SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8462 | snp | A/G | 0.3512 | 0.228601 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121424268 | TCACTATACAAAACA[A/G]TGTAAACTGATTACA | 80196 |
rs750008 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419701 | TTTGTGTTTTCTAAA[C/G]TGTTCTGATTGAGAA | 80196 |
rs889970 | snp | C/T | 0.47852 | 0.101384 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418414 | TGTCCAAGGACCTCA[C/T]TGGGACAATATTATT | 80196 |
rs1110337 | snp | A/G | 0 | 0 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420730 | AAATGGGAACTGGTA[A/G]AGAAAGTAAACCGGT | 80196 |
rs1177625 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408270 | tatttttagtagaga[C/G/T]ggggtttcaccatgt | 80196 |
rs1177626 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408190 | gcctcccaaagtgtt[A/G]ggattacaggcgtga | 80196 |
rs1177634 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410070 | acctcccaggttcaa[C/G]cgattctcctgcctc | 80196 |
rs1182952 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408229 | ggtctcgaactcctg[A/G]cctcaggtgatctgc | 80196 |
rs1305816 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410142 | tttgagacggagttt[C/T]gctcttgtcacccag | 80196 |
rs1305817 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410125 | ctcttgttgcccagg[C/T]tggagtgcagtggcg | 80196 |
rs1612971 | snp | A/C/G | 0 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410916 | CCAAGCCAACCTCCA[A/C/G]AGTGTCCCAGGCAAA | 80196 |
rs1706458 | snp | A/G | 0.200182 | 0.244986 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413641 | gcagtgagcccagat[A/G]gcaccactgcactcc | 80196 |
rs1706459 | snp | A/G | 0.390277 | 0.206936 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413428 | caaaactccgtctca[A/G]aaaaaaaaaaaaGGA | 80196 |
rs2293462 | snp | C/T | 0.350982 | 0.228698 | intron-variant | RNF34 | GRCh38.p7 | 12:121401051 | ACTTTCAGACCTAGA[C/T]GGTTTCGTTAATCTC | 80196 |
rs2293463 | snp | A/G | 0.350764 | 0.228794 | intron-variant | RNF34 | GRCh38.p7 | 12:121401153 | TCAAAGATTTACTAT[A/G]GAAGATTGAAAAAGA | 80196 |
rs2552078 | snp | C/T | | | | | GRCh38.p7 | 12:121415017 | cgtccgcctcccggg[C/T]tcaagcgattctcct | 80196 |
rs2668257 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415000 | gctggggaggctgag[A/G]caggagaatcgcttg | 80196 |
rs2668258 | snp | G/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415038 | gaggcggacgttgca[G/T]tgagccgagatcacg | 80196 |
rs2695150 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414937 | agctaattttttgta[C/G/T]ttttggtagacacag | 80196 |
rs3080027 | in-del | -/TA/TAG | 0 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419578 | GTGCCTGGCAATCAG[-/TA/TAG]GGTGGAATATTTGAA | 80196 |
rs3751132 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423998 | GAGCCACTGCTCAGC[A/C]TGTTCCATGTCGGCC | 80196 |
rs3751133 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422743 | TAAGAAAGACGATGA[A/G]TAAGTTAAAAAAAAG | 80196 |
rs3751134 | snp | A/C | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420409 | CCTGTACTAATCTAG[A/C]GAATGTCCACAGGGC | 80196 |
rs3751135 | snp | A/T | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420405 | TACTAATCTAGCGAA[A/T]GTCCACAGGGCACTG | 80196 |
rs3763973 | snp | C/T | 0.350764 | 0.228794 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399338 | TATTTTTGACAAGGT[C/T]TTGCTCTTGCCCAGG | 80196 |
rs3842646 | in-del | -/T | 0.351418 | 0.228505 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422916 | GAGCCTTAGTTCCCC[-/T]CTTAGGAAAGTTAGG | 80196 |
rs4081775 | snp | C/T | 0.416218 | 0.186739 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409776 | TTTTAGTCCTGTACC[C/T]TCGTAGCTGCTGTCA | 80196 |
rs4640009 | snp | C/T | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422116 | ATGTACAGTGCACAA[C/T]GATAATGCCATTCCC | 80196 |
rs7132130 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410581 | TGGGAAAAAAAAAAA[A/T]ACTTCAAATATACTA | 80196 |
rs7296507 | snp | A/G | 0.478603 | 0.101197 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409332 | ACCAAAGTGGGATGC[A/G]AAATACTACATATCC | 80196 |
rs7301132 | snp | G/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410410 | ggtgtggtggtgggt[G/T]cctgtaatcccggct | 80196 |
rs7311543 | snp | A/C | 0.350982 | 0.228698 | intron-variant | RNF34 | GRCh38.p7 | 12:121400757 | ACGTCGGGGCCGCGA[A/C]CTAGAGAAGGCTGGA | 80196 |
rs7311592 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421684 | ttatttttttctttt[A/T]aattgtaaaaaaaat | 80196 |
rs7311596 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421690 | ttttctttttaattg[A/T]aaaaaaaatatatat | 80196 |
rs7311769 | snp | C/T | 0.029116 | 0.117091 | intron-variant | RNF34 | GRCh38.p7 | 12:121400818 | CAAGGAATTTGGCAG[C/T]TTGAGTTCTCCAAGG | 80196 |
rs7961800 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422024 | GAGCTTTCAGAGGTC[A/G]TAGGCTGCTGGCTGG | 80196 |
rs10744761 | snp | C/T | 0.492727 | 0.0598633 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398223 | TAAAAATACAAAAAA[C/T]TAGCCGGGCGCGGTG | 80196 |
rs10744762 | snp | A/C | 0.492435 | 0.0610346 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121401898 | GACATCAGCCTGTGC[A/C]AGATGACAGTTATAA | 80196 |
rs10774594 | snp | A/G | 0.416218 | 0.186739 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404917 | CTTGAGGCCATTTGA[A/G]AATCCTGGCACTGTG | 80196 |
rs10849875 | snp | A/G | 0.415891 | 0.18703 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398176 | CAGGAGATCGAGACC[A/G]TCCTGGCTAACACGG | 80196 |
rs10849876 | snp | A/G | 0.479014 | 0.100263 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398302 | gcgtgaacccaggag[A/G]cggagcttgcagtga | 80196 |
rs10849877 | snp | A/G | 0.416218 | 0.186739 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404465 | GGTGGCACCATCTCA[A/G]CTTACTGCAGTCTCC | 80196 |
rs10849878 | snp | A/G | 0.417196 | 0.185864 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406489 | ATGGCGTTTCACCAC[A/G]TTGCCCACGCTGGTC | 80196 |
rs10849879 | snp | A/T | 0.416218 | 0.186739 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411512 | TTGTATTCTTCCCTA[A/T]TTCATTGTAAAACTA | 80196 |
rs10849880 | snp | A/C | 0.416708 | 0.186302 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422041 | AGGCTGCTGGCTGGG[A/C]AATGGTTTTCTGGCA | 80196 |
rs11065555 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398385 | TCAAAAAAAAAAAAA[A/T]TTTTTTTTTTAAGAA | 80196 |
rs11065556 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398614 | TTAACTCTGGAGGTA[A/G]ACCTGCCAGGCCTTT | 80196 |
rs11065557 | snp | A/C/G | 0 | 0 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398664 | GGCTTTGTACCCCAA[A/C/G]AACATTTTTATTGAG | 80196 |
rs11065558 | snp | A/G | 0.00649344 | 0.0566088 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398813 | GACTATTATGGATAA[A/G]AAGTGACATTATCTG | 80196 |
rs11065559 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404658 | AAAGTGCTGGGATTA[A/G]AGGTGTGAGCTACTG | 80196 |
rs11065560 | snp | A/G | 0 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407760 | AAGAACATGAACTTA[A/G]GTCTCTAAAGCTTTT | 80196 |
rs11065561 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412169 | TGGGTTCAAGCGATT[C/T]TCCTGCCTCAGCCTC | 80196 |
rs11065562 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413101 | TGCGATCTAGGCTCA[C/G]TGCAACCTCCGCCTC | 80196 |
rs11065563 | snp | C/T | 0.416218 | 0.186739 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413466 | GCCCAAGCTGGAGTG[C/T]GGTGGCACAATCTTG | 80196 |
rs11065564 | snp | A/G | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414327 | GGCAAAAGCCTATTC[A/G]TTCTAAACACTATAG | 80196 |
rs11065565 | snp | C/T | 0.445196 | 0.1562 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415361 | CATAGTGGCTCACAC[C/T]TGTAATCTGAGCACT | 80196 |
rs11065566 | snp | C/T | 0.478354 | 0.101757 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415570 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGTACTCC | 80196 |
rs11065567 | snp | C/T | 0.01233 | 0.0775433 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421247 | TGAGGTTAAGAACTT[C/T]TGAACTAggctgggc | 80196 |
rs11398833 | in-del | -/A/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421372 | GAGATCCCATCTCTA[-/A/C]AAAAAAAAAAAAAAA | 80196 |
rs11446752 | in-del | -/A | | | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424725 | AAAAAAAAAAAAAAA[-/A]GAAAAAAAAGAAAAA | 80196 |
rs11545004 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417600 | CACTTATTACAAGAG[A/G]CAGCATTTCAGCGCC | 80196 |
rs11545005 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121424187 | TGTTCAGGTATAGCT[C/T]TTTATAGCAAGGGCT | 80196 |
rs11610134 | snp | A/G | 0.00934559 | 0.067716 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417375 | CATGAAAATACCTCT[A/G]GAAATAGTCTGGTGC | 80196 |
rs11612856 | snp | G/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412706 | TAAATTAACTCTTAG[G/T]GAATCTAGATGTTCA | 80196 |
rs11615530 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121401872 | TCAGAAGCAAAATAT[A/G]GACCTGAATAGACAT | 80196 |
rs11829166 | snp | G/T | 0.350982 | 0.228698 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404784 | TTAAAAGTTTAGGGT[G/T]GAAAATTTGTGGTAA | 80196 |
rs11830100 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410150 | caagagcgaaactcc[A/G]tctcaaaaaaaaaga | 80196 |
rs11830307 | snp | A/T | 0.34659 | 0.230587 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398384 | CTCAAAAAAAAAAAA[A/T]TTTTTTTTTTTAAGA | 80196 |
rs11831204 | snp | C/T | 0.350764 | 0.228794 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408206 | AACACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 80196 |
rs11831315 | snp | C/T | 0.245452 | 0.249959 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402831 | TGTATCTATAGCACA[C/T]GTTATTGTAATAATC | 80196 |
rs11833355 | snp | A/G | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408127 | CCTGGGCAGCATATC[A/G]AGACCCCGTCTCTAA | 80196 |
rs11837988 | snp | C/T | 0.350764 | 0.228794 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398486 | TCCACATCCTCACCA[C/T]CTATTTTCTTTCTTT | 80196 |
rs12099579 | snp | A/G | 0.184838 | 0.241358 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412187 | CTGCCTCAGCCTCCC[A/G]ACTAGCTGGGACTAC | 80196 |
rs12314670 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404415 | tttttttttttttga[A/G]atggagtctctcttt | 80196 |
rs12321719 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404417 | tttttttttttgaga[A/T]ggagtctctctttgt | 80196 |
rs12368549 | snp | A/T | | | intron-variant | RNF34 | GRCh38.p7 | 12:121401352 | CAGAAGGCTATAGGT[A/T]TCaaaaaaaaaaaaa | 80196 |
rs12369641 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421285 | ctcacaactgtaatt[C/T]taggactttgggagg | 80196 |
rs12371831 | snp | C/T | | | intron-variant | RNF34 | GRCh38.p7 | 12:121401344 | TTACAAGGCAGAAGG[C/T]TATAGGTATCaaaaa | 80196 |
rs12810275 | snp | C/G | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399544 | AGAGCCCTTGGTTTT[C/G]TAAGTGTTTTCAATA | 80196 |
rs12811672 | snp | G/T | 0 | 0 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399520 | TTTTCAAAGAGCCCT[G/T]GGGATTTGAGAGCCC | 80196 |
rs12812023 | snp | A/T | 0 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408913 | AAAAGTTACAGGCCA[A/T]TCTGTGGTAAAAAGG | 80196 |
rs12813638 | snp | G/T | 0 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408914 | AAAGTTACAGGCCAA[G/T]CTGTGGTAAAAAGGA | 80196 |
rs12815395 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412786 | ctggagtgcagtggc[A/G]tgatctcggctcact | 80196 |
rs28398328 | snp | A/G | | | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424737 | AAAAGAAAAAAAAGA[A/G]AAAAACAATGCCACA | 80196 |
rs28493526 | snp | A/G | | | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424726 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAGAAAAAA | 80196 |
rs28557279 | snp | A/C | 0.255521 | 0.249939 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423621 | CCCAAACTTGACCCC[A/C]AACATTTCAATGCAC | 80196 |
rs34194877 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403128 | GAGGCCGGGCGCGGT[A/G]GCTCACGCCTGTAGT | 80196 |
rs34621569 | in-del | -/G | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398881 | ATTATTTCAGTCTAA[-/G]GGAAGTGGCCTGCCA | 80196 |
rs34735211 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422155 | GTACTTTGCGGCGTA[A/G/T]GATATAACATGGTTG | 80196 |
rs34812514 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420664 | ATGAGCGTGCGCCAG[C/G]TGAAGGAAATTCTGG | 80196 |
rs34892758 | in-del | -/G | | | intron-variant | RNF34 | GRCh38.p7 | 12:121400617 | ACTAACCCAAGTGTT[-/G]GGGGACATCGTGGGA | 80196 |
rs35270866 | in-del | -/AGT | 0.492484 | 0.0608394 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419576 | TGGTGCCTGGCAATC[-/AGT]AGGGTGGAATATTTG | 80196 |
rs35375423 | in-del | -/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416859 | AGACCCATCATATTG[-/G]GTAGGCCTCCTTGCT | 80196 |
rs35628523 | in-del | -/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407799 | GTGCAGAAGAGGGAT[-/C]CCTTGTTGGTTATGA | 80196 |
rs35917782 | in-del | -/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413575 | GCCACCATGCCCAGC[-/T]TTTTTTTTTTTTTTT | 80196 |
rs35925457 | in-del | -/A/ACAA | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421371 | AGAGATCCCATCTCT[-/A/ACAA]AAAAAAAAAAAAAAA | 80196 |
rs36077205 | in-del | -/G | | | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424549 | TAGCTTGGACAACAT[-/G]GGCGAAACCCTGTCT | 80196 |
rs41367546 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417432 | ATTAAATTTTAGTAG[A/C]AGGCRGAAAGAAAAC | 80196 |
rs41422244 | snp | C/T | 0.00161617 | 0.0283809 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402846 | YGTTATTGTAATAAT[C/T]GATCAGTTTGGCCAA | 80196 |
rs41468645 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417437 | ATTTTAGTAGMAGGC[A/G]GAAAGAAAACTCATG | 80196 |