| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs182594 | snp | C/G | 0.495596 | 0.0467178 | intron-variant | PHF14 | GRCh38.p7 | 7:11005495 | GACAAAACAGAGAAA[C/G]AGTGAGAGAAAGAGA | 9678 |
| rs190074 | snp | A/G | 0 | 0 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974321 | GGATACACTTACTAA[A/G]GAATCCGTGAGGTGG | 9678 |
| rs190075 | snp | G/T | 0.453453 | 0.145282 | | | GRCh38.p7 | 7:10969845 | TGGAGATCCGAATTT[G/T]GGTCTAGGCTTGGCC | 9678 |
| rs191984 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11075701 | Ttgatatagtttgga[A/T]atatgtctcctccaa | 9678 |
| rs218962 | snp | C/T | 0.455144 | 0.142885 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966431 | ttctttgatgccttt[C/T]ggccaatcagatggt | 9678 |
| rs218963 | snp | A/G | 0.46865 | 0.121211 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964631 | gatcttccccaacct[A/G]gcaagacaggccaac | 9678 |
| rs218964 | snp | C/T | 0.476401 | 0.106032 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963566 | acatctacagaactc[C/T]ccaccccaaatcaac | 9678 |
| rs218965 | snp | C/T | 0.446602 | 0.154427 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982937 | TCCCTCTTTCTGAGA[C/T]GCAGATCTCCCTTTT | 9678 |
| rs218966 | snp | C/T | 0.452541 | 0.146551 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982603 | TCCTTCTCTTTCTCC[C/T]TTTTCTTTCTAGGTC | 9678 |
| rs218973 | snp | A/G | 0.4444 | 0.15719 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960237 | ggggtggggtgctgg[A/G]gaagggatagtgttg | 9678 |
| rs218974 | snp | A/G | 0.446771 | 0.154211 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959665 | tccagctacagcctc[A/G]cagagagccggtgcc | 9678 |
| rs218975 | snp | A/G | 0.435837 | 0.167226 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959557 | ctcactcactcacat[A/G]cctctcaccactctg | 9678 |
| rs218976 | snp | C/G | 0.468047 | 0.122292 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956775 | ATCTTCCAGTTCCTA[C/G]TGGCTTCTGGTGTTC | 9678 |
| rs218980 | snp | C/G | 0.409041 | 0.192888 | | | GRCh38.p7 | 7:10971592 | acaatattgcattta[C/G]gttattaATCTTTTG | 9678 |
| rs218981 | snp | C/T | 0.405776 | 0.195535 | | | GRCh38.p7 | 7:10970547 | ATTGCTTTGTTGCCC[C/T]GGCTGGAGTGTGTAG | 9678 |
| rs218982 | snp | A/G | 0.456332 | 0.141164 | | | GRCh38.p7 | 7:10970108 | TTTCCAAAAAACAGC[A/G]AGCACAAACTGCCTC | 9678 |
| rs218983 | snp | C/T | 0.427879 | 0.175668 | | | GRCh38.p7 | 7:10969465 | AAAGAGATGAAGTGC[C/T]TAGGGAAAGTAAAAT | 9678 |
| rs220089 | snp | C/T | 0.491157 | 0.065903 | intron-variant | PHF14 | GRCh38.p7 | 7:11007460 | TTAGATAAAAATTCA[C/T]TTTGAAACTTAAAAA | 9678 |
| rs220090 | snp | A/G | 0.444533 | 0.157025 | intron-variant | PHF14 | GRCh38.p7 | 7:11006683 | CAGATATCCTCGGAA[A/G]AGCTCCCCCAGGAGA | 9678 |
| rs220091 | snp | C/T | 0.496105 | 0.0439572 | intron-variant | PHF14 | GRCh38.p7 | 7:11005425 | CTCTCACTGGTCAAA[C/T]TTGGACAATGTAATA | 9678 |
| rs220092 | snp | A/G | 0.434831 | 0.168337 | intron-variant | PHF14 | GRCh38.p7 | 7:11004091 | CTGGCTGATTTTTCT[A/G]TATTTTGTAGAGACA | 9678 |
| rs220093 | snp | G/T | 0.438806 | 0.163867 | intron-variant | PHF14 | GRCh38.p7 | 7:11027126 | TCACTCTGAAATCCC[G/T]TGCTCAATTTCAACA | 9678 |
| rs220094 | snp | C/T | 0.49607 | 0.0441545 | intron-variant | PHF14 | GRCh38.p7 | 7:11027234 | TCTCTTTATCTCTCT[C/T]GCTCAATCTCATGTT | 9678 |
| rs220095 | snp | A/T | 0.496105 | 0.0439572 | intron-variant | PHF14 | GRCh38.p7 | 7:11017344 | gttgcatgaaatgta[A/T]attagtacaaccatg | 9678 |
| rs220096 | snp | C/T | 0.445724 | 0.155538 | intron-variant | PHF14 | GRCh38.p7 | 7:11013097 | GTTGGCAAACACTTA[C/T]TGAGGTCCCTTTGTA | 9678 |
| rs220097 | snp | A/G | 0.497211 | 0.037236 | intron-variant | PHF14 | GRCh38.p7 | 7:11009896 | TTTAAACCTCCTACA[A/G]TTAATCTTAGGAATG | 9678 |
| rs220098 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065172 | GTAGATGGCAAAAAA[A/C]CAGCACTTAAAAAAA | 9678 |
| rs220099 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064837 | TGTGATCATGTACAA[C/T]GGGGGGAAAACCAAG | 9678 |
| rs220100 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | PHF14 | GRCh38.p7 | 7:11078627 | TCAGGTGTAAGGAAT[C/G]TGAGTCATTTATAGA | 9678 |
| rs721028 | snp | A/G | 0.167158 | 0.235875 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065358 | TTGGAAGTAGTTATG[A/G]AACTACTTAGTGATA | 9678 |
| rs766817 | snp | C/G | 0 | 0 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958691 | taaaataaaaCTACA[C/G]AAGTAAGCAGTTGGC | 9678 |
| rs1026903 | snp | C/T | 0.174288 | 0.23826 | intron-variant | PHF14 | GRCh38.p7 | 7:11022248 | TTACCATACAATCTA[C/T]ATACTAAAATTTATA | 9678 |
| rs1029583 | snp | C/G | 0.492137 | 0.0622048 | intron-variant | PHF14 | GRCh38.p7 | 7:11134941 | TCAGCATGTTTATGT[C/G]CAAGTATTCATATTA | 9678 |
| rs1029584 | snp | G/T | 0.492727 | 0.0598633 | intron-variant | PHF14 | GRCh38.p7 | 7:11109711 | TTGTTCTGGCATTAA[G/T]AAAGAATAATAAATA | 9678 |
| rs1057436 | snp | C/G | 0.487809 | 0.0771174 | intron-variant | PHF14 | GRCh38.p7 | 7:11126591 | AAATCCCTAACTTTT[C/G]TCTTCCTGTCTACTC | 9678 |
| rs1057437 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11126619 | CTCCTTCCTTTCTCC[C/T]TCACATTTCCAAGCA | 9678 |
| rs1154920 | snp | C/T | 0.406986 | 0.194565 | intron-variant | PHF14 | GRCh38.p7 | 7:10978615 | ACAAAATGCCAATAG[C/T]GCCAAGGTTGAGAAA | 9678 |
| rs1154921 | snp | A/G | 0.45946 | 0.136478 | intron-variant | PHF14 | GRCh38.p7 | 7:10978597 | CAAGGTTGAGAAACC[A/G]TTAACTCGTATATAC | 9678 |
| rs1154922 | snp | C/T | 0.409382 | 0.192607 | intron-variant | PHF14 | GRCh38.p7 | 7:10978420 | GTTCATAGTTCCACT[C/T]TTACCTCCTCTCCTC | 9678 |
| rs1154923 | snp | G/T | 0.171704 | 0.237423 | intron-variant | PHF14 | GRCh38.p7 | 7:10978365 | AATCTCATTTCCTAT[G/T]AAAGACTTGAACTAC | 9678 |
| rs1483201 | snp | C/T | 0.499424 | 0.0169631 | intron-variant | PHF14 | GRCh38.p7 | 7:11058143 | GGTCCTTTTCTGATA[C/T]ATTTTGAGGCTGAAA | 9678 |
| rs1483202 | snp | C/T | 0.495855 | 0.045338 | intron-variant | PHF14 | GRCh38.p7 | 7:11058025 | AACACAGATACGTTA[C/T]CTGGAAATTCCACAT | 9678 |
| rs1483203 | snp | C/T | 0.44333 | 0.158505 | intron-variant | PHF14 | GRCh38.p7 | 7:11057956 | TTTGACAGTAATTAG[C/T]TAACCTATTAAAAGT | 9678 |
| rs1483204 | snp | A/C | 0.499295 | 0.0187567 | intron-variant | PHF14 | GRCh38.p7 | 7:11057666 | TTTATTCAGGCCGGG[A/C]ACAGTGGCTCAGGCC | 9678 |
| rs1483205 | snp | A/T | 0.437542 | 0.165312 | intron-variant | PHF14 | GRCh38.p7 | 7:11051295 | TGCTGGGATTATGGG[A/T]GTGAGCCACTGCAGC | 9678 |
| rs1531834 | snp | A/T | 0.44858 | 0.151875 | intron-variant | PHF14 | GRCh38.p7 | 7:11044327 | CTTTTCTTTTTTTTT[A/T]AATTTCAACTTTTAT | 9678 |
| rs1547944 | snp | C/G | 0.499982 | 0.00299515 | intron-variant | PHF14 | GRCh38.p7 | 7:11119430 | TAATATATTCCACAC[C/G]ACTTCTGAATTTTAT | 9678 |
| rs1547945 | snp | A/T | 0.491473 | 0.0647364 | intron-variant | PHF14 | GRCh38.p7 | 7:11119374 | TTGATTATATAACCT[A/T]ATTTTAATATTTCAA | 9678 |
| rs1625381 | snp | A/G | 0.44651 | 0.154543 | intron-variant | PHF14 | GRCh38.p7 | 7:11026109 | ttttttttttttttt[A/G]atggagtctcacact | 9678 |
| rs1629587 | snp | A/G | 0.435263 | 0.167862 | intron-variant | PHF14 | GRCh38.p7 | 7:11025651 | cctgctaccatgccc[A/G]gctaattttttgtat | 9678 |
| rs1636753 | snp | C/T | 0.449853 | 0.150196 | intron-variant | PHF14 | GRCh38.p7 | 7:11021324 | TTTATAACTTTGTAA[C/T]TAAGACAAATCTACA | 9678 |
| rs1636754 | snp | A/G | 0.438806 | 0.163867 | intron-variant | PHF14 | GRCh38.p7 | 7:11019075 | taggatttatccctg[A/G]gttgcaagcatggtt | 9678 |
| rs1636755 | snp | C/T | 0.438386 | 0.164349 | intron-variant | PHF14 | GRCh38.p7 | 7:11019031 | tcaatcaacatgata[C/T]atcacatcaacagga | 9678 |
| rs1636756 | snp | C/T | 0.492871 | 0.0592773 | intron-variant | PHF14 | GRCh38.p7 | 7:11018379 | aaaaatattccatgt[C/T]cacaaactggaagaa | 9678 |
| rs1636757 | snp | A/T | 0.449218 | 0.151037 | intron-variant | PHF14 | GRCh38.p7 | 7:11018083 | agaactcagaaacaa[A/T]tccacgcacctaagt | 9678 |
| rs1640699 | snp | C/G | 0.499663 | 0.0129749 | intron-variant | PHF14 | GRCh38.p7 | 7:10977986 | GTCTGGTTAATAGAA[C/G]TAATACATGTCTGCA | 9678 |
| rs1640700 | snp | A/C | 0.475081 | 0.108804 | intron-variant | PHF14 | GRCh38.p7 | 7:10977651 | TCAATCAAAAATGAG[A/C]AGCTTACTTTTGCTT | 9678 |
| rs1640701 | snp | C/G | 0.459914 | 0.13578 | intron-variant | PHF14 | GRCh38.p7 | 7:10977063 | TAATCTAGAGTAAGC[C/G]AATATCTCAGCTATG | 9678 |
| rs1640702 | snp | A/G | 0.457154 | 0.139954 | intron-variant | PHF14 | GRCh38.p7 | 7:10976987 | TTTCTGTTGACTACT[A/G]ATCATTTTAAATACA | 9678 |
| rs1640703 | snp | A/G | 0.448708 | 0.151707 | intron-variant | PHF14 | GRCh38.p7 | 7:10976893 | CTGAGACCACAGATC[A/G]CAAATTTAAGCTCCC | 9678 |
| rs1640704 | snp | C/T | 0.497722 | 0.0336691 | intron-variant | PHF14 | GRCh38.p7 | 7:10992004 | AATTTTTTAAGAATG[C/T]TTTCTATCAGACTAA | 9678 |
| rs1640705 | snp | C/T | 0.435119 | 0.16802 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968594 | TCTCTGCCAGGTGAA[C/T]AGGGCTTCTTATTTG | 9678 |
| rs1640710 | snp | A/C | 0.40733 | 0.194287 | intron-variant | PHF14 | GRCh38.p7 | 7:10988697 | GTTCAAAAAGAGGAA[A/C]ATGAACTGATAATTT | 9678 |
| rs1640712 | snp | A/G | 0.476918 | 0.104919 | intron-variant | PHF14 | GRCh38.p7 | 7:10986011 | actgcaccccagtcc[A/G]ggaaacaaagcgaga | 9678 |
| rs1640713 | snp | A/C | 0.45866 | 0.137698 | intron-variant | PHF14 | GRCh38.p7 | 7:10986008 | gcaccccagtccagg[A/C]aacaaagcgagaatc | 9678 |
| rs1681281 | snp | A/G | 0.439641 | 0.162899 | intron-variant | PHF14 | GRCh38.p7 | 7:11021696 | AATATAAAGATACAC[A/G]TCTTCAACAAGCAGC | 9678 |
| rs1681283 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11068920 | atgcaagattcctaa[A/G]gtcgaaactacatca | 9678 |
| rs1681284 | snp | C/T | 0.474723 | 0.109542 | intron-variant | PHF14 | GRCh38.p7 | 7:10989047 | GGGCTGACAAATGGC[C/T]GGCAAATAAAACTGA | 9678 |
| rs1681285 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:10988434 | GTGGAATTAAAATTA[A/T]TCAGCCCTGGAAAAA | 9678 |
| rs1681286 | snp | C/T | 0.462144 | 0.132269 | intron-variant | PHF14 | GRCh38.p7 | 7:10988127 | AAATATTTCCCTAAC[C/T]AAATGGCTAGCAGAC | 9678 |
| rs1681290 | snp | A/G | 0.498109 | 0.0306926 | intron-variant | PHF14 | GRCh38.p7 | 7:10991692 | GTTTCTTTAAAGGTC[A/G]GTGTTCTGGTATTGT | 9678 |
| rs1681291 | snp | A/G | 0.497803 | 0.033074 | intron-variant | PHF14 | GRCh38.p7 | 7:10991721 | GTATTTTATGGTACT[A/G]tttcttgtttgtttt | 9678 |
| rs1681292 | snp | A/G | 0.43978 | 0.162738 | intron-variant | PHF14 | GRCh38.p7 | 7:10991785 | ttttttttggtagag[A/G]cagggttttgctatg | 9678 |
| rs1681293 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020605 | gatcacttaagctca[A/G]gagtttgagaccagc | 9678 |
| rs1681302 | snp | C/G | 0.41275 | 0.189769 | intron-variant | PHF14 | GRCh38.p7 | 7:10978907 | TTGAAGACAGCCAAT[C/G]AGTCAACACAACTCA | 9678 |
| rs1681305 | snp | C/T | 0.404209 | 0.196773 | intron-variant | PHF14 | GRCh38.p7 | 7:10977213 | ATTTAATCTCCTATT[C/T]GTAAGTAGGGCTGGG | 9678 |
| rs1681309 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11075366 | atttggcccacggat[C/T]tgccggctgtacaag | 9678 |
| rs1681310 | snp | C/T | 0.410399 | 0.191761 | intron-variant | PHF14 | GRCh38.p7 | 7:10986797 | TTCCCATTTTCAAGA[C/T]TTTGAAACTAAAGTT | 9678 |
| rs1681311 | snp | C/T | 0.45866 | 0.137698 | intron-variant | PHF14 | GRCh38.p7 | 7:10987188 | GTCCTAAAAAAAGGT[C/T]AGTTCTGTAACATTT | 9678 |
| rs1681312 | snp | C/T | 0.410399 | 0.191761 | intron-variant | PHF14 | GRCh38.p7 | 7:10987342 | ATTTTACAGGAAATG[C/T]GCTGGAATTTCCTTG | 9678 |
| rs1833011 | snp | C/T | 0.490398 | 0.0686206 | intron-variant | PHF14 | GRCh38.p7 | 7:11091683 | GCAACCTCTGCCTCC[C/T]GGGTTCAGGTGATTC | 9678 |
| rs2020391 | snp | C/G | 0.454904 | 0.143228 | intron-variant | PHF14 | GRCh38.p7 | 7:11081712 | cgtgccaccacaccc[C/G]gctaattttttgtat | 9678 |
| rs2108111 | snp | C/T | 0.438246 | 0.16451 | intron-variant | PHF14 | GRCh38.p7 | 7:11034042 | GAAGACATAAAAACC[C/T]GGATACAAATCTTGG | 9678 |
| rs2108112 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11032742 | ATGGGTGAAGGAGAC[C/T]TAAAAGATGCCAGAA | 9678 |
| rs2108114 | snp | C/T | 0.437683 | 0.165152 | intron-variant | PHF14 | GRCh38.p7 | 7:11057398 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAATAA | 9678 |
| rs2110376 | snp | G/T | 0.499722 | 0.0117779 | intron-variant | PHF14 | GRCh38.p7 | 7:10990005 | AGAGAACTCTATTAA[G/T]TAGGTCTCTATCAAG | 9678 |
| rs2110377 | snp | G/T | 0.234401 | 0.249513 | intron-variant | PHF14 | GRCh38.p7 | 7:10989998 | TCTATTAAGTAGGTC[G/T]CTATCAAGAAATATC | 9678 |
| rs2158780 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11045290 | GAAATTTGATCACTA[A/G]AAACAAGGAGAAATT | 9678 |
| rs2160059 | snp | C/T | 0.189261 | 0.242509 | intron-variant | PHF14 | GRCh38.p7 | 7:10990121 | GCATTATCAAACTAC[C/T]GTAAGACAGATCCAT | 9678 |
| rs2190293 | snp | C/T | 0.493658 | 0.0559517 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104451 | TTCTCCTTATAGTAG[C/T]TGGACCGATTATGGA | 9678 |
| rs2190294 | snp | C/T | 0.436408 | 0.16659 | intron-variant | PHF14 | GRCh38.p7 | 7:11051110 | GAGGCTGCAGTGAGC[C/T]ATGATCTCAACACTG | 9678 |
| rs2190295 | snp | G/T | 0.441158 | 0.161117 | intron-variant | PHF14 | GRCh38.p7 | 7:11050834 | AAAAAGGTCATATTA[G/T]TTGGTGGCCCCTACT | 9678 |
| rs2214858 | snp | A/G | 0.437259 | 0.165632 | intron-variant | PHF14 | GRCh38.p7 | 7:11050919 | TTTTAATTGTAGTCA[A/G]TGACAACTTGTGCTG | 9678 |
| rs2301959 | snp | C/G | 0.497959 | 0.0318836 | intron-variant | PHF14 | GRCh38.p7 | 7:11061679 | TAACTAATTTTGCAA[C/G]TGCCTAACCTAAGCA | 9678 |
| rs2301960 | snp | C/T | 0.0221176 | 0.102809 | intron-variant | PHF14 | GRCh38.p7 | 7:11028840 | GAACATGTTCACCAA[C/T]TATGGGTTTAAATAA | 9678 |
| rs2301961 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11023147 | ATAGAAGAATTTATG[C/T]ATTATTGGCTTTCTA | 9678 |
| rs2301962 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11022793 | ACAAACATATAAAAC[A/G]CTTGCCATCTCAAAA | 9678 |
| rs2353338 | snp | C/T | 0.255503 | 0.249939 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959648 | TTCCAGGTGCCAGCA[C/T]AGGCACCGGCTCTCT | 9678 |
| rs2353339 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11001666 | TTTTAATTTCAATTC[C/T]ACTTGTTCATTGCTT | 9678 |
| rs2353340 | snp | A/G | 0.487572 | 0.0778428 | intron-variant | PHF14 | GRCh38.p7 | 7:11035636 | CTGTGCTTTCTTTGT[A/G]TAGGATATAGCAGAT | 9678 |