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 |
rs41507449 | snp | A/G | 0.00902168 | 0.0665541 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417808 | CTAGCTTTTTTACAC[A/G]TTCGTTTTTTTCAAA | 80196 |
rs55639228 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409467 | CTCAGGAATTTGTGG[A/C]GGGTGATGTCCCAGC | 80196 |
rs56174403 | snp | C/T | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403600 | TTGAGTTTTAGCAAA[C/T]TGAAGGTTGTCCAGA | 80196 |
rs56196633 | snp | C/T | 0.333261 | 0.235728 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406745 | ATTTTTAGTAATCAC[C/T]GATGACTAGAAAATA | 80196 |
rs57206363 | snp | G/T | 0.3512 | 0.228601 | intron-variant, utr-variant-3-prime | RNF34, KDM2B | GRCh38.p7 | 12:121402436 | CTTTCTCCCTTTGGC[G/T]TTTTGGTTTGGTTTG | 80196 |
rs57222350 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418926 | TGGTCAGGCTGGTCT[C/T]GAATACCTGACCTCA | 80196 |
rs57636873 | snp | C/T | 0.3512 | 0.228601 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121402001 | CTTAATGTTGATTTA[C/T]ATTGAAATTGTTTAA | 80196 |
rs57703781 | snp | C/G | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410253 | TTTTCAAATATGCTG[C/G]ATGGGGCTGGCGTGG | 80196 |
rs57800170 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421370 | AGAGAGATCCCATCT[C/T]TAAAAAAAAAAAAAA | 80196 |
rs57913468 | snp | A/C | 0.0596104 | 0.162024 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399906 | GGTCTTCGCTCGGGG[A/C]GGAAAAGAATCCTCC | 80196 |
rs58583717 | snp | C/T | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411503 | TTTGAAAAATTGTAT[C/T]CTTCCCTAATTCATT | 80196 |
rs58750993 | in-del | -/C | 0.5 | 0 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399644 | GCCCCGAGGTCATCA[-/C]CGAGCATGAACGCGG | 80196 |
rs59183074 | in-del | -/A | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410163 | CGTCTCAAAAAAAAA[-/A]GAAAAGGAATTATGT | 80196 |
rs59199848 | snp | A/G | 0.390651 | 0.206682 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403345 | AGTTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 80196 |
rs59253955 | in-del | -/A | 0.487871 | 0.076925 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410546 | TGTCTCAAAACCACC[-/A]AAAAAAAAAAAATGC | 80196 |
rs59558352 | snp | C/T | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412388 | GGGACTACAGGTGCC[C/T]GCCACCACGCCAGGC | 80196 |
rs59645029 | snp | A/G | 0.350982 | 0.228698 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409918 | CCCAGCACTTTGGGA[A/G]GCCGAGGCGGGCGGA | 80196 |
rs59697780 | snp | A/G | 0.350982 | 0.228698 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407566 | TACGCCTAGTATGCT[A/G]TCTTTCCAGGAATTG | 80196 |
rs59746769 | in-del | -/AATAAA | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408464 | AAAAATAAAAATAAA[-/AATAAA]TAAAAACTAGAAAAT | 80196 |
rs59834647 | snp | C/G | 0.0726307 | 0.176182 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398244 | GGGCGCGGTGGCGGG[C/G]GCCTGTAGTCCCAGC | 80196 |
rs59966462 | snp | A/G | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419018 | CAAGAGTGTCTTTTA[A/G]TTAGTAAATGAATAA | 80196 |
rs60270456 | snp | C/T | 0.350982 | 0.228698 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409814 | TTCACTGAAGGGCAG[C/T]GGGGGTGGGTGTTAC | 80196 |
rs60582822 | snp | A/G | 0.350982 | 0.228698 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411756 | AAGAAGTTTTTGTCC[A/G]TGAGGAACTTTCACT | 80196 |
rs60801024 | snp | A/G | 0.350982 | 0.228698 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410687 | ATGATAACTATAAGT[A/G]GATTTGCCCTTCAAT | 80196 |
rs60900182 | in-del | -/A | 0 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403426 | AAACAAAAAAAAAAA[-/A]GGATAAAGATTTTGC | 80196 |
rs60970745 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421368 | ATAGAGAGATCCCAT[C/T]TCTAAAAAAAAAAAA | 80196 |
rs61079975 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414821 | CTGGGAGGCTGGGCA[C/T]GGTGGCTCATGCCTG | 80196 |
rs61201057 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418229 | AAGTAGCACATACAC[A/G]TTTGTAGTGTTATGT | 80196 |
rs61221047 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399777 | CCTCCCCGGAAACTT[G/T]ACCACCTAGCCCAGA | 80196 |
rs61659403 | in-del | -/TTG | 0.350982 | 0.228698 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405405 | GTATATTATCCAGAC[-/TTG]TTGGCTACAGAGCTA | 80196 |
rs61733229 | snp | A/G | 0.029116 | 0.117091 | utr-variant-5-prime, nc-transcript-variant | RNF34 | GRCh38.p7 | 12:121400138 | CCGCCCAGAGGGAAG[A/G]AGGTCGGCAGTGTGA | 80196 |
rs61739898 | snp | A/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420310 | TGAGGATGATGATGA[A/T]GAAGAAGAAAACGCA | 80196 |
rs61751317 | snp | A/T | 0.000446488 | 0.0149347 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420313 | GGATGATGATGATGA[A/T]GAAGAAAACGCAGAG | 80196 |
rs61754471 | snp | A/G | 1.67604e-05 | 0.00289481 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423512 | CCAAGTGCGGCAAGC[A/G]CATGAGTGAGTGTCC | 80196 |
rs61760895 | snp | A/C | 1.64727e-05 | 0.00286986 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416316 | ACCCACCAGCAGCTA[A/C]GGAAGGGCCCAACAT | 80196 |
rs61955092 | snp | A/T | 0.416218 | 0.186739 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415083 | CCTGGGCAACAAGAG[A/T]GAAGTTCCATCTCAA | 80196 |
rs61955093 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423365 | CTGAAGCCGAGGCCT[A/T]AGCTCTCTGTTGCCT | 80196 |
rs67472562 | in-del | -/T | 0 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404412 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCTC | 80196 |
rs68064188 | in-del | -/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413595 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC | 80196 |
rs71454696 | snp | G/T | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404452 | CAGGCTGGAGTGCGG[G/T]GGCACCATCTCAGCT | 80196 |
rs73407605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402729 | TTCCTTTTCCTTTTT[C/T]TTTCTCTGAAAGGTG | 80196 |
rs73407607 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403614 | ACTGAAGGTTGTCCA[C/G]AGTTTGAAACAAACC | 80196 |
rs74709796 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414248 | ACTAATACCTCAGCT[A/G]TCTCGACTTCCATTA | 80196 |
rs75522792 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408814 | TTCACACAAGAAAAC[A/G]TGCAGAGGAGTTAAG | 80196 |
rs75616931 | snp | A/G | 0.185155 | 0.241444 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421197 | TAGTTCTTAGCATCA[A/G]CTATCTGTAGATTTC | 80196 |
rs75714012 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424710 | AGCCAGACCTTGTCT[A/C]AAAAAAAAAAAAAAA | 80196 |
rs75734449 | snp | A/C | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403397 | CAAGACTCTGTCTCC[A/C]AAAAAAAAAACCAAA | 80196 |
rs75804679 | snp | A/C | 0.0733688 | 0.176922 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405506 | TTTTTCTTTTTGAGA[A/C]AGGGTCTTGCTCTGT | 80196 |
rs75955894 | snp | C/T | 0.390651 | 0.206682 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409477 | TGTGGAGGGTGATGT[C/T]CCAGCTGAAACAGTG | 80196 |
rs76518376 | snp | A/C | 0 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421373 | GAGATCCCATCTCTA[A/C]AAAAAAAAAAAAAAA | 80196 |
rs76542175 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414340 | TCGTTCTAAACACTA[C/T]AGCTTTTATTTTAAG | 80196 |
rs76598395 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423074 | CTTTTTCTAGTTACA[-/G]AAGTAATATATCCCT | 80196 |
rs76652312 | snp | C/T | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403734 | CTGAGACAATTATTT[C/T]TGAATTTAAAACTTC | 80196 |
rs77286564 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423650 | ACAGAAGGGACTGGA[A/G]AGTTATGTTCAAAGG | 80196 |
rs77443157 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | RNF34 | GRCh38.p7 | 12:121401157 | AGATTTACTATAGAA[A/G]ATTGAAAAAGAGTGT | 80196 |
rs77507303 | in-del | -/T | 0 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413021 | ATTGTGCCCAGGCTA[-/T]TTTTTTTTTCCTTCC | 80196 |
rs77552790 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415878 | CATGCCTGTGTACAT[G/T]TATCTGTTTTGGGTG | 80196 |
rs77730756 | snp | A/C | 0.350764 | 0.228794 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399517 | AGCTTTTCAAAGAGC[A/C]CTTGGGATTTGAGAG | 80196 |
rs77821626 | snp | A/C | 0.350982 | 0.228698 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409567 | TGTATATCAGAATTA[A/C]CCAGGGAGTTTTCAA | 80196 |
rs77970809 | snp | A/G | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412850 | CTGCCTTAGCCTCCC[A/G]AGTAGCTGGGATTAC | 80196 |
rs78030102 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420796 | AGGTTTATCTTTTCA[G/T]TTTTTCCCTGTAGTA | 80196 |
rs78071836 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422074 | GAGGGGAGAAGTCAG[C/T]TGACTTCATAAATGT | 80196 |
rs78146460 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421844 | CTAGCTTAAACAGCC[C/T]TCCCATCATTAACTT | 80196 |
rs78166997 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417092 | AGATCAGTTGCCTTT[C/T]TCTTTCCCTGTCAGT | 80196 |
rs78205157 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399863 | AAAGCAGCGCCGCAG[C/G]GCGCCTTCCGCCACG | 80196 |
rs78415178 | snp | A/T | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410580 | ATGGGAAAAAAAAAA[A/T]TACTTCAAATATACT | 80196 |
rs78570062 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402951 | AGAGAAATAATTTAG[A/G]ATGTAGAATTCCTTC | 80196 |
rs78573621 | in-del | -/T | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413137 | TTCAAGCGATTCTCC[-/T]GCCTCGGCCTTCCAA | 80196 |
rs78719350 | snp | A/C | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416797 | TTAGAGATTCAACAT[A/C]AAATACTTAGCTAAC | 80196 |
rs78901279 | snp | A/G | 0 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403411 | CAAAAAAAAAAACCA[A/G]AACAAAAAAAAAAAA | 80196 |
rs79012375 | snp | A/G | 0.350982 | 0.228698 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405588 | TCCCAGGTTCAAGCA[A/G]TTCTCCTGCCTCACC | 80196 |
rs79084421 | snp | A/C | 0.0807149 | 0.183963 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414270 | CTTCCATTACCTATC[A/C]CATTATCTAGATTCT | 80196 |
rs79123623 | snp | G/T | 0.3512 | 0.228601 | intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420940 | TATAGATCTGGAAAG[G/T]AGTAACTTCATTATG | 80196 |
rs79172008 | snp | C/G | 0.184838 | 0.241358 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419610 | TTGGGAACCGACCTA[C/G]CTTATTGGAGAGCTA | 80196 |
rs79330682 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398371 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAATT | 80196 |
rs79540358 | in-del | -/GTTGTTGTTGTTGTT | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406304 | GTTGTTGTTGTTGTT[-/GTTGTTGTTGTTGTT]TGAGACAGACTCTTG | 80196 |
rs79602836 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418255 | TATGTGTTAGTGCAC[A/G]TGTTTCAGTGACCAC | 80196 |
rs79716797 | snp | A/C | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412645 | TGGCCTCCCAAAGTG[A/C]TGAGATTACAGATGT | 80196 |
rs79807208 | in-del | -/T | 0.0737376 | 0.17729 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406453 | CCTGACTAATTTTTT[-/T]GTATTTCAGTAGAGA | 80196 |
rs111378433 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407309 | GGTTTTTTTCCCCCA[A/G]TGAACAAATAATGGA | 80196 |
rs111388380 | snp | G/T | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404636 | CCTCAAGTGATTCTG[G/T]CCTCCTAAAGTGCTG | 80196 |
rs111466028 | snp | A/G | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420236 | AGATACGTTGTATAA[A/G]TGTAGGTACAAAGTG | 80196 |
rs111571472 | snp | A/C/T | 0 | 0 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423622 | CCAAACTTGACCCCC[A/C/T]ACATTTCAATGCACA | 80196 |
rs111780423 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410095 | GGAGGTAGAGGTTGC[A/G]GTGAGCCAAGATCGT | 80196 |
rs111951207 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399797 | CCTAGCCCAGAAAGC[C/T]GCAGCAGCTTCCTCA | 80196 |
rs112083066 | snp | C/G | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403212 | CCATCCTGGCTAACA[C/G]AGTGAAACCCTGTCT | 80196 |
rs112104048 | snp | A/G | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418023 | CAAGTCATGTGCTGG[A/G]GTGAAGCTTCCACAC | 80196 |
rs112166347 | snp | A/G | 0.0325976 | 0.123435 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424434 | GGTGGGAGCACCTTC[A/G]AAGATGTCACATGGG | 80196 |
rs112382698 | snp | C/T | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412230 | CCATGCCCAACTAAT[C/T]TTTTTTTTTTTTTTT | 80196 |
rs112419342 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404342 | CATAAACTTTCTTTT[C/T]CCACTCTCCCCCTAT | 80196 |
rs112532382 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418897 | TTTTTAGTAAAGATG[G/T]GGTTTCACCATGTTG | 80196 |
rs112607887 | snp | A/G | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402873 | CCAATGTCTTGTCTA[A/G]AAGTATTACATTTTA | 80196 |
rs112773484 | snp | A/G | 0.000181185 | 0.00951628 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416261 | TTTGCAGGAGCCACC[A/G]GTCCATTCAGATTTA | 80196 |
rs112786606 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400010 | GCCTCCCGAAAGTCG[C/G]CTTCCTATTGGTCGT | 80196 |
rs112812260 | in-del | -/A | 0.5 | 0 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424710 | GCCAGACCTTGTCTC[-/A]AAAAAAAAAAAAAAA | 80196 |
rs112921407 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398264 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 80196 |
rs113095218 | in-del | -/A | 0.350546 | 0.22889 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410154 | GCGAAACTCCGTCTC[-/A]AAAAAAAAAGAAAAG | 80196 |
rs113326640 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398838 | TATCTGAGCAGCACT[C/T]GAAGCAAGAGAAATA | 80196 |
rs113356293 | snp | C/T | 0 | 0 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400060 | TTTTACCGGGGCACG[C/T]GGCGAGCGTGACCAC | 80196 |
rs113384828 | snp | C/G | | | intron-variant | RNF34 | GRCh38.p7 | 12:121400375 | CTTCAGGTGCCCCAA[C/G]CGAGCCAGGGCAGGC | 80196 |
rs113432721 | snp | A/G | 0.5 | 0 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420734 | GGGAACTGGTAGAGA[A/G]AGTAAACCGGTTATA | 80196 |
rs113535252 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405903 | GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCT | 80196 |
rs113569984 | snp | A/G | 0.3512 | 0.228601 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413112 | CTCACTGCAACCTCC[A/G]CCTCCCCGGTTCAAG | 80196 |
rs113603645 | snp | A/G | 0.5 | 0 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404644 | GATTCTGGCCTCCTA[A/G]AGTGCTGGGATTAGA | 80196 |
rs113741957 | snp | A/G | 0.5 | 0 | intron-variant | RNF34 | GRCh38.p7 | 12:121401771 | AGACGTGTGTTTTGA[A/G]TTGAAGTGGAAGGTA | 80196 |
rs113850313 | snp | C/T | 0.0325976 | 0.123435 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424452 | GATGTCACATGGGGG[C/T]CGGGTGCGGTGGCTC | 80196 |
rs114043273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419792 | TAGATTGTCTAAGTA[C/T]GCTGTGGTAGGACTG | 80196 |
rs114179027 | snp | G/T | 0.0547245 | 0.156101 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399908 | TCTTCGCTCGGGGCG[G/T]AAAAGAATCCTCCCC | 80196 |
rs114285155 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422518 | TCCACACCAGTAGTC[A/G]TGGGCCATGAACTAA | 80196 |
rs115198333 | snp | G/T | 0.0547245 | 0.156101 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405109 | CTCTTACGCAGATTA[G/T]TTAGGTTTGTATTCT | 80196 |
rs115618932 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404249 | TGAGCTCAGGCAGTC[C/T]ACTTGCCTTGGCCTC | 80196 |
rs115944827 | snp | G/T | 0.0554779 | 0.157039 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421602 | TTGGCACAGAAATTC[G/T]TCCTCAGCTGGTAAC | 80196 |
rs117056373 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399919 | GGCGGAAAAGAATCC[C/T]CCCCGCGCACTCCCA | 80196 |
rs117120114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121402159 | GCAAGTATACCTGGC[C/T]GGGTGCAATAGCTCA | 80196 |
rs117160881 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414102 | ATTTTAAGGTTGAGG[G/T]CTTTTTATTTGCTTT | 80196 |
rs117220933 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402983 | TTTGTGGTATATGGT[C/T]GGATATTTGGTCACT | 80196 |
rs117736614 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409219 | TCCTGTCCTCAGGTG[A/G]CCTGCTGGCCTCGGC | 80196 |
rs118005823 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF34 | GRCh38.p7 | 12:121400624 | CCAAGTGTTGGGGAC[A/G]TCGTGGGACCGAGGA | 80196 |
rs137857947 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403960 | TGGCATTATTATTAC[A/C]TTGCTATTTACCTAG | 80196 |
rs138143734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422365 | TGGCTCCTCTGCTTT[A/C]CTAAGTTCTAAAGAG | 80196 |
rs138199363 | snp | A/G | 2.14034e-05 | 0.00327128 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420247 | ATAAGTGTAGGTACA[A/G]AGTGAAATCACTTCA | 80196 |
rs138299103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405210 | GGGAACAGTATGGGA[A/G]AAACACTGTCAGTCT | 80196 |
rs138379218 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417246 | TATACCAAGGGGTGG[A/T]AAGGTTTTAATTCAT | 80196 |
rs138434056 | in-del | -/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419989 | ACCTTCCTGAGAGAG[-/T]TAATACTCTGGTTAG | 80196 |
rs138681520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417994 | TTTAGTGCTTGATGA[C/T]TTCTGATAAACTTCA | 80196 |
rs139024381 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419336 | TACACTGTGATGTTC[A/G]CACAATGACAAAATC | 80196 |
rs139160366 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406443 | AGGCACTTGCCACCA[C/T]GCCTGACTAATTTTT | 80196 |
rs139170044 | in-del | -/CCCCCC/GAAACCCCC | | | cds-indel, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423422 | GGATGAGGAAGACGA[-/CCCCCC/GAAACCCCC]CAGCCTGTGTCGCAT | 80196 |
rs139288912 | snp | G/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420602 | TCTCCAAGGAGAGAG[G/T]GAGAGCTTCACTGTC | 80196 |
rs139296354 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413702 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 80196 |
rs139336092 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418456 | TAACATGTAAAGGCT[C/T]GTAATTAATATTTAC | 80196 |
rs139422249 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412882 | GGTGCCTGGGCCAGC[C/T]ATTTTTGTATTTTTA | 80196 |
rs139546535 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422544 | ACTAAGACCCCAGAT[C/T]ACAAGAATCTCTCCC | 80196 |
rs139787083 | snp | A/G | | | intron-variant | RNF34 | GRCh38.p7 | 12:121401247 | AGGGAGACATGGTGA[A/G]GAGAAGTAATTCAAA | 80196 |
rs139825196 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407031 | AGGTAGTGAACACAG[G/T]ACCCAACAGTTAGTT | 80196 |
rs140143041 | in-del | -/C | 0.445196 | 0.1562 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415089 | AACAAGAGTGAAGTT[-/C]CCATCTCAAGAAAAA | 80196 |
rs140213777 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423844 | AGTCAGCCTGTTTGC[A/G]CCATGTGGGCATCAG | 80196 |
rs140252700 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403297 | GCTACTCTGGAGGCT[A/G]AGGCAGGAGAATGGC | 80196 |
rs140742825 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415367 | GGCTCACACTTGTAA[C/T]CTGAGCACTTCAGGA | 80196 |
rs140745383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121400520 | TGTGCGCCTCCTCGG[C/G]GGCCTGAGGCAGAGC | 80196 |
rs140798762 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408962 | ATCAGATTGTTAAAA[A/C]CTCAGGTGACCCTTT | 80196 |
rs141042508 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121424305 | ATTTTCAGTGCTACC[C/T]GCTAGCTGATTTTAA | 80196 |
rs141081411 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410445 | GGGAGGCTGAAGCAG[A/G]AGAATTGCTTGAACC | 80196 |
rs141105657 | snp | A/G | 8.24654e-05 | 0.00642074 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417540 | AAGGATTTTTGCTCC[A/G]TTTGTTCAGTCTTAC | 80196 |
rs141404014 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421619 | CCTCAGCTGGTAACA[C/T]GATCAAGCCACGGAA | 80196 |
rs141526270 | in-del | -/TC | 0.0185938 | 0.0946107 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418279 | GACCACAGAAAACAA[-/TC]TCAGTAGTGTAAGTT | 80196 |
rs141745301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416634 | TTTTATTTTCTATTA[C/T]GTTTATTTCCAAAAG | 80196 |
rs141786813 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419649 | TATAGTCAAAAGAAA[A/G]TATGTGAAGGAAGGT | 80196 |
rs141914430 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399855 | CAACCGAGAAAGCAG[C/T]GCCGCAGCGCGCCTT | 80196 |
rs142087959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419121 | ATAGACCACATACAC[A/G]GCAGTGGTTCTGTAA | 80196 |
rs142217962 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398658 | AACCATGGCTTTGTA[C/T]CCCAAGAACATTTTT | 80196 |
rs142305118 | in-del | -/A | 0.0310518 | 0.120672 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411279 | TAAGTGTTTTTCTTC[-/A]TTTTCTTTCTGGGGA | 80196 |
rs142546121 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418502 | TCTAAACTGCTGAAA[C/G]AAATGTTTTGAACAA | 80196 |
rs142639830 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422407 | CCTCCACACAGAAGG[A/G]GAGACCAAGGCCCAC | 80196 |
rs142733577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407111 | TGTTCTTTCTAAACT[A/G]TTAGAAAAAGGGTTA | 80196 |
rs142943995 | in-del | -/A | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398372 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAATTT | 80196 |
rs143025348 | in-del | -/AT | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418014 | GATAAACTTCAAGTC[-/AT]GTGCTGGAGTGAAGC | 80196 |
rs143077452 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406507 | GCCCACGCTGGTCTC[A/G]AACTCCTGAGCTCAA | 80196 |
rs143103429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403032 | TGCATATTGTATTTC[A/G]GTTGAAGCAGCAGTT | 80196 |
rs143117593 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412270 | TTTGAGATGGAGTCC[C/T]GCTCTGTTGCCCAGG | 80196 |
rs143210041 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417696 | GATACTTGTCGTGAG[A/G]AAGAAGACTTGGTGG | 80196 |
rs143217753 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420744 | AGAGAAAGTAAACCG[G/T]TTATACAAAGAGAAT | 80196 |
rs143285387 | snp | A/G/T | 6.59287e-05 | 0.00574113 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420583 | TGGTTTCAGAACCCC[A/G/T]GGCTCTCCAAGGAGA | 80196 |
rs143648835 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412260 | TTTTTTTTTTTTTGA[A/G]ATGGAGTCCCGCTCT | 80196 |
rs143834959 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409582 | CCCAGGGAGTTTTCA[A/G]AAAAATTCTGGTGCC | 80196 |
rs144021288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408305 | AAATTACCAGGGTGT[A/G]ATGGCAGGCACTTGT | 80196 |
rs144069576 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413872 | GAGCCACCGCGCCCG[G/T]CTTCACCTGACTTTT | 80196 |
rs144086612 | snp | C/G | 1.64727e-05 | 0.00286986 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416329 | TACGGAAGGGCCCAA[C/G]ATAGTTTGTAAAGCC | 80196 |
rs144288733 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404191 | TCTTCGTATTTAGTA[A/C/G]AGACGGAGTTTCACA | 80196 |
rs144296164 | in-del | -/AA | | | intron-variant | RNF34 | GRCh38.p7 | 12:121401162 | TACTATAGAAGATTG[-/AA]AAAGAGTGTCAGCTG | 80196 |
rs144358195 | in-del | -/GTTGTTGTTGTTGTT | 0.416545 | 0.186448 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406283 | TTATGGAATGTGTAA[-/GTTGTTGTTGTTGTT]GTTGTTGTTGTTGTT | 80196 |
rs144493337 | snp | G/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423040 | CAAAGCCCATCTACA[G/T]AAGACCAGCTGAGGG | 80196 |
rs144605495 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RNF34 | GRCh38.p7 | 12:121400725 | ATGCCACCCGGAAGG[A/G]GTGCTTCGTAGGCTG | 80196 |
rs144703856 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414501 | CCTGGTGGCTCAAAG[A/G]GAGGGAAGAGACAAG | 80196 |
rs144788428 | snp | A/T | 0.0310518 | 0.120672 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399306 | CAGTGAGCCGAGATC[A/T]CACTATTGCACTCCA | 80196 |
rs144819272 | snp | A/G | 0.00257381 | 0.035781 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423457 | ATGGATGCCGTCATC[A/G]ACTGTGTCCTACTGG | 80196 |
rs144970416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419386 | AGAACGTCTCCTAGT[C/T]GTCAAGCAACACATA | 80196 |
rs145004602 | snp | A/G | 0.0263992 | 0.111815 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121402254 | AACAGCTTGGCCAAC[A/G]TAGCAAAACCCTGTC | 80196 |
rs145010576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423147 | ACATAGCTAACATTT[A/G]TTGGGTACGTCAAGC | 80196 |
rs145447461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415450 | ACATGGTGAAACCCA[A/G]TCTCTACTAAAAATA | 80196 |
rs145495936 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416207 | GGGCTGCTGAATGAA[A/G]TCATGGGAACTGGAG | 80196 |
rs145599445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422029 | TTCAGAGGTCGTAGG[C/T]TGCTGGCTGGGAAAT | 80196 |
rs145652750 | in-del | -/T | 0.00780721 | 0.0619891 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417484 | ATCTTGCTGTCATCA[-/T]AATGCTTTTCTTTCT | 80196 |
rs146001775 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422454 | GTTGCCTAGTGCCTT[C/T]TCCATTGGCATATCT | 80196 |
rs146436628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408617 | ATTTCTGAAATTTAT[A/G]AGAAAGTACAGGAAG | 80196 |
rs146497196 | snp | A/G/T | 0.000164724 | 0.00907396 | intron-variant, synonymous-codon, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416350 | TTGTAAAGCCTGTGG[A/G/T]CTTTCATTTTCAGTC | 80196 |
rs146717385 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408119 | GAGATCAGCCTGGGC[A/G]GCATATCAAGACCCC | 80196 |
rs146824763 | in-del | -/AAAAAAA | | | intron-variant | RNF34 | GRCh38.p7 | 12:121401353 | GAAGGCTATAGGTAT[-/AAAAAAA]CAAAAAAAAAAAAAA | 80196 |
rs147032853 | in-del | -/AGT | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419577 | GGTGCCTGGCAATCA[-/AGT]GGGTGGAATATTTGA | 80196 |
rs147069367 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417234 | TAATTACATGTTTAT[A/C]CCAAGGGGTGGAAAG | 80196 |
rs147092139 | snp | A/G | 0.000473391 | 0.0153776 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420227 | GACCTAATCAGATAC[A/G]TTGTATAAGTGTAGG | 80196 |
rs147553178 | snp | A/G/T | 3.72682e-05 | 0.00431656 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423595 | AGGCTCCCCTCACCA[A/G/T]GACAGTCACCCCCAA | 80196 |
rs147866946 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF34 | GRCh38.p7 | 12:121400786 | GATGTGCCTCCATCG[C/T]CACTAGGTAAACGCA | 80196 |
rs147940397 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415896 | TCTGTTTTGGGTGGG[C/T]AGGGAGGTTTTTTGT | 80196 |
rs147950606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419547 | GGGTGATGTGGATTG[C/T]TGGATGCTACAGTAT | 80196 |
rs148275322 | snp | C/G/T | 4.94192e-05 | 0.00497067 | intron-variant, synonymous-codon, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417740 | CCATCATGGACTAGG[C/G/T]TCTGAGGACGACATG | 80196 |
rs148311487 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421488 | AGCCTGCAGGGAGCC[A/G]TGGTCATGCCACTGC | 80196 |
rs148409841 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423096 | TATATCCCTATCACA[C/G]ATGTCTTGAATTAGA | 80196 |
rs148549696 | snp | A/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399475 | CAAATTCTTTTATTA[A/T]GCTACGATTTTGGTT | 80196 |
rs148644546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419037 | GTAAATGAATAAATG[C/T]AGAGGGAAATTTGGT | 80196 |
rs148694694 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413224 | TAGAGACGGCGTTTC[A/G]CCATGTTGTCCAGGC | 80196 |
rs149083024 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402927 | CCTGCTTAATGTCCA[A/G]ATGGTATGAGAGAAA | 80196 |
rs149335072 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418115 | GCTCCAAAGTCTGCT[A/G]TCTGAAGGGTCCCAA | 80196 |
rs149598276 | in-del | -/CC | | | intron-variant | RNF34 | GRCh38.p7 | 12:121400227 | CATGAAGGTGAGGGG[-/CC]GGTGGAGCCGGACAG | 80196 |
rs149671327 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415412 | GATCACTTGAGGCCA[C/T]GCATCTGAGACCAGC | 80196 |
rs149715112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407822 | GGTTATGACCCTACC[A/G]GATATGGTAACTGGG | 80196 |
rs150250138 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410971 | ACAGGGTCTCACTCC[A/G]TCACCCAGGCTGGAG | 80196 |
rs150408238 | snp | C/T | 1.65894e-05 | 0.00288 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417894 | GACCAAACATCCAGA[C/T]CTGGAGTGCCGGCAC | 80196 |
rs150480808 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404590 | GAGACCGGGTTTCAC[C/T]ATCTTGGCTAGGCTG | 80196 |
rs150552544 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412358 | CATTCTCCCACCTTA[A/G]CCTCCCGAGTAGCTG | 80196 |
rs150587957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407398 | AAATTCAGAAGCCAA[A/G]AGGGTATGCCTAGTA | 80196 |
rs151100805 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121424042 | CTTTATTAGTCATGT[A/G]TATTTTAAATGCTAA | 80196 |
rs151144914 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419252 | CACTAACGTGATGTA[C/T]GGCTTCGTAGCCGGC | 80196 |
rs151187360 | in-del | -/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412230 | CCATGCCCAACTAAT[-/C]TTTTTTTTTTTTTTT | 80196 |
rs180874457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418584 | AGGAAAGCTGGATGC[A/G]GTGGTGTGAGCCTGC | 80196 |
rs180884285 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403703 | GCTCCTTGGTCCTTG[C/T]AGATTCATGTAGCAT | 80196 |
rs181069525 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399501 | TGGTTATTTTGAATA[A/C]AGCTTTTCAAAGAGC | 80196 |
rs181081695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421414 | CCAAAAAAACCTGGT[A/G]TGGTGGCACCAGCCT | 80196 |
rs181595445 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418432 | AGGTCCTTGGACATC[A/C]TGATTGAATAACATG | 80196 |
rs181602120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411433 | TTACCAGAGCTGTGT[A/G]GTTGAAAAAAAAATT | 80196 |
rs181816892 | snp | C/G | 1.64735e-05 | 0.00286993 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417717 | GACTTGGTGGATCTA[C/G]TACTGTGCCATCATG | 80196 |
rs181975056 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404761 | TGATAATATATTTAA[C/T]GGAATCATTAAAAGT | 80196 |
rs182001879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421787 | TGGGCCACCATGCCT[C/G]ACCCTCAGTGGTGTT | 80196 |
rs182007925 | snp | A/C | 0.0142736 | 0.0832652 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398975 | AATGTATATAAATAA[A/C]AGAACAGTCTTAGGT | 80196 |
rs182031296 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RNF34 | GRCh38.p7 | 12:121400143 | CAGAGGGAAGGAGGT[C/G]GGCAGTGTGAGGAGC | 80196 |
rs182375659 | snp | C/T | 0.000445857 | 0.0149241 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402827 | CATTTGTATCTATAG[C/T]ACATGTTATTGTAAT | 80196 |
rs182581069 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410869 | GTTAATATGTGTCTG[A/G]GTTGTACTGAATATT | 80196 |
rs182812926 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405673 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 80196 |
rs182932415 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407756 | AGGAAAGAACATGAA[C/G]TTAGGTCTCTAAAGC | 80196 |
rs182966689 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414797 | CGTGCCTTTGGCCCT[C/T]GCTGAAAGCTGGGAG | 80196 |
rs183191791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418782 | CTAGAGTGAAGTGGC[A/G]AGATCTTAGTTCACT | 80196 |
rs183199831 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398233 | AAAAACTAGCCGGGC[A/G]CGGTGGCGGGCGCCT | 80196 |
rs183486512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419100 | CTAATAATGTTTTGG[C/T]CAGTGATAGACCACA | 80196 |
rs183521191 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423826 | CCCGTGAACACTCAT[G/T]GAAGTCAGCCTGTTT | 80196 |
rs183599162 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416645 | ATTATGTTTATTTCC[A/G]AAAGCAAGAAATTTG | 80196 |
rs183699148 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF34 | GRCh38.p7 | 12:121400912 | GTTTCCGGCCTACTT[C/G]TGAGAGATGATTCTC | 80196 |
rs183786304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408813 | TTTCACACAAGAAAA[C/T]GTGCAGAGGAGTTAA | 80196 |
rs183849858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419410 | ACACATACTGTAGTC[A/G]TAAATTAGATAAGTC | 80196 |
rs183880893 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398359 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 80196 |
rs183982568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403342 | CAGAGTTTGCAGTGA[A/G]CCAAGATTGCGCCAC | 80196 |
rs184201950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409680 | AAGACTTGCCTGGTG[A/T]GTCCAACATGCAGCC | 80196 |
rs184217302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413864 | ACAGGTGTGAGCCAC[C/T]GCGCCCGGCTTCACC | 80196 |
rs184548290 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410403 | TTAGCCGGGTGTGGT[C/G]GTGGGTGCCTGTAAT | 80196 |
rs184665845 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417924 | CAGGTACGAGGGGGT[A/G]ACTAATTACACCCAG | 80196 |
rs184732914 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415897 | CTGTTTTGGGTGGGT[A/G]GGGAGGTTTTTTGTT | 80196 |
rs184892121 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398479 | CAAATTCTCCACATC[C/T]TCACCATCTATTTTC | 80196 |
rs184904177 | snp | A/C/T | 6.96064e-05 | 0.00589901 | synonymous-codon, missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420332 | GAAAACGCAGAGGAT[A/C/T]GGGTGAGGCCACCTA | 80196 |
rs184979349 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418599 | GGTGGTGTGAGCCTG[C/T]AGTCTGATACTTGGC | 80196 |
rs184984405 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399089 | AATCGGCTGGGCCCG[G/T]TGGCTAATCTCAGCA | 80196 |
rs185096803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421191 | GTTACATAGTTCTTA[A/G]CATCAACTATCTGTA | 80196 |
rs185211970 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399622 | TTACCGGACCCACGA[A/G]TGAGGAGCCCCGAGG | 80196 |
rs185216751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421457 | ACTTGGGAGGCTGAG[C/G]GGGGAGGATTGCTTG | 80196 |
rs185345399 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403123 | ATAAAGAGGCCGGGC[A/G]CGGTGGCTCACGCCT | 80196 |
rs185506667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411017 | ATAGCTCACCATAGT[C/T]TCAACCTCCCAGGCT | 80196 |
rs185731627 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405973 | TAATTTTTTGTATTT[C/T]TAGTAGAGACGGGGT | 80196 |
rs185775166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404074 | GGCTGGAGTGCAGTG[A/G]CACGATCTCAGCTCA | 80196 |
rs185979955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412165 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 80196 |
rs186280175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422808 | GCCAAGAGCCAGGAC[A/G]GCCCATCTCTTTCAA | 80196 |
rs186317006 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418453 | GAATAACATGTAAAG[G/T]CTTGTAATTAATATT | 80196 |
rs186646962 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF34 | GRCh38.p7 | 12:121400920 | CCTACTTCTGAGAGA[G/T]GATTCTCAACCCGAT | 80196 |
rs186729070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419704 | GTGTTTTCTAAAGTG[C/T]TCTGATTGAGAAATT | 80196 |
rs186833228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424749 | AGAAAAAAACAATGC[C/T]ACATGAGCAACAGTG | 80196 |
rs186959684 | snp | C/T | | | intron-variant | RNF34 | GRCh38.p7 | 12:121401411 | CCAGAAAGGATACTT[C/T]TGGCTACAGAAAGCA | 80196 |
rs187073342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405075 | TTATAACCTTATTGG[C/T]TGGAAACTGTCATTC | 80196 |
rs187266213 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414854 | ATCCCAGCACTTCGG[A/G]AGGCCGAGGTGGGTG | 80196 |
rs187357001 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RNF34 | GRCh38.p7 | 12:121400475 | GTCCCTAGCGTTCGC[G/T]CCGGGTGGGCCCCTC | 80196 |
rs187480409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418888 | ATTTTTGTATTTTTA[A/G]TAAAGATGGGGTTTC | 80196 |
rs187484706 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408419 | CGCACTCCAGCCTGG[C/G]TAACAAGAGTGAAAC | 80196 |
rs187530348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409190 | TTACCATGTTGGCCA[G/T]GCTGGTCTCAAACTC | 80196 |
rs187798086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414337 | TATTCGTTCTAAACA[C/T]TATAGCTTTTATTTT | 80196 |
rs187985452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419199 | TTTAGATACACAAAT[A/G]CTTATTACTGTGTTA | 80196 |
rs188015976 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416398 | TTGGATGAAATGTTA[C/T]ATAACAACACACATG | 80196 |
rs188072787 | snp | A/G | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399859 | CGAGAAAGCAGCGCC[A/G]CAGCGCGCCTTCCGC | 80196 |
rs188076750 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421478 | GGATTGCTTGAGCCT[A/G]CAGGGAGCCGTGGTC | 80196 |
rs188311504 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398290 | GGCAGGAGAATGGCG[C/T]GAACCCAGGAGACGG | 80196 |
rs188318418 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403360 | AAGATTGCGCCACTG[C/T]ACTCCAGCCTGGGCA | 80196 |
rs188565453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409860 | TAAAATGAATGTAAA[G/T]AAATTATGTTCATGG | 80196 |
rs189063926 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402978 | CTTCCTTTGTGGTAT[A/T]TGGTCGGATATTTGG | 80196 |
rs189121012 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410494 | GTGAGCCGAGATTGC[A/G]CCACTGCATTCCATC | 80196 |
rs189301389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411085 | AGCACAGGCACATGC[C/T]ACCACACCTGGCTAA | 80196 |
rs189546046 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416988 | CCTCTTTAAGCTTCT[C/G/T]TAGTGGCAAGGCTTT | 80196 |
rs189677321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421200 | TTCTTAGCATCAACT[A/C]TCTGTAGATTTCTGT | 80196 |
rs189899657 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418175 | AATTTCTCTGTCTTA[C/T]ACAGTTAGACACTAA | 80196 |
rs189926709 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399105 | TGGCTAATCTCAGCA[C/G]TTTGGAAGGCCGAGG | 80196 |
rs189929462 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403245 | ACTAAAAATACAAAA[A/C]ATTAGCTGGATGTGG | 80196 |
rs190055090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406569 | TAGGATTACAGGCGT[A/G]AGCCACCGCGCCGGG | 80196 |
rs190300694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413223 | GTAGAGACGGCGTTT[C/T]GCCATGTTGTCCAGG | 80196 |
rs190315684 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | RNF34 | GRCh38.p7 | 12:121400932 | AGATGATTCTCAACC[C/G]GATCACTGAGAGTTC | 80196 |
rs190400029 | snp | A/G | 3.29837e-05 | 0.00406088 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420567 | GCTAATGGATGCTCT[A/G]TGGTTTCAGAACCCC | 80196 |
rs190612857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405258 | AGAGGGACTTGAATA[C/T]TGAGGAGTTTCAGTG | 80196 |
rs190717761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414457 | CAGTAAAAAGGAGAC[A/G]GGTTACTCTGGGCAG | 80196 |
rs190734520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404421 | TTTTTTTGAGATGGA[A/G]TCTCTCTTTGTTGCC | 80196 |
rs190770382 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413671 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 80196 |
rs190921881 | snp | C/T | 0.000172048 | 0.00927331 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420283 | CACAGAAGATGATGA[C/T]GACGACGATGATGAG | 80196 |
rs190962060 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418709 | GTACCCCCAGCCTGG[G/T]CAACATAGCAAGACT | 80196 |
rs191269243 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418454 | AATAACATGTAAAGG[C/T]TTGTAATTAATATTT | 80196 |
rs191315620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424793 | CTTGCTTATCAGTAA[A/G]GTTAACTGCTGATGT | 80196 |
rs191383778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121401455 | GAATAGGTAACTTTG[A/G]AACTGTGCCTTGAAG | 80196 |
rs191630627 | snp | A/G | 0.0275645 | 0.114116 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398357 | AGCCTGGGCGACAGA[A/G]CGAGACTCCGTCTCA | 80196 |
rs191800360 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403321 | GAATGGCGTGAACCC[A/G]GGAGGCAGAGTTTGC | 80196 |
rs191830083 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398189 | CCATCCTGGCTAACA[C/T]GGTGAAACCCGTCTC | 80196 |
rs191831301 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF34 | GRCh38.p7 | 12:121400640 | TCGTGGGACCGAGGA[C/G]AACAGGAGGGGTGCA | 80196 |
rs192062634 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409331 | AACCAAAGTGGGATG[C/T]AAAATACTACATATC | 80196 |
rs192094523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423050 | CTACAGAAGACCAGC[C/T]GAGGGTTTCTTTTTC | 80196 |
rs192352613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416515 | AGCCATTTTCCATCT[A/G]GAAAAATACTTAATT | 80196 |
rs192604672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419827 | CTTTCAAATCAGATG[C/T]CCCTGATGCTTGGGC | 80196 |
rs192617912 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410218 | AAATATGGGGCTTAA[A/G]GGGGAGATGGAAATT | 80196 |
rs192853497 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419396 | CTAGTCGTCAAGCAA[C/T]ACATACTGTAGTCGT | 80196 |
rs192923920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420929 | ATGAGCCTGTTTATA[A/G]ATCTGGAAAGGAGTA | 80196 |
rs192985562 | snp | A/T | 0.00516221 | 0.0505416 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415248 | GTTTTCCAAGTCATT[A/T]AAAAAATTATTTACA | 80196 |
rs193045780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403086 | CTAAGGAGCATATGT[G/T]TCTCAAATGGCTCTA | 80196 |
rs193286748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408434 | GTAACAAGAGTGAAA[C/T]TCTGTCTAAAAAATA | 80196 |
rs199515654 | snp | A/G | 0.000181703 | 0.00952986 | utr-variant-5-prime, nc-transcript-variant | RNF34 | GRCh38.p7 | 12:121400203 | CGGCCGAGCTGAGGC[A/G]GTCGCGGCCATGAAG | 80196 |
rs199695141 | in-del | -/GCCT | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413527 | GCGATTCTCCTGCCT[-/GCCT]CAGCCTCCCGAGTAG | 80196 |
rs199742513 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415840 | AGACTTTTGTCCAGT[C/T]TTTTTTTTTTTTTTT | 80196 |
rs200116682 | snp | A/G | 1.6486e-05 | 0.00287102 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417549 | TGCTCCGTTTGTTCA[A/G]TCTTACAAGAAAATC | 80196 |
rs200273600 | snp | C/T | 3.51624e-05 | 0.00419284 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423572 | TGCACGTGTTCAAGT[C/T]CTGAAACAGGCTCCC | 80196 |
rs200332742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417825 | TCGTTTTTTTCAAAC[G/T]ATACAGCCCCCTCTG | 80196 |
rs200478156 | in-del | -/TTGGGA | 0.030665 | 0.119967 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421443 | TGTGGTCCCAGCTAC[-/TTGGGA]TTGGGAGGCTGAGGG | 80196 |
rs200480167 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406318 | TTTGAGACAGACTCT[A/T]GCTGTGTCGCCCAGG | 80196 |
rs200513045 | snp | C/T | 0.000166503 | 0.00912271 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423390 | TTGCCTTTCAGATGG[C/T]GAGCGGCTGCAGCTG | 80196 |
rs200788702 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant, synonymous-codon, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416290 | TACACCAAACCCTGA[A/G]TTTTCCACCTACCCA | 80196 |
rs201019913 | snp | A/G | 6.59055e-05 | 0.00574007 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420695 | CTCGGAATTTTGTCA[A/G]CTATTCTGGCTGTTG | 80196 |
rs201069572 | in-del | -/A | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413020 | CATTGTGCCCAGGCT[-/A]TTTTTTTTTTCCTTC | 80196 |
rs201157520 | in-del | -/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422915 | TCCTAACTTTCCTAA[-/G]GGGGGAACTAAGGCT | 80196 |
rs201172818 | snp | C/T | 0.000462008 | 0.0151918 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402836 | CTATAGCACATGTTA[C/T]TGTAATAATCGATCA | 80196 |
rs201204148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417770 | GGACACAAGCAGTCT[C/G]AATTCTTCAAGGTCC | 80196 |
rs201268373 | in-del | -/A | 0.386884 | 0.209196 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402557 | GATTAAAAAAAAAAA[-/A]TCCAAATTGGTGCCC | 80196 |
rs201362422 | snp | A/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403612 | AAACTGAAGGTTGTC[A/C]AGAGTTTGAAACAAA | 80196 |
rs201432830 | in-del | -/A | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414167 | ATTTTACATGCTATT[-/A]TAAAATGTTTGACAG | 80196 |
rs201536085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416124 | AGCCCAGATTCCACT[C/T]AGCTTTAAACTGTGG | 80196 |
rs201673963 | snp | A/C/T | 9.9148e-05 | 0.00704026 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420542 | GAGGGTCTGGACTTA[A/C/T]GGGACCAGGGCTAAT | 80196 |
rs201929209 | snp | A/G | 4.94181e-05 | 0.00497057 | intron-variant, synonymous-codon, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416185 | GTCTATGTGGGCTTC[A/G]TGCTGTGGGCTGCTG | 80196 |
rs201968366 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418176 | ATTTCTCTGTCTTAC[A/T]CAGTTAGACACTAAC | 80196 |
rs202010836 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417680 | GAGAAATATACCCAT[A/G]GATACTTGTCGTGAG | 80196 |
rs202069016 | snp | A/C | 0.00199792 | 0.0315431 | intron-variant, utr-variant-5-prime | RNF34, KDM2B | GRCh38.p7 | 12:121402764 | AGTGGTACTAAGGAT[A/C]AAGTATACTGTTAAA | 80196 |
rs202132357 | snp | C/T | 8.86171e-05 | 0.00665588 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420286 | AGAAGATGATGATGA[C/T]GACGATGATGAGGAT | 80196 |
rs367629594 | snp | A/C/T | 4.9498e-05 | 0.00497459 | intron-variant, synonymous-codon, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417539 | GAAGGATTTTTGCTC[A/C/T]GTTTGTTCAGTCTTA | 80196 |
rs367644293 | in-del | -/A | 0.361684 | 0.223667 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403415 | AAAAAAAACCAAAAC[-/A]AAAAAAAAAAAGGAT | 80196 |
rs367731648 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422917 | CCTAACTTTCCTAAG[A/G]GGGAACTAAGGCTCC | 80196 |
rs368005152 | snp | G/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420323 | GATGAAGAAGAAAAC[G/T]CAGAGGATCGGGTGA | 80196 |
rs368018624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403224 | ACACAGTGAAACCCT[C/G]TCTCTACTAAAAATA | 80196 |
rs368030223 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403135 | GGCGCGGTGGCTCAC[A/G]CCTGTAGTCCCAGCA | 80196 |
rs368081105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406575 | TACAGGCGTGAGCCA[C/T]CGCGCCGGGCTGGTG | 80196 |
rs368172717 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422915 | TTCCTAACTTTCCTA[A/G]GGGGGAACTAAGGCT | 80196 |
rs368256317 | snp | A/T | 0.000153988 | 0.00877328 | utr-variant-5-prime, nc-transcript-variant | RNF34 | GRCh38.p7 | 12:121400164 | TGTGAGGAGCTGCTA[A/T]GGTGCTGAGTTTCCT | 80196 |
rs368392505 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407196 | CAACTAAGGTCCCCA[A/G]GTAGGTCATGAAAGC | 80196 |
rs368427013 | snp | C/T | 4.95421e-05 | 0.00497681 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417853 | CTGCTACTATGTCTT[C/T]GTTTCAGGGAGAGCT | 80196 |
rs368457083 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404215 | TTTCACAATGTTGCC[C/T]AGGCTGGTCCCAAAC | 80196 |
rs368558209 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407777 | TCTCTAAAGCTTTTA[A/C]AAGGAGGGTGCAGAA | 80196 |
rs368630147 | snp | A/G | 4.95127e-05 | 0.00497533 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402847 | GTTATTGTAATAATC[A/G]ATCAGTTTGGCCAAT | 80196 |
rs368767001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34 | GRCh38.p7 | 12:121401008 | TGCCGAACTCAAACC[A/G]AGTGGGATGAGTCAT | 80196 |
rs368822975 | snp | G/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417473 | ATAATGGTTTATATC[G/T]TGCTGTCATCAAATG | 80196 |
rs368849518 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418930 | CAGGCTGGTCTCGAA[C/T]ACCTGACCTCAGGTT | 80196 |
rs369125307 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413932 | GGGTGTGAAGACTTA[C/T]AATATTGAAATCCTT | 80196 |
rs369150251 | snp | A/G | | | intron-variant | RNF34 | GRCh38.p7 | 12:121401694 | ATTAAGGAACTAGCT[A/G]TCGAAGGAAAGAATT | 80196 |
rs369386826 | snp | A/G | | | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424735 | AAAAAAGAAAAAAAA[A/G]AAAAAAACAATGCCA | 80196 |
rs369500317 | snp | A/G | 1.64876e-05 | 0.00287116 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416386 | AAAGAAGGTGAGTTG[A/G]ATGAAATGTTACATA | 80196 |
rs369581058 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405561 | CAATCTCTGCTTACC[A/G]CAACCTCCGTCTCCC | 80196 |
rs369707785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406084 | ATGAGCCACCGTGCC[C/T]GGCCTGTCTTATTTC | 80196 |
rs369744462 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415578 | CCGAGATTGCGCCAC[C/T]GTACTCCAGCCTGGT | 80196 |
rs369744966 | snp | A/G | 0.000177289 | 0.00941346 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423395 | TTTCAGATGGCGAGC[A/G]GCTGCAGCTGCAGGA | 80196 |
rs369753490 | snp | G/T | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398166 | ATCACGAGGTCAGGA[G/T]ATCGAGACCATCCTG | 80196 |
rs369952588 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412682 | TTGTGCCTGGCTGAA[C/T]ACTAACTTTAAATTA | 80196 |
rs370193799 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402823 | GTAACATTTGTATCT[A/G]TAGCACATGTTATTG | 80196 |
rs370203859 | snp | A/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403071 | AAATCCTTTCACATT[A/C]TAAGGAGCATATGTT | 80196 |
rs370330071 | snp | A/G | 0.000206686 | 0.0101637 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423562 | GTGCGAGCCGTGCAC[A/G]TGTTCAAGTCCTGAA | 80196 |
rs370393586 | snp | A/G | 0.000181185 | 0.00951628 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416312 | ACCTACCCACCAGCA[A/G]CTACGGAAGGGCCCA | 80196 |
rs370473629 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403144 | GCTCACGCCTGTAGT[C/G]CCAGCACTTTGGGAG | 80196 |
rs370507061 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410230 | TAAAGGGGAGATGGA[A/T]ATTAAAATTTTCAAA | 80196 |
rs370548063 | snp | A/G | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399790 | TTGACCACCTAGCCC[A/G]GAAAGCCGCAGCAGC | 80196 |
rs370594485 | snp | G/T | 0.000155988 | 0.00883004 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420374 | TTCCCTGACATGTCA[G/T]CCTGACAGGAAGGGA | 80196 |
rs370713779 | in-del | -/A | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399360 | CAAAAATAAAAAAAA[-/A]GGTGTAGGAAAATAA | 80196 |
rs370728950 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405807 | ATTTCTTTTTTTTTT[C/T]TCTTGAGACGGAGTC | 80196 |
rs370742713 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417944 | ATTACACCCAGGGCC[C/T]GGCACGCTTATTCTT | 80196 |
rs370848382 | snp | C/T | 1.675e-05 | 0.00289391 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423535 | GAGTGTCCCATCTGC[C/T]GGCAGTATGTGGTGC | 80196 |
rs370917565 | in-del | -/T | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398385 | TCAAAAAAAAAAAAA[-/T]TTTTTTTTTTAAGAA | 80196 |
rs371007642 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412534 | AGGGGTGAGCCACCA[C/T]GCCTGGCCTAATTTT | 80196 |
rs371429893 | snp | C/G | 0 | 0 | utr-variant-5-prime, nc-transcript-variant | RNF34 | GRCh38.p7 | 12:121400158 | CGGCAGTGTGAGGAG[C/G]TGCTATGGTGCTGAG | 80196 |
rs371610614 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411794 | AGGAGGCAACATCAG[A/T]CATGAATTAGAAGGG | 80196 |
rs371636385 | snp | G/T | 1.64738e-05 | 0.00286995 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417636 | TTAATGCGACTGAAG[G/T]TGAAGGACCTGCGGC | 80196 |
rs371660693 | snp | A/G | 1.65067e-05 | 0.00287282 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420555 | TATGGGACCAGGGCT[A/G]ATGGATGCTCTGTGG | 80196 |
rs371667128 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424604 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGTAGG | 80196 |
rs371779349 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422916 | TCCTAACTTTCCTAA[A/G]GGGGAACTAAGGCTC | 80196 |
rs371889967 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398099 | CATTTTTGGGCCGGG[C/T]GCGGTGGCTCACGCC | 80196 |
rs371944541 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409232 | TGACCTGCTGGCCTC[C/G]GCCTCCCAAACTGCT | 80196 |
rs372006434 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416420 | ACACACATGGGTCAG[C/T]ATTCTTGATTGTAGG | 80196 |
rs372156640 | in-del | -/T | 0.384976 | 0.210431 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404163 | GCCATGCCCGGCTAA[-/T]TTTTTTTTTTTTTCT | 80196 |
rs372267828 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423631 | ACCCCCAACATTTCA[A/G]TGCACAGAAGGGACT | 80196 |
rs372273481 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408032 | AAATGTGGGCCAAGC[A/G]TGGTAGCTCATGCCT | 80196 |
rs372445215 | snp | C/T | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400011 | CCTCCCGAAAGTCGG[C/T]TTCCTATTGGTCGTC | 80196 |
rs372493833 | snp | C/T | 4.3123e-05 | 0.00464323 | intron-variant | RNF34 | GRCh38.p7 | 12:121400258 | GACCCTCCTCGCCAA[C/T]CCTATCCTGCCAGGG | 80196 |
rs372732361 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121401966 | TTGAGGATTTGGGCT[-/G]TTAAATGTTTATTAT | 80196 |
rs372744345 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF34 | GRCh38.p7 | 12:121400681 | AGGCTAGGGCCAGGC[C/T]AACGGGTTAAAGAAC | 80196 |
rs372804221 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404991 | ACCTTTCCTCTTGCT[G/T]TTGTTGACTGTAATG | 80196 |
rs372856839 | snp | C/T | 3.39127e-05 | 0.00411767 | stop-gained, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423550 | CGGCAGTATGTGGTG[C/T]GAGCCGTGCACGTGT | 80196 |
rs372895681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403521 | TTAAACTGTAAAACC[A/G]ATTATTTTATATCAC | 80196 |
rs373171102 | snp | C/T | 1.92509e-05 | 0.00310243 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423450 | CATCTGCATGGATGC[C/T]GTCATCGACTGTGTC | 80196 |
rs373182097 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406195 | AGAGGAGAACTGGCA[C/T]TGGATACCAGAATGA | 80196 |
rs373273712 | snp | A/G | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398173 | GGTCAGGAGATCGAG[A/G]CCATCCTGGCTAACA | 80196 |
rs373330201 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417926 | GGTACGAGGGGGTAA[C/T]TAATTACACCCAGGG | 80196 |
rs373551359 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403117 | AATAGGATAAAGAGG[C/T]CGGGCGCGGTGGCTC | 80196 |
rs373568534 | snp | A/G | 4.95954e-05 | 0.00497948 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420743 | TAGAGAAAGTAAACC[A/G]GTTATACAAAGAGAA | 80196 |
rs373607538 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411592 | GTGTCATTTGAGATT[C/T]TTGGTTTTCTTTACC | 80196 |
rs373649845 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413288 | TTCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 80196 |
rs373654787 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421827 | AAATCTTATGTTCCT[A/C]TCTAGCTTAAACAGC | 80196 |
rs373863873 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414343 | TTCTAAACACTATAG[C/G/T]TTTTATTTTAAGCAT | 80196 |
rs373896354 | snp | G/T | 3.31087e-05 | 0.00406857 | intron-variant, utr-variant-5-prime | RNF34, KDM2B | GRCh38.p7 | 12:121402753 | AAAGGTGGGGGAGTG[G/T]TACTAAGGATCAAGT | 80196 |
rs373942453 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407042 | ACAGTACCCAACAGT[C/T]AGTTTTTCACCCCTT | 80196 |
rs373966078 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402695 | AGATATCAAGGAGAA[A/T]GTAATCTACTGAATG | 80196 |
rs374047813 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399823 | CCTCAGGGACGCTAT[C/T]TCCCATTTCAAACAC | 80196 |
rs374173829 | snp | C/T | 1.6507e-05 | 0.00287284 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402850 | ATTGTAATAATCGAT[C/T]AGTTTGGCCAATGTC | 80196 |
rs374432244 | snp | A/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408070 | CAGTGATTTGGGAGG[A/C]TGAAGCAGAAGGATC | 80196 |
rs374454541 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, synonymous-codon, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416356 | AGCCTGTGGGCTTTC[A/G]TTTTCAGTCTTTAGA | 80196 |
rs374643962 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410966 | TTGAGACAGGGTCTC[A/G]CTCCGTCACCCAGGC | 80196 |
rs374654278 | in-del | -/CT | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398901 | GTGGCCTGCCACGCA[-/CT]CTCTCTCTCTCCGTG | 80196 |
rs374677569 | snp | A/G | 0.000307953 | 0.0124049 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423615 | GTCACCCCCAAACTT[A/G]ACCCCCAACATTTCA | 80196 |
rs374827363 | snp | G/T | 1.65045e-05 | 0.00287263 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402838 | ATAGCACATGTTATT[G/T]TAATAATCGATCAGT | 80196 |
rs374975607 | snp | A/G | 0.000437904 | 0.0147905 | utr-variant-5-prime, upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400119 | TCCCGGGGCGCGGTA[A/G]TCACCGCCCAGAGGG | 80196 |
rs375023523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413866 | AGGTGTGAGCCACCG[C/T]GCCCGGCTTCACCTG | 80196 |
rs375145025 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409277 | GGACCACAACACTTG[A/G]CCAAAACTTAGCTGA | 80196 |
rs375234075 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406843 | ATTCTCTTATTCTCT[A/G]TGTTGTTTTAAACTA | 80196 |
rs375326843 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409128 | TGGACCACAGGCGTG[C/T]ACCACCATGCCCGGC | 80196 |
rs375341078 | snp | A/G | 1.75906e-05 | 0.00296564 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417950 | CCCAGGGCCCGGCAC[A/G]CTTATTCTTGGCCGT | 80196 |
rs375421973 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414891 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCATGGT | 80196 |
rs375473478 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407682 | AAAGAAAAATAAAGG[A/T]ATACAGGCTAATTTA | 80196 |
rs375539157 | snp | A/G | 0.000437904 | 0.0147905 | utr-variant-5-prime, nc-transcript-variant | RNF34 | GRCh38.p7 | 12:121400160 | GCAGTGTGAGGAGCT[A/G]CTATGGTGCTGAGTT | 80196 |
rs375929001 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420684 | GGAAATTCTGGCTCG[A/G]AATTTTGTCAACTAT | 80196 |
rs376080046 | snp | C/G/T | 6.58908e-05 | 0.0057395 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417690 | CCCATAGATACTTGT[C/G/T]GTGAGAAAGAAGACT | 80196 |
rs376390193 | snp | A/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403414 | AAAAAAAAACCAAAA[A/C]AAAAAAAAAAAAGGA | 80196 |
rs376437787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405787 | CCGTGTCCGGCCTCT[A/G]TCTTATTTCTTTTTT | 80196 |
rs376542969 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413089 | GGAGTGCAATGGTGC[A/G]ATCTAGGCTCACTGC | 80196 |
rs376656619 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418429 | GTGAGGTCCTTGGAC[A/C]TCCTGATTGAATAAC | 80196 |
rs376706808 | snp | C/T | 6.73911e-05 | 0.0058044 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423504 | TACCTGCACCAAGTG[C/T]GGCAAGCGCATGAGT | 80196 |
rs376707194 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413414 | TATAATTTTACCTGT[C/T]CTTTTTTTTTTTTTT | 80196 |
rs376734127 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121401921 | AGTTATAAATGATGC[C/T]TTTGTTTTTGTGAAA | 80196 |
rs376776911 | snp | A/C | 0.0107246 | 0.0724382 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398148 | GGAGGCCGAGGTGGG[A/C]GGATCACGAGGTCAG | 80196 |
rs376909182 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405998 | CGGGGTTTCACCATG[C/T]TAGCCAGGATGGTCT | 80196 |
rs377017432 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420289 | AGATGATGATGACGA[C/T]GATGATGAGGATGAT | 80196 |
rs377078507 | snp | C/T | 1.72074e-05 | 0.00293316 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423561 | GGTGCGAGCCGTGCA[C/T]GTGTTCAAGTCCTGA | 80196 |
rs377206024 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416213 | CTGAATGAAGTCATG[A/G]GAACTGGAGCTGTCA | 80196 |
rs377270647 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423784 | GACACGTGAGCTTCC[C/T]GGGCTCAGCTGGGCT | 80196 |
rs377330563 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419946 | GTGCTGTCCCATATC[C/T]TTAATGGCTTTGGCA | 80196 |
rs377368194 | in-del | -/GA | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409978 | TGACCAACATGGAGA[-/GA]AACCCTGCCTCTACT | 80196 |
rs377482605 | in-del | -/T | 0.00350982 | 0.0417443 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402732 | TTTTCCTTTTTTTTT[-/T]CTCTGAAAGGTGGGG | 80196 |
rs377499687 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413385 | GTATATAATCATTTA[A/G]AGGTATGGACTGTTA | 80196 |
rs377505318 | snp | C/T | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398401 | TTTTTTTTTTAAGAA[C/T]TGTCAGGCATTTTCA | 80196 |
rs377505774 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407301 | AACTGTAGGGTTTTT[C/T]TCCCCCAATGAACAA | 80196 |
rs377533837 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417937 | GTAACTAATTACACC[C/T]AGGGCCCGGCACGCT | 80196 |
rs377619856 | in-del | -/G | | | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398607 | GTGCTTATTAACTCT[-/G]GAGGTAGACCTGCCA | 80196 |
rs377629063 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418361 | TGAAAGAGCCATCTG[-/A]ATTAGTGAAAAAATG | 80196 |
rs377645969 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410637 | ATTTCTGAACTTTCC[A/G]GAAGGCTGGAGTGTT | 80196 |
rs386767036 | multinucleotide-polymorphism | CA/TG | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409331 | AACCAAAGTGGGATG[CA/TG]AAATACTACATATCC | 80196 |
rs397850094 | in-del | -/C | | | intron-variant, frameshift-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417644 | ACTGAAGGTGAAGGA[-/C]CTGCGGCAGTATCTC | 80196 |
rs397963490 | in-del | -/TTG | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405408 | TATTATCCAGACTTG[-/TTG]GCTACAGAGCTAAGG | 80196 |
rs398098552 | in-del | -/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406459 | CCTGACTAATTTTTT[-/T]GTATTTCAGTAGAGA | 80196 |
rs527273232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121400301 | CTCCTTTCTTTCCGC[C/G]TTAGCGGTTACCTAG | 80196 |
rs527296454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407483 | TGACTGCAAATGCAG[A/G]AGCCAAAGGCATATG | 80196 |
rs527309225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415801 | AATTTTTAGTATATG[C/T]ATATCCCAAATATAC | 80196 |
rs527332802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121401190 | GCTGGTCACAGAAAT[G/T]CAGCACATGTTTTGT | 80196 |
rs527338372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415210 | CAAAAAAATCTAGAG[A/T]GAGTTTCAGTTGGTG | 80196 |
rs527477378 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422156 | TACTTTGCGGCGTAG[A/G]ATATAACATGGTTGT | 80196 |
rs527829751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406356 | GCAGTGGCGTGATCT[C/T]AGCTCACTGCAGCCT | 80196 |
rs527829798 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399265 | CTGAGGCAGGAGAAT[C/G]CTTTGAACCCGGGAG | 80196 |
rs527867628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405736 | TGATCCTCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 80196 |
rs527905830 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413434 | TTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTTT | 80196 |
rs527937942 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413023 | TGTGCCCAGGCTATT[A/T]TTTTTTTCCTTCCTC | 80196 |
rs527945351 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420412 | CTGTGGACATTCGCT[A/C]GATTAGTACAGGATG | 80196 |
rs528021951 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411721 | CAGTCATACCATGGT[A/G]GAAAGAGGAGCAGGA | 80196 |
rs528070903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419710 | TCTAAAGTGTTCTGA[C/T]TGAGAAATTTTAAAA | 80196 |
rs528253912 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398363 | GGCGACAGAGCGAGA[C/T]TCCGTCTCAAAAAAA | 80196 |
rs528419692 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405094 | AAACTGTCATTCCTA[C/T]TCTTACGCAGATTAT | 80196 |
rs528534112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418565 | AGGGGGTTATTAAAA[A/G]TAGAGGAAAGCTGGA | 80196 |
rs528862322 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421848 | CTTAAACAGCCCTCC[C/T]ATCATTAACTTTTAT | 80196 |
rs528916658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402882 | TGTCTAAAAGTATTA[C/T]ATTTTAGAGTTCATC | 80196 |
rs529016037 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406996 | ACGCTAAAGTTTGGG[A/G]TACAGTTGGTCCCGC | 80196 |
rs529106684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416640 | TTTCTATTATGTTTA[C/T]TTCCAAAAGCAAGAA | 80196 |
rs529154386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415960 | AAACAAGAGATCATG[A/G]GTATTGGCAATGCCA | 80196 |
rs529293094 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412365 | CCACCTTAGCCTCCC[A/G]AGTAGCTGGGACTAC | 80196 |
rs529430682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34 | GRCh38.p7 | 12:121400762 | GGGGCCGCGAACTAG[A/G]GAAGGCTGGATGTGC | 80196 |
rs529512856 | snp | A/G | 1.98214e-05 | 0.00314806 | utr-variant-5-prime, nc-transcript-variant | RNF34 | GRCh38.p7 | 12:121400163 | GTGTGAGGAGCTGCT[A/G]TGGTGCTGAGTTTCC | 80196 |
rs529650241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415052 | AGTGAGCCGAGATCA[C/T]GCCATTACACTCCAG | 80196 |
rs529671435 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414314 | GAATTAGGACAAAGG[A/C]AAAAGCCTATTCGTT | 80196 |
rs529685193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422138 | GCCATTCCCACCCTT[A/G]AGTACTTTGCGGCGT | 80196 |
rs530061643 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398551 | ATCCATGGATTTGAT[G/T]TGCATTTCCTTGATA | 80196 |
rs530092259 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399179 | AACACAGTGAAAACC[A/C]GTCTCTACTAAAAAT | 80196 |
rs530170124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413338 | GGCCAGATTTTCATG[C/T]TTTTAAGCACACCAT | 80196 |
rs530307748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412898 | ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 80196 |
rs530347549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419698 | AGATTTGTGTTTTCT[A/G]AAGTGTTCTGATTGA | 80196 |
rs530401918 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418528 | AACAAATTTTTTCAC[A/G]CTTAATTTTCTTCTC | 80196 |
rs530839243 | snp | G/T | 1.65231e-05 | 0.00287424 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417871 | TTCAGGGAGAGCTTA[G/T]GGATGGAGACCAAAC | 80196 |
rs531081110 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414332 | AAGCCTATTCGTTCT[A/G]AACACTATAGCTTTT | 80196 |
rs531162515 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423774 | TCTGCCTGTGGACAC[C/G]TGAGCTTCCCGGGCT | 80196 |
rs531194831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121401481 | TGAAGTATGAGGATA[C/T]TGTAAAAGCTTATTT | 80196 |
rs531346080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409180 | AGACGGGGTTTTACC[A/G]TGTTGGCCAGGCTGG | 80196 |
rs531386204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416521 | TTTCCATCTAGAAAA[A/G]TACTTAATTGGAGGG | 80196 |
rs531433780 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423017 | AAATTCCAATAGCAT[C/G]CTGACTCCAAAGCCC | 80196 |
rs531521434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415913 | GGGAGGTTTTTTGTT[A/C]TGTAAAATTTGGATC | 80196 |
rs531599397 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422352 | CCTGACAAGATACTG[G/T]CTCCTCTGCTTTCCT | 80196 |
rs531787629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407278 | TTGGGCTTTATTCAC[G/T]GAGGAGTAACTGTAG | 80196 |
rs531789356 | snp | A/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407840 | TATGGTAACTGGGTT[A/C]CAAGGAAATATAACA | 80196 |
rs531846866 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414168 | TTTTACATGCTATTA[A/T]AAAATGTTTGACAGA | 80196 |
rs531910098 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399893 | GCCCAGGTCCGCAGG[A/T]CTTCGCTCGGGGCGG | 80196 |
rs531969313 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413520 | GGGTTCAAGCGATTC[G/T]CCTGCCTCAGCCTCC | 80196 |
rs532006940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420518 | GGCCAGTGATGAGTT[C/T]AGAGTGGGGAGGGTC | 80196 |
rs532311942 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398395 | AAAAATTTTTTTTTT[A/T]AAGAATTGTCAGGCA | 80196 |
rs532415138 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404309 | ATGGCACCTGGCCTA[C/G]TTGTCTGTTTTCATA | 80196 |
rs532448868 | in-del | -/GGG | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416911 | TTCTGAAATACTTAA[-/GGG]GGAAAAAAAATGTTA | 80196 |
rs532472791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403645 | CTGGACATATAGTGG[G/T]TGAGTTCTCTGAGGA | 80196 |
rs532514962 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404910 | GCTGAACCTTGAGGC[C/T]ATTTGAAAATCCTGG | 80196 |
rs532561720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412740 | TTTTTTTTTTTTTTT[C/T]TTGAGATGGAGTCTC | 80196 |
rs532752292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419120 | GATAGACCACATACA[C/T]GGCAGTGGTTCTGTA | 80196 |
rs532789510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418624 | CTTGGCAGGCTGAGG[C/T]AAGAGGATTGCTTTA | 80196 |
rs532960766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402942 | AATGGTATGAGAGAA[A/G]TAATTTAGGATGTAG | 80196 |
rs533134411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410850 | TAGTATTTGGCTGAC[A/T]GTAGTTAATATGTGT | 80196 |
rs533153209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416792 | ACTCTTTAGAGATTC[A/G]ACATCAAATACTTAG | 80196 |
rs533191154 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423714 | AAGTGGGGACAGAAA[C/G]ATCCATCCTGAGTTG | 80196 |
rs533557952 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400003 | GTGACCGGCCTCCCG[A/G]AAGTCGGCTTCCTAT | 80196 |
rs533605067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406590 | CCGCGCCGGGCTGGT[G/T]TTAAGTTTTTAAATA | 80196 |
rs533842380 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419375 | ACACATTACTCAGAA[C/T]GTCTCCTAGTCGTCA | 80196 |
rs533948661 | snp | A/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422096 | CATAAATGTAAATAG[A/C]AACTATGTACAGTGC | 80196 |
rs534053105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420882 | ATTTTTGAGAAAGCT[A/G]TGTACCATTTTACTG | 80196 |
rs534090055 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121424306 | TTTTCAGTGCTACCC[A/G]CTAGCTGATTTTAAC | 80196 |
rs534144227 | snp | A/G | | | intron-variant, splice-acceptor-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402741 | TTTTTTTCTCTGAAA[A/G]GTGGGGGAGTGGTAC | 80196 |
rs534393092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418812 | TGCAACCTCTGCCCC[C/G]CTGGGTTCAAGCAAT | 80196 |
rs534409955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405166 | TTGCTCCTACAGAGG[C/G]GAGGGGGCTTCTAAT | 80196 |
rs534410058 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398232 | AAAAAACTAGCCGGG[C/T]GCGGTGGCGGGCGCC | 80196 |
rs534447804 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404531 | AGCTGGGACTACAGT[G/T]GTGCACCACCACACC | 80196 |
rs534749271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402568 | GGATTAAAAAAAAAA[A/G]TCCAAATTGGTGCCC | 80196 |
rs534884139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409494 | CAGCTGAAACAGTGT[A/G]GGCAGGAAGAAGACA | 80196 |
rs534940579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417174 | GGAAAAGACCAGGAA[A/G]TGTGATTCTGCTTTC | 80196 |
rs534977403 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423986 | GTGTCCACAAGTGGC[C/T]GACATGGAACATGCT | 80196 |
rs535074870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410366 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 80196 |
rs535216026 | snp | A/G | 3.59479e-05 | 0.00423942 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417964 | CGCTTATTCTTGGCC[A/G]TATATGGTGGGGCCT | 80196 |
rs535514291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422436 | ACTCTGATTTCATCT[C/T]GAGTTGCCTAGTGCC | 80196 |
rs535611735 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406244 | TCTGAGGCAGTCCAG[C/G]CAGGTTTTAGAATTT | 80196 |
rs535639770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121400942 | CAACCCGATCACTGA[A/G]AGTTCTGAAGAGCTT | 80196 |
rs535678224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408405 | CAAGATCATACCACC[A/G]CACTCCAGCCTGGGT | 80196 |
rs535703945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407711 | TAACTGGAGGAAGAT[C/T]TTAAAGTATAGGGAA | 80196 |
rs535742857 | snp | C/G | | | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121402033 | TGTGGGTATGCTCAT[C/G]TGTAGATTTCTGGGC | 80196 |
rs535875353 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414758 | GATCACAACAATCTC[C/T]GCCTCCCGAATTCAA | 80196 |
rs535876851 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405956 | CTGCTACCACGTCCA[A/G]CTAATTTTTTGTATT | 80196 |
rs535910696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413670 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 80196 |
rs535912618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405329 | CTCACATTTGTCTTC[C/T]TGTAGTGAAGATGGA | 80196 |
rs535948816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413142 | GCGATTCTCCTGCCT[C/T]GGCCTTCCAAGTAGC | 80196 |
rs536213548 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413328 | CACTGAGCCTGGCCA[A/G]ATTTTCATGCTTTTA | 80196 |
rs536489502 | snp | A/T | 1.86879e-05 | 0.00305673 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420211 | ATACAGATTGATTCC[A/T]GACCTAATCAGATAC | 80196 |
rs536709655 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398200 | AACACGGTGAAACCC[A/G]TCTCTACTAAAAATA | 80196 |
rs536876100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412148 | CTCACTGCAAACTCC[A/G]CCTCCTGGGTTCAAG | 80196 |
rs536914107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411290 | CTTCATTTTCTTTCT[C/G]GGGAACAAAGAGGAA | 80196 |
rs536956148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418757 | GCAGAGTCTCACTCT[A/G]TTGCCCAGGCTAGAG | 80196 |
rs537087822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418254 | TTATGTGTTAGTGCA[C/T]GTGTTTCAGTGACCA | 80196 |
rs537114455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408744 | AAAACACTTTGAACA[A/G]TGGCTGCTTTTGATA | 80196 |
rs537289756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423335 | CTGGGAGGGTGGCTG[A/G]CTGACTGGCCATGCC | 80196 |
rs537333760 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410045 | CTGTAATCCCAGCTA[C/T]TAGGAGGCTGAGGCA | 80196 |
rs537504031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121400404 | GCTGCCGGACCCTCT[C/G]GAGCTCCTCCAGTGC | 80196 |
rs537636270 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant, synonymous-codon, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416170 | TTAGGCGGGTGCCAC[A/G]TCTATGTGGGCTTCG | 80196 |
rs537778311 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410743 | GGGAGATCATGTTCT[C/T]ATTGGAAGATTTTGC | 80196 |
rs538042011 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400057 | CGCTTTTACCGGGGC[A/G]CGCGGCGAGCGTGAC | 80196 |
rs538065666 | snp | C/T | 0.000174688 | 0.00934416 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415281 | TGCTATAGTATATTA[C/T]ACCCAATTACAAATG | 80196 |
rs538080699 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399366 | ATAAAAAAAAGGTGT[A/G]GGAAAATAAACTGTC | 80196 |
rs538140958 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421760 | TTGCCCAGACTAGTG[A/C]TGAATTAGGCGTGGG | 80196 |
rs538273518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413056 | TTCGAGGCAGAGTCT[C/T]ACTCTGTCACCCAAG | 80196 |
rs538292340 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404615 | AGGCTGGTCTTGAAC[G/T]CCTGACCTCAAGTGA | 80196 |
rs538310229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419898 | CAGGCTCCAGTTAAA[C/T]TAGCCATTTGCAGGT | 80196 |
rs538310409 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412396 | AGGTGCCCGCCACCA[C/T]GCCAGGCTAATTTTG | 80196 |
rs538349327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419335 | GTACACTGTGATGTT[C/T]GCACAATGACAAAAT | 80196 |
rs538989285 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419977 | TTCCATTATGGGACC[C/T]TCCTGAGAGAGTTAA | 80196 |
rs539222818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411092 | GCACATGCCACCACA[A/C]CTGGCTAATTTTATT | 80196 |
rs539342428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417267 | TTTAATTCATTAACA[A/C]AAGAGTGTGTTTTTC | 80196 |
rs539448073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408579 | GTAGAGATGCCTTTG[C/T]CCTGAGGAGGCATGC | 80196 |
rs539486553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416053 | AATATAGTAATCTCA[A/G]AGTTATTGAGGGCAA | 80196 |
rs539519797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423238 | AACCAAAGTGCAGAG[A/G]AGTTGGGATTATTTC | 80196 |
rs539521866 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412821 | CCTCTGCCTCCTGGG[C/T]TCAAGTAATTCTCCT | 80196 |
rs539877379 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417204 | CTGCTCTGTGTGGTT[C/T]AAGCTCTGTTTTGTT | 80196 |
rs540029238 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399047 | AAATACTGGTTAAGT[C/T]AGAGGTGAGATTAAA | 80196 |
rs540081406 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405471 | CAAACATTTTAATTT[A/C]CATTTGTCTTCTTGC | 80196 |
rs540130898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413182 | AGGCATCTGCCAATA[C/T]GCCCAGCTAATTTTT | 80196 |
rs540172137 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417143 | TGCTCTTTAAATGGA[A/G]GAAATTGTTCATGTA | 80196 |
rs540231602 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399922 | GGAAAAGAATCCTCC[C/G]CGCGCACTCCCAGCC | 80196 |
rs540470027 | in-del | -/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421108 | CTAATGCCTTTGGCC[-/G]GGCCAGTACCTTGGT | 80196 |
rs540532499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412707 | AAATTAACTCTTAGT[C/G]AATCTAGATGTTCAT | 80196 |
rs540672550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419498 | ATAAGGCACAGCTGA[C/T]TTACATACCCCTTTT | 80196 |
rs540784278 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423093 | TAATATATCCCTATC[A/T]CAGATGTCTTGAATT | 80196 |
rs541018409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403757 | AAAACTTCTAGGTTC[A/T]TCCTTAAAATAACTG | 80196 |
rs541055430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403264 | AGCTGGATGTGGTGG[C/T]GGGCGCCTGTAGTCC | 80196 |
rs541217333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121401326 | TATTTGTAAGTAACC[A/G]TATTACAAGGCAGAA | 80196 |
rs541255451 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF34 | GRCh38.p7 | 12:121400778 | GAAGGCTGGATGTGC[C/T]TCCATCGCCACTAGG | 80196 |
rs541296878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408131 | GGCAGCATATCAAGA[C/T]CCCGTCTCTAAAAAA | 80196 |
rs541370805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415593 | TGTACTCCAGCCTGG[G/T]TGACAATGAGACCCT | 80196 |
rs541374474 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411222 | TGTGAGCCACCATTC[C/T]TGGCCTGTTTTTAAT | 80196 |
rs541509653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422759 | TCATCGTCTTTCTTA[C/T]TCACAGACTGGATTT | 80196 |
rs541894466 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422151 | TTAAGTACTTTGCGG[C/T]GTAGGATATAACATG | 80196 |
rs541930136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413918 | TCTTGAGAATTATAG[A/G]GTGTGAAGACTTATA | 80196 |
rs541967110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421092 | AAATGCTTATTTTCT[A/C]ACTAATGCCTTTGGC | 80196 |
rs542072626 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412164 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 80196 |
rs542101589 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400101 | TCCGGACGCTCGGTC[G/T]CCTCCCGGGGCGCGG | 80196 |
rs542237745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406982 | GGGTATATTGAGTGA[C/T]GCTAAAGTTTGGGGT | 80196 |
rs542272806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406339 | GTCGCCCAGGCTGGA[A/G]TGCAGTGGCGTGATC | 80196 |
rs542290556 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398972 | TATAATGTATATAAA[C/T]AACAGAACAGTCTTA | 80196 |
rs542350542 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413346 | TTTCATGCTTTTAAG[C/T]ACACCATGGCTGTAG | 80196 |
rs542407829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404752 | CTGGCTGGTTGATAA[C/T]ATATTTAATGGAATC | 80196 |
rs542442994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404181 | TTTTTTTTTTTCTTC[G/T]TATTTAGTAGAGACG | 80196 |
rs542445003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412535 | GGGGTGAGCCACCAC[A/G]CCTGGCCTAATTTTT | 80196 |
rs542768426 | snp | G/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405480 | TAATTTCCATTTGTC[G/T]TCTTGCTTTTTTTTT | 80196 |
rs542816906 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407018 | TGGTCCCGCCAGCAG[A/G]TAGTGAACACAGTAC | 80196 |
rs542907333 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403240 | TCTCTACTAAAAATA[C/G]AAAAAATTAGCTGGA | 80196 |
rs542914194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418911 | GGGGTTTCACCATGT[C/T]GGTCAGGCTGGTCTC | 80196 |
rs543410838 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406649 | CAGGCAGACCATGGT[C/T]CTATGGTGGCTCTAC | 80196 |
rs543435955 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405908 | ACGCCATTCTCCTGC[C/G]TCAGCCTCCTGAGTA | 80196 |
rs543515213 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408055 | TCATGCCTGTAATCC[C/T]AGTGATTTGGGAGGC | 80196 |
rs543520616 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424379 | CTTGGTCAGTTCCTA[A/C]ATCAAGTGACCTGGC | 80196 |
rs543522964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121400726 | TGCCACCCGGAAGGG[C/G]TGCTTCGTAGGCTGC | 80196 |
rs543550025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416560 | ACTGCTCAAGTTTTA[C/T]AGACATTGTTTCTCA | 80196 |
rs543650240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415540 | AGAATCGCTTGAACC[C/T]AGGAGGTGGAGGTTG | 80196 |
rs543778079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422103 | GTAAATAGCAACTAT[A/G]TACAGTGCACAACGA | 80196 |
rs543904299 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RNF34 | GRCh38.p7 | 12:121400157 | TCGGCAGTGTGAGGA[G/T]CTGCTATGGTGCTGA | 80196 |
rs544074648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422645 | GTTCCAACTATTCAT[C/G]ATTCCCTTTGATCTC | 80196 |
rs544095678 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413663 | GCTCACTGCAAGCTC[C/G]GCCTCCCGGGTTCAC | 80196 |
rs544113736 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399664 | CATGAACGCGGGAAC[A/G]TCTGGGAAGGAAATC | 80196 |
rs544151049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406269 | GAATTTGATTTCTTA[C/T]TATGGAATGTGTAAG | 80196 |
rs544466350 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399156 | AGGAGTTCTAGACCA[C/G]CCTGGCCAACACAGT | 80196 |
rs544505005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405510 | TCTTTTTGAGACAGG[G/T]TCTTGCTCTGTCACC | 80196 |
rs544658836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413225 | AGAGACGGCGTTTCG[A/C]CATGTTGTCCAGGCT | 80196 |
rs544697639 | snp | C/T | 5.69071e-05 | 0.00533388 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420322 | TGATGAAGAAGAAAA[C/T]GCAGAGGATCGGGTG | 80196 |
rs544697783 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412756 | TTGAGATGGAGTCTC[A/G]CTGTGTCACCCAGGC | 80196 |
rs544786415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403303 | CTGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 80196 |
rs544791890 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418365 | AGAGCCATCTGAATT[A/C]GTGAAAAAATGTAGT | 80196 |
rs544840841 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411864 | TAGTAGGAAGCTAAA[C/G]TTGTAAAACTGCACT | 80196 |
rs544843564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418869 | TAGGATTACACCCCA[A/G]TTAATTTTTGTATTT | 80196 |
rs544957295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424633 | GGAGGATGGCTTGAG[C/T]CTTGGGTGTGGAGGT | 80196 |
rs545020514 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398269 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 80196 |
rs545076929 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417568 | TACAAGAAAATCTCC[A/G]TAGATGTTCTACTTG | 80196 |
rs545229348 | snp | C/T | | | intron-variant | RNF34 | GRCh38.p7 | 12:121400313 | CGCCTTAGCGGTTAC[C/T]TAGTCGTCATCTCGG | 80196 |
rs545379395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409040 | GCAGTGGTACAGTGG[C/T]GTGATATCTGCTCAC | 80196 |
rs545596191 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405704 | GACCAGGCTGGTCTG[A/G]AACTCCTGACCTCAG | 80196 |
rs545893040 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423423 | GGATGAGGAAGACGA[C/T]AGCCTGTGTCGCATC | 80196 |
rs545927737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422880 | GATTCTAAGGCTAGG[C/G]AGGGAAGGATGCACA | 80196 |
rs545992841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414822 | TGGGAGGCTGGGCAC[A/G]GTGGCTCATGCCTGT | 80196 |
rs546221864 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423640 | ATTTCAATGCACAGA[A/G]GGGACTGGAAAGTTA | 80196 |
rs546453476 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398100 | ATTTTTGGGCCGGGC[A/G]CGGTGGCTCACGCCT | 80196 |
rs546490493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404224 | GTTGCCCAGGCTGGT[C/G]CCAAACTCCTGAGCT | 80196 |
rs546639457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403456 | CTTTTTTATCAACTG[G/T]TTTTTCTGCTTTGCT | 80196 |
rs546726587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411847 | TGGTTTAGTAGCTAC[A/G]TTAGTAGGAAGCTAA | 80196 |
rs546990930 | snp | A/G | | | intron-variant | RNF34 | GRCh38.p7 | 12:121401470 | GAACTGTGCCTTGAA[A/G]TATGAGGATATTGTA | 80196 |
rs547046076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411057 | CTTTTGCCTCAGCCT[C/T]CGAGTAGCTGGGAGC | 80196 |
rs547310761 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423687 | CTATTTTAAAACATT[A/G]TTTTGACTACTAAGT | 80196 |
rs547313369 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121424307 | TTTCAGTGCTACCCG[C/T]TAGCTGATTTTAACT | 80196 |
rs547338011 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411944 | AGTTGAGGTATTTTT[C/T]TCCCCAAAAAATGTA | 80196 |
rs547348227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423100 | TCCCTATCACAGATG[C/T]CTTGAATTAGACAAA | 80196 |
rs547399001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415961 | AACAAGAGATCATGG[G/T]TATTGGCAATGCCAG | 80196 |
rs547546223 | snp | C/G | | | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424579 | TTTGGAAAAAATTAG[C/G]CAGGCGTGGTAGTCC | 80196 |
rs547619569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409289 | TTGGCCAAAACTTAG[C/T]TGACCCTTTCTTAAA | 80196 |
rs547687687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407421 | GCCTAGTATACTGTC[A/G]GAAGCCAGAGGTGGG | 80196 |
rs547749063 | snp | G/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405203 | TTGGGGAGGGAACAG[G/T]ATGGGAGAAACACTG | 80196 |
rs547820821 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406576 | ACAGGCGTGAGCCAC[C/T]GCGCCGGGCTGGTGT | 80196 |
rs547928605 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421971 | ATCCTACTTCAAAGA[C/T]GATGTCACAGTGGTA | 80196 |
rs547962647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414323 | CAAAGGCAAAAGCCT[A/G]TTCGTTCTAAACACT | 80196 |
rs548321215 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399188 | AAAACCAGTCTCTAC[C/T]AAAAATAGAAAAAAT | 80196 |
rs548327206 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420633 | TGACTTGTCAAGCCT[C/T]GATGATGTGGAAGGA | 80196 |
rs548629660 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398559 | ATTTGATGTGCATTT[C/T]CTTGATAGTTAATGA | 80196 |
rs548668886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405617 | CCCTTCTGAGTAGCT[A/G]GGATTACAGGCATCC | 80196 |
rs548797351 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408587 | GCCTTTGCCCTGAGG[A/G]GGCATGCAGAATAAA | 80196 |
rs548846218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412914 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC | 80196 |
rs548885650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419206 | ACACAAATACTTATT[A/T]CTGTGTTATAGCTGC | 80196 |
rs548977121 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412380 | GAGTAGCTGGGACTA[C/T]AGGTGCCCGCCACCA | 80196 |
rs549087125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417020 | ATTGTGATTAGGCTG[C/T]GTAGTTTACAGATTA | 80196 |
rs549153257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418478 | AATATTTACTTGTAC[A/G]TGAGTGATTCTAAAC | 80196 |
rs549441736 | snp | C/G | 1.66252e-05 | 0.00288311 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417900 | ACATCCAGATCTGGA[C/G]TGCCGGCACAGGTAC | 80196 |
rs549734944 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410149 | ACAAGAGCGAAACTC[C/T]GTCTCAAAAAAAAAG | 80196 |
rs549793312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121401780 | TTTTGAATTGAAGTG[A/G]AAGGTACTACTTTCT | 80196 |
rs549908728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408319 | TGATGGCAGGCACTT[A/G]TAATCCCAGCTACTT | 80196 |
rs549987247 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412835 | GTTCAAGTAATTCTC[C/T]TGCCTTAGCCTCCCA | 80196 |
rs550042926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407628 | GGTTTGTAGAAGATG[C/T]TTCAATCTTACTATC | 80196 |
rs550045118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415930 | GTAAAATTTGGATCA[C/T]GTTCTCTTTTTGTTA | 80196 |
rs550081780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415290 | ATATTATACCCAATT[A/G]CAAATGCGAAAACAG | 80196 |
rs550116853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413528 | GCGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC | 80196 |
rs550156574 | snp | A/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407776 | GTCTCTAAAGCTTTT[A/C]AAAGGAGGGTGCAGA | 80196 |
rs550189865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406529 | TGAGCTCAAGCAATC[C/T]GCCCACTTCAGCCTC | 80196 |
rs550280561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419910 | AAACTAGCCATTTGC[A/G]GGTACTTTGATAATG | 80196 |
rs550468683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405916 | CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAC | 80196 |
rs551113250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412010 | CAGTTTTAAGAGTGC[A/G]TACTCTAAAGAACTG | 80196 |
rs551150356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411166 | GACCTGGCCTCAAAC[A/G]ATCCTCCCACCTTGG | 80196 |
rs551402731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409428 | TAGGGCCACAGGCTT[C/T]CAAAGTAACCACAGC | 80196 |
rs551491860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423247 | GCAGAGAAGTTGGGA[C/T]TATTTCTTGTACAAC | 80196 |
rs551632043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410108 | GCGGTGAGCCAAGAT[A/C]GTGCCATCGCACTCC | 80196 |
rs551662505 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412771 | GCTGTGTCACCCAGG[C/T]TGGAGTGCAGTGGCG | 80196 |
rs551804664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121400312 | CCGCCTTAGCGGTTA[C/T]CTAGTCGTCATCTCG | 80196 |
rs552001630 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415221 | AGAGAGAGTTTCAGT[G/T]GGTGTTTTGATGTTT | 80196 |
rs552029784 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417901 | CATCCAGATCTGGAG[C/T]GCCGGCACAGGTACG | 80196 |
rs552061403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34 | GRCh38.p7 | 12:121400851 | GGAGTGAGAGCGTGG[A/G]AGCATTACTGATGAG | 80196 |
rs552183261 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412506 | CCTTGTCCTCCCAAA[C/G]TGCTAGGATTACAGG | 80196 |
rs552352113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422253 | ATCTCTGGCTTGGGT[A/G]GAACACACATTTTGT | 80196 |
rs552464462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420466 | CAGTATACTGAAACA[C/T]TTCTAGGACTGCTGA | 80196 |
rs552543818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405761 | AGTGCTGGGATCACA[A/G]GCGTGAGCCACCGTG | 80196 |
rs552570553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413464 | TTGCCCAAGCTGGAG[C/T]GCGGTGGCACAATCT | 80196 |
rs552640635 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419296 | CTAGGTGTGTAGCAG[C/G]CTGTGCCATCTAGGT | 80196 |
rs552647261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412340 | TGCCTCCCGGGTTCA[C/T]GCCATTCTCCCACCT | 80196 |
rs552849269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413038 | TTTTTTTTCCTTCCT[C/G]TTTTCGAGGCAGAGT | 80196 |
rs552964821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403783 | AACTGTGTAAATAAT[A/C]TATTTAACTTAGAGT | 80196 |
rs553019955 | in-del | -/GAGGTATATAATCATTTA | 0.0807149 | 0.183963 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413366 | ATGGCTGTAGAGTTT[-/GAGGTATATAATCATTTA]GAGGTATATAATCAT | 80196 |
rs553022776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411446 | GTAGTTGAAAAAAAA[A/T]TTTTCAGCCTAGAAT | 80196 |
rs553035564 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403122 | GATAAAGAGGCCGGG[C/T]GCGGTGGCTCACGCC | 80196 |
rs553059394 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418832 | GTTCAAGCAATTCTC[C/T]TGCCTCAGCCTTCCG | 80196 |
rs553074342 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402670 | TCTGGGTTCTTCCAA[G/T]CTCAAAATGAGATAT | 80196 |
rs553205364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410383 | CTCTACTAAAAATAC[A/G]AAAATTAGCCGGGTG | 80196 |
rs553219149 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414517 | AGGGAAGAGACAAGG[-/A]AAAAAACCATAGAAA | 80196 |
rs553418450 | snp | C/G | 1.64727e-05 | 0.00286986 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416298 | ACCCTGAGTTTTCCA[C/G]CTACCCACCAGCAGC | 80196 |
rs553482643 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409531 | CTTTGACTGAGCAGG[A/T]CTTAAGCTTTTAACC | 80196 |
rs553768457 | snp | G/T | | | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424687 | CTGAAATCCAACTTG[G/T]GTAACAGAGCCAGAC | 80196 |
rs553999305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421956 | CAAAATATTTTGGCA[A/G]TCCTACTTCAAAGAT | 80196 |
rs554046703 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF34 | GRCh38.p7 | 12:121400961 | TCTGAAGAGCTTTGT[C/G]AACAGCAGTCAGTTC | 80196 |
rs554084808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121400547 | GAGCCGCCAGGGCTC[G/T]CCTGAGCCTCGGTCC | 80196 |
rs554086502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415375 | CTTGTAATCTGAGCA[C/G]TTCAGGAGGCCAAGG | 80196 |
rs554182016 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399523 | TCAAAGAGCCCTTGG[A/G]ATTTGAGAGCCCTTG | 80196 |
rs554257671 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405366 | GTCTCCACTCAACTA[A/C/G]CTGGTAAGCTGCTCT | 80196 |
rs554329296 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419057 | GGAAATTTGGTCTAA[C/T]TGCCTTCTAGATATA | 80196 |
rs554382799 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405135 | ATTCTTTCCCCTCCC[A/G]TTTGCTTCCTCTCCT | 80196 |
rs554430671 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413143 | CGATTCTCCTGCCTC[C/G]GCCTTCCAAGTAGCT | 80196 |
rs554797649 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421631 | ACACGATCAAGCCAC[A/G]GAACATTTATGGACA | 80196 |
rs555022639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418760 | GAGTCTCACTCTGTT[A/G]CCCAGGCTAGAGTGA | 80196 |
rs555050713 | snp | A/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422782 | CTGGATTTTCTCAGA[A/T]GTAAAGGTGGGCCAA | 80196 |
rs555243879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424394 | AATCAAGTGACCTGG[A/C]CTAGCACCCCTCTTC | 80196 |
rs555279401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403669 | CTGAGGAAGCTTTCA[C/T]TGATGGAAGAACAGT | 80196 |
rs555316463 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403228 | AGTGAAACCCTGTCT[A/C/T]TACTAAAAATACAAA | 80196 |
rs555324590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411328 | TCCTTGTATAGAAAC[A/G]TGAGGAATGGGACAA | 80196 |
rs555363388 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410544 | TCTGTCTCAAAACCA[C/G]CAAAAAAAAAAAAAT | 80196 |
rs555440509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418316 | ATGCCCATTTGTCTT[A/G]CTACAGTGAAATTGT | 80196 |
rs555463139 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408747 | ACACTTTGAACAATG[G/T]CTGCTTTTGATAGAC | 80196 |
rs555501715 | snp | A/G | 0.00110307 | 0.0234589 | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416231 | ACTGGAGCTGTCAGG[A/G]GCCAGCAGTCAGCAT | 80196 |
rs555555558 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406326 | AGACTCTTGCTGTGT[C/T]GCCCAGGCTGGAGTG | 80196 |
rs555771925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RNF34, KDM2B | GRCh38.p7 | 12:121402500 | TAGGTCTTACCTCTC[A/G]GACTCAAGTAACTTT | 80196 |
rs555823341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422709 | ATAGCCCTATGGCCA[A/G]ATCTCAGGCTGGGGT | 80196 |
rs555865152 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402723 | TGTAATTCCTTTTCC[-/T]TTTTTTTTTCTCTGA | 80196 |
rs556023779 | snp | C/T | 0.000348129 | 0.0131888 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423357 | GGCCATGCCTGAAGC[C/T]GAGGCCTTAGCTCTC | 80196 |
rs556125439 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400091 | GCCCCTTACGTCCGG[A/G]CGCTCGGTCGCCTCC | 80196 |
rs556230423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34 | GRCh38.p7 | 12:121400470 | CGGGCGTCCCTAGCG[C/T]TCGCGCCGGGTGGGC | 80196 |
rs556378668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420984 | GGCTGCGAGACCACC[A/G]CTGCCAAGTGAGTTA | 80196 |
rs556518285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414690 | TTGTTGTTGTTTTTT[C/T]GAGATGGACTCTCGC | 80196 |
rs556557001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413870 | GTGAGCCACCGCGCC[C/T]GGCTTCACCTGACTT | 80196 |
rs556584334 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398904 | GCCTGCCACGCACTC[A/T]CTCTCTCTCCGTGTG | 80196 |
rs556657886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412433 | TTTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 80196 |
rs556701475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403201 | GGAGGTTGAGACCAT[C/T]CTGGCTAACACAGTG | 80196 |
rs556724817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405306 | GGCTCAGTACTTTCT[A/G]GGACCTTCTCACATT | 80196 |
rs556981433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410961 | TGTTTTTGAGACAGG[A/G]TCTCACTCCGTCACC | 80196 |
rs556998348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404714 | TGGAAACTACCATAG[C/T]TTTTCTGATTCTTCG | 80196 |
rs557321241 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404553 | ACCACACCCAGCTAA[-/T]TTTTTTTTGGTATTT | 80196 |
rs557485368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403132 | CCGGGCGCGGTGGCT[C/T]ACGCCTGTAGTCCCA | 80196 |
rs557821046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416085 | CTTACCTCTCCAGAA[G/T]AGCATTCCCTGAGGA | 80196 |
rs557896634 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422588 | AAAACATTTCTCTTA[A/C]ATCTAGAGACTACTG | 80196 |
rs558215799 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400024 | GGCTTCCTATTGGTC[A/G]TCGTGGCCGCCGCTC | 80196 |
rs558250781 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399645 | CCCCGAGGTCATCAC[A/C]GAGCATGAACGCGGG | 80196 |
rs558330013 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405681 | TAGAGACGGGGTTTC[-/A]CCATGTTGACCAGGC | 80196 |
rs558426432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406096 | GCCCGGCCTGTCTTA[C/T]TTCTTAATTAGCTCC | 80196 |
rs558557741 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404907 | ACAGCTGAACCTTGA[A/G]GCCATTTGAAAATCC | 80196 |
rs558564784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413722 | AGCTGGGACTACAGG[C/T]CCCACCAGCATGCCC | 80196 |
rs558641438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406591 | CGCGCCGGGCTGGTG[G/T]TAAGTTTTTAAATAC | 80196 |
rs558920463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420903 | CATTTTACTGAGTAT[C/G]AGTTAGTTACATGAG | 80196 |
rs558958221 | snp | A/G | 3.44489e-05 | 0.00415009 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420290 | GATGATGATGACGAC[A/G]ATGATGAGGATGATG | 80196 |
rs559212100 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410733 | TTCTCTCACTGGGAG[A/T]TCATGTTCTCATTGG | 80196 |
rs559243669 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398776 | GAAAGGCTTTCTGTA[A/C/G]ATTTTTCCAAAAAAA | 80196 |
rs559265552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424460 | ATGGGGGCCGGGTGC[A/G]GTGGCTCACGCCTGT | 80196 |
rs559299836 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423707 | GACTACTAAGTGGGG[A/G]CAGAAAGATCCATCC | 80196 |
rs559449494 | in-del | -/CAAC | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421385 | TAAAAAAAAAAAAAA[-/CAAC]AAAAAAAAAAAAACC | 80196 |
rs559481976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121401423 | CTTCTGGCTACAGAA[A/T]GCAAGGAATATTTTT | 80196 |
rs559487139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403265 | GCTGGATGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 80196 |
rs559727039 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414162 | CCAGCATTTTACATG[C/G]TATTATAAAATGTTT | 80196 |
rs559896971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415173 | ATTAAAATCTATTCT[G/T]GTTTGTCTACAACTT | 80196 |
rs560023039 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408154 | CTAAAAAAATAAAAA[A/T]AAATGGCCAGGTGTG | 80196 |
rs560059835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415798 | AAGAATTTTTAGTAT[A/G]TGCATATCCCAAATA | 80196 |
rs560190992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422798 | GTAAAGGTGGGCCAA[A/G]AGCCAGGACGGCCCA | 80196 |
rs560193157 | snp | C/T | | | intron-variant | RNF34 | GRCh38.p7 | 12:121401313 | TCAAAAGAAGAGTTA[C/T]TTGTAAGTAACCATA | 80196 |
rs560471513 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400106 | ACGCTCGGTCGCCTC[C/T]CGGGGCGCGGTAATC | 80196 |
rs560481052 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399847 | CAAACACCCAACCGA[C/G]AAAGCAGCGCCGCAG | 80196 |
rs560567381 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406348 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 80196 |
rs560661573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413931 | AGGGTGTGAAGACTT[A/C]TAATATTGAAATCCT | 80196 |
rs560698486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421132 | CCTTGGTTCTCTCAA[C/T]TTTTAAATCTAACAG | 80196 |
rs560699835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404756 | CTGGTTGATAATATA[C/T]TTAATGGAATCATTA | 80196 |
rs560795713 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421155 | TCTAACAGTAGGGGG[A/C]AAATTCCCTATAGCC | 80196 |
rs560847736 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412545 | ACCACGCCTGGCCTA[A/T]TTTTTGTGTTTTTAG | 80196 |
rs560873975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411745 | AGCAGGAGAAAAAGA[A/G]GTTTTTGTCCATGAG | 80196 |
rs560910665 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410995 | GCTGGAGTGCGGTGG[C/T]GTAAGCATAGCTCAC | 80196 |
rs561190929 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407433 | TCAGAAGCCAGAGGT[-/G]GGGGGTATGCCTAGT | 80196 |
rs561412769 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121424069 | CTAACATTTGATGAA[C/T]GTAAGTTTCCACATT | 80196 |
rs561455551 | in-del | -/T | 0.00706837 | 0.0590273 | intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420811 | TTTTTCCCTGTAGTA[-/T]TTTTTCCTTAGGCTT | 80196 |
rs561575037 | in-del | -/TT | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412231 | CATGCCCAACTAATC[-/TT]TTTTTTTTTTTTTTT | 80196 |
rs561619970 | snp | A/C | 6.60164e-05 | 0.0057449 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121402851 | TTGTAATAATCGATC[A/C]GTTTGGCCAATGTCT | 80196 |
rs561803185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409206 | GCTGGTCTCAAACTC[C/G]TGTCCTCAGGTGACC | 80196 |
rs561873903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423071 | TTTCTTTTTCTAGTT[A/G]CAGAAGTAATATATC | 80196 |
rs562033009 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411262 | TATAATGAGGGCTAA[A/G]TTAAGTGTTTTTCTT | 80196 |
rs562141916 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423692 | TTAAAACATTATTTT[A/G]ACTACTAAGTGGGGA | 80196 |
rs562356831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421456 | TACTTGGGAGGCTGA[A/G]GGGGGAGGATTGCTT | 80196 |
rs562656629 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399176 | GCCAACACAGTGAAA[A/C]CCAGTCTCTACTAAA | 80196 |
rs562781161 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399673 | GGGAACGTCTGGGAA[A/G]GAAATCTGAGGCCCT | 80196 |
rs562989707 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404968 | CTGCTCTTGCAAAGA[A/C]ACAGAACACCTTTCC | 80196 |
rs563044413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419689 | AAACTGAAGAGATTT[A/G]TGTTTTCTAAAGTGT | 80196 |
rs563070119 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407532 | AGTGAACTGACTGCA[A/G]ATTCGGAAGCCCAAG | 80196 |
rs563255908 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404013 | AGATCATTTAGTTTT[C/T]TGTTTCTTTTTTTTT | 80196 |
rs563285897 | in-del | -/AAAAAAAAA | 0.492727 | 0.0598633 | intron-variant | RNF34 | GRCh38.p7 | 12:121401354 | AAGGCTATAGGTATC[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 80196 |
rs563330029 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412324 | GGCTCACTGCAAGCT[C/T]TGCCTCCCGGGTTCA | 80196 |
rs563519344 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415508 | GTAATCCTAGTTACT[C/T]GGGAGGCTGAGGCAG | 80196 |
rs563595496 | snp | C/T | | | intron-variant, synonymous-codon | RNF34, KDM2B | GRCh38.p7 | 12:121408659 | TAAAGGAGAGCCAGG[C/T]AGATGGAGTCCAGGC | 80196 |
rs563708245 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424725 | CAAAAAAAAAAAAAA[A/G]GAAAAAAAAGAAAAA | 80196 |
rs563945980 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403538 | TTATTTTATATCACC[A/G]TTGCTAAGATTTAAT | 80196 |
rs564021654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408294 | AAAAATACAAAAAAT[C/T]ACCAGGGTGTGATGG | 80196 |
rs564026513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34 | GRCh38.p7 | 12:121401460 | GGTAACTTTGGAACT[A/G]TGCCTTGAAGTATGA | 80196 |
rs564067256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409067 | TCACTGCAACCTCCA[C/T]CTCCCAGGTTCAAAC | 80196 |
rs564166371 | snp | C/T | | | intron-variant | RNF34 | GRCh38.p7 | 12:121401592 | AAAACCACCCTCTGC[C/T]GTGTTAAGATCCAAA | 80196 |
rs564241770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422943 | GCTCCTTTTCCTACT[A/G]AGATGAGGCTCCAGA | 80196 |
rs564309364 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414852 | TAATCCCAGCACTTC[A/G]GGAGGCCGAGGTGGG | 80196 |
rs564509403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420490 | CTGCTGAGATGGCTG[G/T]GAGAATATTCAGGGC | 80196 |
rs564599430 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RNF34 | GRCh38.p7 | 12:121400141 | CCCAGAGGGAAGGAG[A/G]TCGGCAGTGTGAGGA | 80196 |
rs564602418 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399888 | GCCACGCCCAGGTCC[A/G]CAGGTCTTCGCTCGG | 80196 |
rs564619232 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414167 | ATTTTACATGCTATT[A/T]TAAAATGTTTGACAG | 80196 |
rs564636012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407197 | AACTAAGGTCCCCAA[G/T]TAGGTCATGAAAGCC | 80196 |
rs564742373 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | RNF34 | GRCh38.p7 | 12:121400341 | GGAGAGCTGCGCTGA[-/G]GGGGGGTCGCTTGCC | 80196 |
rs564831922 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398386 | CAAAAAAAAAAAAAT[A/T]TTTTTTTTTAAGAAT | 80196 |
rs565065750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404904 | AAGACAGCTGAACCT[C/T]GAGGCCATTTGAAAA | 80196 |
rs565102518 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412725 | TCTAGATGTTCATGC[C/T]TTTTTTTTTTTTTTT | 80196 |
rs565110096 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412092 | TTTGAGATGGAGTCT[C/T]GCTCTGTCACCCAGG | 80196 |
rs565181731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405497 | CTTGCTTTTTTTTTC[C/T]TTTTGAGACAGGGTC | 80196 |
rs565287200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411909 | AATGAAGAGAAGTTT[A/T]TCCTGGGAGTACTTT | 80196 |
rs565340310 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417646 | TGAAGGTGAAGGACC[C/T]GCGGCAGTATCTCAT | 80196 |
rs565878281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416700 | TGATTTACTGTAACT[A/G]TGATTCAGATTCAAG | 80196 |
rs565889491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121400989 | TTCAGGGTATTGATT[C/G]ATTTGCCGAACTCAA | 80196 |
rs565958374 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415405 | GTAGGCAGATCACTT[C/G]AGGCCACGCATCTGA | 80196 |
rs565988493 | snp | A/G | | | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121401916 | ATGACAGTTATAAAT[A/G]ATGCTTTTGTTTTTG | 80196 |
rs566045979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415976 | GTATTGGCAATGCCA[A/G]ATATTCTTTGGAAAT | 80196 |
rs566065726 | snp | C/G | 4.24574e-05 | 0.00460727 | intron-variant | RNF34 | GRCh38.p7 | 12:121400241 | GCCGGTGGAGCCGGA[C/G]AGACCCTCCTCGCCA | 80196 |
rs566102452 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399973 | CGCCCAATCCCTGTC[G/T]CTTCATTGGCTCTGG | 80196 |
rs566102821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407467 | CAACAACTCAGTGAA[C/T]TGACTGCAAATGCAG | 80196 |
rs566140739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406582 | GTGAGCCACCGCGCC[A/G]GGCTGGTGTTAAGTT | 80196 |
rs566276345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405983 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 80196 |
rs566339806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418847 | CTGCCTCAGCCTTCC[A/G]AGTAGCTAGGATTAC | 80196 |
rs566527964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413687 | GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCC | 80196 |
rs566564625 | snp | C/T | 1.71228e-05 | 0.00292594 | intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420815 | TTCCCTGTAGTATTT[C/T]TCCTTAGGCTTTTAA | 80196 |
rs566637758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421587 | ATACATTGATGAAAT[C/T]TGGCACAGAAATTCT | 80196 |
rs566968792 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399194 | AGTCTCTACTAAAAA[C/T]AGAAAAAATTAGCCG | 80196 |
rs567044208 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398229 | TACAAAAAACTAGCC[A/G]GGCGCGGTGGCGGGC | 80196 |
rs567057952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413020 | CATTGTGCCCAGGCT[A/G]TTTTTTTTTTCCTTC | 80196 |
rs567079374 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404477 | TCAGCTTACTGCAGT[C/G]TCCGCCTCAAGTGAT | 80196 |
rs567295692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403055 | CAGCAGTTTTGATAA[G/T]AAATCCTTTCACATT | 80196 |
rs567324827 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410259 | AATATGCTGCATGGG[G/T]CTGGCGTGGTGGCTC | 80196 |
rs567460066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409485 | GTGATGTCCCAGCTG[A/G]AACAGTGTAGGCAGG | 80196 |
rs567695152 | snp | A/G | 0.000302867 | 0.0123021 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121417916 | TGCCGGCACAGGTAC[A/G]AGGGGGTAACTAATT | 80196 |
rs567734553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424806 | AAGGTTAACTGCTGA[C/T]GTGCTGTTTCTTGTG | 80196 |
rs567861217 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423960 | ACTTCTGTCCTCTTT[G/T]GATGAGATCAGTGTC | 80196 |
rs567926125 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415050 | GCAGTGAGCCGAGAT[C/G]ACGCCATTACACTCC | 80196 |
rs567955868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419243 | TATTCAGTACACTAA[C/T]GTGATGTACGGCTTC | 80196 |
rs568108928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409774 | ACTGACAGCAGCTAC[A/G]AAGGTACAGGACTAA | 80196 |
rs568162588 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415939 | GGATCATGTTCTCTT[G/T]TTGTTAAACAAGAGA | 80196 |
rs568184110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121400933 | GATGATTCTCAACCC[G/T]ATCACTGAGAGTTCT | 80196 |
rs568224604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121408341 | CAGCTACTTGGGAGG[C/T]TGAGGCACAAGAATC | 80196 |
rs568273746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407658 | CAGTATGGAAGCAAT[C/G]AATGAATAAAAGAAA | 80196 |
rs568458511 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419930 | CTTTGATAATGACAC[A/G]GTGCTGTCCCATATC | 80196 |
rs568476746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405918 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 80196 |
rs568571722 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418515 | AAGAAATGTTTTGAA[C/G]AAATTTTTTCACGCT | 80196 |
rs568585813 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419004 | CAACCGCGCCTGGCC[A/G]AGAGTGTCTTTTAAT | 80196 |
rs568859609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416089 | CCTCTCCAGAATAGC[A/G]TTCCCTGAGGATCCC | 80196 |
rs568934658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121420076 | GTAGGTTCTTCATGC[A/G]ATTTTGTAGGGCCCA | 80196 |
rs569279560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404346 | AACTTTCTTTTCCCA[C/T]TCTCCCCCTATACTT | 80196 |
rs569447439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412111 | CTGTCACCCAGGCTG[C/G]AGTGCAGTGGCGCAA | 80196 |
rs569482058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419189 | TTTAGATATGTTTAG[A/G]TACACAAATACTTAT | 80196 |
rs569484009 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121411285 | TTTTTCTTCATTTTC[A/T]TTCTGGGGAACAAAG | 80196 |
rs569620270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418755 | AGGCAGAGTCTCACT[C/G]TGTTGCCCAGGCTAG | 80196 |
rs569650243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410111 | GTGAGCCAAGATCGT[A/G]CCATCGCACTCCAAC | 80196 |
rs569726001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121416836 | TCACTAAGATGGAAA[C/G]TCATTCAGAGACCCA | 80196 |
rs569901935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423316 | GTGGCTGCTCAGCTT[C/T]GGACTGGGAGGGTGG | 80196 |
rs569923568 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121404743 | CGTTCTAGTCTGGCT[A/G]GTTGATAATATATTT | 80196 |
rs569961240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RNF34, KDM2B | GRCh38.p7 | 12:121402305 | AAAGAAAAAAAGGAA[A/G]AAAAAAGTTAAGCAG | 80196 |
rs570005587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121409451 | ACCACAGCCCTTTCC[A/G]CTCAGGAATTTGTGG | 80196 |
rs570098861 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423813 | CTTTATCACACATCC[C/T]GTGAACACTCATTGA | 80196 |
rs570168559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121415591 | ACTGTACTCCAGCCT[A/G]GTTGACAATGAGACC | 80196 |
rs570517350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34 | GRCh38.p7 | 12:121400370 | CCCGGCTTCAGGTGC[C/T]CCAACCGAGCCAGGG | 80196 |
rs570519893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406714 | AAGGGATTAGACTAT[C/G]AAGAACAAGTCATTT | 80196 |
rs570530800 | snp | C/T | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121412140 | AATCTTGGCTCACTG[C/T]AAACTCCGCCTCCTG | 80196 |
rs570556065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407537 | ACTGACTGCAAATTC[A/G]GAAGCCCAAGGGCTA | 80196 |
rs570590000 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF34, KDM2B | GRCh38.p7 | 12:121424830 | TCTTGTGTCCAGGTA[C/T]TGCGCTAGGTGCTGT | 80196 |
rs570667681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422301 | TCTTTCCTAGCTTGA[C/T]TGGCTCCAAGTCACT | 80196 |
rs570696212 | snp | A/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121422157 | ACTTTGCGGCGTAGG[A/C]TATAACATGGTTGTT | 80196 |
rs570792463 | snp | A/C | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405362 | TCTGGTCTCCACTCA[A/C]CTAGCTGGTAAGCTG | 80196 |
rs570806194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121421630 | AACACGATCAAGCCA[C/T]GGAACATTTATGGAC | 80196 |
rs570822139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407536 | AACTGACTGCAAATT[C/T]GGAAGCCCAAGGGCT | 80196 |
rs571056174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419324 | GGTTTGTGGAAGTAC[A/G]CTGTGATGTTCGCAC | 80196 |
rs571085404 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121419224 | GTGTTATAGCTGCCT[A/G]CAGTATTCAGTACAC | 80196 |
rs571087595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121405219 | ATGGGAGAAACACTG[A/T]CAGTCTCTGCTATGG | 80196 |
rs571126155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121413048 | TTCCTCTTTTCGAGG[C/T]AGAGTCTCACTCTGT | 80196 |
rs571155668 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398828 | GAAGTGACATTATCT[A/G]AGCAGCACTTGAAGC | 80196 |
rs571238898 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121398140 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 80196 |
rs571558432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121403482 | TTGCTTTTAGTTATG[C/T]AGGAAAGTTTAACCT | 80196 |
rs571782647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410399 | AAAATTAGCCGGGTG[G/T]GGTGGTGGGTGCCTG | 80196 |
rs571822272 | snp | C/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121410688 | TGATAACTATAAGTG[C/G]ATTTGCCCTTCAATA | 80196 |
rs571877949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121418022 | TCAAGTCATGTGCTG[A/G]AGTGAAGCTTCCACA | 80196 |
rs572055216 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121424041 | ACTTTATTAGTCATG[C/T]ATATTTTAAATGCTA | 80196 |
rs572090476 | snp | A/G | 9.54289e-05 | 0.00690691 | missense, intron-variant, nc-transcript-variant | RNF34, KDM2B | GRCh38.p7 | 12:121423415 | CAGCTGCAGGATGAG[A/G]AAGACGACAGCCTGT | 80196 |
rs572374805 | snp | A/G | | | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121406349 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 80196 |
rs572409987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121407105 | GATTATTGTTCTTTC[C/T]AAACTGTTAGAAAAA | 80196 |
rs572439985 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121400111 | CGGTCGCCTCCCGGG[G/T]CGCGGTAATCACCGC | 80196 |
rs572514910 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF34 | GRCh38.p7 | 12:121399582 | TTTTTAAAGGCCGCG[C/T]CCTAGCGAGTGCAGC | 80196 |
rs572530134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF34, KDM2B | GRCh38.p7 | 12:121414034 | CAACATTACTTCTGG[A/G]TAATAGCAGAAACAG | 80196 |