SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3719 | snp | C/T | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180008118 | ACTTCCCCCATAGAT[C/T]CCTGACAATGTGCTG | 55819 |
rs9202 | snp | A/T | 0 | 0 | missense | RNF130 | GRCh38.p7 | 5:179970434 | CAGGGCCTTCAATAT[A/T]TTAAGTTTGCACATA | 55819 |
rs14755 | snp | A/T | 0 | 0 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955597 | GTAAATGATGCACAA[A/T]AATAGGTTCTTTTTT | 55819 |
rs26073 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | RNF130 | GRCh38.p7 | 5:179974287 | ATACGTTCATCCACG[C/T]GGCAACTCCACTTCT | 55819 |
rs27010 | snp | A/C | 0.496279 | 0.0429702 | intron-variant | RNF130 | GRCh38.p7 | 5:179963003 | CAGCGGGTCTTTCAA[A/C]CTGCTTCTTTCCTGC | 55819 |
rs27011 | snp | C/T | 0.499203 | 0.0199521 | intron-variant | RNF130 | GRCh38.p7 | 5:179973446 | GCTACAACAGTCTGG[C/T]GCTCGGCAAACCACC | 55819 |
rs27012 | snp | A/C | 0.257454 | 0.249889 | intron-variant | RNF130 | GRCh38.p7 | 5:179975211 | GCGTCCCAAGGCAGA[A/C]GGAATTCTGTAAGCG | 55819 |
rs27013 | snp | G/T | 0.499913 | 0.00658888 | intron-variant | RNF130 | GRCh38.p7 | 5:179975275 | TGGCATCTGCTGGGG[G/T]GAGGCTTGAAGAGCC | 55819 |
rs27014 | snp | A/C | 0.495634 | 0.0465208 | intron-variant | RNF130 | GRCh38.p7 | 5:179976258 | AAGTTCCCAGAATAA[A/C]CTACTTTAGGCCGAG | 55819 |
rs27015 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976707 | TTTTTTTTTTTTTTT[A/T]AAAAACAGATCTTCC | 55819 |
rs27016 | snp | A/C | 0.494609 | 0.0516363 | intron-variant | RNF130 | GRCh38.p7 | 5:179977008 | GCTGTTTCCAGGGCA[A/C]CCAGGCACAGGCGAG | 55819 |
rs27017 | snp | A/G | 0.48546 | 0.0840147 | intron-variant | RNF130 | GRCh38.p7 | 5:179977375 | CTCACTGAAGGGCTT[A/G]GAGATGTAGTCTAAG | 55819 |
rs27018 | snp | A/G | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:179978144 | GATGCCCACCCTGAA[A/G]AGGAGGCATACAAAG | 55819 |
rs27019 | snp | C/G | 0.494896 | 0.0502606 | intron-variant | RNF130 | GRCh38.p7 | 5:179978399 | AGCAAGTGTTATAAA[C/G]TGAAAAATGATTAAA | 55819 |
rs28011 | snp | C/T | 0.405379 | 0.195851 | intron-variant | RNF130 | GRCh38.p7 | 5:179980229 | AAATAAAAACAGATA[C/T]TAAGTGTAAGATCTC | 55819 |
rs32469 | snp | A/C | 0.49423 | 0.0534032 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919897 | CACCTGTACTCCACG[A/C]GGGTAGGAAGCTTCT | 55819 |
rs36750 | snp | C/G | 0.444444 | 0.157135 | intron-variant | RNF130 | GRCh38.p7 | 5:179968493 | caacatggggaaacc[C/G]catctctactaaaaa | 55819 |
rs42414 | snp | G/T | 0.415563 | 0.18732 | intron-variant | RNF130 | GRCh38.p7 | 5:179941681 | TTCTCTAGGATCTTT[G/T]CTCCTCAAGTCATCA | 55819 |
rs149558 | snp | C/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179927004 | ataacagtcaacaca[C/G]aagacttccgtgacc | 55819 |
rs152232 | snp | A/G | 0.474634 | 0.109726 | intron-variant | RNF130 | GRCh38.p7 | 5:179926282 | CAAAAGAAAATTTTA[A/G]CAGTGGCCCATGATG | 55819 |
rs152236 | snp | C/T | 0.490943 | 0.0666801 | intron-variant | RNF130 | GRCh38.p7 | 5:179922987 | gcaaatatttcctcc[C/T]agtctgtgacttgcc | 55819 |
rs152237 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | RNF130 | GRCh38.p7 | 5:179923061 | aattttggtaagatc[A/G]aatttattgattttt | 55819 |
rs152238 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | RNF130 | GRCh38.p7 | 5:179923140 | cactaagattttctc[A/G]tacatgttcatctag | 55819 |
rs152253 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | RNF130 | GRCh38.p7 | 5:179925982 | GAAAGGGGGAGCAGC[A/G]GAGGCGAGGCAGGGA | 55819 |
rs155574 | snp | C/T | 0.441705 | 0.160466 | intron-variant | RNF130 | GRCh38.p7 | 5:179927665 | ttgatcttggctcac[C/T]gcaagctctgcctcc | 55819 |
rs155575 | snp | C/G | 0.49706 | 0.0382258 | intron-variant | RNF130 | GRCh38.p7 | 5:179953854 | aaaatatttgcaaat[C/G]acctatctgataaag | 55819 |
rs155576 | snp | C/T | 0.478768 | 0.100824 | intron-variant | RNF130 | GRCh38.p7 | 5:179956815 | CATAGCCCTGAGCTC[C/T]GGCGGGGCCAGACCA | 55819 |
rs155577 | snp | G/T | 0.464947 | 0.127663 | intron-variant | RNF130 | GRCh38.p7 | 5:179945108 | TAGTCAGTTATCACT[G/T]TATTTTTTTAACCAT | 55819 |
rs155784 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | RNF130 | GRCh38.p7 | 5:179927966 | gactctgtctgacac[A/G]caaatgtctgacatt | 55819 |
rs155785 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179927716 | gcctcagtctcctga[A/G]tatgggactacaggt | 55819 |
rs156096 | snp | A/G | 0.441432 | 0.160792 | intron-variant | RNF130 | GRCh38.p7 | 5:179929450 | tctttccatttccac[A/G]taaattctaggatca | 55819 |
rs156097 | snp | A/G | 0.317451 | 0.240729 | intron-variant | RNF130 | GRCh38.p7 | 5:179946655 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 55819 |
rs156098 | snp | A/T | 0.0482946 | 0.147699 | intron-variant | RNF130 | GRCh38.p7 | 5:179945381 | GCTGAGTGGTACCTG[A/T]GCAAGGCGTTCCTAT | 55819 |
rs156099 | snp | C/T | 0.104504 | 0.2033 | intron-variant | RNF130 | GRCh38.p7 | 5:179943614 | aagatagatgtgtca[C/T]tatttcatacacaga | 55819 |
rs156100 | snp | A/G | 0.451359 | 0.148171 | intron-variant | RNF130 | GRCh38.p7 | 5:179943127 | TTCAACCAGAGAGGC[A/G]GAGGTTGCAGTGAGC | 55819 |
rs166032 | snp | C/T | 0.497776 | 0.0332724 | intron-variant | RNF130 | GRCh38.p7 | 5:179937627 | aaatggtttagccat[C/T]gtgtaaaagagtttg | 55819 |
rs171580 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179937126 | TATCATCAAAACGAA[A/G]TATCATCAAAACGAA | 55819 |
rs173560 | snp | C/T | 0.454664 | 0.143571 | intron-variant | RNF130 | GRCh38.p7 | 5:179937186 | GAAGTATcatcaaaa[C/T]gaaatatcatcaaaa | 55819 |
rs173562 | snp | G/T | 0.494609 | 0.0516363 | intron-variant | RNF130 | GRCh38.p7 | 5:179981358 | GAAAAGGCAGATGCC[G/T]CTCCTGACGGAGCAA | 55819 |
rs182085 | snp | A/G | 0.498832 | 0.0241331 | intron-variant | RNF130 | GRCh38.p7 | 5:179926626 | gagtcttgttctgtc[A/G]cccaggctggagtgc | 55819 |
rs183849 | snp | A/C | 0 | 0 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954751 | CCTTTCAGCCCCCTG[A/C]TGATTTGAGCATGAC | 55819 |
rs185076 | snp | C/G | 0.494733 | 0.0510469 | intron-variant | RNF130 | GRCh38.p7 | 5:179995047 | ccccagtagcaggca[C/G]aagcactggctctga | 55819 |
rs190328 | snp | C/G | 0.495855 | 0.045338 | intron-variant | RNF130 | GRCh38.p7 | 5:179971318 | CAGGACAGACGTTCA[C/G]GGCAGCTTTGGAAGA | 55819 |
rs190604 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF130 | GRCh38.p7 | 5:179946256 | AGTGACTCTTCACTG[C/T]CCATGTGTATAGGGT | 55819 |
rs193718 | snp | C/T | 0.461068 | 0.133979 | intron-variant | RNF130 | GRCh38.p7 | 5:179982108 | ttttgctgtaacagt[C/T]tgcaacatcatgagt | 55819 |
rs193720 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997268 | tgccttagcctcctg[A/T]gtagctgggattaca | 55819 |
rs248216 | snp | C/T | 0.450985 | 0.148678 | intron-variant | RNF130 | GRCh38.p7 | 5:179965313 | TGCCAGCGGGAGGCA[C/T]TGTGGTTGCTACGGT | 55819 |
rs248221 | snp | C/T | 0.242201 | 0.249878 | intron-variant | RNF130 | GRCh38.p7 | 5:179969502 | TCTAAAGGTAGGTAC[C/T]GGAATGAAGAAAAAT | 55819 |
rs248227 | snp | A/G | 0.491629 | 0.0641526 | intron-variant | RNF130 | GRCh38.p7 | 5:179930848 | gttcaagaccagccc[A/G]gtaaacataacaaaa | 55819 |
rs248228 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | RNF130 | GRCh38.p7 | 5:179930424 | tgttaaatttactta[C/T]tcattttaagagctg | 55819 |
rs248229 | snp | C/G | 0.499575 | 0.0145705 | intron-variant | RNF130 | GRCh38.p7 | 5:179929461 | ccacgtaaattctag[C/G]atcaggctgggcgtg | 55819 |
rs248230 | snp | C/T | 0.49975 | 0.0111793 | intron-variant | RNF130 | GRCh38.p7 | 5:179927082 | CTAACAAAAAAGATT[C/T]GGTCATTTCCACTTC | 55819 |
rs248232 | snp | C/T | 0.430285 | 0.173197 | intron-variant | RNF130 | GRCh38.p7 | 5:179923387 | ggcactattctgttc[C/T]agcaatccatttgtc | 55819 |
rs248257 | snp | G/T | 0.494855 | 0.0504572 | intron-variant | RNF130 | GRCh38.p7 | 5:179981536 | ttaccagtactttac[G/T]tctatttttcatctg | 55819 |
rs248258 | snp | C/T | 0.494896 | 0.0502606 | intron-variant | RNF130 | GRCh38.p7 | 5:179980987 | CACAGAGGAGGCGAC[C/T]AGGAGGGGTGGGGCG | 55819 |
rs248315 | snp | A/G | 0.492533 | 0.0606443 | intron-variant | RNF130 | GRCh38.p7 | 5:179994883 | tatctttgttaacca[A/G]gagaagtacttaagt | 55819 |
rs248316 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | RNF130 | GRCh38.p7 | 5:179996519 | aacttgttaagagtt[C/T]atatcatgaagccac | 55819 |
rs248317 | snp | C/T | 0.494187 | 0.0535994 | intron-variant | RNF130 | GRCh38.p7 | 5:180003266 | CTTCTGGCTCGGTGA[C/T]GAGCCGTGTGAGAGC | 55819 |
rs248318 | snp | C/T | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180003530 | TTTCTTTGGACTTGG[C/T]TTCAGTATTACTACC | 55819 |
rs248319 | snp | G/T | 0.421842 | 0.181577 | intron-variant | RNF130 | GRCh38.p7 | 5:180003727 | AGTCTATTTGCATCC[G/T]GCTAACTCTCAAGTA | 55819 |
rs248320 | snp | A/G | 0.256897 | 0.249905 | intron-variant | RNF130 | GRCh38.p7 | 5:180005096 | CTCCCTAAGTCTCTC[A/G]CACCAGAAAAGAATT | 55819 |
rs248321 | snp | A/C | 0.312104 | 0.242163 | intron-variant | RNF130 | GRCh38.p7 | 5:179944900 | GCCCTGTTTCCAGAT[A/C]AGGCACATATATTTG | 55819 |
rs248322 | snp | C/T | 0.451732 | 0.147663 | intron-variant | RNF130 | GRCh38.p7 | 5:179959443 | CCAGCCTGGCCAAGA[C/T]AGTGAAACCCCATCT | 55819 |
rs248327 | snp | C/T | 0.467744 | 0.122832 | intron-variant | RNF130 | GRCh38.p7 | 5:179950650 | GAAGTCCCAATCTAT[C/T]AATTCACTCATTTCG | 55819 |
rs248328 | snp | C/T | 0.49607 | 0.0441545 | intron-variant | RNF130 | GRCh38.p7 | 5:179950085 | ctcattatttaaggt[C/T]gacaGTTGATAGCAT | 55819 |
rs248329 | snp | C/G | 0.466412 | 0.125164 | intron-variant | RNF130 | GRCh38.p7 | 5:179949068 | CCTCCCGGGTTCAAG[C/G]GATTCTCCTGCCTCA | 55819 |
rs248330 | snp | C/T | 0.463559 | 0.129972 | intron-variant | RNF130 | GRCh38.p7 | 5:179948727 | GGAACTTGGCATAAC[C/T]AAATAATTTGGAAGA | 55819 |
rs248331 | snp | C/T | 0.248188 | 0.249993 | intron-variant | RNF130 | GRCh38.p7 | 5:179946616 | tggagtgcagtggtg[C/T]gatcttggctcactg | 55819 |
rs248332 | snp | A/C | 0.428484 | 0.175052 | intron-variant | RNF130 | GRCh38.p7 | 5:179946399 | CCATTGTCTTGCCTG[A/C]CCAAAGGCAAGCATT | 55819 |
rs270335 | snp | C/T | 0.089084 | 0.191327 | intron-variant | RNF130 | GRCh38.p7 | 5:179946708 | acaggcgcccgccac[C/T]acgcccggctaattt | 55819 |
rs270336 | snp | G/T | 0.163892 | 0.234703 | intron-variant | RNF130 | GRCh38.p7 | 5:179940320 | ggcaggagaaccgct[G/T]gaacctgggaagcgg | 55819 |
rs375133 | snp | A/C | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179952912 | tgatctcgtagggaa[A/C]acctttccatctgtc | 55819 |
rs379655 | snp | A/G | 0.375 | 0.216506 | intron-variant | RNF130 | GRCh38.p7 | 5:179990797 | catacagagatagta[A/G]ctgaaggggcatggt | 55819 |
rs389849 | snp | A/C | 0.495782 | 0.0457324 | intron-variant | RNF130 | GRCh38.p7 | 5:179958672 | GGACGGACAATTTTA[A/C]CTACTACAAAGTTGt | 55819 |
rs394588 | snp | C/G | 0.421368 | 0.182025 | intron-variant | RNF130 | GRCh38.p7 | 5:179999698 | ctccagcctaggcga[C/G]caagcgagactccgt | 55819 |
rs394616 | snp | G/T | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:179991134 | cattctcttctggct[G/T]gtgtagtgtatcttt | 55819 |
rs413344 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | RNF130 | GRCh38.p7 | 5:180000060 | ctgcatgttttcctg[C/G]tagtgaatactgtct | 55819 |
rs415979 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997647 | Gtttgtattttaatt[C/T]gtagagatggggttt | 55819 |
rs418384 | snp | C/T | 0.494143 | 0.0537956 | intron-variant | RNF130 | GRCh38.p7 | 5:179992220 | gatctcggctcactg[C/T]aaactctgcctcccg | 55819 |
rs423635 | snp | A/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180004960 | AAAAGAAGCCTCTGT[A/T]AACTCTTTTGCAAGA | 55819 |
rs427178 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936650 | CTTTCATTGCTACTT[G/T]AAAGTAAAGCATCTC | 55819 |
rs438050 | snp | C/T | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:179987645 | gtatctttcactata[C/T]tgaagtatgttactt | 55819 |
rs442181 | snp | A/T | 0.444444 | 0.157135 | intron-variant | RNF130 | GRCh38.p7 | 5:179991116 | ccagaagagaatggg[A/T]tgctattttcaaagt | 55819 |
rs449511 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | RNF130 | GRCh38.p7 | 5:180000400 | gatttactcttattt[A/G]ggaaccactgggcta | 55819 |
rs456377 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923550 | accaaggagctgagt[C/T]tcagccaatcccagc | 55819 |
rs456456 | snp | G/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179952678 | ttgtcccacaattgg[G/T]tcaatgtaagaaaat | 55819 |
rs456480 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934560 | TTTTTTTTTTTTTGG[G/T]GGTGGGGACAGGGTC | 55819 |
rs456958 | snp | A/G | 0.497502 | 0.035255 | intron-variant | RNF130 | GRCh38.p7 | 5:179934493 | ctgttaattttattc[A/G]tcattttaaaggaac | 55819 |
rs457048 | snp | C/T | | | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920168 | CACCTTGGGGGAACT[C/T]TGCAAATTAACCCTG | 55819 |
rs457610 | snp | A/G | 0.497558 | 0.0348586 | intron-variant | RNF130 | GRCh38.p7 | 5:179934206 | TAGCAGCCTGGCGGC[A/G]TGGAAAGGTGGTGGG | 55819 |
rs457952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003364 | TCTTCAGCAAGCTGA[C/T]GTGAATGCATGTAGG | 55819 |
rs459085 | snp | A/C | 0.497416 | 0.0358495 | intron-variant | RNF130 | GRCh38.p7 | 5:179934295 | gtgaaatgcatctcc[A/C]gaactttttcatctt | 55819 |
rs461613 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934563 | ttttttttttggtgg[G/T]ggggacagggtctga | 55819 |
rs464219 | snp | G/T | 0.49152 | 0.0645617 | intron-variant | RNF130 | GRCh38.p7 | 5:179936784 | agacatacagattaa[G/T]ggaataaaattgaga | 55819 |
rs464939 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952855 | agactatagactaga[C/T]acctttatcaagttg | 55819 |
rs466269 | snp | C/T | 0.184838 | 0.241358 | intron-variant | RNF130 | GRCh38.p7 | 5:179943780 | AATCACTGTTAAATA[C/T]ACTTTGCGGTTTAAT | 55819 |
rs467480 | snp | C/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179928059 | attgtgtggtggcca[C/G]acagtggaacatgat | 55819 |
rs467493 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928187 | atccgagggaaaggc[A/G]tgtccatgtgtacaa | 55819 |
rs467764 | snp | A/G | 0.452103 | 0.147154 | intron-variant | RNF130 | GRCh38.p7 | 5:179938910 | GTACAATCTTGTCCT[A/G]CCACTAAAGAGTCAA | 55819 |
rs467877 | snp | G/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179949898 | gtgacatactcacta[G/T]cctcacgtggaaaat | 55819 |
rs468160 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179956833 | CTGAAGGTAATGGAG[A/G]CCTGGTCTGGCCCCG | 55819 |
rs468208 | snp | A/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179946485 | AGTAAGAAAGTGGAT[A/T]ATTTCTACAAATGTA | 55819 |
rs468507 | snp | C/G | 0.185155 | 0.241444 | intron-variant | RNF130 | GRCh38.p7 | 5:179943514 | AAATTGTTTTAAATT[C/G]TTTTTCTGAATAAGT | 55819 |
rs468622 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179949885 | caatcggatcactgt[A/G]acatactcactatcc | 55819 |
rs495267 | snp | C/T | 0.409041 | 0.192888 | intron-variant | RNF130 | GRCh38.p7 | 5:179990645 | tggtctagcggtagc[C/T]gtcagtgccaaggaa | 55819 |
rs518075 | snp | C/T | 0.497613 | 0.0344622 | intron-variant | RNF130 | GRCh38.p7 | 5:179935964 | AGGGATGAGTATCAG[C/T]GTCTCACACATCGAG | 55819 |
rs578582 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953032 | ttcttcctttccaat[C/G]tggatgcttatttat | 55819 |
rs594202 | snp | C/T | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:179990335 | agagaggacagctta[C/T]gtcatcatttcttct | 55819 |
rs705448 | snp | C/T | 0.45198 | 0.147323 | intron-variant | RNF130 | GRCh38.p7 | 5:179958131 | atccgcccgcctcgg[C/T]ctcccaaagtgctgg | 55819 |
rs764959 | snp | A/T | 0.143959 | 0.226396 | intron-variant | RNF130 | GRCh38.p7 | 5:179920797 | TATATATATATATAT[A/T]TTTTTTTTTGAGATG | 55819 |
rs764960 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920795 | tatatatatatatat[A/T]tatttttttttgaga | 55819 |
rs836255 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF130 | GRCh38.p7 | 5:179936185 | ggagtgcagaggcac[A/G]atcatggctcaccac | 55819 |
rs844377 | snp | A/C | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179968134 | ccccgtctctactaa[A/C]aatacaaaacattag | 55819 |
rs857181 | snp | C/T | 0.492484 | 0.0608394 | intron-variant | RNF130 | GRCh38.p7 | 5:179989699 | gctgtatcttttaag[C/T]ggagcatttgatcca | 55819 |
rs857182 | snp | A/G | 0.49423 | 0.0534032 | intron-variant | RNF130 | GRCh38.p7 | 5:179990034 | agggtccagccccac[A/G]gggttggtgggtttt | 55819 |
rs857183 | snp | C/T | 0.494187 | 0.0535994 | intron-variant | RNF130 | GRCh38.p7 | 5:179990078 | ggagacgagagattg[C/T]agaaataaagacaca | 55819 |
rs857184 | snp | A/G | 0.492484 | 0.0608394 | intron-variant | RNF130 | GRCh38.p7 | 5:179990185 | cgaatgcctggctgc[A/G]ctgttatttattgga | 55819 |
rs857187 | snp | C/T | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:179993013 | gtttgctgagaatga[C/T]ggtttccagcttcat | 55819 |
rs857188 | snp | A/C | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:179993113 | ccacattttcttaat[A/C]cagtctatcgttgtt | 55819 |
rs857189 | snp | C/T | 0.494143 | 0.0537956 | intron-variant | RNF130 | GRCh38.p7 | 5:180001735 | TGACAGCAAGTATCC[C/T]AGCTTAGGGGAGCAG | 55819 |
rs857190 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937933 | gtgtgtgtgtgtgtg[A/T]gagagagagagagag | 55819 |
rs860707 | snp | A/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179928557 | cttcttCTCCTTTAT[A/T]GTGACTGTGAGTCCT | 55819 |
rs863231 | snp | C/T | 0.419135 | 0.184101 | intron-variant | RNF130 | GRCh38.p7 | 5:179982613 | caaggtcttgctctg[C/T]ttcccaaactggagt | 55819 |
rs863904 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179982878 | tgtgagccacggcac[A/G]cagcctccttacagt | 55819 |
rs864137 | snp | A/G | 0.488485 | 0.0749998 | intron-variant | RNF130 | GRCh38.p7 | 5:179985482 | tctggggtcaagaag[A/G]ccactctgaagcctt | 55819 |
rs864138 | snp | G/T | 0.488485 | 0.0749998 | intron-variant | RNF130 | GRCh38.p7 | 5:179985707 | tcccttccaggctgg[G/T]gtttagtagctttat | 55819 |
rs864481 | snp | A/G | 0.432457 | 0.170908 | intron-variant | RNF130 | GRCh38.p7 | 5:179984289 | tcctttttacttact[A/G]tgctggctagaatct | 55819 |
rs864482 | snp | A/G | 0.255782 | 0.249933 | intron-variant | RNF130 | GRCh38.p7 | 5:180000873 | ttctggcaattcatt[A/G]agttttttcccattg | 55819 |
rs864485 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937166 | AAACGAAATATCATC[A/C]AAACGAAGTATcatc | 55819 |
rs1102190 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | RNF130 | GRCh38.p7 | 5:179989059 | taatcaactcagttc[C/T]gcatggctaagaagg | 55819 |
rs1102191 | snp | C/T | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:179989210 | actcactctctatca[C/T]gagaacaacatggag | 55819 |
rs1103811 | snp | A/G | 0.40733 | 0.194287 | intron-variant | RNF130 | GRCh38.p7 | 5:179986168 | taaaggctgcaaaag[A/G]tatttagcaaaaagt | 55819 |
rs1160931 | in-del | -/CT | 0.485392 | 0.0842056 | intron-variant | RNF130 | GRCh38.p7 | 5:179976000 | TTTCCAGACCTGACT[-/CT]GCATCAGAGTCAGTG | 55819 |
rs1348523 | snp | A/G | 0.241053 | 0.24984 | intron-variant | RNF130 | GRCh38.p7 | 5:180068532 | ATTTTGGCAAGTGCT[A/G]TACTTTACGTAGTAT | 55819 |
rs1500142 | snp | A/C | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179984674 | tttgcatctatgttc[A/C]agaggggtcctggtc | 55819 |
rs1650806 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179997424 | cgcctcccaggttca[A/C]gccattctcctgcct | 55819 |
rs1650809 | snp | A/C | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180005274 | ctctactaaaaatac[A/C]aaaattagtcgggcc | 55819 |
rs1697029 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967966 | TTTAGGAGGATTTTG[G/T]TATAAACAGAGGAGA | 55819 |
rs1697036 | snp | A/T | 0.491732 | 0.0637633 | intron-variant | RNF130 | GRCh38.p7 | 5:179998859 | TAGATCTAGTATTTT[A/T]TATATATATATATAT | 55819 |
rs1808088 | snp | C/T | 0.197393 | 0.244402 | intron-variant | RNF130 | GRCh38.p7 | 5:179991800 | aattatacaaatcac[C/T]ataacgtagaatcag | 55819 |
rs1909707 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | RNF130 | GRCh38.p7 | 5:179988561 | ACTTCCCTCTTAGCA[A/C]TGCTTTTGCTGTATC | 55819 |
rs1978603 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960983 | TTTCTCCTGGGAACT[A/T]AAATCAGTAGGAATT | 55819 |
rs1991464 | snp | A/C | 0.10237 | 0.201756 | intron-variant | RNF130 | GRCh38.p7 | 5:179949225 | ctgccttggcctccc[A/C]aagttgcagggatta | 55819 |
rs2069332 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | RNF130 | GRCh38.p7 | 5:180001177 | CAGTGGTATAAGCTG[C/T]GGATGTCTGCTGCAG | 55819 |
rs2115042 | snp | A/G | 0.203882 | 0.245709 | intron-variant | RNF130 | GRCh38.p7 | 5:179995835 | cccagtgtctgaaat[A/G]ttctgttcaattcct | 55819 |
rs2115043 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RNF130 | GRCh38.p7 | 5:179923197 | ttagatggtccactt[C/T]aagtaaatctttgaa | 55819 |
rs2162760 | snp | A/G | 0.137867 | 0.223442 | intron-variant | RNF130 | GRCh38.p7 | 5:179964811 | GCTTAGTAAACCCCT[A/G]TCTTTTAGACACCAG | 55819 |
rs2218423 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RNF130 | GRCh38.p7 | 5:180066788 | CGGTGAGCCGAGATC[A/G]CGCCATTGCACTCCG | 55819 |
rs2386704 | snp | C/T | 0.495445 | 0.0475058 | intron-variant | RNF130 | GRCh38.p7 | 5:180062199 | agctgggactacagg[C/T]acgcacagccacgcc | 55819 |
rs2450481 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952949 | cacatggatgtctgt[G/T]tgcaccatttctatt | 55819 |
rs2450482 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952994 | ttgaggtgctagcca[C/G]aacaattaagcatga | 55819 |
rs2454856 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984965 | TTATCCAAAATGCTT[G/T]GGACCAGAAAttttt | 55819 |
rs2454857 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952986 | aattgttctggctag[A/C]acctcaaatagtaga | 55819 |
rs2560867 | snp | C/G | | | | | GRCh38.p7 | 5:179968706 | gagaaAGTTTCTAAA[C/G]TGTGCTAGGCATCAT | 55819 |
rs2650369 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968704 | gagagaaAGTTTCTA[A/C]ACTGTGCTAGGCATC | 55819 |
rs2937020 | snp | G/T | 0.491732 | 0.0637633 | intron-variant | RNF130 | GRCh38.p7 | 5:179984660 | aattttttagaattt[G/T]tgcatctatgttcaa | 55819 |
rs3078899 | in-del | -/ACAA | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179931789 | AAAACAAACAAACAA[-/ACAA]CAAAACTACAGTACA | 55819 |
rs3078901 | in-del | -/AG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937969 | gagagagagagagag[-/AG]acagagacagacagg | 55819 |
rs3084833 | in-del | -/AAT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179927345 | TGTTATTGGCTACAT[-/AAT]GTTATTAAGTAAACT | 55819 |
rs3209571 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNF130 | GRCh38.p7 | 5:179955920 | TGTATTTAAACAACA[C/T]GCCATGGGCCTGACC | 55819 |
rs3734002 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963915 | AAATATGCTTAGTCT[A/G]CTTTACTGTCATTTA | 55819 |
rs3749821 | snp | A/G | 0.454944 | 0.143172 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071595 | CCAGGAGTACTACAC[A/G]GCGCTCATCAACGTG | 55819 |
rs3756615 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179974890 | GTGCTGACCCGGGTG[C/T]GCAGGCCGGAGAGGC | 55819 |
rs3756616 | snp | G/T | 0.492337 | 0.0614248 | intron-variant | RNF130 | GRCh38.p7 | 5:179973847 | TGCTTGTGCTTTTCA[G/T]GTTTCACTGTCCACG | 55819 |
rs3776946 | snp | C/T | 0.253824 | 0.249971 | intron-variant | RNF130 | GRCh38.p7 | 5:179976606 | ACATATAAAGGAAAA[C/T]CTATAAAACTAAATG | 55819 |
rs3776948 | snp | A/G | 0.252983 | 0.249982 | intron-variant | RNF130 | GRCh38.p7 | 5:179976061 | GTGCTGGGATCACAG[A/G]CATGAGCCTGACGTC | 55819 |
rs3797763 | snp | A/G | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180012516 | AGTTCCACTGACAGC[A/G]CATCTATTTTGGTTG | 55819 |
rs3797764 | snp | C/T | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180012345 | CTCTCCTAGACTTTT[C/T]GTGTAGAAAACTAAG | 55819 |
rs3797769 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | RNF130 | GRCh38.p7 | 5:179961586 | TTCGAGAATTATTGG[A/G]TAGTTTAATAGTCAC | 55819 |
rs3797770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961495 | CTCAGTAGACATGTT[A/G]CCTATTAGAAATCAT | 55819 |
rs3797771 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | RNF130 | GRCh38.p7 | 5:179961363 | CTCCCATTAGCAGTT[A/G]TAGAGGGTTGATTTC | 55819 |
rs3797772 | snp | A/G | 0.128632 | 0.218563 | intron-variant | RNF130 | GRCh38.p7 | 5:179960369 | AATACTGTTTATTTA[A/G]TACTGCGACTGATTA | 55819 |
rs3828698 | snp | A/C | 0.479632 | 0.0988382 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071658 | ccggctcgccgcgcT[A/C]GCCCTGCTGACCTGC | 55819 |
rs3839292 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003689 | AAAATTTTAAAAAAA[-/A]TAGTGGCTTTTAGAC | 55819 |
rs4009657 | in-del | -/AGGAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977426 | GTTTTTGAAACCCAC[-/AGGAA]TCACAAAACAATGCC | 55819 |
rs4129403 | snp | A/G | 0.248755 | 0.249997 | intron-variant | RNF130 | GRCh38.p7 | 5:180049610 | CCCAAGTATACTGAA[A/G]CAATGTATCAAAGTA | 55819 |
rs4130025 | snp | A/G | 0.417196 | 0.185864 | intron-variant | RNF130 | GRCh38.p7 | 5:180048239 | AGTTGAAATCTTGGA[A/G]AACTCCTATTAACTC | 55819 |
rs4130027 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180048515 | aaagtgctgggatta[C/T]aggcatgagccaccg | 55819 |
rs4235504 | snp | C/T | 0.258288 | 0.249863 | intron-variant | RNF130 | GRCh38.p7 | 5:180026680 | GGTACATACAGTATA[C/T]AGGGAATACTTATAT | 55819 |
rs4235505 | snp | C/T | 0.256619 | 0.249912 | intron-variant | RNF130 | GRCh38.p7 | 5:180038470 | TGGATTATAGGATTA[C/T]AGGTGTGAGCCACTG | 55819 |
rs4264913 | snp | A/G | 0.256619 | 0.249912 | intron-variant | RNF130 | GRCh38.p7 | 5:180045728 | tagacacagagtgcc[A/G]attggtgcatttaca | 55819 |
rs4298216 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | RNF130 | GRCh38.p7 | 5:180048279 | GGAAGGGGCACGGAA[A/G]GGAGTCTGTAGTCCG | 55819 |
rs4340879 | snp | A/G | 0.472989 | 0.113031 | intron-variant | RNF130 | GRCh38.p7 | 5:180054302 | AAAAATGATACAATC[A/G]CTTTCTTCCCAATTT | 55819 |
rs4389651 | snp | A/T | 0.255224 | 0.249945 | intron-variant | RNF130 | GRCh38.p7 | 5:180033968 | taatgagagtggaca[A/T]ccttggcttgttcct | 55819 |
rs4466125 | snp | C/T | 0.417359 | 0.185718 | intron-variant | RNF130 | GRCh38.p7 | 5:180045394 | tcgtggtctcactga[C/T]ttcaagagtgaagct | 55819 |
rs4623110 | snp | C/G | 0.245916 | 0.249967 | intron-variant | RNF130 | GRCh38.p7 | 5:180031761 | ttttcatttctctta[C/G]atatctgggagtggg | 55819 |
rs4700703 | snp | A/C | 0.160938 | 0.233598 | intron-variant | RNF130 | GRCh38.p7 | 5:179938562 | ATTTATTTTCACCAA[A/C]CACATTCTCATTTCT | 55819 |
rs4700705 | snp | A/T | 0.410737 | 0.191478 | intron-variant | RNF130 | GRCh38.p7 | 5:180033791 | gtttattacatctag[A/T]ggtttttaataaatt | 55819 |
rs4700852 | snp | A/G | 0.27856 | 0.248363 | intron-variant | RNF130 | GRCh38.p7 | 5:180045187 | TGCAATGAGAGAAGG[A/G]GAAGAATATTCAGGT | 55819 |
rs4700853 | snp | A/G | 0.248755 | 0.249997 | intron-variant | RNF130 | GRCh38.p7 | 5:180046328 | CCTCAAGCGTGGCCA[A/G]AGCAGACACCAAGGC | 55819 |
rs4700854 | snp | C/T | 0.256897 | 0.249905 | intron-variant | RNF130 | GRCh38.p7 | 5:180054789 | tggagggcacaggta[C/T]cttaacaaaacaagt | 55819 |
rs4700855 | snp | A/T | 0.495708 | 0.0461266 | intron-variant | RNF130 | GRCh38.p7 | 5:180060258 | TGCTGTGAGCCACCT[A/T]GTTTTTGGTGATTTG | 55819 |
rs4700857 | snp | A/C | 0.226484 | 0.248892 | intron-variant | RNF130 | GRCh38.p7 | 5:180065773 | tcaaaaaaaaaaaaa[A/C]aaCTATGTAAAGAAA | 55819 |
rs4700858 | snp | C/T | 0.467132 | 0.12391 | intron-variant | RNF130 | GRCh38.p7 | 5:180070249 | AGTTGTTTCTACGGC[C/T]AAGCTGGGACCCTAA | 55819 |
rs4700859 | snp | C/T | 0.38555 | 0.210062 | intron-variant | RNF130 | GRCh38.p7 | 5:180070748 | ATCAACTAAACAAAG[C/T]CCTTGTTCATAGGAA | 55819 |
rs4700860 | snp | A/G | 0.489893 | 0.0703642 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073287 | GGCGCGGTGGCTCAC[A/G]CCCGTAATCGCAGCA | 55819 |
rs4700861 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073410 | aaattagtcgtggtg[A/G]tgcgtgcctgtagtc | 55819 |
rs4700862 | snp | A/G | 0.47709 | 0.104548 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073722 | CAAGTACAGACCCTA[A/G]GCCAAAGCAGCGGGG | 55819 |
rs5873672 | in-del | -/TA | 0.493703 | 0.0557558 | intron-variant | RNF130 | GRCh38.p7 | 5:179920779 | CTGGGCATATATATT[-/TA]TATATATATATATAT | 55819 |
rs5873673 | in-del | -/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179927606 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 55819 |
rs5873675 | in-del | -/G | 0.498733 | 0.0370934 | intron-variant | RNF130 | GRCh38.p7 | 5:179938439 | ACTGCTTAATGAGTA[-/G]GGGGGTTTCTTTTTG | 55819 |
rs5873676 | in-del | -/A | 0.465263 | 0.127129 | intron-variant | RNF130 | GRCh38.p7 | 5:179960846 | AGGGCAATTAAGGTG[-/A]AAAAAAAAAAAATCT | 55819 |
rs6601077 | snp | C/T | 0.248755 | 0.249997 | intron-variant | RNF130 | GRCh38.p7 | 5:179975769 | CCATAGAGGGTGCAG[C/T]GAAATTCCGTGAACC | 55819 |
rs6601078 | snp | C/T | 0.222333 | 0.248464 | intron-variant | RNF130 | GRCh38.p7 | 5:180018248 | ttcagtgagccgaga[C/T]tgtgccactgcactc | 55819 |
rs6859628 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF130 | GRCh38.p7 | 5:179981895 | ATAATTGACTTAAAA[C/T]AGACTGCATATATTT | 55819 |
rs6862105 | snp | A/G | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180043642 | AAGGGGTGCAACCAC[A/G]GAGCAAAAGTTATCA | 55819 |
rs6869040 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RNF130 | GRCh38.p7 | 5:180065739 | cattctagcctgggc[A/G]acagagtgagactct | 55819 |
rs6869349 | snp | A/G | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180009499 | acataaaaaatgtct[A/G]attagagaaatgcaa | 55819 |
rs6870903 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | RNF130 | GRCh38.p7 | 5:180013908 | AGCTGGTAACAGAGC[C/T]ACAAAGTGCCAAATG | 55819 |
rs6871596 | snp | A/T | 0.421209 | 0.182174 | intron-variant | RNF130 | GRCh38.p7 | 5:180014331 | ACAGAGAAACTTCTA[A/T]CAATCTATCAGCGAT | 55819 |
rs6873317 | snp | C/T | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180009278 | attagaaatttttgc[C/T]tttcaaagaccttgt | 55819 |
rs6873639 | snp | C/T | 0.222333 | 0.248464 | intron-variant | RNF130 | GRCh38.p7 | 5:180009466 | tcactgaagaggata[C/T]acggatggcaaacaa | 55819 |
rs6873781 | snp | A/C | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180009734 | ttggaatttacactg[A/C]actcagaaattacac | 55819 |
rs6873994 | snp | G/T | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180009696 | aaatatgcacttatc[G/T]taacagcccaaaaac | 55819 |
rs6876648 | snp | C/T | 0.256061 | 0.249927 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180014842 | AACAGGAACATTAGC[C/T]AGGCATGGTGGCACA | 55819 |
rs6877436 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937174 | TATCATCAAAACGAA[A/G]TATcatcaaaacgaa | 55819 |
rs6877900 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045876 | caatcctttagctag[A/C]cagaaaagttctcca | 55819 |
rs6878695 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937170 | GAAATATCATCAAAA[C/T]GAAGTATcatcaaaa | 55819 |
rs6880962 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | RNF130 | GRCh38.p7 | 5:179976708 | ttttttttttttttt[A/T]aaaaCAGATCTTCCT | 55819 |
rs6881316 | snp | C/T | 0.246769 | 0.249979 | intron-variant | RNF130 | GRCh38.p7 | 5:179990449 | gatggaacatgagag[C/T]ggaccaggggcgtga | 55819 |
rs6881735 | snp | G/T | 0.437824 | 0.164991 | intron-variant | RNF130 | GRCh38.p7 | 5:180038411 | AAAAAAGCCTGTTTT[G/T]TTTTTTTTTTTATTT | 55819 |
rs6883196 | snp | A/G | 0.497933 | 0.032082 | intron-variant | RNF130 | GRCh38.p7 | 5:179968325 | aaacaaaaaaaGAAG[A/G]CGGCGGCTAGCGGTA | 55819 |
rs6884272 | snp | A/C | 0.497933 | 0.032082 | intron-variant | RNF130 | GRCh38.p7 | 5:179968326 | aacaaaaaaaGAAGG[A/C]GGCGGCTAGCGGTAA | 55819 |
rs6884290 | snp | A/G | 0.494013 | 0.0543839 | intron-variant | RNF130 | GRCh38.p7 | 5:180050847 | gggtttcactctgtc[A/G]cccagggtggagtgc | 55819 |
rs6884565 | snp | C/G | 0.256619 | 0.249912 | intron-variant | RNF130 | GRCh38.p7 | 5:180043773 | CCTGTATAAGCAAAA[C/G]AATGTTCCTGTTTCC | 55819 |
rs6888883 | snp | C/T | 0.422 | 0.181428 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017395 | aaataaatgttttcc[C/T]cttaattaataagca | 55819 |
rs6893619 | snp | A/T | 0.2462 | 0.249971 | intron-variant | RNF130 | GRCh38.p7 | 5:179993614 | aagttctttgtagat[A/T]ctggatattagccct | 55819 |
rs6894363 | snp | C/G | 0.029116 | 0.117091 | intron-variant | RNF130 | GRCh38.p7 | 5:180070439 | AGCTTAGCACTTTGG[C/G]ATACAAATACAGACC | 55819 |
rs7381056 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949105 | tgagtagctgggatt[A/G]caggcatgtgccacc | 55819 |
rs7448551 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180002883 | aagttctaaggattt[C/T]taatgggtcattttc | 55819 |
rs7448914 | snp | A/C | 0.16846 | 0.236329 | intron-variant | RNF130 | GRCh38.p7 | 5:179998132 | gcgtgagccactgtg[A/C]ttggcctgtttttgc | 55819 |
rs7705292 | snp | A/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179937935 | gtgtgtgtgtgtgtg[A/T]gagagagagagagag | 55819 |
rs7706543 | snp | C/G | 0.0607341 | 0.163335 | intron-variant | RNF130 | GRCh38.p7 | 5:179992779 | gtgcacaacgtgcag[C/G]tttgttacatatgta | 55819 |
rs7706570 | snp | A/G | 0.470521 | 0.117772 | intron-variant | RNF130 | GRCh38.p7 | 5:180053027 | GTCAAGATAATGTAC[A/G]TCCTTCAAGGAATCC | 55819 |
rs7706876 | snp | A/G | 0.229429 | 0.249152 | intron-variant | RNF130 | GRCh38.p7 | 5:180053172 | ACAGATCTCAAAACT[A/G]GCAGACAGGATAGGG | 55819 |
rs7709697 | snp | G/T | 0.147321 | 0.227941 | intron-variant | RNF130 | GRCh38.p7 | 5:179938140 | ttttgtatttttttg[G/T]agagatggggttttg | 55819 |
rs7713656 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | RNF130 | GRCh38.p7 | 5:179944320 | GCTATTTCCAATAAA[G/T]TAAATAACTAAAGGA | 55819 |
rs7718851 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179928595 | TTAAGCATTGCAGGT[A/G]CCTTCTTCCAAAACT | 55819 |
rs7722611 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | RNF130 | GRCh38.p7 | 5:179986190 | gcaaaaagtataaag[A/T]ttttgtgcctgttgg | 55819 |
rs7727946 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNF130 | GRCh38.p7 | 5:179931827 | TGTAACTGTGATTCA[A/G]GCCCCCCAGCACCCC | 55819 |
rs7729516 | snp | C/G | 0.200182 | 0.244986 | intron-variant | RNF130 | GRCh38.p7 | 5:180057265 | caatcatgtctgtgt[C/G]ggggtgggcacagtg | 55819 |
rs7734329 | snp | A/C | 0.385359 | 0.210185 | intron-variant | RNF130 | GRCh38.p7 | 5:180057838 | tcaaactgagtaggg[A/C]gttacgggaacctcc | 55819 |
rs7734867 | snp | A/G | 0.388587 | 0.208071 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072292 | GGTTGTTTCTCTGTC[A/G]GGCGTGATAGCCGCA | 55819 |
rs9329090 | snp | A/C | 0.0752113 | 0.178743 | intron-variant | RNF130 | GRCh38.p7 | 5:179940026 | ATTTTCTCTCTGCTT[A/C]TTCTTTAGTCTCAGG | 55819 |
rs9329091 | snp | G/T | 0.375 | 0.216506 | intron-variant | RNF130 | GRCh38.p7 | 5:179957999 | tctcctgcctcagcc[G/T]cccaagtagctggga | 55819 |
rs9329092 | snp | C/T | 0.190519 | 0.242821 | intron-variant | RNF130 | GRCh38.p7 | 5:179980885 | CCACAGATGAAGAGA[C/T]GGTGATCCCTACCCT | 55819 |
rs9329095 | snp | A/G | 0.257732 | 0.24988 | intron-variant | RNF130 | GRCh38.p7 | 5:180029155 | TAGAGGTACTATATC[A/G]TCCAACTAAAACATT | 55819 |
rs9329096 | snp | G/T | 0.482534 | 0.0918038 | intron-variant | RNF130 | GRCh38.p7 | 5:180052621 | AAGACTGGGCTATCT[G/T]GACCATAATTTAAAA | 55819 |
rs9654545 | snp | C/T | 0.201727 | 0.245295 | intron-variant | RNF130 | GRCh38.p7 | 5:179978025 | TGCAGCCCGCACCTG[C/T]TGAACAGCACCACTC | 55819 |
rs9885239 | snp | A/C | 0.145642 | 0.227177 | intron-variant | RNF130 | GRCh38.p7 | 5:179938842 | CAGCAGGCTGACACC[A/C]CATGGCTCACATTTC | 55819 |
rs10036834 | snp | A/G | 0.369142 | 0.219784 | intron-variant | RNF130 | GRCh38.p7 | 5:180027428 | AGAGTTATGGCATAC[A/G]AAAGTCAGAAGAGGA | 55819 |
rs10042725 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179948484 | agacaagcctagcca[A/C]catggtgaaaccccc | 55819 |
rs10045755 | snp | A/G | 0.421209 | 0.182174 | intron-variant | RNF130 | GRCh38.p7 | 5:180019371 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA | 55819 |
rs10045882 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027200 | CTGTCTGGGGTGGGG[G/T]GGGGGGAGGATCCTG | 55819 |
rs10045947 | snp | C/T | 0.284471 | 0.247612 | intron-variant | RNF130 | GRCh38.p7 | 5:180027508 | CAGAGAAGCTTCTGA[C/T]AGTGTGTGTGTTCTC | 55819 |
rs10051632 | snp | C/T | 0.395453 | 0.203331 | intron-variant | RNF130 | GRCh38.p7 | 5:180058000 | tagttagtgtcagaa[C/T]tgaattaaactgtag | 55819 |
rs10051694 | snp | C/T | 0.256897 | 0.249905 | intron-variant | RNF130 | GRCh38.p7 | 5:180058038 | aattgatgtTGAAAA[C/T]CCACACATTTGGTAT | 55819 |
rs10054685 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | RNF130 | GRCh38.p7 | 5:179965728 | AACTACACTCAAAGC[A/G]CAGTTTTCTCTATTG | 55819 |
rs10054689 | snp | A/G | 0.245916 | 0.249967 | intron-variant | RNF130 | GRCh38.p7 | 5:179996860 | gttcccttctcttca[A/G]ttttctggaggagta | 55819 |
rs10054764 | snp | A/G | 0.190205 | 0.242744 | intron-variant | RNF130 | GRCh38.p7 | 5:179997001 | taattactcataact[A/G]gtctgtttgatcagg | 55819 |
rs10056316 | snp | A/G | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180060935 | TTAGCTGGGCGAGGT[A/G]GTGGGCGCCTGTAGT | 55819 |
rs10056758 | snp | A/G | 0.039522 | 0.134904 | intron-variant | RNF130 | GRCh38.p7 | 5:179962836 | ACAGCAAACCATCCC[A/G]CCACTAACCAACCCC | 55819 |
rs10056991 | snp | A/G | 0.255503 | 0.249939 | intron-variant | RNF130 | GRCh38.p7 | 5:180058315 | gtgtatgtTACAGCT[A/G]GTAAAAATGTGTGCT | 55819 |
rs10058085 | snp | C/T | 0.19646 | 0.2442 | intron-variant | RNF130 | GRCh38.p7 | 5:179985870 | tcaatattaaaaatc[C/T]gttcacaaaaataac | 55819 |
rs10059400 | snp | A/T | 0.221141 | 0.248329 | intron-variant | RNF130 | GRCh38.p7 | 5:180066833 | gcgaaactctgtctc[A/T]aaaaaataaaataca | 55819 |
rs10059710 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | RNF130 | GRCh38.p7 | 5:179972274 | CTCCCTTAGATCTGA[C/T]AGAAGTTACAGAACC | 55819 |
rs10060093 | snp | C/T | 0.0138388 | 0.0820237 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966867 | ATCCTGAGGAAGAGG[C/T]GAGATCCCCGAAGTT | 55819 |
rs10061208 | snp | C/G | 0.0383715 | 0.133092 | intron-variant | RNF130 | GRCh38.p7 | 5:179965075 | GCAGACTACCTTGTA[C/G]AACTTCGTCACATCT | 55819 |
rs10061480 | snp | A/G | 0.482609 | 0.0916147 | intron-variant | RNF130 | GRCh38.p7 | 5:180043930 | AAGAGGTTTTCATAA[A/G]CAGGAACTTAATACT | 55819 |
rs10064979 | snp | A/G | 0.067446 | 0.170804 | intron-variant | RNF130 | GRCh38.p7 | 5:179972307 | CCTCTGAAAAGTCAC[A/G]GGGACGCAAATGCCT | 55819 |
rs10066845 | snp | A/C | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180020200 | AAGTGGAATGACTGA[A/C]GGGCCTGTGGAAGGA | 55819 |
rs10066848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180050299 | aagaccagcaggctc[C/T]gcgcccacaagagtc | 55819 |
rs10067073 | snp | A/G | 0.194902 | 0.243853 | intron-variant | RNF130 | GRCh38.p7 | 5:180068265 | TAGCTAGGCTGCTCC[A/G]CAAAGGTACTAAATA | 55819 |
rs10068039 | snp | C/T | 0.421051 | 0.182323 | intron-variant | RNF130 | GRCh38.p7 | 5:180010800 | tccttgtgatggaac[C/T]ggtctgtatcctgac | 55819 |
rs10068529 | snp | A/G | 0.492823 | 0.0594727 | intron-variant | RNF130 | GRCh38.p7 | 5:180044040 | CTTTTCATGACTGAT[A/G]ACTATAATTAAGTAG | 55819 |
rs10068594 | snp | A/G | 0.492823 | 0.0594727 | intron-variant | RNF130 | GRCh38.p7 | 5:180044145 | TATCTATATAATTAT[A/G]AGCCTTTAAAATTTG | 55819 |
rs10070664 | snp | A/C | 0.247053 | 0.249983 | intron-variant | RNF130 | GRCh38.p7 | 5:179988654 | ttaatatattcatca[A/C]ccttatggcagtgat | 55819 |
rs10071652 | snp | C/T | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180047975 | CAGGACTCTCCAGGG[C/T]TCATGTTCACCATGT | 55819 |
rs10073876 | snp | A/C | 0.190205 | 0.242744 | intron-variant | RNF130 | GRCh38.p7 | 5:180003960 | aggtactgttctaag[A/C]ccttcacaagtactg | 55819 |
rs10075627 | snp | C/T | 0.284733 | 0.247575 | intron-variant | RNF130 | GRCh38.p7 | 5:180025549 | TTTAAAATGGAACCA[C/T]TGCATTTATTTTATT | 55819 |
rs10076682 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | RNF130 | GRCh38.p7 | 5:179965325 | GCACTGTGGTTGCTA[C/T]GGTGCCCAGGGCTTC | 55819 |
rs10078845 | snp | A/T | 0.245916 | 0.249967 | intron-variant | RNF130 | GRCh38.p7 | 5:180031940 | actttttaattatga[A/T]cattctagaggatgt | 55819 |
rs10078977 | snp | C/T | 0.493881 | 0.054972 | intron-variant | RNF130 | GRCh38.p7 | 5:180031527 | gaggcaaaagttata[C/T]gtagctttttgactg | 55819 |
rs10079029 | snp | C/T | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180061660 | TTCTCTGTGTGTCTT[C/T]CTGTATCTTTTCCTC | 55819 |
rs10080045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179941745 | aatgttttaaaaata[C/T]tttttCCATATTTCT | 55819 |
rs10464058 | snp | C/T | 0.256619 | 0.249912 | intron-variant | RNF130 | GRCh38.p7 | 5:180055821 | CTggtgcgtggctca[C/T]ggctgtaatcctctc | 55819 |
rs10464097 | snp | A/G | 0.471863 | 0.115225 | intron-variant | RNF130 | GRCh38.p7 | 5:180055472 | tgtgtgtgtgtgtgc[A/G]cgcgcgcacgcgtat | 55819 |
rs10479453 | snp | C/T | 0.466618 | 0.124806 | intron-variant | RNF130 | GRCh38.p7 | 5:180030898 | taccaccagtgtgaa[C/T]tgtccagatccactt | 55819 |
rs10479455 | snp | C/T | 0.493881 | 0.054972 | intron-variant | RNF130 | GRCh38.p7 | 5:180031665 | gttgatgaacaactg[C/T]gttgtctctactttt | 55819 |
rs10479551 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | RNF130 | GRCh38.p7 | 5:179929352 | tactgtcttaattac[C/T]gtggctttgtcaaaa | 55819 |
rs10479552 | snp | C/T | 0.040671 | 0.13668 | intron-variant | RNF130 | GRCh38.p7 | 5:179956575 | CTGTCTCCTGCCTAC[C/T]GTCACCACCACCTAC | 55819 |
rs10479553 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179983010 | gcctatatgtgtaca[C/T]tgtctgtggtgaagt | 55819 |
rs10479556 | snp | C/T | 0.197082 | 0.244335 | intron-variant | RNF130 | GRCh38.p7 | 5:179992623 | attatctttttcata[C/T]ttcctatagtattat | 55819 |
rs10479557 | snp | A/G | 0.421051 | 0.182323 | intron-variant | RNF130 | GRCh38.p7 | 5:180028852 | GAATGAAGAAAAAGT[A/G]TACTTAGAAATTTTT | 55819 |
rs10491478 | snp | C/T | 0.421526 | 0.181876 | intron-variant | RNF130 | GRCh38.p7 | 5:179942288 | AAGATTACAAAGGTT[C/T]TAAATAACTGAAACA | 55819 |
rs10516141 | snp | C/T | 0.103806 | 0.202799 | intron-variant | RNF130 | GRCh38.p7 | 5:180013358 | GACATTTAAAACTTA[C/T]GGAAACATCAAATGT | 55819 |
rs10547660 | in-del | -/TC | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:180064928 | AGGATTCCACTTACT[-/TC]TCTCTAGGATTCACA | 55819 |
rs10556651 | in-del | -/AAG | 0.186421 | 0.24178 | intron-variant | RNF130 | GRCh38.p7 | 5:180041536 | GCAAATCTTAAGAAG[-/AAG]CCCCCGGCTGCTCTT | 55819 |
rs10565684 | in-del | -/ATA | 0.499631 | 0.0135733 | intron-variant | RNF130 | GRCh38.p7 | 5:179927343 | TTTGTTATTGGCTAC[-/ATA]ATGTTATTAAGTAAA | 55819 |
rs10577251 | in-del | -/TC | 0.242775 | 0.249896 | intron-variant | RNF130 | GRCh38.p7 | 5:180038248 | TTTGTAGAGATGGGG[-/TC]TCCCTATGTTGCCCA | 55819 |
rs10645011 | in-del | -/AAC | 0.255782 | 0.249933 | intron-variant | RNF130 | GRCh38.p7 | 5:180005433 | CCTCTGTCTCAGAAA[-/AAC]AACAACAACAACAAC | 55819 |
rs10706357 | in-del | -/A | 0.494719 | 0.0511129 | intron-variant | RNF130 | GRCh38.p7 | 5:179939278 | CAACTTTTAAGACAG[-/A]AAAAAAGTGGTCCTA | 55819 |
rs10794702 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180018797 | ATTTATGCTTTAGTT[C/T]AGAAAGTGAGTCTAC | 55819 |
rs10903246 | snp | A/C | 0.420892 | 0.182472 | intron-variant | RNF130 | GRCh38.p7 | 5:180020755 | AGCAAGCACCTGCCC[A/C]GAACAGAAAGCTTTC | 55819 |
rs11249663 | snp | A/C | 0.256619 | 0.249912 | intron-variant | RNF130 | GRCh38.p7 | 5:180008621 | aggacacagtggctc[A/C]tgtctgtaatcccag | 55819 |
rs11249664 | snp | C/T | 0.25634 | 0.24992 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017267 | ACCACAAGGTGATGG[C/T]GTGTCCCTCCTCAGC | 55819 |
rs11249665 | snp | A/C | 0.230669 | 0.249252 | intron-variant | RNF130 | GRCh38.p7 | 5:180048818 | GACTGCCAGCAGCAA[A/C]TGAAGTCACACAGCT | 55819 |
rs11249666 | snp | A/T | 0.385359 | 0.210185 | intron-variant | RNF130 | GRCh38.p7 | 5:180057896 | tgtgggtaccctttg[A/T]cccactacctacaac | 55819 |
rs11333596 | in-del | -/G | 0.498852 | 0.0239341 | intron-variant | RNF130 | GRCh38.p7 | 5:179925289 | CGCCCATGGCCAACA[-/G]TTTAATCAGTCATGC | 55819 |
rs11346161 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928632 | TTTTAATTGTTGTTG[-/T]TTTTTTTTTTTTTTG | 55819 |
rs11359101 | in-del | -/C | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180070982 | CATTTTCCATTTACA[-/C]CCCCCCCCCAATTTA | 55819 |
rs11397024 | in-del | -/T/TT/TTT | 0.44651 | 0.154543 | intron-variant | RNF130 | GRCh38.p7 | 5:180029852 | GCCACTATCCACCTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 55819 |
rs11424965 | in-del | -/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179945922 | AAAAAGGCGGGGGCA[-/G]GGGATATTTAAATGG | 55819 |
rs11443491 | in-del | -/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015666 | TAGGAAAGGAGTAGG[-/G]AAAGGAGTAGGGAAA | 55819 |
rs11443741 | in-del | -/T/TT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029865 | CCACCTCTTTTTTTT[-/T/TT]TTTTTTGAGACAAGG | 55819 |
rs11739706 | snp | C/G | 0.254105 | 0.249966 | intron-variant | RNF130 | GRCh38.p7 | 5:180014648 | AGCTAAAAGAACCAT[C/G]TTTGTGTTACATGCA | 55819 |
rs11739898 | snp | C/T | 0.235564 | 0.249583 | intron-variant | RNF130 | GRCh38.p7 | 5:179974490 | CCACAGTAAATAGTG[C/T]GACAGAAGAGGAAAA | 55819 |
rs11740637 | snp | A/G | 0.120674 | 0.21395 | intron-variant | RNF130 | GRCh38.p7 | 5:180003261 | CCAGACTTCTGGCTC[A/G]GTGATGAGCCGTGTG | 55819 |
rs11742990 | snp | A/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180014674 | ATGCAGTCACAGAAG[A/T]CTACACGCAACTGAA | 55819 |
rs11745588 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | RNF130 | GRCh38.p7 | 5:180055812 | CCATTACAACTGGTG[C/T]gtggctcatggctgt | 55819 |
rs11746941 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015504 | taggaaaggagtagg[A/G]aaaggagtaggaaag | 55819 |
rs11747468 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179923339 | cacctttatggaaaa[A/T]ctattgattgtaaat | 55819 |
rs11748441 | snp | A/G | 0.256619 | 0.249912 | intron-variant | RNF130 | GRCh38.p7 | 5:179992332 | atttttagtagagac[A/G]gggtttcaccatgtt | 55819 |
rs11750102 | snp | A/G | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180023851 | gggctgtgcacagtg[A/G]tgtcaaaagttatca | 55819 |
rs11948891 | snp | C/T | 0.201727 | 0.245295 | intron-variant | RNF130 | GRCh38.p7 | 5:180038486 | aggtgtgagccactg[C/T]gaccagccAAAACAG | 55819 |
rs11949896 | snp | A/C/T | 0.0414363 | 0.137845 | intron-variant | RNF130 | GRCh38.p7 | 5:179968789 | ggggacatctggcaa[A/C/T]gtctggagacatttc | 55819 |
rs11953118 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | RNF130 | GRCh38.p7 | 5:179952755 | actcacatgatcatc[C/T]caatagacacaaagc | 55819 |
rs11954181 | snp | A/G | 0.202959 | 0.245534 | intron-variant | RNF130 | GRCh38.p7 | 5:180037076 | ACTTACTGTGTTTGG[A/G]AGACTTATTCATGTA | 55819 |
rs11955147 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNF130 | GRCh38.p7 | 5:179940568 | aaatggttactttta[C/T]gttatgagaatttca | 55819 |
rs11955292 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | RNF130 | GRCh38.p7 | 5:179973634 | CCCGCACGCCTGACC[A/G]CGCTCACCCTCACTA | 55819 |
rs11956412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002358 | cctggagatgtgggg[C/T]cactgtgctggggtg | 55819 |
rs11958554 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | RNF130 | GRCh38.p7 | 5:179964584 | TGCACAAGCTGTATA[C/T]AGCATGTGTGTTTCT | 55819 |
rs11958600 | snp | C/T | 0.138546 | 0.223781 | intron-variant | RNF130 | GRCh38.p7 | 5:179934654 | gttcaagtgatcctg[C/T]tgcctcagcctccca | 55819 |
rs11959514 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | RNF130 | GRCh38.p7 | 5:179950878 | AATCACCGTTAAATA[A/T]GGAGAGAAGGAAAGA | 55819 |
rs12108932 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RNF130 | GRCh38.p7 | 5:179930203 | gctgggattacaggc[A/G]tctgccaccacaccc | 55819 |
rs12108997 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF130 | GRCh38.p7 | 5:179930204 | ctgggattacaggca[C/T]ctgccaccacacccg | 55819 |
rs12152713 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | RNF130 | GRCh38.p7 | 5:180007232 | atggtgaaatcccat[C/T]tctactaaaaataca | 55819 |
rs12153395 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | RNF130 | GRCh38.p7 | 5:179984477 | tcgatgttggacttc[A/G]gcaaatatcttttct | 55819 |
rs12153541 | snp | A/G | 0.417359 | 0.185718 | intron-variant | RNF130 | GRCh38.p7 | 5:180046346 | CAGACACCAAGGCGA[A/G]GAGGCACCGAGAGCG | 55819 |
rs12332469 | snp | C/T | 0.040671 | 0.13668 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955594 | TTGGTAAATGATGCA[C/T]AAAAATAGGTTCTTT | 55819 |
rs12514260 | snp | A/G | 0.19459 | 0.243782 | intron-variant | RNF130 | GRCh38.p7 | 5:180026403 | TTTTCAGACAAGTAT[A/G]CATTATTGTAAACTA | 55819 |
rs12514644 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | RNF130 | GRCh38.p7 | 5:180059400 | TCTGCTTTCCCCAGA[C/T]AGGACACAAGAGCTG | 55819 |
rs12516233 | snp | A/G | 0.187369 | 0.242028 | intron-variant | RNF130 | GRCh38.p7 | 5:180034313 | TTTGTGCCTACATTC[A/G]TAAGGGATATTGGTA | 55819 |
rs12516364 | snp | C/T | 0.195214 | 0.243923 | intron-variant | RNF130 | GRCh38.p7 | 5:180011891 | cttacaaattttttg[C/T]taagtctaaaattac | 55819 |
rs12516629 | snp | C/T | 0.194902 | 0.243853 | intron-variant | RNF130 | GRCh38.p7 | 5:180052146 | TCTGTCCCAGGCCCT[C/T]TTTTCTCAGTGGACA | 55819 |
rs12516762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037953 | CCCCTGCATTTCTTT[A/C]ATTTGTGCTGTTATA | 55819 |
rs12516767 | snp | C/T | 0.193966 | 0.243639 | intron-variant | RNF130 | GRCh38.p7 | 5:180007725 | TGCTAGGAAACAAGC[C/T]CGCAGTTTGTGGCCT | 55819 |
rs12519642 | snp | G/T | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180011626 | taaaaaattagccag[G/T]catggtggtgcatac | 55819 |
rs12520005 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF130 | GRCh38.p7 | 5:179981366 | AGATGCCGCTCCTGA[C/T]GGAGCAAGGCGGGGA | 55819 |
rs12521479 | snp | C/T | 0.452227 | 0.146984 | intron-variant | RNF130 | GRCh38.p7 | 5:180034093 | ctaatgtgttaaatg[C/T]ttttttttttttaaa | 55819 |
rs12521533 | snp | G/T | 0.019229 | 0.0961495 | intron-variant | RNF130 | GRCh38.p7 | 5:180021891 | CTTTACAGCAGCCCA[G/T]GTCCGAGTCACATGC | 55819 |
rs12522345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980010 | TAAAGCATTAGGTAG[G/T]GTAGTTGGAGAAAAT | 55819 |
rs12652904 | snp | C/T | 0.194902 | 0.243853 | intron-variant | RNF130 | GRCh38.p7 | 5:180069422 | CCCTCACCCCCACCC[C/T]GAGAAAACCTGGAGC | 55819 |
rs12653312 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060242 | aggagtaaattggtg[C/T]tgctgtgagccacct | 55819 |
rs12653944 | snp | C/T | 0.421526 | 0.181876 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016133 | AGGAGGACAGCAGAA[C/T]GAAAGCCCGCCACCA | 55819 |
rs12654148 | snp | A/T | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180011920 | ACAAATATAAAAATT[A/T]TCAAAATAAAAAAAA | 55819 |
rs12654523 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038391 | gtctcggggaggggg[A/G]aaaaaaaaaAGCCTG | 55819 |
rs12655422 | snp | A/C | 0.206947 | 0.246265 | intron-variant | RNF130 | GRCh38.p7 | 5:180053825 | AAAAGCAAATACATT[A/C]TTTTTTTTTTTTTTT | 55819 |
rs12656219 | snp | A/G | 0.49306 | 0.0584955 | intron-variant | RNF130 | GRCh38.p7 | 5:180071189 | GCAAACTCCTAGCTC[A/G]ATGCCCTCCAGCAAA | 55819 |
rs12656814 | snp | A/G | 0.247905 | 0.249991 | intron-variant | RNF130 | GRCh38.p7 | 5:180044556 | AGCCTCCACATGGCC[A/G]GGCGCGGTGGCTCAC | 55819 |
rs13158571 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNF130 | GRCh38.p7 | 5:180056059 | accgtactctggcct[A/G]ggcgacagagcgaaa | 55819 |
rs13160016 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922322 | AAAtttcttttttta[A/T]ttttttttgagacag | 55819 |
rs13161042 | snp | C/T | 0.217851 | 0.247924 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073771 | CACCTAAAGAGTGCT[C/T]TAATCTGGTCCCCTC | 55819 |
rs13161895 | snp | C/T | 0.248755 | 0.249997 | intron-variant | RNF130 | GRCh38.p7 | 5:180044201 | GAATAACGGTACTTC[C/T]GTTTTTCTTACCTGC | 55819 |
rs13162328 | snp | A/G | 0.466721 | 0.124627 | intron-variant | RNF130 | GRCh38.p7 | 5:180069239 | ATGCTTCATAGAGAC[A/G]GATTTTTTTAAATCT | 55819 |
rs13164090 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922320 | AAAAAtttctttttt[A/T]aattttttttgagac | 55819 |
rs13164817 | snp | C/T | 0.156319 | 0.231784 | intron-variant | RNF130 | GRCh38.p7 | 5:179938949 | AGTGCATACACAGGC[C/T]GGGCACAGCAGCTCA | 55819 |
rs13166286 | snp | C/T | 0.167484 | 0.23599 | intron-variant | RNF130 | GRCh38.p7 | 5:180027656 | ACTCCATTAAGAACC[C/T]TAGCAGCCAGGACGC | 55819 |
rs13169458 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010441 | catggctcactgcag[C/G]ctctgcctcccaagt | 55819 |
rs13170926 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989346 | aatcgtatcagccgg[A/C]tactgaatttcccaa | 55819 |
rs13177634 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922519 | ggtttcaccatgttg[C/G]ccaggctggtctcga | 55819 |
rs13179406 | snp | A/C | 0.16911 | 0.236552 | intron-variant | RNF130 | GRCh38.p7 | 5:180026077 | GAGAATATGATGGAA[A/C]AAAGGTGAAGAGCCA | 55819 |
rs13188665 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010275 | aaaaaaaaaaaaagt[A/T]tctcaaggtaattat | 55819 |
rs13354862 | snp | A/G | 0.200492 | 0.245049 | intron-variant | RNF130 | GRCh38.p7 | 5:180065396 | GTTTTATGGCTGTGT[A/G]ACACTCCACTGAGTG | 55819 |
rs13355074 | snp | C/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179961737 | CTGTGGGTGAAATAA[C/G]TGTTTCCCTCTAAAC | 55819 |
rs13355237 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179997550 | agccaggatggtctt[A/C/G]atctcctgacctcgt | 55819 |
rs13362131 | snp | C/T | 0.195526 | 0.243993 | intron-variant | RNF130 | GRCh38.p7 | 5:180000836 | ctctgagtttccata[C/T]gatcataattttgaa | 55819 |
rs13435998 | snp | C/G | 0.375 | 0.216506 | intron-variant | RNF130 | GRCh38.p7 | 5:180021057 | CGCAATCTCTGCCTC[C/G]CGGGTTCAACTGATT | 55819 |
rs17079808 | snp | C/T | 0.183568 | 0.241012 | intron-variant | RNF130 | GRCh38.p7 | 5:179935813 | CCCTGGATTATGACA[C/T]GTATCCTTGATTTAT | 55819 |
rs17079813 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RNF130 | GRCh38.p7 | 5:179939824 | GAAGTTGAATGAAAA[C/T]GGGTCCCTCCCACCA | 55819 |
rs17079821 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF130 | GRCh38.p7 | 5:179942833 | ATGGGTGACATATTT[C/T]CAGTTATGTGTAACT | 55819 |
rs17079827 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | RNF130 | GRCh38.p7 | 5:179943767 | GATTGCAGCTATGAT[C/T]AAACCGCAAAGTATA | 55819 |
rs17079839 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | RNF130 | GRCh38.p7 | 5:179960366 | GTATAATCAGTCGCA[A/G]TACTAAATAAACAGT | 55819 |
rs17079854 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | RNF130 | GRCh38.p7 | 5:179970697 | GAGCCCAACCTCATA[A/T]GTACAACACCGTGTA | 55819 |
rs17079857 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | RNF130 | GRCh38.p7 | 5:179973353 | TCATCACCCATTGTC[C/T]AACCCTCCTGCTAGT | 55819 |
rs17079867 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RNF130 | GRCh38.p7 | 5:179973870 | CACAAGCATACTGAG[C/T]GCCAACAAAGTCCTT | 55819 |
rs17079868 | snp | A/G | 0.100231 | 0.200173 | intron-variant | RNF130 | GRCh38.p7 | 5:179974333 | ACGACTACACACTCC[A/G]ATGGCCGACCTTTAA | 55819 |
rs17079875 | snp | A/G | 0.130694 | 0.219696 | intron-variant | RNF130 | GRCh38.p7 | 5:179974542 | GCAGGCAATCCATGA[A/G]CGGCTTGACAGCTCT | 55819 |
rs17079876 | snp | A/G | 0.152001 | 0.229992 | intron-variant | RNF130 | GRCh38.p7 | 5:179974699 | CAGTACTTGGAGGGC[A/G]ATGGCTTTGAAAGAG | 55819 |
rs17079880 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | RNF130 | GRCh38.p7 | 5:179977973 | GAGTCTGGAGGCCGC[A/G]TGCCACATCGCATAT | 55819 |
rs17079941 | snp | C/T | 0.196149 | 0.244131 | intron-variant | RNF130 | GRCh38.p7 | 5:180004684 | TACGGCTTAATCTAA[C/T]AGGAATAGTTGGTTC | 55819 |
rs17079966 | snp | G/T | 0.254944 | 0.249951 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016190 | CTTAAATCTTTTACA[G/T]AATCTGGCGAAAGTT | 55819 |
rs17079968 | snp | C/T | 0.256061 | 0.249927 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016423 | TGAAGAATAATTAGA[C/T]TGTAACGCTGTAAAT | 55819 |
rs17616317 | snp | A/G | 0.116838 | 0.211584 | intron-variant | RNF130 | GRCh38.p7 | 5:179941372 | ATTAGAGATTGAACA[A/G]ATTCACAGTTGGGCT | 55819 |
rs17619391 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | RNF130 | GRCh38.p7 | 5:180004140 | ACGATCTTGGAAATT[G/T]GCAATTTTAAAAAGT | 55819 |
rs17673499 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF130 | GRCh38.p7 | 5:179976334 | ATGGTTTTGGAGGCC[C/T]GTAGTTTTAGGTGCC | 55819 |
rs17673520 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:179976347 | CCCGTAGTTTTAGGT[C/G]CCATATGGTTCTGGA | 55819 |
rs17681274 | snp | C/T | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180004306 | TCACACTGTGCCCTA[C/T]TCCTTTAATAATAAA | 55819 |
rs17681505 | snp | A/C | 0.0607341 | 0.163335 | intron-variant | RNF130 | GRCh38.p7 | 5:180013576 | ATTAACTTGTCTGAC[A/C]ACTACATTTTTAAAA | 55819 |
rs17681729 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RNF130 | GRCh38.p7 | 5:180020221 | TGTGGAAGGAATTTT[C/T]GGTTAGGTGTTCACT | 55819 |
rs28478989 | snp | C/T | 0.191775 | 0.243125 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073185 | CCGGAAAAGAGGTGG[C/T]TCCCCAAAAAGAAAT | 55819 |
rs28754309 | snp | C/G | 0.189576 | 0.242588 | intron-variant | RNF130 | GRCh38.p7 | 5:180046460 | TCATTTCTTAGAAAT[C/G]TAAACACGCCACATA | 55819 |
rs33940528 | in-del | -/GACT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180019192 | GATCAAAACCATCCT[-/GACT]AACACGGTGAAACCC | 55819 |
rs33997180 | in-del | -/A | 0.279461 | 0.248258 | intron-variant | RNF130 | GRCh38.p7 | 5:180006296 | CTTCCAATGTGGAAG[-/A]AAAAAAAAAACCTTT | 55819 |
rs34027780 | snp | A/C | 0.249038 | 0.249998 | intron-variant | RNF130 | GRCh38.p7 | 5:180051891 | AACAGATACTTCATG[A/C]AAGATGCTACAGATC | 55819 |
rs34035683 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945407 | CCTATCATCAGTGCT[-/A]AAAAGGGCTCTGATG | 55819 |
rs34044107 | snp | G/T | 0.242201 | 0.249878 | intron-variant | RNF130 | GRCh38.p7 | 5:180056360 | TGTGTCCTGTTACTA[G/T]AGAGAATGGGCTAGA | 55819 |
rs34048926 | in-del | -/TG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992084 | ATGCTCAGCTCCTGC[-/TG]TGTGTCCTGTATCCA | 55819 |
rs34086692 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053855 | TTAATTTGAGACAGA[-/A]GTCTCACTCTGTCGC | 55819 |
rs34097796 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008920 | AATATCTAAACTACT[-/G]GGAAATTCAATAACA | 55819 |
rs34132233 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923719 | CCAACCACGGTGCAG[-/C]CCCTGGAGTTGCTTT | 55819 |
rs34171983 | in-del | -/C | 0.475525 | 0.107882 | intron-variant | RNF130 | GRCh38.p7 | 5:179932217 | TTGTAATTTTAAGTT[-/C]CATGTGTTTAATCAT | 55819 |
rs34223050 | in-del | -/G | 0.0558544 | 0.157504 | intron-variant | RNF130 | GRCh38.p7 | 5:179952851 | TCTCAACTTGATAAA[-/G]GGTATCTAGTCTATA | 55819 |
rs34253318 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037292 | ATCAGTGCTTGTGTG[-/A]AGTATATGAAATCTG | 55819 |
rs34262739 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNF130 | GRCh38.p7 | 5:179973505 | GACTGGGCCAGGGGC[A/G]TTTAATCTACCTTGG | 55819 |
rs34266288 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931032 | CCAAACCTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55819 |
rs34286978 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044157 | ATGAGCCTTTAAAAT[-/C]TTGTCAATAGCAATT | 55819 |
rs34316343 | in-del | -/TGTG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055452 | GTGTGTGTGTGTGTG[-/TGTG]CGTGTGTGTGTGTGT | 55819 |
rs34319790 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928006 | CATCCATCCGCCTCA[-/G]GGGAATATAGCAACA | 55819 |
rs34322803 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963658 | AACGAAGCAGACGTC[-/T]AACGGAGGTGTAAGC | 55819 |
rs34326515 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024858 | CTCCTCAAACTTAAG[-/A]CATCTGACAGTGGGT | 55819 |
rs34333417 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058741 | TAATTTTTGTATTTT[-/T]AGTGGAGATGGGGTT | 55819 |
rs34345494 | snp | A/C | 0.497695 | 0.0338674 | intron-variant | RNF130 | GRCh38.p7 | 5:179932967 | TCAAGAAAGAAGACC[A/C]AAATGACCATTATCA | 55819 |
rs34361237 | in-del | -/A | 0.26078 | 0.249767 | intron-variant | RNF130 | GRCh38.p7 | 5:180026118 | TTTGTTCAACCATCC[-/A]AAAAAAAAAAAGAAA | 55819 |
rs34421268 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057559 | CTCAAAAAAAAAAAA[-/A]TCATGTGTAATGTGT | 55819 |
rs34434279 | snp | A/G | 0.21725 | 0.247846 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073291 | CGGTGGCTCACGCCC[A/G]TAATCGCAGCACTTT | 55819 |
rs34442402 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065149 | TTAAAAAAAAAAAAA[-/A]TCTTGCAAAGACCTA | 55819 |
rs34448835 | in-del | -/A | 0.370162 | 0.219229 | intron-variant | RNF130 | GRCh38.p7 | 5:180030040 | TTGGTAGAGATGAGG[-/A]TTTCATCATGTTGGC | 55819 |
rs34450878 | snp | A/C | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180026938 | CATGAAAGGAAAAGG[A/C]CAATACTGTCATGGA | 55819 |
rs34492552 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928668 | AGTCTCGCTCTATCA[-/C]CCCAGGCTGGAGTGC | 55819 |
rs34526086 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922314 | TTTAAAAAAAATTTC[-/T]TTTTTTAATTTTTTT | 55819 |
rs34559470 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037772 | CCACATAATGCCAAA[-/T]TTTCTCTCCAAAGTA | 55819 |
rs34603792 | snp | A/G | 0.255224 | 0.249945 | intron-variant | RNF130 | GRCh38.p7 | 5:180032287 | ACAGACTATCTTCTA[A/G]AAGTTTACAGTTTTA | 55819 |
rs34628274 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921942 | GGAGAATCACTTGAA[-/C]CCCAGGAGGCGGAGG | 55819 |
rs34636313 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963076 | GCCGGGGCTTCCCCA[-/G]GAAGCTAGACATGCC | 55819 |
rs34642514 | in-del | -/T | | | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954720 | AGCATGTGAATTACA[-/T]TTTGATTGCAAAAAT | 55819 |
rs34647134 | in-del | -/GAAC | 0.420892 | 0.182472 | intron-variant | RNF130 | GRCh38.p7 | 5:180028563 | TCCAGACCTGGGTCA[-/GAAC]CCCTTTCGTAATAAC | 55819 |
rs34664226 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990171 | CCAGTAGTGGCCCCG[-/A]AATGCCTGGCTGCAC | 55819 |
rs34674199 | snp | A/G | 0.248755 | 0.249997 | intron-variant | RNF130 | GRCh38.p7 | 5:180046900 | TCTAGCATCTCCTGC[A/G]AATATGTCTGGCACA | 55819 |
rs34688572 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020730 | TCAAGAGAAAGAAAA[-/G]GGGGGCAGGAGCAAG | 55819 |
rs34690283 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986345 | ATCAAGCAATACAAC[-/T]TTTTTCTTGTAACGT | 55819 |
rs34698128 | in-del | -/A | 0.26271 | 0.249677 | intron-variant | RNF130 | GRCh38.p7 | 5:180033697 | CGAGACTCTGCCTTT[-/A]AAAAAAAAAAAGAGA | 55819 |
rs34733825 | in-del | -/T | 0.4973 | 0.0366419 | intron-variant | RNF130 | GRCh38.p7 | 5:179935780 | TTTTACTTTTTTTTT[-/T]AGTTGTTACCCTGGA | 55819 |
rs34754560 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041798 | ATAAAAGCAAGGCGA[-/G]GGTGTGGTGGCTCAC | 55819 |
rs34771874 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973518 | CGTTTAATCTACCTT[-/G]GGGAAGTGTCTGGAG | 55819 |
rs34822130 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960526 | CCTTGTGGGGATCCT[-/C]CCTTGTGTAGTTAGC | 55819 |
rs34823714 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RNF130 | GRCh38.p7 | 5:180018029 | GGCTGGGCGTGGTGG[C/T]TCACACCTGTAATCT | 55819 |
rs34837643 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037268 | TGGAAAGAAGGACAG[-/T]AGAGAGGCTATCAGT | 55819 |
rs34848443 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939952 | TGTCATAAACGTCCC[-/T]TTTTTTTTTTTTCTA | 55819 |
rs34866732 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942897 | TGACAGAAGAGCCTC[-/A]AAAATGTCTTTTCTT | 55819 |
rs34870362 | in-del | -/T | 0.480223 | 0.0974544 | intron-variant | RNF130 | GRCh38.p7 | 5:180034093 | TGCTTTTTTTTTTTT[-/T]AAATCATGATGGGTA | 55819 |
rs34882290 | snp | A/C | 0.255224 | 0.249945 | intron-variant | RNF130 | GRCh38.p7 | 5:180036836 | GTCTGTCTACCCCCA[A/C]ACTCAGCTTAAGAAA | 55819 |
rs34891287 | in-del | -/T | 0.270351 | 0.24917 | intron-variant | RNF130 | GRCh38.p7 | 5:179981174 | GGTGTAAAGAACAGG[-/T]TATGTGAAGAAAACT | 55819 |
rs34898419 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059896 | GTGAATACATCAGGT[-/T]ACAGAGCAAGGGGGA | 55819 |
rs34904822 | in-del | -/G | | | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919873 | TCCAGAGCCAGGTCA[-/G]GGGAGCAGCACCTGT | 55819 |
rs34918177 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013033 | TCTGGCTGTTACGAA[-/C]CCAATCACTGTTGAG | 55819 |
rs34934872 | in-del | -/A/AA | 0.556718 | 0.144294 | intron-variant | RNF130 | GRCh38.p7 | 5:179929747 | CTCAAAAAAAAAAAA[-/A/AA]TTCTAGGATCAATTG | 55819 |
rs34976451 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953890 | TATCTAGAACATACA[-/G]AAGAACTCTTACAAC | 55819 |
rs34977597 | in-del | -/GT | 0.546917 | 0.0934366 | intron-variant | RNF130 | GRCh38.p7 | 5:179935515 | AAGATATGTCAGCAC[-/GT]GTGTGTGTGTGTGTG | 55819 |
rs34980840 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004149 | GAAATTTGCAATTTT[-/A]AAAAGTGCTCCAGCC | 55819 |
rs34998254 | in-del | -/T/TT/TTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985153 | CCTTTACCCCCTAAC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 55819 |
rs35013583 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012465 | CCAGGCCCTCACACC[-/G]GGGGAAGCACACTGC | 55819 |
rs35045213 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978832 | AATACTCGGTCTTCA[-/T]TTAAGAGTGAGAAAG | 55819 |
rs35058229 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980457 | CAATTCTCCAGCAGT[-/A]AAAAAGTTAGGTGTC | 55819 |
rs35118830 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | RNF130 | GRCh38.p7 | 5:180050787 | TTCTCTCAGCACTTC[G/T]GGGTTGTTCTTGCAC | 55819 |
rs35135297 | snp | C/T | 0.247905 | 0.249991 | intron-variant | RNF130 | GRCh38.p7 | 5:180042532 | AAATCCTGAAACAGA[C/T]TGTTTACTTTCATCA | 55819 |
rs35149336 | in-del | -/AG/GC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976001 | ACTGACTCTGATGCA[-/AG/GC]GTCAGGTCTGGAAAG | 55819 |
rs35151349 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964953 | TGTTTTAAGTTAGGG[-/A]AAAATGTATATGGCA | 55819 |
rs35188893 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020761 | ACCTGCCCCGAACAG[-/A]AAAGCTTTCTTCCTT | 55819 |
rs35203472 | in-del | -/T | 0.496175 | 0.0435625 | intron-variant | RNF130 | GRCh38.p7 | 5:180065812 | AAACACAGAAAAAAA[-/T]GTTTCCTTCCTTTAT | 55819 |
rs35206203 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959277 | ACCAAGCATCCCCAA[-/G]GACATCAAATAATTA | 55819 |
rs35210948 | in-del | -/TA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920780 | TATATATTTATATAT[-/TA]ATATATATATTTTTT | 55819 |
rs35214110 | in-del | -/A | 0.273318 | 0.24891 | intron-variant | RNF130 | GRCh38.p7 | 5:179924494 | GCAAAACTCTGTCTG[-/A]AAAAAAAAAAAAATA | 55819 |
rs35245433 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971815 | TCTAGAGAACTCAGT[-/G]TTCTACTGGGATCTG | 55819 |
rs35245733 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934209 | AGCCTGGCGGCATGG[-/C]AAAGGTGGTGGGAAG | 55819 |
rs35253256 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953649 | GATCATCAAAGATCT[-/A]AAAGTTAAGAGCAAA | 55819 |
rs35328290 | in-del | -/TC | 0.482683 | 0.0914256 | intron-variant | RNF130 | GRCh38.p7 | 5:180047009 | TTTGTGGCAAAGAGT[-/TC]TCTGTTTCACGTGGT | 55819 |
rs35364071 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179955888 | TGCTTTAATACTCCC[-/A]AAAGGATGAAGGAAA | 55819 |
rs35391995 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963843 | CACCAAAAAGTGTGC[-/T]GGTGAAAATATGTAT | 55819 |
rs35437763 | snp | C/T | | | splice-acceptor-variant | RNF130 | GRCh38.p7 | 5:179978286 | GTCTGGGTCAGTTTC[C/T]TAAAATGAAAAGTAC | 55819 |
rs35447931 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050198 | AGGAATTGGCTCTGG[-/G]CAATTATGGAGACAG | 55819 |
rs35468324 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992894 | CCAACCCATGACAGG[-/C]CCCCAGTGTGTGATG | 55819 |
rs35503311 | in-del | -/G | 0.447032 | 0.153878 | intron-variant | RNF130 | GRCh38.p7 | 5:179926551 | TACTCGGGAGGCTGA[-/G]GCAGGGGAATTGCTT | 55819 |
rs35516757 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060827 | TAATCCCAGCACTTT[-/T]GGGAGGCCGAGGTGG | 55819 |
rs35592104 | snp | A/T | 0.254944 | 0.249951 | intron-variant | RNF130 | GRCh38.p7 | 5:180020661 | TAGGGCCAAGGGGCC[A/T]CAGTACAGCACTTGA | 55819 |
rs35598193 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980381 | TCAGCATTCTGGTTG[-/A]AAAGTAAAAAGTGTT | 55819 |
rs35608303 | snp | A/G | 0.248755 | 0.249997 | intron-variant | RNF130 | GRCh38.p7 | 5:180047637 | TAATCCTAGCTACTC[A/G]GGAGGCTGAGGCAGA | 55819 |
rs35629659 | in-del | -/T | 0.470034 | 0.11868 | intron-variant | RNF130 | GRCh38.p7 | 5:179957882 | AAAAATTCAAAATTC[-/T]TTTTTTTTTTTTTGA | 55819 |
rs35729589 | in-del | -/A | 0.486398 | 0.0813386 | intron-variant | RNF130 | GRCh38.p7 | 5:180056254 | ATAGTATCTGTGGGG[-/A]AAAAAAAAAAAACCC | 55819 |
rs35735455 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954263 | TATCAAAGAGAACTG[-/A]AAAATATATGTTCAG | 55819 |
rs35800495 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021528 | TTCAACATAACAATT[-/G]CTTAAAATGTGCAAA | 55819 |
rs35802224 | in-del | -/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179983353 | TTTTTTTTTTTTTTT[-/T]GCATATGGACATACA | 55819 |
rs35806855 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021447 | CTGTCAAGCAACTCT[-/A]AAGATGTCATGGAAT | 55819 |
rs35844702 | in-del | -/TGAC | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180019191 | AGATCAAAACCATCC[-/TGAC]TAACACGGTGAAACC | 55819 |
rs35911906 | in-del | -/A | 0.255224 | 0.249945 | intron-variant | RNF130 | GRCh38.p7 | 5:180036757 | TTATAAATATTTCAC[-/A]AAGTTTTTCTCTAAT | 55819 |
rs35928331 | snp | A/G | 0.485596 | 0.0836329 | intron-variant | RNF130 | GRCh38.p7 | 5:180023080 | GATGTAGGATGGCAA[A/G]AGCCAGGTTTTTCAT | 55819 |
rs35941932 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968668 | GAGACTCTGTCTCAT[-/A]AAAAAAAAAAAAAAA | 55819 |
rs35973843 | snp | C/T | 0.247905 | 0.249991 | intron-variant | RNF130 | GRCh38.p7 | 5:180039502 | CTTGGCCTCCTAAAG[C/T]ATATCTTACTTCTAA | 55819 |
rs35988237 | snp | C/T | 0.251014 | 0.249998 | intron-variant | RNF130 | GRCh38.p7 | 5:180051528 | AGGCGTGAGCCACCG[C/T]GCCCCGGCCTTTGTA | 55819 |
rs35995020 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926717 | AGCAAATTAACCAAA[-/C]CTAAGGAGGGGGCGG | 55819 |
rs35997713 | in-del | -/ATTT | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:179988610 | TTTATTTCCATTTTC[-/ATTT]ATTTCAAGAACTTAA | 55819 |
rs35998925 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009153 | CATAATATAAAACTT[-/C]CCAGGAAAAATAGTA | 55819 |
rs36014571 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972298 | CAGAACCTCCCTCTG[-/A]AAAGTCACGGGGACG | 55819 |
rs36031769 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924492 | AGAGCAAAACTCTGT[C/T]TGAAAAAAAAAAAAA | 55819 |
rs55716450 | in-del | -/GGAGGGATACACA | 0 | 0 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016344 | TCTGGCCCAGTTTCA[-/GGAGGGATACACA]CGCCAAAGGAAATGT | 55819 |
rs55734821 | snp | A/G | 0.493881 | 0.054972 | intron-variant | RNF130 | GRCh38.p7 | 5:180031847 | TTTTCCAAACTGGTT[A/G]TACCATTTCACATTT | 55819 |
rs55755063 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998471 | AATTTTTAAAAAGTT[C/T]TTAAAACTAAGAAAC | 55819 |
rs55761202 | in-del | -/GAAA | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180036848 | CCACACTCAGCTTAA[-/GAAA]TAAAACATTATAGAT | 55819 |
rs55805918 | in-del | -/CG/GC | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072920 | AACGCGCGCGCGCGC[-/CG/GC]ACACACACACGACTC | 55819 |
rs55808906 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179971140 | GTAGAAAGTCACAGT[C/T]TTGTGACTGGAAATA | 55819 |
rs55837514 | snp | A/C | 0.113685 | 0.209567 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180014952 | GATCACGCCACTGCA[A/C]GCCAGCCTGGGTGAC | 55819 |
rs55862338 | in-del | -/CT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064933 | TCCACTTACTTCTCT[-/CT]AGGATTCACAAACTG | 55819 |
rs55965907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922437 | TGTGCCTCAGCCTCC[C/T]AAGTAGCTGAGATTA | 55819 |
rs56015351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041654 | CTGCAGACTGCTGGC[A/G]CACAGTGGCAGAGGG | 55819 |
rs56130424 | in-del | -/T | 0.39325 | 0.204889 | intron-variant | RNF130 | GRCh38.p7 | 5:180053826 | AAAGCAAATACATTC[-/T]TTTTTTTTTTTTTTT | 55819 |
rs56235463 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922415 | CCTCCTGGGTTCAAG[A/C]GATTCTTGTGCCTCA | 55819 |
rs56691249 | in-del | -/A | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180019400 | AAAAAAAAAAAAAAA[-/A]TCACTTTGAAGTTCC | 55819 |
rs56821111 | snp | A/C | 0.121022 | 0.21416 | intron-variant | RNF130 | GRCh38.p7 | 5:179948444 | GGAGGCTGAGGCGAG[A/C]GGATCACCTGAGGTC | 55819 |
rs57000847 | snp | G/T | 0.0711525 | 0.174681 | intron-variant | RNF130 | GRCh38.p7 | 5:179967810 | GCTTCCTGGGCAAAA[G/T]AACTGTTTCAGGTCA | 55819 |
rs57008562 | snp | A/C | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:179990170 | GACCAGTAGTGGCCC[A/C]GAATGCCTGGCTGCA | 55819 |
rs57087166 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055281 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAACAGCAA | 55819 |
rs57117216 | snp | A/C | 0.222333 | 0.248464 | intron-variant | RNF130 | GRCh38.p7 | 5:179987050 | TATGAGTTTTTGGTG[A/C]ACTCTTTGTTTTTTT | 55819 |
rs57141821 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | RNF130 | GRCh38.p7 | 5:180033936 | AAATGTTGAGTAAGT[A/G]TAATGTTGAATACAA | 55819 |
rs57144908 | snp | A/G | 0.195214 | 0.243923 | intron-variant | RNF130 | GRCh38.p7 | 5:180019500 | CTGCCTGTGTCTCAG[A/G]GAGACTGCTGGCTCC | 55819 |
rs57266236 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | RNF130 | GRCh38.p7 | 5:180010934 | AGATTTCAGTGTATT[C/T]AGGAAGATCAGTGGA | 55819 |
rs57346064 | in-del | -/TTCAT | 0.258288 | 0.249863 | intron-variant | RNF130 | GRCh38.p7 | 5:180034591 | TAGGAATTTGTTCAT[-/TTCAT]CTAAGGTGTCTAATT | 55819 |
rs57356486 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF130 | GRCh38.p7 | 5:180029289 | AGACAGCTATGGAAA[C/T]AGTGATCTATAAATT | 55819 |
rs57623727 | in-del | -/CACAAAACAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977432 | GAAACCCACAGGAAT[-/CACAAAACAA]TGCCAAGCACAGTGA | 55819 |
rs57674660 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933001 | ATGAAAAAGACATCA[C/T]TGCAAAGCCTACAGA | 55819 |
rs57744473 | in-del | -/A | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180061069 | AAAAAAAAAAAAAAA[-/A]GCTATGTTCATGCAT | 55819 |
rs57844233 | in-del | -/GTTT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180033776 | ATTCTTTCAAGACTT[-/GTTT]ATTACATCTAGTGGT | 55819 |
rs57927481 | in-del | -/C/CTGTGTG | 0.295088 | 0.245901 | intron-variant | RNF130 | GRCh38.p7 | 5:180055440 | AATGTCAGATGACTT[-/C/CTGTGTG]TGTGTGTGTGTGCGT | 55819 |
rs57945500 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RNF130 | GRCh38.p7 | 5:179968687 | AAAAAAAAAAAAAAA[A/G]AGAGAGAAAGTTTCT | 55819 |
rs58007232 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | RNF130 | GRCh38.p7 | 5:179998750 | CAGTTTAAACCCAAT[A/G]TTTCTTTATTTTCTG | 55819 |
rs58271600 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | RNF130 | GRCh38.p7 | 5:179930106 | CTTGTCGCCCAGGCT[A/G]GAGTGCAATGGCGTG | 55819 |
rs58286692 | snp | C/T | 0.196149 | 0.244131 | intron-variant | RNF130 | GRCh38.p7 | 5:180070641 | AAAGTTCAGCGTGGG[C/T]CAAAACCCAAAAAAT | 55819 |
rs58518365 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | RNF130 | GRCh38.p7 | 5:179989221 | ATCACGAGAACAACA[C/T]GGAGTTAACCACCCT | 55819 |
rs58548426 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF130 | GRCh38.p7 | 5:180060691 | ATCTCTACATAAATA[C/T]GTAGTCTTCTGGAGA | 55819 |
rs58899481 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | RNF130 | GRCh38.p7 | 5:179980965 | CATGCCCAGGGCCAG[C/G]TGGCAGCACAGAGGA | 55819 |
rs58904455 | in-del | -/AAAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968688 | AAAAAAAAAAAAAAA[-/AAAA]GAGAGAAAGTTTCTA | 55819 |
rs59011938 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920777 | CATCTGGGCATATAT[A/T]TTTATATATATATAT | 55819 |
rs59121777 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | RNF130 | GRCh38.p7 | 5:180066308 | TTCTCTTGCTGCCGC[A/C]ATGTAAGAAGTACCT | 55819 |
rs59150995 | snp | A/C | 0.187685 | 0.242109 | intron-variant | RNF130 | GRCh38.p7 | 5:180060648 | TCAAGAGGCAACTGG[A/C]CTCCTAACCTTATTA | 55819 |
rs59240958 | in-del | -/G | 0.418653 | 0.184544 | intron-variant | RNF130 | GRCh38.p7 | 5:180038411 | AAAAAAGCCTGTTTT[-/G]TTTTTTTTTTTATTT | 55819 |
rs59273081 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920779 | TCTGGGCATATATAT[A/T]TATATATATATATAT | 55819 |
rs59354197 | in-del | -/A | 0.308166 | 0.243139 | intron-variant | RNF130 | GRCh38.p7 | 5:180018295 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAGA | 55819 |
rs59577461 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179922494 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 55819 |
rs59639284 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951389 | TTGTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC | 55819 |
rs59706994 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068632 | AAATGTTATTCAGAA[A/T]TTCACACGTGCCAAA | 55819 |
rs59826561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179992568 | AGGATTTAAGGATCC[A/G]TTGTTGGAGAATTAC | 55819 |
rs60044157 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | RNF130 | GRCh38.p7 | 5:180056405 | CAGAGGAGGCTGCAA[C/G]AGGTGTGGAGAGAAA | 55819 |
rs60202107 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933178 | TGTGGAAGACTGGTG[A/C]TACTTTTTCCCTCAA | 55819 |
rs60246221 | in-del | -/CAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067569 | GCTAATGGAAATCAT[-/CAT]TCAAATGTGAAGGAA | 55819 |
rs60269817 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179985499 | CACTCTGAAGCCTTC[A/G]GTATTGAATTCATGG | 55819 |
rs60320083 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922551 | CTCCTGAGCTCAAGC[C/G]ATCTGCATCAGCCTC | 55819 |
rs60388708 | snp | C/T | 0.197082 | 0.244335 | intron-variant | RNF130 | GRCh38.p7 | 5:180063597 | CTAAAAATCAAGATA[C/T]GGGAGGAGGTAACAG | 55819 |
rs60407359 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | RNF130 | GRCh38.p7 | 5:179975025 | CACACCTGCAGGTGC[C/T]GCTGTGCCGAATGCG | 55819 |
rs60509028 | in-del | -/T/TT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180029866 | CTTTTTTTTTTTTTT[-/T/TT]GAGACAAGGTCTTGC | 55819 |
rs60567501 | in-del | -/GT/GTGT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179935533 | TGTGTGTGTGTGTGT[-/GT/GTGT]ATACATTTTAAATCT | 55819 |
rs60717527 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF130 | GRCh38.p7 | 5:179929944 | TCGATAACACATAAT[C/T]GTTCTCTGTATAAAA | 55819 |
rs61092349 | in-del | -/GACTCACTGCAATCTC | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180021050 | CAGTGGCGCAATCTC[-/GACTCACTGCAATCTC]TGCCTCGCGGGTTCA | 55819 |
rs61232613 | in-del | -/ATATAT/ATATATATATATATATATATAT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179998884 | TATATATATATATAT[lengthTooLong]GTTTTATATATCTGA | 55819 |
rs61340522 | in-del | -/ATTTATTTATTT/ATTTATTTATTTATTTATTT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180051267 | TTTATTTATTTATTT[lengthTooLong]GAGACAGAGTCTCGA | 55819 |
rs61356660 | snp | A/G | 0.221737 | 0.248397 | intron-variant | RNF130 | GRCh38.p7 | 5:179988985 | CGGGTGTATTAGTCC[A/G]TTTTTATGCTGCTAT | 55819 |
rs61675210 | in-del | -/T/TT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180048014 | ACTTTTTTTTTTTTT[-/T/TT]ATTGGAACAACAATG | 55819 |
rs61701033 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179930205 | TGGGATTACAGGCAT[C/G]TGCCACCACACCCGG | 55819 |
rs61754470 | snp | C/T | 0.00552073 | 0.0522483 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180040553 | TATTTTCTCTTTAAA[C/T]GTGCAGTTTCCCCTC | 55819 |
rs62404969 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179975689 | AAAACTCTACACTCA[A/G]CCAGGGCAGTAAGCA | 55819 |
rs62404970 | snp | C/T | 0.254385 | 0.249962 | intron-variant | RNF130 | GRCh38.p7 | 5:179977114 | CATTTCTGAATTGTG[C/T]GACCCTGGAACCTGC | 55819 |
rs62404971 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980465 | CAGCAGTAAAAAAGT[A/T]AGGTGTCATAATTGC | 55819 |
rs62404973 | snp | C/T | 0.203882 | 0.245709 | intron-variant | RNF130 | GRCh38.p7 | 5:179991172 | TGCTGAGAAAGTCTG[C/T]TGTTTGTCTGATGGA | 55819 |
rs62404974 | snp | C/T | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:179993991 | ATAGGGAATCCTTTC[C/T]CCATTTCTTGTTTTT | 55819 |
rs62404976 | snp | A/G | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180000089 | CTTTTCAAAATGTAA[A/G]ACTCTCTCAAGATGT | 55819 |
rs62404977 | snp | A/G | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180001887 | GTACTAGAGTTCTAC[A/G]GCCTGTAAGGGCAAG | 55819 |
rs62404978 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006016 | CAGTCTCTGTATATG[A/G]AAAGTGTTATTTATT | 55819 |
rs62404979 | snp | A/G | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:180008348 | CTCACAGAGCCCAGT[A/G]GGAATAGGCTCTCCC | 55819 |
rs62405015 | snp | C/T | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180011433 | TTAAGGGTAACAGGG[C/T]ATCATATCTCAAACT | 55819 |
rs62405016 | snp | A/G | 0.256061 | 0.249927 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015551 | AGGAAAGGAGTAGGG[A/G]AAGGAGTAGGGAAGG | 55819 |
rs62405017 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180029836 | GTGGGTCACCATGCC[G/T]GGCCACTATCCACCT | 55819 |
rs62405019 | snp | C/G | 0.0383715 | 0.133092 | intron-variant | RNF130 | GRCh38.p7 | 5:180034974 | TCTATCTAAAGGTTT[C/G]TCAATTTTATTGATA | 55819 |
rs62405020 | snp | A/G | 0.417359 | 0.185718 | intron-variant | RNF130 | GRCh38.p7 | 5:180046129 | GCGGTGGACCGCGGC[A/G]CGTGCAGGCCCACAG | 55819 |
rs62405021 | snp | A/T | 0.482609 | 0.0916147 | intron-variant | RNF130 | GRCh38.p7 | 5:180046218 | GACCGGGGCAGGTGC[A/T]GGGCCCGCCAAGCTC | 55819 |
rs62405022 | snp | C/T | 0.18989 | 0.242666 | intron-variant | RNF130 | GRCh38.p7 | 5:180047219 | CTATCTTTCCTTATT[C/T]TCCTTTGTCAAATTC | 55819 |
rs62405023 | snp | C/T | 0.188946 | 0.24243 | intron-variant | RNF130 | GRCh38.p7 | 5:180051287 | CAGAGTCTCGATCTG[C/T]CACCCAGGCTGGAAT | 55819 |
rs62405024 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180056250 | TAAGATAGTATCTGT[A/G]GGGAAAAAAAAAAAA | 55819 |
rs62405046 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180069599 | GAGATTCCTCTAGGT[C/T]AACAAATCTCCTCTT | 55819 |
rs62407265 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924580 | AGGTGGGTGGATCAC[C/T]TGAGGTCAGGAGGAG | 55819 |
rs62407266 | snp | C/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179954145 | GCATACTCTCTTGGT[C/G]AGAATGCAAAATGGT | 55819 |
rs62407267 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957976 | TCCGCCTCCCGGGTT[A/C]ACGCCATTCTCCTGC | 55819 |
rs62407268 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179960190 | TTGGGAATTGAAATT[C/T]AGTAACCTCGCTTAC | 55819 |
rs62407269 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179963597 | GGAGGAAATCACTCT[G/T]GGGAGAAGGTTTAAG | 55819 |
rs66520412 | in-del | -/CT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180047012 | GTGGCAAAGAGTTCT[-/CT]GTTTCACGTGGTAAT | 55819 |
rs66616765 | in-del | -/G | 0.447032 | 0.153878 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015619 | GTAGGGAAAGGAGTA[-/G]GGAAAGGAGTAGGGA | 55819 |
rs66797381 | in-del | -/G | 0.473451 | 0.112115 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015525 | AGTAGGAAAGGAGTA[-/G]GGAAAGGAGTAGGAA | 55819 |
rs66823881 | in-del | -/CTGA | 0.421051 | 0.182323 | intron-variant | RNF130 | GRCh38.p7 | 5:180019190 | AAGATCAAAACCATC[-/CTGA]CTAACACGGTGAAAC | 55819 |
rs66864272 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179956376 | ACACAACTCTCTAGC[-/A]ACTCCTGATTTCAGC | 55819 |
rs67369864 | in-del | -/CAGGAGGGATACA | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016343 | CTCTGGCCCAGTTTC[-/CAGGAGGGATACA]ACGCCAAAGGAAATG | 55819 |
rs67542237 | multinucleotide-polymorphism | AA/GC | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179968325 | AAACAAAAAAAGAAG[AA/GC]GGCGGCTAGCGGTAA | 55819 |
rs67545539 | in-del | -/T/TT/TTTT | 0.406641 | 0.194842 | intron-variant | RNF130 | GRCh38.p7 | 5:180048001 | ATGTCAACAGCACAC[-/T/TT/TTTT]CTTTTTTTTTTTTTA | 55819 |
rs67726603 | in-del | -/GCAATCTCGACTCACT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021043 | TGGAGTGCAGTGGCG[-/GCAATCTCGACTCACT]CAATCTCTGCCTCGC | 55819 |
rs71001059 | in-del | -/A | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179931057 | AAAAAAAAAAAAAAA[-/A]TCAAGAATAGGTGTT | 55819 |
rs71001060 | in-del | -/TGTGTG/TGTGTGTG/TGTGTGTGTGTG/TGTGTGTGTGTGTG | 0.172351 | 0.237636 | intron-variant | RNF130 | GRCh38.p7 | 5:179933398 | GTGTGTGTGTGTGTG[lengthTooLong]AGTGTGTGGTAAAAA | 55819 |
rs71001061 | in-del | -/TATCATCAAAACGAAG/TGAAATATCATCAAAACGAAATATCATCAAAA | 0.625 | 0.125 | intron-variant | RNF130 | GRCh38.p7 | 5:179937137 | GAAATATCATCAAAA[lengthTooLong]CGAAATATCATCAAA | 55819 |
rs71001067 | in-del | -/A | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180010272 | AAAAAAAAAAAAAAA[-/A]GTATCTCAAGGTAAT | 55819 |
rs71281057 | in-del | -/GAAATATCATCAAAACGAAATATCATCAAAAT | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179937106 | GGATATCATTAAAAC[lengthTooLong]GAAATATCATCAAAA | 55819 |
rs71281059 | in-del | -/C/CTAA | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179953124 | AAAAAAATATGAGAA[-/C/CTAA]TAAATGAGTTCAGCA | 55819 |
rs71577408 | multinucleotide-polymorphism | ACA/CAG | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180008010 | TTTTTTTTTTTTTAA[ACA/CAG]GTTATATTACATGTT | 55819 |
rs71591446 | in-del | -/CAAA | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179931778 | GACTCTGTCTTAAAA[-/CAAA]CAAACAAACAACAAA | 55819 |
rs71591448 | in-del | -/TG | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179937934 | GTGTGTGTGTGTGTG[-/TG]AGAGAGAGAGAGAGA | 55819 |
rs71591449 | in-del | -/TGTTT | 0.390763 | 0.206606 | intron-variant | RNF130 | GRCh38.p7 | 5:179982566 | TATGGTGAGATTTTG[-/TGTTT]TGTTTTGTTTTGTTT | 55819 |
rs71591450 | in-del | -/A | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180019383 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55819 |
rs71591451 | in-del | -/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180032363 | TCTAAATCCCTTCCT[-/C]CCCTCCCTCCCTTCT | 55819 |
rs71591452 | in-del | -/TTGT | 0.493013 | 0.058691 | intron-variant | RNF130 | GRCh38.p7 | 5:180033774 | ACATTCTTTCAAGAC[-/TTGT]TTATTACATCTAGTG | 55819 |
rs71591454 | in-del | -/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180038407 | AAAAAAAAAAGCCTG[-/T]TTTTTTTTTTTTTTT | 55819 |
rs71596443 | snp | A/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180008008 | TTTTTTTTTTTTTTT[A/T]ACAGGTTATATTACA | 55819 |
rs71613434 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179989795 | TTTGTAAATTCTTTG[G/T]TTTATTTTTTCTTCT | 55819 |
rs71613435 | snp | A/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180026111 | AACTAATTTTGTTCA[A/C]CCATCCAAAAAAAAA | 55819 |
rs71613436 | snp | C/T | 0.170733 | 0.237101 | intron-variant | RNF130 | GRCh38.p7 | 5:180031009 | TCAATGGGAAGAAGA[C/T]AAGGATGAAAACCAT | 55819 |
rs71613437 | snp | C/T | 0.247905 | 0.249991 | intron-variant | RNF130 | GRCh38.p7 | 5:180045985 | GGCGGTGGATGGGAC[C/T]GAGCCCCGTGGAGCA | 55819 |
rs71613438 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180046044 | GTGGCGTGGACGGAG[A/G]GGGGTGGGGCTCGGG | 55819 |
rs71613439 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF130 | GRCh38.p7 | 5:180063127 | GATGATGACGAGCCA[C/T]TGCAGGGGTTTAAGC | 55819 |
rs71613440 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180068179 | CTCCCAACCCCCACT[C/T]TGGGGCCAAACAAAA | 55819 |
rs71769924 | in-del | -/GT | 0.189261 | 0.242509 | intron-variant | RNF130 | GRCh38.p7 | 5:180068312 | AAGCTCACCATTTGA[-/GT]AAGTAATAAGAAAGC | 55819 |
rs71769985 | in-del | -/ACA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005434 | ACAACAACAACAACA[-/ACA]CCAACAGAAACCATA | 55819 |
rs71924344 | in-del | -/ATC | 0.0271762 | 0.113356 | intron-variant | RNF130 | GRCh38.p7 | 5:180067564 | TATAGGCTAATGGAA[-/ATC]ATCATTCAAATGTGA | 55819 |
rs71959214 | in-del | -/AT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920795 | ATATATATATATATA[-/AT]TTTTTTTTTTTGAGA | 55819 |
rs72813770 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179927333 | AATTATTATCTTTGT[C/T]ATTGGCTACATAATG | 55819 |
rs72813773 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933423 | GTGTGTGTGTGTGTG[A/T]GTGTGTGGTAAAAAG | 55819 |
rs72813780 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179966542 | TGATTTCAAAACAAG[A/G]TTTATAAAACAGCGA | 55819 |
rs72813783 | snp | C/T | 0.0165326 | 0.0894035 | missense | RNF130 | GRCh38.p7 | 5:179980158 | TTACTGTCCTGGTTG[C/T]CAATTTACTGATGGC | 55819 |
rs72813784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179989815 | TTTTTTCTTCTGTCT[C/T]TGTGGTTTCATGGAG | 55819 |
rs72813785 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179999998 | AGATTTGATTCCCTT[C/T]TCTTTCTCCTTTGTG | 55819 |
rs72813786 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180000807 | ATTGATTGTCTACAC[A/G]TTTTCTTGTATCTCT | 55819 |
rs72813787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002288 | AAGAACAGGTGGAGC[A/G]GCTCCATCTCTGCTG | 55819 |
rs72813801 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | RNF130 | GRCh38.p7 | 5:180030643 | CTCCGATGTAGCTGG[G/T]ATTACTGATGCTTGC | 55819 |
rs72815707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044491 | CAGCTACACGCTAAG[C/T]ACCAAAGAGAGATAC | 55819 |
rs73335521 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | RNF130 | GRCh38.p7 | 5:180048403 | CAGGATTAACCTCCG[A/T]ATCTAGGCAATTTCT | 55819 |
rs73338298 | snp | C/T | 0.02016 | 0.0983543 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919947 | CGTAAGCAGGGACCA[C/T]AAAAGGATGTTAAAA | 55819 |
rs73338301 | snp | A/T | 0.0825414 | 0.185628 | intron-variant | RNF130 | GRCh38.p7 | 5:179920738 | GGGCACATGATCTTA[A/T]GGAGGACTGCCCCCC | 55819 |
rs73340208 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | RNF130 | GRCh38.p7 | 5:179922205 | CTGATGACTAGTGAC[A/G]TTGAGCATCTTTTCA | 55819 |
rs73340210 | snp | G/T | 0.0829062 | 0.185956 | intron-variant | RNF130 | GRCh38.p7 | 5:179922249 | CAACCGTGTATCTTC[G/T]TTTGTGAAGTGTTTT | 55819 |
rs73342216 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RNF130 | GRCh38.p7 | 5:179945229 | ACCTGTGACCCCTTT[C/T]CCTCCACTACGATGA | 55819 |
rs73342221 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | RNF130 | GRCh38.p7 | 5:179948304 | CAACAGTTAACAGTT[A/T]CTTCCTGCCCAGCTT | 55819 |
rs73342229 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | RNF130 | GRCh38.p7 | 5:179951899 | CAAAATTTACAAATG[A/G]GTGAAATAGGACTCA | 55819 |
rs73342289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952651 | GGATTGTACATTATG[A/G]CCAAGTGGGATTTGT | 55819 |
rs73342292 | snp | C/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179952707 | ATCAATGTAATGCAC[C/G]ACATTCATAGGATAG | 55819 |
rs73344319 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | RNF130 | GRCh38.p7 | 5:179966440 | GTGGAGAGCACGAGC[A/G]CTCACAGCATACAAC | 55819 |
rs73344328 | snp | A/T | 0.0685596 | 0.171987 | intron-variant | RNF130 | GRCh38.p7 | 5:179970937 | TTTTTTGGCACCCTG[A/T]TTGAATGTCATTTAA | 55819 |
rs73344340 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RNF130 | GRCh38.p7 | 5:179973650 | CGCTCACCCTCACTA[C/T]GGCTCTGGGCTCTCA | 55819 |
rs73344346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973970 | AATCATGAAATTCAG[C/T]GCCCTCCCCTTTCCT | 55819 |
rs73348242 | snp | A/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179985370 | GTTTTATCTGGATTC[A/T]ATTCTACAGCATTAA | 55819 |
rs73348244 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179985653 | CTATTCGGTCCTCCC[A/T]GTTTTGCAATTAAAA | 55819 |
rs73348268 | snp | C/T | 0.197703 | 0.244469 | intron-variant | RNF130 | GRCh38.p7 | 5:179994634 | GGTGGCTTTCTCAAA[C/T]GCTGGTTACAGTAGT | 55819 |
rs73348273 | snp | C/T | 0.190205 | 0.242744 | intron-variant | RNF130 | GRCh38.p7 | 5:179997765 | AGCCACCATGCCTGG[C/T]CCTTTAGTCTTGATT | 55819 |
rs73348275 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | RNF130 | GRCh38.p7 | 5:179997821 | TTATTTTTTTTTGCT[G/T]CTTCTGACTTTGGGT | 55819 |
rs73350018 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180054250 | TGAGATGATTTGTAA[C/T]GACCCAGCTTTCTTT | 55819 |
rs73350028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057649 | TGCCAAGAGGATTAT[C/T]ACACCCCCGCAATAC | 55819 |
rs73350044 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180064461 | CCAACAGTTTTTAGT[C/T]CTTCTGGTGGTCTAT | 55819 |
rs73350154 | snp | C/T | 0.19459 | 0.243782 | intron-variant | RNF130 | GRCh38.p7 | 5:180010519 | CGCATGGCACCTTGC[C/T]CAGCTACATTTTTGT | 55819 |
rs73350172 | snp | A/G | 0.186105 | 0.241697 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016563 | CCGCCAGTACTAACT[A/G]TCAGAGATGGCAATC | 55819 |
rs73350175 | snp | C/T | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016664 | AACAGGAACTTCTGT[C/T]TCCACACTGCTTGAG | 55819 |
rs73810488 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | RNF130 | GRCh38.p7 | 5:179921054 | ATTATTTGACTATCT[C/G]TGCTACTCAAAGCTG | 55819 |
rs73810492 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | RNF130 | GRCh38.p7 | 5:179977227 | ATAGTCTGCTCAGAG[A/C]AGAGCATCTGAACCA | 55819 |
rs73810493 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | RNF130 | GRCh38.p7 | 5:179981279 | GACAAGGGGCAAAAA[C/T]CGCGACTGTCCCAGG | 55819 |
rs73810929 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RNF130 | GRCh38.p7 | 5:180028601 | CAGCTGATCCCGCTA[C/T]GTAGGTATGCAAAGT | 55819 |
rs73810932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037288 | AGGCTATCAGTGCTT[A/G]TGTGAGTATATGAAA | 55819 |
rs73810939 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF130 | GRCh38.p7 | 5:180063652 | CCTGTCTCAGTGTTG[C/T]CTTATTTCATTACAA | 55819 |
rs73810942 | snp | A/C | 0.232651 | 0.249397 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072267 | GGCAGCCGGGTCAGC[A/C]GCTGGTGCTGGTTGT | 55819 |
rs74293464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179968236 | GGAGGCGGAGSTTGC[A/G]GTGAGCCGAGATCGC | 55819 |
rs74347382 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | RNF130 | GRCh38.p7 | 5:180053650 | TATTCAGAGCAAGAA[A/G]AGTTGGAAAGAAATA | 55819 |
rs74428116 | snp | A/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179928613 | TTCTTCCAAAACTGT[A/T]TTTTTTTAATTGTTG | 55819 |
rs74444675 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179982405 | CCTGAGGTAAATACT[C/G]CAAGTAGAAAGATGG | 55819 |
rs74445981 | snp | A/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179976693 | CTTCTTCAGTTTGAT[A/T]TTTTTTTTTTTTTTA | 55819 |
rs74496447 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RNF130 | GRCh38.p7 | 5:180020528 | CGAATGTGTAAGCCA[C/T]TGAGTGGTAGTCACT | 55819 |
rs74507840 | snp | A/G | 0.195214 | 0.243923 | intron-variant | RNF130 | GRCh38.p7 | 5:180060430 | ATTATGTCTTTTATG[A/G]TATCATAAGCTGAAG | 55819 |
rs74514672 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180059267 | TCAGCTGAAACATCA[G/T]TTCTTCAGGGACGCC | 55819 |
rs74521660 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | RNF130 | GRCh38.p7 | 5:179967249 | GAAAACTAAAATTCA[C/T]TGCAGATCAGAGAAG | 55819 |
rs74522366 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | RNF130 | GRCh38.p7 | 5:179977327 | AAGTCCCTGGAGTTG[C/T]TGTACCCAGAGCCAG | 55819 |
rs74550372 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180039258 | TTTTCTTTTTTTTTT[G/T]AGATGGAGTCTTGCT | 55819 |
rs74563387 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044789 | GTGAGCCAAGATTGT[A/G]CCACTGGACTCCAGC | 55819 |
rs74642151 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | RNF130 | GRCh38.p7 | 5:180032895 | ACCACAAGGAATTTA[A/T]ATATCCATTTTAAGA | 55819 |
rs74662248 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF130 | GRCh38.p7 | 5:179973232 | CCATGGCACATCCCT[C/T]GCTTCCACAAAGCTG | 55819 |
rs74696544 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RNF130 | GRCh38.p7 | 5:179939850 | CACCAAAAATTCCCT[C/G]AAGACATCATCTGAG | 55819 |
rs74716751 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179973589 | TGCAGGGCCATCACA[C/T]GGGCAGAGCGGCCCC | 55819 |
rs74719337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035919 | TGCTGCCATTCATTA[A/T]TGTCATACTTTATTT | 55819 |
rs74723068 | snp | G/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179943990 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 55819 |
rs74723130 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180017732 | GAAAATATGATAATA[A/C]TGCTATAATCCTGAC | 55819 |
rs74736185 | snp | A/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179935807 | TTGTTACCCTGGATT[A/C]TGACACGTATCCTTG | 55819 |
rs74752505 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | RNF130 | GRCh38.p7 | 5:180001867 | TACAGGTTCAAGCAA[A/G]CAGGGTACTAGAGTT | 55819 |
rs74762373 | snp | C/G | 0.111606 | 0.2082 | intron-variant | RNF130 | GRCh38.p7 | 5:179962879 | CCTTCCTTTTACCGA[C/G]GTGAAGCCTGCCGTC | 55819 |
rs74810404 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | RNF130 | GRCh38.p7 | 5:180041039 | TGTTCATGTACTAGC[C/T]TCTCCACACACCGCC | 55819 |
rs74826507 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179928500 | GTTCGCTCTGAAATG[A/T]CTCTTTGTTTCTTTT | 55819 |
rs74853987 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | RNF130 | GRCh38.p7 | 5:179923069 | TAAGATCAAATTTAT[C/T]GATTTTTTCCTATTA | 55819 |
rs74869820 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179948693 | AAAAGAGAGAGAGAG[A/G]AAAAAAGAGTCTTGA | 55819 |
rs74871978 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924293 | CTGAGGTTGGGAGTG[C/G]GAGACCAGCCTGACC | 55819 |
rs74901885 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179935089 | AATAATTTCCACTGC[A/G]ATTTCTTCTTTGATT | 55819 |
rs74903646 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNF130 | GRCh38.p7 | 5:179962801 | GCCTCTGCCTACATT[C/T]CCAGTCCTGAGCGTG | 55819 |
rs74931337 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RNF130 | GRCh38.p7 | 5:180035233 | ATGTGTTTTCATTTT[C/T]GTTTGGTTCCAAATG | 55819 |
rs74944136 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934364 | GTAATCGCTCCTCTG[A/C]ACTCTACTTCTTTGC | 55819 |
rs74968201 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180037958 | GCATTTCTTTAATTT[C/G]TGCTGTTATACACTC | 55819 |
rs75001477 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180033706 | GCCTTTAAAAAAAAA[A/G]AAGAGAGAGAGAGAG | 55819 |
rs75064908 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RNF130 | GRCh38.p7 | 5:179984482 | GTTGGACTTCGGCAA[A/G]TATCTTTTCTCCATC | 55819 |
rs75068914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976123 | GCCAGGAGTTCAGAG[C/T]GGCCTGGGCAACATA | 55819 |
rs75076075 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013664 | AGAGAAGTGTATCAA[C/T]ATCATGGTAGATTTA | 55819 |
rs75149321 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179928488 | TTTGTGTATCTGGTT[A/C]GCTCTGAAATGTCTC | 55819 |
rs75358254 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | RNF130 | GRCh38.p7 | 5:180000658 | GAGATTCTTTCTTAC[A/G]TATGATCAAGTTTGC | 55819 |
rs75373521 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | RNF130 | GRCh38.p7 | 5:179960632 | ACAGTGAGTAGACAG[A/G]GTCAAGGACTTGCTT | 55819 |
rs75377277 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF130 | GRCh38.p7 | 5:180044532 | ACGCCTTGCTCTTGA[C/T]TCTTAAAGAGCCTCC | 55819 |
rs75461572 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | RNF130 | GRCh38.p7 | 5:179988451 | CAATTTTGGGTTTGG[A/T]TTATTCTTGCTTTTC | 55819 |
rs75467146 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033529 | AGGAGTTCGAGACCA[G/T]CCCGGCCAACATGGT | 55819 |
rs75469689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179973504 | GGACTGGGCCAGGGG[C/T]GTTTAATCTACCTTG | 55819 |
rs75484205 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179986465 | ACTGCACTAAACACA[C/T]TGAAAACTATGTGAG | 55819 |
rs75515933 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:179945749 | TTATGAGCGGTGTCC[A/G]GCCTCGGCAGGAACC | 55819 |
rs75530468 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180053772 | GAACTGCAACAAGCA[C/T]GGCTACATGACACTG | 55819 |
rs75552254 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF130 | GRCh38.p7 | 5:180041234 | GCTTATATTTGAAAG[C/T]TGAAGTAGTTAAAAT | 55819 |
rs75568109 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044715 | TGGGTGCCTGTAATC[C/T]CAGCTACTCAGAAGG | 55819 |
rs75610202 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044746 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 55819 |
rs75616919 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:180040721 | AAAGTGTCAACTGCT[C/T]TCTGAATACCACACA | 55819 |
rs75637356 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044747 | TGAGGCAGGAGAATT[G/T]CTTGAACCCAGGAGG | 55819 |
rs75650050 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044763 | CTTGAACCCAGGAGG[C/T]GGAGGTTACAGTGAG | 55819 |
rs75654641 | snp | C/T | 0.212728 | 0.247206 | intron-variant | RNF130 | GRCh38.p7 | 5:180059021 | CCAACAAAAATCCCT[C/T]CAATAGTTTTCCATT | 55819 |
rs75680454 | snp | C/G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179982903 | TACAGTTTTAATTTG[C/G/T]ATTTCCCTATTGTAA | 55819 |
rs75682967 | snp | G/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179943989 | ATTTTTTTTTTTTTT[G/T]GAGACGGAGTCTTGC | 55819 |
rs75683123 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | RNF130 | GRCh38.p7 | 5:179972125 | TGTTACTCGTAGCCT[C/G]TGTGTGTGGAGTGGT | 55819 |
rs75689110 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | RNF130 | GRCh38.p7 | 5:179943565 | ATAAAGAGGAAAAGG[C/T]GTAACATGTATACTT | 55819 |
rs75691177 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | RNF130 | GRCh38.p7 | 5:179985337 | TTCAACAGTGCCATC[G/T]TTCCAGACTTTTGTG | 55819 |
rs75767476 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | RNF130 | GRCh38.p7 | 5:180034835 | CATGGGGACCCCAGA[C/T]ATAGTTACCATAAAG | 55819 |
rs75808567 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RNF130 | GRCh38.p7 | 5:179982434 | GGGCTCACCTGATAG[C/T]TGTCTGACTTTTATT | 55819 |
rs75873408 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | RNF130 | GRCh38.p7 | 5:179991271 | TAAGCAATCTGATGA[A/C]TATATGTCATGGTGA | 55819 |
rs75878040 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | RNF130 | GRCh38.p7 | 5:179954188 | AAGAACATTTTGGCA[G/T]CTTCTCAAGAAGTTA | 55819 |
rs75894617 | snp | C/G | 0.178785 | 0.239642 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072854 | TGCTCTAGTGACTAG[C/G]TGAACTACTCCAGGG | 55819 |
rs75997440 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179945564 | CCACTGGTGAGAAAA[C/G]AGAGGCTGGGAGAGG | 55819 |
rs76013390 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RNF130 | GRCh38.p7 | 5:180036057 | CTTTTGTTTTCCTGA[A/G]TATGAGTCAAACATC | 55819 |
rs76045688 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:180049272 | AACATGAGCTATTTG[G/T]GAGTGGAGAGCCCCA | 55819 |
rs76062962 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179988689 | TTGTTTAGTTTCCAC[A/G]TAGATACTGTTTCCA | 55819 |
rs76085741 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982593 | GTTTTGTTTTGTTTT[G/T]AAGACAAGGTCTTGC | 55819 |
rs76085989 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180034811 | TGAGTCACTGAACCT[G/T]TGGATGGTCATGGGG | 55819 |
rs76087345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976135 | GAGCGGCCTGGGCAA[C/T]ATAGTGAGACCCCAA | 55819 |
rs76107111 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044691 | ACAAAAATTAGCTGG[A/G]CATGGTGGTGGGTGC | 55819 |
rs76143069 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179996947 | GAATCAAGTGCTGGA[C/G]TTTTCTTTAATGGGA | 55819 |
rs76181655 | snp | C/G | 0.021333 | 0.101051 | intron-variant | RNF130 | GRCh38.p7 | 5:180068669 | GTAGCACTGCAAAGC[C/G]AACAGGAAGGTTTCT | 55819 |
rs76193404 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RNF130 | GRCh38.p7 | 5:180024532 | AACAACAAACAACAC[C/T]TTTGAAGTGCTGAAA | 55819 |
rs76198375 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:180069579 | TCTGAAATCTCACCA[A/G]CTGAGAGATTCCTCT | 55819 |
rs76281164 | snp | A/T | 0.0970103 | 0.197722 | intron-variant | RNF130 | GRCh38.p7 | 5:180061372 | CTAACCCTGCATGCC[A/T]GTGTTCAACGCTGGG | 55819 |
rs76315806 | snp | C/G | 0.212122 | 0.247114 | intron-variant | RNF130 | GRCh38.p7 | 5:180058515 | TGTTCGCAGGGGCTG[C/G]GGCAGAGGGGGTAAT | 55819 |
rs76367065 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RNF130 | GRCh38.p7 | 5:180070476 | GGGCATAATATGTTA[A/G]TATCTTAAGAGTGTA | 55819 |
rs76369889 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | RNF130 | GRCh38.p7 | 5:180039673 | ATAATTATGTAAAAA[A/T]TACACGATGAAAAGT | 55819 |
rs76422845 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053971 | AGTAGCTGGGACTAC[A/T]ACACCCAGCTAATTT | 55819 |
rs76443222 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RNF130 | GRCh38.p7 | 5:180024222 | TAAATGTAATGTGGT[A/G]TCCTGGGTGGGATCC | 55819 |
rs76445930 | snp | A/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044793 | GCCAAGATTGTGCCA[A/C]TGGACTCCAGCCTGG | 55819 |
rs76458747 | snp | C/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044699 | TAGCTGGGCATGGTG[C/G]TGGGTGCCTGTAATC | 55819 |
rs76550516 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RNF130 | GRCh38.p7 | 5:179998773 | ATTTTCTGTCTAGAT[A/G]ATCTGTCTAATGCTA | 55819 |
rs76559407 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:179974742 | TGGACTGGGAAATGC[A/G]AGTGTCACGAGATGC | 55819 |
rs76560434 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179950963 | ATACCATGAATCTAC[A/G]AAATACCACCAGAGG | 55819 |
rs76597950 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033527 | TCAGGAGTTCGAGAC[C/T]AGCCCGGCCAACATG | 55819 |
rs76598499 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180033927 | CCACAAGAAAAATGT[G/T]GAGTAAGTATAATGT | 55819 |
rs76652572 | snp | A/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179931056 | AAAAAAAAAAAAAAA[A/T]ATCAAGAATAGGTGT | 55819 |
rs76713133 | snp | G/T | 0.030278 | 0.119257 | intron-variant | RNF130 | GRCh38.p7 | 5:179928357 | ATAATGGATATTTTG[G/T]TTTTTTTTTTCATTT | 55819 |
rs76722385 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180044323 | CAAGATAGATAATAC[A/G]AAATATTTTACTACA | 55819 |
rs76731983 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RNF130 | GRCh38.p7 | 5:179939750 | AAAGCGGAGAAAAAC[A/G]ACCCCCTCCCTTGGC | 55819 |
rs76734684 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180041212 | AAAATTTAAAAGTTT[C/G]GTTTTGGCTTATATT | 55819 |
rs76761674 | snp | C/G | 0.0134861 | 0.0810011 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954758 | GCCCCCTGCTGATTT[C/G]AGCATGACTACTGGA | 55819 |
rs76795296 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015737 | TAGGAAAGGAGTAGG[A/G]AAAGGAGTAGGAAAG | 55819 |
rs76856600 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | RNF130 | GRCh38.p7 | 5:180022121 | ACACCACCAGGCGGC[A/C]GAGAGCTTTTTTTTA | 55819 |
rs76878788 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | RNF130 | GRCh38.p7 | 5:180004703 | AATAGTTGGTTCAAA[C/G]CCAAATGGTTCAGAG | 55819 |
rs76898970 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072314 | ATAGCCGCAGGGCGT[A/G]GAGCCCGGGAGATTT | 55819 |
rs76952307 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968231 | ACCCAGGAGGCGGAG[C/G/T]TTGCRGTGAGCCGAG | 55819 |
rs76980863 | snp | A/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179944758 | TGAGACCCTGTCTCA[A/C]AAAAAAAAAAAGTTC | 55819 |
rs76982304 | snp | A/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044347 | TACTACAGAACTTAA[A/T]TTTTTTTTTCCTCTA | 55819 |
rs76990465 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976428 | CTGGTCATTCCAGTG[C/T]TGAAGCAGGCAAGTG | 55819 |
rs77024076 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RNF130 | GRCh38.p7 | 5:179977330 | TCCCTGGAGTTGTTG[C/T]ACCCAGAGCCAGGTG | 55819 |
rs77046728 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:180046116 | CGAGAATCTGTGCGC[A/G]GTGGACCGCGGCGCG | 55819 |
rs77065082 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF130 | GRCh38.p7 | 5:179989765 | TGTTACTGAAATATA[C/T]TGTTATCTAGCTGTT | 55819 |
rs77069807 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:180017511 | TGCCTGAATCTGTTA[A/C]GACAATGGTATTTGT | 55819 |
rs77120209 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179981367 | GATGCCGCTCCTGAC[A/G]GAGCAAGGCGGGGAC | 55819 |
rs77130801 | snp | A/G | 0.32 | 0.24 | intron-variant | RNF130 | GRCh38.p7 | 5:179938159 | ACCAGCCTGGGCAAC[A/G]TGGTGAAACCACTCG | 55819 |
rs77134873 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179934117 | TTGAAGCACGGCCTA[A/G]TAAGAACCTGGTGTT | 55819 |
rs77158606 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044674 | CCATCTCTACTAAAA[A/G]TACAAAAATTAGCTG | 55819 |
rs77174409 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179973625 | CTGGCCATTCCCGCA[C/T]GCCTGACCGCGCTCA | 55819 |
rs77191311 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | RNF130 | GRCh38.p7 | 5:180032965 | GATATGAAAGGTCTC[C/T]CCATTTATCCAGATT | 55819 |
rs77199759 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003696 | AGCCACTATTTTTTT[A/T]AAATTTTTCATTCTA | 55819 |
rs77210669 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021649 | TATTTAAAGAATCTA[A/C]AACTTACAGAAAAAT | 55819 |
rs77217566 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180006023 | TGTATATGAAAAGTG[C/T]TATTTATTTACAAAA | 55819 |
rs77241190 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RNF130 | GRCh38.p7 | 5:180064667 | CGCAACTAGAAACTA[C/T]CTCTTGAATCCCCAT | 55819 |
rs77255015 | snp | C/T | 0.030665 | 0.119967 | intron-variant | RNF130 | GRCh38.p7 | 5:179969340 | GGCTCCAGTCACTGC[C/T]TGCCTTCTCTGCTTG | 55819 |
rs77261059 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033528 | CAGGAGTTCGAGACC[A/C]GCCCGGCCAACATGG | 55819 |
rs77281718 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF130 | GRCh38.p7 | 5:180032933 | CACCCTGACAATACT[A/G]AACAATGGAATCAAA | 55819 |
rs77282554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179950114 | ATCATGCTTATTAAA[C/T]AACTTTTTTTTTTCT | 55819 |
rs77293047 | snp | C/T | 0.42666 | 0.176893 | intron-variant | RNF130 | GRCh38.p7 | 5:179931018 | AGCCTGGGCTGCAGA[C/T]CAAACCTCTGTCTCA | 55819 |
rs77343601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945533 | GTGCTACGTTGCTGT[C/T]ACAGTGACTTTTATT | 55819 |
rs77344164 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044768 | ACCCAGGAGGCGGAG[A/G]TTACAGTGAGCCAAG | 55819 |
rs77372818 | in-del | -/CAGGAATCACAAAACAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977425 | TGTTTTTGAAACCCA[-/CAGGAATCACAAAACAA]TGCCAAGCACAGTGA | 55819 |
rs77381803 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180057969 | TACCTGTGGGGTCTG[C/T]GCTAACTTTACCAGG | 55819 |
rs77383912 | snp | A/G | 0.170084 | 0.236883 | intron-variant | RNF130 | GRCh38.p7 | 5:180059525 | TGAATACTTGAGGCA[A/G]CTGTCCCACAGGAAT | 55819 |
rs77406192 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | RNF130 | GRCh38.p7 | 5:179987911 | CTATGTTCAAGGACA[C/T]TGGCCTGCCATTTTC | 55819 |
rs77406634 | snp | G/T | 0.103082 | 0.202275 | intron-variant | RNF130 | GRCh38.p7 | 5:179991534 | AGGCCTTGTTCTTTT[G/T]AAGTTTTTCTTTTCT | 55819 |
rs77419386 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RNF130 | GRCh38.p7 | 5:180031913 | ATCCTCAACAAAACT[C/T]GGTACTGTATGACTT | 55819 |
rs77430120 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | RNF130 | GRCh38.p7 | 5:180042646 | AATACTGTATCCAAA[C/T]GGGGAATAACCAAGG | 55819 |
rs77437890 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179973323 | AGCTGCCCTGAACAC[A/G]GCACCTTTTTCTCCT | 55819 |
rs77462542 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180055323 | ATGCAATTTTTTTTT[C/T]CTTTGAGAAGGAGTC | 55819 |
rs77474502 | snp | A/G | 0.10624 | 0.204532 | intron-variant | RNF130 | GRCh38.p7 | 5:179967027 | TGCAAAATATTTCCA[A/G]GTTAAAAATAATTGT | 55819 |
rs77492992 | snp | A/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180034216 | TGTAAAAAAAAAAAC[A/C]ATATATCCCATTCCT | 55819 |
rs77499741 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | RNF130 | GRCh38.p7 | 5:180040971 | AAAGGCCAACACAGA[C/T]GAGAAACCCAGGTGA | 55819 |
rs77617244 | snp | C/G | 0.0295035 | 0.117819 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072384 | GAAAAAAAGCCATAA[C/G]TTTAAAAGAAATGTT | 55819 |
rs77627621 | snp | C/G | 0.031825 | 0.122064 | intron-variant | RNF130 | GRCh38.p7 | 5:180022010 | AGACTACATTCGGCC[C/G]AGTTGATCTGTCGAA | 55819 |
rs77646575 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179966237 | CACGGTATTTTTTTT[C/T]CAGGCAGATTGTCCT | 55819 |
rs77688984 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RNF130 | GRCh38.p7 | 5:179992070 | CAGTCACTCACCTGA[C/T]GCTCAGCTCCTGCTG | 55819 |
rs77734594 | snp | A/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044697 | ATTAGCTGGGCATGG[A/T]GGTGGGTGCCTGTAA | 55819 |
rs77753345 | snp | C/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044730 | CCAGCTACTCAGAAG[C/G]CTGAGGCAGGAGAAT | 55819 |
rs77786230 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | RNF130 | GRCh38.p7 | 5:179989507 | ACTATTATCTATTTA[C/T]GTTTTTTAATTTTTA | 55819 |
rs77853588 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984231 | TCTGTAAATGAAGAC[A/G]GCTTACTTCTCCATT | 55819 |
rs77864449 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF130 | GRCh38.p7 | 5:180004193 | CTCACATGATTCTTT[C/T]GTATACTAAAGTTTG | 55819 |
rs77873467 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | RNF130 | GRCh38.p7 | 5:180069232 | AGAAGCTATGCTTCA[C/T]AGAGACGGATTTTTT | 55819 |
rs77878471 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180061094 | AAAAAAAAAAAAAAA[A/G]CTATGTTCATGCATT | 55819 |
rs77889528 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | RNF130 | GRCh38.p7 | 5:180067958 | ACATTTTTAAACATG[A/G]AAACCTAAGATTCAC | 55819 |
rs77947924 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | RNF130 | GRCh38.p7 | 5:180022370 | TGAAACAGCTACTAA[C/T]GTTATTCATTTTGAT | 55819 |
rs77948565 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180035801 | CCTCTAGTGAATTTT[C/T]CATTTCCAAAATTGT | 55819 |
rs77951890 | snp | A/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179956033 | GTTGTCTTTAAAAAA[A/T]GCTCCTCTTACCTCT | 55819 |
rs77952531 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | RNF130 | GRCh38.p7 | 5:179988259 | CTCTAATGATCCTTT[G/T]TATTTTGTTGGTTTC | 55819 |
rs77954316 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950115 | TCATGCTTATTAAAT[A/T]ACTTTTTTTTTTCTT | 55819 |
rs77978373 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044796 | AAGATTGTGCCACTG[G/T]ACTCCAGCCTGGGCG | 55819 |
rs78137208 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179963181 | CTCTAAGACTATACT[G/T]CTCCTTTGCCACTTG | 55819 |
rs78170657 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180055324 | TGCAATTTTTTTTTT[C/T]TTTGAGAAGGAGTCA | 55819 |
rs78179066 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF130 | GRCh38.p7 | 5:180059244 | TAATATCTGCTCATG[C/T]TGCCGTCTCAGCTGA | 55819 |
rs78193509 | snp | C/T | 0.235854 | 0.249599 | intron-variant | RNF130 | GRCh38.p7 | 5:180063261 | AGTAGGAAATGATAG[C/T]TGCCTGAACTAAGGC | 55819 |
rs78271874 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | RNF130 | GRCh38.p7 | 5:180055478 | TGTGTGTGCGCGCGC[A/G]CACGCGTATGTGTCT | 55819 |
rs78276257 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180033020 | CGCTCTGTTGCCCGG[A/C]GAGAATGCAGCAGCA | 55819 |
rs78282770 | snp | A/T | 0.210301 | 0.246828 | intron-variant | RNF130 | GRCh38.p7 | 5:180056686 | TTATGGACACTCAAA[A/T]GTATTCCCAATAAAA | 55819 |
rs78284088 | snp | C/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044740 | AGAAGGCTGAGGCAG[C/G]AGAATTGCTTGAACC | 55819 |
rs78300177 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950113 | CATCATGCTTATTAA[A/C]TAACTTTTTTTTTTC | 55819 |
rs78338559 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | RNF130 | GRCh38.p7 | 5:180004934 | ACCATTTTTTCCCAT[G/T]TTTTTTTCTCAAAAG | 55819 |
rs78391628 | snp | C/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179982902 | TTACAGTTTTAATTT[C/G]CATTTCCCTATTGTA | 55819 |
rs78399743 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179941619 | GGCAGATGCCACAAG[A/G]AAAAAAGTAGTGTTG | 55819 |
rs78413790 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180008890 | CCCTCTCTCAAAAGG[A/G]AAAAAAAAAAAGTAA | 55819 |
rs78425170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056871 | CATGCAGTAACATGA[A/G]TTCATCTCACTAACA | 55819 |
rs78439747 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180030108 | CTACCTCGGCCTCCT[C/G]AAGCGTTGGGATTAC | 55819 |
rs78534180 | snp | A/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044831 | AAGTAGACTCCGTCT[A/C]AAAAAAAAAAAATAA | 55819 |
rs78563146 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RNF130 | GRCh38.p7 | 5:179975137 | TTAGCAACATGAGGT[A/G]CAGAAAGCCACAGCA | 55819 |
rs78604443 | snp | A/C | 0.237014 | 0.249662 | intron-variant | RNF130 | GRCh38.p7 | 5:180049195 | TCTTTGGTTTCCAAG[A/C]GCTTTGACACAGGGA | 55819 |
rs78617726 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | RNF130 | GRCh38.p7 | 5:179931229 | GGACTGTAACACTGA[C/T]GGCGATACAGTGTGG | 55819 |
rs78654932 | snp | A/T | 0.172674 | 0.237741 | intron-variant | RNF130 | GRCh38.p7 | 5:180000246 | CATTCTCTCCTAGGC[A/T]GTAAGATTTCTCTGG | 55819 |
rs78678378 | snp | A/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044673 | CCCATCTCTACTAAA[A/C]ATACAAAAATTAGCT | 55819 |
rs78715016 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:180043395 | TTGTTTGTTTCACTG[A/G]CATTCATCCTATGTT | 55819 |
rs78725605 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF130 | GRCh38.p7 | 5:180014199 | GACCTTTCCCCTACA[C/T]AATTTCCAGAAGTAG | 55819 |
rs78761438 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180052288 | CCATGAATACTGAGC[A/C]GTCCAAACTTATTAG | 55819 |
rs78842864 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954692 | AATACACACTTTAAA[C/T]GGGTAATTTTATAGC | 55819 |
rs78852847 | snp | C/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179974982 | GTGAAGAACAAGCGT[C/G]TGAGTTAAGGTGTTG | 55819 |
rs78920061 | snp | A/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044723 | TGTAATCCCAGCTAC[A/T]CAGAAGGCTGAGGCA | 55819 |
rs78936657 | snp | C/G | 0.0733688 | 0.176922 | intron-variant | RNF130 | GRCh38.p7 | 5:179944631 | TTTTTTTTGAATTTT[C/G]TAGAGACAGTCCCCC | 55819 |
rs78943184 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | RNF130 | GRCh38.p7 | 5:179960882 | TGGTTGTAAGTTTAT[C/T]GGTAGATAAAGGCAA | 55819 |
rs78954427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179984595 | TATTCCTGGAGTAAA[C/T]ATCACCTGGTCATGA | 55819 |
rs78967753 | snp | C/G | 0.155128 | 0.231299 | intron-variant | RNF130 | GRCh38.p7 | 5:180049388 | ATCATCTTTATTTCT[C/G]CTAAAATCTAACTGA | 55819 |
rs78998001 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF130 | GRCh38.p7 | 5:179974874 | TGGACCGCAGCAGAC[A/G]GCCTCTCCGGCCTGC | 55819 |
rs79017176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179974096 | CCTCTTGGTGCCATG[C/T]AAGAACCTGGCAAAT | 55819 |
rs79067939 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180027651 | CACCCACTCCATTAA[A/G]AACCCTAGCAGCCAG | 55819 |
rs79102171 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | RNF130 | GRCh38.p7 | 5:179926875 | CAGGTAGACAGCGTT[G/T]GAACTGAATTGAATT | 55819 |
rs79108955 | snp | A/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179929748 | GTGAGACTGTGTCTC[A/C]AAAAAAAAAAATTCT | 55819 |
rs79118463 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | RNF130 | GRCh38.p7 | 5:179931200 | CCCGCCTGAAGTACC[A/G]CACATCTGAACTGGG | 55819 |
rs79132122 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:180058954 | ACCATGACTTAACAG[C/T]TAGATGGTCAATTTA | 55819 |
rs79135377 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179989908 | AATTTTATACTTTCA[G/T]GTGTTTTTATGATGG | 55819 |
rs79150913 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179964902 | ATCAGCATGAACATT[C/T]AAAAACACATATAAA | 55819 |
rs79155895 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF130 | GRCh38.p7 | 5:179953349 | GTTGATTCTAAAATT[C/T]ATGCAAGGGACCCTG | 55819 |
rs79156725 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179939964 | TCCCTTTTTTTTTTT[C/T]CTAGCATCAGACAGC | 55819 |
rs79156819 | snp | A/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179961124 | GTTAAAAAAAAAAAA[A/C]ACAACACATAAAAGC | 55819 |
rs79171112 | snp | G/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179982901 | CTTACAGTTTTAATT[G/T]GCATTTCCCTATTGT | 55819 |
rs79178067 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179939965 | CCCTTTTTTTTTTTT[C/T]TAGCATCAGACAGCA | 55819 |
rs79193977 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998857 | TTTAGATCTAGTATT[A/T]TTTATATATATATAT | 55819 |
rs79213209 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179920723 | TGAAGACTTCTTCCT[A/G]GGCACATGATCTTAT | 55819 |
rs79221887 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RNF130 | GRCh38.p7 | 5:180052589 | ACTAATGACTCGATG[C/T]AATGACAGTAATGAC | 55819 |
rs79347818 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF130 | GRCh38.p7 | 5:180039044 | GTGTTTCCACATAGA[C/T]GTCCAGCTAAATTAA | 55819 |
rs79411593 | snp | C/G | 0.235564 | 0.249583 | intron-variant | RNF130 | GRCh38.p7 | 5:180063447 | GGGAAAGACTGGAGA[C/G]CAGTGGTAGCAGATA | 55819 |
rs79415650 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033526 | GTCAGGAGTTCGAGA[C/T]CAGCCCGGCCAACAT | 55819 |
rs79421803 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF130 | GRCh38.p7 | 5:180070300 | GAGATGAGATATGCA[C/T]CTTAAGCACCTGATT | 55819 |
rs79422868 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | RNF130 | GRCh38.p7 | 5:180013002 | AAGATGCATGGTCAC[A/G]ACAGATGACTGTGAA | 55819 |
rs79448685 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | RNF130 | GRCh38.p7 | 5:179938649 | CTAAGCTTAACATTA[C/T]ATATTTAAATAATTG | 55819 |
rs79458933 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179987162 | TTTCCTTCCTTCCTT[C/T]CTTTCTTCTATTTTT | 55819 |
rs79532913 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF130 | GRCh38.p7 | 5:180069787 | CCTACAATGCTGCCT[C/T]CCCACTGAGAGGGGA | 55819 |
rs79556046 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | RNF130 | GRCh38.p7 | 5:179950498 | CAAATGCATGCACAT[A/G]TGCACACAAAATATA | 55819 |
rs79571478 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180008888 | GACCCTCTCTCAAAA[A/G]GAAAAAAAAAAAAGT | 55819 |
rs79597811 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF130 | GRCh38.p7 | 5:180066510 | ACTGTCCCTCATGGG[C/T]ATAGTCTAGCAAGTT | 55819 |
rs79620642 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011778 | CTTAAAAAAAAAAAA[-/A]GTTTTTTAAATTAAA | 55819 |
rs79667040 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:180042612 | CCTGTTACGATAATC[A/T]CCTCTTAGAAAAATG | 55819 |
rs79674876 | snp | A/C | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180028562 | TTCCAGACCTGGGTC[A/C]GAACCCCTTTCGTAA | 55819 |
rs79679842 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | RNF130 | GRCh38.p7 | 5:180068607 | TGCTCTTTAAAGGGA[C/T]AGGACAAATAAATGT | 55819 |
rs79682342 | snp | A/G | 0.030278 | 0.119257 | intron-variant | RNF130 | GRCh38.p7 | 5:179995460 | AGACCCAGTGTTCCA[A/G]TCCTGGCATGAGACT | 55819 |
rs79700017 | snp | G/T | 0.0433465 | 0.140692 | intron-variant | RNF130 | GRCh38.p7 | 5:179992594 | ATTACTGTGTTTTTT[G/T]GGGGGGGTGTCATAT | 55819 |
rs79701638 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | RNF130 | GRCh38.p7 | 5:179977069 | ATGTGGGGAGCACCA[A/C]ATTAAAGGCAGGCCT | 55819 |
rs79716036 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | RNF130 | GRCh38.p7 | 5:179952455 | AATTCTTCTTAAGAT[C/T]TTCCAAAAAACAGAA | 55819 |
rs79739726 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179942706 | GTTTAAACTGTAATC[A/G]TTAGAGTACATTTGT | 55819 |
rs79782985 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | RNF130 | GRCh38.p7 | 5:179954324 | ACATTCATAACAGCC[A/G]AACAGCGGAAACAAG | 55819 |
rs79815382 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | RNF130 | GRCh38.p7 | 5:180067341 | ATTCTGACCCTGCTA[C/T]CAAATATATGTTACA | 55819 |
rs79815759 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044696 | AATTAGCTGGGCATG[A/G]TGGTGGGTGCCTGTA | 55819 |
rs79845995 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180039257 | CTTTTCTTTTTTTTT[G/T]GAGATGGAGTCTTGC | 55819 |
rs79892587 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | RNF130 | GRCh38.p7 | 5:180030177 | ACCATTCTATCCTTA[C/T]ATGCTCTTTTAATTT | 55819 |
rs79900141 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022818 | TAGTTTTGTGCCTCT[A/T]TCAAGTAAGATGCTT | 55819 |
rs79920794 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179930376 | TTTCATTTTAAATTG[C/T]TTATTGTTAGTCTAT | 55819 |
rs79936788 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF130 | GRCh38.p7 | 5:179941563 | GCTCTCCTTCTCTCT[C/T]GGTCTTTGGGCCATC | 55819 |
rs79938184 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179928367 | TTTTGTTTTTTTTTT[C/T]CATTTTAGCATTCCA | 55819 |
rs79938689 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180033707 | CCTTTAAAAAAAAAA[A/G]AGAGAGAGAGAGAGA | 55819 |
rs80030936 | snp | C/T | 0.169435 | 0.236663 | intron-variant | RNF130 | GRCh38.p7 | 5:179937138 | GAAATATCATCAAAA[C/T]GAAATATCATCAAAA | 55819 |
rs80091215 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180044770 | CCAGGAGGCGGAGGT[C/T]ACAGTGAGCCAAGAT | 55819 |
rs80095176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180028095 | ACTTAAAATTACTTT[C/T]GTTTTGCTTTTCCCC | 55819 |
rs80121882 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179928633 | TTTAATTGTTGTTGT[G/T]TTTTTTTTTTTTTGA | 55819 |
rs80191022 | snp | C/T | 0.107341 | 0.205301 | intron-variant | RNF130 | GRCh38.p7 | 5:180036899 | ATCCTATTTCCTTTC[C/T]TCCCTCTCCAGAGAC | 55819 |
rs80193351 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179953305 | CCTATAAAATCCTAG[C/T]TTTTTTTTTTTTTTA | 55819 |
rs80291090 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | RNF130 | GRCh38.p7 | 5:179934638 | CACTGCGAACTTATG[A/G]GTTCAAGTGATCCTG | 55819 |
rs80296369 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972675 | GGGGGATGGAGGTGC[A/G]GCTCTGGTGCTCCCT | 55819 |
rs111296472 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179962938 | GCCCATGGAGATAGC[A/G]CTTAGACTTATTTTC | 55819 |
rs111297502 | snp | A/G | 0.040671 | 0.13668 | intron-variant | RNF130 | GRCh38.p7 | 5:179951423 | GAGTCTCGCTTTGTC[A/G]CCCAGGCTGGAGTGC | 55819 |
rs111304982 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | RNF130 | GRCh38.p7 | 5:179922779 | TCTCTACTAAAAATA[C/T]AAAAAGTAGCCAGGT | 55819 |
rs111321644 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180008011 | TTTTTTTTTTTTTAA[C/T]AGGTATATTACATGT | 55819 |
rs111375098 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179947514 | GGGGTTTGGAACACA[A/G]ACCCTGGGGGCCAGC | 55819 |
rs111393394 | in-del | -/A | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179944757 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAGTT | 55819 |
rs111474156 | snp | C/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180011744 | CACTCCAGCCTGGGT[C/G]ACAGGGCAAGACCCT | 55819 |
rs111476720 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072931 | GAAACGCGCGCGCGC[A/G]CACACACACACGACT | 55819 |
rs111513318 | snp | C/T | 0.48 | 0.0979796 | intron-variant | RNF130 | GRCh38.p7 | 5:180013450 | ACTTCTCAACTGAAA[C/T]GTAGATGCAGCTGGG | 55819 |
rs111532634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948543 | AGGCATGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 55819 |
rs111551681 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180033717 | AAAAAAAGAGAGAGA[C/G]AGAGAAATACAATTG | 55819 |
rs111595347 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | RNF130 | GRCh38.p7 | 5:180068549 | GCACTTGCCAAAATA[A/T]ACTTTTAAAATACCA | 55819 |
rs111727034 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF130 | GRCh38.p7 | 5:180050649 | CCTTATTCTACATCC[C/T]TCAGAAGTTCTTTCA | 55819 |
rs111748122 | in-del | -/G | 0.161299 | 0.233735 | intron-variant | RNF130 | GRCh38.p7 | 5:179944164 | ATTTTTAGTAGAGAC[-/G]GGGGGGTTCACCATA | 55819 |
rs111872107 | snp | C/T | 0.194278 | 0.243711 | intron-variant | RNF130 | GRCh38.p7 | 5:180066693 | ATACAAAAAATTAGC[C/T]GTGCTTGGTGGCACA | 55819 |
rs111887415 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | RNF130 | GRCh38.p7 | 5:179921525 | GGTCCTGGCTGGGTG[C/T]GGTGGCTCATGCCTG | 55819 |
rs111916049 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179920897 | TATGTTGATCCTTCC[A/C/G]AATTTTTTTCAGTCT | 55819 |
rs111926782 | in-del | -/AAAC | 0.461037 | 0.134028 | intron-variant | RNF130 | GRCh38.p7 | 5:179931775 | CCAGACTCTGTCTTA[-/AAAC]AAAACAAACAAACAA | 55819 |
rs111940876 | snp | A/C | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179966362 | GGCTATGTTCCAAGA[A/C]CTGTGAATTTTTAGG | 55819 |
rs111954563 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RNF130 | GRCh38.p7 | 5:179971563 | TTTAGTAGAGACGGG[A/G]TTTCACCATGTTAGC | 55819 |
rs112297602 | snp | C/T | 0.187369 | 0.242028 | intron-variant | RNF130 | GRCh38.p7 | 5:180044810 | GGACTCCAGCCTGGG[C/T]GACGGAAGTAGACTC | 55819 |
rs112460090 | snp | C/T | 0.196149 | 0.244131 | intron-variant | RNF130 | GRCh38.p7 | 5:180008705 | GCCTGGGCAACACAG[C/T]GAAACCTCATCTCTA | 55819 |
rs112492503 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179977453 | ACAATGCCAAGCACA[C/G]TGACTCATGCCTGTA | 55819 |
rs112515113 | in-del | -/CAGGAGGGATACA | 0.23031 | 0.249223 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016342 | GCTCTGGCCCAGTTT[-/CAGGAGGGATACA]CACGCCAAAGGAAAT | 55819 |
rs112594478 | snp | C/T | 0.111576 | 0.20818 | intron-variant | RNF130 | GRCh38.p7 | 5:179948481 | TTGAGACAAGCCTAG[C/T]CAACATGGTGAAACC | 55819 |
rs112690516 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931640 | CGGGCGTGGTGGTGC[A/C]TGCCTGTAATCCCAA | 55819 |
rs112710637 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180066063 | TGCATAATATGTGCA[C/T]ATATGTGTACACATA | 55819 |
rs112715721 | in-del | -/A | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179939073 | ATCTCTACTAAAAAT[-/A]CAAAAATTAGCCGGG | 55819 |
rs112745383 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926589 | GGAGGTGGAGGTGGC[A/T]GTGAGCCGAGATAGC | 55819 |
rs112752025 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:180057798 | GTGTTTTCCTGAGTT[C/T]TATGAGCTGTTATAT | 55819 |
rs112794723 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179947450 | TGGTCAGGACACCCC[A/G]CAGCCTGCCCCTGAC | 55819 |
rs112834074 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180055620 | AATACTGCCAACAGT[A/G]TAATAGCCATACACT | 55819 |
rs112853530 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179993058 | AGGACATGAACACAT[C/G]CTTTTTTATGGCTGC | 55819 |
rs112920284 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF130 | GRCh38.p7 | 5:179998486 | CTTAAAACTAAGAAA[C/T]GCCATCTCACTATAT | 55819 |
rs112922629 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180041579 | CTTTCACATTTATAA[C/T]AGGTTCAAATGAGAG | 55819 |
rs112924412 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180052777 | AAAATCAGTCCCTAC[A/G]GAGGATTACAGAAAA | 55819 |
rs112943408 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:180063158 | AAGCAGTAACATGAC[C/T]GGGTGAACCTTTAAG | 55819 |
rs112946567 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF130 | GRCh38.p7 | 5:179953537 | GGAGGAAAAAAGTCT[C/T]TTAAACAAATGGCAC | 55819 |
rs112960734 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179939635 | ACTACCACAAATGAC[A/G]TGGAAGAGAATGAAG | 55819 |
rs113009837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179934707 | GCCACCACATCCGGC[C/T]ACTTTATTTTTATTC | 55819 |
rs113028734 | snp | A/G | 0.192088 | 0.2432 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073300 | ACGCCCGTAATCGCA[A/G]CACTTTGGGAGGCCT | 55819 |
rs113076515 | snp | A/C | 0.197703 | 0.244469 | intron-variant | RNF130 | GRCh38.p7 | 5:179994191 | TTCTTTTGGCTTATG[A/C]GGGCTCTTTTTTGGT | 55819 |
rs113082029 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179980584 | TGGCTTTTGGATTCT[A/G]CTCAACGAATGATCA | 55819 |
rs113083691 | in-del | -/ATC | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179933281 | ATTCAATTTATTACC[-/ATC]TAGATGTAGGAGAAT | 55819 |
rs113094456 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994337 | TATTGATTCTTCCTA[C/T]CCATGAGCATGGAAT | 55819 |
rs113132832 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180035273 | TTTCCTTTTGAATTT[G/T]TTATTGGACCCGTGT | 55819 |
rs113149932 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010164 | AGGCAGGAGAATGGC[A/G]TGAACCTGGGAGGCG | 55819 |
rs113175823 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179947360 | CGTCTCTCACCCACC[C/T]CACCTGTGTCCTAAA | 55819 |
rs113228082 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | RNF130 | GRCh38.p7 | 5:179944238 | CCTCCCAAAGTGTTG[A/G]GATTACAGGCGTGAG | 55819 |
rs113246643 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957894 | TTCTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 55819 |
rs113251520 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030041 | TTGGTAGAGATGAGG[A/T]TTCATCATGTTGGCC | 55819 |
rs113298248 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:179965358 | AGGGAAAGCAGAGGT[A/G]GCTGTGGTTTAGTTC | 55819 |
rs113300961 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017049 | TGTCCAGGATTCAAT[C/T]GGGGCTGTCGGCATC | 55819 |
rs113358173 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179934703 | GTGCGCCACCACATC[C/T]GGCTACTTTATTTTT | 55819 |
rs113363635 | snp | G/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179991669 | GTGACTGGTTTTGTG[G/T]AAGACAATTTTTCCA | 55819 |
rs113372912 | snp | C/G/T | 0 | 0 | intron-variant, splice-acceptor-variant | RNF130 | GRCh38.p7 | 5:179963565 | TAATAAACCATTCTT[C/G/T]TGTTGACAAAGGAAA | 55819 |
rs113384829 | snp | A/C | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179942636 | TCTATACAGCAAAGC[A/C]ATTTAGGAGAAAATT | 55819 |
rs113440216 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:179967096 | TCTAAACTTTGACGC[C/T]CTGTTGCAAAGACCT | 55819 |
rs113457529 | in-del | -/A | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179961111 | TTCATGCTTACTGTT[-/A]AAAAAAAAAAAACAC | 55819 |
rs113492228 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179953712 | TAAATTAGGTAATAC[A/T]TTCTTAGACATCTAA | 55819 |
rs113509176 | snp | A/G | 0.5 | 0 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180040508 | ATTGTAGATGACTAC[A/G]GCAACTGCATTGTGG | 55819 |
rs113541882 | snp | C/T | 0.0818113 | 0.184966 | intron-variant | RNF130 | GRCh38.p7 | 5:179997244 | CCTCCTGGGCTCAAG[C/T]GATTCTTCCATCTCA | 55819 |
rs113571106 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | RNF130 | GRCh38.p7 | 5:179951206 | CCCCAAACTACATGA[A/G]GCAAAACAGACAGAA | 55819 |
rs113576113 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | RNF130 | GRCh38.p7 | 5:179933061 | ATAGAGCGCAGAGGA[A/G]CGATTACCAGGGTGT | 55819 |
rs113595771 | snp | A/G | 0.5 | 0 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013214 | CATTCGAGTTCCAAC[A/G]GCTATTGTCATTTGT | 55819 |
rs113607945 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036848 | CCACACTCAGCTTAA[G/T]AAATAAAACATTATA | 55819 |
rs113641887 | in-del | -/CG | 0.479857 | 0.108604 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072919 | CTCCACCTTCCGAAA[-/CG]CGCGCGCGCGCGCAC | 55819 |
rs113657185 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179987991 | TGGTAGAATGAGTTA[A/G]AAAGAATTCTCTCTT | 55819 |
rs113691041 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | RNF130 | GRCh38.p7 | 5:179920823 | AGATGGAGTTTTGCT[C/T]TTGTTGCCCAGACTG | 55819 |
rs113708481 | in-del | -/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179931424 | CTTTTTTGTTTTTTG[-/T]TTTTTTTTCTTTTTT | 55819 |
rs113717114 | snp | C/T | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179978170 | CAAAGCACATTAATA[C/T]CATTCTTTCTCAAAC | 55819 |
rs113722320 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF130 | GRCh38.p7 | 5:180034837 | TGGGGACCCCAGACA[C/T]AGTTACCATAAAGTT | 55819 |
rs113770489 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF130 | GRCh38.p7 | 5:179922495 | TTTTTGTATTTTTAA[C/T]AGAGATGGGGTTTCA | 55819 |
rs113802460 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | RNF130 | GRCh38.p7 | 5:179957945 | TGCAGTGGCGGGATC[C/T]CGGCTCACTGCAAGC | 55819 |
rs113816511 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RNF130 | GRCh38.p7 | 5:179969866 | GGTGGTGACGGGCAC[C/T]TGCAATCCCAGCTAC | 55819 |
rs113842479 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016908 | CTCCTAAGAACAAGG[C/T]TAGCTACGTGGCCAC | 55819 |
rs113869116 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041061 | CACACCGCCACCACC[A/G]CTATCCCCACAGTGA | 55819 |
rs113897224 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | RNF130 | GRCh38.p7 | 5:179971400 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 55819 |
rs113903683 | snp | A/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179986988 | AAATGATACTAACTT[A/T]TGTACACAAACTTTG | 55819 |
rs113906174 | snp | A/G | 0.5 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179957982 | TCCCGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 55819 |
rs113929250 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:179979793 | AATGCAGGTCTTCAA[C/T]TCTCCATGTATCTAG | 55819 |
rs113963802 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179962329 | ATAACACATGCCACT[A/G]CAAGTGGAGGCCACT | 55819 |
rs114017300 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | RNF130 | GRCh38.p7 | 5:180045498 | TCTCAAACAGGGAAA[A/G]AACAAAGCTCCCACA | 55819 |
rs114135949 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF130 | GRCh38.p7 | 5:180061688 | CTCTTCTTATAAGGA[C/T]ATTAGTCGTTGGATT | 55819 |
rs114136241 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179945292 | CTGACTGCACCTGGG[A/G]AAACAGTGGGACCCA | 55819 |
rs114141691 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919847 | GGAAGTAGAATAAGC[A/G]AGAGGGGAACATCCA | 55819 |
rs114206662 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RNF130 | GRCh38.p7 | 5:180051055 | CAATCTGCCCACCTC[A/G]ACCTCCCAAACTGCT | 55819 |
rs114208464 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:179931223 | GAACTGGGACTGTAA[C/T]ACTGATGGCGATACA | 55819 |
rs114211674 | snp | A/C | 0.213937 | 0.247385 | intron-variant | RNF130 | GRCh38.p7 | 5:180057518 | GTACCACTGCGCTCC[A/C]GCCTGGGTGACAGAG | 55819 |
rs114213141 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | RNF130 | GRCh38.p7 | 5:180027537 | TCTGTGCTACTTAAC[C/G]TGCACTTCTCACCCC | 55819 |
rs114246269 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180025259 | GTTAAGAACATCCTC[C/T]GTCCTGGAACCTAGG | 55819 |
rs114261335 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179923278 | TCCAATTGTTCCGTC[A/G]TCGATTGTTTAAAAG | 55819 |
rs114330569 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF130 | GRCh38.p7 | 5:179995646 | TCTCTCAGCTACTCC[C/T]TAAGTAAGATCCAGG | 55819 |