| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs1035276 | snp | A/C | 0.244898 | 0.249948 | intron-variant | GRAP | GRCh38.p7 | 17:19037583 | tgattagcagtcccc[A/C]tgaatgggattggtg | 10750 |
| rs1057399 | snp | A/G | 0 | 0 | synonymous-codon, utr-variant-3-prime | GRAP | GRCh38.p7 | 17:19021835 | CCTTGGACTGAACGT[A/G]GGCTCCTAACTGCCT | 10750 |
| rs1057400 | snp | C/G | 0 | 0 | utr-variant-3-prime | GRAP | GRCh38.p7 | 17:19021812 | ACTGCCTCCCGGCCG[C/G]TCTGCACAAACTGGG | 10750 |
| rs1621499 | snp | C/T | 0.496483 | 0.0417852 | downstream-variant-500B, utr-variant-3-prime | SLC5A10, GRAP | GRCh38.p7 | 17:19020875 | CTGGCATTTGGGAGC[C/T]GGTGGGTGGAGGGAG | 10750 |
| rs1624825 | snp | C/T | 0.408017 | 0.193729 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020505 | TGCCCCTCTTGGGGC[C/T]TCGGGATCCCCATGA | 10750 |
| rs1634412 | snp | C/T | 0.46875 | 0.121031 | intron-variant | GRAP | GRCh38.p7 | 17:19027484 | GTGTGTGTGTGTGTG[C/T]GCGCGCGCGCGCGCA | 10750 |
| rs2074269 | snp | G/T | 0 | 0 | intron-variant | GRAP | GRCh38.p7 | 17:19031506 | CTGCCCCCCACCCCC[G/T]GCCCATGAATCCAAC | 10750 |
| rs2074277 | snp | C/T | 0.243633 | 0.249919 | intron-variant | GRAP | GRCh38.p7 | 17:19023630 | TGGGGGGTGGGGGGT[C/T]GGGGTCATCCACCCC | 10750 |
| rs2430875 | snp | A/G | 0.375 | 0.216506 | intron-variant | GRAP | GRCh38.p7 | 17:19045771 | CCCAGCATAGAGAAG[A/G]AGGAATTGCTCCTCC | 10750 |
| rs2472705 | snp | A/G | 0.5 | 0 | intron-variant | GRAP | GRCh38.p7 | 17:19032975 | TGTGCGCTTGTGTGT[A/G]CTGGGGGTTTACTGT | 10750 |
| rs9893211 | snp | A/G/T | 0 | 0 | intron-variant, missense, synonymous-codon | GRAP | GRCh38.p7 | 17:19024233 | GAGCAAGGGCTCCTC[A/G/T]TCGCGCAGGAAGATC | 10750 |
| rs9896426 | snp | A/G | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | SLC5A10, GRAP | GRCh38.p7 | 17:19021032 | CTCATATCCCTGATC[A/G]TGGCACATTCTCTGG | 10750 |
| rs11867753 | snp | C/T | 0.141258 | 0.225111 | downstream-variant-500B, utr-variant-3-prime | SLC5A10, GRAP | GRCh38.p7 | 17:19020807 | GGAGGAAGAGCCCCA[C/T]ATGCCCAGAGCAAGG | 10750 |
| rs17847612 | snp | G/T | | | missense | GRAP | GRCh38.p7 | 17:19021996 | GCGGGCGCGTTGGCT[G/T]CTTCCCACGGAGTTA | 10750 |
| rs56745876 | snp | C/T | 0.00835141 | 0.0640778 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020579 | GCCAAGCCAGCAAAG[C/T]GGGAGCCCTGAAAAA | 10750 |
| rs58536605 | snp | A/G | 0.139903 | 0.224452 | intron-variant | GRAP | GRCh38.p7 | 17:19023540 | ATTGTTGGCATCCCA[A/G]TCAGCTTCAGAGCTG | 10750 |
| rs58803056 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | GRAP | GRCh38.p7 | 17:19025143 | AATCGCCCCGAGTAC[C/T]TTCTAGCCCAGCGGA | 10750 |
| rs59708379 | snp | C/G | 0.137867 | 0.223442 | intron-variant | GRAP | GRCh38.p7 | 17:19022373 | ATAGAACACGGCTTT[C/G]CCAGCCGCCCAGCTG | 10750 |
| rs59794490 | snp | A/T | | | intron-variant | GRAP | GRCh38.p7 | 17:19024028 | TCTCCTTTCCCACCC[A/T]TGCAAGTCTCACCAT | 10750 |
| rs61749864 | snp | A/G | | | missense, synonymous-codon | GRAP | GRCh38.p7 | 17:19022064 | CAGGACCTCAATGAT[A/G]TCGCCACGGCGGAAG | 10750 |
| rs62066654 | snp | A/G | | | intron-variant | GRAP | GRCh38.p7 | 17:19027480 | CACATGCGCGCGCGC[A/G]CGCGCACACACACAC | 10750 |
| rs62066655 | snp | A/G | | | intron-variant | GRAP | GRCh38.p7 | 17:19027482 | CATGCGCGCGCGCGC[A/G]CGCACACACACACAC | 10750 |
| rs62066656 | snp | G/T | | | intron-variant | GRAP | GRCh38.p7 | 17:19040453 | GCCTCTGTGGGGGAG[G/T]CTGGGAGTGCCTGCA | 10750 |
| rs62066657 | snp | A/G | | | upstream-variant-2KB, intron-variant | GRAP | GRCh38.p7 | 17:19048309 | AAGCACAGCTGTATT[A/G]TTTGGAACCAGGGTT | 10750 |
| rs71155385 | in-del | -/ACACAC | 0 | 0 | intron-variant | GRAP | GRCh38.p7 | 17:19027525 | CACACACACACACAC[-/ACACAC]CCCTACCTCTCCTGG | 10750 |
| rs74935822 | snp | A/G | 0.5 | 0 | intron-variant | GRAP | GRCh38.p7 | 17:19027472 | TGATGGGACACATGC[A/G]CGCGCGCGCGCGCAC | 10750 |
| rs75913841 | in-del | -/TT | | | intron-variant | GRAP | GRCh38.p7 | 17:19024575 | CCCATCTGGCAGTGG[-/TT]AATATGGGGTTAATT | 10750 |
| rs76020008 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | GRAP | GRCh38.p7 | 17:19022849 | ATCTCATCCAGGATG[G/T]GTGATAGGATCAGCA | 10750 |
| rs77000553 | snp | C/T | 6.59957e-05 | 0.005744 | synonymous-codon, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020332 | CCCTCCAGGTGATGG[C/T]CAAACACCCCAGAAA | 10750 |
| rs78368288 | snp | A/C | 0.249603 | 0.25 | intron-variant | GRAP | GRCh38.p7 | 17:19023919 | ATTTATTGAGCACCT[A/C]CTGTGTGCCACATGC | 10750 |
| rs79681382 | snp | A/G | 0.46875 | 0.121031 | intron-variant | GRAP | GRCh38.p7 | 17:19027486 | CGCGCGCGCGCGCGC[A/G]CACACACACACACAC | 10750 |
| rs79973350 | snp | A/G | 0.5 | 0 | intron-variant | GRAP | GRCh38.p7 | 17:19027476 | GGGACACATGCGCGC[A/G]CGCGCGCGCACACAC | 10750 |
| rs80209928 | snp | C/T | 0.249603 | 0.25 | intron-variant | GRAP | GRCh38.p7 | 17:19024683 | GTTTTCTCATAATGA[C/T]AACATCTCCGTTATG | 10750 |
| rs111271912 | snp | A/G | | | intron-variant | GRAP | GRCh38.p7 | 17:19031893 | GCCTGGGCCCAGGCA[A/G]GAAGAAGCCAAGGGT | 10750 |
| rs111420837 | snp | A/G | | | intron-variant | GRAP | GRCh38.p7 | 17:19045253 | GGCCTATCAGGGAGG[A/G]AGGCTTTGTCCCAGG | 10750 |
| rs111538159 | snp | G/T | | | intron-variant | GRAP | GRCh38.p7 | 17:19039342 | TGTGAGATCCTGGGG[G/T]GGCACTCAACCTCTC | 10750 |
| rs111636163 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | GRAP | GRCh38.p7 | 17:19021331 | ACCTTCCCTACTGCC[C/T]GCCCCTTTTTCAGGG | 10750 |
| rs111741299 | snp | A/G | | | intron-variant | GRAP | GRCh38.p7 | 17:19031474 | ACTCCCTGTGCTGCT[A/G]CCTCTTCTCTAAGAG | 10750 |
| rs111811667 | snp | A/C | 0.029116 | 0.117091 | intron-variant | GRAP | GRCh38.p7 | 17:19024638 | TCACTGTGTGACCTC[A/C]TGCAAGTCTCTCAAC | 10750 |
| rs112396407 | snp | C/T | | | upstream-variant-2KB, intron-variant | GRAP | GRCh38.p7 | 17:19047814 | CAACATGGTGAAGCC[C/T]CATCTCTAATAAAAA | 10750 |
| rs112655941 | snp | C/T | | | intron-variant | GRAP | GRCh38.p7 | 17:19025281 | ACTGCAAGCTCCGCC[C/T]CCCAGGTTCATGCCA | 10750 |
| rs113267681 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | SLC5A10, GRAP | GRCh38.p7 | 17:19020680 | AAATTAGATTTCTGA[C/T]GGACATCCTGATGTT | 10750 |
| rs113565327 | snp | A/G | | | intron-variant | GRAP | GRCh38.p7 | 17:19045243 | AGAAACGCCTGGCCT[A/G]TCAGGGAGGGAGGCT | 10750 |
| rs113703856 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | GRAP | GRCh38.p7 | 17:19021791 | TTGCTGGGGGACCTG[A/G]GCCATCCCAGTTTGT | 10750 |
| rs114171855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GRAP | GRCh38.p7 | 17:19022482 | GGGATCTTATTTACC[C/T]GACTCTGCAGCAGCC | 10750 |
| rs114301648 | snp | A/G | 0.021333 | 0.101051 | intron-variant | GRAP | GRCh38.p7 | 17:19023657 | CCCACCCCCCACCCC[A/G]CGGCTTGCCAGGATC | 10750 |
| rs115496750 | snp | A/G | 0.151668 | 0.229849 | intron-variant | GRAP | GRCh38.p7 | 17:19023232 | TCAAGGCACTGTTTG[A/G]CTCCCCTGGCATATC | 10750 |
| rs115811363 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | GRAP | GRCh38.p7 | 17:19022302 | ATGGTAGTGCCACCA[A/C]TGGGCCTCCTGCTGC | 10750 |
| rs117355297 | snp | C/T | 0.052506 | 0.153284 | synonymous-codon, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020368 | CTTCTGGGCCCGTGT[C/T]TGTGGCTTCAATGCC | 10750 |
| rs138402616 | snp | C/T | 0.00060018 | 0.0173127 | missense | GRAP | GRCh38.p7 | 17:19022074 | ATGATGTCGCCACGG[C/T]GGAAGCTGAGCTGCG | 10750 |
| rs140507873 | snp | C/T | 0.000798403 | 0.0199641 | missense, utr-variant-3-prime | GRAP | GRCh38.p7 | 17:19021852 | CGTTCAGTCCAAGGC[C/T]GTCCACTGAGCCCCG | 10750 |
| rs140671488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GRAP | GRCh38.p7 | 17:19024612 | TGTGGGCTCTGAACC[A/T]GGCCACTTTCTCACT | 10750 |
| rs140715864 | snp | A/C/G | 0.0105829 | 0.0719742 | missense, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020426 | TTTTATGCCTACTTC[A/C/G]CCTGACACTGCCATC | 10750 |
| rs140799294 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GRAP | GRCh38.p7 | 17:19024047 | AAGTCTCACCATAGC[C/T]GCCACCAGGATATAA | 10750 |
| rs141313902 | snp | C/T | 0.000153988 | 0.00877327 | missense | GRAP | GRCh38.p7 | 17:19022122 | AAGTCAAACTGGGCC[C/T]GGGCAAAGCAGGCCC | 10750 |
| rs141697248 | in-del | -/C | 0.115438 | 0.210697 | intron-variant | GRAP | GRCh38.p7 | 17:19032174 | ACACACCCCTCGCTT[-/C]CCCCACCTCTAGATC | 10750 |
| rs141856816 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020548 | AGCTGCACAGCAGCT[C/T]GGTGCCCAAGAACTG | 10750 |
| rs143281137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | GRAP | GRCh38.p7 | 17:19024235 | GCAAGGGCTCCTCGT[C/T]GCGCAGGAAGATCTG | 10750 |
| rs143302839 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, missense | GRAP | GRCh38.p7 | 17:19024256 | GGAAGATCTGCCGCT[C/T]CTTGGCGATGGTGGT | 10750 |
| rs143618306 | snp | A/G | 0.0130921 | 0.0798413 | downstream-variant-500B, utr-variant-3-prime | SLC5A10, GRAP | GRCh38.p7 | 17:19021076 | TCTCGGGTAGGGGCC[A/G]TGCCCCACCTAGGTA | 10750 |
| rs144488147 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | GRAP | GRCh38.p7 | 17:19022614 | TCAGCCGTTGAGGGA[C/G]AGAATTGTCACTTTG | 10750 |
| rs144628398 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | GRAP | GRCh38.p7 | 17:19022840 | ATCTGCAGAATCTCA[G/T]CCAGGATGGGTGATA | 10750 |
| rs145421074 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | GRAP | GRCh38.p7 | 17:19025242 | TGTCACCCAGGCTAG[A/C]GTGCAATGGCGCTAT | 10750 |
| rs145838566 | snp | C/G/T | 3.81832e-05 | 0.00436923 | synonymous-codon, missense | GRAP | GRCh38.p7 | 17:19022066 | GGACCTCAATGATGT[C/G/T]GCCACGGCGGAAGCT | 10750 |
| rs145881467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GRAP | GRCh38.p7 | 17:19025112 | GCCCTGCCTTCCAGC[C/T]AGCCCACTACCGCCA | 10750 |
| rs145906142 | snp | A/G | 0.00118882 | 0.0243516 | missense, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020351 | ACACCCCAGAAACAC[A/G]CCTTCTGGGCCCGTG | 10750 |
| rs147067630 | snp | C/T | | | intron-variant | GRAP | GRCh38.p7 | 17:19028006 | CTCATCTAAGCCTTC[C/T]GAGTAGCTGGGATTA | 10750 |
| rs147181892 | snp | C/T | 0.0134861 | 0.0810011 | utr-variant-3-prime | GRAP | GRCh38.p7 | 17:19021686 | AGGTGGGCGGGGCCT[C/T]CACAGACTCCGCCCT | 10750 |
| rs148398873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GRAP | GRCh38.p7 | 17:19023006 | TGGGTGTAGGGGAGC[C/T]CTCAGTTGCCCCTGC | 10750 |
| rs149136744 | snp | C/T | | | intron-variant | GRAP | GRCh38.p7 | 17:19025635 | TTTTTTTTTTTGAGG[C/T]GTAGTCTCGCTCTGT | 10750 |
| rs149655640 | snp | C/T | 3.30682e-05 | 0.00406608 | missense, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020363 | CACGCCTTCTGGGCC[C/T]GTGTCTGTGGCTTCA | 10750 |
| rs150271742 | snp | C/T | | | upstream-variant-2KB, intron-variant | GRAP | GRCh38.p7 | 17:19048969 | CCGGCTCTGTTGCAG[C/T]TGAGGTTTCAAAGCC | 10750 |
| rs150950085 | snp | C/T | 1.6492e-05 | 0.00287154 | synonymous-codon, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020197 | GCTCAGGATGTGCCC[C/T]TGGGAACTAAAGCAG | 10750 |
| rs180846047 | snp | A/G/T | 0.000399281 | 0.0141238 | synonymous-codon, missense, utr-variant-3-prime | GRAP | GRCh38.p7 | 17:19021867 | CGTCCACTGAGCCCC[A/G/T]TGTGACTCTGACAGA | 10750 |
| rs181171065 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GRAP | GRCh38.p7 | 17:19021591 | CACCCACCATGGCCA[C/G]GGTTCCTTAGGTTGA | 10750 |
| rs182375043 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GRAP | GRCh38.p7 | 17:19024693 | AATGATAACATCTCC[A/G]TTATGGATAAGTGCA | 10750 |
| rs182750946 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GRAP | GRCh38.p7 | 17:19025090 | CTTTCTCTCATTTCC[A/C]GTCTGTGCCCTGCCT | 10750 |
| rs183572042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GRAP | GRCh38.p7 | 17:19023790 | CACTCTCTGAGCCTC[A/G]GTTTCCTCATCTGTA | 10750 |
| rs183598688 | snp | C/T | | | intron-variant | GRAP | GRCh38.p7 | 17:19025616 | TCTTTTTTCTTTTCT[C/T]TTTTTTTTTTTTTTG | 10750 |
| rs185228977 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020557 | GCAGCTCGGTGCCCA[A/C]GAACTGGCCAAGCCA | 10750 |
| rs185265231 | snp | G/T | | | intron-variant | GRAP | GRCh38.p7 | 17:19031912 | GAAGCCAAGGGTCAA[G/T]GGCTCCACCTGCTGG | 10750 |
| rs185335436 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | GRAP | GRCh38.p7 | 17:19021626 | CCAGTGGGTGAAACC[C/T]GGGAGTCCTCAACCT | 10750 |
| rs186833107 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | GRAP | GRCh38.p7 | 17:19023819 | TATAATGGGCATGAT[A/G]AGGCTCCCAGAGTAC | 10750 |
| rs186974309 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GRAP | GRCh38.p7 | 17:19024833 | TGCTCCCCTGCTCCT[C/T]CCATGCCCCAGAGTC | 10750 |
| rs187374701 | snp | A/C | | | intron-variant | GRAP | GRCh38.p7 | 17:19041389 | CCCTCTCCCAGCCAC[A/C]ACCCAGGGCCGGGCC | 10750 |
| rs187397886 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GRAP | GRCh38.p7 | 17:19022261 | GGTCTCGGGCAGCAC[C/T]GGAGTTGAACTTTAA | 10750 |
| rs188114963 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GRAP | GRCh38.p7 | 17:19021673 | CATTGACAAGAGGAG[G/T]TGGGCGGGGCCTCCA | 10750 |
| rs188747641 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SLC5A10, GRAP | GRCh38.p7 | 17:19020685 | AGATTTCTGACGGAC[A/G]TCCTGATGTTGGTTT | 10750 |
| rs188919341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GRAP | GRCh38.p7 | 17:19025223 | TTGAGGCGGAGTCTC[A/G]CTCTGTCACCCAGGC | 10750 |
| rs189900767 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | GRAP | GRCh38.p7 | 17:19025075 | GAAGCAAGCAGGCCC[C/T]TTTCTCTCATTTCCC | 10750 |
| rs190188279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GRAP | GRCh38.p7 | 17:19023862 | AGTGCATGGTACCCA[A/G]TATGCTCAGTGGGGG | 10750 |
| rs192191761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GRAP | GRCh38.p7 | 17:19023368 | GGAGCTTCTCTTCAG[C/T]GGTTATCAGCCTCTC | 10750 |
| rs192961679 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant, downstream-variant-500B | SLC5A10, GRAP | GRCh38.p7 | 17:19020549 | GCTGCACAGCAGCTC[A/G]GTGCCCAAGAACTGG | 10750 |
| rs193221319 | snp | C/T | | | intron-variant | GRAP | GRCh38.p7 | 17:19031492 | TCTTCTCTAAGAGTG[C/T]TGGATTCATGGGCCG | 10750 |
| rs199803859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | GRAP | GRCh38.p7 | 17:19024231 | TTGAGCAAGGGCTCC[C/T]CGTCGCGCAGGAAGA | 10750 |
| rs200039222 | snp | A/G | | | intron-variant | GRAP | GRCh38.p7 | 17:19027346 | TAGGGGCACAGGATG[A/G]CCACTGGGAGGTAGA | 10750 |
| rs200201794 | snp | C/T | 0.000231938 | 0.0107664 | intron-variant, synonymous-codon | GRAP | GRCh38.p7 | 17:19024254 | CAGGAAGATCTGCCG[C/T]TTCTTGGCGATGGTG | 10750 |
| rs200251709 | snp | C/T | | | intron-variant | GRAP | GRCh38.p7 | 17:19040876 | ACACATCCTTCAAAA[C/T]CTCACTCATTGCCAC | 10750 |
| rs200266407 | snp | A/G | 0.417034 | 0.18601 | intron-variant | GRAP | GRCh38.p7 | 17:19043652 | AAAACAACTCCCCCA[A/G]CCTAAGGAGAAAATG | 10750 |
| rs201111642 | snp | A/G | 0.0158563 | 0.0876169 | synonymous-codon | GRAP | GRCh38.p7 | 17:19041812 | GTCCACTCACGGATG[A/G]GGCTTGACGCGGATG | 10750 |