SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs718182 | snp | A/G | 0 | 0 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109336001 | GAGACATTCGGGCTG[A/G]TTTAAGTGACTGGCA | 344558 |
rs720978 | snp | C/G | 0.373799 | 0.217195 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109335475 | TGAGCGAGGGCTAGT[C/G]GACGAGCATGTCCCA | 344558 |
rs720979 | snp | A/G | 0.376989 | 0.215346 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109335254 | GTTCTCGTGTGGGAC[A/G]GGCGAGGGGCCTTGC | 344558 |
rs730491 | snp | A/C | 0.495174 | 0.0488838 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109284557 | GACTGCTCCACACAT[A/C]ATTCAAACACAGGGT | 344558 |
rs732476 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109326069 | GAAAATGTGGCATAC[A/G]CCCAGGATACCCCTG | 344558 |
rs732477 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109325876 | TTTCAACCCTCTCTG[A/G]ACTTTTTCCCAGGAG | 344558 |
rs735373 | snp | A/T | 0.0944967 | 0.195752 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109214449 | ATGACTCTTTTTTTT[A/T]Aatactttaagttct | 344558 |
rs736303 | snp | C/T | 0.44768 | 0.153045 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109319704 | CACACCATTTGGCTC[C/T]GGCACGGCACTCTTC | 344558 |
rs736304 | snp | C/T | 0.448323 | 0.15221 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109319523 | CTCAGAATACACATC[C/T]GTACTAACATGTGTT | 344558 |
rs736505 | snp | C/T | 0.373598 | 0.21731 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109225365 | CAAAATGTGGGTTTC[C/T]GGGCTCCGCTTGGAC | 344558 |
rs737478 | snp | A/G | 0.20511 | 0.245937 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109152690 | TCCAATGATGAGCTG[A/G]GTTCAGCAGTCTTGA | 344558 |
rs744898 | snp | A/G | 0.45692 | 0.1403 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109277423 | TGAAATTATACAGTC[A/G]TAGTAATTGAGAACA | 344558 |
rs748410 | snp | A/G | 0.497829 | 0.0328757 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109258240 | GCCCCTACAAACAGC[A/G]CCAGGCTGTCCCCCA | 344558 |
rs748411 | snp | A/G | 0.496245 | 0.0431677 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109258235 | TACAAACAGCGCCAG[A/G]CTGTCCCCCACTCCT | 344558 |
rs752272 | snp | G/T | 0.282369 | 0.247896 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109213647 | CAGGGCAGCAAACTG[G/T]GTGTCTACACAGGCA | 344558 |
rs752311 | snp | A/G | 0.470424 | 0.117954 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109215230 | CCCTGCCCCCTTACT[A/G]ATGTCACGGGCAGAG | 344558 |
rs879546 | snp | A/G | 0.400147 | 0.19989 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109136925 | TTGAACCAGGGTAAA[A/G]ATGGCTCCCTGCGAA | 344558 |
rs879964 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109136264 | AAGCATTTGCTGGGG[A/G]AAATGCTCTTGATAG | 344558 |
rs891414 | snp | C/T | 0.305436 | 0.243776 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109325567 | CTTTACAACATCCCT[C/T]AATATGGCTGCTCTG | 344558 |
rs891415 | snp | A/G | 0.305436 | 0.243776 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109325750 | TGTCCTGCAGACTCT[A/G]CCAGCCTGGAGTAGT | 344558 |
rs891417 | snp | A/G | 0.258565 | 0.249853 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109171886 | TGGGAACACAGAATG[A/G]GAGTTTCAAAGTGAA | 344558 |
rs891418 | snp | C/T | 0.25634 | 0.24992 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109171775 | TGAGCGTGGCCGGGA[C/T]GCACGGCAGGGAGCC | 344558 |
rs891419 | snp | C/G | 0.258565 | 0.249853 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109171753 | CAGGGAGCCAGCCAG[C/G]GTGGGCACCAGGAGG | 344558 |
rs891420 | snp | C/G | 0.419776 | 0.18351 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109171720 | AGCGCCAGGCGCAGG[C/G]GCTGGGCCTCTGGAA | 344558 |
rs891421 | snp | C/T | 0.269538 | 0.249235 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109160110 | TCTGGGCCCATAAAT[C/T]GACTGATAATGTCAT | 344558 |
rs891422 | snp | A/G | 0.298651 | 0.24522 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109264751 | ATGAGATGCCCGCCC[A/G]GTGGGCCTGGGAAGG | 344558 |
rs891423 | snp | C/T | 0.299916 | 0.244966 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109257923 | AGCTGGTCTAATTCA[C/T]TCTGAGCCCAGGACA | 344558 |
rs891425 | snp | A/G | 0.453209 | 0.145623 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109276754 | TCAGCCTTCTCTGTT[A/G]TTTTGTTTCTAGAGA | 344558 |
rs891426 | snp | A/G | 0.448452 | 0.152042 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109319214 | CAGATAGTGACAGTG[A/G]CATCGTTTTGCAGGA | 344558 |
rs891427 | snp | C/T | 0.4231 | 0.180378 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109319336 | TAAGCCAGTGCAGGT[C/T]AGTTGACTGCAAAGA | 344558 |
rs891428 | snp | C/T | 0.448323 | 0.15221 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109319458 | GATTTACAAGTGATT[C/T]GTTTTCTTACTCTTG | 344558 |
rs919508 | snp | C/T | 0.278399 | 0.248382 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109188711 | TGACGGCAAGCACCA[C/T]GTGGTGGGAGGTGGT | 344558 |
rs919509 | snp | C/T | 0.186105 | 0.241697 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109188459 | CAGGGGGAAACAATG[C/T]GCATGCTTCATCCAC | 344558 |
rs919510 | snp | A/C | 0.285257 | 0.247501 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109198077 | CACACTCCCGAGCAC[A/C]CCCAACTGACACACT | 344558 |
rs934288 | snp | G/T | 0.161596 | 0.233848 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109170987 | CGGGCTTGGTTCCTG[G/T]GGGGAGCGCCCTGTG | 344558 |
rs934289 | snp | C/T | 0.259951 | 0.249802 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109185785 | TAACTGAAGTATTAG[C/T]GTGCCAAGTTAATTT | 344558 |
rs934290 | snp | A/G | 0.25634 | 0.24992 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109185597 | TCTCTGCCAACCCCA[A/G]AGGCAGGAAAACCAA | 344558 |
rs934291 | snp | A/G | 0.420144 | 0.183169 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109185491 | TTCAACATGCTCTGT[A/G]ACTCAAGTAAATGTG | 344558 |
rs964158 | snp | A/G | 0.481319 | 0.0948228 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109147596 | ATGAGACCTTGATAT[A/G]ACCCTCCTGAATAAT | 344558 |
rs987841 | snp | A/G | 0.376989 | 0.215346 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109326305 | TTTTCATGGATCTGA[A/G]TATATCATAGACTAT | 344558 |
rs1001172 | snp | A/G | 0.407502 | 0.194147 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109324460 | AAATCACAAAGACTG[A/G]CAATAATGAATGTTG | 344558 |
rs1019838 | snp | C/T | 0.448836 | 0.15154 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109317125 | tttcatgagtgggtt[C/T]ctcatgaaatgtttt | 344558 |
rs1025374 | snp | C/T | 0.448708 | 0.151707 | intron-variant, upstream-variant-2KB | SH3RF3, MIR4266, RANBP2 | GRCh38.p7 | 2:109314888 | TGGTAGAGATTGAAG[C/T]AGAGCTAAGCCCTCG | 344558 |
rs1025375 | snp | A/G | 0.449091 | 0.151204 | intron-variant, upstream-variant-2KB | SH3RF3, MIR4266, RANBP2 | GRCh38.p7 | 2:109315005 | GAGCTGCACTGTCCC[A/G]TAAGGTAGCCACCGA | 344558 |
rs1025376 | snp | C/T | 0.449091 | 0.151204 | intron-variant, upstream-variant-2KB | SH3RF3, MIR4266, RANBP2 | GRCh38.p7 | 2:109315018 | CCATAAGGTAGCCAC[C/T]GACCACACTCAGTGA | 344558 |
rs1025377 | snp | C/T | 0.448836 | 0.15154 | intron-variant, upstream-variant-2KB | SH3RF3, MIR4266, RANBP2 | GRCh38.p7 | 2:109315172 | TAGCAGAAAGTCTTA[C/T]TTGATGACTTTTCTC | 344558 |
rs1025378 | snp | A/G | 0.433236 | 0.170072 | intron-variant, upstream-variant-2KB | SH3RF3, MIR4266, RANBP2 | GRCh38.p7 | 2:109315455 | ATAGCTTGTGTCTGT[A/G]GAATGCACTTGCTTT | 344558 |
rs1025379 | snp | A/G | 0.389903 | 0.207189 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109315890 | ACCAGTTCCCAGAAC[A/G]TCACCTGCGACCAGC | 344558 |
rs1025380 | snp | C/T | 0.433818 | 0.169443 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109315898 | CCAGAACGTCACCTG[C/T]GACCAGCATAGGTCT | 344558 |
rs1036029 | snp | C/T | 0.448836 | 0.15154 | intron-variant, upstream-variant-2KB | SH3RF3, MIR4266, RANBP2 | GRCh38.p7 | 2:109314736 | GTGCATAATATCCAC[C/T]AGCCAATTTCTTATT | 344558 |
rs1075813 | snp | C/T | 0.498206 | 0.0298983 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109171128 | CTCAGTAATCTGCAG[C/T]ACCTAGATCATTCAG | 344558 |
rs1078251 | snp | A/T | 0.447938 | 0.152711 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109304634 | TTAATTCATTTAAAT[A/T]CAAACTCAAATAGCT | 344558 |
rs1078252 | snp | A/G | 0.442385 | 0.15965 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109304554 | GCAGCGGAGTTAACC[A/G]CTCTTACCCAGTCAG | 344558 |
rs1078253 | snp | C/T | 0.451608 | 0.147832 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109304453 | GGAACCCCTAGCAGA[C/T]AACGTGGGGCAACTC | 344558 |
rs1078254 | snp | C/T | 0.451483 | 0.148002 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109304440 | GACAACGTGGGGCAA[C/T]TCAGCCTTAAAAAAG | 344558 |
rs1107234 | snp | C/T | 0.25801 | 0.249872 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109138637 | GAGTGACCCACTTCC[C/T]CACTGCAGATGAACA | 344558 |
rs1367274 | snp | C/G | 0.25455 | 0.249959 | upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime, intron-variant | SH3RF3, SH3RF3-AS1, RANBP2 | GRCh38.p7 | 2:109129473 | GTGGAGCCCGCCACC[C/G]GCAGCCAGCATCAGG | 344558 |
rs1430302 | snp | A/G | 0.442249 | 0.159814 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109319284 | GAGTTGGTTCCTGGC[A/G]TCGTGATATGAACTC | 344558 |
rs1430303 | snp | C/T | 0.447421 | 0.153379 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109319396 | GGCTCAGTGGGGTCC[C/T]GGGGATCACCCAGGC | 344558 |
rs1430304 | snp | G/T | 0.447809 | 0.152878 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109307236 | ACACACAAGTCCAAT[G/T]TGCAAAAAGGTAATT | 344558 |
rs1430305 | snp | A/G | 0.447809 | 0.152878 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109307209 | AATTATGAATATTCA[A/G]TTTTCAAATGTGCAC | 344558 |
rs1430306 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109191429 | TTGATTTATAACTCA[C/T]CCCACTTTCTTCTAA | 344558 |
rs1430307 | snp | A/G | 0.256061 | 0.249927 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109191263 | CTCCCTTTCCTCTTG[A/G]TGTCAGAAACAACCT | 344558 |
rs1465630 | snp | A/C | 0.370568 | 0.219005 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109264780 | GATGGCCAGACTCCA[A/C]GGCCCTCAGAAGAAT | 344558 |
rs1465631 | snp | A/G | 0.193966 | 0.243639 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109225337 | TTGAAACTTCCCTTG[A/G]TTACTTGCAGGTCTC | 344558 |
rs1465632 | snp | A/G | 0.311614 | 0.242289 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109225306 | TCCACCCAGCTGAGT[A/G]CAATGGTTTGAGGAC | 344558 |
rs1469529 | snp | C/T | 0.497121 | 0.0378299 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109132165 | GGTTACCTGCTATCA[C/T]GGCATATTAGTTAAA | 344558 |
rs1529573 | snp | C/T | 0.257176 | 0.249897 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109176606 | GGGACTACAGGCATG[C/T]GCCACCACACCTGGC | 344558 |
rs1529574 | snp | C/T | 0.499942 | 0.00539106 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109176548 | GATAGGGTCTCATTA[C/T]GTTGCCAAGGCTGAT | 344558 |
rs1560385 | snp | A/G | 0.256897 | 0.249905 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109187561 | GCATGGACTGTACTA[A/G]ACACCTTAGGAGCTG | 344558 |
rs1560386 | snp | A/C | 0.492484 | 0.0608394 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109219138 | TGAATGGGGTGTGAG[A/C]GAGAGAGGTGGAACT | 344558 |
rs1560387 | snp | A/G | 0.185472 | 0.241529 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109218932 | CTACAAGCCTGGTCC[A/G]TGCAGGGAAGGCAGG | 344558 |
rs1560388 | snp | C/T | 0.492727 | 0.0598633 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109216509 | GGCACTTAAGCTTTG[C/T]GGCCAGGTGGGCGTG | 344558 |
rs1835356 | snp | G/T | 0.447809 | 0.152878 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109307398 | TATCTGCTCCAAGCT[G/T]CCGCCCAGAGCATGG | 344558 |
rs1835357 | snp | C/T | 0.450231 | 0.149691 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109304114 | gcagagtagatcttt[C/T]ttttttttttttgag | 344558 |
rs1864473 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109243129 | ATAGCCTGCTCCCAA[C/T]TGTCTGCCTGAAAGA | 344558 |
rs1864474 | snp | G/T | 0.319856 | 0.240042 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109243063 | GGAATATGAACAGCC[G/T]ATTTCATTGTTCTCA | 344558 |
rs1864475 | snp | A/G | 0.447938 | 0.152711 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109306406 | GGAATCGGAAGCCCC[A/G]GGAAGCCTCCAGGAG | 344558 |
rs1864476 | snp | A/G | 0.448195 | 0.152377 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109306329 | TGGAGGCAGGGACAC[A/G]CAGGGGTCAGAACAA | 344558 |
rs1864477 | snp | C/T | 0.256061 | 0.249927 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109192957 | ACAATACCTCTTCTT[C/T]TTGCAAAACACCCTT | 344558 |
rs1864478 | snp | C/T | 0.278399 | 0.248382 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109189358 | AAAAAAGTCAAACGA[C/T]TGAACACGTAAGTTC | 344558 |
rs1864479 | snp | C/T | 0.256061 | 0.249927 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109188964 | ACAAGATGAAAAGAG[C/T]ACTTCACAAACATTT | 344558 |
rs1971765 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109264336 | CGGAGTGGATCCTGG[A/G]GAGGTGAACGGGGAG | 344558 |
rs1972285 | snp | C/T | 0.371177 | 0.218669 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109264443 | GATGGGGAGCACACA[C/T]AGACTTGGGGTGGAT | 344558 |
rs2007790 | snp | A/T | 0.466515 | 0.124985 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109138200 | CCCGGCTAATTTTTT[A/T]ATATTTTTAGTAGAG | 344558 |
rs2008775 | snp | G/T | 0.448452 | 0.152042 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109303923 | GTAGAGACGGGGTTA[G/T]ATCTTATAGTAAGGA | 344558 |
rs2014263 | snp | C/T | 0.306182 | 0.243605 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109240437 | GCAGAGGTGCGATCT[C/T]GGCTCACTGCAAGCT | 344558 |
rs2043076 | snp | A/G | 0.308414 | 0.24308 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109280625 | AAAACAATCTACACT[A/G]ATAGATCTGCTCATC | 344558 |
rs2043077 | snp | C/T | 0.260504 | 0.249779 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109197458 | TTGGGGAGAGCCTCA[C/T]CCCCATTTACTGATG | 344558 |
rs2069246 | snp | C/T | 0.419776 | 0.18351 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109171638 | GAGACATTTCCTGTG[C/T]GGGAATGAATCCAGG | 344558 |
rs2115898 | snp | C/T | | | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109334814 | TCTCCAACTAGAATG[C/T]TATGTGCCACTTGCT | 344558 |
rs2115899 | snp | C/T | 0.490287 | 0.0690083 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109210753 | GAGGAAAGGGAGAAA[C/T]GCTGTGAATTAGTCG | 344558 |
rs2115900 | snp | C/G | 0.0926964 | 0.194308 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109210785 | CTGCTTCTCTGGCAA[C/G]CACGACCTATTTCTA | 344558 |
rs2163259 | snp | A/G | 0.256897 | 0.249905 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109173565 | TTCCCCGCAGCCACC[A/G]GCTCTGCTGTTAGAG | 344558 |
rs2163260 | snp | C/T | 0.292523 | 0.246357 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109210391 | AAGCCTGGTCTTTTC[C/T]GTGCTCCCTCGTTTT | 344558 |
rs2163261 | snp | A/G | 0.419936 | 0.183362 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109279375 | AATCGGCAGTGGCAG[A/G]TTCTTGCATGGAAGT | 344558 |
rs2378299 | snp | C/T | 0.490997 | 0.0664859 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109211259 | CAGCTGGCTAGGTGG[C/T]GAGGGGATGTCCTGC | 344558 |
rs2378300 | snp | A/G | 0.451608 | 0.147832 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109304368 | TGACTGGCTTATTTC[A/G]TTTAACATAATGTCC | 344558 |
rs2378301 | snp | G/T | 0.256061 | 0.249927 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109187986 | ATTGTAAGGAAGGGG[G/T]GCACAGCGGGGGTTG | 344558 |
rs2378302 | snp | A/T | 0.481319 | 0.0948228 | intron-variant | SH3RF3, RANBP2 | GRCh38.p7 | 2:109147595 | AATTATTCAGGAGGG[A/T]TATATCAAGGTCTCA | 344558 |