SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs773308555 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF41, NABP2 | GRCh38.p7 | 12:56221844 | CTGCCCTGGTGCCGG[A/G]TCCCAGCCTCTCCCG | 10193 |
rs773431925 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF41, NABP2 | GRCh38.p7 | 12:56220958 | TGCCCTATTGTCAGA[A/C]TCTAAAACCCCTGTA | 10193 |
rs773517056 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant | RNF41 | GRCh38.p7 | 12:56208144 | AGGGATATGTTCTCC[C/T]CCGTGTCTTGGGGCC | 10193 |
rs773662119 | in-del | -/AAA | | | intron-variant | RNF41 | GRCh38.p7 | 12:56215718 | GCACGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 10193 |
rs773719764 | snp | C/T | 1.65021e-05 | 0.00287241 | synonymous-codon, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56208247 | CTGTACCACTGAGCG[C/T]AGGTGCTTAATGCAG | 10193 |
rs774073863 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF41 | GRCh38.p7 | 12:56217957 | TGCTTTCACATAAAT[C/T]ATTATTATTATTTCG | 10193 |
rs774161113 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56208668 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 10193 |
rs774190140 | snp | A/G | 3.15981e-05 | 0.00397467 | intron-variant | RNF41 | GRCh38.p7 | 12:56206850 | ATCTCCTTTCTCTGT[A/G]TTGGCTTTTTCTGCT | 10193 |
rs774559826 | snp | A/G | 1.65395e-05 | 0.00287567 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56210530 | AGAGAACCACTGGGT[A/G]ATGCAGGCGTTGCAG | 10193 |
rs774588272 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56213412 | ACCATGTTGGCCAGG[A/G]TGGCTCTTGAACTCG | 10193 |
rs774809907 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56214379 | TACAAAAATTAGCTG[A/G]GTGTGGTATGCGCAT | 10193 |
rs774897383 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNF41, NABP2 | GRCh38.p7 | 12:56221724 | CCCCTCCCACACCCT[C/T]TTTTAGGTGGAAGAT | 10193 |
rs774953461 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56207725 | TTGCACGCATGTATG[C/T]CTTTAGCAGCTGGAT | 10193 |
rs775004661 | snp | G/T | 1.64876e-05 | 0.00287116 | intron-variant | RNF41 | GRCh38.p7 | 12:56208131 | TTATCTGCATATGAG[G/T]GATATGTTCTCCCCC | 10193 |
rs775031054 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56204661 | GACAGGACAGTATGA[C/G]CCTTGGTTAAGGCAG | 10193 |
rs775086939 | snp | C/T | 3.29571e-05 | 0.00405924 | intron-variant | RNF41 | GRCh38.p7 | 12:56213944 | CCACCAAACCTGCCA[C/T]CAGACCAACTCACCT | 10193 |
rs775127855 | snp | A/T | | | intron-variant | RNF41 | GRCh38.p7 | 12:56212766 | GAGTAGTACTGGGAG[A/T]AAAAATAAAGGCTCA | 10193 |
rs775270365 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56206549 | CATCACGACAACAGC[C/T]TGCTTGCCAGGGATG | 10193 |
rs775468696 | snp | C/G | 1.67711e-05 | 0.00289573 | intron-variant | RNF41 | GRCh38.p7 | 12:56208310 | CAGGCTGCAGACCAG[C/G]GTGGGGAAAGAGCAG | 10193 |
rs775582891 | snp | C/T | | | intron-variant | RNF41 | GRCh38.p7 | 12:56208927 | TGGAGTGCAATGGCA[C/T]GGTCTCAGCTCACTG | 10193 |
rs775735983 | snp | C/T | 3.31472e-05 | 0.00407093 | missense, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56210346 | GGTTGTGCTCACAGT[C/T]GCTGAGGTGAGACAT | 10193 |
rs776121028 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF41 | GRCh38.p7 | 12:56216881 | CGTGGTGGCTCACGC[A/C]TGTAATCCCAGCTCT | 10193 |
rs776149944 | snp | C/T | 1.64754e-05 | 0.00287009 | intron-variant | RNF41 | GRCh38.p7 | 12:56207603 | TCCTTTCAGGCCTTG[C/T]TGTCAGGACATGAAA | 10193 |
rs776260977 | snp | G/T | | | intron-variant | RNF41 | GRCh38.p7 | 12:56211364 | ATAAATATATATATA[G/T]ATATTCCCTGTGCTC | 10193 |
rs776343820 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56207719 | TGCGGATTGCACGCA[C/T]GTATGCCTTTAGCAG | 10193 |
rs776381579 | snp | C/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56214086 | CTGAAAGGACAACAG[C/G]AAAAAGAGGCCAGTT | 10193 |
rs776402446 | snp | C/T | | | intron-variant | RNF41 | GRCh38.p7 | 12:56212452 | CTCAGAAGATAAAGC[C/T]TGGAGGTAGATGGGT | 10193 |
rs776479109 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | RNF41, NABP2 | GRCh38.p7 | 12:56222090 | GTCTAGTCTAGAGTC[C/T]ATATGGTCCCAGCCA | 10193 |
rs776808054 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56205107 | CTTAGAACCCAGCTA[C/T]ACAGCTCCAAGGAAA | 10193 |
rs776849265 | snp | A/G | 1.65693e-05 | 0.00287826 | synonymous-codon, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56208276 | AGTTATGGTTGGGCA[A/G]CTCATCTTTGGGCAT | 10193 |
rs776921587 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56216507 | AGTGCCACTGAAGAG[A/G]TTCTCCCAGTAACCC | 10193 |
rs777045424 | snp | C/T | 4.97673e-05 | 0.00498811 | missense, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56210327 | CAGGTCACAGGCCGC[C/T]TCGGGTTGTGCTCAC | 10193 |
rs777198394 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF41 | GRCh38.p7 | 12:56217446 | CAGCTACTCAGGAGG[C/T]TGAGGCAGGGAGAAT | 10193 |
rs777204332 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56214623 | GAGCTGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 10193 |
rs777315691 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF41, NABP2 | GRCh38.p7 | 12:56221284 | ATGGAGGGCTGGGAG[C/G]GGGTGAGGAGCGGGG | 10193 |
rs777423759 | in-del | -/A/TA | | | intron-variant | RNF41 | GRCh38.p7 | 12:56219198 | TTTATTTATTTATTT[-/A/TA]ATTTTTTTTTTGAGA | 10193 |
rs777452893 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF41 | GRCh38.p7 | 12:56218322 | TGGAGTACAGTGGCA[C/T]GATCATAGCTCACTA | 10193 |
rs777483024 | snp | C/G | 3.29457e-05 | 0.00405854 | intron-variant | RNF41 | GRCh38.p7 | 12:56207785 | AGGAATAATGGTTAA[C/G]GCAGACAGCAGAAAA | 10193 |
rs777483595 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56207696 | GTTCTGAAGGTTGGG[A/G]TTGACACTGCGGATT | 10193 |
rs777962986 | snp | C/G | | | upstream-variant-2KB, intron-variant | RNF41, NABP2 | GRCh38.p7 | 12:56223596 | CAGGTTCCATTTCTT[C/G]CAAGAAGGGTGAGCC | 10193 |
rs778065480 | snp | C/T | 1.65081e-05 | 0.00287293 | splice-acceptor-variant | RNF41 | GRCh38.p7 | 12:56214071 | ACTGAAACCCAGGTC[C/T]TGAAAGGACAACAGG | 10193 |
rs778144429 | snp | C/T | 0.00023298 | 0.0107905 | missense, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56210306 | TCTCACCCACAGCCC[C/T]GTTCACAGGTCACAG | 10193 |
rs778162442 | snp | C/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56207958 | ATGTGATAACTGGTA[C/G]GTGAATTAATGCTAT | 10193 |
rs778162723 | snp | A/C | | | downstream-variant-500B | RNF41 | GRCh38.p7 | 12:56202032 | CTACCTAAGAGGCTG[A/C]GGTAGGAGGATCACT | 10193 |
rs778333547 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF41 | GRCh38.p7 | 12:56218010 | CTAGGCTAGAGTGCA[A/G]TGGCGCGATCTTGGC | 10193 |
rs778541493 | snp | A/G | 6.60437e-05 | 0.00574608 | synonymous-codon, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56210404 | ACAGCCGAACACAGC[A/G]TTGTCACAGGCAATC | 10193 |
rs778568033 | snp | A/C | | | intron-variant | RNF41 | GRCh38.p7 | 12:56209855 | GTGACTTGCCCACTT[A/C]GGCCTCCCAAAGTGC | 10193 |
rs778798724 | in-del | -/TGTG | | | intron-variant | RNF41 | GRCh38.p7 | 12:56219662 | GTGTGTGTGTATATA[-/TGTG]TATATACACGCGCGC | 10193 |
rs778799698 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56207657 | TCACTCTAGGATCTC[A/G]TTGTATTCAATTGTC | 10193 |
rs778814117 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56202559 | TACAAAAGCAGGCAG[C/T]GGGGTTGTAACCTGT | 10193 |
rs778867163 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56204172 | CAAAGGAAAAAGATA[C/T]ATACATATCTTCTGT | 10193 |
rs778930429 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56218767 | GGAGTACAGTGGCAC[A/G]ATCTTGGCTCACTGC | 10193 |
rs779027557 | in-del | -/A | 0.000709958 | 0.0188275 | intron-variant | RNF41 | GRCh38.p7 | 12:56214087 | TGAAAGGACAACAGG[-/A]AAAAGAGGCCAGTTC | 10193 |
rs779214645 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56211845 | GGCGTGGTGGCGGGT[A/G]CCTGTAGTCTCAGCT | 10193 |
rs779256471 | snp | A/G | 6.78346e-05 | 0.00582346 | synonymous-codon, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56206462 | TTATATCTCTTCCAC[A/G]CCATGCGCAAATATC | 10193 |
rs779316077 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNF41, NABP2 | GRCh38.p7 | 12:56222836 | GTTTATACACAACAA[C/T]ACAGAGCTAGCTACC | 10193 |
rs779365423 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56205930 | TGCTTGGCACAGAGG[G/T]CCAGTCTTTCCCTAA | 10193 |
rs779596851 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56213487 | TGAGCCACTGTGCCC[A/G]GCCTTCCTATTTGTT | 10193 |
rs779627739 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RNF41 | GRCh38.p7 | 12:56203030 | AAACATACCTTGTGT[C/G]CATAGAAGCGCAGAC | 10193 |
rs779940450 | snp | A/G/T | 6.58896e-05 | 0.00573943 | synonymous-codon, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56207651 | TGACACTCACTCTAG[A/G/T]ATCTCGTTGTATTCA | 10193 |
rs780074577 | snp | A/G | 4.0235e-05 | 0.00448507 | intron-variant | RNF41 | GRCh38.p7 | 12:56206805 | TTCACCCACCTGTGT[A/G]GAGGTGGTTAAAGAT | 10193 |
rs780128243 | in-del | -/T | | | upstream-variant-2KB, intron-variant | RNF41, NABP2 | GRCh38.p7 | 12:56223820 | TACATATTTTTTGTC[-/T]TTTTTTCCCTTTTTG | 10193 |
rs780145933 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, utr-variant-5-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56210477 | CGCAGATGGGCGACC[A/G]TCACAACACTACGGT | 10193 |
rs780170511 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56209584 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 10193 |
rs780288436 | in-del | -/C | | | intron-variant | RNF41 | GRCh38.p7 | 12:56211796 | GCTAACATAGCGAAA[-/C]CCTGTCTCTACTAAA | 10193 |
rs780792583 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56215227 | AGCAAGGGCCATGCT[A/G]TGAAAAGTCTGTGAG | 10193 |
rs780893150 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56204452 | TAAGGTGAGAGAAAG[A/G]CAAAAGCAGAGGGGA | 10193 |
rs780961663 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNF41, NABP2 | GRCh38.p7 | 12:56222616 | GATGTGGGCGGTAGA[A/G]AACGTGGGATCCAAG | 10193 |
rs781015009 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56205643 | TATCAAAGTAACTAA[C/G]TACAGTCACAGGGCT | 10193 |
rs781025263 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56208205 | AGCTGACGTCTTCTC[C/T]AGCTCTGCGATGCGT | 10193 |
rs781220038 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56213117 | TCAAAATGCAGAGTG[C/T]ATGGCTGTATCAAAA | 10193 |
rs781243134 | snp | C/T | 1.68801e-05 | 0.00290512 | missense, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56206763 | ATCATCCCTCCCCAG[C/T]GGGTCACTCTTGCTG | 10193 |
rs781563996 | in-del | -/AA | | | intron-variant | RNF41 | GRCh38.p7 | 12:56214521 | CGAGCCTCAGTCTCT[-/AA]AAAAAAAAAAAAAAT | 10193 |
rs781645291 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56210467 | AGGTACTGGGCGCAG[A/G]TGGGCGACCGTCACA | 10193 |
rs781689655 | snp | C/T | 0.000135727 | 0.0082368 | intron-variant | RNF41 | GRCh38.p7 | 12:56210596 | ACAAGGCAAAAGGGG[C/T]GCAAGGGAATTAGCA | 10193 |
rs781700266 | snp | C/T | | | intron-variant | RNF41 | GRCh38.p7 | 12:56210080 | CACAAATTTACTAAA[C/T]TGCTGTGCCCCTTCT | 10193 |
rs796126131 | in-del | -/A | | | intron-variant | RNF41 | GRCh38.p7 | 12:56211184 | ATCTCGAAAAAAAAA[-/A]GCTGGGCCTGGTGGC | 10193 |
rs796226237 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56205574 | AAAAAAAAGAGGGGG[-/C]GGGGGCAGTAGGTGG | 10193 |
rs796231451 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56215741 | AAAAAAAAAAAAAGA[A/G]AGGTCCAAAAGAGCA | 10193 |
rs796248392 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56203188 | CCTTTTTCTTTTCTT[-/TT]CTTTTTTTTTTTTGA | 10193 |
rs796258832 | in-del | -/T | | | intron-variant | RNF41 | GRCh38.p7 | 12:56213205 | TCCTATTTGTTTTTG[-/T]TTTTTTTTTTTTTGA | 10193 |
rs796264790 | in-del | -/TA | | | intron-variant | RNF41 | GRCh38.p7 | 12:56219198 | ATTTATTTATTTATT[-/TA]TTTTTTTTTTGAGAC | 10193 |
rs796314078 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56205552 | ATAGCCATGATCAGG[C/T]CATTCTTAAAAAAAA | 10193 |
rs796362219 | snp | G/T | | | intron-variant | RNF41 | GRCh38.p7 | 12:56215905 | GGTGGGTGGATCACC[G/T]GAGGTCAGGAGTTCA | 10193 |
rs796549473 | snp | A/G | | | intron-variant | RNF41 | GRCh38.p7 | 12:56211635 | GATAATTCAGATGAT[A/G]GATTTAGAGAGGAGG | 10193 |
rs796642921 | in-del | -/GG | | | utr-variant-3-prime, nc-transcript-variant | RNF41 | GRCh38.p7 | 12:56203399 | ATACTTATGAAGACT[-/GG]TTTTTTTTTTTTTTT | 10193 |
rs796908541 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF41 | GRCh38.p7 | 12:56218336 | ATGATCATAGCTCAC[C/T]ACAGCCTCGCCTTCC | 10193 |
rs796980194 | in-del | -/C | | | intron-variant | RNF41 | GRCh38.p7 | 12:56215946 | GCCAACATGGTGAAA[-/C]CCCCATCTCTACTAA | 10193 |