SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs178746 | snp | A/G | 0.497803 | 0.033074 | intron-variant | RNF212B | GRCh38.p7 | 14:23219216 | caatctgaaagaaaa[A/G]gatgctaatgagcaa | 100507650 |
rs178747 | snp | A/G | 0.486984 | 0.079614 | intron-variant | RNF212B | GRCh38.p7 | 14:23219253 | atcatcggaaggtac[A/G]aaactcactggtaag | 100507650 |
rs178748 | snp | A/G | 0.243633 | 0.249919 | intron-variant | RNF212B | GRCh38.p7 | 14:23219541 | cagtggcaagatctc[A/G]gctcactgcaacctc | 100507650 |
rs178749 | snp | A/C | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23219669 | tagagatggggtttc[A/C]ccatgttggtcaggc | 100507650 |
rs178750 | snp | C/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23220010 | ccaacatggtgaaac[C/T]ccatctctaccaaaa | 100507650 |
rs178751 | snp | A/G | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23220855 | acaaaaaacaaatac[A/G]caaaaaataaaagca | 100507650 |
rs178752 | snp | A/G | 0.488606 | 0.0746142 | intron-variant | RNF212B | GRCh38.p7 | 14:23221160 | gggaggctgaggtgg[A/G]cagatcacttgaggt | 100507650 |
rs178753 | snp | C/T | 0.461923 | 0.132621 | intron-variant | RNF212B | GRCh38.p7 | 14:23222021 | gtatagctataagtg[C/T]ctacatcaaaaagga | 100507650 |
rs178754 | snp | A/G | 0.242488 | 0.249887 | intron-variant | RNF212B | GRCh38.p7 | 14:23222721 | gatgaatattgatgc[A/G]aaaatgctagtaaac | 100507650 |
rs178755 | snp | C/T | 0.240765 | 0.249829 | intron-variant | RNF212B | GRCh38.p7 | 14:23224206 | ttcttatcaaaatac[C/T]gatgacattctccac | 100507650 |
rs178756 | snp | A/C | 0.499722 | 0.0117779 | intron-variant | RNF212B | GRCh38.p7 | 14:23226628 | agagcgagactctgt[A/C]tcaaaaacaaaacaa | 100507650 |
rs178757 | snp | A/G | 0.499673 | 0.0127754 | intron-variant | RNF212B | GRCh38.p7 | 14:23227859 | ccatcttagcccccc[A/G]aagtgctgggattac | 100507650 |
rs178758 | snp | A/G | 0.247337 | 0.249986 | intron-variant | RNF212B | GRCh38.p7 | 14:23229855 | CTATATTCCCAATAA[A/G]ACATGCCCAACTGTC | 100507650 |
rs178759 | snp | A/G | 0.499673 | 0.0127754 | intron-variant | RNF212B | GRCh38.p7 | 14:23230649 | acagagcgagactcc[A/G]tctcaaaaaaaaaaa | 100507650 |
rs178761 | snp | A/G | 0.458545 | 0.137872 | intron-variant | RNF212B | GRCh38.p7 | 14:23232847 | ggggtgcctctgccc[A/G]gctgccccgtctggg | 100507650 |
rs178762 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236511 | CAGAGTGAGACTCTG[C/T]TTCAAAAAACAACAA | 100507650 |
rs178763 | snp | G/T | 0.287085 | 0.247234 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236714 | aacaaaagctctttg[G/T]agggtcttcaataat | 100507650 |
rs178764 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236961 | TTATTCTGTCTCTCt[C/T]ttttttttttttttt | 100507650 |
rs178765 | snp | A/G | 0.43655 | 0.16643 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23237529 | TTTTTAAATTTTCCT[A/G]TTTCCGATTTTACGC | 100507650 |
rs178766 | snp | C/G | 0.163236 | 0.234461 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23237716 | GGGGACAAATAAACA[C/G]TGTAACCTAATCCCA | 100507650 |
rs178767 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23237775 | GGCTGCTGGGAAAAG[G/T]CTCCTACACCCCTCT | 100507650 |
rs178768 | snp | A/G | 0.499234 | 0.0195537 | intron-variant | RNF212B | GRCh38.p7 | 14:23239033 | GAACAAACATTAAGT[A/G]ATTTTTCAAAGTCCA | 100507650 |
rs178769 | snp | C/T | 0.499265 | 0.0191552 | intron-variant | RNF212B | GRCh38.p7 | 14:23239178 | TTATCATGCCTCAGC[C/T]TCCCAAGTAGCTGGG | 100507650 |
rs178770 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | RNF212B | GRCh38.p7 | 14:23239351 | AGGTGTGAGACACCA[C/T]GCTTGGCCTGATTCT | 100507650 |
rs178771 | snp | G/T | 0.136166 | 0.22258 | intron-variant | RNF212B | GRCh38.p7 | 14:23239560 | GAAGTAGTTAAAAAA[G/T]AAATGGACGATTCAT | 100507650 |
rs178772 | snp | A/G | 0.17138 | 0.237316 | intron-variant | RNF212B | GRCh38.p7 | 14:23240631 | GAATGGTCCTAAATT[A/G]TTTAGCAAATGATTT | 100507650 |
rs178773 | snp | C/T | 0.172028 | 0.23753 | intron-variant | RNF212B | GRCh38.p7 | 14:23242036 | gcagtgagccaagat[C/T]gtgccactgcactcc | 100507650 |
rs178774 | snp | A/G | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23242098 | aaaaaaaaaaaaaaa[A/G]aaaaaaaaagaaaAG | 100507650 |
rs178775 | snp | A/G | 0.17461 | 0.238362 | intron-variant | RNF212B | GRCh38.p7 | 14:23243418 | AAAGAAAAGAAgacc[A/G]ggcgtggtggctcag | 100507650 |
rs178776 | snp | C/T | 0.499203 | 0.0199521 | intron-variant | RNF212B | GRCh38.p7 | 14:23243540 | gtctctactaaaata[C/T]aaaaaattagccagg | 100507650 |
rs178777 | snp | C/G | 0.438666 | 0.164028 | intron-variant | RNF212B | GRCh38.p7 | 14:23243911 | aggaaaccctcgtct[C/G]tactaaaaatacaaa | 100507650 |
rs178778 | snp | C/T | 0.49917 | 0.0203505 | intron-variant | RNF212B | GRCh38.p7 | 14:23245039 | ACTTTGGTTTTTTTC[C/T]TTCTACTCCCCATTT | 100507650 |
rs729531 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | RNF212B | GRCh38.p7 | 14:23187209 | TCTAAATCCATATTT[A/G]TAAGAAAACGGCCTT | 100507650 |
rs742874 | snp | C/G | 0.175897 | 0.238765 | intron-variant | RNF212B | GRCh38.p7 | 14:23249460 | TGAGGTGGGAGAATT[C/G]CTTGATCCCAAGAGG | 100507650 |
rs755575 | snp | C/T | 0.445592 | 0.155704 | intron-variant | RNF212B | GRCh38.p7 | 14:23249459 | CTGAGGTGGGAGAAT[C/T]GCTTGATCCCAAGAG | 100507650 |
rs761875 | snp | G/T | 0.488846 | 0.0738428 | intron-variant | RNF212B | GRCh38.p7 | 14:23187672 | AGATTTGGGTCCTTT[G/T]TTGGTAACCTCAGAC | 100507650 |
rs977870 | snp | G/T | 0.497502 | 0.035255 | intron-variant | RNF212B | GRCh38.p7 | 14:23255938 | TCAGGCAAAATCACT[G/T]CTTCTTTAATACTCC | 100507650 |
rs977871 | snp | C/T | 0.495174 | 0.0488838 | intron-variant | RNF212B | GRCh38.p7 | 14:23256030 | GTAGACAAAGTAGGT[C/T]TGCTTAGGCCTGGCA | 100507650 |
rs1055375 | snp | A/G | 0.0329836 | 0.124112 | utr-variant-3-prime, downstream-variant-500B | RNF212B | GRCh38.p7 | 14:23273087 | GTCTTACAAAAGGCT[A/G]GTGCTTCAGGAAGAT | 100507650 |
rs1569952 | snp | C/T | 0.478768 | 0.100824 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23184262 | GCTCACGTGATCCTC[C/T]CCTGTCAGCCTCCCA | 100507650 |
rs1569953 | snp | A/G | 0 | 0 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23184149 | AAGAACCTTTTTCCC[A/G]TTGTTAATTCCTTCC | 100507650 |
rs1884543 | snp | A/C | 0.031825 | 0.122064 | intron-variant | RNF212B | GRCh38.p7 | 14:23188456 | AAAAAAAAAAACCCT[A/C]ATCTTTGTCAAACAT | 100507650 |
rs1884544 | snp | A/G | 0.118933 | 0.212888 | intron-variant | RNF212B | GRCh38.p7 | 14:23188392 | ATTTAAGTATTCAAA[A/G]CTGGAGTCACTTAAA | 100507650 |
rs1955560 | snp | A/G | 0.25912 | 0.249834 | intron-variant | RNF212B | GRCh38.p7 | 14:23252548 | ggggtttaatcataa[A/G]acagctgaacaagga | 100507650 |
rs1955561 | snp | A/G | 0.136847 | 0.222927 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23259581 | CAAGATGGAGTCCTT[A/G]ATAAAAATTTTTAGA | 100507650 |
rs1963151 | snp | A/G | 0.46974 | 0.119223 | intron-variant | RNF212B | GRCh38.p7 | 14:23263529 | TCTCGGCTTAAGGGA[A/G]TTAAGTTTATGCTGA | 100507650 |
rs2064482 | snp | C/T | 0.353803 | 0.227431 | intron-variant | RNF212B | GRCh38.p7 | 14:23240106 | ATGTATATATATATA[C/T]ACACACACACATTTA | 100507650 |
rs2064483 | snp | A/G | 0.475525 | 0.107882 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260541 | TTCCTCCTACTGGGA[A/G]TCTTAGCAACCATGA | 100507650 |
rs2064750 | snp | A/C | 0.177503 | 0.239258 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213702 | TTTGGCATGCAGTCA[A/C]CCTGTTTAGGTAGAG | 100507650 |
rs2064751 | snp | A/C | 0.177503 | 0.239258 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213701 | TTGGCATGCAGTCAC[A/C]CTGTTTAGGTAGAGC | 100507650 |
rs2064752 | snp | C/G | 0.177503 | 0.239258 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213693 | CAGTCACCCTGTTTA[C/G]GTAGAGCACACAGTT | 100507650 |
rs2064753 | snp | A/G | 0.178465 | 0.239547 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213490 | ATACTTCTTCTTTCC[A/G]CCTCATGACTCCTGG | 100507650 |
rs2064754 | snp | A/C | 0.178144 | 0.239451 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213426 | GATCAAATTGGGAAA[A/C]ATTGACTTCTTAACA | 100507650 |
rs2092706 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | RNF212B | GRCh38.p7 | 14:23243907 | CATGAGGAAACCCTC[A/G]TCTCTACTAAAAATA | 100507650 |
rs2092708 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23222040 | catcaaaaaggaaga[A/C]gaacttcaaacaaat | 100507650 |
rs2092709 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23222103 | caagagcaaaccaaa[A/C]ccaaaattaggagaa | 100507650 |
rs2092710 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23222132 | aaaaaaagcaaaaat[A/C]tggatcagagcagaa | 100507650 |
rs2092711 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23222136 | aaagcaaaaatatgg[A/C]tcagagcagaaataa | 100507650 |
rs2144037 | snp | A/G | 0.198634 | 0.244666 | intron-variant | RNF212B | GRCh38.p7 | 14:23218331 | caagattgcacctct[A/G]cactatagcctgggt | 100507650 |
rs2144038 | snp | C/T | 0.313741 | 0.241738 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23259979 | CTTATTATTATTTTC[C/T]CTCTTACTTTTCTCA | 100507650 |
rs2144039 | snp | A/G | 0.475525 | 0.107882 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260193 | TGACCTACCAGTTGG[A/G]AAGCTCTCTTATAGA | 100507650 |
rs2144828 | snp | A/T | 0.463851 | 0.12949 | intron-variant | RNF212B | GRCh38.p7 | 14:23218375 | TCTTTTTATTTATTT[A/T]TTTTTTTGAGATAGA | 100507650 |
rs2144829 | snp | C/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23217442 | ggccaaggcccttct[C/T]ttcagggcagcgagt | 100507650 |
rs2179931 | snp | A/G | 0.349671 | 0.229272 | intron-variant | RNF212B | GRCh38.p7 | 14:23265184 | AAAATAAAGATTTGA[A/G]TGATAGAAAGTCATT | 100507650 |
rs2331938 | snp | C/T | 0.029116 | 0.117091 | intron-variant | RNF212B | GRCh38.p7 | 14:23186913 | TGGTCAAAGCCTCAA[C/T]TTCTTTCACCTGAGG | 100507650 |
rs2331939 | snp | A/G | 0.0744748 | 0.178019 | utr-variant-5-prime, nc-transcript-variant | RNF212B | GRCh38.p7 | 14:23193372 | agggaataagtaaag[A/G]aggaagaagaccctg | 100507650 |
rs2331940 | snp | A/G | 0.408017 | 0.193729 | intron-variant | RNF212B | GRCh38.p7 | 14:23194476 | ggcgcagtgacacac[A/G]cctataatcccagca | 100507650 |
rs2331941 | snp | A/T | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205300 | tttttctcttttttt[A/T]aaaaaaaggacaccc | 100507650 |
rs2331942 | snp | C/G | 0.49975 | 0.0111793 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205479 | tattttattttaatt[C/G]tttacctagattatt | 100507650 |
rs2331943 | snp | C/G | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213689 | TAGGAACTGTGTGCT[C/G]TACCTAAACAGGGTG | 100507650 |
rs2331944 | snp | C/T | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213690 | AGGAACTGTGTGCTC[C/T]ACCTAAACAGGGTGA | 100507650 |
rs2331945 | snp | A/G | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213695 | CTGTGTGCTCTACCT[A/G]AACAGGGTGACTGCA | 100507650 |
rs2331946 | snp | A/T | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213697 | GTGTGCTCTACCTAA[A/T]CAGGGTGACTGCATG | 100507650 |
rs2331947 | snp | G/T | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213700 | TGCTCTACCTAAACA[G/T]GGTGACTGCATGCCA | 100507650 |
rs2331948 | snp | C/T | 0.26818 | 0.249338 | intron-variant | RNF212B | GRCh38.p7 | 14:23218174 | gagatcgagaccctc[C/T]tggctaacacggtga | 100507650 |
rs2474013 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF212B | GRCh38.p7 | 14:23227850 | gtgattcacccacct[C/T]agccccccgaagtgc | 100507650 |
rs2474514 | snp | A/G | 0.249038 | 0.249998 | intron-variant | RNF212B | GRCh38.p7 | 14:23227847 | CTTCGGGGGGCTGAG[A/G]TGGGTGAATCACCTG | 100507650 |
rs2877514 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23271263 | gaccaatatggtaaa[A/C]ccccgtctctctcta | 100507650 |
rs2877535 | snp | A/G | 0.482979 | 0.0906686 | intron-variant | RNF212B | GRCh38.p7 | 14:23194524 | gggcagatcatctga[A/G]ctcaggagtttgaga | 100507650 |
rs2877536 | snp | A/G | 0.496842 | 0.0396107 | intron-variant | RNF212B | GRCh38.p7 | 14:23217262 | GGCAGTGGTGGGGGG[A/G]GGGCTCCTCTGCCTG | 100507650 |
rs3045528 | in-del | -/AAAAAAAAA | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23193110 | AAAAAAAAAAAAAAA[-/AAAAAAAAA]GAATGTTACCAGAAT | 100507650 |
rs3045551 | in-del | -/CCT | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213692 | GAACTGTGTGCTCTA[-/CCT]AAACAGGGTGACTGC | 100507650 |
rs3811180 | snp | A/G | 0.421368 | 0.182025 | intron-variant | RNF212B | GRCh38.p7 | 14:23264516 | ATATATTGTTCTACT[A/G]CAGTGGGCATACTAG | 100507650 |
rs4375573 | snp | C/T | 0.352287 | 0.228117 | intron-variant | RNF212B | GRCh38.p7 | 14:23271029 | AGGAAAAACCACATT[C/T]ACTTCTCCAGAGACC | 100507650 |
rs4619311 | snp | C/T | 0.158632 | 0.232706 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209263 | GTGGGTTTTGGCCGG[C/T]TCCTTTACCGCAACC | 100507650 |
rs4981460 | snp | A/C | 0.3744 | 0.216852 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23212467 | AATAATGGGGTTTGA[A/C]AAGTTTGTAGAATAC | 100507650 |
rs4981462 | snp | C/T | 0.236144 | 0.249616 | intron-variant | RNF212B | GRCh38.p7 | 14:23216669 | CAGATTGCTTGAGCT[C/T]AGGAGTTCAAGACAA | 100507650 |
rs4982739 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | RNF212B | GRCh38.p7 | 14:23189848 | cttcccttgatgctc[C/T]attcctttcagctac | 100507650 |
rs4982740 | snp | C/T | 0.483272 | 0.0899109 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195437 | ACCATATCTCTTGTC[C/T]ACCTCTAAGGCTTCG | 100507650 |
rs4982745 | snp | C/T | 0.0685596 | 0.171987 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23237422 | ggcgtgagccaccgc[C/T]cctggccAAAAATTT | 100507650 |
rs4982747 | snp | C/G | 0.381697 | 0.212499 | intron-variant | RNF212B | GRCh38.p7 | 14:23272380 | agcggagatgcacca[C/G]tgcactccagcctgg | 100507650 |
rs5807213 | in-del | -/A | | | intron-variant | RNF212B | GRCh38.p7 | 14:23240047 | CTCAAAAAAAAAAAA[-/A]TCTCACCACTGTCTG | 100507650 |
rs5807215 | snp | A/T | 0.42357 | 0.179927 | intron-variant | RNF212B | GRCh38.p7 | 14:23264828 | ACAAGGTTTTTTTTT[A/T]TTTTTTTGGTGAGAT | 100507650 |
rs6573018 | snp | A/G | 0.0310518 | 0.120672 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23184075 | GGAGAGAACGTTGAA[A/G]GGACATCATCTTCGA | 100507650 |
rs6573034 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200384 | AGGCTAGAGTGCAAT[C/G]GCATGATCTTGGCCC | 100507650 |
rs6573044 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23206222 | TGGGATTATAGGTGC[A/G]CACCACCATGGCCAG | 100507650 |
rs6573045 | snp | A/G | 0.175254 | 0.238565 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213140 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAAAT | 100507650 |
rs6573046 | snp | C/T | 0.227664 | 0.249 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213169 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCAGG | 100507650 |
rs6573047 | snp | A/G | 0.16846 | 0.236329 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213176 | AAATTAGCCGGGCGT[A/G]GTGGCAGGCGCCTGT | 100507650 |
rs6573048 | snp | A/G | 0.174288 | 0.23826 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213182 | GCCGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 100507650 |
rs6573049 | snp | A/G | 0.178144 | 0.239451 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213300 | CCTGGGCGACAGAGT[A/G]AGACTCCGTCTTAAA | 100507650 |
rs6573050 | snp | A/C | 0.428333 | 0.175206 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214709 | AGAGAGAAAACGGGC[A/C]TAACTAATGTCAGGA | 100507650 |
rs6573079 | snp | A/G | 0.497502 | 0.035255 | intron-variant | RNF212B | GRCh38.p7 | 14:23258905 | AAAACTGCTTCCCAg[A/G]ccaggtgcagtggct | 100507650 |
rs6573081 | snp | A/C | 0.24932 | 0.249999 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260096 | CACTATAGTAAATGG[A/C]TGAGGTCTCAGCAGA | 100507650 |
rs6573082 | snp | A/C | 0.281841 | 0.247964 | intron-variant | RNF212B | GRCh38.p7 | 14:23263754 | TGTGCCCCTTCCCCC[A/C]AAAAAAACGAGTGTT | 100507650 |
rs6573084 | snp | A/G | 0.4983 | 0.0291038 | intron-variant | RNF212B | GRCh38.p7 | 14:23265459 | TTACCATTTTCAAGG[A/G]CATTAGCCAGTACCT | 100507650 |
rs7141429 | snp | C/T | 0.340333 | 0.233109 | intron-variant | RNF212B | GRCh38.p7 | 14:23271778 | CTACAAATATATGGC[C/T]CCTAATTGGATCTTG | 100507650 |
rs7141505 | snp | A/C | 0.478685 | 0.10101 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23183979 | AGGGAACAGTTGTGC[A/C]GATACTTTTAATGCC | 100507650 |
rs7141796 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208969 | TTCATCGTGTTAGCC[A/G]GGATGGTCTCGATCT | 100507650 |
rs7142071 | snp | A/T | 0.093777 | 0.195178 | intron-variant | RNF212B | GRCh38.p7 | 14:23257169 | cacacacaaaaaaaa[A/T]aaaataaaataaatc | 100507650 |
rs7142944 | snp | C/T | 0.422787 | 0.180679 | intron-variant | RNF212B | GRCh38.p7 | 14:23266107 | gggactacaggcacg[C/T]gccaccatgcttggc | 100507650 |
rs7149073 | snp | A/C | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23267728 | agccactgtgcctgg[A/C]ccaacaattttgtct | 100507650 |
rs7149081 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213483 | AATTCCACCAGGAGT[C/T]ATGAGGCGGAAAGAA | 100507650 |
rs7149680 | snp | C/T | 0.0693013 | 0.172766 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260808 | TAGCTTTCACTTCTC[C/T]GAGGAAGAGTTAGTT | 100507650 |
rs7149868 | snp | A/C | 0.475613 | 0.107697 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260887 | GTCATCTTATGAAAT[A/C]CTAGtgtttgaaatg | 100507650 |
rs7150075 | snp | A/G | 0.250732 | 0.249999 | intron-variant | RNF212B | GRCh38.p7 | 14:23252231 | GGTATGGTTGAAAGG[A/G]GCTTGTTATGAATAA | 100507650 |
rs7150196 | snp | A/G | 0.248471 | 0.249995 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23259557 | gtgtatgtgctgcca[A/G]agcaatcacAAGATG | 100507650 |
rs7150224 | snp | A/G | 0.243061 | 0.249904 | intron-variant | RNF212B | GRCh38.p7 | 14:23252264 | AAAGATGCTCCTATC[A/G]CTCAGGAAATGCCAA | 100507650 |
rs7150714 | snp | C/T | 0.360632 | 0.224189 | intron-variant | RNF212B | GRCh38.p7 | 14:23254838 | CAGTTATTTCTCCTT[C/T]ACTCTTTCCAACCTT | 100507650 |
rs7150951 | snp | A/G | 0.475613 | 0.107697 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23261100 | ccattggctggaacc[A/G]gacctcacattctgt | 100507650 |
rs7151703 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | RNF212B | GRCh38.p7 | 14:23190910 | tccttgaacactaag[A/C]tctgcctcagggcct | 100507650 |
rs7151923 | snp | C/T | 0.174288 | 0.23826 | intron-variant | RNF212B | GRCh38.p7 | 14:23233802 | aaataaacaacccaa[C/T]taaaaatgggtaggt | 100507650 |
rs7152378 | snp | C/G | 0.0905309 | 0.192535 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23198544 | AGCTGGGCGTGGTGG[C/G]GGGTACCTGTAATCC | 100507650 |
rs7154448 | snp | A/T | 0.0991586 | 0.199366 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213482 | AAATTCCACCAGGAG[A/T]CATGAGGCGGAAAGA | 100507650 |
rs7155747 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23198692 | AAAAAAAAGGTCCAC[A/G]TACTGTATGTAAACA | 100507650 |
rs7155912 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | RNF212B | GRCh38.p7 | 14:23253017 | tttcatgcatccatc[A/C]ctccacttcaacaat | 100507650 |
rs7156407 | snp | C/T | 0.21875 | 0.248039 | intron-variant | RNF212B | GRCh38.p7 | 14:23262071 | TATGGATTAAAGAGA[C/T]ACTGCCCCTACATTC | 100507650 |
rs7156827 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RNF212B | GRCh38.p7 | 14:23232257 | cctctgccccgccgc[C/T]ccatctgggatgtga | 100507650 |
rs7157342 | snp | A/G | 0.475702 | 0.107512 | intron-variant | RNF212B | GRCh38.p7 | 14:23257326 | catgcctggctTAAA[A/G]TAAACATTTTCTTTT | 100507650 |
rs7158499 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211089 | TGGTCGTGATGGCGT[A/G]CGCCTGTAATCCCAG | 100507650 |
rs7158521 | snp | A/G | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23191927 | AAATTTTATTCAGTT[A/G]CTGTAAATTATTGGA | 100507650 |
rs7158649 | snp | A/C | 0.0360663 | 0.129354 | intron-variant, downstream-variant-500B | RNF212B, LOC105370406 | GRCh38.p7 | 14:23199262 | ATATGTAAGAAGTAC[A/C]TTGGTTCAGTCTGGA | 100507650 |
rs7160550 | snp | A/T | 0.248755 | 0.249997 | intron-variant | RNF212B | GRCh38.p7 | 14:23252988 | tcttgttaaacccta[A/T]gaggacggtttattt | 100507650 |
rs7161362 | snp | A/T | 0.039522 | 0.134904 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195883 | aacgggttcaaaatt[A/T]tgtgacttgccaagg | 100507650 |
rs7342547 | snp | C/G/T | 0.0326558 | 0.123885 | intron-variant | RNF212B | GRCh38.p7 | 14:23231786 | ctgcgattgcaggca[C/G/T]gcgccgccacgcctg | 100507650 |
rs7493317 | snp | A/T | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213011 | atgtaaaagacctgt[A/T]cactaaaaattataa | 100507650 |
rs7493814 | snp | A/C | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23265132 | ggccTACAAGTTTTT[A/C]AAATAATGATATTTT | 100507650 |
rs8003873 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | RNF212B | GRCh38.p7 | 14:23272355 | aacccgggaggcgga[A/G]cttgcagtaagcgga | 100507650 |
rs8004063 | snp | C/T | 0.471004 | 0.116864 | intron-variant | RNF212B | GRCh38.p7 | 14:23263270 | CTTCATCTCATGCTC[C/T]GAACAGGGAAAGTTG | 100507650 |
rs8004773 | snp | C/G | 0.321053 | 0.23969 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209154 | ataagataacttcct[C/G]acgttgccatggcat | 100507650 |
rs8005697 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209624 | taaataatatatgta[C/G]atactttttcttgca | 100507650 |
rs8006954 | snp | C/G | 0.0737376 | 0.17729 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209585 | ggaaacaaatcttta[C/G]agaatactttgactt | 100507650 |
rs8007396 | snp | C/T | 0.352721 | 0.227922 | intron-variant | RNF212B | GRCh38.p7 | 14:23267588 | catgtgccaccacgc[C/T]tagctaatttttgta | 100507650 |
rs8007591 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209625 | aaataatatatgtag[A/G]tactttttcttgcag | 100507650 |
rs8009209 | snp | C/T | 0.469937 | 0.118861 | intron-variant | RNF212B | GRCh38.p7 | 14:23263296 | AGTTGAGAGTGAGGG[C/T]TGACATTTCACATTT | 100507650 |
rs8009590 | snp | A/C | 0.327914 | 0.237549 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23197530 | gactccatctcaaaa[A/C]TAATTTTCACTAATT | 100507650 |
rs8009627 | snp | A/G | 0.182614 | 0.240747 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213044 | caggccgggcatggt[A/G]ggttatgcctgtaat | 100507650 |
rs8010663 | snp | C/T | 0.493523 | 0.0565391 | utr-variant-3-prime, downstream-variant-500B | RNF212B | GRCh38.p7 | 14:23273126 | CTCTTCCAGAAGACA[C/T]TGGTAGCTCCCCTCA | 100507650 |
rs8010666 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210102 | gttgcagggagccaa[A/G]attgcaccactgcac | 100507650 |
rs8011838 | snp | A/T | 0.0737376 | 0.17729 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209533 | gcctccatactgata[A/T]aaacaaatgattgac | 100507650 |
rs8011991 | snp | G/T | 0.0737376 | 0.17729 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209590 | caaatctttacagaa[G/T]actttgacttccaaa | 100507650 |
rs8012162 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209876 | atctatgactggccc[A/G]gtgaggtgactcaaa | 100507650 |
rs8013737 | snp | C/G | 0.260504 | 0.249779 | intron-variant | RNF212B | GRCh38.p7 | 14:23189543 | ctgggtggctcacgt[C/G]tataatcccatcact | 100507650 |
rs8014241 | snp | C/T | 0.157972 | 0.232445 | intron-variant | RNF212B | GRCh38.p7 | 14:23225886 | acgaggggatcgata[C/T]cctatctttcatgat | 100507650 |
rs8014783 | snp | G/T | 0.478685 | 0.10101 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23184840 | ATTTATAATTGTAAA[G/T]TATTTCGAAAAAACA | 100507650 |
rs8015398 | snp | A/C | 0.172674 | 0.237741 | intron-variant | RNF212B | GRCh38.p7 | 14:23226579 | gagcttgcagtgagc[A/C]gagatcgcgccacca | 100507650 |
rs8015556 | snp | C/T | 0.449984 | 0.150021 | intron-variant | RNF212B | GRCh38.p7 | 14:23258710 | TTTTTTTTTTTTTTT[C/T]TTCTAAGAAGTGACA | 100507650 |
rs8015767 | snp | C/T | 0.486133 | 0.082104 | intron-variant | RNF212B | GRCh38.p7 | 14:23250439 | AGTGAGCCTAGAATG[C/T]GCCACTGCACTCCAG | 100507650 |
rs8015922 | snp | A/C | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | RNF212B, HOMEZ | GRCh38.p7 | 14:23273913 | ACTACTTCCTTTTTA[A/C]AGTTTTTGTTCTTTT | 100507650 |
rs8016285 | snp | A/C | | | intron-variant, downstream-variant-500B | RNF212B, LOC105370406 | GRCh38.p7 | 14:23194758 | aaaaaaaaaaaaaaa[A/C]aacgctgctgtatca | 100507650 |
rs8017553 | snp | C/T | 0.422473 | 0.180978 | intron-variant | RNF212B | GRCh38.p7 | 14:23268313 | GACTGTTGGGTTTCA[C/T]CATGAGCATGCCCTG | 100507650 |
rs8017619 | snp | C/T | 0.078151 | 0.181571 | intron-variant | RNF212B | GRCh38.p7 | 14:23223150 | atgcaaatcaatata[C/T]gtcgtacatcatatc | 100507650 |
rs8018227 | snp | C/T | 0.475613 | 0.107697 | intron-variant | RNF212B | GRCh38.p7 | 14:23262016 | CTCTCTCTATATATA[C/T]ACACACACACATATA | 100507650 |
rs8020924 | snp | A/T | | | utr-variant-3-prime | RNF212B, HOMEZ | GRCh38.p7 | 14:23274041 | GGAGTGGCAAAGTGG[A/T]TGAGAGAGAAACAAT | 100507650 |
rs8021381 | snp | A/G | 0 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23196161 | TTACTCTGCAAATCA[A/G]AGCCTAGACACTTAG | 100507650 |
rs8021709 | snp | A/G | 0.129664 | 0.219133 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236085 | cgtactgcaaaagtt[A/G]atgcagaagcaaata | 100507650 |
rs9652343 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RNF212B | GRCh38.p7 | 14:23245905 | TAATAAGTAGTGGAC[A/G]CTCAAGACGTTGTCA | 100507650 |
rs9671711 | snp | A/G | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23239976 | CAGAAAACCTGGGGG[A/G]AAAAAAAGTAAAGGA | 100507650 |
rs9743682 | snp | A/T | 0.135143 | 0.222054 | intron-variant | RNF212B | GRCh38.p7 | 14:23232424 | gccgccctgtctgag[A/T]agtgaggagcgcctc | 100507650 |
rs9919908 | snp | G/T | 0.499918 | 0.00638925 | intron-variant | RNF212B | GRCh38.p7 | 14:23248121 | gcctctttttattta[G/T]ttttttgagacaggg | 100507650 |
rs9919912 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF212B | GRCh38.p7 | 14:23248423 | aggcatgagccacca[C/T]gcccaaccccaagcc | 100507650 |
rs10047910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212B | GRCh38.p7 | 14:23220480 | gaggttgctgtgagc[C/T]gagatcacaccactg | 100507650 |
rs10130376 | snp | A/T | 0.374 | 0.217081 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211788 | agtgcagtggtgcaa[A/T]cttggctcactgaaa | 100507650 |
rs10130456 | snp | A/G | 0.374 | 0.217081 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211880 | ggcacatgccaccat[A/G]cctggctaatttttt | 100507650 |
rs10134378 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23202800 | aggttgcagtgagcc[A/G]agattggtcactgca | 100507650 |
rs10137582 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | RNF212B | GRCh38.p7 | 14:23223312 | aaaagccacatatga[C/G]agacccacagctaat | 100507650 |
rs10139243 | snp | C/T | 0.365024 | 0.221967 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200984 | agagaaacaaatatg[C/T]tccaaattttgttca | 100507650 |
rs10139654 | snp | G/T | 0.115438 | 0.210697 | intron-variant | RNF212B | GRCh38.p7 | 14:23223767 | agagaaagaaataaa[G/T]ggcatccaaattgga | 100507650 |
rs10141064 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | RNF212B | GRCh38.p7 | 14:23242160 | AGAAAGAACAGTCAA[C/G]TTAAGTAGCCTCAGG | 100507650 |
rs10141797 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF212B | GRCh38.p7 | 14:23272227 | tcgagaccatcctgg[C/T]taacatggtgaaacc | 100507650 |
rs10141978 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF212B | GRCh38.p7 | 14:23272367 | ggagcttgcagtaag[C/T]ggagatgcaccactg | 100507650 |
rs10144176 | snp | A/T | 0.485049 | 0.0851591 | intron-variant | RNF212B | GRCh38.p7 | 14:23216580 | AGTAAAAAAAAAAAA[A/T]AATAATAAGGCCAAT | 100507650 |
rs10144491 | snp | A/G | 0.482159 | 0.0927485 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213174 | aaaaattagccgggc[A/G]tggtggcaggcgcct | 100507650 |
rs10145356 | snp | A/G | 0.48435 | 0.0870631 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203346 | ttgggttggttccac[A/G]attttgcaattgtga | 100507650 |
rs10145616 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF212B | GRCh38.p7 | 14:23259065 | gacatggtggttcac[A/G]cctgtagtcccagct | 100507650 |
rs10151351 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF212B | GRCh38.p7 | 14:23222749 | aaccaaattcaacaa[C/T]acattaaaaagattg | 100507650 |
rs10151903 | snp | C/G | 0.132066 | 0.220435 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205395 | aaaatacctattatt[C/G]aatttaactttattt | 100507650 |
rs10400701 | snp | A/T | 0.499977 | 0.00339449 | intron-variant | RNF212B | GRCh38.p7 | 14:23254344 | AACAAAAACAAAAAC[A/T]AAAACTAAAACTGGG | 100507650 |
rs10459510 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23196833 | attcatccttctgat[C/T]tagcacaattgttac | 100507650 |
rs10547691 | in-del | -/TTT | 0.000940291 | 0.0216624 | intron-variant | RNF212B | GRCh38.p7 | 14:23258694 | AAGTCCCAAGAGAGC[-/TTT]TTTTTTTTTTTTTTT | 100507650 |
rs10555690 | in-del | -/CAATT | 0.497641 | 0.0342639 | intron-variant | RNF212B | GRCh38.p7 | 14:23251249 | CAACTAGGTATGCAA[-/CAATT]CAATTCAATTCAATT | 100507650 |
rs10651792 | in-del | -/CTT | 0.24932 | 0.249999 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260268 | AGATACCTCAGGACC[-/CTT]CTTCCTCTGCATCAC | 100507650 |
rs10676306 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260269 | ACCTCAGGACCCTTC[-/TTC]CTCTGCATCACACTC | 100507650 |
rs10707951 | in-del | -/A | 0.289942 | 0.246789 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213313 | GTAAGACTCCGTCTT[-/A]AAAAAAAAAAAAATT | 100507650 |
rs10782427 | snp | C/T | 0.124444 | 0.216185 | intron-variant | RNF212B | GRCh38.p7 | 14:23192071 | ggagaaataggaaca[C/T]ttttacactgttggt | 100507650 |
rs10782428 | snp | A/G | 0.124444 | 0.216185 | intron-variant | RNF212B | GRCh38.p7 | 14:23192087 | ttttacactgttggt[A/G]ggactgtaaactagt | 100507650 |
rs10873088 | snp | A/C | 0.227745 | 0.249007 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23185265 | AACAACAAACAACAA[A/C]AAAAAAAACCAGACA | 100507650 |
rs11158038 | snp | A/G | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23192148 | cctcaaggatctaga[A/G]ctagaaataccattt | 100507650 |
rs11158076 | snp | A/G | 0.259674 | 0.249813 | intron-variant | RNF212B | GRCh38.p7 | 14:23261704 | TGGTGGCTCACACCC[A/G]TAATCACAGCACTTT | 100507650 |
rs11299802 | in-del | -/T | 0.477768 | 0.103061 | intron-variant | RNF212B | GRCh38.p7 | 14:23271502 | GCCTTTTTTTGTTTG[-/T]TTTTTTTAATGGCTT | 100507650 |
rs11325258 | snp | A/T | 0.351968 | 0.22826 | intron-variant | RNF212B | GRCh38.p7 | 14:23257386 | TTAAAAATGAGGGTT[A/T]AAAAAAATAGACTAG | 100507650 |
rs11352293 | in-del | -/A | 0.158302 | 0.232576 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23198672 | AAGAAAACTCTGTCC[-/A]AAAAAAAAAAAAGGT | 100507650 |
rs11378662 | in-del | -/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23242216 | CATGACCTTTTAAAG[-/T]TTCGCTAATGTAAAA | 100507650 |
rs11448890 | in-del | -/T | 0.375 | 0.216506 | intron-variant | RNF212B | GRCh38.p7 | 14:23256377 | AATTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 100507650 |
rs11621567 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23267268 | ttataggcatgagca[A/C]ccatgcccagtccct | 100507650 |
rs11622160 | snp | G/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23272285 | attagccgggcatgg[G/T]ggcgggcgcctgtag | 100507650 |
rs11622414 | snp | C/T | 0.21845 | 0.248001 | intron-variant | RNF212B | GRCh38.p7 | 14:23259002 | GCCTGGGCAACACAG[C/T]GAGACTCTGTTTCTA | 100507650 |
rs11622474 | snp | C/T | 0.21845 | 0.248001 | intron-variant | RNF212B | GRCh38.p7 | 14:23259163 | ACCACGACACTCCAG[C/T]GTGGGTGAAAAAGTG | 100507650 |
rs11622605 | snp | C/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23267415 | tttatcattatttaa[C/T]gcctttgtctcttgt | 100507650 |
rs11623639 | snp | A/G | 0.203882 | 0.245709 | intron-variant | RNF212B | GRCh38.p7 | 14:23230603 | agcttgcagtgagcc[A/G]agatcgcgccactgc | 100507650 |
rs11623889 | snp | C/T | 0.239902 | 0.249796 | intron-variant | RNF212B | GRCh38.p7 | 14:23230470 | ccatcctggctaaca[C/T]ggtgaaaccccgtct | 100507650 |
rs11624060 | snp | A/G | 0.257176 | 0.249897 | intron-variant | RNF212B | GRCh38.p7 | 14:23248528 | ctcactgcaatctcc[A/G]cctcccgggttcaag | 100507650 |
rs11624694 | snp | A/G | 0.221141 | 0.248329 | intron-variant | RNF212B | GRCh38.p7 | 14:23227458 | agggtggctgattac[A/G]tgggtgtgttgagtt | 100507650 |
rs11625329 | snp | C/T | 0.262985 | 0.249663 | intron-variant | RNF212B | GRCh38.p7 | 14:23248831 | ctccatctcttaata[C/T]tattgcattgggagt | 100507650 |
rs11625337 | snp | A/G | 0.499943 | 0.00533303 | intron-variant | RNF212B | GRCh38.p7 | 14:23262882 | CCAGGCAAGGCAGGC[A/G]TACCATTGATGGCAA | 100507650 |
rs11625545 | snp | G/T | 0.221439 | 0.248363 | intron-variant | RNF212B | GRCh38.p7 | 14:23227212 | tatagctattttatt[G/T]tattattataatttt | 100507650 |
rs11626224 | snp | A/T | 0.288127 | 0.247076 | intron-variant | RNF212B | GRCh38.p7 | 14:23240048 | TCAAAAAAAAAAAAA[A/T]CTCACCACTGTCTGT | 100507650 |
rs11626235 | snp | C/T | 0.499944 | 0.00527116 | intron-variant | RNF212B | GRCh38.p7 | 14:23262883 | CAGGCAAGGCAGGCA[C/T]ACCATTGATGGCAAC | 100507650 |
rs11628689 | snp | A/T | 0.42357 | 0.179927 | intron-variant | RNF212B | GRCh38.p7 | 14:23264823 | ATATTACAAGGTTTT[A/T]TTTTTTTTTTTTGGT | 100507650 |
rs11628821 | snp | A/G | 0.263535 | 0.249633 | intron-variant | RNF212B | GRCh38.p7 | 14:23248503 | ctggagtgcagtggc[A/G]cgatctcggctcact | 100507650 |
rs11629105 | snp | G/T | 0.239326 | 0.249772 | intron-variant | RNF212B | GRCh38.p7 | 14:23252671 | tgattggttaaggaa[G/T]gcaggttgaagtcat | 100507650 |
rs11845597 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209049 | aggcgtgagccaccg[C/T]gcccggcctggttgc | 100507650 |
rs11848278 | snp | C/T | 0.248471 | 0.249995 | intron-variant | RNF212B | GRCh38.p7 | 14:23254585 | TTTTGGTAGAGATAG[C/T]ATTTTGCCACGTTGC | 100507650 |
rs12147242 | snp | G/T | 0.251296 | 0.249997 | intron-variant | RNF212B | GRCh38.p7 | 14:23255554 | ATCAATAGAACTACT[G/T]TTATTATTATCAGCT | 100507650 |
rs12323394 | snp | C/T | 0.49753 | 0.0350569 | intron-variant | RNF212B | GRCh38.p7 | 14:23253937 | GTTCAAAAATTAAAT[C/T]GCGTGCAAAAATAAA | 100507650 |
rs12323468 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | RNF212B | GRCh38.p7 | 14:23189574 | ttgggaggccaaggc[A/G]ggaggatcgcttgag | 100507650 |
rs12323469 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | RNF212B | GRCh38.p7 | 14:23189583 | caaggcgggaggatc[A/G]cttgagtccaggaat | 100507650 |
rs12323882 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23189647 | gtttctactaaaaat[C/T]aaaaaaaaaaaatta | 100507650 |
rs12432395 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | RNF212B | GRCh38.p7 | 14:23249206 | CAGGTCAAGATTTGA[A/T]CTCATCAATAGACCA | 100507650 |
rs12586324 | snp | C/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23233522 | gttgagcccaggagt[C/T]tgagaccagcctggg | 100507650 |
rs12717441 | snp | C/G | 0.239326 | 0.249772 | intron-variant | RNF212B | GRCh38.p7 | 14:23252751 | gtgggggtctttaga[C/G]tcactgttccactgg | 100507650 |
rs12879214 | snp | C/G | 0.267364 | 0.249396 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208830 | atggcgcgatctcag[C/G]tcactgcaagctctg | 100507650 |
rs12879346 | snp | A/T | 0.4862 | 0.0819127 | utr-variant-5-prime, upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23183499 | TGGTTTCCACCTGCT[A/T]TGGGTTTCTTTTCCC | 100507650 |
rs12879411 | snp | A/G | 0.494896 | 0.0502606 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208960 | agacggggtttcatc[A/G]tgttagccgggatgg | 100507650 |
rs12879493 | snp | A/T | 0 | 0 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23183764 | CCTCCCTCCTCTGCA[A/T]TTTAAGTATTAGCAC | 100507650 |
rs12879494 | snp | A/T | 0 | 0 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23183768 | CCTCCTCTGCAATTT[A/T]AGTATTAGCACAAAG | 100507650 |
rs12879505 | snp | A/C | | | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23183789 | TAGCACAAAGCCCCC[A/C]AACAGCACTGAGAAA | 100507650 |
rs12879509 | snp | A/C | | | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23183800 | CCCCAAACAGCACTG[A/C]GAAAATGGACTAAGT | 100507650 |
rs12880128 | snp | A/G | 0.473726 | 0.111565 | intron-variant | RNF212B | GRCh38.p7 | 14:23241910 | acacggtgaaacccc[A/G]tctctactaaaacta | 100507650 |
rs12880452 | snp | C/T | 0.475789 | 0.107327 | intron-variant | RNF212B | GRCh38.p7 | 14:23258128 | TAGATCACCTGAGGT[C/T]GGAAGTTCAAGACTA | 100507650 |
rs12880488 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23242107 | AAAAAAAAAAAAAAA[A/G]GAAAAGAAAAAGAAA | 100507650 |
rs12880612 | snp | C/T | 0.493748 | 0.0555599 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208948 | tatttttagtagaga[C/T]ggggtttcatcgtgt | 100507650 |
rs12881129 | snp | G/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23266436 | ttttttttgagatgg[G/T]gtttctttcttgttg | 100507650 |
rs12881746 | snp | C/T | 0.365024 | 0.221967 | intron-variant | RNF212B | GRCh38.p7 | 14:23251586 | tttgggaggctgagg[C/T]gggcagatcacctga | 100507650 |
rs12882182 | snp | A/G | 0.477684 | 0.103247 | intron-variant | RNF212B | GRCh38.p7 | 14:23251531 | taaaagatacaacat[A/G]ggggccaggtgcagt | 100507650 |
rs12885446 | snp | C/T | 0.496034 | 0.0443518 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208958 | agagacggggtttca[C/T]cgtgttagccgggat | 100507650 |
rs12885940 | snp | C/G | 0.365024 | 0.221967 | intron-variant | RNF212B | GRCh38.p7 | 14:23251847 | aagaaaaccatatat[C/G]atggaaatagccaaa | 100507650 |
rs12887796 | snp | A/C/G | 0.233527 | 0.249457 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203561 | ttggctcactgcaat[A/C/G]tccaccttccgggtt | 100507650 |
rs12888111 | snp | G/T | 0.282895 | 0.247826 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23198445 | agcactttgggaggc[G/T]gaggagggtggatca | 100507650 |
rs12888165 | snp | C/T | 0.229723 | 0.249176 | intron-variant | RNF212B | GRCh38.p7 | 14:23238598 | TAAAAAATAGCCAGG[C/T]GTGGTGGTGCTCGCC | 100507650 |
rs12888598 | snp | C/T | 0.0139463 | 0.0823326 | intron-variant | RNF212B | GRCh38.p7 | 14:23231622 | AGctccccctctccc[C/T]tctcccctctcccct | 100507650 |
rs12888887 | snp | A/G | 0.286042 | 0.247388 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23197799 | TTTtttttttgagca[A/G]catggctgtttattt | 100507650 |
rs12889946 | snp | A/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23234335 | GCAAAAAGTTTTTTT[A/T]AAAATTACTTAGTCA | 100507650 |
rs12892123 | snp | C/G | 0.234109 | 0.249494 | intron-variant | RNF212B | GRCh38.p7 | 14:23223577 | agccaggatggtctc[C/G]atctcctgaccccgt | 100507650 |
rs12892157 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | RNF212B | GRCh38.p7 | 14:23223647 | ggcgtgagccaccgc[A/G]cccggccaagccttt | 100507650 |
rs12892307 | snp | A/C | 0.483199 | 0.0901004 | intron-variant, downstream-variant-500B | RNF212B, LOC105370406 | GRCh38.p7 | 14:23194993 | acagattcttgggtc[A/C]caatgaaattaaatt | 100507650 |
rs12892513 | snp | C/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23223160 | atatacgtcgtacat[C/G]atatcaatagaacga | 100507650 |
rs12892827 | snp | C/T | 0.233527 | 0.249457 | intron-variant | RNF212B | GRCh38.p7 | 14:23223285 | tatagaagaatgata[C/T]ctcaatataataaaa | 100507650 |
rs12893027 | snp | G/T | 0.453087 | 0.145793 | intron-variant | RNF212B | GRCh38.p7 | 14:23216878 | gaatgtgaccctgtc[G/T]caaaaaaaaaaaaaa | 100507650 |
rs12893114 | snp | A/G | 0.233527 | 0.249457 | intron-variant | RNF212B | GRCh38.p7 | 14:23223147 | gatatgcaaatcaat[A/G]tacgtcgtacatcat | 100507650 |
rs12893769 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23257086 | tgaacgtgggtggcg[A/G]aggttgcagtgagct | 100507650 |
rs12895279 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23266431 | tttttttttttttga[A/G]atggtgtttctttct | 100507650 |
rs12895345 | snp | C/T | 0.430583 | 0.172886 | intron-variant | RNF212B | GRCh38.p7 | 14:23192347 | tacaccaaggaatac[C/T]atgcagccataaaaa | 100507650 |
rs12896519 | snp | C/T | 0.220843 | 0.248294 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236375 | aaaaaattagctggg[C/T]gtaatggcaggcgcc | 100507650 |
rs12896531 | snp | C/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23266480 | gcagtggtgcaatct[C/T]ggctcaccgcaacct | 100507650 |
rs13379479 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23215661 | aaggtgaactcaaga[A/C]attcccaaatgaagg | 100507650 |
rs17093607 | snp | C/G | 0.0543475 | 0.155628 | utr-variant-3-prime, downstream-variant-500B | RNF212B, HOMEZ | GRCh38.p7 | 14:23273834 | TGTTACTCCTGAAGC[C/G]TCAGAAATTTTAGTC | 100507650 |
rs17127493 | snp | C/T | 0.15665 | 0.231917 | intron-variant | RNF212B | GRCh38.p7 | 14:23186295 | CCTTGGTGTAATATG[C/T]TGACAAAAATCTGTA | 100507650 |
rs17128047 | snp | A/G | 0.0894459 | 0.191631 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23237768 | TTTCCTGGGCTGCTG[A/G]GAAAAGTCTCCTACA | 100507650 |
rs17128051 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RNF212B | GRCh38.p7 | 14:23238198 | GGGCTCATCTGGTCA[A/G]TTCAGGGGATGACAT | 100507650 |
rs17128091 | snp | C/G | 0.357451 | 0.225731 | intron-variant | RNF212B | GRCh38.p7 | 14:23245473 | GTAGAGAAATCATAT[C/G]TAGTCTGAATCCTAA | 100507650 |
rs17128153 | snp | A/C | 0.248188 | 0.249993 | intron-variant | RNF212B | GRCh38.p7 | 14:23257625 | TACTGCTGTGTACTC[A/C]AAAGTAGAGCCTGAC | 100507650 |
rs17128209 | snp | C/T | 0.247905 | 0.249991 | intron-variant | RNF212B | GRCh38.p7 | 14:23262536 | GCTACCTATAATACA[C/T]GAGAGTAAGCAATTT | 100507650 |
rs17183905 | snp | C/T | 0.0898077 | 0.191933 | upstream-variant-2KB, intron-variant | SLC7A8, RNF212B | GRCh38.p7 | 14:23185592 | GTCTCTTGCTAAAAC[C/T]AGTGCAAACTGATAA | 100507650 |
rs17183940 | snp | A/G | 0.259397 | 0.249823 | intron-variant | RNF212B | GRCh38.p7 | 14:23257417 | AGTAAATTCTTATCT[A/G]TCTAAAACTAGTTTA | 100507650 |
rs17199051 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF212B | GRCh38.p7 | 14:23240716 | CAGGGAAAGCCACAA[A/G]GCATCAGATTCTTCA | 100507650 |
rs17256106 | snp | C/T | 0.249603 | 0.25 | intron-variant | RNF212B | GRCh38.p7 | 14:23191859 | AAATACATACTTATT[C/T]GATATTCATTGTATA | 100507650 |
rs17256127 | snp | G/T | 0.397452 | 0.201886 | intron-variant | RNF212B | GRCh38.p7 | 14:23242216 | TCATGACCTTTTAAA[G/T]TTCGCTAATGTAAAA | 100507650 |
rs17256134 | snp | A/G | 0.261056 | 0.249755 | intron-variant | RNF212B | GRCh38.p7 | 14:23257552 | CAAGATCTAGGAAAG[A/G]ACCCTAGACAAAAGA | 100507650 |
rs17256141 | snp | A/G | 0.259397 | 0.249823 | intron-variant | RNF212B | GRCh38.p7 | 14:23257605 | GGAAGCAGATGAGAC[A/G]TAAATACTGCTGTGT | 100507650 |
rs28368866 | snp | C/T | 0.248755 | 0.249997 | intron-variant | RNF212B | GRCh38.p7 | 14:23257107 | GCAGTGAGCTGAGAT[C/T]GTGCCATTGCACTCC | 100507650 |
rs28404192 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | RNF212B | GRCh38.p7 | 14:23231921 | TGCCGGGATTGCAGA[A/C]GGAGTCTCGTTCACT | 100507650 |
rs28463155 | snp | A/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23249529 | CAGCTTGTGTAAAAA[A/T]AAAAAATTAAAAAGA | 100507650 |
rs28474668 | snp | A/C | 0.482757 | 0.0912364 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213237 | AGAATGGCGTGAACC[A/C]GTGAGGCGGAGCTTG | 100507650 |
rs28535403 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF212B | GRCh38.p7 | 14:23264766 | TATAATGCCATTTCA[C/T]TTGTTTTTTTTTCCT | 100507650 |
rs28541470 | snp | A/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23249528 | CCAGCTTGTGTAAAA[A/T]TAAAAAATTAAAAAG | 100507650 |
rs28662173 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | RNF212B | GRCh38.p7 | 14:23186665 | TTATTCTATTCTCTA[C/T]GTTTAAATAGTGCTT | 100507650 |
rs28674982 | snp | C/T | 0.248755 | 0.249997 | intron-variant | RNF212B | GRCh38.p7 | 14:23257121 | TCGTGCCATTGCACT[C/T]CAGCCTGGGCGACAG | 100507650 |
rs28734785 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF212B | GRCh38.p7 | 14:23247094 | GCGGTGAGCCAAGAT[C/T]GCACCATTGCACTCC | 100507650 |
rs28813416 | snp | A/T | 0.121717 | 0.214577 | intron-variant | RNF212B | GRCh38.p7 | 14:23217109 | AACCTGCTATGGACC[A/T]GAGTGGAGCCCCCTG | 100507650 |
rs28856273 | snp | A/G | 0.49975 | 0.0111793 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205646 | GCATGGGCTGAACTA[A/G]CTTTGGGAAGGAACT | 100507650 |
rs28872333 | snp | A/T | 0.499741 | 0.0113788 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23204997 | TTAAAAAAAGTTTTA[A/T]CTCAGTTTTTTTCCT | 100507650 |
rs34014159 | in-del | -/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23257963 | TTGAAAAACAGTTTT[-/T]AAAAAAAATCTCTCT | 100507650 |
rs34019946 | in-del | -/A | 0 | 0 | intron-variant, downstream-variant-500B | RNF212B, LOC105370406 | GRCh38.p7 | 14:23194735 | AAAAAAAAAAAAAAA[-/A]ACAACGCTGCTGTAT | 100507650 |
rs34046498 | snp | A/G | 0.233818 | 0.249476 | intron-variant | RNF212B | GRCh38.p7 | 14:23221823 | TAAAACTAAAAATCA[A/G]TAACAGGAGGAATTT | 100507650 |
rs34087069 | in-del | -/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23250238 | TAATCCCAGCACTTT[-/T]GGAGGCTGAGGGGGT | 100507650 |
rs34135364 | in-del | -/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23227586 | CATTGAATATACATT[-/C]AAATCGAACAAAAAG | 100507650 |
rs34181212 | in-del | -/A | 0.499999 | 0.000599041 | intron-variant | RNF212B | GRCh38.p7 | 14:23235215 | ATACTCTGTCTCAGG[-/A]AAAAAAAAAAATAGC | 100507650 |
rs34210072 | snp | A/G | 0.240478 | 0.249819 | intron-variant | RNF212B | GRCh38.p7 | 14:23216233 | CCTGGGTGACAGAGC[A/G]AGACTCCATTTCAAA | 100507650 |
rs34260336 | in-del | -/T | 0.464841 | 0.127841 | intron-variant | RNF212B | GRCh38.p7 | 14:23263091 | AGGGTTTTTTTTTTT[-/T]CCCTAAGCCAAACTG | 100507650 |
rs34262711 | snp | C/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23258708 | CTTTTTTTTTTTTTT[C/T]TTTTCTAAGAAGTGA | 100507650 |
rs34272224 | in-del | -/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23227195 | CAATTTCCTATGAAT[-/G]CTATAGCTATTTTAT | 100507650 |
rs34288769 | in-del | -/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23248459 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 100507650 |
rs34293089 | in-del | -/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23242588 | ATCTTGTACTCTTCC[-/C]TCACTCTTGTAAATG | 100507650 |
rs34344413 | snp | A/G | 0.357024 | 0.225933 | intron-variant | RNF212B | GRCh38.p7 | 14:23238708 | TGCCACTGCACTCCA[A/G]CCTGGAGACAGAGCC | 100507650 |
rs34425415 | snp | A/C/T | 0.02016 | 0.0983543 | intron-variant | RNF212B | GRCh38.p7 | 14:23222219 | GTTCTTTTGAAAAGA[A/C/T]GAACAAAATTGATAA | 100507650 |
rs34428427 | snp | G/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23272274 | AAGTACAAAAAATTA[G/T]CCGGGCATGGTGGCG | 100507650 |
rs34447558 | in-del | -/C | 0.444267 | 0.157354 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23216069 | GCTAACACGGTGAAA[-/C]CCCCATCTCTACTAA | 100507650 |
rs34490261 | in-del | -/C | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203971 | TGATTTGCATTTCCC[-/C]TGATCACTAGTGATG | 100507650 |
rs34583422 | snp | G/T | 0.347694 | 0.230122 | intron-variant | RNF212B | GRCh38.p7 | 14:23248022 | AACAGATTCAGTGTC[G/T]GGGGAGGGCTTACTC | 100507650 |
rs34648124 | snp | A/G | 0.475613 | 0.107697 | intron-variant | RNF212B | GRCh38.p7 | 14:23254100 | CCTGGGCAACATAGT[A/G]AGACCCTTTCTCTTA | 100507650 |
rs34659222 | in-del | -/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23221014 | TCAATAATAACATTG[-/G]AATGTAAATGGACTA | 100507650 |
rs34688858 | in-del | -/AAT | | | intron-variant | RNF212B | GRCh38.p7 | 14:23238782 | AATAATAATAATAAT[-/AAT]CCCACAAAGAAACCT | 100507650 |
rs34688870 | in-del | -/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23222810 | TAATCCTAGCACTTT[-/T]GGGAGGCTGAGGCGG | 100507650 |
rs34738962 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23217460 | AAGGGCCTTGGCCAA[A/G]AAATAGTGCTGTGCT | 100507650 |
rs34772395 | in-del | -/A | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23233405 | TAAAAAAAAAAAAAA[-/A]GAATATTTAAAGAAA | 100507650 |
rs34797222 | snp | A/C | 0.237593 | 0.249692 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205237 | TTCCTGGTTCCTTTT[A/C]CCTTGTTTTATACAG | 100507650 |
rs34808245 | in-del | -/G | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23196489 | TGTCACACGGGCTGG[-/G]AGGGCAGTGGAGTGA | 100507650 |
rs34823941 | in-del | -/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23247837 | TATATTTAACTTTTT[-/T]AGGAACTGCCAGACT | 100507650 |
rs34825470 | in-del | -/A | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23250483 | AAAAAAAAAAAAAAA[-/A]GACTGAATTAATAAT | 100507650 |
rs34895919 | in-del | -/TT | 0.498568 | 0.0267188 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23197780 | CTATGTCTTGTCTTC[-/TT]TTTTTTTTTTTTGAG | 100507650 |
rs34943878 | in-del | -/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23227779 | TAATTTTGTACTTTT[-/T]GTAGAGACAGGATTT | 100507650 |
rs34974601 | in-del | -/A | | | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23185241 | TCAGCAAAAAAAAAA[-/A]CAACAAACAACAACA | 100507650 |
rs34991646 | in-del | -/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23219491 | GTTTTTTTTTTTTTT[-/T]GAGACAGTCTCACTC | 100507650 |
rs34992150 | in-del | -/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23221860 | TATATGAACACATGG[-/G]AAATTAAACAGTATG | 100507650 |
rs35011486 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23228487 | AAAAAAAAAAAAAAA[A/T]TTAACAGGTGTGGTG | 100507650 |
rs35033427 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RNF212B | GRCh38.p7 | 14:23246556 | ATCCAATGAGACAAT[A/G]TTTATGGAAATATTT | 100507650 |
rs35054545 | in-del | -/A | | | intron-variant | RNF212B | GRCh38.p7 | 14:23187156 | TGCTTCAGATCAGAA[-/A]GAAATTGATCCCTTT | 100507650 |
rs35099689 | in-del | -/T | | | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23237146 | TTTTTTTTTTTTTTT[-/T]AAAGACGGAGTCTCT | 100507650 |
rs35114789 | in-del | -/G | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23228340 | TCTGCAAAAGAACAG[-/G]CTGGCCAGGCGCAGT | 100507650 |
rs35172299 | in-del | -/A | 0.232651 | 0.249397 | intron-variant | RNF212B | GRCh38.p7 | 14:23220909 | AAAATCACCTTCACT[-/A]AAAAGGAAGAGAGGA | 100507650 |
rs35175826 | snp | A/C | 0.252702 | 0.249985 | intron-variant | RNF212B | GRCh38.p7 | 14:23228839 | TTGAATATGTATAGA[A/C]CACTGATTTTCCTTT | 100507650 |
rs35188230 | snp | C/T | 0.234109 | 0.249494 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23206221 | CTGGGATTATAGGTG[C/T]ACACCACCATGGCCA | 100507650 |
rs35193725 | in-del | -/TT | 0.499 | 0.0223418 | intron-variant | RNF212B | GRCh38.p7 | 14:23258694 | AAGTCCCAAGAGAGC[-/TT]TTTTTTTTTTTTTTT | 100507650 |
rs35208170 | in-del | -/T | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203490 | CTTTTTTTTTTTTTT[-/T]GAGATGGAGCCTTGC | 100507650 |
rs35253799 | snp | A/C | 0.203267 | 0.245593 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236551 | CAAAAAGCAAAAAAA[A/C]CCCAAACAACAACAA | 100507650 |
rs35272583 | in-del | -/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23264819 | ACATATATTACAAGG[-/T]TTTTTTTTTTTTTTT | 100507650 |
rs35354365 | in-del | -/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23228050 | GCCTGACCAACATGG[-/G]AGAAACCTCGTCTCT | 100507650 |
rs35356471 | in-del | -/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23239757 | TGATTAGCTGGGATT[-/C]ACAGGTGCCTGCCAC | 100507650 |
rs35431756 | snp | C/T | 0.249038 | 0.249998 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203729 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 100507650 |
rs35441124 | in-del | -/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23266884 | TTCTGTTTCCTTTCC[-/C]TTGCTGATCTTCTGT | 100507650 |
rs35468129 | in-del | -/T | 0.314057 | 0.241654 | intron-variant | RNF212B | GRCh38.p7 | 14:23238265 | GGGCCTTTTCAGTGG[-/T]GTTTTTTAGACTCAC | 100507650 |
rs35477689 | snp | C/T | 0.221439 | 0.248363 | intron-variant | RNF212B | GRCh38.p7 | 14:23234954 | TACGGTGGCTCATAC[C/T]TGTAATCCCAGCACT | 100507650 |
rs35491816 | snp | G/T | 0.340559 | 0.233022 | intron-variant | RNF212B | GRCh38.p7 | 14:23250541 | TTATCTCTATATCTT[G/T]TAAGTACTTGTGTTC | 100507650 |
rs35528372 | snp | G/T | 0.347694 | 0.230122 | intron-variant | RNF212B | GRCh38.p7 | 14:23248025 | AGATTCAGTGTCGGG[G/T]GAGGGCTTACTCTTT | 100507650 |
rs35529368 | in-del | -/A | | | utr-variant-5-prime, upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23183340 | TAATAAAACAGGAGA[-/A]CTGCCTTTACCTCCC | 100507650 |
rs35546234 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260254 | TTCAAGAAACTCAAA[-/A]GATACCTCAGGACCC | 100507650 |
rs35558599 | in-del | -/TTTG | | | intron-variant | RNF212B | GRCh38.p7 | 14:23227615 | GTGTTTTTTTGTTTG[-/TTTG]TTTTGAGACTAGTTC | 100507650 |
rs35565260 | in-del | -/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23218536 | TCATGTGAGTCTGGG[-/G]AAGTTGAGGCTGCAG | 100507650 |
rs35568266 | in-del | -/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23249445 | GCTACTCAGGAGGCT[-/T]GAGGTGGGAGAATTG | 100507650 |
rs35577263 | in-del | -/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23240200 | TACATATACTTCTTT[-/T]ACAACCAATTGGAAT | 100507650 |
rs35628249 | in-del | -/A | | | intron-variant | RNF212B | GRCh38.p7 | 14:23218375 | TCTATCTCAAAAAAA[-/A]TAAATAAATAAAAAG | 100507650 |
rs35632337 | in-del | -/T | 0.498927 | 0.0231381 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205316 | AAAAAAAGGACACCC[-/T]TTTTTTTTTTTAAGC | 100507650 |
rs35654046 | in-del | -/A | 0.375 | 0.216506 | intron-variant | RNF212B | GRCh38.p7 | 14:23233563 | AAAAAAAAAAAAAAA[-/A]TAGAAAAATTAGCCG | 100507650 |
rs35659718 | in-del | -/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23223363 | TTCCTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 100507650 |
rs35681305 | snp | A/G | 0.201727 | 0.245295 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210223 | CATCAGACAAGCCCA[A/G]ACTGAGGGACATTCT | 100507650 |
rs35693171 | snp | A/C | 0.229429 | 0.249152 | intron-variant | RNF212B | GRCh38.p7 | 14:23225081 | TGATGCCACCCCACA[A/C]AAAAAAAAAACACCT | 100507650 |
rs35728517 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | RNF212B | GRCh38.p7 | 14:23251801 | AGTCTGGCAACAGAG[C/T]GAGACTCTGTCTCAA | 100507650 |
rs35758292 | snp | A/T | 0.273049 | 0.248935 | intron-variant | RNF212B | GRCh38.p7 | 14:23222237 | ACAAAATTGATAAAC[A/T]TTTAGCCAGACTGAA | 100507650 |
rs35771944 | in-del | -/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23261246 | AAGGAAGAGGAACAG[-/C]ACTATAACCTAATGC | 100507650 |
rs35811048 | in-del | -/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23258066 | AAAGGGGCCGGGTGC[-/C]GGTGGCTCACGCCTG | 100507650 |
rs35812759 | snp | A/G | 0.353371 | 0.227628 | intron-variant | RNF212B | GRCh38.p7 | 14:23249378 | TAGTGAAACCCCTTC[A/G]CTACAAAAAATTTAA | 100507650 |
rs35841884 | in-del | -/AAA | | | intron-variant, downstream-variant-500B | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195024 | AGCAATCAACAATTA[-/AAA]TAGAAAATAAGGTAA | 100507650 |
rs35862886 | snp | A/C | 0.468047 | 0.122292 | intron-variant | RNF212B | GRCh38.p7 | 14:23250544 | TCTCTATATCTTGTA[A/C]GTACTTGTGTTCTGC | 100507650 |
rs35882294 | in-del | -/T | | | intron-variant, nc-transcript-variant | RNF212B | GRCh38.p7 | 14:23270388 | TATATTGGCTATTTT[-/T]CCCACTCATAGTTAA | 100507650 |
rs35886483 | snp | A/G | 0.221141 | 0.248329 | intron-variant | RNF212B | GRCh38.p7 | 14:23226028 | AACTCGGCTGGGCGC[A/G]GTGGCTCACGCCTGT | 100507650 |
rs35936290 | in-del | -/A | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23201046 | TAGCTCAAAAGAAAA[-/A]GTTTTAAGACTCTGA | 100507650 |
rs35948084 | in-del | -/AC/ACAC | 0.297444 | 0.251919 | intron-variant | RNF212B | GRCh38.p7 | 14:23239993 | CACACACACACACAC[-/AC/ACAC]TCATAACCTCACCAC | 100507650 |
rs35983702 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23204022 | CATTTGTATATCTTC[C/T]CTTGAGAATTGTCTA | 100507650 |
rs35985078 | in-del | -/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23263358 | CCCTGACTTTCAGGG[-/G]AATGAAATGAAAATG | 100507650 |
rs35991567 | in-del | -/AAC | 0.499154 | 0.0205497 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209758 | GCAACCACTCTCTTA[-/AAC]AACAACTCAAAATTA | 100507650 |
rs36074283 | in-del | -/A | 0.476314 | 0.106217 | intron-variant | RNF212B | GRCh38.p7 | 14:23247140 | CAAAAAAAAAAAAAA[-/A]TTGTTTTCAAGGGGA | 100507650 |
rs36088546 | in-del | -/T | | | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23183660 | GCTTCTCCACACACT[-/T]AACGTGCTTCTCTTT | 100507650 |
rs45453094 | snp | C/T | 0.0295544 | 0.117914 | missense, stop-lost, synonymous-codon, intron-variant, nc-transcript-variant | RNF212B | GRCh38.p7 | 14:23270624 | AGAGCACAACTACAC[C/T]AGAGAGTCTTCCTAG | 100507650 |
rs45582142 | snp | G/T | 0.0150606 | 0.0854603 | downstream-variant-500B, utr-variant-3-prime | RNF212B, HOMEZ | GRCh38.p7 | 14:23274337 | AGGAGGTAGTTAACA[G/T]GTTTGTAAAACCAAA | 100507650 |
rs55661012 | in-del | -/T/TT | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23262655 | CGCCTCTTTTTTTTT[-/T/TT]CCCTTGCAGGTCAAT | 100507650 |
rs55663511 | in-del | -/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23254302 | AAAAACAAAACAAAA[-/C]AAAACAAAACAAAAC | 100507650 |
rs55683744 | snp | C/T | 0.266546 | 0.249452 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208844 | GGTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAC | 100507650 |
rs55694130 | in-del | -/A | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23223071 | AAAAAAAAAAAAAAA[-/A]GGAAAAGAAAAGATT | 100507650 |
rs55731601 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214122 | TATCTTTTTTAAAAA[-/A]GCTTCAATAAACAAT | 100507650 |
rs55763514 | snp | A/C | 0.233818 | 0.249476 | intron-variant | RNF212B | GRCh38.p7 | 14:23254292 | TCTTTATCTCAAAAA[A/C]AAAACAAAACAAAAC | 100507650 |
rs55813798 | snp | A/G | 0.0984431 | 0.198823 | intron-variant, nc-transcript-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23207313 | GATGGGTCTCAGGCT[A/G]TAGACTGCTCTCTAC | 100507650 |
rs55869471 | snp | A/C | 0.270351 | 0.24917 | intron-variant | RNF212B | GRCh38.p7 | 14:23254297 | ATCTCAAAAACAAAA[A/C]AAAACAAAACAAAAC | 100507650 |
rs55951877 | snp | C/G | 0.5 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208889 | TCAGCCCCCTGAGTA[C/G]TTGGGACTACAGGTG | 100507650 |
rs55974627 | snp | A/G | 0.264084 | 0.249603 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208852 | CAAGCTCTGCCTCCC[A/G]GGTTCACGCCATTCT | 100507650 |
rs56044467 | snp | A/G | 0.266546 | 0.249452 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208828 | CAATGGCGCGATCTC[A/G]GGTCACTGCAAGCTC | 100507650 |
rs56125059 | snp | C/G | 0.252702 | 0.249985 | intron-variant | RNF212B | GRCh38.p7 | 14:23229828 | CGCACAGCAAATAAA[C/G]AAACAGAAAAACTAT | 100507650 |
rs56126316 | snp | C/T | 0.415399 | 0.187465 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208883 | CCTGACTCAGCCCCC[C/T]GAGTAGTTGGGACTA | 100507650 |
rs56149372 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | RNF212B | GRCh38.p7 | 14:23229596 | CCACATGTGAAATGA[C/T]ATTTCACTGTGGTTT | 100507650 |
rs56183109 | snp | C/T | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209095 | TGTATTGATGATATG[C/T]TAAACAAGGGGTGGA | 100507650 |
rs56220318 | in-del | -/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23254307 | CAAAACAAAACAAAA[-/C]AAAACAAAACAAAAA | 100507650 |
rs56260323 | snp | A/C | 0.262985 | 0.249663 | intron-variant | RNF212B | GRCh38.p7 | 14:23243892 | GACCAGCCTGGCCAA[A/C]ATGAGGAAACCCTCG | 100507650 |
rs56327739 | snp | A/G | 0.150667 | 0.229419 | intron-variant | RNF212B | GRCh38.p7 | 14:23246369 | ATCTTCCCTATTGAA[A/G]TTTTCCTTTAATGTA | 100507650 |
rs56779201 | snp | C/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23239627 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTGAGACG | 100507650 |
rs56879783 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23246179 | TTTGTCTGTCACCCA[A/G]GCTGGAGTGCAGTGG | 100507650 |
rs56902258 | snp | A/T | 0.235854 | 0.249599 | intron-variant | RNF212B | GRCh38.p7 | 14:23263905 | CCAGTGTGGCCAACA[A/T]GGTGAAACCCTGTCT | 100507650 |
rs56932731 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23255759 | AGTTAATCTTCTTTG[A/G]AAAAACGAAAGAGAC | 100507650 |
rs57085489 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23254825 | TCTCAGTATTTTTCA[A/G]TTATTTCTCCTTTAC | 100507650 |
rs57224524 | snp | A/G | 0.229723 | 0.249176 | intron-variant | RNF212B | GRCh38.p7 | 14:23189188 | ACACCCCAAATCTTC[A/G]CTTCTAGTTGACATC | 100507650 |
rs57278320 | snp | A/G | 0.150333 | 0.229274 | intron-variant | RNF212B | GRCh38.p7 | 14:23239658 | GAGTCTGGCTCTGTC[A/G]CCTAGGCTGGAGTGC | 100507650 |
rs57395749 | in-del | -/T/TTT | 0.361053 | 0.22398 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23259444 | TTTCTTCTTTTAAAG[-/T/TTT]TTTTTTTTGTTTTTT | 100507650 |
rs57561951 | snp | C/G | 0.208169 | 0.246476 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23196886 | ACCCCATTCCTGGCC[C/G]TAGAGTGTGTTCTTT | 100507650 |
rs57656091 | in-del | -/AATTC | | | intron-variant | RNF212B | GRCh38.p7 | 14:23251270 | AATTCAATTCAATTC[-/AATTC]TAACACTAATTCCTA | 100507650 |
rs57731750 | in-del | -/TTT | | | intron-variant | RNF212B | GRCh38.p7 | 14:23266428 | TTTTTTTTTTTTTTT[-/TTT]GAGATGGTGTTTCTT | 100507650 |
rs57751160 | in-del | -/GAGA | | | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260773 | GTGAACTCTGAGAGA[-/GAGA]AAATGGTTAATGAAT | 100507650 |
rs57792695 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23271083 | TATGGGACTATGATT[A/C]TGATTCCAGCAACAA | 100507650 |
rs57941268 | in-del | -/GAAA | | | intron-variant | RNF212B | GRCh38.p7 | 14:23242098 | AAAAAAAAAAAAAAA[-/GAAA]AAAAAAAAAGAAAAG | 100507650 |
rs58028274 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | RNF212B | GRCh38.p7 | 14:23246999 | TAAAAAATTAGCCAG[C/G]TGTGGTGGCACGTGC | 100507650 |
rs58134677 | in-del | -/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23254292 | TCTTTATCTCAAAAA[-/C]AAAACAAAACAAAAC | 100507650 |
rs58145978 | snp | C/T | 0.127599 | 0.217986 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23197974 | GTACATTCTTAAGGG[C/T]GGGGGAGATTACAAA | 100507650 |
rs58202235 | snp | C/T | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23204835 | TTTTCACAATATTGA[C/T]TCTACCCATCCATGA | 100507650 |
rs58290003 | snp | C/T | 0.039522 | 0.134904 | intron-variant | RNF212B | GRCh38.p7 | 14:23187845 | ATCACTGCCTATGGT[C/T]GATTAGATGGGGCCT | 100507650 |
rs58402786 | in-del | -/T/TA | | | intron-variant | RNF212B | GRCh38.p7 | 14:23218376 | TATCTCAAAAAAAAA[-/T/TA]AATAAATAAAAAGAA | 100507650 |
rs58497672 | in-del | -/A | | | intron-variant | RNF212B | GRCh38.p7 | 14:23242107 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAAGAAA | 100507650 |
rs58565146 | in-del | -/AA | 0 | 0 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214649 | ATAAAGCATAGGAAA[-/AA]GTCAGTGAACTTGAA | 100507650 |
rs58592582 | snp | C/G | 0.154993 | 0.231244 | intron-variant | RNF212B | GRCh38.p7 | 14:23247482 | TTTTCCTGTTCAGGG[C/G]ATTTCATAAATATGG | 100507650 |
rs58719841 | snp | A/G | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203614 | CTCTCAAGTAGCTGA[A/G]ATTATAAGTGTGTGC | 100507650 |
rs58810022 | in-del | -/GAAAAA | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23242130 | AAAGAAAAAGAAAAA[-/GAAAAA]CCTTTAGTCCCCAGA | 100507650 |
rs59063249 | snp | A/C | 0.137867 | 0.223442 | intron-variant | RNF212B | GRCh38.p7 | 14:23264814 | TCCATACATATATTA[A/C]AAGGTTTTTTTTTTT | 100507650 |
rs59228982 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23233744 | GAGACCCTGTCTCAA[A/C]AAAAAAAAAAAAAAA | 100507650 |
rs59257853 | snp | A/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23255720 | AATTTTTTTAATTTT[A/T]AAAAAAGCAAGCAAG | 100507650 |
rs59279931 | in-del | -/C/CT | | | intron-variant | RNF212B | GRCh38.p7 | 14:23226814 | TTTCTTCTTCTTCTT[-/C/CT]TTTTTTTTTTTTAAT | 100507650 |
rs59357260 | in-del | -/G | 0.239037 | 0.24976 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211229 | TCTCAAAAAAAAAAA[-/G]AAAGAAAAAGCAACA | 100507650 |
rs59515753 | in-del | -/T | 0.159622 | 0.233092 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209309 | TATGACCTGTATTTT[-/T]GTGCTGACCTATCTC | 100507650 |
rs59611077 | in-del | -/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23252097 | TCAGGGGTTGGGGGG[-/G]CGTGGGAAGAAAGGT | 100507650 |
rs59884945 | snp | C/T | 0.458315 | 0.13822 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210543 | AGAACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 100507650 |
rs59923716 | in-del | -/AAAA/AAAAA | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23216904 | AAAAAAAAAAAAAAA[-/AAAA/AAAAA]GACCAATCTCAAAGG | 100507650 |
rs59972093 | snp | A/G | 0.100588 | 0.200439 | intron-variant | RNF212B | GRCh38.p7 | 14:23190631 | TCAGCTCTCACCTAC[A/G]CTGTTTCAATAGCCT | 100507650 |
rs59984693 | in-del | -/T | 0.423881 | 0.179625 | intron-variant | RNF212B | GRCh38.p7 | 14:23264770 | ATGCCATTTCACTTG[-/T]TTTTTTTTCCTGACA | 100507650 |
rs60085951 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200053 | CGATAGTACACTCGT[C/T]GTTAGAGTCTAGTCT | 100507650 |
rs60122483 | in-del | -/A | | | intron-variant | RNF212B | GRCh38.p7 | 14:23230683 | AAAAAAAAAAAAAAA[-/A]CCATTGCCAAATACA | 100507650 |
rs60125066 | snp | G/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23255757 | AAAGTTAATCTTCTT[G/T]GGAAAAACGAAAGAG | 100507650 |
rs60293319 | in-del | -/GCA | | | intron-variant | RNF212B | GRCh38.p7 | 14:23243732 | AAAGCAAGCAAGCAA[-/GCA]AGCAAGCAAGCAAAG | 100507650 |
rs60476895 | snp | A/G | 0.151334 | 0.229706 | intron-variant | RNF212B | GRCh38.p7 | 14:23247184 | AAGTATAAACACCCC[A/G]TCTACTTTTTTTTTT | 100507650 |
rs60478967 | snp | A/C | 0.131723 | 0.220251 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23197963 | GATCTCACAAAGTAC[A/C]TTCTTAAGGGCGGGG | 100507650 |
rs60659225 | in-del | -/T/TT | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23188477 | TTTTTTTTTTTTTTT[-/T/TT]AGAGATAGGGTCTCA | 100507650 |
rs60746817 | in-del | -/A | 0.255047 | 0.249949 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23185265 | CAACAACAAAAAAAA[-/A]CCAGACAAGGCAGGG | 100507650 |
rs60915610 | in-del | -/T | 0.371987 | 0.218218 | intron-variant | RNF212B | GRCh38.p7 | 14:23186347 | ATTAAATTTTGAGCA[-/T]TTTTTTTTTTTTTGA | 100507650 |
rs60929844 | in-del | -/CAGTGGTGGG | | | intron-variant | RNF212B | GRCh38.p7 | 14:23217249 | TGGTGGCAGTGGTGG[-/CAGTGGTGGG]GGGGGGGCTCCTCTG | 100507650 |
rs60933668 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203739 | TGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 100507650 |
rs61199624 | in-del | -/AA | | | intron-variant, downstream-variant-500B | RNF212B, LOC105370406 | GRCh38.p7 | 14:23194756 | AAAAAAAAAAAAAAA[-/AA]CAACGCTGCTGTATC | 100507650 |
rs61203381 | in-del | -/T | 0.127254 | 0.217792 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23259453 | TTGTTTTTTTTTTTT[-/T]ATGGAATGCTTCAAG | 100507650 |
rs61397282 | snp | C/G | 0.353587 | 0.22753 | intron-variant | RNF212B | GRCh38.p7 | 14:23252098 | TCAGGGGTTGGGGGG[C/G]GTGGGAAGAAAGGTT | 100507650 |
rs61588912 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | RNF212B | GRCh38.p7 | 14:23267125 | AGGCATGCACCACCA[C/T]GCCTGGCTAGTTTTT | 100507650 |
rs61614521 | snp | C/T | 0.178785 | 0.239642 | intron-variant | RNF212B | GRCh38.p7 | 14:23190373 | GCCCAAAAGAGAGTG[C/T]GTGCTTTCCGCTCCA | 100507650 |
rs61656270 | in-del | -/TATATATATATATATA | | | intron-variant | RNF212B | GRCh38.p7 | 14:23229247 | ATATATATATATATA[-/TATATATATATATATA]CCACATTGTTTATCC | 100507650 |
rs61682325 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF212B | GRCh38.p7 | 14:23190982 | ACCGTCTTGGGGGTG[C/T]CCTCCCTTTCTCACA | 100507650 |
rs61701886 | in-del | -/AAAAACAAAAAC | | | intron-variant | RNF212B | GRCh38.p7 | 14:23220228 | AACAAAAACAAAAAC[-/AAAAACAAAAAC]CATACAACAAGGCCA | 100507650 |
rs61976533 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF212B | GRCh38.p7 | 14:23190381 | GAGAGTGCGTGCTTT[C/T]CGCTCCAAACCTGAT | 100507650 |
rs61976534 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205889 | TTTATAGTTTTGTAA[C/G]TTCTATGCCAAATTT | 100507650 |
rs61976536 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23216666 | AGGCAGATTGCTTGA[A/G]CTTAGGAGTTCAAGA | 100507650 |
rs61976537 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23216877 | TGAATGTGACCCTGT[A/C]TCAAAAAAAAAAAAA | 100507650 |
rs61976538 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23233403 | CCCAAGAATGATCAA[A/T]TAAAAAAAAAAAAAA | 100507650 |
rs61976539 | snp | G/T | | | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23237150 | TTTTTTTTTTTTAAA[G/T]ACGGAGTCTCTCTCT | 100507650 |
rs61976540 | snp | C/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23250365 | GCGCGTGCCTGTAAT[C/G]CCAGCTGCTTGGGAG | 100507650 |
rs61976541 | snp | G/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23250375 | GTAATGCCAGCTGCT[G/T]GGGAGGCTGAGGCAT | 100507650 |
rs61976542 | snp | A/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23255796 | CTTCATGAGGCTGAG[A/G]GATTTGAAAGATTGC | 100507650 |
rs62213660 | snp | A/C | 0.243061 | 0.249904 | intron-variant | RNF212B | GRCh38.p7 | 14:23233255 | ATCTCAAGTACCCAG[A/C]GACACAAACACTGCG | 100507650 |
rs63566862 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23198673 | AGAAAACTCTGTCCA[A/C]AAAAAAAAAAAGGTC | 100507650 |
rs66588201 | in-del | -/T | 0.253824 | 0.249971 | intron-variant | RNF212B | GRCh38.p7 | 14:23234328 | TGTACATGCAAAAAG[-/T]TTTTTTTAAAATTAC | 100507650 |
rs67344644 | snp | A/G | 0.242488 | 0.249887 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211229 | TCTCAAAAAAAAAAA[A/G]AAAGAAAAAGCAACA | 100507650 |
rs71115601 | in-del | -/A | 0.380724 | 0.213099 | intron-variant | RNF212B | GRCh38.p7 | 14:23193752 | AGTAGAAGATTTAAC[-/A]AAAAAAAAAAAGGAA | 100507650 |
rs71119003 | in-del | -/TTTT | 0 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208776 | TTTTTTTTTTTTTTT[-/TTTT]GAGACGGAGTCTCAC | 100507650 |
rs71119004 | in-del | -/A | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23221248 | AAAAAAAAAAAAAAA[-/A]GAAAGAAACACGCTT | 100507650 |
rs71119005 | in-del | -/A | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23226316 | AAAAAAAAAAAAAAA[-/A]TTAAATAAATAAATA | 100507650 |
rs71119006 | in-del | -/T/TC | | | intron-variant | RNF212B | GRCh38.p7 | 14:23226813 | CTTTTTTTTTTTTTT[-/T/TC]AATAGAGAGGAGGTC | 100507650 |
rs71119007 | in-del | -/TA | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23229262 | ATATATATATATATA[-/TA]CCACATTGTTTATCC | 100507650 |
rs71119008 | in-del | -/TTG | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23231952 | CAGTGCTCAATGTTG[-/TTG]CCCAGGCTGGAGTGC | 100507650 |
rs71119010 | in-del | -/AA | | | intron-variant | RNF212B | GRCh38.p7 | 14:23240035 | TCAAAAAAAAAAAAA[-/AA]TCTCACCACTGTCTG | 100507650 |
rs71119011 | in-del | -/AAAA | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23251825 | TCTCAAAAAAAAAAA[-/AAAA]GAAAGAAAGAAAACC | 100507650 |
rs71313499 | in-del | -/A | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23258356 | AAAAAAAAAAAAAAA[-/A]GACAGTAGAAGGCTA | 100507650 |
rs71413971 | snp | C/T | 0.376791 | 0.215463 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208903 | AGTTGGGACTACAGG[C/T]GCCCGCCACTACGCC | 100507650 |
rs71413972 | snp | C/T | 0.378174 | 0.214642 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208915 | AGGTGCCCGCCACTA[C/T]GCCTGGCTAATTTTT | 100507650 |
rs71413973 | snp | C/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23216762 | GCATGCATCTGTGGT[C/T]TCAGCTACTTGGGAA | 100507650 |
rs71413974 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23242445 | GCAGAGCTTCAAAGC[A/C]AGATTAACAAATATT | 100507650 |
rs71413975 | snp | G/T | 0.239902 | 0.249796 | intron-variant | RNF212B | GRCh38.p7 | 14:23254202 | AAGTGGGAGGATCAC[G/T]TGAGTCCAGGAGGTT | 100507650 |
rs71413976 | snp | A/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23258054 | CATTAAGATAGTAAA[A/G]GGGGCCGGGTGCGGT | 100507650 |
rs71413977 | snp | C/T | 0.263535 | 0.249633 | intron-variant | RNF212B | GRCh38.p7 | 14:23263853 | AGCACTTTGGGAGGC[C/T]GAGGCGAGTGGATCA | 100507650 |
rs71418271 | snp | A/C | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23231629 | CCTCTCCCCTCTCCC[A/C]TCTCCCCTCTCCCCA | 100507650 |
rs71425068 | in-del | -/A | 0.110167 | 0.207236 | intron-variant | RNF212B | GRCh38.p7 | 14:23218367 | GTGAGAGTCTATCTC[-/A]CAAAAAAAAAAATAA | 100507650 |
rs71425070 | in-del | -/C | 0.222928 | 0.24853 | intron-variant | RNF212B | GRCh38.p7 | 14:23224569 | AAGAATGAAACGAAA[-/C]CCCCTAGCTCTTGCC | 100507650 |
rs71425075 | in-del | -/ATA | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23238738 | AGACCCTGTCTCAAA[-/ATA]ATAATAATAATAATA | 100507650 |
rs71425076 | in-del | -/A/AAAAGA | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23242108 | AAAAAAAAAAAAAGG[-/A/AAAAGA]AAAAGAAAAAGAAAA | 100507650 |
rs71425078 | in-del | -/A/AA/AAA | 0.451732 | 0.147663 | intron-variant | RNF212B | GRCh38.p7 | 14:23250482 | GCGAGACTCTGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 100507650 |
rs71425079 | in-del | -/T | 0.36021 | 0.224397 | intron-variant | RNF212B | GRCh38.p7 | 14:23257384 | TATTAAAAATGAGGG[-/T]TTAAAAAAATAGACT | 100507650 |
rs72488269 | snp | A/G | 0.259397 | 0.249823 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23261166 | AAAAGGGGCAAAGGT[A/G]GAGGAGAACAAAGGA | 100507650 |
rs72684354 | snp | A/G | 0.264358 | 0.249587 | intron-variant | RNF212B | GRCh38.p7 | 14:23186451 | GGCTCCTAGGTTCAA[A/G]TGATTCTCCTGCCTC | 100507650 |
rs72684356 | snp | A/G | 0.247053 | 0.249983 | intron-variant | RNF212B | GRCh38.p7 | 14:23191700 | TTGTTTAAGTGGGAT[A/G]ATGGGTAATAGTCCA | 100507650 |
rs72684361 | snp | A/G | 0.249886 | 0.25 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23196364 | CCAAGCCCACTCTGC[A/G]TCACCACTGCTCTCT | 100507650 |
rs72684368 | snp | C/G | 0.255782 | 0.249933 | intron-variant | RNF212B | GRCh38.p7 | 14:23251246 | CACCAACTAGGTATG[C/G]AACAATTCAATTCAA | 100507650 |
rs72684370 | snp | C/T | 0.25912 | 0.249834 | intron-variant | RNF212B | GRCh38.p7 | 14:23251849 | GAAAACCATATATCA[C/T]GGAAATAGCCAAATG | 100507650 |
rs72684372 | snp | C/T | 0.260504 | 0.249779 | intron-variant | RNF212B | GRCh38.p7 | 14:23253562 | AAGACCACTTTATTC[C/T]AGTGTTGTATTCCAC | 100507650 |
rs72684373 | snp | C/T | 0.26078 | 0.249767 | intron-variant | RNF212B | GRCh38.p7 | 14:23253631 | GAGGGTAGCCATTGA[C/T]GAACTTTGCAGAGAT | 100507650 |
rs72684374 | snp | A/G | 0.26078 | 0.249767 | intron-variant | RNF212B | GRCh38.p7 | 14:23254042 | CCAACACTTTGGGAG[A/G]CCGAAGTGGGAGAAC | 100507650 |
rs72684376 | snp | A/G | 0.25912 | 0.249834 | intron-variant | RNF212B | GRCh38.p7 | 14:23256821 | CCTTTCAGGTAGTTG[A/G]GATTACAGGAATGTA | 100507650 |
rs72684381 | snp | G/T | 0.259397 | 0.249823 | intron-variant | RNF212B | GRCh38.p7 | 14:23258068 | AAGGGGCCGGGTGCG[G/T]TGGCTCACGCCTGTA | 100507650 |
rs72684391 | snp | G/T | 0.263809 | 0.249618 | intron-variant | RNF212B | GRCh38.p7 | 14:23267744 | CCAACAATTTTGTCT[G/T]AAAGTCTATTTTGTC | 100507650 |
rs73600435 | snp | C/T | 0.131381 | 0.220067 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23184318 | AACAGAGCGAGACCC[C/T]GTCTACTAAAAATTT | 100507650 |
rs73600436 | snp | G/T | 0.203575 | 0.245652 | intron-variant | RNF212B | GRCh38.p7 | 14:23186194 | ATTAAGTGCCTCTCT[G/T]TAGGTTGGAATCTTT | 100507650 |
rs73600449 | snp | A/T | 0.0391387 | 0.134304 | intron-variant | RNF212B | GRCh38.p7 | 14:23189803 | ACAGAGTGAGTTCTT[A/T]TCTGAAAATATGTGA | 100507650 |
rs73600451 | snp | A/G | 0.100231 | 0.200173 | intron-variant | RNF212B | GRCh38.p7 | 14:23190278 | GTCCTAATCTCTTGC[A/G]TAAACTCTAGAATGA | 100507650 |
rs73600459 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195343 | CAGATTTAGAAAACA[C/T]GGAAGATTTATAATA | 100507650 |
rs73600460 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195401 | ATGGAATTATAAGCG[C/G]TTGACTCGTAGCCCA | 100507650 |
rs73600465 | snp | G/T | 0.095934 | 0.196885 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200132 | GATAAATCATGGTAG[G/T]ATTGGTTTGCTTATT | 100507650 |
rs73600479 | snp | G/T | 0.375 | 0.216506 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208777 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCACT | 100507650 |
rs73600489 | snp | A/C | 0.0777841 | 0.181223 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23212049 | GAAAAATTATATTAA[A/C]AGATACAGCAAAAGC | 100507650 |
rs73600490 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23212414 | ACGGCATGATTATCT[A/G]TCTAGAAAATCAAAT | 100507650 |
rs73602407 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | RNF212B | GRCh38.p7 | 14:23221259 | AAAAAGAAAGAAACA[C/T]GCTTCACTTATACAG | 100507650 |
rs73602428 | snp | C/G | 0.172028 | 0.23753 | intron-variant | RNF212B | GRCh38.p7 | 14:23248346 | TTACCATGTTGCCCA[C/G]GTCTCGAACCCCTGG | 100507650 |
rs73602441 | snp | A/G | 0.0341408 | 0.126114 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23259503 | ATGTTAACTTTCTTT[A/G]GGGGCTATGTTAATC | 100507650 |
rs73602447 | snp | C/T | 0.138886 | 0.22395 | intron-variant | RNF212B | GRCh38.p7 | 14:23265843 | TCCTAAGGTGGAAGT[C/T]TCGATTATTGATTTG | 100507650 |
rs74036943 | snp | A/C | 0.126033 | 0.21761 | intron-variant | RNF212B | GRCh38.p7 | 14:23193729 | AGATAGTCATAATAA[A/C]GCATACCAGTAGAAG | 100507650 |
rs74036945 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195382 | AAGCTATCAGAGGAA[C/G]CAAATGGAATTATAA | 100507650 |
rs74036951 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211384 | AAATCTTCCCACAAA[A/G]AAAACTCCAGGCTTA | 100507650 |
rs74036953 | snp | C/T | 0.178144 | 0.239451 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213901 | AACCCCAACAGTCAA[C/T]AGGCACTAACATTTC | 100507650 |
rs74036954 | snp | A/T | 0.157972 | 0.232445 | intron-variant | RNF212B | GRCh38.p7 | 14:23227331 | TATTTTAAAACAAAA[A/T]GTTACAATTTATGGT | 100507650 |
rs74036958 | snp | G/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23245128 | TTATCACTGTTCCCT[G/T]TCTATACTCTTACTT | 100507650 |
rs74036959 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | RNF212B | GRCh38.p7 | 14:23245972 | TCTATTTATGTTTTT[A/G]TGTTCTCCAATCTCT | 100507650 |
rs74036960 | snp | A/C | 0.150333 | 0.229274 | intron-variant | RNF212B | GRCh38.p7 | 14:23246474 | CTTATAGCTTTATTT[A/C]TTTGAACCAGTCATA | 100507650 |
rs74036961 | snp | A/C | 0.151334 | 0.229706 | intron-variant | RNF212B | GRCh38.p7 | 14:23249061 | ACTTATTTACAAAAA[A/C]AGACAGCTGGTTATG | 100507650 |
rs74036966 | snp | A/C | 0.118933 | 0.212888 | intron-variant | RNF212B | GRCh38.p7 | 14:23262178 | GATTTTTTTTTTCAT[A/C]TCTCCCACTAGCCTG | 100507650 |
rs74036969 | snp | A/C | 0.115088 | 0.210473 | utr-variant-3-prime | RNF212B, HOMEZ | GRCh38.p7 | 14:23274081 | GGCCTTTTTATTATT[A/C]TTCTAGCATTTTAGG | 100507650 |
rs74276786 | in-del | -/TTA | | | intron-variant | RNF212B | GRCh38.p7 | 14:23234321 | TGTGTGTGTACATGC[-/TTA]AAAAAGTTTTTTTTA | 100507650 |
rs74347789 | snp | C/T | 0.00205674 | 0.0320022 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260650 | CACTCCTGGTTTTTT[C/T]ACCTATAGGAATCTC | 100507650 |
rs74457033 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23229844 | AAACAGAAAAACTAT[A/T]TTCCCAATAAAACAT | 100507650 |
rs74548561 | snp | A/G | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23212028 | CCACCGTGCCTGACC[A/G]AAAAAGAAAAATTAT | 100507650 |
rs74550688 | snp | G/T | 0 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23197793 | TCTTTTTTTTTTTTT[G/T]GAGCAACATGGCTGT | 100507650 |
rs74604003 | snp | C/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23256845 | GAATGTATTATCACG[C/T]CTGGCTAAATTTTTT | 100507650 |
rs74604409 | snp | G/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23248303 | TGGCTAGTTTTTGTG[G/T]TTTTTTTTTTTTAAT | 100507650 |
rs74605022 | snp | A/G | 0.159951 | 0.233219 | intron-variant | RNF212B | GRCh38.p7 | 14:23225165 | CAATAACAAGTGCTG[A/G]CGAGGATGTGGAGAA | 100507650 |
rs74633866 | snp | A/G | 0.234109 | 0.249494 | intron-variant | RNF212B | GRCh38.p7 | 14:23219815 | TTGTATATGCAATCA[A/G]TGTTGTCATCAGTTT | 100507650 |
rs74681162 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203874 | TGTTCTCTGATCACC[A/G]TATCCATGCCAACAT | 100507650 |
rs74742188 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23235680 | TAGATAGTGATATTA[A/G]CAAAAGTGATTTTTT | 100507650 |
rs74808752 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211247 | AGAAAAAGCAACAAA[C/T]TGAACAACTTAGATA | 100507650 |
rs74840007 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF212B | GRCh38.p7 | 14:23232036 | GGCCTCCCAAAGTGC[C/T]GAGATTGCAGCCTCT | 100507650 |
rs74860143 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF212B | GRCh38.p7 | 14:23253519 | GGTTTATCACCATCA[C/T]TGGTTTGGGGGCGGG | 100507650 |
rs74907575 | snp | A/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23224769 | TGTGCAGAATCTTTT[A/T]AACTTAATGTGATTC | 100507650 |
rs74909030 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23224684 | TTTTTGCCCAAACCA[A/G]TGTTCTAGAGAGTTC | 100507650 |
rs74936928 | snp | A/G | 0.0244538 | 0.107838 | utr-variant-3-prime | RNF212B, HOMEZ | GRCh38.p7 | 14:23274213 | AATTCACTTAAAGAC[A/G]ATGGTCCCTCTGTCC | 100507650 |
rs75041578 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23258338 | AGCGAAACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 100507650 |
rs75063414 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | RNF212B | GRCh38.p7 | 14:23227396 | GATGGTGTATGGAAG[C/G]GGGCACAGGGGTTTT | 100507650 |
rs75074019 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF212B | GRCh38.p7 | 14:23248870 | AACAAATGAATTTTT[A/G]TGGGACACAAATATT | 100507650 |
rs75170914 | snp | C/T | 0.350764 | 0.228794 | intron-variant | RNF212B | GRCh38.p7 | 14:23229357 | GAATATTGGTGTACA[C/T]ATATCTGTTTGAGCC | 100507650 |
rs75211252 | snp | A/G | 0.0287284 | 0.116357 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23215488 | CTAGCCTGGGTGACA[A/G]AGCAAGACTCTGTAT | 100507650 |
rs75248021 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23224785 | TGATTGTTTCCTTTG[A/C]TGTGCAGAAGCTTTT | 100507650 |
rs75265229 | snp | C/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23263793 | TAACAACATATAAAG[C/T]TAGGTTTTCTGAGGC | 100507650 |
rs75371684 | snp | C/T | 0.112983 | 0.209108 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210347 | GACATGACAATGAAA[C/T]GCAGTGCGGTATATA | 100507650 |
rs75396926 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23262165 | TAAACACTGTTCTGA[A/T]TTTTTTTTTCATCTC | 100507650 |
rs75411423 | snp | C/T | 0.243919 | 0.249926 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23207681 | ATGGTTACCAAAATG[C/T]GAATCCTGAAAATTT | 100507650 |
rs75433614 | snp | A/G | 0.046775 | 0.145601 | intron-variant, nc-transcript-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214072 | AGGTTGTAGTGTGCT[A/G]TAATGTAATCCATAG | 100507650 |
rs75438563 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | RNF212B | GRCh38.p7 | 14:23249262 | TAAGAATTTGAACAA[C/G]TGAGGTACTCAGTGG | 100507650 |
rs75462546 | snp | A/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260580 | CACTGAGCTTAGTTA[A/T]CTCGCAAGTAAGACT | 100507650 |
rs75483267 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23262164 | TTAAACACTGTTCTG[A/T]TTTTTTTTTTCATCT | 100507650 |
rs75508225 | snp | C/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23190847 | TTGGACTTCATACCC[C/T]TCTCTTCCTTTCACG | 100507650 |
rs75513058 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | RNF212B | GRCh38.p7 | 14:23194370 | AAATAGATGAAGAAA[A/C]AATTGATAGAATTGA | 100507650 |
rs75533286 | snp | A/G | 0.188946 | 0.24243 | intron-variant | RNF212B | GRCh38.p7 | 14:23224443 | AGAACCCAGAAACAA[A/G]TCCACACAACAACAG | 100507650 |
rs75599183 | snp | C/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23224734 | GTCAATTTTTTGCTT[C/T]GGTTGCCTGTGCTTA | 100507650 |
rs75606957 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205002 | AAAAGTTTTAACTCA[G/T]TTTTTTTCCTAAGCA | 100507650 |
rs75616952 | in-del | -/A | 0.475702 | 0.107512 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23259203 | CTCAAAAACAAAAAC[-/A]AAAAAAAACATCTGC | 100507650 |
rs75617306 | snp | G/T | 0 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208775 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCA | 100507650 |
rs75715208 | snp | C/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23188367 | GCCTTAACAGTCTTC[C/T]TTCTCAGGATTTAAG | 100507650 |
rs75723791 | snp | C/T | 0.046775 | 0.145601 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214859 | AAAGAAATAAGGCCA[C/T]AAATTCAAAAAGCTG | 100507650 |
rs75739051 | snp | C/T | 0.107694 | 0.205546 | intron-variant | RNF212B | GRCh38.p7 | 14:23189343 | TGAATGTGCTGTCTG[C/T]GTTCCTATGTATCTC | 100507650 |
rs75791045 | snp | G/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23219491 | AGTTTTTTTTTTTTT[G/T]GAGACAGTCTCACTC | 100507650 |
rs75935177 | snp | A/T | 0.0539704 | 0.155153 | intron-variant | RNF212B | GRCh38.p7 | 14:23219439 | TTAAAAGCAGAGGAA[A/T]GAAGTTGAAGTGTAG | 100507650 |
rs75940808 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | RNF212B | GRCh38.p7 | 14:23190782 | TCAAAACCCTCCAAC[A/G]CTGCCTGTCACAGCT | 100507650 |
rs75994736 | snp | A/T | 0.0803491 | 0.183626 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211490 | GTTAAAGAGAAAGGA[A/T]TAGTTCCCCAATGAT | 100507650 |
rs76036479 | snp | A/G | 0.179105 | 0.239737 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23212615 | GAGTCTCGCTCTGTC[A/G]CCCAGGCCCAGGCTG | 100507650 |
rs76042481 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF212B | GRCh38.p7 | 14:23253515 | TTAGGGTTTATCACC[A/G]TCATTGGTTTGGGGG | 100507650 |
rs76045372 | snp | A/G | 0.17332 | 0.23795 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210706 | TGCATGAGCCCAGGA[A/G]GTGGAGGTTGCAGTG | 100507650 |
rs76104030 | snp | A/G | 0.123105 | 0.215401 | intron-variant | RNF212B | GRCh38.p7 | 14:23193814 | ATTAGAAGTTTTGTA[A/G]TACAATATGACTTTT | 100507650 |
rs76151034 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23233405 | CAAGAATGATCAATT[A/T]AAAAAAAAAAAAAGA | 100507650 |
rs76172455 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23235682 | GATAGTGATATTAAC[A/C]AAAGTGATTTTTTAT | 100507650 |
rs76177148 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236861 | AGGGGATATAAATTT[C/T]TGGGATCATAGTTTC | 100507650 |
rs76189105 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23217712 | AAAATCACAGTATTA[C/T]AGGGCTTGGGACCCA | 100507650 |
rs76242999 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23251283 | TCAATTCTAACACTA[A/G]TTCCTAGAGTTTTAG | 100507650 |
rs76297481 | snp | C/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, downstream-variant-500B | RNF212B, HOMEZ | GRCh38.p7 | 14:23273146 | AGCTCCCCTCATTTC[C/G]TACAATTTGGAACAA | 100507650 |
rs76357328 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23243168 | TTCTTCCTTTGCTAG[A/C]ATACTAGATTGTTGC | 100507650 |
rs76361569 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RNF212B | GRCh38.p7 | 14:23245258 | CCTCACTCTAGAGAT[A/G]GAGTAAGGGGAATTA | 100507650 |
rs76379565 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23230655 | CGAGACTCCATCTCA[A/T]AAAAAAAAAAAAAAA | 100507650 |
rs76438043 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF212B | GRCh38.p7 | 14:23190553 | AAATCTCGCAAATAT[C/T]GAGAGACTGATCACT | 100507650 |
rs76562743 | snp | A/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23224761 | AGCTTTATAACTTGA[A/T]GTGATCTCATTTGTT | 100507650 |
rs76574853 | in-del | -/AA | 0.232359 | 0.249377 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214646 | TGAATAAAGCATAGG[-/AA]AAAGTCAGTGAACTT | 100507650 |
rs76611083 | snp | C/T | 0.24019 | 0.249807 | intron-variant | RNF212B | GRCh38.p7 | 14:23229200 | TCAAAACTTTATTTC[C/T]TTTATGGCTGAATAA | 100507650 |
rs76619918 | snp | C/T | 0.158302 | 0.232576 | intron-variant | RNF212B | GRCh38.p7 | 14:23231350 | AATTTTTGACAAAGG[C/T]AATTTAGTTGAGAAA | 100507650 |
rs76648624 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23242085 | AGACTCCGTCTCAAA[A/C]AAAAAAAAAAAAAAA | 100507650 |
rs76663998 | snp | C/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23224790 | TTTGTTGATTGTTTC[C/T]TTTGCTGTACAGAAG | 100507650 |
rs76671935 | snp | C/T | 0.263809 | 0.249618 | intron-variant | RNF212B | GRCh38.p7 | 14:23248378 | CTCACGCAATCTGCC[C/T]GCCTCAGCCTCCCAA | 100507650 |
rs76728966 | snp | A/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23242106 | AAAAAAAAAAAAAAA[A/G]AGAAAAGAAAAAGAA | 100507650 |
rs76758830 | snp | A/C | 0.040671 | 0.13668 | intron-variant | RNF212B | GRCh38.p7 | 14:23189870 | TTCAGCTACCACCCA[A/C]CTTCTCTGCTCCCAT | 100507650 |
rs76767785 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | RNF212B | GRCh38.p7 | 14:23270829 | TCAATTTCAGATTTT[A/T]TCCTACTGTTAGATT | 100507650 |
rs76791338 | snp | C/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23224760 | GGACAAATGGAAACA[C/T]ATCAAGTTAAAAAGC | 100507650 |
rs76797975 | snp | C/T | 0.0399052 | 0.1355 | utr-variant-5-prime, upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23183430 | AGCAATCCTCAGGTA[C/T]TTTCTTCTCTTCTAG | 100507650 |
rs76849305 | snp | G/T | 0.0766824 | 0.180169 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23212270 | AACATTATGCCGATG[G/T]CTATGGCCACTGCAG | 100507650 |
rs76878940 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RNF212B | GRCh38.p7 | 14:23235767 | TGTATAACTCAGTGA[A/C]CCAAAATTTTTGAAA | 100507650 |
rs76922999 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF212B | GRCh38.p7 | 14:23251512 | TATTATTACCAGTTT[A/G]TTATAAAAGATACAA | 100507650 |
rs76997816 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF212B | GRCh38.p7 | 14:23186750 | AGTATCTTGGGCAGA[C/T]GAGGCAGTTATCTTA | 100507650 |
rs77051883 | snp | A/G | 0.5 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209001 | CTGACCTCGTGATCC[A/G]CCCGCCTTGGCCTCC | 100507650 |
rs77087749 | snp | C/G/T | 0.0197687 | 0.0974348 | intron-variant | RNF212B | GRCh38.p7 | 14:23263073 | AATTTTAGGTCTATG[C/G/T]AGAAGTTTAAAGCTA | 100507650 |
rs77145952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23235685 | AGTGATATTAACAAA[A/G]GTGATTTTTTATATT | 100507650 |
rs77333446 | snp | A/G | 0.0471551 | 0.14613 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214880 | CAAAAAGCTGAGTGA[A/G]CTTCAAGAAGAATAA | 100507650 |
rs77354234 | snp | G/T | 0.276723 | 0.258991 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23206908 | AAGAAAAACAAACTT[G/T]CGTTAAAAAAAAAAA | 100507650 |
rs77380542 | snp | A/G | 0.046775 | 0.145601 | intron-variant, nc-transcript-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214027 | GCTTGAGAGGCTAGC[A/G]CAGGAGGATCACTTG | 100507650 |
rs77383580 | snp | G/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23246148 | TCTTTTTTTTTTTTT[G/T]AGATGGAGTCTTGCT | 100507650 |
rs77433216 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, nc-transcript-variant | RNF212B | GRCh38.p7 | 14:23270435 | CCAGTACCTGGTCCT[C/T]ACAGGAAAAGAACAG | 100507650 |
rs77520325 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23235679 | ATAGATAGTGATATT[A/G]ACAAAAGTGATTTTT | 100507650 |
rs77578089 | snp | C/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23224728 | TTTTTGCTTTGATTG[C/T]CTGTGCTTGTGGGGT | 100507650 |
rs77661932 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211582 | GACCAGTTCCTCTCA[C/T]GAACATAAATGCAGC | 100507650 |
rs77738001 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23217046 | AAAGCAACAAGAAGG[C/T]TCCCGGGGTCCCTGA | 100507650 |
rs77740723 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23198674 | GAAAACTCTGTCCAA[A/C]AAAAAAAAAAGGTCC | 100507650 |
rs77756749 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | RNF212B, HOMEZ | GRCh38.p7 | 14:23273719 | CCCATACCCTTTCTG[C/G]TACTCTGAATTTATT | 100507650 |
rs77766165 | snp | C/T | 0.171704 | 0.237423 | intron-variant | RNF212B | GRCh38.p7 | 14:23245750 | CAACATTTTCTACTC[C/T]TTACCATGCTTTTTT | 100507650 |
rs77767864 | snp | A/C | 0.0872718 | 0.189788 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23212961 | TATGATAATATCAGC[A/C]AATATAAAATTATTA | 100507650 |
rs77768167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23199685 | GAAGTCTCATGTCCT[A/G]TGAAGGAAAAATAGT | 100507650 |
rs77806128 | snp | C/T | 0.151334 | 0.229706 | intron-variant | RNF212B | GRCh38.p7 | 14:23248896 | ATATTCAGACCACAG[C/T]AGGCCAGTAAATATT | 100507650 |
rs77834476 | snp | A/T | 0 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213326 | TTAAAAAAAAAAAAA[A/T]TTATAAAACGTTACT | 100507650 |
rs77865500 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23190849 | GGACTTCATACCCTT[A/C/T]TCTTCCTTTCACGTG | 100507650 |
rs77900996 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | RNF212B | GRCh38.p7 | 14:23271697 | GGAAGTAACATTCCT[C/T]CCTAAAATCCTCAAA | 100507650 |
rs77977007 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23258340 | CGAAACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 100507650 |
rs78065582 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23258339 | GCGAAACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 100507650 |
rs78108194 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | RNF212B | GRCh38.p7 | 14:23245179 | CCTTTTCTAAACCTC[A/G]AGATGATCCTTAGTC | 100507650 |
rs78158415 | snp | C/T | 0.152219 | 0.230085 | intron-variant | RNF212B | GRCh38.p7 | 14:23229261 | ATATATATATATATA[C/T]ACCACATTGTTTATC | 100507650 |
rs78166639 | snp | C/T | 0.453209 | 0.145623 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203160 | AAGATCCCAAAGTCC[C/T]CAAAGTCCATTATAT | 100507650 |
rs78188920 | snp | A/C | 0.0295035 | 0.117819 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23215942 | TGTATAATGTAATCT[A/C]TAGAGCAACCATTAA | 100507650 |
rs78315826 | snp | C/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23243869 | GGATGGTCTCGATCT[C/T]CTGACCCCGTTATTC | 100507650 |
rs78376273 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RNF212B | GRCh38.p7 | 14:23231167 | AATAGTTGGAATTTT[A/G]ATAGGGATGACATTG | 100507650 |
rs78431243 | snp | G/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23219492 | GTTTTTTTTTTTTTT[G/T]AGACAGTCTCACTCT | 100507650 |
rs78443060 | snp | A/G | 0.0410537 | 0.137264 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23237487 | GTTAGTTCTCAATTA[A/G]TATCACACTGTTCTT | 100507650 |
rs78466639 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF212B | GRCh38.p7 | 14:23250004 | TACCTTAACGTTCTG[A/G]TTCCTCCTAACCTCT | 100507650 |
rs78526319 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23251282 | TTCAATTCTAACACT[A/G]ATTCCTAGAGTTTTA | 100507650 |
rs78592089 | snp | A/C/T | 0.0221141 | 0.102801 | intron-variant | RNF212B | GRCh38.p7 | 14:23244069 | GGTGACAACAGCAAA[A/C/T]CTCTGTCTCAAAGAA | 100507650 |
rs78635142 | snp | A/G | 0 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210796 | AAAAAAAAAAAAAAA[A/G]AAATGTAGGATGATA | 100507650 |
rs78638638 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | RNF212B | GRCh38.p7 | 14:23248080 | TGCATCCTCACATGG[C/T]AAAAGTGGCAAACAG | 100507650 |
rs78677707 | snp | A/C/T | 0.0185938 | 0.0946107 | intron-variant | RNF212B | GRCh38.p7 | 14:23271490 | AAGTCCAGTCTTGCC[A/C/T]TTTTTTGTTTGTTTT | 100507650 |
rs78754462 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23185266 | ACAACAAACAACAAC[A/C]AAAAAAACCAGACAA | 100507650 |
rs78768452 | snp | A/C | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23206694 | TAGCAAAATTTACAT[A/C]ATAAGGTAGAGAGAG | 100507650 |
rs78826045 | snp | A/G | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23233760 | AAAAAAAAAAAAAAA[A/G]AGAGTTCTCAAAACT | 100507650 |
rs78867575 | snp | A/T | 0.151668 | 0.229849 | intron-variant | RNF212B | GRCh38.p7 | 14:23248315 | GTGTTTTTTTTTTTT[A/T]AATAGATACAGGGTT | 100507650 |
rs78898862 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23259453 | TTTAAAGTTTTTTTT[G/T]TTTTTTTTTTTTATG | 100507650 |
rs78930188 | snp | A/G | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23215487 | TCTAGCCTGGGTGAC[A/G]GAGCAAGACTCTGTA | 100507650 |
rs78940944 | in-del | -/AAAAAAAAGAA | | | intron-variant | RNF212B | GRCh38.p7 | 14:23193111 | AAAAAAAAAAAAAAA[-/AAAAAAAAGAA]TGTTACCAGAATGGC | 100507650 |
rs79002170 | snp | A/G | 0.077417 | 0.180873 | intron-variant | RNF212B | GRCh38.p7 | 14:23217723 | ATTACAGGGCTTGGG[A/G]CCCAGGTCTGTTTGA | 100507650 |
rs79080542 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236200 | TCTTGTTTTGGAAAA[C/T]ATATTTTCCATAGAT | 100507650 |
rs79116791 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF212B | GRCh38.p7 | 14:23252947 | TTAATTATAACTATA[C/T]TTCTGTCCAGAGCCA | 100507650 |
rs79130251 | snp | C/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23224721 | TTTGGTTGTTTGAGC[C/T]TATGGGGTATTACTC | 100507650 |
rs79134746 | snp | G/T | 0.237303 | 0.249677 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205005 | AGTTTTAACTCAGTT[G/T]TTTTCCTAAGCAAAC | 100507650 |
rs79162506 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236963 | ATTCTGTCTCTCTCT[C/T]TTTTTTTTTTTTTTG | 100507650 |
rs79186565 | snp | C/T | 0.245631 | 0.249962 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208176 | TCCTTGGAGAAATGG[C/T]TTTTAGAGCTGGGTC | 100507650 |
rs79244614 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23198961 | GTATATACATGAGTC[A/G]GTATACACACAAATA | 100507650 |
rs79280035 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23201733 | ATTTCAGGTCATTGT[A/G]AAGTCATCTGTTTAA | 100507650 |
rs79311109 | snp | A/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23269724 | CTCAAAAAAAAAAAA[A/G]GAAAAAATTATCATC | 100507650 |
rs79400276 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RNF212B | GRCh38.p7 | 14:23245017 | AGAGAGTTCCCAAGT[G/T]GTAAAAACTTTGGTT | 100507650 |
rs79422196 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23229842 | AGAAACAGAAAAACT[A/G/T]TATTCCCAATAAAAC | 100507650 |
rs79431488 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23216416 | CATACAGAAAACAAA[C/G]AATCAAATAGCATAC | 100507650 |
rs79472264 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | RNF212B | GRCh38.p7 | 14:23259121 | CGTTTGAGCCCAGGA[C/G]TCTGAGTTACAGTGA | 100507650 |
rs79474428 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF212B | GRCh38.p7 | 14:23227379 | TGGTTGCCTTTAGGG[A/G]AGATGGTGTATGGAA | 100507650 |
rs79585794 | snp | A/G | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23206700 | AATTTACATCATAAG[A/G]TAGAGAGAGAAAAAA | 100507650 |
rs79686616 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF212B | GRCh38.p7 | 14:23245239 | CAGTGTCCTGCCTCT[C/T]AATCCTCACTCTAGA | 100507650 |
rs79690340 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195384 | GCTATCAGAGGAACC[A/G]AATGGAATTATAAGC | 100507650 |
rs79733711 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RNF212B | GRCh38.p7 | 14:23238117 | AGGCCCCATCGCCTC[C/T]GGAAAGCAGGGGAAT | 100507650 |
rs79741004 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23191348 | AGTGAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 100507650 |
rs79761343 | snp | C/G | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23243668 | GCCACTGCACTCCAG[C/G]TTGGGCTCAGAGTAA | 100507650 |
rs79765476 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | RNF212B | GRCh38.p7 | 14:23250702 | AGATTGAGGACATGC[A/G]CCTCAGAAGGTTCAG | 100507650 |
rs79767824 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23220863 | CAAATACACAAAAAA[A/T]AAAAGCAGGAAATTA | 100507650 |
rs79784741 | snp | A/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23269725 | TCAAAAAAAAAAAAA[A/G]AAAAAATTATCATCA | 100507650 |
rs79788596 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23201608 | TTGGACTTTAGGGAA[C/T]GTAATATCTTAAAGG | 100507650 |
rs79825285 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF212B | GRCh38.p7 | 14:23235399 | GGAATAGTTTGATTT[A/G]TAACCTGAGCTAATC | 100507650 |
rs79841659 | snp | C/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23224792 | ACTTTGTTGATCGTT[C/T]CCTTTGCTGTGCAGA | 100507650 |
rs79848972 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | RNF212B | GRCh38.p7 | 14:23218885 | AAAGAAGAGTACCTC[C/T]GGGCATTTAATAATC | 100507650 |
rs79888369 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23196280 | TCATTATTCTTTCTG[C/T]TCTTTCTCCAGCCTG | 100507650 |
rs80034041 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | RNF212B | GRCh38.p7 | 14:23250037 | AATTTCAATCACAAC[C/T]ACCATCTCACCTCTC | 100507650 |
rs80066843 | snp | C/T | 0.233527 | 0.249457 | intron-variant | RNF212B | GRCh38.p7 | 14:23220180 | CAAGAGCAAAACTGT[C/T]TCGGGAAAAACAAAA | 100507650 |
rs80160033 | in-del | -/G | 0.262985 | 0.249663 | intron-variant | RNF212B | GRCh38.p7 | 14:23242917 | GGGAGGTTGAGGCTG[-/G]CAGTGAGCCATAATT | 100507650 |
rs80166631 | snp | G/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23224726 | TTTGCTTCGGTTGCC[G/T]GTGCTTATGGGATAT | 100507650 |
rs80176989 | snp | G/T | 0.0810805 | 0.184299 | intron-variant | RNF212B | GRCh38.p7 | 14:23190607 | CCCTGGTTCATCACC[G/T]CTTCACCATCAGCTC | 100507650 |
rs80261976 | snp | A/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23229222 | GCTGAATAATATTTT[A/T]TATATATATATATAT | 100507650 |
rs80347140 | snp | G/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23246147 | TTCTTTTTTTTTTTT[G/T]GAGATGGAGTCTTGC | 100507650 |
rs111272087 | snp | A/G | 0 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209026 | GCCTCCCAGAGTGCT[A/G]GGATTACAGGCGTGA | 100507650 |
rs111325777 | snp | A/G | 0.00993419 | 0.0697739 | downstream-variant-500B, utr-variant-3-prime | RNF212B, HOMEZ | GRCh38.p7 | 14:23274634 | TGAAAATAGCCGGGC[A/G]CGGTGGCTCATGCCT | 100507650 |
rs111329180 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | RNF212B | GRCh38.p7 | 14:23238758 | TAATAATAATAATAA[C/T]AATAATAATAATAAT | 100507650 |
rs111355403 | snp | A/C | | | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236443 | TCGCTTGAACCCAGG[A/C]GGCGGAGGTTGCAGT | 100507650 |
rs111358545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200417 | TGCAACCTCTGCCTC[C/T]TGGGATCAAGCAATT | 100507650 |
rs111367485 | snp | A/C | 0 | 0 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23184879 | CAATATAGTGGACAA[A/C]ACTATAAGTCTAAAA | 100507650 |
rs111371651 | snp | A/T | 0.0539704 | 0.155153 | intron-variant | RNF212B | GRCh38.p7 | 14:23219791 | TTAGTTTTCTTTTAG[A/T]GTGTTTGTTTGTATA | 100507650 |
rs111442300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212B | GRCh38.p7 | 14:23223601 | ACCCCGTGATCTGCC[C/T]GCCTCAGCCTCCCAA | 100507650 |
rs111444328 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23217577 | CACACAGAGAGAGAG[A/C]TTCCATTTTGGGGTG | 100507650 |
rs111445723 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23227738 | CTTAGTAGCTGGGAC[A/T]ACAGGCATGCATCAG | 100507650 |
rs111452590 | in-del | -/T | 0.154661 | 0.231107 | intron-variant | RNF212B | GRCh38.p7 | 14:23226812 | TCTTTCTTCTTCTTC[-/T]TTTTTTTTTTTTTTA | 100507650 |
rs111619751 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23216924 | AATCTCAAAGGTTAC[A/G]GATTGTATGATTCCA | 100507650 |
rs111643346 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200951 | AATAGTTTTCAAATT[C/T]TGGAGAAAATCAATT | 100507650 |
rs111645127 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | RNF212B | GRCh38.p7 | 14:23270290 | AGGCCAATATCCATT[A/C]TTCTCCCCATCTTTT | 100507650 |
rs111651247 | snp | G/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23266413 | TTAAATGTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 100507650 |
rs111658604 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23220641 | TCACCCTGGCTAACA[C/T]GGTGAAATCCCATCT | 100507650 |
rs111664938 | snp | C/T | 0.213635 | 0.247341 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208986 | GATGGTCTCGATCTC[C/T]TGACCTCGTGATCCG | 100507650 |
rs111666600 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23237868 | GCACGCCACGGAGCC[A/T]CGCCCACTGATTTAG | 100507650 |
rs111703730 | snp | C/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23251335 | GGCTCAGCCTCACAA[C/G]ACTGCCCCGACTCTG | 100507650 |
rs111734570 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | RNF212B | GRCh38.p7 | 14:23218225 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCACAC | 100507650 |
rs111749220 | snp | A/G | 0.046775 | 0.145601 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214464 | GCGCCAATGTACTCC[A/G]GCCTGGGCAACAGAG | 100507650 |
rs111752217 | snp | C/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23221751 | GGTCACCAAACAAAT[C/T]TGAAAACTTTAAAAA | 100507650 |
rs111777843 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | RNF212B | GRCh38.p7 | 14:23251642 | CCAACATGGTGAAAC[C/T]CTGCCTCTACTAAAA | 100507650 |
rs111789827 | snp | A/G | 0.122411 | 0.214991 | intron-variant | RNF212B | GRCh38.p7 | 14:23189614 | TTGAGACCAGCCTGG[A/G]CAATATAGCAAAACC | 100507650 |
rs111815958 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | RNF212B | GRCh38.p7 | 14:23216840 | AGCTGAGATTGCCCT[A/G]CTGCATCCTAGTGTG | 100507650 |
rs111824086 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | RNF212B | GRCh38.p7 | 14:23248029 | TCAGTGTCGGGGGAG[G/T]GCTTACTCTTTGCTT | 100507650 |
rs111836469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23207821 | GTACAGCTTAGTTTT[A/G]TACATTTTAGGAAGA | 100507650 |
rs111862404 | snp | C/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23264711 | AGAAATCAACTTACT[C/G]TATGCGAAGATCTGC | 100507650 |
rs111894649 | in-del | -/T | 0.26271 | 0.249677 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23259423 | GCTGGTCTGGAATCC[-/T]TTTTTTTTTCTTCTT | 100507650 |
rs111936229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212B | GRCh38.p7 | 14:23230725 | ATTTTCCCCTATATT[C/T]TCTTCTAAGAGTTTT | 100507650 |
rs111944897 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF212B | GRCh38.p7 | 14:23228612 | TGTGATCACATTAAC[A/G]CAATCCAGCCTGGGT | 100507650 |
rs111950236 | snp | A/G | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23191223 | ACCAGGGCTGGTGGC[A/G]GTGCACACCTGTAGT | 100507650 |
rs111975257 | in-del | -/GA | 0.127254 | 0.217792 | intron-variant | RNF212B | GRCh38.p7 | 14:23255047 | CTTCCAAGAAATCAG[-/GA]GAGAGAGAGGTAATA | 100507650 |
rs111984144 | snp | A/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23252845 | TATTCTATTTATGAG[A/G]ACAATGAGGATGCAA | 100507650 |
rs111984672 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23220257 | TACAACAAGGCCAGG[C/T]AAGGTGGCTTATGCC | 100507650 |
rs112047673 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | RNF212B | GRCh38.p7 | 14:23222197 | AGGTCAATGAAACAG[-/A]AAAAAAGTTCTTTTG | 100507650 |
rs112136297 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF212B | GRCh38.p7 | 14:23233770 | AAAAAAAGAGTTCTC[A/G]AAACTCAACAATAAG | 100507650 |
rs112180476 | snp | A/G | 0 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195409 | ATAAGCGCTTGACTC[A/G]TAGCCCATCTTCACC | 100507650 |
rs112211676 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | RNF212B | GRCh38.p7 | 14:23261817 | ATACAAAAACAAAAT[C/T]AGCCGGGCGTGGTGG | 100507650 |
rs112232473 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF212B | GRCh38.p7 | 14:23228213 | CTCCAGCCTGGGTGA[C/T]GAGAGCGAAACTCTG | 100507650 |
rs112252494 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | RNF212B | GRCh38.p7 | 14:23219964 | CGAGGCAGGTGGATC[A/G]TTTGACGTCAGGAGT | 100507650 |
rs112262745 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200517 | TTTCAGCAGAGATGG[A/G]GTTTCACCATGTTGG | 100507650 |
rs112319515 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23216925 | ATCTCAAAGGTTACA[G/T]ATTGTATGATTCCAC | 100507650 |
rs112322139 | snp | C/G/T | 0.048722 | 0.148516 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23215100 | GGTGATTGGATCATG[C/G/T]GGGCAGTTTCCCCCA | 100507650 |
rs112330230 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210342 | AATGAGACATGACAA[A/T]GAAACGCAGTGCGGT | 100507650 |
rs112399990 | snp | A/G | 0.0341408 | 0.126114 | downstream-variant-500B, utr-variant-3-prime | RNF212B, HOMEZ | GRCh38.p7 | 14:23274650 | CGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 100507650 |
rs112433437 | snp | A/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23271448 | ACTCCATCTCAAAAA[A/G]AAAAAGAAAAAGAAA | 100507650 |
rs112446583 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23207067 | ATTGAGCTGCTTAAA[A/T]TTTTTTTTCTTTAAA | 100507650 |
rs112463333 | in-del | -/A | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23216568 | TAAATTATGCTAAGT[-/A]AAAAAAAAAAAAAAT | 100507650 |
rs112503892 | snp | C/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23256923 | ACTTTGGGAGGCTGA[C/G]GCAGGTGGATCACGA | 100507650 |
rs112506638 | snp | A/C | 0.5 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23202280 | AAAAGCAGTTGGTTA[A/C]TGCTTCACAAAAAAC | 100507650 |
rs112509370 | snp | A/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23187184 | TTTAACTAGGGAAAA[A/T]TATGGATGAAAGGCC | 100507650 |
rs112561149 | snp | C/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23229347 | ATGCTGGTAGGAATA[C/T]TGGTGTACACATATC | 100507650 |
rs112562358 | snp | C/T | 0.151334 | 0.229706 | intron-variant | RNF212B | GRCh38.p7 | 14:23248438 | CGCCCAACCCCAAGC[C/T]TCTTTTTTTTTTTTT | 100507650 |
rs112569978 | snp | A/G | 0.5 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23198660 | CAGCCTGAGAACAAG[A/G]AAACTCTGTCCAAAA | 100507650 |
rs112574204 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23222276 | AAAAAGAAGACCCAA[A/G]GAAATAAAATCAGAG | 100507650 |
rs112580616 | in-del | -/GAGA | 0.126909 | 0.217598 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260767 | GGCTGTGTGAACTCT[-/GAGA]GAGAGAAAATGGTTA | 100507650 |
rs112629843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF212B | GRCh38.p7 | 14:23270062 | GAGGTTTGCCCCCCA[A/G]AGAGCATTGTCTCTA | 100507650 |
rs112658764 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RNF212B | GRCh38.p7 | 14:23225650 | GATGGTTATTAGAGG[C/T]GGGGAAGGGTAGTGG | 100507650 |
rs112665506 | snp | A/G | 0.444444 | 0.157135 | intron-variant | RNF212B | GRCh38.p7 | 14:23257024 | CAGGCGTGGTGGCGG[A/G]CGCCTGTAATCCCAG | 100507650 |
rs112733170 | in-del | -/G | 0.029116 | 0.117091 | intron-variant | RNF212B | GRCh38.p7 | 14:23220800 | ACTGCACTCCAGCCT[-/G]GGAGACAGAGCAAGA | 100507650 |
rs112744416 | in-del | -/A | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23189648 | TTTCTACTAAAAATT[-/A]AAAAAAAAAAATTAG | 100507650 |
rs112806216 | snp | A/C/G/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23216291 | TGTTTTGGAATGTAT[A/C/G/T]ATCTTGTATAGATTT | 100507650 |
rs112846128 | snp | A/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23191332 | GCACCCTGGGCGACA[A/T]AGTGAGACCCTGTCT | 100507650 |
rs112849992 | snp | C/T | 0.039522 | 0.134904 | intron-variant | RNF212B | GRCh38.p7 | 14:23186593 | AACCTTGTGATCCAC[C/T]CGCCTCGGCCTCCCA | 100507650 |
rs112900184 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | RNF212B | GRCh38.p7 | 14:23230218 | AAACCTTATCAGATA[G/T]ATGATTTACTAATAT | 100507650 |
rs112901482 | snp | A/G | 0.26078 | 0.249767 | intron-variant | RNF212B | GRCh38.p7 | 14:23256877 | AATTATTTTTTGGCC[A/G]GGCATGGTGGCTCAC | 100507650 |
rs112942248 | in-del | -/A | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23259017 | CGAGACTCTGTTTCT[-/A]AAAAAAAAAAAATTT | 100507650 |
rs113034894 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23216464 | AATAAGTACATTAAA[C/T]TTAAATGGTTTAACT | 100507650 |
rs113091529 | snp | A/G | 0.257454 | 0.249889 | intron-variant | RNF212B | GRCh38.p7 | 14:23238632 | AGTCCCAGCTACTCC[A/G]GAGGCTGAGGTGGGA | 100507650 |
rs113099525 | in-del | -/AT/T | 0.511465 | 0.191219 | intron-variant | RNF212B | GRCh38.p7 | 14:23218375 | CTATCTCAAAAAAAA[-/AT/T]AAATAAATAAAAAGA | 100507650 |
rs113113199 | in-del | -/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23186346 | ATTAAATTTTGAGCA[-/T]TTTTTTTTTTTTTTG | 100507650 |
rs113119233 | snp | A/G | 0.046775 | 0.145601 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214222 | ACTAAGGCTGGGCAT[A/G]GCGGCTCAAGCCTGT | 100507650 |
rs113161009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212B | GRCh38.p7 | 14:23222508 | AAAGTCTCCCAATAA[A/G]GAAAAGCCTGAGACC | 100507650 |
rs113168237 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | RNF212B | GRCh38.p7 | 14:23219606 | CCTCCCAAGTAGCTG[A/G]AATGATAGGCGTGCA | 100507650 |
rs113181269 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195974 | CTCTTTTCACTGTGC[C/T]ACGGGAGAAAAAAGG | 100507650 |
rs113199228 | in-del | -/AACACGGTGAAACCCCGTC | 0.0283406 | 0.115616 | intron-variant | RNF212B | GRCh38.p7 | 14:23218180 | GAGACCCTCTTGGCT[-/AACACGGTGAAACCCCGTC]TCTACTAAAAATACA | 100507650 |
rs113212464 | snp | C/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23243874 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 100507650 |
rs113220943 | in-del | -/GC | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23243720 | AAAAAAAAAAAAAAA[-/GC]AAGCAAGCAAGCAAG | 100507650 |
rs113252658 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23221224 | AAACCCTGTCTCTAC[C/T]GAAAATAGGAAAAAA | 100507650 |
rs113272723 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF212B | GRCh38.p7 | 14:23187363 | CCTACTCCCCCCTTT[A/T]TTAGAGACAAGGTCT | 100507650 |
rs113374158 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23220268 | CAGGCAAGGTGGCTT[A/T]TGCCTGTAATTTCAG | 100507650 |
rs113399445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF212B | GRCh38.p7 | 14:23272733 | CAGTGGTGTCTGTCT[C/T]GATAAGCTTCATACA | 100507650 |
rs113457346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212B | GRCh38.p7 | 14:23239274 | CACGTTGGCCAGGCT[A/G]GTCTTGAACTCCTGG | 100507650 |
rs113459800 | snp | C/T | 0.213937 | 0.247385 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23208662 | AACTCAGGGTGAGTC[C/T]GCAGTGCAAAGTGAA | 100507650 |
rs113470620 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF212B | GRCh38.p7 | 14:23254066 | GGAGAACGGCTAGAT[C/T]CCAGGAGTTTGAGAT | 100507650 |
rs113481207 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23217101 | CATTTCTGAACCTGC[C/T]ATGGACCAGAGTGGA | 100507650 |
rs113536128 | snp | A/G | 0.26326 | 0.249648 | intron-variant | RNF212B | GRCh38.p7 | 14:23266691 | GCTGAGATTACAGGC[A/G]TGAGCCACCACACCC | 100507650 |
rs113548803 | snp | A/G | 0.0209421 | 0.100162 | intron-variant, nc-transcript-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23199732 | AAAACAACAACAAAC[A/G]AAAGAACATTCTTGG | 100507650 |
rs113554615 | in-del | -/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23265997 | TGTGTTTTTTTTTGA[-/G]ATGGGGTCTCACTCT | 100507650 |
rs113567062 | snp | A/G | 0.236724 | 0.249647 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209019 | CGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 100507650 |
rs113591281 | snp | C/G | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23252096 | TGTCAGGGGTTGGGG[C/G]GCGTGGGAAGAAAGG | 100507650 |
rs113619264 | snp | C/G | 0.0539704 | 0.155153 | intron-variant | RNF212B | GRCh38.p7 | 14:23219903 | AACACACAACAAGGG[C/G]CTGGGCACGGTGGCT | 100507650 |
rs113621122 | in-del | -/T | 0.5 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203483 | TACTTTTAGTCCCCC[-/T]TTTTTTTTTTTTTGA | 100507650 |
rs113629984 | snp | A/G | 0.5 | 0 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23202952 | AACTCAATGTTACAA[A/G]GACTTTATTTTATTT | 100507650 |
rs113642577 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | RNF212B | GRCh38.p7 | 14:23223634 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 100507650 |
rs113648285 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | RNF212B | GRCh38.p7 | 14:23219191 | ACAAGAAATGCTAAA[C/T]GGAGTTCTTCAATCT | 100507650 |
rs113676327 | snp | C/T | 0.046775 | 0.145601 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214221 | AACTAAGGCTGGGCA[C/T]GGCGGCTCAAGCCTG | 100507650 |
rs113701708 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23192858 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 100507650 |
rs113842189 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | RNF212B | GRCh38.p7 | 14:23219023 | GAAGACTTACAAGCC[C/T]GGAGAGAGTGGCATG | 100507650 |
rs113848305 | snp | A/C | 0 | 0 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23184099 | TCTTCGAGTTTCCTA[A/C]AAATAGGGGGAATCG | 100507650 |
rs113859440 | snp | G/T | 0.5 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23240905 | ACCAATTTTATGTAA[G/T]CCTCACCACAAGCCC | 100507650 |
rs113872988 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF212B | GRCh38.p7 | 14:23228581 | TTGAGCCCAGGACTT[C/G]CAGGTTGCAGTGACT | 100507650 |
rs113873723 | in-del | -/T | 0.499527 | 0.0153681 | intron-variant | RNF212B | GRCh38.p7 | 14:23257162 | GTCACACACACACAA[-/T]AAAAAATAAAATAAA | 100507650 |
rs113879977 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | RNF212B | GRCh38.p7 | 14:23251628 | CGAGACCAGCCTGGC[C/T]AACATGGTGAAACCC | 100507650 |
rs113922819 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | RNF212B | GRCh38.p7 | 14:23219970 | AGGTGGATCGTTTGA[C/G]GTCAGGAGTTCGAGA | 100507650 |
rs113949295 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF212B | GRCh38.p7 | 14:23223449 | CAACCTCCGCCTCAC[A/G]GGTTCACGCCATTCT | 100507650 |
rs113991587 | snp | A/C | | | intron-variant | RNF212B | GRCh38.p7 | 14:23230622 | TCGCGCCACTGCACT[A/C]CAGCCTGGACGACAG | 100507650 |
rs114075158 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | RNF212B | GRCh38.p7 | 14:23229992 | AATCTTCTCCAATGT[A/C]TCCTTTTAAAGTTGT | 100507650 |
rs114113457 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23218091 | TGAAAATTGCAGGCC[A/G]GGCGCTGTGGCTCAT | 100507650 |
rs114146292 | snp | A/G | 0.109108 | 0.206518 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23215290 | GCCGTGCAGAACTGT[A/G]AGTCAATTAAATCTC | 100507650 |
rs114165456 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23221416 | CATTCTATAATGATA[A/C]AGGGGTCAATTCAGC | 100507650 |
rs114185968 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23207538 | GATCAGGCATTCTCT[A/G]TAGAGGGTATTTTCA | 100507650 |
rs114210812 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF212B | GRCh38.p7 | 14:23249214 | GATTTGATCTCATCA[A/G]TAGACCAGAGCTTCT | 100507650 |
rs114212673 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNF212B | GRCh38.p7 | 14:23266070 | CCACCTTCGCCTCCC[A/G]GGTTCAGCCTCCCAA | 100507650 |
rs114237040 | snp | C/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23226812 | TTCTTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTA | 100507650 |
rs114247555 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | RNF212B | GRCh38.p7 | 14:23229030 | CTTCCTATCTCTCAT[A/T]CCCCTAGTTCCTGCT | 100507650 |
rs114249093 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200215 | ATAGGCTTTTAAATG[A/G]GCTTTGATGAAACTT | 100507650 |
rs114254540 | snp | C/T | 0.164873 | 0.23506 | intron-variant | RNF212B | GRCh38.p7 | 14:23194555 | CCACCCTGGGCAACA[C/T]GGTGAAACTGCATCT | 100507650 |
rs114409404 | snp | A/C/G | 0.0626037 | 0.165477 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23204845 | ATTGATTCTACCCAT[A/C/G]CATGAGCATGGGGTA | 100507650 |
rs114490160 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | RNF212B | GRCh38.p7 | 14:23248051 | TCTTTGCTTCCAAGA[A/T]AATGCCTTCTTGCTG | 100507650 |
rs114495516 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214059 | GCCCAGGAGTTCGAG[A/G]TTGTAGTGTGCTGTA | 100507650 |
rs114609236 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RNF212B | GRCh38.p7 | 14:23221987 | TGGGATATAGTGAAA[A/G]CAGTATTAAGAGGGA | 100507650 |
rs114624142 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | RNF212B | GRCh38.p7 | 14:23218694 | AAAATAGCCTCAAAA[C/G]GGCAAATGTGAGTTA | 100507650 |
rs114645978 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF212B | GRCh38.p7 | 14:23250185 | TGATTTCTACACTTT[A/G]AAAACTAAGTTAGGC | 100507650 |
rs114658057 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | RNF212B | GRCh38.p7 | 14:23228334 | AGCAACTCTGCAAAA[C/G]AACAGGCTGGCCAGG | 100507650 |
rs114709939 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | RNF212B | GRCh38.p7 | 14:23223979 | AAATAAAAAAGTAAT[A/C]TTATTTACAACAGCC | 100507650 |
rs114752063 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RNF212B | GRCh38.p7 | 14:23223154 | AAATCAATATACGTC[A/G]TACATCATATCAATA | 100507650 |
rs114761390 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | RNF212B | GRCh38.p7 | 14:23224240 | TATAGAATGTCAAAA[A/T]AAAAAAGCTATCCTA | 100507650 |
rs114764308 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23212266 | CTTCAACATTATGCC[A/G]ATGGCTATGGCCACT | 100507650 |
rs114807922 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | RNF212B | GRCh38.p7 | 14:23222451 | AAGAAAACCAAAACC[C/T]AAACAGAAAAATAAC | 100507650 |
rs114949924 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23204869 | TGGGGTATATTTTCA[C/T]TTGTTTCTGTCGTCT | 100507650 |
rs115009908 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | RNF212B | GRCh38.p7 | 14:23221428 | ATAAAGGGGTCAATT[C/T]AGCATGAGAGTGTAA | 100507650 |
rs115017737 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23206892 | GATAACTGAGAAGAA[A/G]AAGAAAAACAAACTT | 100507650 |
rs115049677 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | RNF212B, LOC105370406 | GRCh38.p7 | 14:23199303 | GACTTGAAGTGGGGA[A/G]GAGGCTTCCAGGTCA | 100507650 |
rs115075063 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203282 | TACAATAATAGTCTC[C/T]AATCTCATCTACCAC | 100507650 |
rs115178154 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23237689 | ACCTTTTTGTTTCCA[C/T]AGTAACATGTATGGG | 100507650 |
rs115209322 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | RNF212B | GRCh38.p7 | 14:23189995 | CATCTACTCTATCAG[G/T]TGGACCACCGGTGGT | 100507650 |
rs115292557 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF212B | GRCh38.p7 | 14:23238292 | CACTTGCTGGTGAAA[A/G]TTAGTGTATCACGAT | 100507650 |
rs115328395 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF212B | GRCh38.p7 | 14:23227633 | TTGAGACTAGTTCTC[A/G]CCCTGTCACCCAGGC | 100507650 |
rs115333390 | snp | C/T | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214458 | CAAATTGCGCCAATG[C/T]ACTCCGGCCTGGGCA | 100507650 |
rs115486126 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF212B | GRCh38.p7 | 14:23252171 | AAGTCCCCATTTTGA[C/T]GCTACCTAGGACCCA | 100507650 |
rs115535354 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF212B | GRCh38.p7 | 14:23219971 | GGTGGATCGTTTGAC[A/G]TCAGGAGTTCGAGAC | 100507650 |
rs115555984 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | RNF212B | GRCh38.p7 | 14:23235525 | CAAAACTGCCTTGCC[A/C]CTTCAAGGAAAACCA | 100507650 |
rs115565115 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23197245 | AAAAATATAACGAGA[A/G]GCCAGGCACTGTGGC | 100507650 |
rs115572952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210270 | ATTTTCCTTAAAACC[A/G]TCAAGCTCATGAAAC | 100507650 |
rs115602423 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | RNF212B | GRCh38.p7 | 14:23224174 | GCTACCCAAAGTAAT[C/G]TACAGATTCAATGCA | 100507650 |
rs115752347 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | RNF212B | GRCh38.p7 | 14:23221306 | GGATGTAAAAAGATG[G/T]GCCATGACAATGGAA | 100507650 |
rs115778121 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RNF212B | GRCh38.p7 | 14:23234798 | GAATTAAGATTACTC[A/G]GGCATGATGCTACAT | 100507650 |
rs115897383 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | RNF212B | GRCh38.p7 | 14:23190383 | GAGTGCGTGCTTTCC[A/G]CTCCAAACCTGATTT | 100507650 |
rs115900278 | snp | A/T | 0.039522 | 0.134904 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23184494 | CCCTGTCTCAAAAAC[A/T]AAACAAAACAAAAAG | 100507650 |
rs115949741 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210986 | TCACTTTGGGAGGCC[A/G]AGGTGGACAGATCAC | 100507650 |
rs115951747 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205071 | GTCCTGAACATCCCT[A/C]CTTCTTAATCAACCA | 100507650 |
rs116059090 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | RNF212B | GRCh38.p7 | 14:23265310 | AAAAGAAGGTTCACA[G/T]GATGCTGATTGTTGG | 100507650 |
rs116104975 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF212B | GRCh38.p7 | 14:23190733 | GCCAGAATGATCCTT[C/T]GTAATCACAGATCAG | 100507650 |
rs116167411 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF212B | GRCh38.p7 | 14:23224487 | GGCAAGGATGCCAAC[A/G]ACGTACACTGGGGAA | 100507650 |
rs116237035 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RNF212B | GRCh38.p7 | 14:23240907 | CAATTTTATGTAAGC[C/T]TCACCACAAGCCCAG | 100507650 |
rs116251303 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF212B | GRCh38.p7 | 14:23264509 | TCTTTGACTAGTATG[C/T]CCACTGCAGTAGAAC | 100507650 |
rs116324557 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF212B | GRCh38.p7 | 14:23248735 | ATGAGCCATCACGCC[C/T]GGCCCCCAAGCCTCT | 100507650 |
rs116353153 | snp | A/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23257164 | TCACACACACACAAA[A/T]AAAATAAAATAAAAT | 100507650 |
rs116409043 | snp | C/T | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23215967 | CATTAAAACATTTGC[C/T]GGGTGTGGTGGCTCA | 100507650 |
rs116426468 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200472 | ATGGGATTACAGGTG[C/T]GTGCCACTGTGTCTG | 100507650 |
rs116442694 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RNF212B | GRCh38.p7 | 14:23188639 | GCCTGGCAAATTTTT[A/T]AAAAATTTTTAGTAA | 100507650 |
rs116450656 | snp | C/T | 0.230896 | 0.249269 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23207926 | TAGGCAGACTCTAAG[C/T]GGAGAGGGGGCTTCC | 100507650 |
rs116483162 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | RNF212B | GRCh38.p7 | 14:23219168 | TTCATTAACACCAGA[A/C]CTGTCTTACAAGAAA | 100507650 |
rs116510179 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | RNF212B | GRCh38.p7 | 14:23234433 | TAAGAGTATTTACTA[A/T]TATTTTCGTCTGGTA | 100507650 |
rs116577138 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF212B | GRCh38.p7 | 14:23258400 | GAGTGCTGAGCTCTC[C/T]AGTTCTGGGAAGTTG | 100507650 |
rs116580013 | snp | A/G | 0.0988009 | 0.199095 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23215186 | TTGGCAGTTCCCCCC[A/G]CCCCTCTGCCTCTCC | 100507650 |
rs116640066 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236868 | ATAAATTTCTGGGAT[C/T]ATAGTTTCCGTGAAA | 100507650 |
rs116823274 | snp | A/C | 0.0182019 | 0.0936463 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236558 | CAAAAAAACCCCAAA[A/C]AACAACAACAAACAA | 100507650 |
rs116871688 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212B | GRCh38.p7 | 14:23218945 | AGGATTCTAAAAGTA[C/T]GAGGAGAAAAGAAAC | 100507650 |
rs116877642 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | RNF212B | GRCh38.p7 | 14:23217519 | AGTGGTGGTTGCCAC[A/G]TGGGTGCTTGCATCG | 100507650 |
rs116921841 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RNF212B | GRCh38.p7 | 14:23219413 | AAACATAAAGAGAAA[G/T]AACAAAAAGTTTAAA | 100507650 |
rs116922756 | snp | C/T | 0.110519 | 0.207473 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23197427 | AGCTACTTGGGAGGT[C/T]GAGGCATGAGAATTG | 100507650 |
rs116966948 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200515 | AATTTCAGCAGAGAT[A/G]GGGTTTCACCATGTT | 100507650 |
rs117064099 | snp | A/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23226826 | TCTTTTTTTTTTTTT[A/T]AATAGAGAGGAGGTC | 100507650 |
rs117086416 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | RNF212B | GRCh38.p7 | 14:23261571 | ATTCATTCAATATTA[A/T]GTGCCTACTGTTTAT | 100507650 |
rs117224095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF212B | GRCh38.p7 | 14:23257200 | AAAATTATTTTTCAT[A/G]GAGACAGGGTCTTGC | 100507650 |
rs117225862 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | RNF212B | GRCh38.p7 | 14:23218637 | AGAGTCAGAGGAGAC[A/G]AAAGAAAATAAAAAA | 100507650 |
rs117242259 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23201780 | AGGATTTCAAAAATA[A/G]TGAAAACCTTCATTT | 100507650 |
rs117256132 | snp | A/C | 0.49655 | 0.04139 | intron-variant | RNF212B | GRCh38.p7 | 14:23257160 | TCAGTCACACACACA[A/C]AAAAAAAATAAAATA | 100507650 |
rs117273234 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF212B | GRCh38.p7 | 14:23219513 | GTCTCACTCTGTCGC[A/G]CAGACTGGAGTGCAG | 100507650 |
rs117315937 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF212B | GRCh38.p7 | 14:23226715 | CTTCGTGGTGCTGGA[C/T]CAGTCTCGTCTTATC | 100507650 |
rs117343942 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | RNF212B | GRCh38.p7 | 14:23188556 | ACTGCAACCTTGAAC[C/T]TCTGGGTTCAAGTGA | 100507650 |
rs117345190 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RNF212B | GRCh38.p7 | 14:23222362 | CTATGAACAACTATA[A/T]GTCAATAAATTGGAA | 100507650 |
rs117397554 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | RNF212B | GRCh38.p7 | 14:23191328 | CACTGCACCCTGGGC[A/G]ACAAAGTGAGACCCT | 100507650 |
rs117416903 | snp | C/T | 0.0154087 | 0.0864114 | intron-variant | RNF212B | GRCh38.p7 | 14:23243341 | TGCCACAAACTGTCT[C/T]ATCCCATTCCTGGCC | 100507650 |
rs117684525 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF212B | GRCh38.p7 | 14:23187542 | CAGAGACAAGTTAGA[C/T]GTGTCTGCTAATGCA | 100507650 |
rs117713013 | snp | A/C | 0.440471 | 0.161928 | intron-variant | RNF212B | GRCh38.p7 | 14:23257156 | AGACTCAGTCACACA[A/C]ACACAAAAAAAATAA | 100507650 |
rs117715568 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF212B | GRCh38.p7 | 14:23221777 | AAAAAAACTGAAATA[A/G]TATCAGGCATCTTCT | 100507650 |
rs117735861 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF212B | GRCh38.p7 | 14:23188646 | AAATTTTTAAAAAAT[G/T]TTTAGTAAAGATGAG | 100507650 |
rs117790239 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF212B | GRCh38.p7 | 14:23254068 | AGAACGGCTAGATCC[C/T]AGGAGTTTGAGATCA | 100507650 |
rs117894777 | snp | G/T | 0.203882 | 0.245709 | intron-variant | RNF212B | GRCh38.p7 | 14:23218811 | AACTTCCTAAACCTA[G/T]AGAAAGATATCAACA | 100507650 |
rs117897838 | snp | A/C | 0.441158 | 0.161117 | intron-variant | RNF212B | GRCh38.p7 | 14:23257158 | ACTCAGTCACACACA[A/C]ACAAAAAAAATAAAA | 100507650 |
rs117899116 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260963 | AATTTACTCAGCAAG[G/T]TCATTTTTACTTCCT | 100507650 |
rs117991348 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF212B | GRCh38.p7 | 14:23227158 | AGTCAAGGGTATATG[A/G]AACCTTTCTACACTA | 100507650 |
rs118080461 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF212B | GRCh38.p7 | 14:23227917 | AAAAAGTTCTAAAAA[C/T]ATAAAAGTTTTTTAA | 100507650 |
rs118115930 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23261149 | GCAACTTAGAACTTA[C/T]GAAAAGGGGCAAAGG | 100507650 |
rs118158815 | snp | A/C | 0.177182 | 0.23916 | intron-variant | RNF212B | GRCh38.p7 | 14:23227857 | ACCCACCTCAGCCCC[A/C]CGAAGTGCTGGGATT | 100507650 |
rs118171536 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | RNF212B | GRCh38.p7 | 14:23222026 | GCTATAAGTGTCTAC[A/C]TCAAAAAGGAAGAAG | 100507650 |
rs137863195 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211651 | ATGAACAAATTTATC[A/C]CAGGAACACATAATT | 100507650 |
rs137907017 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF212B | GRCh38.p7 | 14:23265733 | TTCGTTTTGTTGAGA[A/G]TCTGTATTACTTCTT | 100507650 |
rs137925221 | snp | C/T | 0 | 0 | intron-variant | RNF212B | GRCh38.p7 | 14:23186956 | TTTTGCTTTGGTGTC[C/T]TAACTGTGCCTTTTA | 100507650 |
rs137935553 | in-del | -/T | 0.0554779 | 0.157039 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23212905 | TTTTGAAGTAATTTC[-/T]TTTTTTGCCAGCCTA | 100507650 |
rs137955211 | snp | A/C | 0.253264 | 0.249979 | intron-variant | RNF212B | GRCh38.p7 | 14:23238774 | AATAATAATAATAAT[A/C]ATAATAATCCCACAA | 100507650 |
rs138017132 | snp | C/T | 0.0111196 | 0.0737302 | utr-variant-3-prime, downstream-variant-500B | RNF212B, HOMEZ | GRCh38.p7 | 14:23273330 | TTCTTTTCCTTATTA[C/T]ACTTTTTTATTTGTC | 100507650 |
rs138134367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23268733 | CCACAGACTCATGAA[A/G]GGGAGAGGAAAGCAC | 100507650 |
rs138143748 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF212B | GRCh38.p7 | 14:23229852 | AAACTATATTCCCAA[G/T]AAAACATGCCCAACT | 100507650 |
rs138148364 | in-del | -/AAAACT | 0.261608 | 0.24973 | intron-variant | RNF212B | GRCh38.p7 | 14:23254339 | ACAAAAACAAAAACA[-/AAAACT]AAAACTAAAACTGGG | 100507650 |
rs138179941 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23215031 | TGTCCCCACACAAAT[C/G]TCATCTTGAATTGAA | 100507650 |
rs138201299 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23202096 | TCTCTACTAAAAATA[C/T]AAAAATTAGCCAAGC | 100507650 |
rs138225027 | snp | A/G | 0.000390549 | 0.0139686 | intron-variant | RNF212B | GRCh38.p7 | 14:23264682 | TAATGGTGAGGTGGG[A/G]GGAAAAGGGTGTCAG | 100507650 |
rs138247393 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF212B | GRCh38.p7 | 14:23192377 | AAGGATGAGTTCATG[C/T]CCTTTGTAGGGACAT | 100507650 |
rs138247508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23228218 | GCCTGGGTGACGAGA[C/G]CGAAACTCTGTCTAA | 100507650 |
rs138381712 | in-del | -/ATATGGTAAGCTT | 0.448836 | 0.15154 | upstream-variant-2KB, intron-variant | SLC7A8, RNF212B | GRCh38.p7 | 14:23185610 | TGCAAACTGATAACG[-/ATATGGTAAGCTT]TAGCCCTCTCAAATT | 100507650 |
rs138395251 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | RNF212B | GRCh38.p7 | 14:23187881 | AGCCAGTAGTTTTAG[A/T]TGCCTTTACTTCATT | 100507650 |
rs138405188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF212B | GRCh38.p7 | 14:23223173 | ATCATATCAATAGAA[C/T]GAAGGACAAACCATA | 100507650 |
rs138424719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23191565 | AAAAGTTTTATCTTT[C/T]AGATATATATGCCAA | 100507650 |
rs138602611 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23204848 | GATTCTACCCATCCA[C/T]GAGCATGGGGTATAT | 100507650 |
rs138602968 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF212B | GRCh38.p7 | 14:23243185 | TACTAGATTGTTGCC[A/G]TGTACTTTAAGTCTT | 100507650 |
rs138629773 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23202617 | AGCACTTCGGGAGGC[C/T]GAGGCGGGTGGATCA | 100507650 |
rs138653398 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RNF212B | GRCh38.p7 | 14:23235313 | TATGATTGTGCCACT[A/G]AACTCTAGCCTGGGC | 100507650 |
rs138695526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RNF212B, LOC105370406 | GRCh38.p7 | 14:23199258 | CAATATATGTAAGAA[A/G]TACATTGGTTCAGTC | 100507650 |
rs138713179 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203966 | TGGTTTTGATTTGCA[G/T]TTCCCTGATCACTAG | 100507650 |
rs138761490 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF212B | GRCh38.p7 | 14:23261737 | GAGGCCAAGGTGGGC[A/G]GATCATGGGGTCAGG | 100507650 |
rs138790980 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RNF212B | GRCh38.p7 | 14:23232475 | TGAGAAGTGAGGAGC[C/G]CCTCCGCCCGGCAGC | 100507650 |
rs138917685 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23243433 | GGGCGTGGTGGCTCA[A/G]GCCTGTAATCCCAGC | 100507650 |
rs138919960 | snp | C/G | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213991 | TGCTTCAATGAATTG[C/G]GTGTACCTGTAGTCC | 100507650 |
rs138985009 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF212B | GRCh38.p7 | 14:23216952 | CCACTTATACAACAT[C/T]TTAAATGATAAAATT | 100507650 |
rs138988759 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNF212B | GRCh38.p7 | 14:23219026 | GACTTACAAGCCCGG[A/G]GAGAGTGGCATGACA | 100507650 |
rs138993625 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200476 | GATTACAGGTGCGTG[C/T]CACTGTGTCTGGCTA | 100507650 |
rs139001020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260753 | CTTTCTTGACTCCTG[A/G]CTGTGTGAACTCTGA | 100507650 |
rs139024056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23212400 | GTTTTTACTCACAGA[C/T]GGCATGATTATCTAT | 100507650 |
rs139077040 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF212B | GRCh38.p7 | 14:23262105 | GAAGTTACAGTCTAA[C/T]GTTCTTTTGTCCTTC | 100507650 |
rs139083443 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | RNF212B | GRCh38.p7 | 14:23222720 | TGATGAATATTGATG[C/T]GAAAATGCTAGTAAA | 100507650 |
rs139103755 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF212B | GRCh38.p7 | 14:23233887 | GGATCACCTGAGGTC[A/T]GGAGTTCGAGACCAG | 100507650 |
rs139123561 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23197156 | GCCCAGGAGAAAGAT[C/T]TGGGCTAAAAAATCA | 100507650 |
rs139124308 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF212B | GRCh38.p7 | 14:23225117 | AAGATATCATCTTAC[C/T]CCAGTTAAAATGGCT | 100507650 |
rs139147929 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF212B | GRCh38.p7 | 14:23257403 | AAAAAATAGACTAGA[A/G]TAAATTCTTATCTAT | 100507650 |
rs139165117 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF212B | GRCh38.p7 | 14:23244937 | CATATGTTGGCATAC[A/G]ATTGACTTGATCAGG | 100507650 |
rs139180088 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF212B | GRCh38.p7 | 14:23249053 | CCAATAAAACTTATT[G/T]ACAAAAACAGACAGC | 100507650 |
rs139223165 | snp | C/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23258934 | CTCACACCTGTAATC[C/G]CAGCACTTTGGGTGA | 100507650 |
rs139272525 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23242113 | AAAAAAAAAAGAAAA[A/G]AAAAAGAAAAAGAAA | 100507650 |
rs139318359 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210605 | ACATAGTGAAACCCC[A/G]TCTCTACTAAAAATG | 100507650 |
rs139384961 | in-del | -/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23187675 | GAGGTTACCAACAAA[-/G]GGACCCAAATCTCTC | 100507650 |
rs139422700 | snp | G/T | | | synonymous-codon, missense, intron-variant, nc-transcript-variant | RNF212B | GRCh38.p7 | 14:23270619 | GAGGGAGAGCACAAC[G/T]ACACTAGAGAGTCTT | 100507650 |
rs139451786 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF212B | GRCh38.p7 | 14:23255376 | GTAGGAATCCAGAGC[A/G]TGAAGACCATGATAT | 100507650 |
rs139510113 | snp | C/G | 0.0146672 | 0.084371 | utr-variant-5-prime, intron-variant | RNF212B | GRCh38.p7 | 14:23238020 | TGGATGATTTCCTGA[C/G]ATCTGAGGCTTTCTG | 100507650 |
rs139548284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23240641 | AAATTATTTAGCAAA[C/T]GATTTAGCAAATCTA | 100507650 |
rs139585390 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23213026 | ACACTAAAAATTATA[A/G]CACAGGCCGGGCATG | 100507650 |
rs139594837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23193629 | GAACTAGCGATAGTG[A/G]CACAGAAAAGCAAGC | 100507650 |
rs139613192 | in-del | -/AAA | 0.126219 | 0.217206 | intron-variant, downstream-variant-500B | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195023 | TAGCAATCAACAATT[-/AAA]ATAGAAAATAAGGTA | 100507650 |
rs139634901 | snp | C/T | 0.00676609 | 0.0577691 | downstream-variant-500B, utr-variant-3-prime | RNF212B, HOMEZ | GRCh38.p7 | 14:23274766 | AAAAAAGTAGCCGGG[C/T]GTGGTGGCAGGTGCC | 100507650 |
rs139651359 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF212B | GRCh38.p7 | 14:23216114 | AGCTGAGTGTGGTGG[C/T]GGGTGCCTGTAGTCC | 100507650 |
rs139691529 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23184468 | ACTCCAGCCTGGGAG[A/G]TAGAGCAAGACCCTG | 100507650 |
rs139713000 | in-del | -/T | 0.250253 | 0.251622 | intron-variant | RNF212B | GRCh38.p7 | 14:23262646 | GATTAGAGCCGCCTC[-/T]TTTTTTTTTCCCTTG | 100507650 |
rs139750238 | snp | C/G | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB | SLC7A8, RNF212B | GRCh38.p7 | 14:23183614 | CCGTTCTACTGCACA[C/G]CCGGCCCCATCCCTC | 100507650 |
rs139792783 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195328 | AAATGTAAAGTCTCA[A/C]AGATTTAGAAAACAT | 100507650 |
rs139834627 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | RNF212B | GRCh38.p7 | 14:23258276 | CCAGGAGGCAGAGGT[C/T]ACGGTGAGCCGAGAT | 100507650 |
rs139838752 | snp | C/T | 0.118235 | 0.212457 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23197440 | GTCGAGGCATGAGAA[C/T]TGCTTGAACCCGGGA | 100507650 |
rs139878774 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF212B | GRCh38.p7 | 14:23225882 | AAGCACGAGGGGATC[A/G]ATACCCTATCTTTCA | 100507650 |
rs139978932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23200250 | CCATAGGAGGAATCT[C/G]AGATAAGATTTTAAA | 100507650 |
rs139991831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23189309 | CTCCCCACATCCTCT[A/G]CCTTCCCTCCCATTG | 100507650 |
rs140018310 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23207567 | CAGACCTCAGCAAAT[A/T]GTCCTATTAGTTTGA | 100507650 |
rs140038320 | snp | A/G | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210182 | TAAACAAATACCCCT[A/G]TGACTAAGTTGAATC | 100507650 |
rs140073001 | snp | C/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23234093 | TGTATACCATGTGTA[C/T]GAAGGAACACTCAAA | 100507650 |
rs140078361 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF212B | GRCh38.p7 | 14:23241500 | ACAATCTTGGCTCAC[C/T]GCAACCTCTGCTTCC | 100507650 |
rs140114129 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | RNF212B | GRCh38.p7 | 14:23236900 | TCTGGAAAATGTTGT[G/T]TCATTGTTATCTAGA | 100507650 |
rs140123314 | snp | C/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23190078 | GTGGCCAGCTAATGG[C/G]TCTGGAGCACCCACT | 100507650 |
rs140157493 | in-del | -/A | | | intron-variant | RNF212B | GRCh38.p7 | 14:23252385 | AGCCCATTAAAAAAA[-/A]GTTTATTATGATTTC | 100507650 |
rs140261235 | in-del | -/AATAAT | | | intron-variant | RNF212B | GRCh38.p7 | 14:23238738 | CAGACCCTGTCTCAA[-/AATAAT]AATAATAATAATAAT | 100507650 |
rs140267102 | snp | G/T | | | intron-variant | RNF212B | GRCh38.p7 | 14:23256198 | ATTTTGACATAATTT[G/T]ACTCCTGACTAATCC | 100507650 |
rs140389449 | snp | C/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23220191 | CTGTCTCGGGAAAAA[C/G]AAAAACAAAAACAAA | 100507650 |
rs140420240 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203132 | ATCTCTCATCCCCCC[A/G]ACCCTCACCCCCAAG | 100507650 |
rs140442894 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23201777 | TCAAGGATTTCAAAA[A/G]TAGTGAAAACCTTCA | 100507650 |
rs140463391 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF212B | GRCh38.p7 | 14:23189573 | TTTGGGAGGCCAAGG[C/T]GGGAGGATCGCTTGA | 100507650 |
rs140487493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212B | GRCh38.p7 | 14:23248661 | TGGTCAGGCTAGTCT[C/T]GAATTCCTGACCTCG | 100507650 |
rs140538453 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23260085 | TATAACAAGCACACT[A/G]TAGTAAATGGATGAG | 100507650 |
rs140552394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23252728 | TCTCATGCTGATTCA[A/G]TTCCTCTGTGGGGGT | 100507650 |
rs140610060 | in-del | -/C | 0.095934 | 0.196885 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23209215 | TAGCAGTAAGGACGA[-/C]CAGAGGTCACTCTCG | 100507650 |
rs140613416 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF212B | GRCh38.p7 | 14:23235100 | GCCTGTAATCCCAGC[A/T]ACTTGGGAAGCTGAG | 100507650 |
rs140682579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23187497 | GGGACTACAGATGTG[C/T]GCCACCACACCCGGG | 100507650 |
rs140740931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23216226 | ACTCCAGCCTGGGTG[A/T]CAGAGCGAGACTCCA | 100507650 |
rs140753007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23246740 | ATCTGAAAACTGTAC[A/T]TTATTAGTTTAAAGA | 100507650 |
rs140881744 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23203344 | ATTTGGGTTGGTTCC[A/G]CGATTTTGCAATTGT | 100507650 |
rs140899645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23266999 | TTTGAGACAGAGTCT[C/T]GTGCTGTTGTTGATG | 100507650 |
rs140934507 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF212B | GRCh38.p7 | 14:23232212 | GGAGCGTCTCTGCCC[A/G]GCTGCCCATCGTCTG | 100507650 |
rs140962722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF212B | GRCh38.p7 | 14:23269998 | AGGAATGGAGCTTCA[A/C]CTATAGACACATATA | 100507650 |
rs140970941 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23205562 | TTATAACTGAGACAG[C/T]GGAAAAAGTTTTGAC | 100507650 |
rs140982142 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF212B | GRCh38.p7 | 14:23235304 | GTAGCAAGCTATGAT[C/T]GTGCCACTAAACTCT | 100507650 |
rs141061467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23195499 | GCTCTGGAACCAATT[A/G]TTTTGTAATGCTCTT | 100507650 |
rs141141266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212B | GRCh38.p7 | 14:23233835 | GGCATGGTGGCTCAT[A/G]CCTGTAATCCCAGCA | 100507650 |
rs141164376 | snp | C/T | | | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211423 | CACTGGTAAGTTCTA[C/T]CAAACATTTAAGAAA | 100507650 |
rs141186052 | snp | A/C | 0.265453 | 0.249522 | intron-variant | RNF212B | GRCh38.p7 | 14:23254302 | AAAAACAAAACAAAA[A/C]AAAACAAAACAAAAC | 100507650 |
rs141220158 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RNF212B | GRCh38.p7 | 14:23269623 | AGACTAAGACAGGAG[G/T]ATCACTTGAGTTTAG | 100507650 |
rs141248043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23229588 | CCACCCCACCACATG[G/T]GAAATGATATTTCAC | 100507650 |
rs141278927 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23202207 | AGTGAGCCGAGATTG[C/T]GCAACTGCACTCTAG | 100507650 |
rs141364337 | snp | A/G | | | intron-variant | RNF212B | GRCh38.p7 | 14:23242102 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAGAAAA | 100507650 |
rs141450610 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23196624 | TTTAAAATATTTTTA[G/T]AGAGATGGGGTCTTG | 100507650 |
rs141514309 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | RNF212B | GRCh38.p7 | 14:23190152 | GGCTGGATCCTTTCC[-/T]TCTCCAATCTCTTCT | 100507650 |
rs141515427 | in-del | -/G | 0.0232847 | 0.105357 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210597 | TCTTGCCAACATAGT[-/G]AAACCCCGTCTCTAC | 100507650 |
rs141541711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23263950 | AAACTTAGCTGGGCA[C/T]GGTGGTGCACGCCTG | 100507650 |
rs141586640 | in-del | -/TATATATATATATATATATATATATATA | | | intron-variant | RNF212B | GRCh38.p7 | 14:23229221 | GGCTGAATAATATTT[-/TATATATATATATATATATATATATATA]TATATATATATATAC | 100507650 |
rs141599278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23240130 | ACATTTATATATAAA[A/T]TGTTATAACAACCTG | 100507650 |
rs141617422 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23202933 | CCAGGAGTTAAAGCC[C/T]TCTAACTCAATGTTA | 100507650 |
rs141684295 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RNF212B | GRCh38.p7 | 14:23261137 | TCCGATTGGCTAGCA[A/G]CTTAGAACTTATGAA | 100507650 |
rs141685741 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23211834 | TTCAAGCATTTCTCT[C/T]GCCTCAGTCTCCCAA | 100507650 |
rs141730603 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF212B | GRCh38.p7 | 14:23261680 | TATATTTTTAGTATC[A/G]GCTGGGTGTGGTGGC | 100507650 |
rs141820107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212B | GRCh38.p7 | 14:23228192 | AGCTGAGATCGTGCC[A/G]TCACACTCCAGCCTG | 100507650 |
rs141859602 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF212B | GRCh38.p7 | 14:23231334 | TTTTCTCTGGGCAAT[A/C]AATTTTTGACAAAGG | 100507650 |
rs141860449 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23202708 | TACAAAAAATTAGCC[A/G]GGCATGGTGGTGGGC | 100507650 |
rs141877157 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | RNF212B | GRCh38.p7 | 14:23223176 | ATATCAATAGAACGA[A/C]GGACAAACCATATGA | 100507650 |
rs141886921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23264968 | CTAGGATTACAGGCA[C/T]GTGCCACCACGCCTG | 100507650 |
rs141984522 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF212B | GRCh38.p7 | 14:23218273 | CTCAGGAGGCTGAGA[C/T]AGGAGAATTGCTTGA | 100507650 |
rs142011963 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF212B | GRCh38.p7 | 14:23188611 | AGTTGGGACTACAGG[A/T]GCACACCACTATGCC | 100507650 |
rs142028519 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | RNF212B, LOC105370406 | GRCh38.p7 | 14:23210065 | CTGAGGCAGGAAAAT[G/T]GCTTGAACCTGGAAG | 100507650 |
rs142147720 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RNF212B | GRCh38.p7 | 14:23268258 | GGAATGAATCCTTCA[A/T]AAAGCTCCAACCCTG | 100507650 |
rs142194185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212B | GRCh38.p7 | 14:23220327 | GCTTGAGGCCCAGAG[C/T]TCAAGACCAGCCTGG | 100507650 |
rs142230704 | in-del | -/CTC | 0.0995161 | 0.199636 | intron-variant | RNF212B | GRCh38.p7 | 14:23219468 | AGCGCTCTCCTTCTT[-/CTC]CTTCTAGTTTTTTTT | 100507650 |
rs142237665 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF212B | GRCh38.p7 | 14:23242566 | AACTTAAAGTTAAGA[C/T]CTTTGGTATCTTGTA | 100507650 |
rs142255720 | snp | A/G | 0.0988009 | 0.199095 | intron-variant, upstream-variant-2KB | RNF212B, LOC105370406 | GRCh38.p7 | 14:23214383 | CCTGTAATCTCAGCT[A/G]CTTGGGAGGCTGAGT | 100507650 |
rs142278884 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | RNF212B | GRCh38.p7 | 14:23245531 | ATGGTCAAGTATCAA[C/G]ATAAAAGAAATGGAA | 100507650 |
rs142296617 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | RNF212B | GRCh38.p7 | 14:23186054 | GCAATGAGCCAAGAT[C/T]GCACCACTGCACTCC | 100507650 |