 | snp | C/T | 0.0100107 | 0.0700367 | synonymous-codon, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67301059 | GGTGACCCCCATCAT[C/T]GACCTAATGGCCATC | 338692 |
rs61763974 | snp | A/G | 0.00356505 | 0.0420692 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67287597 | GTGAGAGCTGGCTCT[A/G]AAGTGATTGCCTGGT | 338692 |
rs61763975 | snp | C/G | 0.00716837 | 0.0594373 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67287904 | CAATGGGAACGGACA[C/G]TCTCTCTCCCAGGGA | 338692 |
rs61763977 | snp | C/T | 0.0228947 | 0.104514 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288215 | CATAGCGTGGGGTGG[C/T]AAAGTGACCCCAGAT | 338692 |
rs61763978 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288254 | CGCCATGTGACTACA[A/G]GGAGAAGGCAGGGTA | 338692 |
rs61763979 | snp | C/T | 0.0123036 | 0.0774623 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288413 | GCCTTGGCCACCTAG[C/T]AAAACCAGGGCCCCA | 338692 |
rs61763980 | snp | A/G | 0.00353981 | 0.0419211 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288554 | CCTCTCCTGACGCTG[A/G]CAGCCAACCGCAGCC | 338692 |
rs61763981 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288636 | GTCCTCCGCCGGGAC[A/G]GCTCTGCCGCTGCCT | 338692 |
rs61891565 | snp | A/G | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290643 | ACGTGGGAGAGACTG[A/G]ACCCTTTGGAAGAGA | 338692 |
rs61891566 | snp | A/T | 0.177182 | 0.23916 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295209 | GATCACGAGGTCAGG[A/T]GATCGAGACCATCCT | 338692 |
rs71457771 | snp | G/T | 0.5 | 0 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298489 | GTCCAGCTGTAGTGT[G/T]GTTCTTATCTTCTGG | 338692 |
rs71462369 | snp | C/G | 0 | 0 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67289632 | TGGAGCCCCCCCCCC[C/G]CCCCGCCCGCTCAGC | 338692 |
rs72930762 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292622 | GTCAGTGGAAACACT[G/T]AAAAAAAAAAACAAA | 338692 |
rs74475892 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298731 | GTTTCCTAGAGTGTG[C/T]CAAAGCTCATCCCAG | 338692 |
rs74736063 | snp | A/C/G | 0.00954224 | 0.0684493 | upstream-variant-2KB, intron-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67302694 | GCTGGCGAGAGTCAC[A/C/G]TGTCCTTACCAAGCA | 338692 |
rs74885508 | snp | C/G | 0.045891 | 0.144359 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67299933 | GGCGGGGGGCCGAGC[C/G]TGGGCGGGAGGGCAC | 338692 |
rs75299026 | snp | G/T | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67301961 | TATCTGCCACCAAAG[G/T]TGGTGTGAGGGGTGG | 338692 |
rs76001762 | snp | C/T | 0.5 | 0 | intron-variant, synonymous-codon | ANKRD13D | GRCh38.p7 | 11:67300836 | GGCCAGGACACCAGC[C/T]CCCGGGGGAGGCGGG | 338692 |
rs76335959 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292931 | TGCCTTTTGTGTCTG[A/G]CTTCTTTCACTTAGT | 338692 |
rs76353068 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67294110 | TCTGTCTTTATGCCA[A/G]TATTATACTGTCTTA | 338692 |
rs76744563 | snp | A/G/T | 0.0418186 | 0.138422 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296470 | TAGTTTTGGTAGTTT[A/G/T]TGTCTCACTAGGAAT | 338692 |
rs76764674 | snp | A/T | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291027 | CCCTCTCCAGGGCAG[A/T]GTGGTTGGGCGTAGC | 338692 |
rs76948867 | snp | C/T | 0.00703159 | 0.0588757 | synonymous-codon, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67301101 | CTTTGCCAAGCTGCG[C/T]GACTTCATCACTCTG | 338692 |
rs77616840 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300375 | TTCTATTGAATTTCA[C/T]GAGTACCTGCTGGGG | 338692 |
rs77908999 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298859 | GCTAATTCCTCAGTG[A/T]CTTCTAGTCCCAAGT | 338692 |
rs77913150 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, synonymous-codon | ANKRD13D | GRCh38.p7 | 11:67300869 | GCGGCATCTGAGCAG[A/G]GCAGGGCACTCCAGG | 338692 |
rs77994298 | snp | A/C | 0.5 | 0 | intron-variant, missense | ANKRD13D | GRCh38.p7 | 11:67300835 | TGGCCAGGACACCAG[A/C]TCCCGGGGGAGGCGG | 338692 |
rs78472376 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296086 | ACTTGGTTGTGGTGT[A/C]TAATTCTTTTCATAT | 338692 |
rs78657670 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298903 | TCCCCCCCTGTCCAG[A/G]CACCCTCTTCAGGGG | 338692 |
rs78743307 | snp | A/G | 0.123452 | 0.215605 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67293229 | ATTGTTTAATTGACT[A/G]TTTACCAAACGAGCT | 338692 |
rs78822964 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292172 | CACTCGTAATGTGGC[C/G]TTTGAGAGGTCGGTC | 338692 |
rs78926654 | snp | A/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296367 | TGTGTGTGTGTGTGT[A/G]TGTGTGTATAGTTTT | 338692 |
rs78983123 | snp | A/C/G | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300081 | TCAGCCTGGAGTCAC[A/C/G]GAACATTGGCCGCCC | 338692 |
rs79176628 | snp | A/T | 0.5 | 0 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295995 | GATATGATCATGTGA[A/T]TTTTTAAAAAATTCT | 338692 |
rs79226049 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67292351 | CTCACTCAGACTGCC[A/G]GGGTGGTTGGGCTCC | 338692 |
rs79852510 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67297916 | GAGACGTTGGCTATT[G/T]AGGAGTGTGTTGTTT | 338692 |
rs80130094 | snp | C/T | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296993 | TTTTGTTGATGTTTT[C/T]GAAGAGCCAGTTTTT | 338692 |
rs111239786 | snp | C/T | 0.00392295 | 0.0441144 | synonymous-codon, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67299998 | ACCCACGCAGGCCCC[C/T]GTGCAGCAGGCAGCC | 338692 |
rs111345048 | snp | C/G/T | 0.00221253 | 0.0331869 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290064 | GCCCTTTGTGAGTGT[C/G/T]CCGTCTCCCCCAGCA | 338692 |
rs111349378 | snp | G/T | 0.176861 | 0.239062 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67295374 | GTGAGCCAAAATCAC[G/T]CCACTTCACTCCAGC | 338692 |
rs111687572 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292034 | CCATGACCGGCAGGT[A/G]GTGCATGTGGAGACA | 338692 |
rs111935356 | snp | C/G | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67289638 | CCCCCCCCCCCCCCC[C/G]CCCGCTCAGCTCCGC | 338692 |
rs112095274 | snp | C/T | 0.00143431 | 0.0267413 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67299061 | GGTCTGTTTCAGGAA[C/T]AAATGTGGTATCTGG | 338692 |
rs112286896 | snp | C/G | 0.5 | 0 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300129 | AAGTACAGAGGTGAG[C/G]TCTGAGAGCTGGCTG | 338692 |
rs112580474 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288041 | GAGGCTGGAACCAAG[A/G]AAGTCCTGTCGGGGT | 338692 |
rs112865164 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | SSH3, ANKRD13D | GRCh38.p7 | 11:67302475 | TGGAAATAAAGAGAC[C/T]GTCGCAGCAGGGCTG | 338692 |
rs112895629 | snp | A/C | 0.140919 | 0.224948 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67289169 | AGACCCAAGGCCGGG[A/C]ATCTCCTCGGGCGCT | 338692 |
rs112906755 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67291593 | CCAGTGACCCCTGTG[C/T]ACCCTGCAGTGCCCC | 338692 |
rs113207481 | snp | A/G | 0.5 | 0 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67298223 | TCCACCACCGTGCCC[A/G]GCTAATTTTTTGTAT | 338692 |
rs113875221 | snp | A/T | | | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290285 | GCCAGGCCTGGGGTC[A/T]TCTGGAGGGCTCCCC | 338692 |
rs114522764 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67289791 | CCGCATCCTTGCTGA[C/T]CCAAGCTGAGAACAA | 338692 |
rs115593094 | snp | C/T | 0.0178098 | 0.0926698 | upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67288898 | CCTGGGGTAGGAAGA[C/T]CGGGGCGAGCAAGGG | 338692 |
rs115905247 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | ANKRD13D | GRCh38.p7 | 11:67290518 | ACTGTGCCAGGCCTG[A/G]CCTTGGAAAGGCACC | 338692 |
rs117453503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ANKRD13D | GRCh38.p7 | 11:67300472 | AACAGAACAGTTACG[C/T]TCTTGCCTCGTGAGG | 338692 |
rs138195189 | snp | A/G | 1.68783e-05 | 0.00290498 | upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67301610 | CTCCTGCAGTTCGCC[A/G]TCCAGCAGAGCCTGC | 338692 |
rs138406797 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67297286 | GTGATAGCTCACTGC[A/C]ACCTCCGCCTCCCAG | 338692 |
rs138461637 | snp | C/T | 0.000698556 | 0.0186759 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292025 | GGAAGTGGACCATGA[C/T]CGGCAGGTGGTGCAT | 338692 |
rs138486470 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67293564 | TGGAGTGCAGTGACA[A/T]GATCATGGCTCATTG | 338692 |
rs138656438 | snp | A/G | 0.000682611 | 0.0184618 | missense, nc-transcript-variant, downstream-variant-500B | ANKRD13D | GRCh38.p7 | 11:67301359 | GAGCCCCTGAGCTCC[A/G]TGTGGGTGCCGGCCC | 338692 |
rs138792309 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | ANKRD13D | GRCh38.p7 | 11:67294702 | CCCACCACCACTCCT[G/T]GCTAATTTTTGCATT | 338692 |
rs138807212 | snp | C/T | 0.00215163 | 0.032729 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B | SSH3, ANKRD13D | GRCh38.p7 | 11:67301519 | CGAGGTGGACCCCAC[C/T]GTGTTTGAAGTGCCC | 338692 |
rs138888533 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, utr-variant-5-prime | ANKRD13D | GRCh38.p7 | 11:67292104 | GCCATGCGGCCCAGC[A/G]AGGAGCATGTGGCCA | 338692 |
rs138983611 | in-del | -/GT | | | intron-variant | ANKRD13D | GRCh38.p7 | 11:67296339 | GCCATTTGGGCCTGA[-/GT]GTGTGTGTGTGTGTG | 338692 |