SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs764828 | snp | G/T | 0.442385 | 0.15965 | intron-variant | LONRF2 | GRCh38.p7 | 2:100292172 | AATCTTCAGGGCGCC[G/T]CCAGTTTCACCATGC | 164832 |
rs764829 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | LONRF2 | GRCh38.p7 | 2:100292046 | CTTTAGTTTGGGGGA[C/T]GTGTAGTAAAGCTGC | 164832 |
rs920269 | snp | C/T | 0.49907 | 0.0215454 | intron-variant | LONRF2 | GRCh38.p7 | 2:100301901 | ATCATTTCAACTTGT[C/T]AAAATAATATTGCAT | 164832 |
rs920270 | snp | A/G | 0.480853 | 0.0959518 | intron-variant | LONRF2 | GRCh38.p7 | 2:100301499 | GTGCGCATTGCTGCA[A/G]GGCCATGGATTCTAG | 164832 |
rs995110 | snp | C/T | 0.17461 | 0.238362 | intron-variant | LONRF2 | GRCh38.p7 | 2:100314040 | ctttatttatatatg[C/T]cagaaacatttgggg | 164832 |
rs995132 | snp | A/T | 0.127254 | 0.217792 | intron-variant | LONRF2 | GRCh38.p7 | 2:100317296 | TAGGAAGGTAAAATT[A/T]AAAAAAAGCTATAGT | 164832 |
rs995133 | snp | G/T | 0.208474 | 0.246527 | intron-variant | LONRF2 | GRCh38.p7 | 2:100317241 | AATCCAAAAGAAAAT[G/T]GGAGGGAAGAATAGA | 164832 |
rs1437967 | snp | C/G | 0.44755 | 0.153212 | intron-variant | LONRF2 | GRCh38.p7 | 2:100312610 | TTTATGAAATTTGGA[C/G]TTCAGTTAAAGCACC | 164832 |
rs1530028 | snp | G/T | 0.486984 | 0.079614 | intron-variant | LONRF2 | GRCh38.p7 | 2:100311448 | ACAGGATATGAGATC[G/T]CCATTCTCACACAGG | 164832 |
rs1866198 | snp | G/T | 0.499154 | 0.0205497 | intron-variant | LONRF2 | GRCh38.p7 | 2:100301277 | CCTGCCCCCACCAAT[G/T]CCATTCCCTGGTTCT | 164832 |
rs1946799 | snp | G/T | 0.480931 | 0.0957637 | intron-variant | LONRF2 | GRCh38.p7 | 2:100304674 | attgtaccactgcac[G/T]ccagcctggacgagc | 164832 |
rs1967339 | snp | G/T | 0.498323 | 0.0289051 | intron-variant | LONRF2 | GRCh38.p7 | 2:100308193 | tttagtagagacagg[G/T]tttcactgtgttagc | 164832 |
rs1967340 | snp | A/G | 0.4983 | 0.0291038 | intron-variant | LONRF2 | GRCh38.p7 | 2:100308135 | tgatctgcctgcctc[A/G]gcctcccaaagtgct | 164832 |
rs1967341 | snp | A/G | 0.498323 | 0.0289051 | intron-variant | LONRF2 | GRCh38.p7 | 2:100308097 | caggcgtgagccacc[A/G]cgcccggccTCCCTC | 164832 |
rs2033747 | snp | C/T | 0.44333 | 0.158505 | intron-variant | LONRF2 | GRCh38.p7 | 2:100300019 | GTGTATGCCCCCCCC[C/T]TTTTTTTTCCAAAGA | 164832 |
rs2033748 | snp | C/T | 0.42895 | 0.174576 | synonymous-codon | LONRF2 | GRCh38.p7 | 2:100299844 | ACTGGGTCTACACTT[C/T]GAAGAGGATAAAAAG | 164832 |
rs2033749 | snp | A/G | 0.35207 | 0.228214 | intron-variant | LONRF2 | GRCh38.p7 | 2:100299589 | ATTATATCAGCTCTA[A/G]GATTATAGAGCATTT | 164832 |
rs2309816 | snp | C/T | 0.0287284 | 0.116357 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100280997 | CCCAAGTAATTTAAG[C/T]GGTGGGGCACAAAAG | 164832 |
rs2309817 | snp | A/T | 0.283421 | 0.247756 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100281212 | CCTTGATGATTCAAA[A/T]GTCCTGTGGTAAGAC | 164832 |
rs2309818 | snp | G/T | 0.43655 | 0.16643 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100282172 | ACATAACATGCCGAA[G/T]GAGAAGACTCAGAAA | 164832 |
rs2309819 | snp | A/G | 0.436408 | 0.16659 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100283203 | CCTGGTCTGATCACC[A/G]TAAAACTTTCTTTCA | 164832 |
rs2309820 | snp | C/T | 0.436692 | 0.166271 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100283214 | CACCGTAAAACTTTC[C/T]TTCAAAAAAATAAAG | 164832 |
rs2309821 | snp | C/T | 0.337614 | 0.234145 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100283842 | GCCTAAGCGTAGTTT[C/T]GGTTAGCCTGTGTTC | 164832 |
rs2309822 | snp | A/G | 0.283421 | 0.247756 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100283944 | CTGGCAGAGCCAGAT[A/G]CTGACTGGGAAGTGA | 164832 |
rs2309823 | snp | C/T | 0.283421 | 0.247756 | intron-variant | LONRF2 | GRCh38.p7 | 2:100285095 | AGCCGATCATAAACT[C/T]GTTCTCAATATTCTT | 164832 |
rs2309824 | snp | A/G | 0.283421 | 0.247756 | intron-variant | LONRF2 | GRCh38.p7 | 2:100285199 | AATGTGCAGGATGCC[A/G]ATAAGAGCTGGGAGG | 164832 |
rs2309825 | snp | A/C | 0.341137 | 0.235378 | intron-variant | LONRF2 | GRCh38.p7 | 2:100288639 | TCCAGTCAATTACAA[A/C]GCCAACCCCACAAGC | 164832 |
rs2309826 | snp | A/C | 0.436408 | 0.16659 | intron-variant | LONRF2 | GRCh38.p7 | 2:100288812 | acgagtggttcattt[A/C]tttttattgacaggt | 164832 |
rs2871342 | snp | A/G | | | intron-variant | LONRF2 | GRCh38.p7 | 2:100300011 | ACTAGAAATCTTTGG[A/G]AAAAAAAAGGGGGGG | 164832 |
rs3039612 | in-del | -/TTTT | 0 | 0 | intron-variant | LONRF2 | GRCh38.p7 | 2:100304641 | ttttttttttttttt[-/TTTT]gagacagagtcttgc | 164832 |
rs3039614 | in-del | -/TTTT | 0 | 0 | intron-variant | LONRF2 | GRCh38.p7 | 2:100304812 | ttttttttttttttt[-/TTTT]agttgagatggggtt | 164832 |
rs3039770 | in-del | -/TCTG | 0.35445 | 0.227135 | intron-variant | LONRF2 | GRCh38.p7 | 2:100300154 | TATCTTCATATGCAA[-/TCTG]TCTGTCTGTCTATCT | 164832 |
rs3748928 | snp | A/G | 0.41441 | 0.188333 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100283917 | CCAGATGGTAAAGGC[A/G]TGCTTTAGTGTGTAG | 164832 |
rs4069857 | in-del | -/AATTTTTT/TTT | 0 | 0 | intron-variant | LONRF2 | GRCh38.p7 | 2:100304321 | CCTGGCTAATTTTTT[-/AATTTTTT/TTT]TGTAGACTTGGGGTC | 164832 |
rs4264577 | snp | C/T | 0.498206 | 0.0298983 | intron-variant | LONRF2 | GRCh38.p7 | 2:100314200 | CATTTCTTAAGTTGT[C/T]GTACAAACTTATGCT | 164832 |
rs4268944 | snp | C/T | 0.467946 | 0.122472 | intron-variant | LONRF2 | GRCh38.p7 | 2:100297366 | ATGGTCTCTATCTCC[C/T]GCCCTTGTGACCCAC | 164832 |
rs4314007 | snp | A/C | 0.276534 | 0.248588 | intron-variant | LONRF2 | GRCh38.p7 | 2:100297368 | GGTCTCTATCTCCCG[A/C]CCTTGTGACCCACCC | 164832 |
rs4561689 | snp | C/T | 0.233235 | 0.249437 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100275514 | CTCCGGCCATGCGGC[C/T]GGTGAGAGGCACCCT | 164832 |
rs4622752 | snp | A/G | 0.414245 | 0.188477 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100275556 | TGACAGCCGCCAAAA[A/G]GTTTAAATGTTGCTT | 164832 |
rs4635546 | snp | A/G | 0.480931 | 0.0957637 | intron-variant | LONRF2 | GRCh38.p7 | 2:100304663 | gagtcttgctcgctc[A/G]tccaggctggcgtgc | 164832 |
rs4850925 | snp | C/T | 0.467744 | 0.122832 | intron-variant | LONRF2 | GRCh38.p7 | 2:100294116 | ACTTGGACTTTGTTA[C/T]GTAACGGGAGCCACT | 164832 |
rs4851282 | snp | C/T | 0.318896 | 0.240319 | downstream-variant-500B | LONRF2 | GRCh38.p7 | 2:100272924 | TCCACATCTGCACTG[C/T]GTTGAATACTGTTCC | 164832 |
rs4851283 | snp | C/G | 0.25214 | 0.249991 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100278340 | ttcctataaatcttg[C/G]atcttatccccaccc | 164832 |
rs4851284 | snp | C/T | 0.376195 | 0.215812 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100278425 | cagggctcccacagg[C/T]cgtgcagctgctcat | 164832 |
rs4851285 | snp | A/G | 0.270892 | 0.249126 | intron-variant | LONRF2 | GRCh38.p7 | 2:100291136 | GAGAGAGTAGGCAGA[A/G]CCCAGGAAGAGACAC | 164832 |
rs4851286 | snp | C/T | 0.385168 | 0.210309 | intron-variant | LONRF2 | GRCh38.p7 | 2:100299167 | CCCATTACACTTTGG[C/T]ATACATTTCAGAAAG | 164832 |
rs4851287 | snp | A/G | 0.426389 | 0.177163 | missense, intron-variant | LONRF2 | GRCh38.p7 | 2:100299310 | TTTGGGCTCCTTTGA[A/G]GTGAGAGATCTGAAT | 164832 |
rs4851288 | snp | C/T | 0.44858 | 0.151875 | intron-variant | LONRF2 | GRCh38.p7 | 2:100303989 | ttccaagattctttt[C/T]gtttttctttaatct | 164832 |
rs4851289 | snp | C/T | | | intron-variant | LONRF2 | GRCh38.p7 | 2:100304163 | ATTTCCTTTTTTTTT[C/T]TTTTTTAGAGACAGG | 164832 |
rs4851290 | snp | C/T | | | intron-variant | LONRF2 | GRCh38.p7 | 2:100304164 | TTTCCTTTTTTTTTC[C/T]TTTTTAGAGACAGGG | 164832 |
rs4851292 | snp | A/G | 0.495521 | 0.0471118 | intron-variant | LONRF2 | GRCh38.p7 | 2:100308299 | TGCCTAGCCTAGGGG[A/G]CAGAGAGACACTCCG | 164832 |
rs4851293 | snp | A/T | 0.498277 | 0.0293024 | intron-variant | LONRF2 | GRCh38.p7 | 2:100308644 | AGTAAACCTTTCCAA[A/T]CAAAACACAGAGACT | 164832 |
rs4851294 | snp | C/T | 0.498459 | 0.0277128 | upstream-variant-2KB | LONRF2 | GRCh38.p7 | 2:100324647 | ttatcctcagcaaac[C/T]aacacaggaacagaa | 164832 |
rs5832905 | in-del | -/T | 0.498632 | 0.0261223 | intron-variant | LONRF2 | GRCh38.p7 | 2:100307942 | AATTGGAGTCTAAAC[-/T]TTTTTTTTTAGGGAA | 164832 |
rs5832906 | in-del | -/A | 0.486 | 0.0824865 | intron-variant | LONRF2 | GRCh38.p7 | 2:100311357 | CCAAAGGAGATTTGG[-/A]AAAAAAAAATTTTGG | 164832 |
rs6542923 | snp | C/T | 0.306431 | 0.243548 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100276054 | CAATTAGAAATCCAA[C/T]GCTTATACACTAAAA | 164832 |
rs6542924 | snp | A/C | 0.256897 | 0.249905 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100276651 | aaacctggaaaaaaa[A/C]aagtgtgcctcatgg | 164832 |
rs6542925 | snp | C/T | 0.416382 | 0.186593 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100281619 | AAATACAGAACAGCA[C/T]GTATTGTTCCTCAAG | 164832 |
rs6542926 | snp | C/T | 0.271432 | 0.24908 | intron-variant | LONRF2 | GRCh38.p7 | 2:100297273 | AGCTGGGACTACAGG[C/T]GCCCGCCACCATACC | 164832 |
rs6542927 | snp | C/G/T | 0.112983 | 0.209108 | intron-variant | LONRF2 | GRCh38.p7 | 2:100301916 | gacaagttgaaatga[C/G/T]ggccaaaaaccaatg | 164832 |
rs6542928 | snp | A/G | 0.141258 | 0.225111 | intron-variant | LONRF2 | GRCh38.p7 | 2:100302162 | GGTACATTAGAACAC[A/G]TCCAGAAGAGGAAAT | 164832 |
rs6716636 | snp | C/G | 0.485118 | 0.0849685 | upstream-variant-2KB | LONRF2 | GRCh38.p7 | 2:100323605 | CTTATATTTGAGGGT[C/G]ATTTATCCATCAAAT | 164832 |
rs6725052 | snp | A/G | 0.486332 | 0.08153 | intron-variant | LONRF2 | GRCh38.p7 | 2:100319355 | Aaacgtttaaattag[A/G]tctaatatatataca | 164832 |
rs6727252 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100278684 | GGAGACCCCACGTCT[C/T]ACATCCCAGAAGACA | 164832 |
rs6727379 | snp | C/T | 0.149665 | 0.228982 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100278809 | CCCTAGCGATGTCCA[C/T]GGGCTACCTCTCCTG | 164832 |
rs6727623 | snp | A/T | 0.387642 | 0.208697 | intron-variant | LONRF2 | GRCh38.p7 | 2:100300262 | GCTTTATTTTTTTTT[A/T]AATTACACTTTAAGT | 164832 |
rs6731549 | snp | G/T | 0.485118 | 0.0849685 | upstream-variant-2KB | LONRF2 | GRCh38.p7 | 2:100323475 | AGCTGTCTACCTAAC[G/T]TAATTGATAACAGTG | 164832 |
rs6732285 | snp | A/C | 0.151334 | 0.229706 | upstream-variant-2KB | LONRF2 | GRCh38.p7 | 2:100324297 | ggtaaaggtaaaagg[A/C]tggaaaaagatgttc | 164832 |
rs6732839 | snp | C/T | 0.0941369 | 0.195465 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100274941 | AACGTGGGTACATTT[C/T]GATACCACGGGCACA | 164832 |
rs6734881 | snp | C/T | 0.140242 | 0.224618 | intron-variant | LONRF2 | GRCh38.p7 | 2:100301480 | ATGGTTCAAGGTGAG[C/T]GCGCTAGAATCCATG | 164832 |
rs6736666 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | LONRF2 | GRCh38.p7 | 2:100306012 | tcctgcctcagcctc[C/T]ggagtagctgggatt | 164832 |
rs6743347 | snp | A/C | 0.111224 | 0.207945 | intron-variant | LONRF2 | GRCh38.p7 | 2:100304098 | tataatgtgttatta[A/C]ccctacctagaaatt | 164832 |
rs6754867 | snp | A/G | 0.38555 | 0.210062 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100278619 | ctgtttcaaccaaac[A/G]cggcaaatgctggga | 164832 |
rs6755791 | snp | A/G | 0.435837 | 0.167226 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100279410 | gcctaagggactcct[A/G]tatctccacgtgtct | 164832 |
rs7421891 | snp | A/G | 0.436265 | 0.166749 | intron-variant | LONRF2 | GRCh38.p7 | 2:100285704 | CTCTGATGGAGGAAG[A/G]AAGCCGAGGAATGCC | 164832 |
rs7425449 | snp | A/G | 0.48692 | 0.0798058 | intron-variant | LONRF2 | GRCh38.p7 | 2:100311931 | ACACTGCTGGACTCA[A/G]AATACTAAGAAATTT | 164832 |
rs7425797 | snp | C/T | 0.48692 | 0.0798058 | intron-variant | LONRF2 | GRCh38.p7 | 2:100311875 | GTACCGAATTATCCT[C/T]ATGGTCCTAGTATAA | 164832 |
rs7556910 | snp | C/T | 0.467642 | 0.123012 | intron-variant | LONRF2 | GRCh38.p7 | 2:100292534 | TGGCTTCAAGAAATA[C/T]ATGTTCTGTGGTTTA | 164832 |
rs7557575 | snp | A/G | 0.43655 | 0.16643 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100280650 | GCTGGGTGTGGTGGC[A/G]CGTGCCTGTAATCCC | 164832 |
rs7557660 | snp | A/G | 0.43655 | 0.16643 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100280752 | CGCCATTGCACTCCA[A/G]CCTGGGTGACAGAGT | 164832 |
rs7557977 | snp | A/G | 0.43655 | 0.16643 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100281111 | AGTATTTCGATGGTA[A/G]CAACTGCCAATTTTC | 164832 |
rs7558887 | snp | G/T | 0.0618563 | 0.164627 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100275971 | ATAGGCTATTTTAAC[G/T]CAAATATATAATAAA | 164832 |
rs7559464 | snp | A/G | 0.304688 | 0.243945 | intron-variant | LONRF2 | GRCh38.p7 | 2:100289861 | ctttggggctactac[A/G]ctttggttgaggtgg | 164832 |
rs7562372 | snp | C/T | 0.301932 | 0.244547 | intron-variant | LONRF2 | GRCh38.p7 | 2:100289869 | ctactacactttggt[C/T]gaggtgggaggactg | 164832 |
rs7563199 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | LONRF2 | GRCh38.p7 | 2:100299581 | AACATCTAAAATGCT[C/T]TATAATCTTAGAGCT | 164832 |
rs7563954 | snp | A/C/T | 0.0551013 | 0.156571 | intron-variant | LONRF2 | GRCh38.p7 | 2:100300298 | ggtacatgtgtacaa[A/C/T]gtgcaggtttgttac | 164832 |
rs7569170 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100284082 | TTGTTTTCCAACTAT[A/G]GGCTCCATTCAGACT | 164832 |
rs7571306 | snp | C/G | 0.499801 | 0.00998203 | intron-variant | LONRF2 | GRCh38.p7 | 2:100289622 | tttatatttttaata[C/G]agccagggtttcacc | 164832 |
rs7571711 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | LONRF2 | GRCh38.p7 | 2:100296524 | CTTGGGATGGCTCCA[C/T]GTATTTCCAACACAC | 164832 |
rs7573189 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | LONRF2 | GRCh38.p7 | 2:100298464 | ACCTGTGGTCAGAAA[C/T]GATCAAGTCTTCAAT | 164832 |
rs7573523 | snp | C/G | 0.40595 | 0.195396 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100277652 | aagagaatgttgctg[C/G]ttcccatcttttagc | 164832 |
rs7575849 | snp | A/G | 0.077417 | 0.180873 | intron-variant | LONRF2 | GRCh38.p7 | 2:100291256 | AGCTGCACTCACAAA[A/G]GGAGTTTGCATCACA | 164832 |
rs7580252 | snp | G/T | 0.032377 | 0.123046 | intron-variant | LONRF2 | GRCh38.p7 | 2:100286895 | TAACAGAATTATAAA[G/T]GAAAAAGGGAGGGCA | 164832 |
rs7582180 | snp | A/G | 0.3512 | 0.228601 | intron-variant | LONRF2 | GRCh38.p7 | 2:100296001 | AATCTTCCCAACATT[A/G]TGTTTTTTTCTAGCT | 164832 |
rs7582424 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | LONRF2 | GRCh38.p7 | 2:100320945 | GGCTAGAGCCGGAGC[A/G]TTTGACGTGATTACA | 164832 |
rs7588623 | snp | C/T | 0.271432 | 0.24908 | intron-variant | LONRF2 | GRCh38.p7 | 2:100296899 | GCAAAGTCATTTATG[C/T]GCATGATGTGACTCC | 164832 |
rs7590008 | snp | C/T | 0.40595 | 0.195396 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100277653 | agagaatgttgctgc[C/T]tcccatcttttagcc | 164832 |
rs7595580 | snp | A/G | 0.273049 | 0.248935 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100280502 | GGAGATGGGCCGGGC[A/G]CGGTGGCTCACGCCT | 164832 |
rs7599212 | snp | C/T | 0.495963 | 0.0447464 | intron-variant | LONRF2 | GRCh38.p7 | 2:100290116 | tgactcaaaaataaa[C/T]aaatagataaataaa | 164832 |
rs7601442 | snp | A/T | 0.436265 | 0.166749 | utr-variant-3-prime | LONRF2 | GRCh38.p7 | 2:100280889 | ATCACCCACATTTAT[A/T]TTCTTCTAATTTGCT | 164832 |