SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs356636 | snp | C/G | 0.415563 | 0.18732 | intron-variant, upstream-variant-2KB | RNF180 | GRCh38.p7 | 5:64166149 | CTCAGGTGACGCGGC[C/G]GCGGCTTAACTTTCG | 285671 |
rs951960 | snp | A/T | 0.486464 | 0.0811471 | intron-variant | RNF180 | GRCh38.p7 | 5:64177241 | ACACTAAGTCGGGAA[A/T]GTGTAGGGTTGTTTG | 285671 |
rs965491 | snp | G/T | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64309952 | GAATTCATAAAACTT[G/T]GACTACATGAGAGTT | 285671 |
rs965708 | snp | C/T | 0.364609 | 0.222182 | intron-variant | RNF180 | GRCh38.p7 | 5:64252554 | GGAATACATACAAGG[C/T]TTTTTGTCAATTAAA | 285671 |
rs970990 | snp | A/G | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64230097 | TGGGTAGTCTATTTA[A/G]GTTGTCTAATCTGTA | 285671 |
rs970991 | snp | A/G | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64230307 | tattacagttctgta[A/G]gtaagaagttggaaa | 285671 |
rs976692 | snp | A/G | 0.414245 | 0.188477 | intron-variant, utr-variant-3-prime | RNF180 | GRCh38.p7 | 5:64333912 | GTGTCTGGAGTAGCC[A/G]ATTAAAGTATCAAGC | 285671 |
rs1056108 | snp | A/T | 0.0146672 | 0.084371 | utr-variant-3-prime | RNF180 | GRCh38.p7 | 5:64372190 | CACACATTCTTTTTT[A/T]AAAAAATGCCCTAAT | 285671 |
rs1112246 | snp | C/T | 0.485866 | 0.0828688 | intron-variant | RNF180 | GRCh38.p7 | 5:64304191 | ctccagcagagctct[C/T]tggtgactaggtaca | 285671 |
rs1155286 | snp | A/G | 0.488606 | 0.0746142 | intron-variant | RNF180 | GRCh38.p7 | 5:64278601 | AATGTAGAAAGAGAT[A/G]ATAATGGAAGAATCT | 285671 |
rs1307089 | snp | G/T | | | intron-variant | RNF180 | GRCh38.p7 | 5:64359853 | tcagctttctacata[G/T]ggctatccagttttc | 285671 |
rs1348715 | snp | C/T | 0.488118 | 0.0761554 | intron-variant | RNF180 | GRCh38.p7 | 5:64329292 | TTCTCCTTTTTTGTC[C/T]ACCTGTTTATTTCTT | 285671 |
rs1374029 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF180 | GRCh38.p7 | 5:64240965 | CTACTGGACTATAAA[C/T]CTCACAAGAAAAAGG | 285671 |
rs1374030 | snp | A/G | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64296177 | TCTGGAGGGCACTTA[A/G]GTCCACGGAAATTTC | 285671 |
rs1374031 | snp | C/T | 0.438946 | 0.163706 | intron-variant | RNF180 | GRCh38.p7 | 5:64307983 | TCTTTAATTGGACTT[C/T]GGAAGAAATTTTTAA | 285671 |
rs1389862 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | RNF180 | GRCh38.p7 | 5:64220934 | TGCGTAGTGTCTAAA[A/T]CACACCCTTTTAATA | 285671 |
rs1389863 | snp | C/G | 0.109108 | 0.206518 | intron-variant | RNF180 | GRCh38.p7 | 5:64220737 | TCCTGTGGCCTTAAA[C/G]AGACATTTTCTTTTA | 285671 |
rs1389864 | snp | C/T | 0.48995 | 0.0701706 | intron-variant | RNF180 | GRCh38.p7 | 5:64201353 | ACACATAAACTTTCT[C/T]TTCTAGGCCCATAGT | 285671 |
rs1389865 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | RNF180 | GRCh38.p7 | 5:64195516 | ACTTATCAATGACAT[G/T]AAGTGAGGACTTACT | 285671 |
rs1389866 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | RNF180 | GRCh38.p7 | 5:64177247 | GCCAAAACACTAAGT[C/T]GGGAATGTGTAGGGT | 285671 |
rs1389867 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF180 | GRCh38.p7 | 5:64168120 | TGCTTGTAAATTGAC[C/T]AGAAATTTCAAAAAA | 285671 |
rs1445955 | snp | C/T | 0.364193 | 0.222396 | intron-variant | RNF180 | GRCh38.p7 | 5:64239447 | TTTCCTGTCTGCTAG[C/T]AGATAATGCACTTTT | 285671 |
rs1445956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF180 | GRCh38.p7 | 5:64258647 | TGACATGCCTGTGGG[C/G]TGTGAGATATATAGG | 285671 |
rs1445957 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | RNF180 | GRCh38.p7 | 5:64263404 | GAAGAGATGTGCACA[G/T]TTAGCTCTTTTGAGT | 285671 |
rs1445958 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | RNF180 | GRCh38.p7 | 5:64274522 | CTTGGCTGTTCTGAA[C/T]TATGGAAGCAATTCT | 285671 |
rs1445959 | snp | C/T | 0.486595 | 0.0807641 | intron-variant | RNF180 | GRCh38.p7 | 5:64305026 | AGATGATCATTAGTA[C/T]TTTTTAGCAGTAATG | 285671 |
rs1494633 | snp | A/G | 0.390277 | 0.206936 | intron-variant | RNF180 | GRCh38.p7 | 5:64207081 | atttataattgttat[A/G]atattaataGAAGAT | 285671 |
rs1494635 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | RNF180 | GRCh38.p7 | 5:64172458 | GCCATCTACAGGTTC[C/T]TAAATCTTTACTCTT | 285671 |
rs1494636 | snp | A/G | 0.084728 | 0.187577 | intron-variant | RNF180 | GRCh38.p7 | 5:64172058 | TTGCTGGATACTGAT[A/G]CCCAAAGACATTACT | 285671 |
rs1494637 | snp | A/T | 0.0412709 | 0.137594 | intron-variant | RNF180 | GRCh38.p7 | 5:64212044 | AAATAAAAATAAATG[A/T]TATTACTAATTACCA | 285671 |
rs1526874 | snp | C/T | 0.487746 | 0.0773096 | intron-variant | RNF180 | GRCh38.p7 | 5:64361282 | TAAATTCCATATGTC[C/T]TTAATACTGGTTTTT | 285671 |
rs1526875 | snp | C/T | 0.488485 | 0.0749998 | intron-variant | RNF180 | GRCh38.p7 | 5:64361018 | TGAAAGATATTTGCA[C/T]AGCAAACTGTCTCGG | 285671 |
rs1596811 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | RNF180 | GRCh38.p7 | 5:64242729 | AAAGACAAAGATCTC[A/G]AATCAGATTCAATCC | 285671 |
rs1603089 | snp | C/T | 0.109108 | 0.206518 | intron-variant | RNF180 | GRCh38.p7 | 5:64202384 | TTCAGCAGAAAAAAA[C/T]TGATAAACTGTGGTA | 285671 |
rs1603090 | snp | A/C | 0.485118 | 0.0849685 | intron-variant | RNF180 | GRCh38.p7 | 5:64175997 | taaagactccaccaa[A/C]aaactgttagaacta | 285671 |
rs1813341 | snp | C/T | 0.487746 | 0.0773096 | intron-variant | RNF180 | GRCh38.p7 | 5:64281677 | ctaattttgtatttt[C/T]agtagagacaaggtt | 285671 |
rs1874168 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | RNF180 | GRCh38.p7 | 5:64176957 | GCCCCCAATTTACCT[A/G]TAATACCATTGGCCC | 285671 |
rs1918157 | snp | G/T | | | intron-variant | RNF180 | GRCh38.p7 | 5:64306563 | acaatagcaaagact[G/T]ggaaccaacccaaat | 285671 |
rs1947093 | snp | A/G | 0.121022 | 0.21416 | intron-variant | RNF180 | GRCh38.p7 | 5:64276704 | AAAATTTAAAAATAA[A/G]TGAGGGAATACAAAT | 285671 |
rs1947094 | snp | A/G | 0.488846 | 0.0738428 | intron-variant | RNF180 | GRCh38.p7 | 5:64276850 | GATTATTTTGCTTTC[A/G]AAATGTCTTATATTA | 285671 |
rs1991479 | snp | A/T | 0 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RNF180 | GRCh38.p7 | 5:64328089 | GAATCCTTAAGTTGC[A/T]AACTGTTCACCTTCG | 285671 |
rs1994931 | snp | A/G | 0.48955 | 0.071525 | intron-variant | RNF180 | GRCh38.p7 | 5:64207422 | CTATTTTAGTTCCGG[A/G]GATCCACCACAGGGC | 285671 |
rs1994932 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | RNF180 | GRCh38.p7 | 5:64172943 | AGGTCCCCTGAATTC[C/T]AAACAGTTGACAGTG | 285671 |
rs2015822 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RNF180 | GRCh38.p7 | 5:64294749 | GTGCTGTCATAGTTC[A/G]TTACTGATGAATTAT | 285671 |
rs2035998 | snp | C/T | 0.0229869 | 0.104714 | intron-variant | RNF180 | GRCh38.p7 | 5:64200981 | GGCCCACAGCACTCC[C/T]CTACCAGGAAACTGA | 285671 |
rs2035999 | snp | C/G | 0.109461 | 0.206758 | intron-variant | RNF180 | GRCh38.p7 | 5:64199043 | ATCATCTGAGGTCAG[C/G]AGTTCGAAACCAGCC | 285671 |
rs2036000 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | RNF180 | GRCh38.p7 | 5:64198884 | AGGTGGCAGTGGGCC[A/G]AGATCGTGCCACTGC | 285671 |
rs2055134 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | RNF180 | GRCh38.p7 | 5:64212797 | GTCCTACTACTTATA[A/G]TTTTCTAAGACAGGA | 285671 |
rs2055135 | snp | A/G | 0.489376 | 0.0721049 | intron-variant | RNF180 | GRCh38.p7 | 5:64190994 | AAATTTAGTATCAAC[A/G]CTGCTTTTCTAAATG | 285671 |
rs2055136 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF180 | GRCh38.p7 | 5:64189529 | cacaagttctacctt[C/T]cacaaagcactagaa | 285671 |
rs2121168 | snp | C/T | 0.113685 | 0.209567 | intron-variant | RNF180 | GRCh38.p7 | 5:64365867 | AGCTTATAGGTGTCA[C/T]TGCATGTAAGATGAG | 285671 |
rs2121169 | snp | G/T | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64262737 | TGTAATTCTCATGTA[G/T]AAAATTCATTTTGGC | 285671 |
rs2121170 | snp | C/G | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64301638 | TAAATAACCAAATCA[C/G]TTGGAAATTAAAGCT | 285671 |
rs2131997 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF180 | GRCh38.p7 | 5:64192542 | tgggattacaggcac[A/G]cgccaccacgcccag | 285671 |
rs2162804 | snp | A/G | 0.172028 | 0.23753 | intron-variant, downstream-variant-500B | RNF180 | GRCh38.p7 | 5:64328599 | TGTATGCTGGTTCGT[A/G]GGTGTGCAATTGGGA | 285671 |
rs2197521 | snp | A/G | 0.078151 | 0.181571 | intron-variant | RNF180 | GRCh38.p7 | 5:64360290 | aatgtaatccagcat[A/G]taaacagagccaaag | 285671 |
rs2366279 | snp | C/T | 0.093777 | 0.195178 | intron-variant | RNF180 | GRCh38.p7 | 5:64182147 | AGGCGCCCACCACCA[C/T]GCCTGGCTAATTTTT | 285671 |
rs2366280 | snp | G/T | | | intron-variant | RNF180 | GRCh38.p7 | 5:64183505 | caagctggagtgttg[G/T]ggcactatcttgtct | 285671 |
rs2366281 | snp | C/T | 0.484701 | 0.0861117 | intron-variant | RNF180 | GRCh38.p7 | 5:64205706 | GAGATTACCATGCAG[C/T]GTATGAATGGAGTGA | 285671 |
rs2366465 | snp | C/G | | | intron-variant | RNF180 | GRCh38.p7 | 5:64304162 | cttttcaaaatatca[C/G]tgcttgttgacagtg | 285671 |
rs2366466 | snp | A/G | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64307813 | aatggttgcatgggg[A/G]cttgaagtatggttt | 285671 |
rs2366682 | snp | C/T | 0.00914312 | 0.0669923 | utr-variant-3-prime | RNF180 | GRCh38.p7 | 5:64371834 | AAGTATAGCATTTCC[C/T]AGATCTACCAGCTTA | 285671 |
rs2434578 | snp | G/T | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64268950 | GTAATAAGTAAGAGG[G/T]TTGGGGGTTTCCTGA | 285671 |
rs2434579 | snp | A/G | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64260897 | GTTCATGACGGAAAG[A/G]ACATACAACAATATA | 285671 |
rs2434580 | snp | A/G | | | intron-variant | RNF180 | GRCh38.p7 | 5:64292765 | gaagccccatggggg[A/G]ggggctgctgatatc | 285671 |
rs2453815 | snp | A/T | | | intron-variant | RNF180 | GRCh38.p7 | 5:64294934 | aaagatgggacaaaa[A/T]tgaacgagaggggaa | 285671 |
rs2453818 | snp | A/C | | | intron-variant | RNF180 | GRCh38.p7 | 5:64262527 | ACATATTTCCAATTC[A/C]CCCTCATTGGTAGTT | 285671 |
rs2453819 | snp | A/C | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64262525 | ATATTTCCAATTCCC[A/C]CTCATTGGTAGTTTG | 285671 |
rs2453824 | snp | G/T | | | intron-variant | RNF180 | GRCh38.p7 | 5:64319195 | aaaaaAAAAAAACTT[G/T]GTATCTATAAAAAGG | 285671 |
rs2453825 | snp | G/T | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64320528 | CGTTCATTTAGGATT[G/T]CAGTCAATTTCTCTA | 285671 |
rs2463054 | snp | A/T | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64340674 | TCTGAAACTGGAACA[A/T]TTTGTTCACAAGATA | 285671 |
rs2463055 | snp | A/T | | | intron-variant | RNF180 | GRCh38.p7 | 5:64344116 | aaaacatctagaaaa[A/T]aaaaaatgtaaacat | 285671 |
rs2463056 | snp | G/T | | | intron-variant | RNF180 | GRCh38.p7 | 5:64301742 | AGTTTTCAGTCTGGT[G/T]GTTATAAGTCTCTTG | 285671 |
rs2463057 | snp | G/T | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64262493 | ATCACCCGTCTCTTT[G/T]ACCATGGCATAGAGT | 285671 |
rs2463058 | snp | A/T | | | intron-variant | RNF180 | GRCh38.p7 | 5:64327468 | gtgtcctgtagcttt[A/T]ggcgtattatatttc | 285671 |
rs2886681 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RNF180 | GRCh38.p7 | 5:64304348 | gctgccatagatagt[A/G]atgcctgtgatggat | 285671 |
rs2921573 | snp | C/G | | | intron-variant | RNF180 | GRCh38.p7 | 5:64259892 | ctcttgttgcccagg[C/G]tggagttcaatggcg | 285671 |
rs2921574 | snp | C/T | | | intron-variant | RNF180 | GRCh38.p7 | 5:64234745 | aggcgtggtggcggg[C/T]gcctgtagtcccagc | 285671 |
rs2921575 | snp | A/C | 0.0482946 | 0.147699 | intron-variant | RNF180 | GRCh38.p7 | 5:64232001 | TCAAGTGTGTAGTCC[A/C]AAACTGTAATAAAAT | 285671 |
rs2934801 | snp | A/G | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64202694 | atgaaaattaaagct[A/G]taatgatataccact | 285671 |
rs2934802 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | RNF180 | GRCh38.p7 | 5:64198897 | ACTCGGGAGACAGAG[A/G]TGGCAGTGGGCCGAG | 285671 |
rs2934803 | snp | A/C | 0.410568 | 0.191619 | intron-variant | RNF180 | GRCh38.p7 | 5:64194912 | TGTTCATTTTCCTAT[A/C]TGTATATTTCAATAT | 285671 |
rs2934804 | snp | C/T | 0.489259 | 0.0724914 | intron-variant | RNF180 | GRCh38.p7 | 5:64193446 | agctttattaagata[C/T]aattggtatacaaaa | 285671 |
rs2934807 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RNF180 | GRCh38.p7 | 5:64174929 | CTTAAATGTAAAACC[G/T]GAACCTATCAAACTA | 285671 |
rs2934808 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RNF180 | GRCh38.p7 | 5:64172553 | ATCCAAGTCTCCTAA[A/T]AAACTTAGGCTCATC | 285671 |
rs2962997 | snp | C/T | 0.484561 | 0.0864924 | intron-variant | RNF180 | GRCh38.p7 | 5:64195273 | TATTTCATGTAAGTC[C/T]AAAAGTTGAATTTAA | 285671 |
rs2962998 | snp | A/T | 0.489201 | 0.0726845 | intron-variant | RNF180 | GRCh38.p7 | 5:64202009 | TAAAAAGTTTTGGAT[A/T]TTTTCCTAATTAAAA | 285671 |
rs2962999 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RNF180 | GRCh38.p7 | 5:64196733 | ATATTAACTAGACAA[C/G]GAAATATaaaactag | 285671 |
rs2963002 | snp | A/G | 0.489201 | 0.0726845 | intron-variant | RNF180 | GRCh38.p7 | 5:64217272 | ctgaaggacaagtgg[A/G]ttgttttaggttttg | 285671 |
rs2963003 | snp | A/T | | | intron-variant | RNF180 | GRCh38.p7 | 5:64224115 | tgtgtACATACATAT[A/T]TATATCTCAAGTTAT | 285671 |
rs2963004 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | RNF180 | GRCh38.p7 | 5:64232912 | ccaaactagtaagtg[A/T]tgaagcttgaaatca | 285671 |
rs2963005 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | RNF180 | GRCh38.p7 | 5:64187567 | GGACAGTTTAAGTTC[A/T]TAAATTAGCAGTTTC | 285671 |
rs2968284 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | RNF180 | GRCh38.p7 | 5:64174589 | AGCATTTTATCATAT[A/G]CCCGTTGGCCATTTA | 285671 |
rs2968286 | snp | C/T | 0.317451 | 0.240729 | intron-variant | RNF180 | GRCh38.p7 | 5:64182240 | TCGTGATCTGCCCGC[C/T]TTGGCCTCCCAAAGT | 285671 |
rs2968288 | snp | C/G | 0.0998734 | 0.199905 | intron-variant | RNF180 | GRCh38.p7 | 5:64192285 | GTCTCACACCTGTTA[C/G]GATATTACCAAATAA | 285671 |
rs2968289 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | RNF180 | GRCh38.p7 | 5:64193518 | AAATCACAAAGTTAT[C/G]TGTTTTGAGAGGTTC | 285671 |
rs2968291 | snp | A/C | 0.0581099 | 0.160244 | intron-variant | RNF180 | GRCh38.p7 | 5:64203410 | TTTTTAGTTGTGTAA[A/C]CACCACTACATTGCA | 285671 |
rs2968292 | snp | G/T | 0.0995161 | 0.199636 | intron-variant | RNF180 | GRCh38.p7 | 5:64208796 | TTGGTTGTGAGGAGA[G/T]GAAGGTATACTTTAA | 285671 |
rs2968293 | snp | A/T | 0 | 0 | intron-variant | RNF180 | GRCh38.p7 | 5:64210173 | ATTTATAGACACtct[A/T]aggtgtgtcccagga | 285671 |
rs2968294 | snp | A/G | 0.489201 | 0.0726845 | intron-variant | RNF180 | GRCh38.p7 | 5:64216609 | TAGACATCTTTCAGT[A/G]ATCTATGCCATGACA | 285671 |