SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs959022 | snp | A/T | 0.431177 | 0.172264 | intron-variant | RNF19A | GRCh38.p7 | 8:100283764 | AGAAAAAATTCATAA[A/T]TTCACATCTAGCATT | 25897 |
rs962451 | snp | C/T | 0.430732 | 0.172731 | intron-variant | RNF19A | GRCh38.p7 | 8:100318782 | CGGATTTACATAGCC[C/T]AATTTGATAGCATGC | 25897 |
rs962452 | snp | A/G | 0.499587 | 0.0143711 | intron-variant | RNF19A | GRCh38.p7 | 8:100319141 | CCAAGACTCAAAGAT[A/G]GACATTCTATGGATG | 25897 |
rs1020171 | snp | C/T | 0.431325 | 0.172108 | intron-variant | RNF19A | GRCh38.p7 | 8:100276382 | ttttgaaatgtcaaa[C/T]agattagtggttgcc | 25897 |
rs1047901 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258056 | AATTTCATTTTTTTT[C/T]TTCATATGCAATGTG | 25897 |
rs1125706 | snp | A/T | 0.431029 | 0.17242 | intron-variant | RNF19A | GRCh38.p7 | 8:100314511 | TTCACTTAGGCTGTG[A/T]CACCAGGGAAGGGGC | 25897 |
rs1348062 | snp | C/G/T | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100327130 | TTTTCTGTTTTTAAT[C/G/T]TTAGCCTCGCTAACA | 25897 |
rs1371867 | snp | A/C | 0.495855 | 0.045338 | intron-variant | RNF19A | GRCh38.p7 | 8:100317981 | TGGATAGGGCCTAGA[A/C]CACCCCCTCCCCACC | 25897 |
rs1371868 | snp | C/T | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100318039 | GCTCCTTCCTCCCCT[C/T]AGATTTCCTTAAAGA | 25897 |
rs1440572 | snp | G/T | 0.181978 | 0.240568 | intron-variant | RNF19A | GRCh38.p7 | 8:100287125 | AAAAAAATAAAGAAG[G/T]TCATTTGAATTTATG | 25897 |
rs1548046 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | RNF19A | GRCh38.p7 | 8:100326539 | gcagtctagtgaggg[A/G]aactgaGGTAACCCC | 25897 |
rs1548047 | snp | A/C | 0.476574 | 0.105661 | intron-variant | RNF19A | GRCh38.p7 | 8:100327964 | GTAAATAAATCCTAG[A/C]AAACAGGTAGGCTCT | 25897 |
rs1612305 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF19A | GRCh38.p7 | 8:100260775 | AATTTTTCCTACTTA[C/T]CTATATGGCTATTGA | 25897 |
rs1612773 | snp | C/G | 0.496842 | 0.0396107 | intron-variant | RNF19A | GRCh38.p7 | 8:100325590 | ACACCTCTAGCCTAC[C/G]CCCTGGGTCCTCAAG | 25897 |
rs1616833 | snp | C/T | 0.499642 | 0.0133738 | intron-variant | RNF19A | GRCh38.p7 | 8:100259593 | ATCACCACTACCTAA[C/T]TTCAGAACATTTTCA | 25897 |
rs1619759 | snp | C/T | 0.429837 | 0.173662 | intron-variant | RNF19A | GRCh38.p7 | 8:100325332 | TCTTCCAAAAAGTAG[C/T]TACAATGTAACTGTG | 25897 |
rs1629834 | snp | A/G | 0.4231 | 0.180378 | intron-variant | RNF19A | GRCh38.p7 | 8:100305487 | TCATGATAATCTTTC[A/G]GATCTATTGGCTTAA | 25897 |
rs1660310 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100315698 | actctgttgtccagg[G/T]gggagtgcagtggtg | 25897 |
rs1660311 | snp | C/T | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100318351 | TATACTTAACTCACT[C/T]TTGGCTTAAATTCTC | 25897 |
rs1660312 | snp | C/G | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100318406 | AGATTGAATTTTTCT[C/G]GTGCTATATTTTATG | 25897 |
rs1660313 | snp | A/G | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100320484 | TAAAAGTTGAAAAAT[A/G]CTATAACCAACCTCT | 25897 |
rs1660314 | snp | C/T | 0.430732 | 0.172731 | intron-variant | RNF19A | GRCh38.p7 | 8:100320725 | TTAGATAAAATAATA[C/T]ACGTAAAGCATTTAG | 25897 |
rs1660315 | snp | A/G | 0.430732 | 0.172731 | intron-variant | RNF19A | GRCh38.p7 | 8:100320728 | gataaaataatatac[A/G]taaagcatttagcac | 25897 |
rs1660316 | snp | C/T | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100320821 | accaccaaaataaaa[C/T]aaatattgcaataaa | 25897 |
rs1660317 | snp | G/T | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100321024 | ataatctttttgctg[G/T]tggagagtcttgcct | 25897 |
rs1660318 | snp | C/T | 0.495596 | 0.0467178 | intron-variant | RNF19A | GRCh38.p7 | 8:100325051 | AGCTGGAATTACAGG[C/T]GCCTACCACCACAAC | 25897 |
rs1660319 | snp | A/G | 0.496681 | 0.0405994 | intron-variant | RNF19A | GRCh38.p7 | 8:100325302 | AGGGTTTTTGCAGAG[A/G]GTTTGGTTTCTGAGT | 25897 |
rs1660320 | snp | A/C | 0.496714 | 0.0404017 | intron-variant | RNF19A | GRCh38.p7 | 8:100325351 | AATGTAACTGTGTAA[A/C]TTTATAAATTATAAA | 25897 |
rs1660322 | snp | C/T | 0.379158 | 0.214052 | intron-variant | RNF19A | GRCh38.p7 | 8:100265412 | TACCAGAAGACAGGA[C/T]TGAATTCACTCAGCA | 25897 |
rs1660323 | snp | A/T | 0.431769 | 0.17164 | intron-variant | RNF19A | GRCh38.p7 | 8:100266496 | CGATCAGCTAATATA[A/T]TTTGAAATTTTTTAT | 25897 |
rs1660324 | snp | C/T | 0.431029 | 0.17242 | intron-variant | RNF19A | GRCh38.p7 | 8:100269043 | TATTTTTAAAAACTT[C/T]TCATAGTTAGGAGCT | 25897 |
rs1660326 | snp | A/G | 0.431916 | 0.171483 | intron-variant | RNF19A | GRCh38.p7 | 8:100278219 | GCCAAATAAGCACAT[A/G]GCTGCTTTGATAACA | 25897 |
rs1660327 | snp | A/C | 0.431029 | 0.17242 | intron-variant | RNF19A | GRCh38.p7 | 8:100279978 | TTTCTGATTTCTTTT[A/C]ATTTTTCATAACTTC | 25897 |
rs1660328 | snp | A/G | 0.499598 | 0.0141716 | intron-variant | RNF19A | GRCh38.p7 | 8:100291222 | TGTTCTAAGAATAAT[A/G]TGAAATTGACATGTG | 25897 |
rs1660329 | snp | G/T | 0.430434 | 0.173042 | intron-variant | RNF19A | GRCh38.p7 | 8:100291820 | GTCAAAATACTAAAT[G/T]TAAGAGCAGTGTACC | 25897 |
rs1660330 | snp | A/T | 0.430434 | 0.173042 | intron-variant | RNF19A | GRCh38.p7 | 8:100292787 | TTTTTTAATTTCTTA[A/T]TTTTGAGACATTTAT | 25897 |
rs1660331 | snp | C/T | 0.429837 | 0.173662 | intron-variant | RNF19A | GRCh38.p7 | 8:100297228 | TGAAAGAAAGCAATG[C/T]TACTAGATGTACAAT | 25897 |
rs1660332 | snp | C/T | 0.499539 | 0.0151687 | intron-variant | RNF19A | GRCh38.p7 | 8:100297262 | AATACCTTTCAATTA[C/T]TTCAATGTGTCCTTA | 25897 |
rs1660333 | snp | C/T | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100297761 | TCCACCATGAGATTT[C/T]GGGTTTTCTGTTACA | 25897 |
rs1660334 | snp | C/T | 0.430434 | 0.173042 | intron-variant | RNF19A | GRCh38.p7 | 8:100298052 | GAATTACAGTACCTA[C/T]AGTCCATAGATTATA | 25897 |
rs1660339 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100315098 | ttgtcatgttgccta[G/T]gcccaaatcatctgc | 25897 |
rs1660340 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100314932 | GTCTCGCAGCACCTA[G/T]GGAAGGCATGTCATG | 25897 |
rs1660341 | snp | A/C | | | intron-variant | RNF19A | GRCh38.p7 | 8:100314811 | CTACAAATAATGACA[A/C]TGAAGTACTTTATAC | 25897 |
rs1660342 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100314783 | TACACAAAAATTATA[G/T]AGGTAAGCATGGTTG | 25897 |
rs1660343 | snp | C/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100314694 | GAAATGAGCCACGCA[C/G]AGGAGAGGGGAGGGG | 25897 |
rs1660344 | snp | C/T | 0.430732 | 0.172731 | intron-variant | RNF19A | GRCh38.p7 | 8:100312431 | CCAGGCTAATTTTTG[C/T]ATTTTCGCCATCTTG | 25897 |
rs1660345 | snp | G/T | 0.429837 | 0.173662 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310534 | GCAGGTGAACCCTGA[G/T]AACACAAAGGAATGA | 25897 |
rs1660346 | snp | A/G | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100300269 | GAGTATTTTCTAAAG[A/G]CAGAAAAATCTAGGT | 25897 |
rs1660347 | snp | A/G | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100302752 | AGGGGGATCATGGAG[A/G]AATTACACTTTAAAG | 25897 |
rs1660348 | snp | A/G | 0.499587 | 0.0143711 | intron-variant | RNF19A | GRCh38.p7 | 8:100303020 | GTTTAGTCTCTGATC[A/G]TCATAGCACATGATA | 25897 |
rs1660349 | snp | A/G | 0.430732 | 0.172731 | intron-variant | RNF19A | GRCh38.p7 | 8:100307098 | TGGGCTTTTGCCCAA[A/G]GTGGCCTAATTTTTA | 25897 |
rs1660351 | snp | C/T | 0.431769 | 0.17164 | intron-variant | RNF19A | GRCh38.p7 | 8:100262806 | CTAAGGGAAGGACAA[C/T]GAAGAGAGTAAGAAG | 25897 |
rs1788164 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | RNF19A | GRCh38.p7 | 8:100334264 | GTGCTAATTTTGACT[C/T]TTCAACTATTTTGAA | 25897 |
rs1788166 | snp | A/G | 0.4231 | 0.180378 | intron-variant | RNF19A | GRCh38.p7 | 8:100305724 | TAAGTGCTAAGACTT[A/G]AAGAGTGAACAAAGA | 25897 |
rs1788167 | snp | C/T | 0.499575 | 0.0145705 | intron-variant | RNF19A | GRCh38.p7 | 8:100307768 | TTACGACTTCACTTA[C/T]ATTCAAATTTGGGAA | 25897 |
rs1788168 | snp | G/T | 0.499551 | 0.0149693 | intron-variant | RNF19A | GRCh38.p7 | 8:100312732 | agtttgataccagcc[G/T]ggacaacatgatgaa | 25897 |
rs1788169 | snp | C/T | 0.431029 | 0.17242 | intron-variant | RNF19A | GRCh38.p7 | 8:100314086 | gaggttttgccatgt[C/T]gctcaggtgggtctt | 25897 |
rs1788170 | snp | C/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100314794 | ACCTCTATAATTTTT[C/G]TGTATAAAGTACTTC | 25897 |
rs1788173 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | RNF19A | GRCh38.p7 | 8:100318711 | TCAAGCTGGAACACT[C/T]TTAGATATGACCCAG | 25897 |
rs1788174 | snp | C/G | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100318729 | AGATATGACCCAGAA[C/G]CTTGATACCAAATAA | 25897 |
rs1788175 | snp | A/G | 0.499642 | 0.0133738 | intron-variant | RNF19A | GRCh38.p7 | 8:100319861 | ttttttcgagatgga[A/G]ttttgctcttgttgc | 25897 |
rs1788176 | snp | A/G | 0.431029 | 0.17242 | intron-variant | RNF19A | GRCh38.p7 | 8:100319884 | cttgttgcccaggac[A/G]gagtgcaatggtagg | 25897 |
rs1788177 | snp | A/G | 0.431029 | 0.17242 | intron-variant | RNF19A | GRCh38.p7 | 8:100320083 | TCAGGTGACCCAACT[A/G]CCTCAGCCTCCCAAA | 25897 |
rs1788178 | snp | A/C | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100320290 | CCTTTATTTTTTAAA[A/C]AACAACAACAACAAC | 25897 |
rs1788179 | snp | A/G | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100321117 | gtttcttaaaataag[A/G]taacaatgaagtttg | 25897 |
rs1788180 | snp | A/G | 0.49962 | 0.0137727 | intron-variant | RNF19A | GRCh38.p7 | 8:100321140 | gaagtttgccacatc[A/G]attgactcttccttc | 25897 |
rs1788181 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | RNF19A | GRCh38.p7 | 8:100321840 | gaattgtcagtgaga[C/T]ataatattttgaaag | 25897 |
rs1788182 | snp | C/T | 0.499693 | 0.0123764 | intron-variant | RNF19A | GRCh38.p7 | 8:100322392 | tagcttcaaactttt[C/T]ttctgaagcttcctt | 25897 |
rs1788183 | snp | A/C | 0.499693 | 0.0123764 | intron-variant | RNF19A | GRCh38.p7 | 8:100322690 | cttgttttttggttt[A/C]aagtgagaggcatgc | 25897 |
rs1788184 | snp | A/G | 0.499693 | 0.0123764 | intron-variant | RNF19A | GRCh38.p7 | 8:100322878 | aagttcactgtcttc[A/G]gtgggagtggttcat | 25897 |
rs1788185 | snp | C/T | 0.432357 | 0.171014 | intron-variant | RNF19A | GRCh38.p7 | 8:100323301 | TCTCTGTAATATCAT[C/T]TTTGGAAGTTTTATC | 25897 |
rs1788186 | snp | C/T | 0.499693 | 0.0123764 | intron-variant | RNF19A | GRCh38.p7 | 8:100323458 | CCTGTTTTTGCAGGA[C/T]GACCACGTTTCACCC | 25897 |
rs1788187 | snp | A/G | 0.499693 | 0.0123764 | intron-variant | RNF19A | GRCh38.p7 | 8:100323871 | AAATGACTGTGCCAA[A/G]CCAACATTCCTGTCA | 25897 |
rs1788193 | snp | C/T | 0.428333 | 0.175206 | intron-variant | RNF19A | GRCh38.p7 | 8:100264449 | GAAGTGCCAGGCCTC[C/T]GAACTGTACTTGGGG | 25897 |
rs1788194 | snp | C/T | 0.432504 | 0.170857 | intron-variant | RNF19A | GRCh38.p7 | 8:100265688 | TATTACATGGTATAA[C/T]AACACCTTTGGCCTT | 25897 |
rs1788196 | snp | C/T | 0.499587 | 0.0143711 | intron-variant | RNF19A | GRCh38.p7 | 8:100277860 | GTTTTAAAACAATAA[C/T]GTCAGTGAAAAGGAT | 25897 |
rs1788197 | snp | C/T | 0.499673 | 0.0127754 | intron-variant | RNF19A | GRCh38.p7 | 8:100278700 | CTTTGTAGAAGGCTG[C/T]TCAATATACTAGTAT | 25897 |
rs1788198 | snp | A/G | 0.418814 | 0.184396 | intron-variant | RNF19A | GRCh38.p7 | 8:100280132 | TCATTAAGGGGCAGG[A/G]CTGGATTTGAACAAA | 25897 |
rs1788199 | snp | A/G | 0.432797 | 0.170544 | intron-variant | RNF19A | GRCh38.p7 | 8:100280626 | TGTTTTCATAAATGT[A/G]TAATCTGACAACAAA | 25897 |
rs1788201 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100290159 | tgtgtctgttgccca[C/G]gctggagtgcagtga | 25897 |
rs1788202 | snp | C/T | 0.430732 | 0.172731 | intron-variant | RNF19A | GRCh38.p7 | 8:100290328 | gctggcctcgaactc[C/T]tgacctcaagtgatc | 25897 |
rs1788203 | snp | C/T | 0.430285 | 0.173197 | intron-variant | RNF19A | GRCh38.p7 | 8:100291493 | ACATGTTAAGTATCC[C/T]GACACTACAACTTCA | 25897 |
rs1788204 | snp | C/T | 0.43088 | 0.172575 | intron-variant | RNF19A | GRCh38.p7 | 8:100291708 | TACATGGTCAAATAA[C/T]AGTTTTTGCTTCTGT | 25897 |
rs1788205 | snp | C/G | 0.430285 | 0.173197 | intron-variant | RNF19A | GRCh38.p7 | 8:100294318 | GTAGATCTGTGGAAA[C/G]CACCCATGTTTACCA | 25897 |
rs1788206 | snp | A/G | 0.430434 | 0.173042 | intron-variant | RNF19A | GRCh38.p7 | 8:100294738 | ttcatctaggctttg[A/G]gatacagtattcttg | 25897 |
rs1788207 | snp | A/G | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100298495 | CCAACAAGTTCTTTA[A/G]AAAGTAAATGCTTAC | 25897 |
rs1788208 | snp | C/T | 0.430434 | 0.173042 | intron-variant | RNF19A | GRCh38.p7 | 8:100300287 | GAAAAATCTAGGTAA[C/T]AATTACACAGCAGGT | 25897 |
rs1788209 | snp | C/T | 0.495213 | 0.048687 | intron-variant | RNF19A | GRCh38.p7 | 8:100324828 | CTTCCTTCCTTCCTT[C/T]CTCCTTCTTCCTCCC | 25897 |
rs1788210 | snp | A/T | 0.430136 | 0.173352 | intron-variant | RNF19A | GRCh38.p7 | 8:100325084 | GCTAATTTTTTGTAT[A/T]TTTAGTAGAGATGGG | 25897 |
rs1866787 | snp | C/G | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100300199 | GTCTCCCGAAAATGA[C/G]ATTAAAAACTCACGT | 25897 |
rs1962901 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | RNF19A | GRCh38.p7 | 8:100314200 | TATATATAGTATGTA[C/T]GCAATAAAGAGTAGT | 25897 |
rs2033920 | snp | C/T | 0.499396 | 0.0173617 | intron-variant | RNF19A | GRCh38.p7 | 8:100335778 | TTACCTTAGAAAGCA[C/T]CTAGGGACAGGCGGC | 25897 |
rs2033921 | snp | A/G | 0.499653 | 0.0131743 | intron-variant | RNF19A | GRCh38.p7 | 8:100319586 | ccaggctggagtgta[A/G]tggcacaatctcggc | 25897 |
rs2033922 | snp | C/G | 0.431325 | 0.172108 | intron-variant | RNF19A | GRCh38.p7 | 8:100319637 | caggttcaagtgatt[C/G]tcctgcctcagcctc | 25897 |
rs2439452 | snp | C/T | 0.221439 | 0.248363 | intron-variant | RNF19A | GRCh38.p7 | 8:100316993 | ctgggggacccagta[C/T]actctccgcagccgc | 25897 |
rs2439453 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | RNF19A | GRCh38.p7 | 8:100316996 | ggggacccagtacac[C/T]ctccgcagccgctgg | 25897 |
rs2439456 | snp | C/T | 0.502127 | 0.0552246 | intron-variant | RNF19A | GRCh38.p7 | 8:100324646 | TTGATTTTTCACAAA[C/T]GAAGAATTTCCAACC | 25897 |
rs2439458 | snp | C/T | 0.499587 | 0.0143711 | intron-variant | RNF19A | GRCh38.p7 | 8:100285756 | TCCCGTCTTGGCCTC[C/T]CAAAGTGCTGGGATT | 25897 |
rs2439460 | snp | C/T | 0.499563 | 0.0147699 | intron-variant | RNF19A | GRCh38.p7 | 8:100300437 | GGCAGGCAGATTACT[C/T]GAAATTAGGAGTTCA | 25897 |
rs2510206 | snp | A/G | 0.090703 | 0.192677 | intron-variant | RNF19A | GRCh38.p7 | 8:100276738 | caaaaaaaaaaaaaa[A/G]aaaaagaaaaaaagg | 25897 |
rs2849506 | snp | C/G | 0.499767 | 0.0107802 | intron-variant | RNF19A | GRCh38.p7 | 8:100316906 | gcgggctgcaggtcc[C/G]gagccctgccccgcg | 25897 |
rs2861348 | snp | A/G | 0.499713 | 0.0119774 | intron-variant | RNF19A | GRCh38.p7 | 8:100272846 | taagccactgcgccc[A/G]GCCCTCACTGCATTT | 25897 |
rs2861349 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RNF19A | GRCh38.p7 | 8:100284896 | CACTTGAGAAAGAAA[C/T]GTAGTGCTATTAAAA | 25897 |
rs2919465 | snp | C/T | 0.136166 | 0.22258 | intron-variant | RNF19A | GRCh38.p7 | 8:100273489 | TAAAAGTTATGCCAA[C/T]GAGGCATTCCAGGGA | 25897 |
rs2919466 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF19A | GRCh38.p7 | 8:100277281 | AGAGTCAGGGAGTTC[C/T]CTCCATTTTTGGACT | 25897 |
rs2919467 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100299666 | cgggaagctgaggca[A/G]aagaattgcttgaac | 25897 |
rs2919468 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100299669 | gaagctgaggcagaa[A/G]aattgcttgaaccca | 25897 |
rs3808364 | snp | A/C | 0.182296 | 0.240658 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100288380 | CCTTGTTAAAAAAAA[A/C]AACTACTACTAATGG | 25897 |
rs3832572 | in-del | -/TGC | | | cds-indel, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257354 | TCATTGAGGTTAACC[-/TGC]TTTTATTTAAGTGAA | 25897 |
rs4145241 | snp | A/T | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100308701 | CTTTAAAAAAAAAAA[A/T]tgtggaatgtaaaga | 25897 |
rs5893512 | in-del | -/A | 0.0995161 | 0.199636 | intron-variant | RNF19A | GRCh38.p7 | 8:100327086 | TTTTATTTTGCTATG[-/A]AAAAAGTCCCACACA | 25897 |
rs6468708 | snp | C/T | 0.276534 | 0.248588 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311897 | CTTCTGGCTTTCTTG[C/T]CTTCCTAAAAATTAG | 25897 |
rs6468710 | snp | G/T | 0.499437 | 0.0167637 | intron-variant | RNF19A | GRCh38.p7 | 8:100333318 | ttaacaattacccag[G/T]ctgaggtattatatt | 25897 |
rs6468711 | snp | A/T | 0.499437 | 0.0167637 | intron-variant | RNF19A | GRCh38.p7 | 8:100333447 | aagctattaatgaca[A/T]gagaaaatgctcaca | 25897 |
rs6980982 | snp | G/T | 0.276534 | 0.248588 | intron-variant | RNF19A | GRCh38.p7 | 8:100272605 | tgcagtagcacaatg[G/T]cagctcactgcaacc | 25897 |
rs6985608 | snp | C/T | 0.476918 | 0.104919 | intron-variant | RNF19A | GRCh38.p7 | 8:100330371 | CCCATCCCTCCCTCA[C/T]TCTTGGTTCATAATA | 25897 |
rs6986367 | snp | A/G | 0.18134 | 0.240387 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100303756 | tggcaaaacctcgcc[A/G]cttgtaaaaaaaaaa | 25897 |
rs6989703 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | RNF19A | GRCh38.p7 | 8:100316733 | tcccgcaccagggct[A/G]cagttggagctgcct | 25897 |
rs6989921 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | RNF19A | GRCh38.p7 | 8:100317037 | aagtccctcattgcc[C/G]gggaccagcagcgct | 25897 |
rs6989997 | snp | A/C | 0.432063 | 0.171327 | intron-variant | RNF19A | GRCh38.p7 | 8:100279803 | AAGTGCTGGAATTAC[A/C]AGTGTGAGCCACCAC | 25897 |
rs6991563 | snp | G/T | 0.276534 | 0.248588 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100304653 | TTAAATAGATGAGAG[G/T]TTTAAAATCTGGTGC | 25897 |
rs6993210 | snp | C/G | 0.181659 | 0.240478 | intron-variant | RNF19A | GRCh38.p7 | 8:100275590 | ACCAAATTGCATTTA[C/G]CCTAATCTCAATTTT | 25897 |
rs6996156 | snp | C/T | 0.496746 | 0.040204 | intron-variant | RNF19A | GRCh38.p7 | 8:100332286 | attgggtcatggtgg[C/T]aatttcccccatgtt | 25897 |
rs6997022 | snp | A/T | 0.121369 | 0.214369 | intron-variant | RNF19A | GRCh38.p7 | 8:100269034 | AACAATGACTATTTT[A/T]AAAAACTTCTCATAG | 25897 |
rs6997663 | snp | C/G | 0.0592355 | 0.161582 | utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100336150 | GAAATGCAGGGCATG[C/G]GTCCCACACTCAAAT | 25897 |
rs7001993 | snp | A/G | 0.281841 | 0.247964 | intron-variant | RNF19A | GRCh38.p7 | 8:100319578 | tctgtcatccaggct[A/G]gagtgtaatggcaca | 25897 |
rs7002937 | snp | C/T | 0.182614 | 0.240747 | intron-variant | RNF19A | GRCh38.p7 | 8:100290721 | tgtcattaggtgatt[C/T]tgtcgtgtgatcaca | 25897 |
rs7008978 | snp | C/T | 0.476918 | 0.104919 | intron-variant | RNF19A | GRCh38.p7 | 8:100331414 | GTCAAGGTGGGAGGA[C/T]TGCTTGAGCCCAGGA | 25897 |
rs7010782 | snp | A/T | 0.278133 | 0.248412 | intron-variant | RNF19A | GRCh38.p7 | 8:100317474 | TCTTCATGGGACCCA[A/T]GCAATTACTTAGAAT | 25897 |
rs7010789 | snp | A/T | 0.278133 | 0.248412 | intron-variant | RNF19A | GRCh38.p7 | 8:100317484 | ACCCATGCAATTACT[A/T]AGAATCTTCTTTATT | 25897 |
rs7014862 | snp | A/C | 0.423969 | 0.180245 | intron-variant | RNF19A | GRCh38.p7 | 8:100269010 | TAACAAATTAGTGCA[A/C]TATATTAAAACAATG | 25897 |
rs7017969 | snp | C/T | 0.121717 | 0.214577 | intron-variant | RNF19A | GRCh38.p7 | 8:100276219 | ccttcaaaaggtaaa[C/T]ggttaaataagctat | 25897 |
rs7815322 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | RNF19A | GRCh38.p7 | 8:100328541 | cagtggcacaatctc[A/G]gctccctgcaacctc | 25897 |
rs7816489 | snp | C/T | 0.2768 | 0.248559 | intron-variant | RNF19A | GRCh38.p7 | 8:100307148 | AAGATCATAAGCTTA[C/T]TAGTTCAGTACAAAA | 25897 |
rs7816786 | snp | C/T | 0.498871 | 0.0237351 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337434 | TATGGTTTTGAGCTG[C/T]CATGCTGCCAGTTTT | 25897 |
rs7817475 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | RNF19A | GRCh38.p7 | 8:100333810 | gcaatagagtgacac[C/T]ctgtctgtaaacaat | 25897 |
rs7818506 | snp | A/G | 0.499437 | 0.0167637 | intron-variant | RNF19A | GRCh38.p7 | 8:100334299 | CTGTGAAGGCAGGCA[A/G]TATTAATCATTATCT | 25897 |
rs7818852 | snp | A/G | 0.499437 | 0.0167637 | intron-variant | RNF19A | GRCh38.p7 | 8:100334591 | TTCTCCCTTTCTTGT[A/G]CCCCACCTCCGAGCT | 25897 |
rs7819626 | snp | A/C | 0.0655868 | 0.168795 | intron-variant | RNF19A | GRCh38.p7 | 8:100329346 | aaggcctgacttggc[A/C]gccattcatgaggga | 25897 |
rs7819738 | snp | C/T | 0.284471 | 0.247612 | intron-variant | RNF19A | GRCh38.p7 | 8:100312989 | ggtaattgcaatgca[C/T]gaccaaggttggaaa | 25897 |
rs7824192 | snp | C/G | 0.0652144 | 0.168387 | intron-variant | RNF19A | GRCh38.p7 | 8:100265151 | ACCAACAGGATACTT[C/G]CAGCATTCTAAAGGT | 25897 |
rs7824645 | snp | A/T | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100283946 | TGGGGTTTTAATTTT[A/T]AAAAAGGGCGGTCCT | 25897 |
rs7830342 | snp | A/T | 0.499631 | 0.0135733 | intron-variant | RNF19A | GRCh38.p7 | 8:100315510 | GAGAAAGAGATTCTC[A/T]TTCAGCACAATTGAT | 25897 |
rs7831112 | snp | G/T | 0.115088 | 0.210473 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311805 | ACTGGCTTGAAAGGG[G/T]ATTTTGAATAAAGAA | 25897 |
rs7832795 | snp | G/T | 0.498871 | 0.0237351 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337119 | ACTTTTTTACTTTTG[G/T]CTCTAGTCCAGTTGG | 25897 |
rs7833867 | snp | C/G | 0.276534 | 0.248588 | intron-variant | RNF19A | GRCh38.p7 | 8:100267070 | CTGACTCAAACGTAA[C/G]AATTTTGTAACAATT | 25897 |
rs7834075 | snp | G/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258095 | TATAAATAGAAATGT[G/T]ACAGAGTATCATATA | 25897 |
rs7834839 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100325281 | GCAGAGAACTTAAGA[A/G]CCTGAAGGGTTTTTG | 25897 |
rs7836072 | snp | C/G | 0.277067 | 0.24853 | intron-variant | RNF19A | GRCh38.p7 | 8:100282771 | ATCTTTGCAGGATGA[C/G]AATGAGTTACACAGA | 25897 |
rs7837515 | snp | G/T | 0.476574 | 0.105661 | intron-variant | RNF19A | GRCh38.p7 | 8:100329068 | CCAGGTGCCTCCAGA[G/T]CTGTCCTGGCTGCTA | 25897 |
rs7837658 | snp | C/T | 0.276534 | 0.248588 | intron-variant | RNF19A | GRCh38.p7 | 8:100270857 | TACAATGCACAATGG[C/T]GTCAAGTTAAAATCA | 25897 |
rs7837716 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100338171 | tttagtagagatgag[A/G]cttctccatgttggc | 25897 |
rs7839012 | snp | A/G | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100268121 | TTTTTTTTTCTTTTA[A/G]CTATATTCTACTGAA | 25897 |
rs7845921 | snp | A/T | 0.0648419 | 0.167978 | intron-variant | RNF19A | GRCh38.p7 | 8:100315314 | AATAAAGTACATATG[A/T]TATAGACACAGGACA | 25897 |
rs7846076 | snp | A/G | 0.485731 | 0.0832509 | intron-variant | RNF19A | GRCh38.p7 | 8:100315401 | GTTTCACTGGGGGGG[A/G]AAAATGCAACCAGGA | 25897 |
rs9297292 | snp | C/T | 0.120674 | 0.21395 | intron-variant | RNF19A | GRCh38.p7 | 8:100314462 | ccggcaggctggctc[C/T]agagctcatgctctt | 25897 |
rs9642785 | snp | C/G | 3.46675e-05 | 0.00416323 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258568 | GGCCTAAATTTCAGT[C/G]TGAATTGCAACTTTT | 25897 |
rs9774572 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311737 | aaaaaaaaaaaaaaa[A/G]aagaaaagaaAATAG | 25897 |
rs9774618 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311740 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAATAGATC | 25897 |
rs10094622 | snp | A/G | 0.120674 | 0.21395 | intron-variant | RNF19A | GRCh38.p7 | 8:100272094 | GGGTGGTAGCGGTAA[A/G]GGGACAGAGGCAGGA | 25897 |
rs10103544 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF19A | GRCh38.p7 | 8:100282842 | AAGTCTATGGCCCTA[C/T]TTTTTTTAATCCATT | 25897 |
rs10156261 | snp | A/G | 0.121717 | 0.214577 | intron-variant | RNF19A | GRCh38.p7 | 8:100268305 | TTGGACTTTCACAAG[A/G]TTGTTATAATTTGCA | 25897 |
rs10549878 | in-del | -/TTTTC | 0.181659 | 0.240478 | intron-variant | RNF19A | GRCh38.p7 | 8:100282646 | AGTCCCATGTACTTG[-/TTTTC]TCTGGATAAAATCAA | 25897 |
rs10649423 | in-del | -/TC | 0.496382 | 0.0423778 | intron-variant | RNF19A | GRCh38.p7 | 8:100324887 | TTTTTTTTCTTTCTT[-/TC]TCTCTCTCTCTCTTT | 25897 |
rs10670124 | in-del | -/CT/TC | | | intron-variant | RNF19A | GRCh38.p7 | 8:100324900 | TTTCTCTCTCTCTCT[-/CT/TC]TTCTCTCTTTCTTTC | 25897 |
rs10694844 | in-del | -/A/AT | | | intron-variant | RNF19A | GRCh38.p7 | 8:100296600 | TGAATATATATATAT[-/A/AT]TCTAGGCACAGGATA | 25897 |
rs10715614 | in-del | -/T | 0.499587 | 0.0143711 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310761 | ATCTCTTTTATTTCA[-/T]TTTTTTTTTACTATT | 25897 |
rs10718550 | in-del | -/T | 0.418974 | 0.184249 | intron-variant | RNF19A | GRCh38.p7 | 8:100294613 | AAGCCAGTAAGACTC[-/T]TGATTTTCTGCTTGA | 25897 |
rs11308441 | in-del | -/C | 0.430732 | 0.172731 | intron-variant | RNF19A | GRCh38.p7 | 8:100319312 | GATGAAAGTTTTTTT[-/C]TTTTTTAACACAAAA | 25897 |
rs11544133 | snp | A/G | 0 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100288174 | CATGACTTAATGTGA[A/G]TGCAAGAACAAGAAA | 25897 |
rs11544134 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100288166 | AATGTGAATGCAAGA[A/G]CAAGAAATAGGTTTT | 25897 |
rs11777403 | snp | A/T | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100285785 | ttacaggaatgagcc[A/T]ccacgcccagttGTA | 25897 |
rs11779989 | snp | C/G | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100265832 | ATTTCCCAGCATTGA[C/G]TAGAGGTTCCTTGTC | 25897 |
rs11780010 | snp | C/G | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100265782 | GTGATGCATGTATGG[C/G]ACAAGAAACCTTTCT | 25897 |
rs11782660 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100308789 | TAACACTTAAAATTA[A/G]CATTTCTAGCCAACA | 25897 |
rs11985538 | snp | A/G | 0.121369 | 0.214369 | intron-variant | RNF19A | GRCh38.p7 | 8:100308447 | CCATTTTCTAAATAG[A/G]GAAGTATTTACATTT | 25897 |
rs11985901 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100261364 | tggcttcccaacatg[C/T]tgggattacaggcgt | 25897 |
rs11985974 | snp | C/T | 0.117886 | 0.21224 | intron-variant | RNF19A | GRCh38.p7 | 8:100287330 | TAGAAATGAGTAAGA[C/T]AGGATCACTGCCTTT | 25897 |
rs11988199 | snp | C/T | 0.0569829 | 0.158885 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258216 | TTCTTCATTTGAATG[C/T]TGTAGAATTGCATTA | 25897 |
rs11988697 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100274356 | GCTTCTGGACCCATA[A/C]CTACAAATTAACACT | 25897 |
rs11988698 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100274357 | CTTCTGGACCCATAC[C/T]TACAAATTAACACTA | 25897 |
rs11991327 | snp | A/C | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100319412 | GTATTATTATTTAAA[A/C]CAAGATAAATGAAAC | 25897 |
rs11991409 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289532 | caggcatttcacaaa[A/G]ggatatgaaaagtgc | 25897 |
rs11991535 | snp | C/T | 0.414741 | 0.188044 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336858 | GTGTGCTTGCTTCTC[C/T]TGGCCATTCTCTCTG | 25897 |
rs11992025 | snp | A/G | 0.115788 | 0.21092 | intron-variant | RNF19A | GRCh38.p7 | 8:100325395 | TCTGGATCTGCCTCT[A/G]TGGTGTCTGCTAATT | 25897 |
rs11992215 | snp | C/T | 0.2768 | 0.248559 | intron-variant | RNF19A | GRCh38.p7 | 8:100312645 | AGAAAGAAAGAAAAc[C/T]gggcgcagtggctca | 25897 |
rs11994322 | snp | C/G | 0.121022 | 0.21416 | intron-variant | RNF19A | GRCh38.p7 | 8:100284864 | GGATGATCATTAACT[C/G]ACAATCTAAATTGGA | 25897 |
rs11995133 | snp | A/C | 0.0146672 | 0.084371 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257777 | AATCAATGGGGTACA[A/C]ACTTCCCCTTAGAGA | 25897 |
rs11996396 | snp | C/T | 0.121022 | 0.21416 | intron-variant | RNF19A | GRCh38.p7 | 8:100287127 | AAAAATAAAGAAGGT[C/T]ATTTGAATTTATGAC | 25897 |
rs12542891 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257276 | TACCAAAAGAAAACG[C/T]TCAGTAGCACCATAA | 25897 |
rs12544135 | snp | C/T | | | splice-acceptor-variant, intron-variant | RNF19A | GRCh38.p7 | 8:100264196 | TAGGAACACCGATAC[C/T]TAAAGAGAAATTAAA | 25897 |
rs12678088 | snp | A/G | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100306517 | AAAAATAATTCTTCA[A/G]GTGTTAATGACAGTG | 25897 |
rs13275921 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100315392 | CTTATGTTTGTTTCA[C/T]TGGGGGGGAAAAATG | 25897 |
rs13276656 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100315400 | TGTTTCACTGGGGGG[A/G]AAAAATGCAACCAGG | 25897 |
rs13277960 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100315393 | TTATGTTTGTTTCAC[G/T]GGGGGGGAAAAATGC | 25897 |
rs13282313 | snp | C/G | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100298369 | GCTAGTACAAACCTA[C/G]CTCAAGTGGTCTAAT | 25897 |
rs16898112 | snp | A/G | 0.121022 | 0.21416 | intron-variant | RNF19A | GRCh38.p7 | 8:100260190 | ATCCAAATAAAATGG[A/G]GAACATCAGCTGTCT | 25897 |
rs16898115 | snp | C/T | 0.123798 | 0.215808 | intron-variant | RNF19A | GRCh38.p7 | 8:100262164 | TCTGATAACACTATG[C/T]TCCAATTTTACAGTA | 25897 |
rs16898138 | snp | C/G | 0.110519 | 0.207473 | intron-variant | RNF19A | GRCh38.p7 | 8:100272030 | ATTAAGAAAAAACAA[C/G]AGGTTACAAAACACC | 25897 |
rs16898151 | snp | A/G | 0.109108 | 0.206518 | intron-variant | RNF19A | GRCh38.p7 | 8:100273621 | AAAGCCATTTCTGTC[A/G]TTTTTTAATTTAATG | 25897 |
rs16898173 | snp | C/T | 0.121717 | 0.214577 | intron-variant | RNF19A | GRCh38.p7 | 8:100280733 | CATATGTATTCAATC[C/T]TAACCATAACAGTAT | 25897 |
rs16898229 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100323464 | TTTGCAGGATGACCA[C/T]GTTTCACCCTTCTTT | 25897 |
rs16898236 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | RNF19A | GRCh38.p7 | 8:100324688 | AATATGAATCTACGC[A/G]TTTGCTTCAAGAAAA | 25897 |
rs16898242 | snp | A/G | 0.116138 | 0.211142 | intron-variant | RNF19A | GRCh38.p7 | 8:100325715 | TCAATATTGCAGAAA[A/G]TATCTGTGGATGTTT | 25897 |
rs16898244 | snp | G/T | 0.321053 | 0.23969 | intron-variant | RNF19A | GRCh38.p7 | 8:100326029 | TGCTATCTGCTATCC[G/T]GGTGTTTTATGCTCT | 25897 |
rs17337916 | snp | A/G | 0.240765 | 0.249829 | intron-variant | RNF19A | GRCh38.p7 | 8:100305438 | CGCCCCTAGAGCTAC[A/G]CTGTCCAATATGAAT | 25897 |
rs17338532 | snp | A/T | 0.221737 | 0.248397 | intron-variant | RNF19A | GRCh38.p7 | 8:100327985 | GGTAGGCTCTTCAAG[A/T]GTTTGAGGTAAGAGT | 25897 |
rs17422137 | snp | A/G | 0.24134 | 0.24985 | intron-variant | RNF19A | GRCh38.p7 | 8:100285498 | ATATATTATGATGAC[A/G]TTACCAATCAATCTA | 25897 |
rs17422240 | snp | A/C | 0.0460142 | 0.144533 | intron-variant | RNF19A | GRCh38.p7 | 8:100291704 | CTACTACATGGTCAA[A/C]TAACAGTTTTTGCTT | 25897 |
rs28413017 | snp | G/T | 0.116838 | 0.211584 | intron-variant | RNF19A | GRCh38.p7 | 8:100309145 | GTAGTAGTATTACTT[G/T]CCGGGCGAGGGCTGG | 25897 |
rs28461614 | snp | A/C | 0.121369 | 0.214369 | intron-variant | RNF19A | GRCh38.p7 | 8:100307512 | AAAATTTCTATATAA[A/C]TCTAAATAAGTGTTC | 25897 |
rs28502451 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | RNF19A | GRCh38.p7 | 8:100327531 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT | 25897 |
rs28540777 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100299772 | TCAAAATAAAAAAAA[A/G]AAAAAAAAAAGTATT | 25897 |
rs28542923 | snp | A/G | 0.115788 | 0.21092 | intron-variant | RNF19A | GRCh38.p7 | 8:100325789 | CACACACACATTTAT[A/G]TCCATAAAATCTAAG | 25897 |
rs28562556 | snp | G/T | 0.2768 | 0.248559 | intron-variant | RNF19A | GRCh38.p7 | 8:100296837 | GTATTCCAGTTGAAG[G/T]TGCAACTCTTTCCAC | 25897 |
rs28580294 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | RNF19A | GRCh38.p7 | 8:100279746 | TGGCTAGGCTTGTCT[C/T]GAACTCCAGACCTCA | 25897 |
rs28583983 | snp | C/T | 0.175897 | 0.238765 | intron-variant | RNF19A | GRCh38.p7 | 8:100273133 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT | 25897 |
rs28595052 | snp | A/G | 0.430434 | 0.173042 | intron-variant | RNF19A | GRCh38.p7 | 8:100315325 | TATGATATAGACACA[A/G]GACAAGGTACCATTA | 25897 |
rs28612810 | snp | C/T | 0.120326 | 0.21374 | intron-variant | RNF19A | GRCh38.p7 | 8:100273086 | TGCCTAGGCTGGTCT[C/T]GAACTCCTGGGCTCA | 25897 |
rs28651515 | snp | A/C | 0.120674 | 0.21395 | intron-variant | RNF19A | GRCh38.p7 | 8:100309232 | TACTTCACCCCAAGG[A/C]TACACCATTTTGGTG | 25897 |
rs28664006 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100299771 | CTCAAAATAAAAAAA[A/G]GAAAAAAAAAAGTAT | 25897 |
rs34031167 | in-del | -/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100267417 | TCTATCACCCAGGCT[-/G]GGAGTGAAGTGGCAC | 25897 |
rs34033609 | in-del | -/A | | | intron-variant | RNF19A | GRCh38.p7 | 8:100293800 | TTGTAATCTTTTTTT[-/A]CTTCGTTCAGTAGAC | 25897 |
rs34110743 | in-del | -/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100275479 | ATGATGCTGAGGTTT[-/G]GGGCTTCTAATGATT | 25897 |
rs34139640 | in-del | -/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100263950 | GGATGGCAATGGAAA[-/T]TTCTGAGTTGCATGT | 25897 |
rs34159177 | in-del | -/C | | | intron-variant | RNF19A | GRCh38.p7 | 8:100265402 | AATAATGGCTACCAG[-/C]AAGACAGGATTGAAT | 25897 |
rs34277998 | in-del | -/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100263923 | GAATGAATACTATTA[-/G]GGCCTAGTAAAAGGA | 25897 |
rs34297750 | in-del | -/AA | | | intron-variant | RNF19A | GRCh38.p7 | 8:100268684 | AGATACCCTTTGTCT[-/AA]AAAAAAAAAAAAAAA | 25897 |
rs34333820 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100276743 | AAAAAAAAAAAAAAA[A/G]GAAAAAAAGGAGTAA | 25897 |
rs34439933 | in-del | -/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100261097 | AAATCTACCACCAAA[-/T]TTTTTCTTTTTTTTT | 25897 |
rs34452066 | in-del | -/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100313449 | AAAGGTCTTAGCCAG[-/T]AAACACTTGTCAAAT | 25897 |
rs34581644 | in-del | -/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100312678 | CTGTAATCCCGGCAC[-/T]TTTGGGAGGCTTAGG | 25897 |
rs34590798 | in-del | -/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100267678 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTTGC | 25897 |
rs34606154 | snp | C/T | 8.24681e-05 | 0.00642085 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258815 | TTAACAGTAGCAAAG[C/T]GGGTGTGATAATCAC | 25897 |
rs34607904 | in-del | -/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100333774 | GCCAGCTATGATTAT[-/G]GCCACTGCACTCCAG | 25897 |
rs34638933 | in-del | -/A/AA | 0.379942 | 0.213577 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289059 | GCGAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA | 25897 |
rs34698535 | in-del | -/T | 0.499642 | 0.0133738 | intron-variant | RNF19A | GRCh38.p7 | 8:100321991 | GGTTTAGCAAAATTC[-/T]TTTTTTTTTCTTTAT | 25897 |
rs34789960 | in-del | -/C | | | intron-variant | RNF19A | GRCh38.p7 | 8:100260172 | ACTGCATAGTACCAG[-/C]CCATCCAAATAAAAT | 25897 |
rs34977409 | snp | A/C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100266208 | GGTACTTTATTGACT[A/C/T]AGCAGGTTTTCCTAG | 25897 |
rs35099425 | in-del | -/A | | | intron-variant | RNF19A | GRCh38.p7 | 8:100259616 | CATTTTCATGATCCC[-/A]AAAAGGGATCTTGCA | 25897 |
rs35108506 | multinucleotide-polymorphism | AT/CC | | | intron-variant | RNF19A | GRCh38.p7 | 8:100274356 | GCTTCTGGACCCATA[AT/CC]TACAAATTAACACTA | 25897 |
rs35121574 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100304479 | ACGCACTCACACTAC[-/T]TTACCAGTTCCCACC | 25897 |
rs35177403 | snp | A/G | 0.00135113 | 0.0259565 | synonymous-codon, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258634 | TTCTTTTAGTGCATC[A/G]CCAAAATATAAATCA | 25897 |
rs35239143 | in-del | -/A | | | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337849 | ATTATCTAGTCTAGT[-/A]AAATAATTGCTATTT | 25897 |
rs35395830 | in-del | -/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100274496 | AAAATTTCATGTGAC[-/T]TTTTTTTCTAGTAGC | 25897 |
rs35442731 | in-del | -/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100279853 | GTTTTTAGTAGGGAT[-/G]GGGGTTTTGCCATGT | 25897 |
rs35455575 | in-del | -/C | | | intron-variant, utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100309321 | GAACACAGCTCCCCT[-/C]CCTAAGGCCCCAGGC | 25897 |
rs35623170 | in-del | -/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100296867 | AAGAGTTAAGTTTTT[-/G]GGGAAGGTTAAAAAA | 25897 |
rs35692414 | in-del | -/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100286743 | ACCTTACTTATAATC[-/T]TCTGGTTTACTAATA | 25897 |
rs35748790 | in-del | -/A | 0.46885 | 0.12085 | intron-variant | RNF19A | GRCh38.p7 | 8:100298198 | TAAAAAAAAAAAAAA[-/A]CACTTATTACACATT | 25897 |
rs35751827 | in-del | -/T | 0.499609 | 0.0139722 | intron-variant | RNF19A | GRCh38.p7 | 8:100277608 | ACATCTTAAATTCCA[-/T]CTTATTTCTGATAGA | 25897 |
rs35773365 | in-del | -/GAAGA | | | intron-variant | RNF19A | GRCh38.p7 | 8:100291947 | TTACTAGCACTGTTG[-/GAAGA]AACAGAAAGAGGACT | 25897 |
rs36016057 | in-del | -/A | | | intron-variant | RNF19A | GRCh38.p7 | 8:100322142 | TCCTTTGAAGCTTTG[-/A]AAGCCAAGCATTGAC | 25897 |
rs36048267 | in-del | -/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100336030 | TGACTGGTTAGCAGT[-/G]GGGAGCTAAAGGGAT | 25897 |
rs36078674 | in-del | -/A | | | intron-variant | RNF19A | GRCh38.p7 | 8:100260259 | AAAGGATTTTCACTT[-/A]AAATGTACTCCATTA | 25897 |
rs41354249 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF19A | GRCh38.p7 | 8:100299137 | CCTAGTATTAGATCT[C/T]AACCAAGTTTACCTA | 25897 |
rs41528948 | snp | G/T | 0.0655868 | 0.168795 | intron-variant | RNF19A | GRCh38.p7 | 8:100329984 | TTAGGATCCCTTACA[G/T]GACCATCTAAGCTCT | 25897 |
rs55695585 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311738 | AAAAAAAAAAAAAAA[-/AA]GAAAAGAAAATAGAT | 25897 |
rs55697077 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100325218 | CAGCTTAAAAGCATC[G/T]ATTTTTAATAGAAAA | 25897 |
rs56028014 | snp | C/G | 0.232943 | 0.249417 | intron-variant | RNF19A | GRCh38.p7 | 8:100334325 | TATCTTCTTTTCACC[C/G]TCTGCTCTGTTTCCA | 25897 |
rs56077605 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100284515 | CAAAAATTAATGTAT[A/G]GCCAAATTAATCACG | 25897 |
rs56088111 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289821 | ATGAATGTACACATA[C/T]ATTAAAAGACATACT | 25897 |
rs56286818 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100334520 | ACATTGGGGTTCTGA[A/G]CCCTGGCTGCACATT | 25897 |
rs56288024 | in-del | -/TGGCCTTAGCCAACTGAAACA | 0.422158 | 0.181278 | intron-variant | RNF19A | GRCh38.p7 | 8:100283215 | GCGCTGGTAGCAGGG[-/TGGCCTTAGCCAACTGAAACA]TGGCCTTAGCCAACT | 25897 |
rs56298614 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100316990 | CTGCTGGGGGACCCA[G/T]TACACTCTCCGCAGC | 25897 |
rs56356271 | snp | C/T | 0.241053 | 0.24984 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310230 | CCACCGGGCCCGCTG[C/T]GGGCGGCTCTGGACG | 25897 |
rs56737985 | in-del | -/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100291989 | AAAGAGGACTAAGTC[-/T]TTTTTTTTTTTTTTT | 25897 |
rs56814140 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100320020 | TTTGTATTTTTAGTA[A/G]AGATGGAGTTTCACC | 25897 |
rs56838048 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100301296 | CAGAGCTAAAGGCTC[A/C]GCATTCTTTCTACTA | 25897 |
rs56995613 | in-del | -/GGTGTGTG/GGTGTGTGTGTGTG | | | intron-variant | RNF19A | GRCh38.p7 | 8:100292436 | TTGCTATCATATGGG[-/GGTGTGTG/GGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 25897 |
rs58005786 | in-del | -/AC/CA | | | intron-variant | RNF19A | GRCh38.p7 | 8:100325767 | ACACACACACACACA[-/AC/CA]TTTATATCCATAAAA | 25897 |
rs58327820 | snp | A/C | 0.277067 | 0.24853 | intron-variant | RNF19A | GRCh38.p7 | 8:100315619 | AGTTTCTTTCCCAGC[A/C]GGGTCATGGAAATTT | 25897 |
rs58473488 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100321713 | TTCTTAAATAATAAG[A/G]CTTGAAAGTTGAAAT | 25897 |
rs58519471 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336740 | AATGGCCCCAGATTG[-/T]TTTTTTTTTTTTTTC | 25897 |
rs58583120 | snp | C/T | 0.0429648 | 0.14013 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337282 | GCTTCTCTCCCTCTT[C/T]CTGTTCCTCCCTTTG | 25897 |
rs59052712 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100296752 | ACTCTCGCTATTTAC[A/C]TTATTAGTACAGCAT | 25897 |
rs59267635 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100333276 | CTTCCCAGATCCAGA[A/G]CAATGAGCCAAATAC | 25897 |
rs59453379 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100266037 | AAGGCAGGCTGCCAA[C/G]AGAAAGGAGTCTTCT | 25897 |
rs59940122 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100275972 | AAAAAATAAAAAAAA[A/C]CTGTTTTTTTTTCCT | 25897 |
rs59979866 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100296744 | TCATTCCTACTCTCG[C/T]TATTTACATTATTAG | 25897 |
rs60110792 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100303785 | AAAAAAAAAAAAAAA[-/A]TGATTAGCTGGGTGT | 25897 |
rs60231223 | in-del | -/AAGAA/GAGAA | | | intron-variant | RNF19A | GRCh38.p7 | 8:100291949 | ACTAGCACTGTTGAA[-/AAGAA/GAGAA]CAGAAAGAGGACTAA | 25897 |
rs60419107 | in-del | -/A | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100276743 | AAAAAAAAAAAAAAA[-/A]GAAAAAAAGGAGTAA | 25897 |
rs60449074 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF19A | GRCh38.p7 | 8:100274291 | CTACCCAATGGCTAC[C/T]GCTGACTCTTCAGGG | 25897 |
rs60530370 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | RNF19A | GRCh38.p7 | 8:100327004 | CGTTCTGATTAACAG[C/T]TCCTCAGCAGATGTG | 25897 |
rs60744450 | snp | C/T | 0.181659 | 0.240478 | intron-variant | RNF19A | GRCh38.p7 | 8:100269430 | TAACTGAGATTCAGG[C/T]TAAAAATTTATCCCT | 25897 |
rs60819091 | in-del | -/A | 0.439918 | 0.162576 | intron-variant | RNF19A | GRCh38.p7 | 8:100308690 | AGAACCATGTTCTTT[-/A]AAAAAAAAAAATGTG | 25897 |
rs60960956 | snp | G/T | 0.277778 | 0.248452 | intron-variant | RNF19A | GRCh38.p7 | 8:100292437 | TTGCTATCATATGGG[G/T]GTGTGTGTGTGTGTG | 25897 |
rs61063726 | in-del | -/C | 0.0333695 | 0.124785 | intron-variant | RNF19A | GRCh38.p7 | 8:100306579 | TATCAAGAAGTGTTA[-/C]TTTTTCCACTTTGAT | 25897 |
rs61539852 | snp | A/T | 0.2768 | 0.248559 | intron-variant | RNF19A | GRCh38.p7 | 8:100296477 | GCCTAGTAAAGTAAA[A/T]ATATAACAAGCACAT | 25897 |
rs61551559 | in-del | -/TTTCT | | | intron-variant | RNF19A | GRCh38.p7 | 8:100282647 | GTCCCATGTACTTGT[-/TTTCT]CTGGATAAAATCAAA | 25897 |
rs61602271 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100281097 | CCTTCCATGGTCCAT[C/T]ATTTAATTCAAGCCT | 25897 |
rs61711991 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100285916 | AGATGAAACATAACA[C/T]AGACATATTCCTCAG | 25897 |
rs61760886 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100274985 | TGACTATAACTAATG[G/T]ATGAAGAACGTATAG | 25897 |
rs62514973 | snp | A/C | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100276722 | GATCACACCACTGTA[A/C]CAAAAAAAAAAAAAA | 25897 |
rs62514974 | snp | A/T | 0.24134 | 0.24985 | intron-variant | RNF19A | GRCh38.p7 | 8:100294173 | ATAAACTGGATATTG[A/T]GGATATCTTATAGAG | 25897 |
rs62514999 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100300074 | TTCTTCAAACTATAA[A/G]GTAATTCTCAGATGG | 25897 |
rs62515000 | snp | A/C | 0.106987 | 0.205054 | intron-variant | RNF19A | GRCh38.p7 | 8:100327619 | TATAGGTGATGTCAT[A/C]CATGACTTTATTGTG | 25897 |
rs62515001 | snp | G/T | 0 | 0 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337701 | CGAAATTTCTGAATT[G/T]CCGAGCTGTGATAGG | 25897 |
rs71303441 | in-del | -/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100327269 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 25897 |
rs71516861 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100327693 | GTGTCTTATTTTTCA[A/G]AAAGAGGATGCTAGA | 25897 |
rs72544635 | in-del | -/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100277607 | CACATCTTAAATTCC[-/T]ACTTATTTCTGATAG | 25897 |
rs72677945 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310741 | TTGGAGAGTATCTTC[C/T]ATTCATCTCTTTTAT | 25897 |
rs73282705 | snp | A/G | 0.0333695 | 0.124785 | downstream-variant-500B | RNF19A | GRCh38.p7 | 8:100256971 | AGGCAGAATAATCAC[A/G]ATGGCTTGCAATATT | 25897 |
rs73282709 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100261243 | GGGACTACAGGTGCA[G/T]GCCACCAAATCCGGC | 25897 |
rs73282713 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100266180 | TTATTGTTAAGTGAA[A/G]GCTCAGCTTTTGGGT | 25897 |
rs73282714 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF19A | GRCh38.p7 | 8:100271102 | GTCAAACTTTACCTG[C/T]GCTTTATCAGTTAAT | 25897 |
rs73282728 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100286644 | TAATGAGTCTTGAAG[C/T]TGTAATTTGATAAAT | 25897 |
rs73282731 | snp | C/T | 0.00338921 | 0.0410258 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100287584 | TTCGTATTTTTCCAT[C/T]AAGACATCATCACTT | 25897 |
rs73282736 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100293191 | CACACACTGTGGCCC[A/G]AGGGTTGGGGAGCCC | 25897 |
rs73282737 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | RNF19A | GRCh38.p7 | 8:100295561 | ATAAACGTTCCTAAG[A/G]CAATGAAAAAAGGGA | 25897 |
rs73282743 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100297426 | AGATGCTGTTACATG[C/T]TCATCTGCTTCATTT | 25897 |
rs73282749 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100300247 | AACTGTATAAGGAAA[G/T]AAAAGGGAGTATTTT | 25897 |
rs73282752 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100301674 | TCCACAATCATTCTA[A/G]GTCAGTAACTATAAA | 25897 |
rs73282753 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100302168 | TTCTAAAGTGACAGA[G/T]ATAGTTTAAAATCTA | 25897 |
rs73282760 | snp | A/C/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100305873 | GGGCAAATACCAATA[A/C/T]GTGACTTAGAAATCA | 25897 |
rs73282762 | snp | G/T | 0.0681886 | 0.171594 | intron-variant | RNF19A | GRCh38.p7 | 8:100306779 | GGTTAAGTAAATGAG[G/T]TGTTTCAATGTTAGA | 25897 |
rs73282764 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100308908 | CATTAAGCAGAGTAA[A/G]GCATCGTTCGTGTAT | 25897 |
rs73282777 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100321965 | TCCGTTTCTAGAGCA[C/T]GTGTAAAGGAGGTTT | 25897 |
rs73282784 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100324164 | TTTACAGCGGAGGAA[A/G]CCCAATCTAGATTTA | 25897 |
rs73282795 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | RNF19A | GRCh38.p7 | 8:100329200 | AAGGTTGGCAGTGGC[A/T]GACTTGAAACCACAG | 25897 |
rs73282796 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RNF19A | GRCh38.p7 | 8:100329545 | GTCCCACTGAACTCA[A/G]CAATGGTCAGGCCTC | 25897 |
rs73284807 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF19A | GRCh38.p7 | 8:100335653 | TTAAAGACTTCATGT[C/T]ACTGTCATAGACTTT | 25897 |
rs73696623 | snp | C/T | 0.121022 | 0.21416 | intron-variant | RNF19A | GRCh38.p7 | 8:100260293 | TCACTCAGCATATGG[C/T]ACTTTGTAATGTTTC | 25897 |
rs73696625 | snp | A/T | 0.121369 | 0.214369 | intron-variant | RNF19A | GRCh38.p7 | 8:100268079 | TTTTAATTTTTTTGA[A/T]CTTCTTGGATACCAA | 25897 |
rs73696627 | snp | G/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100292439 | GCTATCATATGGGTG[G/T]GTGTGTGTGTGTGTG | 25897 |
rs73696709 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | RNF19A | GRCh38.p7 | 8:100332922 | TTTCAATTTTTTTCT[A/G]TATTGCTGTTTAATC | 25897 |
rs73696710 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | RNF19A | GRCh38.p7 | 8:100335264 | TGTAAACCAGGTACC[C/T]ATCCTAAATGTTTAA | 25897 |
rs74385784 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | RNF19A | GRCh38.p7 | 8:100298421 | TTTAATTCAACTACT[C/T]ATAAATGAGGGAGAT | 25897 |
rs74511587 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100328568 | CCTCCACCTCCCGGG[G/T]TCAGGCGATTCTCTT | 25897 |
rs74610994 | snp | G/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100266527 | TTTTTCTCTCTTTTT[G/T]GGAAATAGGGTCTCT | 25897 |
rs74736045 | snp | C/G | 0.131723 | 0.220251 | intron-variant | RNF19A | GRCh38.p7 | 8:100263435 | AATTCTGGAGTGGTA[C/G]GGACAAAAATCTGAT | 25897 |
rs74756721 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | RNF19A | GRCh38.p7 | 8:100298891 | AAACAATACACCATT[A/C]GGAAAACCACAGGGA | 25897 |
rs74797573 | snp | C/T | 0.125182 | 0.216612 | intron-variant | RNF19A | GRCh38.p7 | 8:100267801 | CCTGCTTCAGCCTCC[C/T]GAGTCTGGGATTACA | 25897 |
rs75058856 | snp | G/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100285653 | TTTTTTTTTTTTTAA[G/T]ACAGGGCTTTGCTCT | 25897 |
rs75064080 | snp | G/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100275421 | AGGGTTTTTTTTTTA[G/T]ATTCAGGGGGTACAT | 25897 |
rs75077164 | snp | C/T | 0.181978 | 0.240568 | intron-variant | RNF19A | GRCh38.p7 | 8:100284064 | AGGTGCATTAAATAT[C/T]TGAATGATTATCTGA | 25897 |
rs75095053 | snp | C/T | 0.111224 | 0.207945 | intron-variant | RNF19A | GRCh38.p7 | 8:100295605 | GTGCAGCATTTACTA[C/T]ATGTAGTGTTGCAAA | 25897 |
rs75110464 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100282739 | GTCAAAAGATAGTCA[A/G]GGTATAGCTAAAACA | 25897 |
rs75115485 | snp | A/C | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100276724 | TCACACCACTGTACC[A/C]AAAAAAAAAAAAAAA | 25897 |
rs75134596 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100320634 | AATGCCCATACATCA[A/G]GGTCCTTTAGGCCTG | 25897 |
rs75176684 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100287800 | TATGAAGTCTCCAAT[C/T]TGTTTGCTGATGGAA | 25897 |
rs75221324 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100292562 | ATATCTTTCTGACTT[C/T]TGACTTCTACACCAG | 25897 |
rs75249837 | snp | C/T | 0.127254 | 0.217792 | intron-variant | RNF19A | GRCh38.p7 | 8:100298982 | GGTTTAAAAAAGATA[C/T]CTAGCTGTCAAAAAT | 25897 |
rs75338507 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | RNF19A | GRCh38.p7 | 8:100330118 | ATTATTCTCTACCGA[C/T]GTTTCCATCCAAACA | 25897 |
rs75406786 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100271331 | AATGATCAAAAGAAC[A/G]TGAAGTCTGCATTTA | 25897 |
rs75479837 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310770 | ATTTCATTTTTTTTT[A/T]ACTATTTTGCAGTCA | 25897 |
rs75637942 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RNF19A | GRCh38.p7 | 8:100293106 | GCCACTGATCTGACA[G/T]GAGGTGGAGCTCAGG | 25897 |
rs75646504 | snp | A/C | 0.181659 | 0.240478 | intron-variant, utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100300637 | CACCCTGGGTGACAC[A/C]GTGAGGCCCTGTCTC | 25897 |
rs75753039 | snp | C/T | 0.181659 | 0.240478 | intron-variant | RNF19A | GRCh38.p7 | 8:100261294 | GTAGAGATGGGGTTT[C/T]GCCATGTTGCCCAGG | 25897 |
rs75819405 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | RNF19A | GRCh38.p7 | 8:100295373 | AAACATTTTGGTAGA[A/C]AATTTAAGTTGCACA | 25897 |
rs75958366 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336963 | CAATGAAACAAGGGT[A/G]AATTTTATAGGATGT | 25897 |
rs76014744 | snp | A/C | 0.182296 | 0.240658 | intron-variant | RNF19A | GRCh38.p7 | 8:100306311 | CTTATTTCAGAGTTA[A/C]AACAACTGAACACTT | 25897 |
rs76023542 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | RNF19A | GRCh38.p7 | 8:100298756 | TACAAGTAATATTCA[C/G]TACTCAAGTTATTAC | 25897 |
rs76081072 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100285652 | TTTTTTTTTTTTTTA[A/G]GACAGGGCTTTGCTC | 25897 |
rs76189693 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | RNF19A | GRCh38.p7 | 8:100262494 | TAGGATAATGCTTGG[A/C]ACCCTCAAAAATCAA | 25897 |
rs76195982 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311724 | CTCCGTCTCAAAAAA[A/C]AAAAAAAAAAAAAAA | 25897 |
rs76232690 | snp | A/G | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100275420 | CAGGGTTTTTTTTTT[A/G]GATTCAGGGGGTACA | 25897 |
rs76256696 | snp | C/T | 0.0232847 | 0.105357 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257644 | TCACATTCATGTTTA[C/T]CTATTTCCTGTATTT | 25897 |
rs76258826 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289061 | CGAGACTCCATCTCA[A/C]AAAAAAAAAAAAAAA | 25897 |
rs76297461 | snp | C/G | 0.11228 | 0.208646 | intron-variant | RNF19A | GRCh38.p7 | 8:100332170 | TCCACTTTCCATACT[C/G]ATATCTGATTTGGTT | 25897 |
rs76362191 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | RNF19A | GRCh38.p7 | 8:100308977 | TCTCTCTCCCATATA[C/T]AGCCTTAACCACTCT | 25897 |
rs76372478 | in-del | -/TT | | | intron-variant | RNF19A | GRCh38.p7 | 8:100271169 | GCTTTTTTTTTTTTT[-/TT]AACTTAAGATCTGGT | 25897 |
rs76415226 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100266795 | TAGGATTACAGGCAT[A/G]AGCCACCACACATGG | 25897 |
rs76435421 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | RNF19A | GRCh38.p7 | 8:100315694 | TCTCACTCTGTTGTC[C/T]AGGTGGGAGTGCAGT | 25897 |
rs76454678 | snp | C/T | 0.127254 | 0.217792 | intron-variant | RNF19A | GRCh38.p7 | 8:100295455 | TTTGCTCACTGGGCA[C/T]AACTTTAGGAACCAA | 25897 |
rs76576998 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | RNF19A | GRCh38.p7 | 8:100292326 | CACTACAAGTCATTT[A/G]CATTTCACTTTCTGT | 25897 |
rs76647332 | snp | C/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100282650 | CCATGTACTTGTTTT[C/G]TCTGGATAAAATCAA | 25897 |
rs76810431 | snp | C/T | 0.126564 | 0.217402 | intron-variant | RNF19A | GRCh38.p7 | 8:100276123 | CAAACAAATGAATAT[C/T]TGTGCTCACACAAAA | 25897 |
rs76872645 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | RNF19A | GRCh38.p7 | 8:100302094 | TGCCAGGTTGTGTGG[A/G]GTTAAGGCCACTGTA | 25897 |
rs76875750 | snp | A/T | 0.0551013 | 0.156571 | downstream-variant-500B | RNF19A | GRCh38.p7 | 8:100257030 | ATTCTCATTCTTATT[A/T]AAAAAAAACACTTGT | 25897 |
rs76902985 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100301998 | GAGGAATGTGTCTGG[C/T]ATGCTCAAGGAATAG | 25897 |
rs76949422 | snp | C/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100266629 | AATCCTCCCATCCCA[C/G]CTTCCTTAATAGCGG | 25897 |
rs77002169 | snp | A/G | 0.126909 | 0.217598 | intron-variant | RNF19A | GRCh38.p7 | 8:100261378 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCT | 25897 |
rs77034032 | snp | A/T | | | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258613 | ATGTGAGTGGTTGTT[A/T]TTTGTTTCTTTTAGT | 25897 |
rs77058623 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF19A | GRCh38.p7 | 8:100299111 | GGTTCTCAACAGAAG[A/G]GAAACACTAACCTAG | 25897 |
rs77096301 | snp | C/T | 0.127599 | 0.217986 | intron-variant | RNF19A | GRCh38.p7 | 8:100286465 | ATGTTGTATATTACA[C/T]AGAAATCCTTGGTGG | 25897 |
rs77162270 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF19A | GRCh38.p7 | 8:100294004 | GTTCGGTCATTATGA[C/T]ATTTCCCCCTTTAAG | 25897 |
rs77166530 | in-del | -/TACA | | | intron-variant | RNF19A | GRCh38.p7 | 8:100320770 | TTAGTAATAGCTCAA[-/TACA]GGCATACCTTGAAGA | 25897 |
rs77173664 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RNF19A | GRCh38.p7 | 8:100297624 | CACAATGACTGGCTG[A/G]ATGGAGTAATTCTAG | 25897 |
rs77189256 | snp | C/T | 0.127254 | 0.217792 | intron-variant | RNF19A | GRCh38.p7 | 8:100296689 | TTAATGCTGAGATGT[C/T]AGATTTAACTTGCCA | 25897 |
rs77215482 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100309082 | GGAAATGGGAAAAAA[A/G]GAGCAACTGCAGAGT | 25897 |
rs77356639 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100297579 | TCTAAATCATCCCTG[A/G]AAAAAACCTTCAAGC | 25897 |
rs77526823 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336927 | AAGCCTGATGGAATT[A/T]AAAAGTTGAAAGTAA | 25897 |
rs77715411 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | RNF19A | GRCh38.p7 | 8:100334958 | TAGACCAGCACTAGG[G/T]TTAAAATAAGCTCAG | 25897 |
rs77764694 | snp | A/G | 0.181659 | 0.240478 | intron-variant | RNF19A | GRCh38.p7 | 8:100299089 | CATTTTGCTTACTGT[A/G]TCCCTTGGTTCTCAA | 25897 |
rs77861393 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311864 | TCTGTACAACGGTAA[C/T]ATTTTCCAGAGATGC | 25897 |
rs77897691 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311723 | ACTCCGTCTCAAAAA[A/C]AAAAAAAAAAAAAAA | 25897 |
rs77955374 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100270462 | CACTAACAGGAGGTG[A/G]CAATTTGATATTAAT | 25897 |
rs78116420 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | RNF19A | GRCh38.p7 | 8:100297625 | ACAATGACTGGCTGA[A/C]TGGAGTAATTCTAGT | 25897 |
rs78190387 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310808 | AGAATTCCTATTTCA[C/T]CTCTAATACATTCCT | 25897 |
rs78192511 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF19A | GRCh38.p7 | 8:100271882 | TATGGTTAGTTGATC[C/T]CCCATTCCCCAAGAA | 25897 |
rs78212368 | in-del | -/A | 0.128632 | 0.218563 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258057 | ACATTGCATATGAAG[-/A]AAAAAAATGAAATTT | 25897 |
rs78212464 | snp | A/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100281587 | ATACCTAACATGAAA[A/T]GTAATCCTAAGAAAG | 25897 |
rs78342209 | snp | A/G | 0.182614 | 0.240747 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289047 | CCTGAGCAACAGTGC[A/G]AGACTCCATCTCAAA | 25897 |
rs78383643 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RNF19A | GRCh38.p7 | 8:100291473 | AGTGCTTCAGGATTC[A/G]TAAAACATGTTAAGT | 25897 |
rs78398927 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF19A | GRCh38.p7 | 8:100334798 | GAGACTCCAAAGAGA[C/T]GGTCTTTAGATAAGT | 25897 |
rs78468581 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289616 | CACACCTAATAGGAT[A/G]GCTAAAATTAAAAGA | 25897 |
rs78506519 | snp | C/T | 0.184203 | 0.241186 | intron-variant | RNF19A | GRCh38.p7 | 8:100319063 | AATAAAGAAATTCAC[C/T]GTAATCAAATTACTG | 25897 |
rs78522436 | snp | G/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100313912 | AACTACTTTTTTTTT[G/T]AGACAGAGTCTTACT | 25897 |
rs78524122 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100319421 | TTTAAAACAAGATAA[A/G]TGAAACATAGAAATG | 25897 |
rs78536573 | snp | A/C | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100268686 | ATACCCTTTGTCTAA[A/C]AAAAAAAAAAAAAAA | 25897 |
rs78641115 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RNF19A | GRCh38.p7 | 8:100331768 | AGACAACTATTATCC[A/G]TTTCATATGTATTGA | 25897 |
rs78701116 | in-del | -/T | 0.127599 | 0.217986 | intron-variant | RNF19A | GRCh38.p7 | 8:100285551 | TAAGTGACCAGAAGG[-/T]TTGTGTCCCTGAATT | 25897 |
rs78800094 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RNF19A | GRCh38.p7 | 8:100280252 | CTATGACGGAGATAC[C/T]TGACTTTGGCCACCT | 25897 |
rs78920522 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100285650 | AATTTTTTTTTTTTT[A/C/T]AAGACAGGGCTTTGC | 25897 |
rs78944033 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100319312 | GATGAAAGTTTTTTT[C/T]TTTTTTAACACAAAA | 25897 |
rs79041835 | snp | C/T | 0.107341 | 0.205301 | intron-variant | RNF19A | GRCh38.p7 | 8:100285527 | TAGTACAAGATAATA[C/T]ACAGCAATTAAGTGA | 25897 |
rs79100573 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100266630 | ATCCTCCCATCCCAG[C/T]TTCCTTAATAGCGGG | 25897 |
rs79231513 | snp | A/C | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100285903 | ACACTCTTTCTGTAG[A/C]TGAAACATAACATAG | 25897 |
rs79312571 | snp | C/T | 0.444444 | 0.157135 | intron-variant | RNF19A | GRCh38.p7 | 8:100328132 | ACTCTCCACCCACTC[C/T]TCACACAATGCACCT | 25897 |
rs79500050 | snp | A/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100285803 | ACGCCCAGTTGTAGA[A/T]TTTTTTTAAGCTATT | 25897 |
rs79618493 | snp | A/G | 0.126909 | 0.217598 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100303619 | TAAAGGATATTTAAC[A/G]TTTGTGCATAATTTT | 25897 |
rs79645148 | snp | G/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100267692 | TCTTTTTTTTTTTTT[G/T]TGAGATGGAGTTTTG | 25897 |
rs79666818 | snp | A/C | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100270249 | AGTAAAACAATGAGA[A/C]CAAAGAATAAAAAAA | 25897 |
rs79689700 | snp | C/T | 0.0452528 | 0.143452 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100309738 | TTTCCCACCGGACTT[C/T]CGAATCCATTTCTGT | 25897 |
rs79714738 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100297578 | CTCTAAATCATCCCT[A/G]AAAAAAACCTTCAAG | 25897 |
rs79721854 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF19A | GRCh38.p7 | 8:100328030 | AGTCTGAGAACTCAG[C/T]TCTTTTATAAGAATG | 25897 |
rs79728316 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100281588 | TACCTAACATGAAAT[A/G]TAATCCTAAGAAAGA | 25897 |
rs79802045 | snp | A/G | 0.0162398 | 0.0886349 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336905 | TAGACTTGGACACTA[A/G]ATCTGGAAGCCTGAT | 25897 |
rs79851129 | snp | G/T | 0.121022 | 0.21416 | intron-variant | RNF19A | GRCh38.p7 | 8:100266594 | CAGCTCACTGTAGCC[G/T]CAACCTCACGGGCTC | 25897 |
rs79882385 | in-del | -/T | 0.181659 | 0.240478 | intron-variant | RNF19A | GRCh38.p7 | 8:100296803 | ACCTCAGTTAGAAAA[-/T]AATTCTATTCCATTA | 25897 |
rs79964347 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF19A | GRCh38.p7 | 8:100334589 | CCTTCTCCCTTTCTT[A/G]TGCCCCACCTCCGAG | 25897 |
rs80052552 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100266631 | TCCTCCCATCCCAGC[C/T]TCCTTAATAGCGGGG | 25897 |
rs80058102 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF19A | GRCh38.p7 | 8:100293440 | TACACTGTCTTCTGG[C/T]CTCCATCGTTTCTGA | 25897 |
rs80062360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100304466 | TATTTTCCCCACTTA[C/T]GCACTCACACTACTT | 25897 |
rs80069661 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310771 | TTTCATTTTTTTTTT[A/C]CTATTTTGCAGTCAA | 25897 |
rs80274458 | snp | A/C | | | intron-variant | RNF19A | GRCh38.p7 | 8:100327976 | TAGAAAACAGGTAGG[A/C]TCTTCAAGTGTTTGA | 25897 |
rs80284607 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100312053 | CCTCAAAGCATGCTT[C/T]TTTCATTCACCCAGA | 25897 |
rs80305103 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100271599 | CCCCATTTATTCTTA[C/T]GGTTCTAAAAACACA | 25897 |
rs80316674 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF19A | GRCh38.p7 | 8:100335538 | TAAATACTTTTTACT[A/G]TTTTTACTTTAATAA | 25897 |
rs111247752 | snp | C/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100326521 | CCTGCCCTAACAGAT[C/T]TTGCAGTCTAGTGAG | 25897 |
rs111354706 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100263884 | ATACACTCCTCCTTG[A/G]CAGTTTATTCACTTA | 25897 |
rs111439164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100302481 | TTTTAGACATTTATA[C/T]TTGAGATATCTCTTA | 25897 |
rs111548832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100327498 | TCAAGTGATGTTCCC[A/G]CCTCGGCCTCCCAAA | 25897 |
rs111593583 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF19A | GRCh38.p7 | 8:100267669 | GCCACCATGCCCAGC[C/T]TGTTAGTTCTTTTTT | 25897 |
rs111664815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100287139 | GGTCATTTGAATTTA[C/T]GACCACAAATAACCC | 25897 |
rs111753150 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF19A | GRCh38.p7 | 8:100319598 | GTAATGGCACAATCT[C/T]GGCTCATTGCAACCT | 25897 |
rs111813122 | in-del | -/ATAC | 0.430732 | 0.172731 | intron-variant | RNF19A | GRCh38.p7 | 8:100320769 | CTTAGTAATAGCTCA[-/ATAC]AGGCATACCTTGAAG | 25897 |
rs111852496 | snp | C/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100301824 | AAGGAGATCAGTGTA[C/T]GTGTGGTGTTGATTA | 25897 |
rs111958165 | snp | C/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100271430 | TAAATTAAGGAAATG[C/T]TAATCCTATCTGCGT | 25897 |
rs111958268 | snp | C/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100334582 | CTGCTCACCTTCTCC[C/T]TTTCTTGTGCCCCAC | 25897 |
rs111964600 | snp | C/T | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100297740 | AGAAATAAATTGTTA[C/T]TGTGTTCCACCATGA | 25897 |
rs112013742 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100259027 | ATTTATCTTCATGTT[A/G]CCCTTTTTCCTCAGT | 25897 |
rs112016844 | in-del | -/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100330863 | CTCCACAACCCTCTT[-/G]GAGACTCTTGCTGTG | 25897 |
rs112122149 | snp | C/T | 0.5 | 0 | utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100288175 | TTCTTGTTCTTGCAT[C/T]CACATTAAGTCATGA | 25897 |
rs112125704 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF19A | GRCh38.p7 | 8:100267494 | CCCACCTCAGCCTCC[C/T]AAGTAGCTGGGACTA | 25897 |
rs112155931 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | RNF19A | GRCh38.p7 | 8:100260552 | TGGGATTATAGGTAT[A/G]AGCCACTGAGCCCAA | 25897 |
rs112273589 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258161 | TCTTTAGTGGTTTCA[A/G]TAAAATATCACTAAC | 25897 |
rs112287939 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | RNF19A | GRCh38.p7 | 8:100315226 | CTGGGAGTTGTAGGG[G/T]GCAGTGAGCCAAGAT | 25897 |
rs112411122 | snp | C/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100306436 | AAATACTAGATAACA[C/T]CAATAGGATAAGACT | 25897 |
rs112461040 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100304499 | CAGTTCCCACCCCCA[A/C]TTACGCACTCACATT | 25897 |
rs112580060 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100302232 | ATGGGGAGGTATTAA[A/G]GATGGTAGCACAGAG | 25897 |
rs112611086 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | RNF19A | GRCh38.p7 | 8:100334657 | GGTATGTTTTCTAAA[A/G]CTCCCTTGTTGATTC | 25897 |
rs112669542 | snp | C/T | 0.0681886 | 0.171594 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311562 | TCTCTACTAAAAATA[C/T]AAAAAATTAGCTGGG | 25897 |
rs112702996 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100288977 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAAGTG | 25897 |
rs112849802 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100279809 | TGGAATTACAAGTGT[A/G]AGCCACCACACCCAG | 25897 |
rs112960156 | snp | A/G/T | 0.000164731 | 0.00907405 | missense, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100287891 | TCAGAATGTATACTT[A/G/T]CAATACTTGCAATTC | 25897 |
rs113021185 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100281032 | GGAAATAACTGAACA[C/G/T]CTCTGACTCAAACAG | 25897 |
rs113067656 | snp | A/G | 4.94385e-05 | 0.0049716 | synonymous-codon, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100264708 | TGGAGACACGATTAC[A/G]GACAACGTTACACCA | 25897 |
rs113154923 | snp | C/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100261377 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 25897 |
rs113168929 | snp | A/T | 0.5 | 0 | utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100313357 | ACGTCAATTCTTCTG[A/T]CATTTGAGCTGGATT | 25897 |
rs113206833 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100276434 | GGGAGGGGAAAGAGT[A/G/T]GGGGGAAGTACATGT | 25897 |
rs113224072 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100283789 | AGCATTTCTGGAAAA[C/G]AACCTTTCAAGTGTG | 25897 |
rs113224282 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100288935 | TGTGGTGGCGGGCCC[C/T]TGTAGTCCCAGCTAT | 25897 |
rs113242112 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100288925 | ACTAGCCGGGTGTGG[C/T]GGCGGGCCCCTGTAG | 25897 |
rs113325558 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | RNF19A | GRCh38.p7 | 8:100260459 | TATATTTTTAGAGAC[A/C]GGGTCTCGTTATGTT | 25897 |
rs113336016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289016 | AGTGAGCCGAGATTG[C/T]GCCGCTGCACTCCAC | 25897 |
rs113349339 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100299513 | GCCTGTAATCCCGGC[A/G]CTTTGGGAGACCAAG | 25897 |
rs113358333 | snp | G/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100279213 | TATCAATAGTGATAT[G/T]AAAGTGAATATTTAG | 25897 |
rs113372400 | in-del | -/CA | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100268543 | AAGTTTTATAATACA[-/CA]AACATACTAAAATTT | 25897 |
rs113440492 | snp | C/T | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100327729 | CCCTTTAGGAAAACA[C/T]CCGGTTCCTCTTTTG | 25897 |
rs113482427 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100301090 | TCACCACTAGTCCCA[G/T]GAGGCTATTTAAATT | 25897 |
rs113489759 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337134 | GCTCTAGTCCAGTTG[A/G]TGCATATCTTACTAA | 25897 |
rs113539393 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100280153 | TTTGAACAAATCTCC[A/G]TTCAGTGCCCGGCCC | 25897 |
rs113554405 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100293329 | TTTATCTGGGGAAAA[A/G]AAATGTTATTTCACC | 25897 |
rs113571856 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100277514 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 25897 |
rs113642454 | snp | A/G | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100274577 | TTTAGTAGAGATGGG[A/G]TTTCACCACGTAGCC | 25897 |
rs113764582 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100262881 | TGACAGATCAATCAG[A/G]TGTAGGACAAGAGGG | 25897 |
rs113783825 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF19A | GRCh38.p7 | 8:100306139 | TCCTCAGGGGTCTCC[C/T]CAACAGGACAGAAGT | 25897 |
rs113821692 | snp | C/T | 0.0973687 | 0.197999 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100338135 | AGGCACCCACTACCA[C/T]GCCCAGATAATTTTT | 25897 |
rs113841272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100286970 | CTTGAGGCAAATCCA[A/G]TATTACATAACCCCT | 25897 |
rs113858289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100292660 | TTTGATAGTTTATGA[A/G]TAAGTAGAGATCAAA | 25897 |
rs113871780 | snp | A/G | 0.5 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100274921 | AGTGTTTTGTGTCAA[A/G]TATTTTATTAGAAAA | 25897 |
rs113920062 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF19A | GRCh38.p7 | 8:100316305 | CAGTAGCAAGATTTA[C/T]TGCAAAGAGCGAAAG | 25897 |
rs113974400 | snp | C/G/T | 7.1837e-05 | 0.00599283 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258530 | CACGGTTGTACAGTG[C/G/T]TAATTATTCTGCAGC | 25897 |
rs114088410 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100303618 | CTAAAGGATATTTAA[C/T]GTTTGTGCATAATTT | 25897 |
rs114134283 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100298550 | GTTCTAGCCTTAAGA[C/T]AGTTTCTATAATCTC | 25897 |
rs114140158 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF19A | GRCh38.p7 | 8:100321460 | CACTTCCAATTCTAG[C/T]TCTCTTGCTATTTCT | 25897 |
rs114169911 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257452 | GTCCATAAACAAAAG[A/C]AAAAGAAAATAATGC | 25897 |
rs114287740 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF19A | GRCh38.p7 | 8:100279672 | CAGATTACAGGGGCG[C/T]ATCACCATGCTTGGC | 25897 |
rs114378893 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RNF19A | GRCh38.p7 | 8:100312575 | CCAGCCTGGGCGACA[A/G]AGTGAGACCCTGTCT | 25897 |
rs114382433 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF19A | GRCh38.p7 | 8:100334227 | CAACATAATGCTTCA[C/T]GGTTCTGCCACCATT | 25897 |
rs114539548 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | RNF19A | GRCh38.p7 | 8:100320327 | CTATTTTCAAGATCT[A/G]CCCATGTTGATACAT | 25897 |
rs114582565 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | RNF19A | GRCh38.p7 | 8:100266761 | AATGCAATCCTCCCT[C/G]CTCACCCTCCCCAAG | 25897 |
rs114822707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100326464 | ATGCTGTATACTGTG[C/T]TGGGCAGAGGGTATT | 25897 |
rs114968943 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100301642 | CTCCTCTTTCAAGGC[C/T]CAACTCCTATCTTAT | 25897 |
rs115110219 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant, utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100309474 | CGCCCTTGGGTCTCC[C/G]CCGCTTTAGGGGCAG | 25897 |
rs115304107 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RNF19A | GRCh38.p7 | 8:100281661 | TCTCTCATGTCACGT[C/T]GATTAAAAGAGAATG | 25897 |
rs115321018 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF19A | GRCh38.p7 | 8:100262807 | TAAGGGAAGGACAAC[A/G]AAGAGAGTAAGAAGT | 25897 |
rs115336389 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100334079 | CATTCTGTTCACTGT[G/T]CTTGTAATGCACTTC | 25897 |
rs115465604 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | RNF19A | GRCh38.p7 | 8:100300480 | GCATCAAGGTGAAAC[A/C]CATCTCTACAAAAAC | 25897 |
rs115597515 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF19A | GRCh38.p7 | 8:100303087 | AGACTTTTGACTGCA[C/T]AGTAGTTTCCTGGGG | 25897 |
rs115601535 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RNF19A | GRCh38.p7 | 8:100290595 | CACCTCATGTCCCTC[A/G]GTTTATATTTCCCTT | 25897 |
rs115684133 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100309760 | CATTTCTGTCCCGGG[C/T]AGGGGCGCTAGGGCT | 25897 |
rs115746827 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | RNF19A | GRCh38.p7 | 8:100331675 | ACGGCGCAAAATTTG[A/C]AAGGAATAAAAGGGT | 25897 |
rs115747289 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RNF19A | GRCh38.p7 | 8:100283240 | CCAACTGAAACAGGT[A/G]ATAGAAACTAAAACA | 25897 |
rs115820721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100263978 | TGTTATCTCTGGCCT[C/T]CCCACTACTTACACT | 25897 |
rs115894333 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF19A | GRCh38.p7 | 8:100295311 | TAGACTTTAGATACT[C/T]TTGACAGCACTCTAT | 25897 |
rs115977382 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF19A | GRCh38.p7 | 8:100314291 | TGAGTACATATACTA[C/T]ATGACAGGCACTATT | 25897 |
rs116158015 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | RNF19A | GRCh38.p7 | 8:100297450 | TTCATTTTCCTTCTG[A/C]GCACAAAGCAGGACT | 25897 |
rs116188546 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100299859 | ACAAATTATTGATAA[C/G]AGTAGCATCCCACCT | 25897 |
rs116266442 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | RNF19A | GRCh38.p7 | 8:100318951 | AAGCACATGGCCCAG[A/G]GCAATCCCCAGGCAA | 25897 |
rs116558160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100334367 | GCAGAGGGTAAGGCT[C/T]GATAAACTGCTGACA | 25897 |
rs116580445 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310865 | TCCTTCGTCTCATAT[C/T]TTTTCAGCCAGTCAT | 25897 |
rs116622816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100279344 | CATTACCACGTCAAA[C/T]ATTTAATATTTGATT | 25897 |
rs116666421 | snp | A/G | 0.00130297 | 0.025491 | intron-variant | RNF19A | GRCh38.p7 | 8:100260009 | CAACCTTAAAGGGGG[A/G]TATGAAATCACCAAA | 25897 |
rs116670424 | snp | C/T | 0.00345019 | 0.0413907 | intron-variant | RNF19A | GRCh38.p7 | 8:100269854 | ACATATAAATAGCTC[C/T]TTCTATAAGCTTACC | 25897 |
rs116670929 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100318338 | AGGATGTATTTTATA[C/T]ACTTAACTCACTCTT | 25897 |
rs116704596 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | RNF19A | GRCh38.p7 | 8:100279020 | AATAATTAAATTTTA[A/C]AACAGCTTCATAAAT | 25897 |
rs116974922 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RNF19A | GRCh38.p7 | 8:100293143 | TGCTCACGGCTGCTC[A/G]CCTCCTGCTGCGTGG | 25897 |
rs117047420 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RNF19A | GRCh38.p7 | 8:100269516 | AAACATGCATATTTT[A/T]AGGCATCAATTATCT | 25897 |
rs117073092 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100275453 | TGCAAGTTTGTTACA[C/T]AGGTCTATTGCATGA | 25897 |
rs117100230 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100305237 | GGGAAAGACAGTAAC[A/G]CGCAAAGTCATTTTG | 25897 |
rs117128128 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100288726 | GTGCTATGCCACAAG[A/G]ATGAATACAAAGACC | 25897 |
rs117141057 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RNF19A | GRCh38.p7 | 8:100300699 | ATAAAAAAACAAAAG[A/C]AACATAATCAGTTTA | 25897 |
rs117207634 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RNF19A | GRCh38.p7 | 8:100328103 | GAAAGGGCAGGTGGT[A/G]TCTACATCCCCCCAC | 25897 |
rs117424046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100262157 | ATTAAGATCTGATAA[C/T]ACTATGTTCCAATTT | 25897 |
rs117443190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF19A | GRCh38.p7 | 8:100291472 | AAGTGCTTCAGGATT[C/T]GTAAAACATGTTAAG | 25897 |
rs117460140 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100330895 | ATACAGCATTAATGC[A/G]AAAAGTGCAGACTGG | 25897 |
rs117489322 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100332520 | CAGTTTCAGGGAAGT[C/T]CTTTATAGCAGTGTG | 25897 |
rs117516282 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | RNF19A | GRCh38.p7 | 8:100335864 | TAAGTGGGCCAGGCT[A/G]CCCCTCAGCCACGGC | 25897 |
rs117541003 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF19A | GRCh38.p7 | 8:100281175 | TGAAATGCTTAACCT[A/G]GGAGTGGATGGACAG | 25897 |
rs117557913 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF19A | GRCh38.p7 | 8:100328859 | GTTATAGACTTGTGC[A/G]AAGGGTCTTCTATAA | 25897 |
rs117606223 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF19A | GRCh38.p7 | 8:100334565 | AGCTTTAAAAAATAT[A/G]GCTGCTCACCTTCTC | 25897 |
rs117699770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100318731 | ATATGACCCAGAAGC[A/T]TGATACCAAATAATG | 25897 |
rs117768463 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF19A | GRCh38.p7 | 8:100322569 | AATTTTAACATCCTT[C/T]AAGAACTTTTCCTTT | 25897 |
rs117886629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100326634 | CTTTGTCCCATGCCA[C/T]CTCTCCCTGCCTTCC | 25897 |
rs117888926 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF19A | GRCh38.p7 | 8:100278436 | TGGATAACTGAGTCA[C/T]TTAAGTATAAATGTC | 25897 |
rs117899045 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100330697 | AAGGCAATAAATTAC[C/G]TGTTTTATTTAGCTC | 25897 |
rs118042897 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | RNF19A | GRCh38.p7 | 8:100318767 | AAGAACACTCACTAC[C/T]GGATTTACATAGCCC | 25897 |
rs118148758 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF19A | GRCh38.p7 | 8:100293004 | TGGGAGCAAGGATGG[C/T]TTCATCAGGCATTAT | 25897 |
rs137880268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100303338 | CCTTTTCTGCGCGTC[A/G]TCTTCTCTGTAATGG | 25897 |
rs137938989 | in-del | -/GGGT/GGGTGT/GT | 0.363359 | 0.222822 | intron-variant | RNF19A | GRCh38.p7 | 8:100292435 | CTTGCTATCATATGG[-/GGGT/GGGTGT/GT]GTGTGTGTGTGTGTG | 25897 |
rs137939840 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337345 | CATCTGCTCCATTTT[C/T]CTTTTGGCAGACTAG | 25897 |
rs138112004 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311440 | TATCAATATGTTGGC[C/T]GGAATTGGTGGCTCA | 25897 |
rs138134161 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100299713 | GAGTAAGCCAAGATT[A/G]TGCCATTGCACTCCA | 25897 |
rs138139483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100316785 | CTCGCACTCCTCAGC[C/T]CTTGGGTGGTCTGTG | 25897 |
rs138210911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100276040 | CAGGAATACCTTTCT[C/T]CGAGTTAATATTTCT | 25897 |
rs138215961 | in-del | -/TTTC | 0.0182019 | 0.0936463 | intron-variant | RNF19A | GRCh38.p7 | 8:100281337 | TAAAGTGGTTTTTGT[-/TTTC]TATTATAGGATTTGC | 25897 |
rs138285169 | snp | C/T | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100268820 | GAATGCCAATAATCA[C/T]TGCAGGAATAGCAAT | 25897 |
rs138402879 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100304548 | CCACTTTCCAAATGA[A/C]CTTATTTCATGATTT | 25897 |
rs138475246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100284077 | ATTTGAATGATTATC[C/T]GATTTAAAAAAAAAA | 25897 |
rs138488051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100272509 | CTTTTTAACTTTCTA[C/T]GAGTCTGCGAGAAGC | 25897 |
rs138526860 | in-del | -/C | 0.432797 | 0.170544 | intron-variant | RNF19A | GRCh38.p7 | 8:100272847 | CACTGCGCCCAGCCC[-/C]TCACTGCATTTCTAA | 25897 |
rs138540569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100298592 | AACTCAAAGTTCAGA[A/G]TAAGCTATTCCCATA | 25897 |
rs138606962 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100303692 | ACTTTGGAAGGCTGA[C/T]GTGGGCGGATCACTT | 25897 |
rs138631931 | in-del | -/CTTC | 0.0267878 | 0.112589 | intron-variant | RNF19A | GRCh38.p7 | 8:100324809 | TTCTTTCTCTTTCTT[-/CTTC]CTTCCTTCCTTCCTT | 25897 |
rs138706259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100328958 | TCCACTAAGGATACC[A/G]AGGTGGATCTAGGAA | 25897 |
rs138730799 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100278004 | GAAGTTGGTTACAAT[C/T]TACAAAGGCAGCAAA | 25897 |
rs138731183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100332478 | AGAACTGTGAGTCAA[C/T]TAAATCTCTTTCCTT | 25897 |
rs138744553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100334506 | GTTGAAGCCCCAGAA[C/T]ATTGGGGTTCTGAGC | 25897 |
rs138764980 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337756 | TTCCTCTTCTTTTTT[C/G]CTCTTTATTCAGCAC | 25897 |
rs138774683 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100312116 | CCCATTCTTTTTGTC[C/T]CTTCCAATTCATAAC | 25897 |
rs138812262 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100265276 | AGTATGAATAAACAG[C/T]ATTATTTTTTTCTCA | 25897 |
rs138812511 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100324012 | GGGTTTAGTATCCTG[C/T]GATAAAAGCAAAACT | 25897 |
rs138824461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100260460 | ATATTTTTAGAGACA[A/G]GGTCTCGTTATGTTG | 25897 |
rs138832531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100271742 | TTTATCTATGAAAGG[C/T]TGTTTAGTTTGCTTT | 25897 |
rs138968684 | snp | A/C/T | 0.00340717 | 0.0411342 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100264775 | TCCTTGCCTTCATAG[A/C/T]GATTGTGAATCTTGA | 25897 |
rs139022096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100318454 | TATCAATTTTGAAAC[A/G]AGGCAAATAAAAAAT | 25897 |
rs139030415 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | RNF19A | GRCh38.p7 | 8:100279338 | ATCCTGCATTACCAC[G/T]TCAAACATTTAATAT | 25897 |
rs139078260 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF19A | GRCh38.p7 | 8:100262410 | CAAATGAAGTAAAAC[A/G]GTGAGTCATGAAATT | 25897 |
rs139099355 | in-del | -/A | 0.430136 | 0.173352 | intron-variant | RNF19A | GRCh38.p7 | 8:100296178 | GCATAATCTCAGCTC[-/A]ACTGCAACCTCTGCC | 25897 |
rs139192508 | snp | A/G | 4.95495e-05 | 0.00497718 | synonymous-codon, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100259192 | TCCACTGTTGTGCCT[A/G]AATTTGGATGGCTTT | 25897 |
rs139196738 | in-del | -/ATC | | | intron-variant | RNF19A | GRCh38.p7 | 8:100265467 | TAAGTAGAATTTGAT[-/ATC]ATCATAGAAGCGGTG | 25897 |
rs139202640 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF19A | GRCh38.p7 | 8:100329217 | ACTTGAAACCACAGG[C/T]CAAAGCTCATCTCAC | 25897 |
rs139233747 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF19A | GRCh38.p7 | 8:100328760 | CAGGCGTGAGACACC[A/G]CACCTGGTCTGCGTT | 25897 |
rs139247062 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | RNF19A | GRCh38.p7 | 8:100306956 | TTAAGCTGAAGTACT[A/C]CTCCATATATAATCA | 25897 |
rs139287506 | snp | C/T | 0.000148286 | 0.00860936 | missense, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100287661 | GGCAACTAATATTAA[C/T]TCTGCTTTCAGAGAT | 25897 |
rs139330248 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF19A | GRCh38.p7 | 8:100334840 | AGCTATAGCCTTTGT[C/T]GTATTTCAAAGGTGT | 25897 |
rs139381790 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100294056 | ATAAAGTCTGTCTGC[C/T]AATTCTGCTAATTGC | 25897 |
rs139392595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100305573 | AGAAAATTTTAAATT[A/G]TATTTGTGGCTCACA | 25897 |
rs139498577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100313742 | ACCAGTTAAGAGGCT[A/G]TTCCAGGAATCCAAT | 25897 |
rs139522288 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100320683 | GAAGGTAATAAAAAT[A/G]CCTTCTTCATAGGGT | 25897 |
rs139628167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100286142 | ATCGCATCTAAGCTG[G/T]TTTTCTGTCAGAATA | 25897 |
rs139686864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100262097 | GTAAGAATAGGCTAA[A/G]AGTTGATTTCTAGAT | 25897 |
rs139721340 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100265930 | TCATTATCCTTCAGC[A/G]CTGCAGCTAATTCCT | 25897 |
rs139776435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100294718 | GCAGTTTTCCAAAGG[A/G]TATCTTCATCTAGGC | 25897 |
rs139856995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100295325 | TTTTGACAGCACTCT[A/G]TTTTTCGTAGTTACA | 25897 |
rs139910707 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF19A | GRCh38.p7 | 8:100329738 | GAAATGAAGTGTCTT[C/T]CAACACTTAAAGGAT | 25897 |
rs139955016 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257565 | AAAAACTGAGGTTAT[A/G]TAAAGTTATTCACTA | 25897 |
rs140103529 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100326871 | ATAGTTTCTAACTCA[G/T]AATTGGCAAGGTTTA | 25897 |
rs140120696 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100313297 | TACACTTACCAGAGT[A/G]ACAGAAACCAAAGAG | 25897 |
rs140187487 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RNF19A | GRCh38.p7 | 8:100261411 | CCCCAAATTTCATTT[G/T]TAACATTACTATTTT | 25897 |
rs140238752 | snp | A/T | 0.0146672 | 0.084371 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336919 | AGATCTGGAAGCCTG[A/T]TGGAATTAAAAAGTT | 25897 |
rs140245860 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100299482 | TTAAGTGTTTGGACC[A/G]GGTGCGGTGGCTCAC | 25897 |
rs140266928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100303271 | CTATAAGCATTCCTC[A/G]GCTTGCGGTTACATC | 25897 |
rs140271806 | snp | A/C | | | intron-variant | RNF19A | GRCh38.p7 | 8:100322510 | TTTAAACTTTCTCCA[A/C]ATTAGCAATAAGGCT | 25897 |
rs140278689 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100325615 | CTCAAGCCCAGCCTA[C/T]ATTTGCCATATCTTG | 25897 |
rs140280695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100268047 | GGGATTAATTTCTTT[G/T]TATTTTTTAAAAAAA | 25897 |
rs140361780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311241 | TTAAGTGTCTTTGGC[C/T]TCGAATCTTAAAGGA | 25897 |
rs140368875 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | RNF19A | GRCh38.p7 | 8:100273183 | AGATTTTTAAACAAA[C/G]ATGGAACAAATTCCA | 25897 |
rs140488457 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF19A | GRCh38.p7 | 8:100272261 | GATGCAGTGCTGTCA[C/T]AATTTAAACACATAT | 25897 |
rs140509691 | snp | C/T | 8.23825e-05 | 0.00641751 | missense, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100287630 | TCATGGGGATTAAAC[C/T]GTTCAGTACATTCTG | 25897 |
rs140579421 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100275585 | AGGATACCAAATTGC[A/G]TTTAGCCTAATCTCA | 25897 |
rs140658482 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100322135 | TCAGCCTCTCCTTTG[A/C]AGCTTTGAAGCCAAG | 25897 |
rs140704903 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100305437 | ACGCCCCTAGAGCTA[C/T]GCTGTCCAATATGAA | 25897 |
rs140741108 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RNF19A | GRCh38.p7 | 8:100324136 | ACACTGAAGCTGCTA[A/C]TATAATTTATTTTTT | 25897 |
rs140802062 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF19A | GRCh38.p7 | 8:100297268 | TTTCAATTACTTCAA[C/T]GTGTCCTTAGACGCG | 25897 |
rs140821883 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100274408 | TCTTTAGGAAAGAGA[A/C]GCAAATCAATCAGCA | 25897 |
rs140904167 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100303507 | GGATTAGGACATGAA[C/T]ATATCTTTTGTGGGG | 25897 |
rs141024607 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100302455 | AGAGTGAGCCAAGAC[C/G]AGAAGTTCATTTTTA | 25897 |
rs141096913 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100264742 | GCTATGGCCAAATTC[C/T]GTTTGTGCTTTGAAA | 25897 |
rs141118360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100331129 | CCATATGGGTCAGGT[A/G]CTGGGCAATTCAATA | 25897 |
rs141148099 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant | RNF19A | GRCh38.p7 | 8:100261602 | ATACTGGCTCCAGCT[A/G]GTGCCATGGTGCTGG | 25897 |
rs141157854 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RNF19A | GRCh38.p7 | 8:100329157 | TTCGTTCATCCAGAA[C/G]TGCTGGCACAAAGCA | 25897 |
rs141211508 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100287953 | ACGTTTGTTATCTTT[C/T]TTCCTCCGAAACAGG | 25897 |
rs141277914 | snp | A/C | | | intron-variant | RNF19A | GRCh38.p7 | 8:100323792 | AGGGAAAATTTAGGG[A/C]CCTGTGTTAACTTGT | 25897 |
rs141308201 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100263714 | GTATTATTGGTCATC[C/T]GTATTTCTTTTATTA | 25897 |
rs141399519 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | RNF19A | GRCh38.p7 | 8:100270070 | GTCTAAAAATAACTT[C/G]TAGCAGTTTACCAAT | 25897 |
rs141413073 | in-del | -/AAAT | | | intron-variant | RNF19A | GRCh38.p7 | 8:100312950 | CAACAACAACAACAA[-/AAAT]AAATACATAACCTCT | 25897 |
rs141453602 | in-del | -/TAAAT | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100296023 | ATTATTTTCCTCTAA[-/TAAAT]TGATTCCCCAACATA | 25897 |
rs141532244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100277343 | TTGAGACAGAGTCTC[A/G]CTTTGTTGCCCAGGT | 25897 |
rs141590285 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100305488 | CATGATAATCTTTCA[A/G]ATCTATTGGCTTAAA | 25897 |
rs141641606 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF19A | GRCh38.p7 | 8:100285577 | GAATTTACTGTCTTA[A/G]TATCTCCTGGCCAAA | 25897 |
rs141765384 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | RNF19A | GRCh38.p7 | 8:100334540 | GGCTGCACATTATAA[C/G]TATCTGGGGAGCTTT | 25897 |
rs141774346 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100331671 | ATATACGGCGCAAAA[G/T]TTGAAAGGAATAAAA | 25897 |
rs141802682 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | RNF19A | GRCh38.p7 | 8:100286215 | CTATTTTCTTCCCAC[A/C]TTTTTCTTGAAAATT | 25897 |
rs141806052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100333865 | GTCTATCTTTATTTA[C/T]GACCCCATAATGACT | 25897 |
rs141813759 | snp | A/G | 0.0166325 | 0.0896639 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336515 | AACCTTGGATTCCCG[A/G]TGACGTCCTGGCTCC | 25897 |
rs141846071 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100338032 | CACCCAGGCTGTAGT[A/G]CAGTAGCACGATCTT | 25897 |
rs141872318 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF19A | GRCh38.p7 | 8:100264587 | AAATTGTCCTCAAAT[C/T]AAAAAACAATTAAAA | 25897 |
rs141886922 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF19A | GRCh38.p7 | 8:100293445 | TGTCTTCTGGCCTCC[A/G]TCGTTTCTGACAAGT | 25897 |
rs141905737 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100290227 | TCAAGCAATTCTCCT[C/G]CCTCAGCTGGGATTA | 25897 |
rs141939349 | in-del | -/GAAAA/GAAGA | 0.524246 | 0.0821164 | intron-variant | RNF19A | GRCh38.p7 | 8:100291946 | TTTACTAGCACTGTT[-/GAAAA/GAAGA]GAACAGAAAGAGGAC | 25897 |
rs141958430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100324497 | GAAATACTACATTTT[A/G]AAGGCTAAGGAAATC | 25897 |
rs141977642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100272586 | TCTGTCGCTCAGGCT[A/G]GCATGCAGTAGCACA | 25897 |
rs142005927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100313154 | ATTTGAATGCTTACT[A/G]TATTGGGGATGGGGT | 25897 |
rs142007721 | in-del | -/A | 0.117886 | 0.21224 | intron-variant | RNF19A | GRCh38.p7 | 8:100299773 | CAAAATAAAAAAAAG[-/A]AAAAAAAAAGTATTA | 25897 |
rs142099297 | snp | A/G/T | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100264776 | CCTTGCCTTCATAGC[A/G/T]ATTGTGAATCTTGAA | 25897 |
rs142104760 | snp | C/G/T | 8.24442e-05 | 0.00641998 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100259932 | CTAACTGTTCCCAAG[C/G/T]TGACTGTGCCAGATT | 25897 |
rs142112554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100318094 | GCCTACATTAAGGGA[A/T]TTATAGGAGCCATGA | 25897 |
rs142162657 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100317649 | TGTGCTGGTGACCTG[G/T]ACCAGAATCCTCCAG | 25897 |
rs142190365 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | RNF19A | GRCh38.p7 | 8:100314804 | TTTTTCTGTATAAAG[A/T]ACTTCATTGTCATTA | 25897 |
rs142203113 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, intron-variant | RNF19A | GRCh38.p7 | 8:100261712 | ACCAACACTTCCCTC[C/T]CCTATGCTTGGGTTG | 25897 |
rs142213702 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100322352 | AAACAAACTCTTTCC[C/T]TATACCTCATGATCC | 25897 |
rs142229355 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNF19A | GRCh38.p7 | 8:100318921 | CAGTGACCCACAAGA[A/G]GGAATTATGGCCAGA | 25897 |
rs142229521 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100260337 | AAGTTAGAATACATT[A/G]TTAATCATTAAACAT | 25897 |
rs142276122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289888 | AAATATTGGAAACAA[C/T]CCATAATTTTATCAA | 25897 |
rs142291451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100265487 | CATAGAAGCGGTGAT[G/T]AAAAACTGGCTTGTG | 25897 |
rs142314060 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF19A | GRCh38.p7 | 8:100263069 | CAAGTGCAGATTAAA[C/G]AGGAAAGTTACACAT | 25897 |
rs142409483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100295862 | CATATATCACTTTCT[C/T]TTAACAGAGAGAAAT | 25897 |
rs142419878 | in-del | -/TA | | | intron-variant | RNF19A | GRCh38.p7 | 8:100263308 | GTATTTCAAGAAGGG[-/TA]GAGTCTCTACCATGT | 25897 |
rs142506110 | in-del | -/GTTTT | | | intron-variant | RNF19A | GRCh38.p7 | 8:100321102 | GGGTAGCTGTGGCGG[-/GTTTT]TTTCTTAAAATAAGA | 25897 |
rs142518876 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | RNF19A | GRCh38.p7 | 8:100291539 | TAATATCCCACCAAT[A/C]AACATCTAACCATAA | 25897 |
rs142576556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100294087 | AGAGTCTGCTACCTA[C/T]TTTTGAGGGAGTCTT | 25897 |
rs142583313 | in-del | -/ATAA | 0.0166325 | 0.0896639 | intron-variant | RNF19A | GRCh38.p7 | 8:100298340 | TCAAAGGTAAATTAT[-/ATAA]ATAATGTACAGCTAG | 25897 |
rs142604505 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100295749 | TCTACTAGAAATGAT[A/G]TATTTCTACCCAAGC | 25897 |
rs142622708 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF19A | GRCh38.p7 | 8:100326727 | TTCCAAGACCTTACT[A/C]CTTATGGGCCTTAAT | 25897 |
rs142690902 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | RNF19A | GRCh38.p7 | 8:100274063 | GTGCTGGGATTACAG[C/G]CATGAGCCACCGTGA | 25897 |
rs142725215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100278367 | TACTCAAAATAAATA[C/T]TGGTTGGCATTTTAG | 25897 |
rs142760961 | in-del | -/CTG | 0.180702 | 0.240204 | cds-indel, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257353 | ATCATTGAGGTTAAC[-/CTG]CTTTTATTTAAGTGA | 25897 |
rs142766664 | in-del | -/A | 0.0448719 | 0.142907 | intron-variant | RNF19A | GRCh38.p7 | 8:100306654 | AAGTACACAAGTTTT[-/A]AACACCCAAAGTGAT | 25897 |
rs142797271 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100330372 | CCATCCCTCCCTCAT[G/T]CTTGGTTCATAATAT | 25897 |
rs142802037 | snp | C/T | 0.000296736 | 0.012177 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100268829 | TAATCATTGCAGGAA[C/T]AGCAATGCCAGCTAT | 25897 |
rs142908263 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF19A | GRCh38.p7 | 8:100302983 | TGATATTTCTCAGAA[C/T]TAGAATTCTAACGAA | 25897 |
rs142992731 | snp | A/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257157 | TATACAAATACCATA[A/T]GCATTATCAAATAAA | 25897 |
rs143013110 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100308497 | CAGTCAGTGTTAAAG[A/C]AGCAAAAACAGGCAA | 25897 |
rs143029905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100293029 | CATTATATTCTCATA[C/T]GGAGTGTGCCATCTA | 25897 |
rs143152009 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100260977 | ATCTAGGCTTAAGTA[C/T]TGCCTTTGCTTCAAT | 25897 |
rs143268683 | snp | A/G | 0.0115144 | 0.0749975 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258458 | ATGATAATGAAACCC[A/G]GCTTTTGCTGGTAAC | 25897 |
rs143307343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100262286 | AGGAAAAATACAAGA[C/G]AGTAAAGGGGAGGAG | 25897 |
rs143385273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100276455 | AAGTACATGTGATTA[C/T]AAGAGAGCAACACAG | 25897 |
rs143395442 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100279718 | CTTTAGTAGACACGG[G/T]GTTTTGCCATGTTGG | 25897 |
rs143426825 | snp | C/T | 1.65029e-05 | 0.00287248 | missense, intron-variant, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100264106 | TAACTCCTTTTCCAT[C/T]GCCTGCTGAGACTCC | 25897 |
rs143470751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100333651 | GCAAGAGCCCATCTC[C/T]AAAAATTTTTTTAAA | 25897 |
rs143521541 | snp | C/T | 0.143284 | 0.226079 | intron-variant | RNF19A | GRCh38.p7 | 8:100325183 | AAAGTCCTGGGATTA[C/T]AGGCATGAGCCACTG | 25897 |
rs143534381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100263751 | TTCCTCTTCATATCC[C/T]TTACTTAGTTATTTA | 25897 |
rs143557819 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100328790 | TAATGTTTTAAGACA[G/T]CAATGGTTGTGCAAA | 25897 |
rs143644146 | in-del | -/AC | 0.430024 | 0.178876 | intron-variant | RNF19A | GRCh38.p7 | 8:100325766 | GTGTGAGTATGTATT[-/AC]ACACACACACACACA | 25897 |
rs143689117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100326882 | CTCAGAATTGGCAAG[C/G]TTTATTTAAGTGTTA | 25897 |
rs143726301 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100329793 | TCATGGTTTGTTAAT[A/C]CAGAGGGCAAACTGA | 25897 |
rs143816995 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257799 | CCTTAGAGAAAGGTG[A/G]ATTTTTTGTAATACT | 25897 |
rs143888775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100305153 | TGTTGGTCAGGCTAG[C/T]CTTGCCCGACCTCAA | 25897 |
rs144035955 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RNF19A | GRCh38.p7 | 8:100307710 | CCCCAATAAAATAGA[C/G]GTGACCCAAGTGTCT | 25897 |
rs144058189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100313477 | AATTCAAGGCAGCTA[C/G]AGGCTGAACATAGCA | 25897 |
rs144085299 | snp | A/C | | | intron-variant | RNF19A | GRCh38.p7 | 8:100300229 | TACAAAGGAAATATT[A/C]TTAACTGTATAAGGA | 25897 |
rs144122203 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF19A | GRCh38.p7 | 8:100279616 | GGAGTGCAGTGGCAC[A/C]ATCTTGGCTCGCTGC | 25897 |
rs144188983 | snp | C/T | 0.000214562 | 0.0103554 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258723 | CTTCTGAACAGGAAG[C/T]AGTTTGGGTAACCAC | 25897 |
rs144211088 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RNF19A | GRCh38.p7 | 8:100261299 | GATGGGGTTTCGCCA[C/T]GTTGCCCAGGCTGGT | 25897 |
rs144216080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100273507 | GGCATTCCAGGGAAG[C/T]ACTGCTGAAATAAAC | 25897 |
rs144221152 | snp | A/T | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100268833 | CATTGCAGGAATAGC[A/T]ATGCCAGCTATTAAA | 25897 |
rs144250472 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF19A | GRCh38.p7 | 8:100335830 | CGGAGGTGCGGGCCT[A/G]GACAGCAGTGCTCTG | 25897 |
rs144282648 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100279841 | CTCAATTTTTTGTGT[C/T]TTTAGTAGGGATGGG | 25897 |
rs144320392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100266665 | ACAGGCATGCACCAC[C/T]ACTCCCAGCTGATTA | 25897 |
rs144324855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100288729 | CTATGCCACAAGGAT[A/G]AATACAAAGACCAGT | 25897 |
rs144412268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100319021 | GTAGGGACTGGCACC[A/C]TGTGGTTTGCAGCTA | 25897 |
rs144485142 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF19A | GRCh38.p7 | 8:100320621 | TATCAGGGTGATGAA[C/T]GCCCATACATCAAGG | 25897 |
rs144543938 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100268537 | ATACTCAAAGTTTTA[C/T]AATACAAACATACTA | 25897 |
rs144581517 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337505 | CTATCCACTTCAGCT[G/T]CTGTGTCTCTCAGAA | 25897 |
rs144590243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100336101 | CTGATAAGAAACCAG[A/G]TATTACCATGAGCAG | 25897 |
rs144629744 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | RNF19A | GRCh38.p7 | 8:100326137 | TGACCTCATTTCCAG[A/C]CTGGCTTTCATCACC | 25897 |
rs144656203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100312460 | GGCATGGTGGCCCAC[A/G]TCTGCAGTCCCAGCT | 25897 |
rs144699385 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100295323 | ACTTTTGACAGCACT[C/T]TATTTTTCGTAGTTA | 25897 |
rs144761383 | in-del | -/AT | 0.429538 | 0.173972 | intron-variant | RNF19A | GRCh38.p7 | 8:100296588 | TATGTTAATTTGTGA[-/AT]ATATATATATATTCT | 25897 |
rs144766005 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF19A | GRCh38.p7 | 8:100317718 | TTTGACAGGATGAGG[C/T]TGGCTCACGAGGTCT | 25897 |
rs144868108 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100262965 | TGGAGAAGCTACTTA[C/T]TGAGTTAAGGAGGAT | 25897 |
rs144871836 | in-del | -/AGTG | 0.0966517 | 0.197444 | intron-variant | RNF19A | GRCh38.p7 | 8:100332313 | TGTTGTTCTCATGAT[-/AGTG]AGTGAGTTCTCACGT | 25897 |
rs144888632 | snp | G/T | 6.72201e-05 | 0.00579703 | missense, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100288138 | CACACAGCCCTTCAT[G/T]ATATTTAGAGATAAA | 25897 |
rs144953980 | snp | A/G | 0.126909 | 0.217598 | intron-variant | RNF19A | GRCh38.p7 | 8:100319630 | CCGCTCCCAGGTTCA[A/G]GTGATTCTCCTGCCT | 25897 |
rs144977769 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100270916 | CAACTACTTTGCATG[C/T]TGGCATCTGTTTAAA | 25897 |
rs144993659 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF19A | GRCh38.p7 | 8:100323958 | TTTATCTGAGGTCTC[A/G]GGGCCAGAGATCTGT | 25897 |
rs144998225 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100259921 | TGGCATTATCACTAA[C/T]TGTTCCCAAGCTGAC | 25897 |
rs145037612 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100320778 | TAGCTCAAGGCATAC[C/G]TTGAAGATATTGTGG | 25897 |
rs145170162 | in-del | -/A | 0.206947 | 0.246265 | downstream-variant-500B | RNF19A | GRCh38.p7 | 8:100256818 | AAGTTAAATTCAACC[-/A]ATTTACTCAAAAAAA | 25897 |
rs145204710 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF19A | GRCh38.p7 | 8:100299596 | GAAACACTGTCTCTA[C/T]TAGAAATACAAAATT | 25897 |
rs145243277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100303335 | CCTCCTTTTCTGCGC[A/G]TCGTCTTCTCTGTAA | 25897 |
rs145257484 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100323398 | ACAGTAAGAAGAAAA[C/T]AGTAGAGAAAGGCAA | 25897 |
rs145312313 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RNF19A | GRCh38.p7 | 8:100318501 | ACACAAAAAAATGGG[C/T]GCTAATTGTTATATA | 25897 |
rs145364336 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100301522 | TAGCCAACTGACCTA[C/T]TTGTTAAATATCTTA | 25897 |
rs145411802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100328472 | TTTTTGTTTTTTGTT[G/T]GTTTGCTTTTTTTTT | 25897 |
rs145436740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100313856 | TATAATCAGTCATAC[C/T]TGCATGGAATGGAAT | 25897 |
rs145479213 | in-del | -/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100268104 | ACCAAAGAAAATTTC[-/T]TTTTTTTTTTCTTTT | 25897 |
rs145481850 | snp | A/C/T | 0.000450348 | 0.0149994 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258517 | AACCAGCTCCAAACA[A/C/T]GGTTGTACAGTGGTA | 25897 |
rs145559673 | snp | A/C | 0.0279526 | 0.114869 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336779 | AATTATTGTACTCCT[A/C]TTTATAGTTTTTCTG | 25897 |
rs145563203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100319171 | GGTTTACTAAGTTAT[C/T]TTATGGATAAATTGA | 25897 |
rs145624476 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RNF19A | GRCh38.p7 | 8:100272458 | ACAATACCAAAATAT[C/G]TGGAATAATAATAAA | 25897 |
rs145643695 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF19A | GRCh38.p7 | 8:100275954 | TGGTGCCAATCTCCT[A/G]CCAAAAAATAAAAAA | 25897 |
rs145835820 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF19A | GRCh38.p7 | 8:100302706 | GTAGGGGAGAAGAGG[C/T]GAATCCAGTAAAGGA | 25897 |
rs145872722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100283034 | TTTTTTATTGAGCAT[A/G]AGGTTAGCCTGTGGT | 25897 |
rs145877424 | snp | A/G/T | 0.00105585 | 0.0229544 | missense, intron-variant | RNF19A | GRCh38.p7 | 8:100261548 | AACACACACCTGTTA[A/G/T]AACAGTTTACCATGG | 25897 |
rs145880682 | snp | C/T | | | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258621 | GGTTGTTATTTGTTT[C/T]TTTTAGTGCATCGCC | 25897 |
rs145915440 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100314941 | CCTTCCCTAGGTGCT[G/T]CGAGACACCAATATG | 25897 |
rs146012675 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100329595 | AGCACATTTTAAAGA[C/G]AGACACATGCAAACT | 25897 |
rs146025017 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100334257 | TTCTTGTGTGCTAAT[C/T]TTGACTTTTCAACTA | 25897 |
rs146040489 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100324881 | CTTTCTCTTTTTTTT[C/T]TTTCTTTCTCTCTCT | 25897 |
rs146085465 | in-del | -/T | 0.2776 | 0.248472 | intron-variant | RNF19A | GRCh38.p7 | 8:100319509 | ACTGCTATCCTGAAG[-/T]TTTTACCTATCTGGT | 25897 |
rs146130198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100263442 | GAGTGGTAGGGACAA[A/G]AATCTGATTGAGGCC | 25897 |
rs146134826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100313233 | TCCGTTTGCATGGTG[C/T]TTACATTGGGGGATG | 25897 |
rs146228620 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | RNF19A | GRCh38.p7 | 8:100334573 | AAAATATGGCTGCTC[A/T]CCTTCTCCCTTTCTT | 25897 |
rs146265711 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100293933 | GTACTTTTCAGTTCT[A/G]TAACATCTATTGTTC | 25897 |
rs146340012 | snp | A/G | 1.6492e-05 | 0.00287154 | synonymous-codon, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100264780 | GCCTTCATAGCGATT[A/G]TGAATCTTGAATTAA | 25897 |
rs146378972 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | RNF19A | GRCh38.p7 | 8:100261993 | TATAAAGAATATGAT[G/T]GTTAAAAAATATCGC | 25897 |
rs146389528 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100265828 | TCCCATTTCCCAGCA[C/T]TGACTAGAGGTTCCT | 25897 |
rs146432983 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF19A | GRCh38.p7 | 8:100308172 | AAAAAAATACACTAA[C/T]ATTAGTTGCCAACTG | 25897 |
rs146460513 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100313643 | AGATGTTTAAGCAGC[A/G]TGACATCTGATTTGT | 25897 |
rs146473099 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100326803 | CAGTCTGTATCAAAC[A/G]CAAAACTGTATTTGA | 25897 |
rs146522290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311885 | CCAGAGATGCTGCTT[C/T]TGGCTTTCTTGTCTT | 25897 |
rs146592466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100306807 | AGACATCTTCTATCT[A/G]CTAACAGAGAACTGG | 25897 |
rs146654179 | in-del | -/C | 0.0240643 | 0.107019 | intron-variant | RNF19A | GRCh38.p7 | 8:100284986 | CAAGTAACTTGGTTA[-/C]CCCCCTGAAGTTCAC | 25897 |
rs146699919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100303256 | TCCAGCTTCTGGTGA[C/G]TATAAGCATTCCTCG | 25897 |
rs146797695 | snp | A/G/T | 0.0379877 | 0.132479 | intron-variant | RNF19A | GRCh38.p7 | 8:100327291 | GAGTCTCACTCTGTC[A/G/T]CCCAGGCTGGGGTGC | 25897 |
rs146823605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100330009 | TCCTAATTTGTTTTT[C/T]TGTGGGGGAGGCAGT | 25897 |
rs146823667 | snp | A/T | 1.9877e-05 | 0.00315247 | intron-variant | RNF19A | GRCh38.p7 | 8:100274908 | AGTTAAAATAACTAG[A/T]GTTTTGTGTCAAATA | 25897 |
rs146835782 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258086 | TTATGCCGATATAAA[C/T]AGAAATGTTACAGAG | 25897 |
rs146916635 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100300980 | CACCAACTTTATGTG[A/G]CTGTGAAACCTATCC | 25897 |
rs146954005 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF19A | GRCh38.p7 | 8:100284506 | CAATAACACCAAAAA[C/T]TAATGTATGGCCAAA | 25897 |
rs146984685 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311281 | GGGTATGTTTATTTT[A/C]ATTTATGGGAAGTTT | 25897 |
rs147007906 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF19A | GRCh38.p7 | 8:100314496 | TTAAACCTACCCCTG[A/G]CCCCTTCCCTGGTGT | 25897 |
rs147079123 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100332106 | CACATATTGTGAATT[A/G]CCTGTAGGATAAATT | 25897 |
rs147088547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100283183 | AGAAGAACTCACATG[A/G]GATGACAGGGATAAT | 25897 |
rs147127748 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100320862 | CAAATTTATGGTTTC[C/G]TATTATATAAAAGTT | 25897 |
rs147213781 | in-del | -/TATAA | 0.122064 | 0.214785 | intron-variant | RNF19A | GRCh38.p7 | 8:100282511 | CAAGCTATTAACTCT[-/TATAA]TATGTTTATGTATGT | 25897 |
rs147234793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100302365 | TGATGGATTACAAGA[G/T]GATTTGGCCTGATTA | 25897 |
rs147258264 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100305358 | TGGCCTCAAAAGACA[C/T]ATCAATCAGTTAGAA | 25897 |
rs147341084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100273781 | TCTTTATTTTATTAT[C/T]ATCATCATTATTATT | 25897 |
rs147365295 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100279079 | TCTGAGTCTAGAGAC[C/T]TAAACTCATGAAAAT | 25897 |
rs147432652 | in-del | -/T | 0.3435 | 0.231857 | intron-variant | RNF19A | GRCh38.p7 | 8:100277790 | AGAAAAAAGACCCTA[-/T]TTTTTTTAATCAAAG | 25897 |
rs147500000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100277800 | CCCTATTTTTTTTAA[C/T]CAAAGTTTTAATCTA | 25897 |
rs147572807 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | RNF19A | GRCh38.p7 | 8:100267820 | TCTGGGATTACAGGC[A/C]CCTGCCACCATGCCT | 25897 |
rs147624532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100314684 | CCTAAAATGCCCCCT[C/T]CCCTCTCCTCTGCCT | 25897 |
rs147645049 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100318891 | AGATTTGGGAATGCA[C/T]AGTCCAGATGATAAC | 25897 |
rs147751679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100295533 | TTTGGATCTGCTCAG[C/T]CTCTGGTGCTACATA | 25897 |
rs147763737 | in-del | -/TTAGG | | | intron-variant | RNF19A | GRCh38.p7 | 8:100314369 | CCTAAAGCTCCCAAA[-/TTAGG]ATCTGAGGCACAAGA | 25897 |
rs147785346 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon, intron-variant | RNF19A | GRCh38.p7 | 8:100261601 | TATACTGGCTCCAGC[C/T]AGTGCCATGGTGCTG | 25897 |
rs147832823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100263685 | TTGAATAACATTGAG[C/T]TGAAGATATTTTTGT | 25897 |
rs147937540 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF19A | GRCh38.p7 | 8:100331664 | AAACCAGATATACGG[C/T]GCAAAATTTGAAAGG | 25897 |
rs147960871 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336328 | ACAATGAGTCTGCAG[A/G]CTGAAATAGGTCAGG | 25897 |
rs147979095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100333838 | AATAACAACAAAAAC[C/T]GAAAACACATTGTCT | 25897 |
rs147989454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100285323 | TGGTGACAATCTAAT[A/G]TTTTCCCCCTCAAAT | 25897 |
rs148057301 | in-del | -/AG | 0.0111196 | 0.0737302 | intron-variant | RNF19A | GRCh38.p7 | 8:100314887 | CACCTAGTGAGAGAA[-/AG]AGGAAGCAGGCACAG | 25897 |
rs148117044 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100264575 | CAGGCTCAATTTAAA[C/T]TGTCCTCAAATTAAA | 25897 |
rs148147966 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100324468 | TTTCTTTAAAACAAA[C/T]AATGGATTCCCTTGA | 25897 |
rs148193031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100293142 | ATGCTCACGGCTGCT[C/T]GCCTCCTGCTGCGTG | 25897 |
rs148327294 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100315832 | TTGTTAAAATAGATT[C/T]CTGAGTTTCATATCA | 25897 |
rs148357865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100276852 | ATACATATAACTAAA[G/T]ACACTGTGCAGAAAT | 25897 |
rs148429927 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF19A | GRCh38.p7 | 8:100267335 | AAATAAGTAAAAGTA[C/T]ATACAACACCTATGA | 25897 |
rs148472375 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNF19A | GRCh38.p7 | 8:100326369 | ACAGCGATTCCCAGC[A/G]TTTTCCATTCTTCTA | 25897 |
rs148483250 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF19A | GRCh38.p7 | 8:100273851 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 25897 |
rs148493533 | snp | C/T | 3.30158e-05 | 0.00406286 | synonymous-codon, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100269937 | ACCACAAACAGCACA[C/T]GTCATGTGATTGCAG | 25897 |
rs148505308 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF19A | GRCh38.p7 | 8:100256669 | CTAATGTTGCTAGAA[C/T]AGAATCTCTTAAAAT | 25897 |
rs148525571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100330015 | TTTGTTTTTTTGTGG[A/G]GGAGGCAGTGGGAGG | 25897 |
rs148586544 | snp | A/T | 0.181978 | 0.240568 | intron-variant | RNF19A | GRCh38.p7 | 8:100312728 | CAGGAGTTTGATACC[A/T]GCCGGGACAACATGA | 25897 |
rs148639618 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100317908 | AGACAATAAATTACA[C/T]GGTCACCCTGGTAAT | 25897 |
rs148683525 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100279670 | CTCAGATTACAGGGG[C/T]GCATCACCATGCTTG | 25897 |
rs148711457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100335946 | GCCGCTTTCTATACT[A/G]TGAACCAACGGGACA | 25897 |
rs148733973 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289403 | TAAGGGTATGGGAGG[A/G]GACTTTTGCCACATA | 25897 |
rs148803630 | in-del | -/A | 0.149999 | 0.229128 | intron-variant | RNF19A | GRCh38.p7 | 8:100307547 | ACAAACTGCCGCAAC[-/A]AAAAAAAAAACCGTG | 25897 |
rs148838495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100333562 | TGTCAAAGCAGCAGT[C/T]ACCTGTGTTTAGAGA | 25897 |
rs148915383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100314324 | GATTGCTTTATAAGT[A/G]TTAAGCCACTTAGTT | 25897 |
rs148964920 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100319463 | TACTTTGCACCTTCC[C/G]CTAGTGCACCATTCC | 25897 |
rs148975194 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF19A | GRCh38.p7 | 8:100302894 | AAAGAAACGATACAA[A/G]CAAAATAACAAAATG | 25897 |
rs148995761 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RNF19A | GRCh38.p7 | 8:100283141 | ATAATAAATGTTCTT[A/G]TATATTCAAAGCTCC | 25897 |
rs149027946 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF19A | GRCh38.p7 | 8:100308217 | AAGACACCTTGCGAT[A/G]ACATTAAAATATTTT | 25897 |
rs149039557 | snp | A/C | | | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337439 | TTTTGAGCTGTCATG[A/C]TGCCAGTTTTGGCAA | 25897 |
rs149229221 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RNF19A | GRCh38.p7 | 8:100276267 | ATCAATAAAGAAAGT[A/C]TTGATGCAAGTAACA | 25897 |
rs149280701 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100320420 | TGCTCATGCAGGAGA[G/T]TTTCTCTAGGTTATA | 25897 |
rs149304257 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100304184 | CCAGGCTGGTCTCGA[A/G]CTCCTAACCTCAGGT | 25897 |
rs149330825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100325674 | CACAACTTAACAGAC[C/T]GATTATCTAGTCATT | 25897 |
rs149354412 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100312170 | TACCCCGGAAATATC[C/G]CTGTGCTCTCTGTTC | 25897 |
rs149473345 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100293025 | CAGGCATTATATTCT[C/T]ATATGGAGTGTGCCA | 25897 |
rs149492589 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100273115 | CAAGCGATCCTCCTG[C/T]CTTGGCCTCCCAAAG | 25897 |
rs149669848 | snp | C/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100313803 | GAGACTGTGGAGACA[C/G]AAGTGGATGGTTTTG | 25897 |
rs149797213 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF19A | GRCh38.p7 | 8:100295305 | TCCTAGTAGACTTTA[A/G]ATACTTTTGACAGCA | 25897 |
rs149806165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100274604 | AGCCCAGGCCGTTCT[C/T]GAACTCCTGGCCTTA | 25897 |
rs149882641 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF19A | GRCh38.p7 | 8:100262766 | GGCTATTACAATAGC[C/T]CAGGAAAGAGGATGG | 25897 |
rs149891168 | snp | G/T | 0.00102106 | 0.0225719 | missense, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100287994 | AAATTCTTCTTTTTT[G/T]GGGTGCCTTTTTGAC | 25897 |
rs149923186 | snp | A/G | 0.00756359 | 0.0610294 | intron-variant | RNF19A | GRCh38.p7 | 8:100323265 | TAGAAAGTTTTTAAG[A/G]AAGAAAGAAAACTTT | 25897 |
rs149932888 | snp | G/T | 0 | 0 | intron-variant | RNF19A | GRCh38.p7 | 8:100270504 | TATCCAAAGCACTAT[G/T]AATTTATTTCTTCTA | 25897 |
rs149938039 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100259914 | TTGGTGCTGGCATTA[C/T]CACTAACTGTTCCCA | 25897 |
rs150006575 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF19A | GRCh38.p7 | 8:100335320 | CAGCCCTGTGAAAGA[C/T]GTACTATTATTATCC | 25897 |
rs150038121 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF19A | GRCh38.p7 | 8:100305851 | TAGGATACCTTACCA[C/T]TTTCAGGGGCAAATA | 25897 |
rs150109937 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100297795 | ACAATTATCTATCTT[A/G]CTCACCTTAAAGCTG | 25897 |
rs150162337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100303531 | TGTGGGGTTACCATG[C/T]AACACACTAAAATAT | 25897 |
rs150238621 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100292255 | TATTTGCATGTGAGA[C/T]TGGGAATCCACGAGG | 25897 |
rs150255906 | snp | C/T | 0.00350377 | 0.0417086 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100264745 | ATGGCCAAATTCCGT[C/T]TGTGCTTTGAAACAT | 25897 |
rs150319511 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337279 | GCAGCTTCTCTCCCT[C/G]TTTCTGTTCCTCCCT | 25897 |
rs150392305 | in-del | -/TAC | | | intron-variant | RNF19A | GRCh38.p7 | 8:100327240 | ATAAAATTCAGCAAT[-/TAC]TTCTTTTTTTTTTTT | 25897 |
rs150424476 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100261214 | ATCCTCCTACCTCAG[A/C]CTCCCGACCAGCTGG | 25897 |
rs150468171 | in-del | -/GG | | | intron-variant | RNF19A | GRCh38.p7 | 8:100292433 | GGCTTGCTATCATAT[-/GG]GGGTGTGTGTGTGTG | 25897 |
rs150500589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100285701 | ATAGTGGCGCAATCA[C/T]GGCTCACTGCAGCCT | 25897 |
rs150550860 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RNF19A | GRCh38.p7 | 8:100294672 | TTTCTTTAGGGGGAA[A/T]GATGTATAAATTTTT | 25897 |
rs150577396 | snp | C/T | 6.59055e-05 | 0.00574007 | missense, utr-variant-5-prime, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100287609 | TCACTTAATATCAAG[C/T]GAATATCATGGGGAT | 25897 |
rs150620903 | in-del | -/GTGTTTTTA | 0.00795532 | 0.062565 | intron-variant | RNF19A | GRCh38.p7 | 8:100279837 | CAGCCTCAATTTTTT[-/GTGTTTTTA]GTAGGGATGGGGTTT | 25897 |
rs150679013 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF19A | GRCh38.p7 | 8:100272684 | TGGCACACACCACTA[C/G]AGATGCACACCACCA | 25897 |
rs150686515 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257204 | TTATAAGCATATTAA[G/T]GGACCTGGTAGGGAA | 25897 |
rs150708646 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | RNF19A | GRCh38.p7 | 8:100329174 | GCTGGCACAAAGCAA[A/C]AGTGGGTGCAAAGGT | 25897 |
rs150729581 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100318336 | AAAGGATGTATTTTA[C/T]ATACTTAACTCACTC | 25897 |
rs150845822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100301070 | GAGCTAGTAGGTTCG[A/C]TGTATCACCACTAGT | 25897 |
rs150890540 | snp | A/G | 0.126909 | 0.217598 | intron-variant | RNF19A | GRCh38.p7 | 8:100319985 | GGATTACAGGTGCCC[A/G]CCACCATGCCTGGCT | 25897 |
rs150910283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100305535 | ATTTTGCCTGTTTCC[C/T]TTTACTTCTTTAATG | 25897 |
rs150994945 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF19A | GRCh38.p7 | 8:100274160 | GAGAATGTGGGATTT[A/G]AATTCAGGCAGTCTG | 25897 |
rs151016009 | snp | C/T | 0.000198682 | 0.00996502 | intron-variant | RNF19A | GRCh38.p7 | 8:100260045 | ATTTAATATCAGCAC[C/T]ACTGTAATATGTATC | 25897 |
rs151035116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100330916 | TGCAGACTGGCTCCA[A/G]GGCTCTGAGCTGGTC | 25897 |
rs151045634 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100280440 | GGAGAGTTTAGTTCA[C/T]GGCATGTTATATTTA | 25897 |
rs151164043 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100262356 | TTTTATATGATGTGA[G/T]GACAGAAGGCCTCTT | 25897 |
rs151203989 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100322489 | TTTAATCTTCTATTC[A/C]GACCATTTAAACTTT | 25897 |
rs151226712 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100258957 | GAGCCTCAAATTCAC[C/T]TGAGTTCGTGCTTTG | 25897 |
rs151226902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310933 | ATTCTTAGTTGAATA[A/G]ACAAATTCCGTCTGG | 25897 |
rs151235464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100290222 | TGGGTTCAAGCAATT[C/T]TCCTGCCTCAGCTGG | 25897 |
rs151288547 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | RNF19A | GRCh38.p7 | 8:100297057 | AATATGTCCATAAAG[A/C]TATTATAATGCTATT | 25897 |
rs180804644 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100321976 | AGCACGTGTAAAGGA[G/T]GTTTAGCAAAATTCT | 25897 |
rs180819312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100283143 | AATAAATGTTCTTGT[A/C]TATTCAAAGCTCCCC | 25897 |
rs180828257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100301635 | AGTCCTACTCCTCTT[C/T]CAAGGCCCAACTCCT | 25897 |
rs180831223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100261133 | ACAGGGTCTCACTGT[C/T]ACTCAGGTTGGAGCT | 25897 |
rs180857375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100330878 | TGAGACTCTTGCTGT[A/G]TATACAGCATTAATG | 25897 |
rs180873432 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310840 | ATTACTTTAATCCAG[C/G]TTTATTTGTTCCTTC | 25897 |
rs180939609 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100325844 | CGTCAAGCAAGACTT[A/T]AACTCATTTTCTTCC | 25897 |
rs180961670 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100287047 | CATACTGTGGCACAT[G/T]CTAAGGTAGGTACCT | 25897 |
rs180969260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100305798 | TCTGCACATTTCACA[G/T]AGTCTCATTTGTGAT | 25897 |
rs180975243 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100266415 | ACAGTCTCTCTTTCC[C/G]TTCTAAGTATCTGAA | 25897 |
rs180981180 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337254 | AACTGAAGAAAGCAT[A/G]TGTGATCAGGCAGCT | 25897 |
rs180986024 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RNF19A | GRCh38.p7 | 8:100316672 | GACATAAAGACTCTC[C/G]ACGTCCCCACCAGAC | 25897 |
rs180987759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100277548 | TGATTTCCTGACCTT[C/G]TGATCTGCCCGCCTC | 25897 |
rs181018512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100296397 | GGCGTAAGCCACCAC[A/G]ACCAGCCTCCGGGCA | 25897 |
rs181062580 | snp | A/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100326697 | GAGCTCTTGAATTCA[A/T]TCCCTTCTTCCCTCT | 25897 |
rs181124165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100306638 | TTTTGAGAAACAAAT[C/G]AAGTACACAAGTTTT | 25897 |
rs181135760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100294703 | TAAGGAAAACATCTT[A/G]CAGTTTTCCAAAGGA | 25897 |
rs181158266 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100336095 | GCAAAACTGATAAGA[A/T]ACCAGATATTACCAT | 25897 |
rs181158910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100276052 | TCTCCGAGTTAATAT[A/T]TCTGACACTTTAAAA | 25897 |
rs181161896 | snp | A/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100267019 | TCGGGTCCCAGAAGT[A/T]AGAAACAGAAATAAA | 25897 |
rs181163223 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100315852 | GTTTCATATCAGACT[A/G]ACAGACTCATTTTCT | 25897 |
rs181289371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100290574 | ACATTTCACTCAAAC[A/G]AACTTCACCTCATGT | 25897 |
rs181372799 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100271062 | AAGCATTAAGCTATA[A/T]TCCATTCTTTCTACA | 25897 |
rs181558318 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336514 | TAACCTTGGATTCCC[G/T]ATGACGTCCTGGCTC | 25897 |
rs181582914 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF19A | GRCh38.p7 | 8:100295808 | TTATAAATCTGAATC[A/G]TATCATTAAGAGAAG | 25897 |
rs181591035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100277140 | TGTCTTTTGTAAATA[C/G]TAAACATTTCCTTTT | 25897 |
rs181595995 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF19A | GRCh38.p7 | 8:100316211 | GTGGGCTTGTGGTCT[C/T]GCTGGCTCAGGAGTG | 25897 |
rs181699764 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100299919 | TCTCCTAAAGGACAC[A/C/T]ATGAGTAAGGGGGAG | 25897 |
rs181704528 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100271839 | CTCCAAATACCCTCA[C/T]GATGCAAAAATCCTA | 25897 |
rs181710675 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF19A | GRCh38.p7 | 8:100281502 | CATCAAGCAAGTAGG[A/G]ATACCAGATAGGGTG | 25897 |
rs181712027 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF19A | GRCh38.p7 | 8:100320960 | ATTTAAAAATACTTC[A/G]TTGCTAAAAAATACT | 25897 |
rs181824178 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100311550 | AGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 25897 |
rs181973236 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100300650 | ACAGTGAGGCCCTGT[C/G]TCTGAAAAAAATGAA | 25897 |
rs181984795 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF19A | GRCh38.p7 | 8:100260864 | ATTATCCCGGTCCCA[C/G]TTCACACATTCCTGG | 25897 |
rs182086555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100291343 | TAGCAAGTGCTTAGT[A/C]TTAAATGAATGAATG | 25897 |
rs182096063 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100331645 | AACAAACAAAACAAA[A/C]CAAAAACCAGATATA | 25897 |
rs182150178 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100286206 | TCATTATTCCTATTT[C/T]CTTCCCACCTTTTTC | 25897 |
rs182224774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100321542 | TGAGAGTTGGAGTCA[A/C]CTTCTTTCAAGCTGC | 25897 |
rs182242141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100323328 | TATCTGAATATTTTC[C/G]TTTTCCTTTCACATT | 25897 |
rs182259773 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RNF19A | GRCh38.p7 | 8:100282812 | AATTCTAAAAATACA[A/T]GTTATTTAGTCCCTA | 25897 |
rs182371469 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF19A | GRCh38.p7 | 8:100317153 | CCCAGCCCGGGTTCC[C/T]GCTCGCGCCTCTCCC | 25897 |
rs182372097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100327399 | TGGAATTACAGGCGT[A/G]TGCCACCATGCCCAG | 25897 |
rs182380901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100307733 | AAGTGTCTTACATCC[G/T]CAACTGCAAACATAC | 25897 |
rs182395324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100268374 | AGCTTTGAACTACAG[C/T]AGAAATAATTCAAGA | 25897 |
rs182396367 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100297556 | GTATGCCCTTTCAAG[A/C/G]ACTGACCTCTAAATC | 25897 |
rs182399729 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF19A | GRCh38.p7 | 8:100278166 | AGCCTCAGTATTCAG[C/T]CAAAATAATCTTTGG | 25897 |
rs182407265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100264945 | TCCTTAAACTATTAT[A/G]TATTCTCACAAATAA | 25897 |
rs182509723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100332913 | TCATATGTGTTTCAA[A/T]TTTTTTCTATATTGC | 25897 |
rs182526306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100292533 | TCAAAAGTTTTTAAC[A/G]TGCTCAAATTCACAT | 25897 |
rs182776187 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100338174 | AGTAGAGATGAGGCT[G/T]CTCCATGTTGGCCAG | 25897 |
rs182788704 | snp | A/G | 0.00608657 | 0.0548292 | intron-variant | RNF19A | GRCh38.p7 | 8:100268774 | GGACTAACAAGAAGT[A/G]TGCATTTTACCTTGC | 25897 |
rs182791848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100307992 | CAGTATGGACAGTTC[C/T]TTATATTAAGTCTAC | 25897 |
rs182812376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100274081 | TGAGCCACCGTGACT[A/G]GCCAGTATCTTTATT | 25897 |
rs182812570 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100313614 | ATGATTGGTATGAAG[A/T]GTGATGAGACAATAG | 25897 |
rs182827361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100318947 | CCAGAAGCACATGGC[C/T]CAGAGCAATCCCCAG | 25897 |
rs182857070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100298153 | TGTAAGTATACTCAT[C/G]TGAGAAGATAGCACA | 25897 |
rs182935075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100314202 | TACTCTTTATTGCAT[A/G]CATACTATATATACT | 25897 |
rs182949989 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF19A | GRCh38.p7 | 8:100322815 | AAGAGGAAGAGATGG[A/G]GGAATGGCTGGTCAG | 25897 |
rs182966854 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF19A | GRCh38.p7 | 8:100293023 | ATCAGGCATTATATT[C/T]TCATATGGAGTGTGC | 25897 |
rs182968253 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100274524 | AGCATAAAGTACATG[A/C]TTATCTCAATACACT | 25897 |
rs183022236 | snp | A/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100267534 | ACTACCATACCCAGA[A/T]AATTTTTAAATTTTT | 25897 |
rs183085404 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100288787 | CCATATAGGCCAGGC[A/G]CGGTGGCTCACGCCT | 25897 |
rs183215256 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF19A | GRCh38.p7 | 8:100332409 | CTTGTGAAGAAGGTG[C/T]CTGCTTCTCGTTCCA | 25897 |
rs183233047 | snp | A/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100291490 | AAAACATGTTAAGTA[A/T]CCTGACACTACAACT | 25897 |
rs183253046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100313132 | ATTTAACATCAATTC[A/G]ATAAACATTTGAATG | 25897 |
rs183389372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100287354 | TGCCTTTAACACCTA[C/G]CATAGTGCCTGACAT | 25897 |
rs183405588 | snp | A/G | 0.0119091 | 0.0762411 | downstream-variant-500B | RNF19A | GRCh38.p7 | 8:100256851 | ATGTTGATGTATACA[A/G]TATCTTTTTTTCTGG | 25897 |
rs183405616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100327202 | ATTGGTAAGGAAGAG[C/T]GTTTGAGTATCTAGG | 25897 |
rs183450753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100328759 | ACAGGCGTGAGACAC[C/T]GCACCTGGTCTGCGT | 25897 |
rs183541152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100284050 | AGTTCCTGGTACATA[A/G]GTGCATTAAATATTT | 25897 |
rs183613809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100278540 | TTTCAAATAATTAAA[C/T]AGGAAAACAATTTAC | 25897 |
rs183615626 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100306906 | ATTTAGCTATTCTCC[A/C/G]TAAGTAGTAAGATGA | 25897 |
rs183641381 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100329532 | AAGGAAGTCAATGGT[C/T]CCACTGAACTCAGCA | 25897 |
rs183643749 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100303332 | CTTCCTCCTTTTCTG[C/T]GCGTCGTCTTCTCTG | 25897 |
rs183645707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310737 | GGGTTTGGAGAGTAT[C/T]TTCCATTCATCTCTT | 25897 |
rs183662065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100262264 | TCACACGGTGACAAA[C/T]GCTATGAGGAAAAAT | 25897 |
rs183673710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289414 | GAGGAGACTTTTGCC[A/T]CATATAACTAATAAA | 25897 |
rs183681038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100270839 | CTTGTATAATAATAT[A/G]GTTACAATGCACAAT | 25897 |
rs183727673 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100284925 | AAATTGTATCAGTAT[A/C]CTAAGCATGAACTGG | 25897 |
rs183730115 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100333466 | AAAATGCTCACACTA[G/T]TATATTAGAGGCAAG | 25897 |
rs183744206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100263003 | AGAAGAGATTTTAGA[A/G]CCAAGAATTTGGCTG | 25897 |
rs183756787 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100302637 | AGATGAAATCACCAA[A/G]AAGTAAATATTAAAG | 25897 |
rs183790833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100261864 | AGGTATAAAATATAC[A/G]CAGACATGGAAAAAT | 25897 |
rs183882105 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF19A | GRCh38.p7 | 8:100323188 | TTAGCTGTTACCCAG[A/G]GTGTTATTTTAAGAT | 25897 |
rs183894647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100284530 | GGCCAAATTAATCAC[A/G]GACAATTATTTGTTA | 25897 |
rs183979441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100259572 | TGTGATCAGAGCTGT[A/G]CAACCATCACCACTA | 25897 |
rs184225339 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100293952 | CATCTATTGTTCTTT[C/T]TCATAGTTTCCATTT | 25897 |
rs184230540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100334839 | CAGCTATAGCCTTTG[C/T]TGTATTTCAAAGGTG | 25897 |
rs184283790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100269692 | TATCCATTTCCTATT[C/T]TGACTAGTTATTAAT | 25897 |
rs184289205 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100289008 | GAGCTTGCAGTGAGC[C/T]GAGATTGCGCCGCTG | 25897 |
rs184329814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100299809 | TTGGACTAATCTTAT[A/C]CTAACCACTTTCTCT | 25897 |
rs184337167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100280962 | TTCCAGGAGTCTCTC[C/T]GCTCTGGTATAATAA | 25897 |
rs184343502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100320703 | CTTCATAGGGTTTCT[A/G]TGTGGATTAGATAAA | 25897 |
rs184356662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100315736 | ATCACCTTGACCTCT[G/T]GGACTCAAGCGATCC | 25897 |
rs184398274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100276048 | CCTTTCTCCGAGTTA[A/G]TATTTCTGACACTTT | 25897 |
rs184420461 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF19A | GRCh38.p7 | 8:100319893 | CAGGACAGAGTGCAA[G/T]GGTAGGGTCTTGGCT | 25897 |
rs184431112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100279755 | TTGTCTCGAACTCCA[A/G]ACCTCAAGTGATCCG | 25897 |
rs184450269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100321010 | AGCAAGTCAAAGACA[C/T]AATCTTTTTGCTGGT | 25897 |
rs184515939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100275417 | GTTCAGGGTTTTTTT[C/T]TTAGATTCAGGGGGT | 25897 |
rs184531365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100293428 | AAAATAGGTTATTAC[A/G]CTGTCTTCTGGCCTC | 25897 |
rs184562199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100294937 | AAACTTTTTGCCTTA[C/T]TTGCTCCAAGTAACC | 25897 |
rs184572396 | snp | A/G | 0.0107246 | 0.0724382 | utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100336208 | ATGAGAGAAGAGGGC[A/G]CGGCGAAGGTGATCC | 25897 |
rs184577747 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RNF19A | GRCh38.p7 | 8:100257147 | TGCAAACAAATATAC[A/C]AATACCATAAGCATT | 25897 |
rs184580877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100315908 | TTTTCCACAAGCTCT[C/T]CAGGTAATTCATATC | 25897 |
rs184863992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100315220 | TTAAGCCTGGGAGTT[A/G]TAGGGTGCAGTGAGC | 25897 |
rs184873503 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100265480 | ATATCATCATAGAAG[C/T]GGTGATTAAAAACTG | 25897 |
rs184875514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100333940 | CCCGATATTCTAACT[G/T]TGGCCCCACTCTACT | 25897 |
rs184880312 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100286339 | TGTTGTTATCTATAT[G/T]ATAGTACAAGCTCCC | 25897 |
rs184956531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100325895 | TTATTTAATTAACAA[A/G]CTGAGCTACTAGAGA | 25897 |
rs184968673 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100306221 | CCAAAGACTCAGTTT[C/T]GAAGTTTCTTTTGGG | 25897 |
rs184985951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100287102 | TGAGAAACATGTCAA[A/C]AAAGAGAAAAAAAAT | 25897 |
rs185002377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100266566 | CTCAGACTAGAGTGC[A/T]GTGGCACGATCACAG | 25897 |
rs185074687 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF19A | GRCh38.p7 | 8:100328983 | TAGGAATCTGGGTCT[C/T]GCGCAGGTTTATCAG | 25897 |
rs185095663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100300067 | TAAAATTTTCTTCAA[A/T]CTATAAGGTAATTCT | 25897 |
rs185102187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100260044 | TATTTAATATCAGCA[C/T]TACTGTAATATGTAT | 25897 |
rs185117238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100260979 | CTAGGCTTAAGTACT[A/G]CCTTTGCTTCAATGT | 25897 |
rs185202271 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100282048 | CTTCAGTTGTTCTCA[A/G]GGCTACATGCCTGAG | 25897 |
rs185206738 | snp | C/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100324102 | TTTTGAGATGACTTT[C/G]TTCAAAGAAAATTCC | 25897 |
rs185221533 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | RNF19A | GRCh38.p7 | 8:100309311 | ACCTTCCTCCGAACA[C/T]AGCTCCCCTCCCTAA | 25897 |
rs185238839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100285380 | GAATAATCAATTCTT[C/T]TCCAGTTGGTTTGGC | 25897 |
rs185315487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100291789 | ATGGAGAAAATCCAG[G/T]AATTTTGTGCTGATG | 25897 |
rs185333237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100313280 | AAATAATGAAAAGGA[A/T]ATACACTTACCAGAG | 25897 |
rs185355523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100305161 | AGGCTAGTCTTGCCC[A/G]ACCTCAAATGATCTG | 25897 |
rs185369773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100264480 | TGGAGTGGGGAGGAA[A/G]GGTATCAGCCACTAA | 25897 |
rs185600238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100322509 | ATTTAAACTTTCTCC[A/G]AATTAGCAATAAGGC | 25897 |
rs185621630 | snp | A/G | | | intron-variant | RNF19A | GRCh38.p7 | 8:100283804 | GAACCTTTCAAGTGT[A/G]TTATATAATAAAAGG | 25897 |
rs185631829 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF19A | GRCh38.p7 | 8:100301915 | GGAGGTAAAGGAGGT[A/G]TTAGCTATGTGGAAA | 25897 |
rs185635355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100261268 | TCCGGCTAATTTTTT[A/G]TATTTTTTTAGTAGA | 25897 |
rs185745146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100305622 | ACACTGCTGAAGAGA[C/T]AGTTATAAAATAAAT | 25897 |
rs185803571 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100337829 | CCTATCAGCACCTGG[A/T]GTTAGATTATCTAGT | 25897 |
rs185844806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100325472 | GAGACCACACCTTGT[C/T]ACCTCTAGGTCCTCC | 25897 |
rs185849970 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF19A | GRCh38.p7 | 8:100296922 | TCCGATTCATCACAC[A/T]AGAATAAACATTATG | 25897 |
rs185944592 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF19A | GRCh38.p7 | 8:100316757 | GCTGCCTGCCAGTCC[C/T]GCACCGTGCGCTCTC | 25897 |
rs185966375 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF19A | GRCh38.p7 | 8:100321637 | TACAGAAAGTTTTCA[A/G]TTCACCCAGATCCAT | 25897 |
rs185978322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100291354 | TAGTATTAAATGAAT[A/G]AATGATGCTTTTCAG | 25897 |
rs185979011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF19A | GRCh38.p7 | 8:100277907 | TCTCTACCTACCTTT[C/T]ATTGAAGGAAGGAAG | 25897 |
rs186002884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100282975 | TTACCCAAATGTATA[G/T]GAGTTATGTTAGTAG | 25897 |
rs186004893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100272011 | AAATATGGGCCATTG[C/T]CATATTAAGAAAAAA | 25897 |
rs186098754 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | RNF19A | GRCh38.p7 | 8:100272851 | CACTGCGCCCAGCCC[G/T]CACTGCATTTCTAAT | 25897 |
rs186127030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF19A | GRCh38.p7 | 8:100300685 | AAAAAAATTAAAAAA[C/T]AAAAAAACAAAAGCA | 25897 |
rs186153165 | snp | G/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100276102 | GGCATTCTTTGGCAT[G/T]TATCCCAAACAAATG | 25897 |
rs186429071 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF19A | GRCh38.p7 | 8:100332683 | TTATTAAACATTTTG[A/G]TCTTTGCAAATTTGT | 25897 |
rs186506414 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100310946 | TAAACAAATTCCGTC[C/T]GGGCCTGGTGCATTT | 25897 |
rs186520989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100271420 | CGTGGTATACTAAAT[G/T]AAGGAAATGCTAATC | 25897 |
rs186535020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100307251 | TCCTATATAACCCGA[C/G]TAGAGAAGATATAAG | 25897 |
rs186539633 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | RNF19A | GRCh38.p7 | 8:100336799 | TAGTTTTTCTGTTTC[C/T]TCCTTTGCTGCTAGG | 25897 |
rs186543477 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100287417 | TTCTCCAGCATGTAA[A/C/G]AATTTTTCTTTTGAG | 25897 |
rs186569066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF19A | GRCh38.p7 | 8:100316243 | AGCAGCAGACCTTCG[A/C]GGTGAGTGTTACAGC | 25897 |
rs186641104 | snp | C/T | | | intron-variant | RNF19A | GRCh38.p7 | 8:100331661 | CAAAAACCAGATATA[C/T]GGCGCAAAATTTGAA | 25897 |