SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs954182 | snp | C/T | 0.140919 | 0.224948 | intron-variant | RNF38 | GRCh38.p7 | 9:36414243 | GCCATTTACATTCAA[C/T]GTTAGTATTGAGATG | 152006 |
rs954779 | snp | A/G | 0.413083 | 0.189483 | intron-variant | RNF38 | GRCh38.p7 | 9:36419532 | TTCACCTCAACTGAG[A/G]GAATAGTCTTATCAA | 152006 |
rs965999 | snp | A/G | 0 | 0 | intron-variant | RNF38 | GRCh38.p7 | 9:36398344 | gaggccaagaaagga[A/G]gatcacctgggccca | 152006 |
rs1106275 | snp | C/T | 0.274124 | 0.248833 | intron-variant | RNF38 | GRCh38.p7 | 9:36457218 | CTTTCTTACCAAACA[C/T]GAAGGCACTGAATTA | 152006 |
rs1106276 | snp | C/T | 0.214843 | 0.247516 | intron-variant | RNF38 | GRCh38.p7 | 9:36457224 | TACCAAACACGAAGG[C/T]ACTGAATTAATAGGA | 152006 |
rs1125295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF38 | GRCh38.p7 | 9:36485344 | cagacatattcattt[A/G]cctaaaatgtccatt | 152006 |
rs1475529 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | RNF38 | GRCh38.p7 | 9:36410918 | ttttcatcttcctaa[A/G]ctgaaattctaccca | 152006 |
rs1889278 | snp | G/T | 0.121022 | 0.21416 | | | GRCh38.p7 | 9:36407387 | CACTACCATGAGCTT[G/T]CCCTCTGTCATTCCA | 152006 |
rs1889279 | snp | A/G | 0.465578 | 0.126594 | | | GRCh38.p7 | 9:36407328 | TCACCTGCACTGTGG[A/G]AACAGCCACCTGACT | 152006 |
rs1889280 | snp | A/C | 0.111576 | 0.20818 | | | GRCh38.p7 | 9:36407319 | CTGTGGAAACAGCCA[A/C]CTGACTAACTCTTCA | 152006 |
rs1962524 | snp | C/T | 0.466824 | 0.124448 | intron-variant | RNF38 | GRCh38.p7 | 9:36485205 | acagaagactacata[C/T]atttttatttattat | 152006 |
rs1970944 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | RNF38 | GRCh38.p7 | 9:36420329 | tagccaggatggtct[C/T]gatctcctgacctcg | 152006 |
rs1980921 | snp | C/T | 0.449345 | 0.150869 | intron-variant | RNF38 | GRCh38.p7 | 9:36355853 | ATTACGTTTGTTTGT[C/T]TGTTTATTTTGGAGA | 152006 |
rs2065607 | snp | C/T | 0.102726 | 0.202016 | intron-variant | RNF38 | GRCh38.p7 | 9:36480136 | caaaacttagctggg[C/T]gtggtggtgtgaacc | 152006 |
rs2065608 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RNF38 | GRCh38.p7 | 9:36444957 | TAACCAGAAATCTCT[A/G]GCGATCACTGATAGG | 152006 |
rs2183265 | snp | A/G | 0.496874 | 0.0394129 | intron-variant | RNF38 | GRCh38.p7 | 9:36411112 | tgtaaatcatgtcta[A/G]taaggggttaatatc | 152006 |
rs2183266 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | RNF38 | GRCh38.p7 | 9:36359550 | TTCATGCTGCTTTAA[C/T]TACAGTATCTTACTG | 152006 |
rs2243798 | snp | A/T | 0.0494327 | 0.149241 | intron-variant | RNF38 | GRCh38.p7 | 9:36398427 | aaaattaaaaaaaaa[A/T]TTTTTTAATGAAAGA | 152006 |
rs2243808 | snp | A/G | 0.111576 | 0.20818 | intron-variant | RNF38 | GRCh38.p7 | 9:36398248 | CTAGATAGAAGAGGT[A/G]AAAAGTTCAGATCCT | 152006 |
rs2243901 | snp | C/T | 0.111576 | 0.20818 | intron-variant | RNF38 | GRCh38.p7 | 9:36397612 | TAGGGTGTGTGAAAA[C/T]AGCCTAAGGCTCCCC | 152006 |
rs2243933 | snp | C/T | 0.497121 | 0.0378299 | intron-variant | RNF38 | GRCh38.p7 | 9:36396772 | ATATAAAACATAACT[C/T]AATAAAGCTTCTTTA | 152006 |
rs2244376 | snp | A/C | 0.102726 | 0.202016 | intron-variant | RNF38 | GRCh38.p7 | 9:36392908 | CAGGGAAAAATTAGG[A/C]GTAAGAGTTCTGAAT | 152006 |
rs2244511 | snp | A/G | 0.121022 | 0.21416 | intron-variant | RNF38 | GRCh38.p7 | 9:36391873 | ccgcctcggcctccc[A/G]aagtgctgggattac | 152006 |
rs2245484 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | RNF38 | GRCh38.p7 | 9:36431076 | gtagtgggtcctcag[A/G]ctaaccacaactttt | 152006 |
rs2247223 | snp | C/T | 0.119978 | 0.213528 | intron-variant | RNF38 | GRCh38.p7 | 9:36391637 | tttttttttttgaga[C/T]ggagtctcgctgtcg | 152006 |
rs2247595 | snp | A/G | 0.465996 | 0.12588 | intron-variant | RNF38 | GRCh38.p7 | 9:36388353 | TAAACGAAAACCCTG[A/G]ATTTTGGGCAATTAA | 152006 |
rs2247795 | snp | A/C | 0.496905 | 0.0392151 | intron-variant | RNF38 | GRCh38.p7 | 9:36386590 | gctgcattcccatca[A/C]gttaggcattctgag | 152006 |
rs2248070 | snp | A/C | 0.110872 | 0.20771 | intron-variant | RNF38 | GRCh38.p7 | 9:36383738 | TGTTTTCAAAAGTTA[A/C]CATGTTGTTTTCAAA | 152006 |
rs2248297 | snp | C/T | 0.127599 | 0.217986 | intron-variant | RNF38 | GRCh38.p7 | 9:36381905 | TCTTTAAAATGTTTT[C/T]ACAGAGTTGGGTCTT | 152006 |
rs2255698 | snp | C/T | 0.47726 | 0.104176 | intron-variant | RNF38 | GRCh38.p7 | 9:36367125 | ACTCCTTAAATAGTC[C/T]TTGATTTTTGTCCCC | 152006 |
rs2265347 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | RNF38 | GRCh38.p7 | 9:36387018 | atgttggccaggctg[A/G]tctcgaactcctgac | 152006 |
rs2265348 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | RNF38 | GRCh38.p7 | 9:36374678 | gcatcttagtagaga[A/C]gaggcttcaccatgt | 152006 |
rs2277171 | snp | C/G | 0.243061 | 0.249904 | intron-variant | RNF38 | GRCh38.p7 | 9:36375712 | GAAAGAGGCTAAAAT[C/G]AGTCGATGCCATTAT | 152006 |
rs2381484 | snp | C/G | 0.114387 | 0.210022 | intron-variant | RNF38 | GRCh38.p7 | 9:36342889 | CACAAGAATTAACAA[C/G]AAAAAAAGAAATGCA | 152006 |
rs2381520 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | RNF38 | GRCh38.p7 | 9:36416057 | caggtgatgggtggc[A/G]ccatagagctctcaa | 152006 |
rs2381521 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | RNF38 | GRCh38.p7 | 9:36366068 | GTTCAaaaacagtag[C/G]ataaacccccatatc | 152006 |
rs2381522 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF38 | GRCh38.p7 | 9:36457560 | TATGTACAAACTTTA[C/T]GGTTGAAGATAATCT | 152006 |
rs2381523 | snp | A/G | 0.460702 | 0.134554 | intron-variant | RNF38 | GRCh38.p7 | 9:36459681 | CTCTAATTATTGTAT[A/G]GTGCTTACAAAGAAA | 152006 |
rs2381524 | snp | A/G | 0.461481 | 0.133325 | intron-variant | RNF38 | GRCh38.p7 | 9:36460942 | AGGAGGCTGGTCGCG[A/G]TGGCTCACAACTGTA | 152006 |
rs2480455 | snp | A/G | 0.46703 | 0.124089 | intron-variant | RNF38 | GRCh38.p7 | 9:36396919 | CTCTAAGCTTCAACA[A/G]TTCTCATACACAAAT | 152006 |
rs2480456 | snp | C/T | 0.111224 | 0.207945 | intron-variant | RNF38 | GRCh38.p7 | 9:36399529 | ttataaataaatata[C/T]tataaatatatattt | 152006 |
rs2480457 | snp | A/G | 0.121022 | 0.21416 | intron-variant | RNF38 | GRCh38.p7 | 9:36399563 | AACCCCAGAGAAAGG[A/G]GTATCTGAAGTGACA | 152006 |
rs2480458 | snp | C/T | 0.121022 | 0.21416 | intron-variant | RNF38 | GRCh38.p7 | 9:36399826 | ATTGAAAAAAATTTA[C/T]GGTAAATTTTCAAGT | 152006 |
rs2480459 | snp | C/T | 0.0352207 | 0.127945 | utr-variant-5-prime, intron-variant | RNF38 | GRCh38.p7 | 9:36400159 | CTCAATAACCTGAAA[C/T]ACTCCCGTTTCAAAA | 152006 |
rs2480460 | snp | A/G | 0.121022 | 0.21416 | utr-variant-5-prime, intron-variant | RNF38 | GRCh38.p7 | 9:36400242 | AACAAAACGCAGCCT[A/G]TCCAGAAACCCACGG | 152006 |
rs2480461 | snp | C/G | 0.02016 | 0.0983543 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RNF38 | GRCh38.p7 | 9:36400965 | CACAGACCCGGGCTC[C/G]CTATGCGCCGGCGCA | 152006 |
rs2480462 | snp | A/C | 0.102726 | 0.202016 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RNF38 | GRCh38.p7 | 9:36401170 | GCACCGCGCGCCGAA[A/C]CCCCTTTGTTTCCAC | 152006 |
rs2480463 | snp | A/G | 0.466721 | 0.124627 | upstream-variant-2KB, intron-variant | RNF38 | GRCh38.p7 | 9:36401355 | GTTCCAATTCCTATA[A/G]ATTTTCTCTTAGTAA | 152006 |
rs2480465 | snp | C/G | 0.112631 | 0.208878 | intron-variant | RNF38 | GRCh38.p7 | 9:36416398 | tgccctgacaacacc[C/G]ttatatccaggcagc | 152006 |
rs2480466 | snp | A/G | 0.168135 | 0.236216 | intron-variant | RNF38 | GRCh38.p7 | 9:36427512 | agagagctcatgaat[A/G]ggatcagtatcctta | 152006 |
rs2483653 | snp | A/G | 0.496874 | 0.0394129 | upstream-variant-2KB, intron-variant | RNF38 | GRCh38.p7 | 9:36401871 | AAACTCGGGTTTTCA[A/G]GTTCTAGTTCTTTTG | 152006 |
rs2483654 | snp | C/G | 0.102726 | 0.202016 | intron-variant | RNF38 | GRCh38.p7 | 9:36411635 | ggtgcaatcttgggt[C/G]actacaacctccgcc | 152006 |
rs2483655 | snp | A/G | 0.111928 | 0.208413 | intron-variant | RNF38 | GRCh38.p7 | 9:36413386 | cagaactgcaagcca[A/G]tgaaacttttcttta | 152006 |
rs2483656 | snp | A/T | 0.081446 | 0.184634 | intron-variant | RNF38 | GRCh38.p7 | 9:36413962 | ttcctgttggaccag[A/T]ccttttatcattaca | 152006 |
rs2483657 | snp | C/T | 0.464735 | 0.128019 | intron-variant | RNF38 | GRCh38.p7 | 9:36415389 | gttgttttattgatt[C/T]tatttctctggagat | 152006 |
rs2890721 | snp | A/G | 0.113685 | 0.209567 | intron-variant | RNF38 | GRCh38.p7 | 9:36341250 | ATTCTCTGTCCGCAC[A/G]TGTCAGGGATTTACA | 152006 |
rs3072687 | in-del | -/TTT | | | intron-variant | RNF38 | GRCh38.p7 | 9:36480569 | ttttttttttttttt[-/TTT]gagacagggtctcac | 152006 |
rs3209858 | snp | A/G | | | utr-variant-3-prime | RNF38 | GRCh38.p7 | 9:36337399 | TGTAAGTTTTTGAGA[A/G]GCAATTGGCAATTTA | 152006 |
rs3808863 | snp | C/G | 0.466515 | 0.124985 | intron-variant | RNF38 | GRCh38.p7 | 9:36376335 | GCTTATTTTTCACTT[C/G]GTATCATTTACTGTG | 152006 |
rs3824425 | snp | A/G | 0.213937 | 0.247385 | upstream-variant-2KB | RNF38 | GRCh38.p7 | 9:36489164 | CTGCTGAGACCTATC[A/G]GAGGAAAGAAGGTGC | 152006 |
rs3832617 | in-del | -/T | 0.0748431 | 0.178382 | intron-variant | RNF38 | GRCh38.p7 | 9:36358055 | CTATTGGAGAGTACA[-/T]TTGTGAAAATCCGTG | 152006 |
rs3930256 | snp | C/T | 0.111576 | 0.20818 | intron-variant | RNF38 | GRCh38.p7 | 9:36356022 | CGGCTAATTTTTGTA[C/T]TTTTAGTAGAGACAG | 152006 |
rs4097501 | snp | A/T | | | intron-variant | RNF38 | GRCh38.p7 | 9:36414498 | gagaccagcctgacc[A/T]acatggagaaatccc | 152006 |
rs4144593 | snp | C/T | 0.411914 | 0.190483 | intron-variant | RNF38 | GRCh38.p7 | 9:36399023 | CTCATCCAATGCTGT[C/T]GGCAGAGAGACAACA | 152006 |
rs4446808 | snp | A/C | 0.498503 | 0.0273153 | intron-variant | RNF38 | GRCh38.p7 | 9:36422433 | CCACCAAAAAACAAA[A/C]AAAAAAAAACAGGAG | 152006 |
rs4590523 | snp | C/T | 0.234692 | 0.249531 | intron-variant | RNF38 | GRCh38.p7 | 9:36418480 | CAGCATGGTGAAACC[C/T]CATCTCTACGAAAAA | 152006 |
rs4878652 | snp | A/T | 0.219648 | 0.248151 | intron-variant | RNF38 | GRCh38.p7 | 9:36342673 | GATTCTATACTATTT[A/T]AAAAAAAATGGTATT | 152006 |
rs4878653 | snp | A/G | 0.110519 | 0.207473 | intron-variant | RNF38 | GRCh38.p7 | 9:36363980 | ctgggataggcaccc[A/G]ccaccacgtctggct | 152006 |
rs4879986 | snp | A/C | 0.0700422 | 0.173537 | intron-variant | RNF38 | GRCh38.p7 | 9:36357609 | TTGCAATAAAATTGG[A/C]CTTTTTACTTGAAAG | 152006 |
rs4879987 | snp | C/T | 0.103082 | 0.202275 | intron-variant | RNF38 | GRCh38.p7 | 9:36361059 | tgagctcatgtgatc[C/T]gcccacttcagcctc | 152006 |
rs4879988 | snp | A/C | 0.466515 | 0.124985 | intron-variant | RNF38 | GRCh38.p7 | 9:36361306 | acaggtgcctgccac[A/C]atgcccagctaattt | 152006 |
rs4879989 | snp | C/T | 0.499354 | 0.0179596 | intron-variant | RNF38 | GRCh38.p7 | 9:36362904 | cccaaagtgctggga[C/T]tacaagcgtgaggca | 152006 |
rs4879991 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | RNF38 | GRCh38.p7 | 9:36364188 | caccagagacagcaa[A/G]accaactcctcctcc | 152006 |
rs4879992 | snp | A/G | 0.443598 | 0.158176 | intron-variant | RNF38 | GRCh38.p7 | 9:36424738 | CCTTACATTTAAACT[A/G]CTTTACCAATTAAAA | 152006 |
rs4879993 | snp | C/T | 0.461813 | 0.132798 | intron-variant | RNF38 | GRCh38.p7 | 9:36473562 | CACTGCACACCAGCT[C/T]GGGCAACAAGAGCGA | 152006 |
rs5897634 | in-del | -/T | 0.0644693 | 0.167566 | intron-variant | RNF38 | GRCh38.p7 | 9:36339987 | GAATTAGCCCAGGAA[-/T]TTTTTTTTTGAGATG | 152006 |
rs6476555 | snp | A/G | 0.467439 | 0.123371 | intron-variant | RNF38 | GRCh38.p7 | 9:36395949 | GGTAGGGTTATATAT[A/G]AACAGGACTTCATAA | 152006 |
rs6476556 | snp | C/T | 0.498632 | 0.0261223 | intron-variant | RNF38 | GRCh38.p7 | 9:36435008 | GGTGGGAAGAGGAAG[C/T]TCTTTATGTACTGAT | 152006 |
rs6476557 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | RNF38 | GRCh38.p7 | 9:36487839 | CCGCCGCTCCCTGAG[A/G]AGGGGAGGCAGAGCG | 152006 |
rs6476558 | snp | A/C | 0.0119091 | 0.0762411 | upstream-variant-2KB | RNF38 | GRCh38.p7 | 9:36487840 | CGCCGCTCCCTGAGA[A/C]GGGGAGGCAGAGCGC | 152006 |
rs7021367 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF38 | GRCh38.p7 | 9:36395110 | AAAGTTTACAGAAAA[C/G]AGTTTAACCTTTTAA | 152006 |
rs7023399 | snp | C/G | 0.479502 | 0.0991411 | intron-variant | RNF38 | GRCh38.p7 | 9:36478557 | GCACGGTGGCTCATA[C/G]TTGTAATCCCAGCAC | 152006 |
rs7024509 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | RNF38 | GRCh38.p7 | 9:36408295 | tttttgtagagacta[A/G]gtttcaccatgttgc | 152006 |
rs7024993 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | RNF38 | GRCh38.p7 | 9:36408611 | TAATCTAGGAGCTGG[A/G]CCTAAACTTGAGCCA | 152006 |
rs7025573 | snp | A/T | 0 | 0 | intron-variant | RNF38 | GRCh38.p7 | 9:36341867 | ATATATATATATATA[A/T]AGAAGCCCCTGCAAT | 152006 |
rs7029289 | snp | A/G | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | RNF38 | GRCh38.p7 | 9:36402529 | CTCCCTACAGAACGC[A/G]GACCACCCTGAAGTA | 152006 |
rs7030510 | snp | C/T | 0.164219 | 0.234823 | intron-variant | RNF38 | GRCh38.p7 | 9:36381034 | agaaggaaacgtcaa[C/T]aaggaaatgtctgct | 152006 |
rs7030673 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF38 | GRCh38.p7 | 9:36416061 | tgatgggtggcacca[C/T]agagctctcaagata | 152006 |
rs7033793 | snp | C/T | 0.413582 | 0.189052 | intron-variant | RNF38 | GRCh38.p7 | 9:36373410 | CAAAAACCAAAATCA[C/T]ATTATCTTAACAGTA | 152006 |
rs7034595 | snp | A/G | 0.0418186 | 0.138422 | utr-variant-3-prime | RNF38 | GRCh38.p7 | 9:36338025 | AGTAGTTAACACTGA[A/G]TGGAAAACTGACACA | 152006 |
rs7037130 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF38 | GRCh38.p7 | 9:36340424 | agggttaaaccctgt[C/T]gcccacaggagcaca | 152006 |
rs7038026 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RNF38 | GRCh38.p7 | 9:36395396 | TAAGCCAGTATGACA[C/T]AACGTACTTCTACAA | 152006 |
rs7038193 | snp | A/T | 0.498632 | 0.0261223 | intron-variant | RNF38 | GRCh38.p7 | 9:36423154 | TGTAGTATACAAAAT[A/T]TTCTGTAGCCAACTA | 152006 |
rs7039144 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | RNF38 | GRCh38.p7 | 9:36362005 | agatgccatcaattg[C/T]gagaagcatccatcc | 152006 |
rs7039946 | snp | C/T | 0.0232847 | 0.105357 | upstream-variant-2KB | RNF38 | GRCh38.p7 | 9:36487825 | GGTATCCTCAGTCTC[C/T]GCCGCTCCCTGAGAA | 152006 |
rs7040334 | snp | A/G | 0.0232847 | 0.105357 | upstream-variant-2KB | RNF38 | GRCh38.p7 | 9:36487942 | GGCCTCTGGGGCCAG[A/G]CCTCGCGCGACCCAG | 152006 |
rs7042226 | snp | C/T | 0.475702 | 0.107512 | intron-variant | RNF38 | GRCh38.p7 | 9:36345154 | tctgagtatctggag[C/T]tacaattgcgtacca | 152006 |
rs7042287 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF38 | GRCh38.p7 | 9:36433011 | TGAAATCTCTAGTAT[C/T]TTCCCTAACTATTAA | 152006 |
rs7044165 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF38 | GRCh38.p7 | 9:36488767 | ATCTTTGACAACAGA[C/T]ATTTCAAATTCCATG | 152006 |
rs7044738 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | RNF38 | GRCh38.p7 | 9:36451917 | CGAGCAAACTTTTTT[A/T]AAAAAAAAACTTTTT | 152006 |