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 |