SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs884273 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | RNFT2 | GRCh38.p7 | 12:116784335 | CAGACCTTCTCCCAA[A/G]AGCTGAACTGGGGAA | 84900 |
rs903771 | snp | G/T | 0.232943 | 0.249417 | downstream-variant-500B | RNFT2 | GRCh38.p7 | 12:116853786 | TCTCGTGGGAGCACT[G/T]CTGTAATAAATCACA | 84900 |
rs903772 | snp | A/G | 0.29175 | 0.246489 | utr-variant-3-prime | RNFT2 | GRCh38.p7 | 12:116852796 | CCTGGAGATGGCTAC[A/G]GGGAGGCTGAGTGAC | 84900 |
rs903773 | snp | A/G | 0.105569 | 0.204058 | utr-variant-3-prime, intron-variant | RNFT2 | GRCh38.p7 | 12:116852350 | GTGGCACACAGGGGC[A/G]AATGTCCTGAATCTA | 84900 |
rs903774 | snp | C/G | 0.292008 | 0.246445 | intron-variant | RNFT2 | GRCh38.p7 | 12:116852291 | AATACTGGCTGACAG[C/G]GAGGTGGCTACAAAG | 84900 |
rs903775 | snp | C/G | 0.481148 | 0.0952395 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851808 | CTGGGCCAAAGCTGA[C/G]CTTTCTTTCTTTCCT | 84900 |
rs924072 | snp | C/G | 0.335559 | 0.234904 | intron-variant | RNFT2 | GRCh38.p7 | 12:116808586 | GATTTATTTATTTAT[C/G]TAGTCCCGCCTGGCT | 84900 |
rs924073 | snp | C/G | 0.186421 | 0.24178 | intron-variant | RNFT2 | GRCh38.p7 | 12:116808831 | AAATTCTTGCTCCCC[C/G]TCCTGTGCTCCCCCT | 84900 |
rs924074 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116808872 | CTCTCACCCCCAGCA[A/C]TGGGCCGTTGGAAAT | 84900 |
rs924075 | snp | C/T | 0.373196 | 0.217538 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812229 | GAACACAGACTTATT[C/T]CCTGCTGCAGCCTTA | 84900 |
rs924076 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116812366 | AGGACGGGGATGGCA[A/G]AGGGAGGAAAGGAGG | 84900 |
rs924077 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812375 | ATGGCAAAGGGAGGA[A/G]AGGAGGGACAGCTCT | 84900 |
rs924078 | snp | A/T | 0.348354 | 0.22984 | intron-variant | RNFT2 | GRCh38.p7 | 12:116816066 | AAGACTATAGCTGAC[A/T]TGGGGACAGATAAGC | 84900 |
rs924079 | snp | C/G | 0.470811 | 0.117228 | intron-variant | RNFT2 | GRCh38.p7 | 12:116816174 | CTTAATCATCAACAT[C/G]TTATAATTAGGCCTC | 84900 |
rs987560 | snp | A/G | 0.142609 | 0.225759 | intron-variant | RNFT2 | GRCh38.p7 | 12:116811074 | TCACCTCCCTTCTCC[A/G]TGCCTCAGTTTCCTC | 84900 |
rs1495933 | snp | A/G | 0.335559 | 0.234904 | intron-variant | RNFT2 | GRCh38.p7 | 12:116805938 | catttacaaaatgcc[A/G]tcacagcaaaaccca | 84900 |
rs1532395 | snp | C/T | 0.260227 | 0.249791 | intron-variant | RNFT2 | GRCh38.p7 | 12:116748511 | TTCCTGAATAGAATT[C/T]CTGGGGGTGGGGGTG | 84900 |
rs1565988 | snp | C/T | 0.111928 | 0.208413 | intron-variant | RNFT2 | GRCh38.p7 | 12:116767339 | tcctcccacctcagc[C/T]tcccaagtagctggt | 84900 |
rs1603327 | snp | C/T | 0.488666 | 0.0744214 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800127 | AGCTTCACCAGAGGC[C/T]GAGCATATGCAGGTG | 84900 |
rs1603328 | snp | A/G | 0.209388 | 0.246679 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800180 | agaaccatgagccaa[A/G]ataaacctcttttct | 84900 |
rs1845777 | snp | A/G | 0.486133 | 0.082104 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800355 | tacaaaaaattggcc[A/G]ggcacagtggcttac | 84900 |
rs1969017 | snp | A/G | 0.229723 | 0.249176 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116740059 | AAAAATACAAAAATT[A/G]GGTGGGCGTGGTGTC | 84900 |
rs1971306 | snp | C/T | 0.348794 | 0.229651 | intron-variant | RNFT2 | GRCh38.p7 | 12:116772468 | AATACAAAAATCAGC[C/T]GGGCGTGGTGGCACA | 84900 |
rs2016622 | snp | A/G | 0.195214 | 0.243923 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806147 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 84900 |
rs2018152 | snp | A/G | 0.37138 | 0.218556 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851609 | GCCGGGCGCGGTGGC[A/G]GGTGCCTGTAATCCC | 84900 |
rs2029852 | snp | C/G | 0.4973 | 0.0366419 | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116737461 | AAGAAAGACGGAAGG[C/G]AAGGGAGAGGAAAAA | 84900 |
rs2029853 | snp | A/G | 0.497933 | 0.032082 | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116737503 | AAGAAAGGGAAGGGG[A/G]AGGAAGGAAAGGGGG | 84900 |
rs2029854 | snp | C/T | 0.211819 | 0.247067 | intron-variant | RNFT2 | GRCh38.p7 | 12:116755245 | ttgttgaaaagggtg[C/T]cctttccccacttta | 84900 |
rs2029855 | snp | A/T | 0.0540123 | 0.155206 | intron-variant | RNFT2 | GRCh38.p7 | 12:116755370 | GCCCAGAGGTCTTTT[A/T]TTTTTTTTTTTTTAA | 84900 |
rs2029856 | snp | C/T | 0.213635 | 0.247341 | intron-variant | RNFT2 | GRCh38.p7 | 12:116755408 | TATGCCATGAATTCA[C/T]AGGGAATAGGTTCCA | 84900 |
rs2088230 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116851764 | cctccctccctccct[G/T]ctttctttctttttt | 84900 |
rs2088231 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116851762 | tccctccctcccttc[G/T]ttctttctttttttt | 84900 |
rs2088232 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116799945 | acaggggtgaatctc[A/C]tgtgaatggcgtggt | 84900 |
rs2088233 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116799951 | gtgaatctcatgtga[A/C]tggcgtggtaccctc | 84900 |
rs2088234 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800012 | tagttcatgcacgat[A/C]tgactgtttaaaaga | 84900 |
rs2088235 | snp | C/T | 0.133435 | 0.221162 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800738 | agaattgcttgagcc[C/T]gggaggtggaggttg | 84900 |
rs2088236 | snp | C/T | 0.47614 | 0.106587 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787273 | GATCATCTGCCAGAT[C/T]GGCCAGGTGCTAGAG | 84900 |
rs2101868 | snp | A/G | 0.106278 | 0.204558 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787118 | tatccttgagtggcc[A/G]ttatttcctttacta | 84900 |
rs2132389 | snp | A/G | 0.450985 | 0.148678 | intron-variant | RNFT2 | GRCh38.p7 | 12:116781553 | TGCCATCACTGACTC[A/G]GAAGACGGaggaaga | 84900 |
rs2172953 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | RNFT2 | GRCh38.p7 | 12:116740307 | GCAGATTCAAGGTAT[C/T]GCAGGGACTGTTCAT | 84900 |
rs2220936 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116739262 | GCCCTTATTACCTTG[A/C]TAGGGTGAAAGGTGG | 84900 |
rs2393084 | snp | A/C | 0.1652 | 0.235179 | intron-variant | RNFT2 | GRCh38.p7 | 12:116791793 | atgatccagaattct[A/C]tgcctatgtatttac | 84900 |
rs2393085 | snp | C/T | 0.165853 | 0.235413 | intron-variant | RNFT2 | GRCh38.p7 | 12:116791734 | gtctgcgaaagctca[C/T]agcagcactattcac | 84900 |
rs2393086 | snp | A/G | 0.208779 | 0.246578 | intron-variant | RNFT2 | GRCh38.p7 | 12:116757392 | tcttcttgtttctct[A/G]gttccttgaggggtg | 84900 |
rs2393087 | snp | C/T | 0.208779 | 0.246578 | intron-variant | RNFT2 | GRCh38.p7 | 12:116757579 | tgatgtcatttttga[C/T]ccaatgctcattcag | 84900 |
rs2393089 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116845262 | tctATATATATATAT[A/T]TAttttttttttttt | 84900 |
rs2393090 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116845260 | tATATATATATATAt[A/T]ttttttttttttttt | 84900 |
rs2393107 | snp | A/G | 0.112631 | 0.208878 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800870 | aaataaaaACCATTT[A/G]ACAGATAAAACAGAG | 84900 |
rs2893689 | snp | A/T | 0.295599 | 0.245806 | intron-variant | RNFT2 | GRCh38.p7 | 12:116847839 | taaattaaaTTTTTT[A/T]AAAAAGAGAGAGggc | 84900 |
rs2893690 | snp | A/C | 0.139903 | 0.224452 | intron-variant | RNFT2 | GRCh38.p7 | 12:116845280 | tctctctctctctct[A/C]tctctATATATATAT | 84900 |
rs2893691 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116845278 | tctctctctctctct[A/C]tctATATATATATAT | 84900 |
rs2893692 | snp | A/G | 0.202959 | 0.245534 | intron-variant | RNFT2 | GRCh38.p7 | 12:116842251 | agtgaaggtgatggg[A/G]tgtcccttctgggat | 84900 |
rs3069215 | in-del | -/CTCT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116845293 | GAGCTCTCTCTCTCT[-/CTCT]CTCTCTATATATATA | 84900 |
rs3069310 | in-del | -/TAAAA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116800813 | AGCAAGACTCCATCT[-/TAAAA]TAAAATAAAATAAAA | 84900 |
rs3088107 | snp | A/G | 0.400282 | 0.220572 | utr-variant-3-prime | RNFT2 | GRCh38.p7 | 12:116853334 | CTCAAGTTCCACGAA[A/G]TCCTTAGAAATGGAC | 84900 |
rs3203930 | snp | C/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116852298 | GCCACCTCCCTGTCA[C/G]CCAGTATTAACATGT | 84900 |
rs3809191 | snp | A/G | 0.0912534 | 0.193131 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738576 | TCGGTGCAGTCCTGT[A/G]ACGGGCCCCAGGGGC | 84900 |
rs3809192 | snp | A/G | 0.247621 | 0.249989 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738747 | GTACGGCCTGCTTCC[A/G]ACAAAGAATCCGAAG | 84900 |
rs3809193 | snp | A/G | 0.114036 | 0.209795 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738900 | TGGAGGGAGGGGCGA[A/G]AGGAGGATTAAGTTG | 84900 |
rs3840786 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738388 | AAAAAGAGAACGCGA[-/T]TTTTTTTTTCTTTTC | 84900 |
rs3863382 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116845276 | TCTCTCTCTCTCTCT[A/C]TATATATATATATAT | 84900 |
rs3926590 | snp | C/G | 0.209084 | 0.246629 | intron-variant | RNFT2 | GRCh38.p7 | 12:116755518 | GGTACCTTTCTCTTC[C/G]GCTTCTTTCTTTTTC | 84900 |
rs3933908 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116737554 | gtgaggaaggtaagg[A/G]aggaagg | 84900 |
rs3933909 | snp | A/C | | | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116737558 | ggaaggtaaggaagg[A/C]agg | 84900 |
rs3941210 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116851745 | tctttcttttttttt[G/T]tagacagagtctcac | 84900 |
rs4238048 | snp | A/G | 0.199564 | 0.24486 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806671 | gatcccttgagcctg[A/G]gagttcgaggctgca | 84900 |
rs4275719 | snp | A/G | 0.379354 | 0.213933 | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116737570 | AGGAAGGGAGGCAGG[A/G]AGAGGGGAAGGAAGG | 84900 |
rs4301877 | snp | C/T | 0.303938 | 0.244112 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750660 | gtgtgatgctaggtg[C/T]attatttaacctctc | 84900 |
rs4326894 | snp | G/T | 0.347253 | 0.230308 | intron-variant | RNFT2 | GRCh38.p7 | 12:116819871 | acagaaatataagag[G/T]agtcacacagacgat | 84900 |
rs4468446 | snp | A/G | 0.208779 | 0.246578 | intron-variant | RNFT2 | GRCh38.p7 | 12:116757413 | ttgaggggtgacctt[A/G]gagtgtcagtttgtg | 84900 |
rs4480639 | snp | A/G | 0.337386 | 0.23423 | intron-variant | RNFT2 | GRCh38.p7 | 12:116807341 | CGTGATAGTAATAAA[A/G]TAAGAAATATTAGAT | 84900 |
rs4486720 | snp | C/G | 0.180383 | 0.240111 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750754 | tgatgttaaatttga[C/G]ttaatatgtgtaaaa | 84900 |
rs4608187 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800813 | AGCAAGACTCCATCT[C/T]AAAATAAAATAAAAT | 84900 |
rs4612912 | snp | A/G | 0.113685 | 0.209567 | intron-variant | RNFT2 | GRCh38.p7 | 12:116753654 | GGCTTAGAGAGGTGC[A/G]GTGACTTGCCCAAGC | 84900 |
rs4766805 | snp | C/T | 0.280256 | 0.248162 | intron-variant | RNFT2 | GRCh38.p7 | 12:116825164 | ACCGTTGGCTGGTTT[C/T]CATGTTTCTCCTCCA | 84900 |
rs4766806 | snp | C/T | 0.28578 | 0.247426 | intron-variant | RNFT2 | GRCh38.p7 | 12:116841465 | ctcaaaaaaataaaa[C/T]gactgggcatggtgg | 84900 |
rs4767443 | snp | C/T | 0.291235 | 0.246576 | intron-variant | RNFT2 | GRCh38.p7 | 12:116745552 | AGGCATGAGCCACCA[C/T]GCCTGGCCTCACTAG | 84900 |
rs4767444 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNFT2 | GRCh38.p7 | 12:116753888 | CTGTCAACTCTGAGG[A/G]GACCAGGGATGTGCC | 84900 |
rs4767445 | snp | C/T | 0.211516 | 0.24702 | intron-variant | RNFT2 | GRCh38.p7 | 12:116754322 | tttatggctgtgtag[C/T]attccaccatgtata | 84900 |
rs4767446 | snp | C/T | 0.209084 | 0.246629 | intron-variant | RNFT2 | GRCh38.p7 | 12:116756722 | gtaatttgttggatt[C/T]ggttagcaagtattt | 84900 |
rs4767447 | snp | A/T | 0.119978 | 0.213528 | intron-variant | RNFT2 | GRCh38.p7 | 12:116756981 | ttgttggtaattttt[A/T]aattaccatttcaat | 84900 |
rs4767448 | snp | A/G | 0.138886 | 0.22395 | intron-variant | RNFT2 | GRCh38.p7 | 12:116759756 | ccagtgcctgttgcc[A/G]tggaggtggtggagg | 84900 |
rs4767449 | snp | A/G | 0.110519 | 0.207473 | intron-variant | RNFT2 | GRCh38.p7 | 12:116771860 | GCCATGCACCTGGAA[A/G]TTCTTTTGAAACGAG | 84900 |
rs4767450 | snp | A/G | 0.110519 | 0.207473 | intron-variant | RNFT2 | GRCh38.p7 | 12:116772009 | CTCCGATGTTTTTTA[A/G]TGAGTTTGTTTCCCC | 84900 |
rs4767451 | snp | A/G | 0.348574 | 0.229746 | intron-variant | RNFT2 | GRCh38.p7 | 12:116774099 | TACCTAAAGTAGTCA[A/G]ATTTATAGACAGAAA | 84900 |
rs4767452 | snp | C/T | 0.206005 | 0.246099 | synonymous-codon, nc-transcript-variant | RNFT2 | GRCh38.p7 | 12:116779336 | CAAGATCATCCTGGC[C/T]GTCAAGTCCAAGGTA | 84900 |
rs4767453 | snp | G/T | 0.449599 | 0.150533 | intron-variant | RNFT2 | GRCh38.p7 | 12:116786754 | CTCACAGTTCTGGAA[G/T]CCAGAAATCCAAAAT | 84900 |
rs4767454 | snp | G/T | 0.11963 | 0.213316 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797922 | tggtaactcctgggt[G/T]ttgccatggcaatgg | 84900 |
rs4767455 | snp | C/G | 0.103438 | 0.202533 | intron-variant | RNFT2 | GRCh38.p7 | 12:116798331 | ATATACAGCTCCCAC[C/G]TTGCTTTTATTATCC | 84900 |
rs4767456 | snp | A/T | 0.0558544 | 0.157504 | intron-variant | RNFT2 | GRCh38.p7 | 12:116798360 | CCATCTATCTTAGAG[A/T]TTGTTCGGATAAATA | 84900 |
rs4767457 | snp | C/G | 0.42803 | 0.175514 | intron-variant | RNFT2 | GRCh38.p7 | 12:116820288 | gatttcattatgttt[C/G]ccagtctggtctcga | 84900 |
rs4767458 | snp | C/T | 0.143284 | 0.226079 | intron-variant | RNFT2 | GRCh38.p7 | 12:116820373 | AGGTGTGAGCCACCA[C/T]GCCCAGCTATCCCTG | 84900 |
rs4767459 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNFT2 | GRCh38.p7 | 12:116825208 | CTGCTCCCCTTCCAC[A/G]TGtcctcttcactgg | 84900 |
rs4767460 | snp | A/T | 0.171057 | 0.237209 | intron-variant | RNFT2 | GRCh38.p7 | 12:116841063 | AAGTCAGATGCTTTT[A/T]gtatcagttatcaat | 84900 |
rs4767461 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | RNFT2 | GRCh38.p7 | 12:116849176 | AGTATTTTGGAGTCG[C/T]ATTGTCTCCCCAACG | 84900 |
rs5801197 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116744226 | GTGAGACTCCTCCTC[-/A]AAAAAAAAAAAAAAA | 84900 |
rs5801198 | in-del | -/A | 0.486 | 0.0824865 | intron-variant | RNFT2 | GRCh38.p7 | 12:116775261 | TGAAACTCCCGTCTC[-/A]AAAAAAAAAAAAAAA | 84900 |
rs5801199 | in-del | -/AAGTCACCAG | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116775332 | TACTGAAGTCACCAG[-/AAGTCACCAG]TCTAGACGGTGCTTG | 84900 |
rs6490086 | snp | A/C | 0.18325 | 0.240924 | intron-variant | RNFT2 | GRCh38.p7 | 12:116752595 | TTAAAAGAGTAAGTG[A/C]GACCAGGTACGGTGG | 84900 |
rs6490091 | snp | A/G | 0.110519 | 0.207473 | intron-variant | RNFT2 | GRCh38.p7 | 12:116776022 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 84900 |
rs6490092 | snp | A/G | 0.416545 | 0.186448 | intron-variant | RNFT2 | GRCh38.p7 | 12:116780472 | AGGCGGAGCTCAGGC[A/G]GTAATGCTTGCTCAC | 84900 |
rs6490093 | snp | C/T | 0.140242 | 0.224618 | intron-variant | RNFT2 | GRCh38.p7 | 12:116803411 | GAAAATAATATATAA[C/T]GGGGATCTCCACACC | 84900 |
rs6490094 | snp | A/G | 0.370568 | 0.219005 | intron-variant | RNFT2 | GRCh38.p7 | 12:116846970 | ctggagtgcagtggc[A/G]cgatcttggctcact | 84900 |
rs6490095 | snp | C/T | 0.105924 | 0.204309 | intron-variant | RNFT2 | GRCh38.p7 | 12:116848074 | attgttcagctctga[C/T]ttatgagtgagaaca | 84900 |
rs7131700 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809750 | caatctcagctcact[A/G]caacctccacctccc | 84900 |
rs7134604 | snp | G/T | 0.304688 | 0.243945 | intron-variant | RNFT2 | GRCh38.p7 | 12:116747482 | GGCTCTAGGGAGCTA[G/T]GATCACACTATTCCA | 84900 |
rs7134617 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806022 | acattaaactaaaca[G/T]ATAGTCCCCCTTTAA | 84900 |
rs7135526 | snp | A/G | 0.110167 | 0.207236 | intron-variant | RNFT2 | GRCh38.p7 | 12:116780364 | CATTGGATTCTCATA[A/G]GGAGCATACAACCTA | 84900 |
rs7136846 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RNFT2 | GRCh38.p7 | 12:116828353 | aaccagctcccaggc[A/G]atgctgatggtgctg | 84900 |
rs7136986 | snp | A/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116832148 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 84900 |
rs7137138 | snp | A/G | 0.182933 | 0.240836 | intron-variant | RNFT2 | GRCh38.p7 | 12:116766477 | AAGGGAAACTGAAAG[A/G]GTTTAAATAACTTGC | 84900 |
rs7137493 | snp | A/G | 0.488118 | 0.0761554 | intron-variant | RNFT2 | GRCh38.p7 | 12:116746186 | aggttgcagtgagcc[A/G]agatcgcgccactgc | 84900 |
rs7138403 | snp | C/T | 0.291493 | 0.246533 | intron-variant | RNFT2 | GRCh38.p7 | 12:116746193 | agtgagccgagatcg[C/T]gccactgcactctag | 84900 |
rs7296142 | snp | A/G | 0.291235 | 0.246576 | intron-variant | RNFT2 | GRCh38.p7 | 12:116746775 | ATGATATTTGTACCT[A/G]TCTAGAGGGTTCCTC | 84900 |
rs7297122 | snp | C/T | 0.000131811 | 0.00811715 | missense, nc-transcript-variant | RNFT2 | GRCh38.p7 | 12:116754035 | CCTATGCCAACTCCA[C/T]GCTTCGAGAACAGGT | 84900 |
rs7297569 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNFT2 | GRCh38.p7 | 12:116799751 | cacctgaggtcacct[C/T]gtgtctactaaaaat | 84900 |
rs7297890 | snp | A/G | 0.381113 | 0.21286 | intron-variant | RNFT2 | GRCh38.p7 | 12:116772260 | CCACACCTGGTCACA[A/G]TTTGTAAAGTTACTT | 84900 |
rs7298317 | snp | C/G | 0.0858192 | 0.188533 | intron-variant | RNFT2 | GRCh38.p7 | 12:116848043 | gttgttcccctccct[C/G]tatccatgtgttctc | 84900 |
rs7298450 | snp | C/G | 0.379354 | 0.213933 | intron-variant | RNFT2 | GRCh38.p7 | 12:116847474 | gtccaagttatacag[C/G]cagagaacggtggaa | 84900 |
rs7299032 | snp | C/G | 0.414741 | 0.188044 | intron-variant | RNFT2 | GRCh38.p7 | 12:116782454 | attgcttgaggccag[C/G]agttccaggcttcag | 84900 |
rs7299363 | snp | A/G | 0.319376 | 0.240181 | intron-variant | RNFT2 | GRCh38.p7 | 12:116805531 | ccaggctggagtgca[A/G]tggcgcaatctcagc | 84900 |
rs7299953 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNFT2 | GRCh38.p7 | 12:116796501 | TAGGCTCTCAATCCT[A/G]TTGGTTTTTCTCTAA | 84900 |
rs7300541 | snp | A/G | 0.295599 | 0.245806 | intron-variant | RNFT2 | GRCh38.p7 | 12:116747842 | GAGCACATCGGCTCC[A/G]CTTGCATCTGTGGTG | 84900 |
rs7301309 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | RNFT2 | GRCh38.p7 | 12:116742505 | ctcccgggctcaagc[G/T]atctgtccgacttgg | 84900 |
rs7301614 | snp | C/T | 0.297382 | 0.245469 | intron-variant | RNFT2 | GRCh38.p7 | 12:116748008 | CCAGCCTGGCCAACG[C/T]GGTGAAACCCTATCT | 84900 |
rs7302199 | snp | A/G | 0.180064 | 0.240019 | intron-variant | RNFT2 | GRCh38.p7 | 12:116818553 | ATCTGCTGCTGGCAA[A/G]TGAGTTGTGAAGCCT | 84900 |
rs7302320 | snp | C/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116818624 | GGCGACCCTGTCGGA[C/G]AGAGAAGGGAGGGTG | 84900 |
rs7302413 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116743287 | Attttttttttttga[A/G]atggagtcttgctct | 84900 |
rs7302953 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809619 | TCTCTCTGGTTCCTC[A/G]AAGACTGGGCTTCAC | 84900 |
rs7304400 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116776887 | tgactccacctctta[A/G]tgccccagtgtcctc | 84900 |
rs7304747 | snp | C/T | 0.145978 | 0.227331 | intron-variant | RNFT2 | GRCh38.p7 | 12:116813805 | GTTGGAAGGGTCTAC[C/T]agacttggagtcaag | 84900 |
rs7305537 | snp | C/T | 0.084364 | 0.187256 | intron-variant | RNFT2 | GRCh38.p7 | 12:116807153 | ggggagaaggaatat[C/T]gggaggcactagcaa | 84900 |
rs7306023 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RNFT2 | GRCh38.p7 | 12:116756847 | gctggcttcatagaa[C/T]gaattagggagggtt | 84900 |
rs7306658 | snp | A/G | 0.110167 | 0.207236 | intron-variant | RNFT2 | GRCh38.p7 | 12:116774271 | ATCATTGAACTGTGC[A/G]CGTAAAAATGGTTAA | 84900 |
rs7307221 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | RNFT2 | GRCh38.p7 | 12:116819372 | CCCGGAGGCCAGACC[C/G]GGAgccggcggcgcg | 84900 |
rs7307465 | snp | A/G | 0.241053 | 0.24984 | intron-variant | RNFT2 | GRCh38.p7 | 12:116780694 | AAAAAAGAGATGTGG[A/G]GAAGAAAGGCCAGAG | 84900 |
rs7310216 | snp | A/G | 0.348354 | 0.22984 | intron-variant | RNFT2 | GRCh38.p7 | 12:116774738 | CAGATCTCATACGCC[A/G]CATTCAGTGCATGGT | 84900 |
rs7310759 | snp | C/T | 0.281313 | 0.248031 | intron-variant | RNFT2 | GRCh38.p7 | 12:116833042 | cctcgcttgagtagc[C/T]tccgagtagctggga | 84900 |
rs7312638 | snp | A/G | 0.291235 | 0.246576 | intron-variant | RNFT2 | GRCh38.p7 | 12:116746679 | AAGATTGGAGTTTGG[A/G]GTCAAATAATCCAGG | 84900 |
rs7313014 | snp | C/T | 0.442113 | 0.159977 | intron-variant | RNFT2 | GRCh38.p7 | 12:116823512 | aatgtggcaaaaccc[C/T]gtctctactaaaaat | 84900 |
rs7313399 | snp | G/T | 0.110519 | 0.207473 | intron-variant | RNFT2 | GRCh38.p7 | 12:116771180 | TAAACATGTGGATAG[G/T]CCAGGTGCGTTGGCT | 84900 |
rs7314211 | snp | G/T | 0.463451 | 0.130149 | intron-variant | RNFT2 | GRCh38.p7 | 12:116796719 | CCTTCCCCTCTCCCC[G/T]CCTTCCCTTCTCCCA | 84900 |
rs7314309 | snp | A/G | 0.110519 | 0.207473 | intron-variant | RNFT2 | GRCh38.p7 | 12:116772066 | GTTGCTGCCCCATCA[A/G]TATTTGTCAAATAAA | 84900 |
rs7314377 | snp | G/T | 0.17138 | 0.237316 | intron-variant | RNFT2 | GRCh38.p7 | 12:116796871 | GAGCCAGCCACACTG[G/T]TTCCAACTACCCACA | 84900 |
rs7315162 | snp | A/G | 0.451483 | 0.148002 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787984 | CCAGGCTGGAGTGCA[A/G]TGGCGCAATCTCGGC | 84900 |
rs7315763 | snp | A/G | 0.372995 | 0.217652 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812604 | CAGTGGCGCGATCTC[A/G]GCTCACTGCAACCTC | 84900 |
rs7316426 | snp | A/G | 0.084364 | 0.187256 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809337 | GAAGTGCTGATGAGA[A/G]GAGAGGTCCTTCCAC | 84900 |
rs7316436 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809369 | TCGTTGTGAGGTTTC[A/G]GCAACTCCTTCATGT | 84900 |
rs7485743 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116841960 | ataAATATATATATa[G/T]agagagagagagaga | 84900 |
rs7953141 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809377 | AGGTTTCGGCAACTC[C/T]TTCATGTGGCCTGGG | 84900 |
rs7953364 | snp | A/G | 0.17654 | 0.238964 | intron-variant | RNFT2 | GRCh38.p7 | 12:116751681 | gctgggattacaggc[A/G]tgagctactgtgcct | 84900 |
rs7953594 | snp | A/G | 0.469839 | 0.119042 | intron-variant | RNFT2 | GRCh38.p7 | 12:116751836 | cgatctcagctcact[A/G]caaacctctacccac | 84900 |
rs7955406 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | RNFT2 | GRCh38.p7 | 12:116845648 | AGGATGGGGCTGGAC[A/G]GGAGACGGGCCATCA | 84900 |
rs7958812 | snp | A/G | 0.107694 | 0.205546 | intron-variant | RNFT2 | GRCh38.p7 | 12:116849868 | tttttttttaaaaca[A/G]ggtctcgctctatca | 84900 |
rs7958828 | snp | A/G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116806389 | aaaaaaaaatatata[A/G/T]atatatatatagata | 84900 |
rs7958834 | snp | G/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806397 | atatatatatatata[G/T]atagatagatagata | 84900 |
rs7960383 | snp | C/G | 0.208474 | 0.246527 | intron-variant | RNFT2 | GRCh38.p7 | 12:116758716 | gcttgtagggtttct[C/G]ctgagaaatctgctg | 84900 |
rs7960408 | snp | G/T | 0.208779 | 0.246578 | intron-variant | RNFT2 | GRCh38.p7 | 12:116758774 | ttagctggtgcttct[G/T]tctcacagctcttaa | 84900 |
rs7960529 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116749158 | gctggaaggctgaga[G/T]cagggtatcagcagg | 84900 |
rs7960557 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RNFT2 | GRCh38.p7 | 12:116846824 | tttagattcttcatc[C/T]ctaaatacttcagtg | 84900 |
rs7960629 | snp | G/T | 0.110872 | 0.20771 | intron-variant | RNFT2 | GRCh38.p7 | 12:116801836 | tttgtttgtttgttt[G/T]tttgagacagagtct | 84900 |
rs7960657 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | RNFT2 | GRCh38.p7 | 12:116811573 | tagagacgagttttc[A/G]ccatgttggccaggc | 84900 |
rs7961400 | snp | A/G | 0.450859 | 0.148847 | intron-variant | RNFT2 | GRCh38.p7 | 12:116782142 | TACTAAAACTGGAAC[A/G]ATACAGAGATTAGCA | 84900 |
rs7961402 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | RNFT2 | GRCh38.p7 | 12:116782148 | aactggaacgataca[A/G]agattagcatggccc | 84900 |
rs7963851 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNFT2 | GRCh38.p7 | 12:116824476 | caaagataagcagcc[C/T]gagcctgggagtatg | 84900 |
rs7964246 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | RNFT2 | GRCh38.p7 | 12:116818298 | actgcactccagcct[C/G]ggtgacagtgaggcc | 84900 |
rs7965007 | snp | A/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750829 | atatattatatatat[A/T]atatatatattatat | 84900 |
rs7965017 | snp | A/G | 0.444444 | 0.157135 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750847 | atatatattatatat[A/G]tataatatatattat | 84900 |
rs7966211 | snp | A/T | 0.104859 | 0.203554 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851230 | ACATCTAAAAAAAAA[A/T]AAAtttattagagat | 84900 |
rs7967983 | snp | A/C/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750831 | atattatatatataa[A/C/T]atatatattatatat | 84900 |
rs7969141 | snp | A/G | 0.450985 | 0.148678 | intron-variant | RNFT2 | GRCh38.p7 | 12:116776812 | AGGAGAGGGACCAGC[A/G]TGGGTTGAGTACTGG | 84900 |
rs7969509 | snp | A/G | 0.325327 | 0.238382 | intron-variant | RNFT2 | GRCh38.p7 | 12:116777090 | gcccagctaattttt[A/G]tatttttagtagaga | 84900 |
rs7971246 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116749294 | tccccccccaccacc[A/C]cttttgagacaggct | 84900 |
rs7974175 | snp | C/T | 0.247621 | 0.249989 | intron-variant | RNFT2 | GRCh38.p7 | 12:116749366 | cactacagcctcaac[C/T]tcctgggctcaagtg | 84900 |
rs7974323 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | RNFT2 | GRCh38.p7 | 12:116785836 | ggtggatcgctcgag[C/T]tcatgagttcgagac | 84900 |
rs7975090 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116744904 | CCCTTGGGTGGCCAC[A/G]GAGAGAGAGTGGCCT | 84900 |
rs7978257 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNFT2 | GRCh38.p7 | 12:116846946 | atctagctcactctg[C/T]tgcccaggctggagt | 84900 |
rs7978279 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNFT2 | GRCh38.p7 | 12:116847001 | gcaacctctgccccc[C/T]gggttcaaacgattc | 84900 |
rs7978853 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | RNFT2 | GRCh38.p7 | 12:116826377 | ATTGCTACCGTTTCC[C/T]CTTCACGGTGGCAGG | 84900 |
rs7980144 | snp | A/G | 0.118933 | 0.212888 | intron-variant | RNFT2 | GRCh38.p7 | 12:116760044 | ctatgggttaagtag[A/G]tgacattcccaggtc | 84900 |
rs7980733 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | RNFT2 | GRCh38.p7 | 12:116805932 | taacaacatttacaa[A/G]atgccatcacagcaa | 84900 |
rs9300333 | snp | C/T | 0.110167 | 0.207236 | intron-variant | RNFT2 | GRCh38.p7 | 12:116772987 | ACACATGCCACCACA[C/T]CCAGCTAATTTTTGT | 84900 |
rs9668850 | snp | A/G | 0.187685 | 0.242109 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116739291 | GGGACAGGGAGCAAG[A/G]GATCTAGAAAAGGGG | 84900 |
rs9668894 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116741825 | agctaatttttaaaa[A/T]tttttggtagagacg | 84900 |
rs9669021 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116742613 | ctggccctagatgat[G/T]taggacaggagaaat | 84900 |
rs9737620 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116806379 | tctcaaaaaaaaaaa[A/T]aaatatatatatata | 84900 |
rs9737621 | snp | A/G/T | 0.625 | 0.125 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806381 | tcaaaaaaaaaaaaa[A/G/T]atatatatatatata | 84900 |
rs9737761 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116806395 | aaatatatatatata[G/T]atatagatagataga | 84900 |
rs10047539 | snp | C/T | 0.102014 | 0.201495 | intron-variant | RNFT2 | GRCh38.p7 | 12:116838412 | TTGGTAGGATAAATT[C/T]CTAGTGGAAGAATTA | 84900 |
rs10161190 | snp | A/C | 0.19459 | 0.243782 | intron-variant | RNFT2 | GRCh38.p7 | 12:116758293 | attctgtgtctttta[A/C]gtggagcatttaggc | 84900 |
rs10527732 | in-del | -/TTCATTCA | 0.372794 | 0.217765 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809188 | TTAGAGCTGAGTTTG[-/TTCATTCA]TTCATTCATTCATTC | 84900 |
rs10558117 | in-del | -/AAA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116743104 | AAAAAAAAAAAAAAA[-/AAA]GGTTAAATGAAGCAG | 84900 |
rs10579273 | in-del | -/ATGG | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116788982 | TGGATGGATGGATGG[-/ATGG]GTAGATAAATGAGAG | 84900 |
rs10629511 | in-del | -/GT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116840932 | GTGTCTGTGTGTGTG[-/GT]TGTGTGTGTGTCCTG | 84900 |
rs10634667 | in-del | -/TT/TTT/TTTT | 0.499984 | 0.00279548 | intron-variant | RNFT2 | GRCh38.p7 | 12:116776916 | CAGCTCAAAATGGGA[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT | 84900 |
rs10637816 | in-del | -/TT/TTT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116745173 | CTCCATTGCACCAGA[-/TT/TTT]TTTTTTTTTTTTTTT | 84900 |
rs10651412 | in-del | -/CTC | 0.439363 | 0.163222 | intron-variant | RNFT2 | GRCh38.p7 | 12:116835300 | CTCCCAACCACACTT[-/CTC]CTACTGAATGTTTTC | 84900 |
rs10735095 | snp | C/T | 0.17654 | 0.238964 | intron-variant | RNFT2 | GRCh38.p7 | 12:116751927 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 84900 |
rs10735096 | snp | G/T | 0.130351 | 0.219509 | intron-variant | RNFT2 | GRCh38.p7 | 12:116767568 | ATATAAAAATTATGT[G/T]TTTTTTTTGTTTGTT | 84900 |
rs10735097 | snp | C/G | 0.116488 | 0.211364 | intron-variant | RNFT2 | GRCh38.p7 | 12:116804073 | TTCTCCTTCCCTAGA[C/G]GTTACCACTGGTTCC | 84900 |
rs10735098 | snp | A/G | 0.373196 | 0.217538 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812883 | GTTCCAAGAGTTTCA[A/G]TACCTTGTCCATAAT | 84900 |
rs10744882 | snp | A/G | 0.344592 | 0.231414 | intron-variant | RNFT2 | GRCh38.p7 | 12:116741840 | TTTTTTGGTAGAGAC[A/G]GGGTCTCACTAAGTT | 84900 |
rs10744883 | snp | C/T | 0.348794 | 0.229651 | intron-variant | RNFT2 | GRCh38.p7 | 12:116781057 | GAGTGCTTTGCTCCA[C/T]GCTCTGCACATAGTA | 84900 |
rs10744884 | snp | C/T | 0.384401 | 0.210799 | intron-variant | RNFT2 | GRCh38.p7 | 12:116781847 | TTTGGGAGGAAGAGG[C/T]GGGTGGACTGCCTGA | 84900 |
rs10774884 | snp | A/G | 0.349233 | 0.229462 | intron-variant | RNFT2 | GRCh38.p7 | 12:116748207 | AAGAAAAAAAAAGAA[A/G]GAAAAGAGGATGAAC | 84900 |
rs10774885 | snp | A/G | 0.303938 | 0.244112 | intron-variant | RNFT2 | GRCh38.p7 | 12:116748225 | AAAGAGGATGAACCC[A/G]AGAATAGAAAGATGG | 84900 |
rs10774886 | snp | A/G | 0.40086 | 0.199352 | intron-variant | RNFT2 | GRCh38.p7 | 12:116758314 | GCATTTAGGCCACTT[A/G]CATTCAATGTTAGTA | 84900 |
rs10774887 | snp | A/G | 0.102726 | 0.202016 | intron-variant | RNFT2 | GRCh38.p7 | 12:116792525 | CTCCGAGCTGTGGGC[A/G]ACAGTTATTAATGCC | 84900 |
rs10774888 | snp | C/T | 0.463451 | 0.130149 | intron-variant | RNFT2 | GRCh38.p7 | 12:116796985 | GGAGGGGGTGTGCTA[C/T]TGGTATTTAGTGGAC | 84900 |
rs10774889 | snp | A/G | 0.134119 | 0.221521 | intron-variant | RNFT2 | GRCh38.p7 | 12:116808236 | TCCTAAAGTGCTCGT[A/G]AGCCACCACACCTGG | 84900 |
rs10774890 | snp | A/C | 0.347253 | 0.230308 | intron-variant | RNFT2 | GRCh38.p7 | 12:116818893 | CCGTTACCACTGTTT[A/C]CACCAGAGCAAGGAG | 84900 |
rs10850707 | snp | C/T | 0.29175 | 0.246489 | intron-variant | RNFT2 | GRCh38.p7 | 12:116743903 | AGGTCTCAGCTTCTC[C/T]ATCCAAAAATGGCAG | 84900 |
rs10850709 | snp | C/T | 0.191461 | 0.24305 | intron-variant | RNFT2 | GRCh38.p7 | 12:116759499 | GTAGACTCCGTCAGA[C/T]GGAAGGTCTAGGGCT | 84900 |
rs10850710 | snp | A/G | 0.185472 | 0.241529 | intron-variant | RNFT2 | GRCh38.p7 | 12:116761114 | GCCCAGTCCCTTTAC[A/G]CCGCAGACATTCAGC | 84900 |
rs10850711 | snp | G/T | 0.208474 | 0.246527 | intron-variant | RNFT2 | GRCh38.p7 | 12:116762107 | AAAAGAGCCAGGCAC[G/T]GTGGCTCATGCATGC | 84900 |
rs10850712 | snp | C/T | 0.398714 | 0.200958 | intron-variant | RNFT2 | GRCh38.p7 | 12:116764823 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAATGAG | 84900 |
rs10850713 | snp | A/G | 0.18134 | 0.240387 | intron-variant | RNFT2 | GRCh38.p7 | 12:116768145 | ACTCTTTGTTGCCCA[A/G]GCTGGGGTGCAGTGG | 84900 |
rs10850714 | snp | C/T | 0.180064 | 0.240019 | intron-variant | RNFT2 | GRCh38.p7 | 12:116768454 | TGATGTTTCTGTCAA[C/T]GATGGACCATATAGA | 84900 |
rs10850715 | snp | A/G | 0.110519 | 0.207473 | intron-variant | RNFT2 | GRCh38.p7 | 12:116769403 | GAAGAAGACATTGCT[A/G]TCGTAGGAGATTACA | 84900 |
rs10850716 | snp | A/G | 0.186737 | 0.241863 | intron-variant | RNFT2 | GRCh38.p7 | 12:116773300 | CCTGTGTGTGTGCCC[A/G]GGACTATATTAAGAA | 84900 |
rs10850718 | snp | A/G | 0.489722 | 0.0709447 | intron-variant | RNFT2 | GRCh38.p7 | 12:116803006 | AGGCTGAGGTGGGAG[A/G]ATCTCTTGAGCCTGG | 84900 |
rs10850719 | snp | G/T | 0.488485 | 0.0749998 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809981 | TGCCTAGGCCAGAAA[G/T]ACCTTCTTATTCTGC | 84900 |
rs10850720 | snp | C/T | 0.354235 | 0.227234 | intron-variant | RNFT2 | GRCh38.p7 | 12:116814835 | aggcatgcaccacca[C/T]gcccagctaagtttt | 84900 |
rs10850721 | snp | C/T | 0.471388 | 0.116136 | intron-variant | RNFT2 | GRCh38.p7 | 12:116817159 | TTGCGTCTACAGGCA[C/T]GCACTACCATGGCCG | 84900 |
rs10850722 | snp | C/G | 0.254105 | 0.249966 | intron-variant | RNFT2 | GRCh38.p7 | 12:116821471 | TCCCCACAACCCCAC[C/G]ATCCTAACAGGCCCG | 84900 |
rs10850723 | snp | A/C | 0.115788 | 0.21092 | intron-variant | RNFT2 | GRCh38.p7 | 12:116821572 | ACTTGTGGCCCCCAT[A/C]CCCTGGGGCTTTTGG | 84900 |
rs10850724 | snp | C/G | 0.49423 | 0.0534032 | intron-variant | RNFT2 | GRCh38.p7 | 12:116822169 | AACCAGCCCTCCTCT[C/G]TGTCCCCTTAGTTCT | 84900 |
rs10850725 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | RNFT2 | GRCh38.p7 | 12:116825755 | TCTATATGTATGTGT[A/G]TATGTATGTGTGTAT | 84900 |
rs10850726 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116850615 | AGTATTTTTTCTTTT[A/C]ttttctttttttttt | 84900 |
rs11068166 | snp | C/G | | | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116737136 | GGTCCTCAACTCGGG[C/G]TTCTAGTCCCAGCTC | 84900 |
rs11068167 | snp | C/T | 0.168135 | 0.236216 | upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738125 | TAGTCGCGCAAGATC[C/T]TCTCACCATTGGTCC | 84900 |
rs11068168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNFT2 | GRCh38.p7 | 12:116741587 | GCACTAATCCCATTC[A/G]TGAAGAGCCCATCTC | 84900 |
rs11068169 | snp | A/G | 0.295599 | 0.245806 | intron-variant | RNFT2 | GRCh38.p7 | 12:116746013 | AGGCCAAGGCGGGTG[A/G]ATCACTTGAGCTCCG | 84900 |
rs11068170 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNFT2 | GRCh38.p7 | 12:116749555 | AAAGTACAGGGATTA[C/T]AGGCATGAGCCACTG | 84900 |
rs11068171 | snp | A/G | 0.170084 | 0.236883 | intron-variant | RNFT2 | GRCh38.p7 | 12:116751648 | tcaggtgttccatcc[A/G]cctcagcctcccaaa | 84900 |
rs11068172 | snp | C/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116752389 | ATTCTGGCATCACAG[C/G]TAAGTTTTGTTTTGT | 84900 |
rs11068174 | snp | A/G | 0.301932 | 0.244547 | intron-variant | RNFT2 | GRCh38.p7 | 12:116764781 | CCTGTAATCCCAGCC[A/G]CTTGGGAGGCTGAGG | 84900 |
rs11068175 | snp | C/T | 0.110872 | 0.20771 | intron-variant | RNFT2 | GRCh38.p7 | 12:116769349 | agtgagactccgtct[C/T]aaagttaactgtaag | 84900 |
rs11068176 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116770605 | GCTCTGTCACCCAGG[C/T]TGGAGTGCAGTGGTG | 84900 |
rs11068177 | snp | A/G | 0.189261 | 0.242509 | intron-variant | RNFT2 | GRCh38.p7 | 12:116771430 | ACACCACTGCACTCC[A/G]GCCTGGGTGACAAAA | 84900 |
rs11068178 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116771494 | AAAAAAAAAAAAAAA[A/T]ATACGTATATGAGCA | 84900 |
rs11068179 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116771528 | TTATTTTTTTCTTTA[A/G]AATTATCTGTATTTT | 84900 |
rs11068180 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116771732 | TGTGACATTGACTCA[A/G]AGTTCTACGCAATGT | 84900 |
rs11068181 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116775929 | gcatctgtaatccca[G/T]ctactcgggaggctg | 84900 |
rs11068182 | snp | C/T | 0.18989 | 0.242666 | intron-variant | RNFT2 | GRCh38.p7 | 12:116776986 | ACAGTGGCACGATCT[C/T]GGCTCACTGCAACCT | 84900 |
rs11068184 | snp | A/G | 0.239614 | 0.249784 | intron-variant | RNFT2 | GRCh38.p7 | 12:116781948 | GCTGGGCGTGGCAGC[A/G]TGCGCCTGTAGTCCT | 84900 |
rs11068185 | snp | C/T | 0.239326 | 0.249772 | intron-variant | RNFT2 | GRCh38.p7 | 12:116782601 | ACATTTTTGGGTGGG[C/T]GCAGCATTCCATTCC | 84900 |
rs11068186 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116786413 | accgcgcccggccGA[A/G]ATCGGGTAGTTCTTA | 84900 |
rs11068187 | snp | A/G | 0.239902 | 0.249796 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787394 | GATGTTAACAGTAGC[A/G]TTCTTTAGATACTGT | 84900 |
rs11068188 | snp | C/T | 0.187685 | 0.242109 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787686 | GTCACTACACTCAGC[C/T]TGGGCAATAGAGGGA | 84900 |
rs11068189 | snp | C/G | 0.239326 | 0.249772 | intron-variant | RNFT2 | GRCh38.p7 | 12:116792262 | ACCATGTTGGCCAGG[C/G]TGGTCTTGAACTCCT | 84900 |
rs11068190 | snp | A/G | 0.239614 | 0.249784 | intron-variant | RNFT2 | GRCh38.p7 | 12:116792342 | GGTATGAGCCACTGC[A/G]CCCAGCCTAGAAAAT | 84900 |
rs11068191 | snp | C/T | 0.188 | 0.24219 | intron-variant | RNFT2 | GRCh38.p7 | 12:116792614 | AATGTGCCAGGTCAG[C/T]GCGTAATCTAGCCTG | 84900 |
rs11068192 | snp | A/G | 0.27893 | 0.24832 | intron-variant | RNFT2 | GRCh38.p7 | 12:116793468 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT | 84900 |
rs11068194 | snp | A/G | 0.138546 | 0.223781 | intron-variant | RNFT2 | GRCh38.p7 | 12:116804868 | GCTATTCAGGAAGCC[A/G]AAGTGGGAGGATTGC | 84900 |
rs11068195 | snp | A/G | 0.135825 | 0.222405 | intron-variant | RNFT2 | GRCh38.p7 | 12:116811650 | CAAAGTGCTGGGATT[A/G]CAGGCGTGAGCCAAC | 84900 |
rs11068196 | snp | A/G | 0.180064 | 0.240019 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812979 | tttttcttttgaaac[A/G]gggtctcactctgtc | 84900 |
rs11068197 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RNFT2 | GRCh38.p7 | 12:116814248 | ATTCTGTACCAGGCC[C/T]AGGACTAGGTCCCAG | 84900 |
rs11068198 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116817052 | gagtctcgctctgtc[A/G]cccaggctagaatac | 84900 |
rs11068199 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116820607 | TACCCCCATAGCTTG[G/T]ATCTTTTCTTTCTCT | 84900 |
rs11068201 | snp | C/T | 0.185155 | 0.241444 | intron-variant | RNFT2 | GRCh38.p7 | 12:116838046 | ACATAAGTTATAGTA[C/T]ATTCTACCTATGCTG | 84900 |
rs11068202 | snp | A/C | 0.325563 | 0.238307 | intron-variant | RNFT2 | GRCh38.p7 | 12:116838420 | ATAAATTTCTAGTGG[A/C]AGAATTACTGGGTCA | 84900 |
rs11068204 | snp | A/G | 0.127944 | 0.218179 | intron-variant | RNFT2 | GRCh38.p7 | 12:116848323 | TGCGTGCATGTATCT[A/G]TTTATCGTAGCACTA | 84900 |
rs11285914 | in-del | -/A | 0.40853 | 0.193309 | intron-variant | RNFT2 | GRCh38.p7 | 12:116803095 | GCAAGACCCTGTCTT[-/A]AAAAAAAAAATCAAA | 84900 |
rs11292371 | in-del | -/G | 0.107694 | 0.205546 | intron-variant | RNFT2 | GRCh38.p7 | 12:116843706 | CCTCAGCTGGGCCCT[-/G]GGGTAAACCTGGTTT | 84900 |
rs11313609 | in-del | -/T | 0.110167 | 0.207236 | intron-variant | RNFT2 | GRCh38.p7 | 12:116772095 | AATGAGTATCTCAGA[-/T]TTTTTTTTATTTTGG | 84900 |
rs11349950 | in-del | -/G | 0.358515 | 0.225221 | intron-variant | RNFT2 | GRCh38.p7 | 12:116785278 | GTGTGTGTGTGTGGC[-/G]GGGGGGGGTTGTTTG | 84900 |
rs11377177 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116753149 | CTTTTTTCTTTTTCT[-/T]TTTTTTTTTTTTTTT | 84900 |
rs11380244 | in-del | -/A | 0.471292 | 0.116318 | intron-variant | RNFT2 | GRCh38.p7 | 12:116818320 | GTGAGGCCCTATCTC[-/A]AAAAAAAAAAAAAAA | 84900 |
rs11411387 | in-del | -/T/TT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116811384 | TGTATTTTTTTTTTT[-/T/TT]CCTTTTTTTGAGACA | 84900 |
rs11436972 | in-del | -/A/AA/AAA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116762080 | AAAAAAAAAAAAAAA[-/A/AA/AAA]CAGAAAAAAAGAAAA | 84900 |
rs11503182 | snp | A/T | 0.190519 | 0.242821 | intron-variant | RNFT2 | GRCh38.p7 | 12:116758937 | GACGTTTTCCTCGAT[A/T]ATTCCCCCAAATATG | 84900 |
rs11608311 | snp | C/T | 0.201418 | 0.245234 | intron-variant | RNFT2 | GRCh38.p7 | 12:116814747 | gcagtggtgcaatct[C/T]ggctggctgcaacct | 84900 |
rs11608314 | snp | C/T | 0.37138 | 0.218556 | intron-variant | RNFT2 | GRCh38.p7 | 12:116849648 | TGGTATAGTGCGTGC[C/T]TCCTTCCCCTGCAAA | 84900 |
rs11609964 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116838890 | CAGTGCTGGTTGAAG[A/C]CTGTACATATGACCA | 84900 |
rs11610151 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116782626 | CATTCCCTGCCACAC[A/C]TGATTTCCTCCCTCC | 84900 |
rs11610785 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116771499 | AAAAAAAAAAAATAC[A/G]TATATGAGCAATTTT | 84900 |
rs11611077 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116780669 | CAAAATGGCATAAAG[A/C]CAAAAAAAAAAAAAA | 84900 |
rs11611604 | snp | G/T | 0.177824 | 0.239355 | intron-variant | RNFT2 | GRCh38.p7 | 12:116751018 | gcctcccaggttggt[G/T]atcctcccacctcag | 84900 |
rs11612320 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | RNFT2 | GRCh38.p7 | 12:116815306 | cttcctgtgagtact[A/G]taacaaataaccaca | 84900 |
rs11614167 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | RNFT2 | GRCh38.p7 | 12:116826804 | GTTACATGAGCACCT[A/G]CTACAtgctagatgc | 84900 |
rs11614883 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116771498 | AAAAAAAAAAAAATA[C/T]GTATATGAGCAATTT | 84900 |
rs11615937 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116839148 | TTTTCCTACTTAGCA[A/C]TTATTCCAATTGTTA | 84900 |
rs11829412 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | RNFT2 | GRCh38.p7 | 12:116780040 | GAAGTCTCCTGCTTT[C/T]CATTCTGTAAAAACA | 84900 |
rs11829788 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RNFT2 | GRCh38.p7 | 12:116776710 | GAAAGCATCCATTCT[A/G]TGCTGAGTGTACTTC | 84900 |
rs11830125 | snp | C/T | 0.147604 | 0.228068 | intron-variant | RNFT2 | GRCh38.p7 | 12:116811444 | GCAGTGGGGCCATCT[C/T]GGCTCACTGCAACCT | 84900 |
rs11831945 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | RNFT2 | GRCh38.p7 | 12:116837388 | TGCAGTGTCTCGGGG[G/T]ACTGAGGCAGAGAGC | 84900 |
rs11832385 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116750830 | tatattatatatata[A/T]tatatatattatata | 84900 |
rs11832387 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116750841 | tataatatatatatt[A/T]tatatatataatata | 84900 |
rs11832734 | snp | A/G | 0.130351 | 0.219509 | upstream-variant-2KB, utr-variant-5-prime | RNFT2, C12orf49 | GRCh38.p7 | 12:116738051 | GCTCCCGGCAGCCTT[A/G]GGCGCAGCCCCACGT | 84900 |
rs11832883 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116750833 | attatatatataata[C/T]atatattatatatat | 84900 |
rs11832884 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116750840 | atataatatatatat[A/T]atatatatataatat | 84900 |
rs11832933 | snp | A/G | 0.15698 | 0.23205 | intron-variant | RNFT2 | GRCh38.p7 | 12:116813728 | AGGTAATTAATTCAT[A/G]AGAATGTTGCAGATA | 84900 |
rs11833084 | snp | A/C | 0.100944 | 0.200705 | intron-variant | RNFT2 | GRCh38.p7 | 12:116752045 | ATTATCTTGTGGTCT[A/C]CTACTTTCCATGAGA | 84900 |
rs11833612 | snp | A/G | 0.15698 | 0.23205 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812478 | ACACTAGGTGAGGCC[A/G]GGAGGTGGCGGGGAG | 84900 |
rs11835089 | snp | A/G | 0.157642 | 0.232314 | intron-variant | RNFT2 | GRCh38.p7 | 12:116811813 | CTGGCTCTTCTCCTC[A/G]GGGCCCAGAAGTGCT | 84900 |
rs11835760 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812647 | ttaaacggttctcct[A/G]cctcagcctcctgag | 84900 |
rs11835957 | snp | C/T | 0.116838 | 0.211584 | intron-variant | RNFT2 | GRCh38.p7 | 12:116775713 | CAATAAAACATTGGA[C/T]ATATATCACAATTAA | 84900 |
rs11835971 | snp | C/T | 0.116838 | 0.211584 | intron-variant | RNFT2 | GRCh38.p7 | 12:116775795 | cgcctgtattcccaa[C/T]actttgggaggccaa | 84900 |
rs11836731 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116794651 | aggggaggggagaag[A/G]aaggaaggaagggag | 84900 |
rs11837091 | snp | G/T | 0.298905 | 0.24517 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797535 | actccagcctgtcta[G/T]ctcaaaaaaaaaaaa | 84900 |
rs12161801 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116783550 | GCGACACAGGTTGCA[A/G]CCACCTGCAGGCACA | 84900 |
rs12231554 | snp | A/G | 0.182933 | 0.240836 | intron-variant | RNFT2 | GRCh38.p7 | 12:116766010 | AAAAATTTGACTTTT[A/G]CCTGTAATTCCAGTG | 84900 |
rs12231952 | snp | A/G | 0.148326 | 0.228391 | intron-variant | RNFT2 | GRCh38.p7 | 12:116767380 | catgccaccacacct[A/G]gctaatttttacatt | 84900 |
rs12296993 | snp | C/T | 0.199564 | 0.24486 | intron-variant | RNFT2 | GRCh38.p7 | 12:116779915 | TTGGAGTTCAGAGGA[C/T]TGAGCAGGGCTCAGA | 84900 |
rs12298519 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116743623 | GGGGGCCTGTTCTCA[A/G]ATTGGGACAGCCTCC | 84900 |
rs12298522 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116743646 | CAGCCTCCAGCCCCA[A/G]AAGCCCTGTCCTAGC | 84900 |
rs12301988 | snp | C/G | 0.470908 | 0.117046 | intron-variant | RNFT2 | GRCh38.p7 | 12:116817850 | TCATATTATGACAGG[C/G]ACTGCGAAGGTGTTG | 84900 |
rs12302528 | snp | C/T | 0.190519 | 0.242821 | intron-variant | RNFT2 | GRCh38.p7 | 12:116752652 | GGAAGCTGAAGTGGG[C/T]GGATCACTTGAGGTC | 84900 |
rs12305605 | snp | A/G | 0.239902 | 0.249796 | intron-variant | RNFT2 | GRCh38.p7 | 12:116780686 | AAAAAAAAAAAAAAG[A/G]GATGTGGAGAAGAAA | 84900 |
rs12306410 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | RNFT2 | GRCh38.p7 | 12:116815554 | aacctctgtgtctgt[C/T]gtctcattgtcttcc | 84900 |
rs12306557 | snp | A/G | 0.2776 | 0.248472 | intron-variant | RNFT2 | GRCh38.p7 | 12:116772557 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 84900 |
rs12307535 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116841908 | aaatatatatatata[A/T]atatatatataaaaa | 84900 |
rs12307537 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116841936 | aaatatatatatata[A/T]atatatatataAATA | 84900 |
rs12307539 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116841948 | ataaatatatatata[A/T]atatatatatagaga | 84900 |
rs12307874 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | RNFT2 | GRCh38.p7 | 12:116821230 | GTTTCTATCCACTTC[C/T]CTCCTTCCTTCCTGT | 84900 |
rs12308482 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738784 | CCAATACAAGCATCC[C/G]AAAGTAGAGTTTCGA | 84900 |
rs12308877 | snp | A/G | 0.191147 | 0.242974 | intron-variant | RNFT2 | GRCh38.p7 | 12:116757583 | gtcatttttgatcca[A/G]tgctcattcaggagc | 84900 |
rs12308981 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116841912 | atatatatataaata[A/T]atatataaaaatata | 84900 |
rs12308987 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116841940 | atatatatataaata[A/T]atatataAATATATA | 84900 |
rs12308990 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116841952 | atatatatataAATA[A/T]ATATATagagagaga | 84900 |
rs12309159 | snp | A/G | 0.264906 | 0.249555 | intron-variant | RNFT2 | GRCh38.p7 | 12:116788223 | tgagccactgcgccc[A/G]gccTCTTTTGCTCct | 84900 |
rs12309982 | snp | A/G | 0.199564 | 0.24486 | intron-variant | RNFT2 | GRCh38.p7 | 12:116779913 | CATTGGAGTTCAGAG[A/G]ACTGAGCAGGGCTCA | 84900 |
rs12312295 | snp | C/T | 0.264906 | 0.249555 | intron-variant | RNFT2 | GRCh38.p7 | 12:116788796 | agatgaatTAGATGA[C/T]CATCTGGGAAGTTTG | 84900 |
rs12313074 | snp | C/T | 0.441021 | 0.161279 | intron-variant | RNFT2 | GRCh38.p7 | 12:116768982 | gtgatctacctgcct[C/T]aacctcccaaagtgc | 84900 |
rs12313689 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116811821 | TCTCCTCGGGGCCCA[A/G]AAGTGCTAAGATCAG | 84900 |
rs12313741 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116841962 | aAATATATATATaga[G/T]agagagagagagaga | 84900 |
rs12313743 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116841968 | ATATATagagagaga[A/G]agagagagagagaga | 84900 |
rs12314052 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116782295 | aggctgaggcaggaa[A/G]attgcttgaggccag | 84900 |
rs12314176 | snp | A/G | 0.190519 | 0.242821 | intron-variant | RNFT2 | GRCh38.p7 | 12:116752445 | TGGCAGGTTTTTTTT[A/G]TTTTGTTTTTTAATC | 84900 |
rs12320723 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116820804 | cctcaccagttaaca[A/G]gggcaaataatttca | 84900 |
rs12320851 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | RNFT2 | GRCh38.p7 | 12:116821051 | acAAGAGGAGCAATT[G/T]GTGTGCCGTTCCTGG | 84900 |
rs12322695 | snp | G/T | 0.185472 | 0.241529 | intron-variant | RNFT2 | GRCh38.p7 | 12:116761609 | tgctcatctcagcag[G/T]ttcatcccagcaacc | 84900 |
rs12369622 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116761954 | cgcctgtaatcccaa[A/C]tactcagaaggctga | 84900 |
rs12371218 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806047 | CTTTAAACAAGAGGG[C/T]AGCTTTGAAGCTGGC | 84900 |
rs12371852 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789960 | ATGGTGGATGGGTGG[A/G]TGGATGGATGGATGG | 84900 |
rs12426049 | snp | A/T | 0.247621 | 0.249989 | intron-variant | RNFT2 | GRCh38.p7 | 12:116766122 | AAAAAAAAATAAAAA[A/T]TTTTTTTTAATTAGC | 84900 |
rs12578311 | snp | A/C | | | synonymous-codon, nc-transcript-variant | RNFT2 | GRCh38.p7 | 12:116750063 | AGGAGGGGGCCGGGG[A/C]GAGGGGGGCGCCTAC | 84900 |
rs12578408 | snp | A/G | 0.128632 | 0.218563 | intron-variant | RNFT2 | GRCh38.p7 | 12:116846983 | gcgcgatcttggctc[A/G]ctgcaacctctgccc | 84900 |
rs12582008 | snp | A/C | | | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116736361 | ACTGTGAGGAGGTGT[A/C]TGAGGTGGCAGAAAA | 84900 |
rs12812873 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789282 | agtagatggatggat[A/G]gatgggtgggtggat | 84900 |
rs12814810 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789220 | ggatggtagatgggt[A/T]aatgggaggagagta | 84900 |
rs12815898 | snp | A/G | 0.487558 | 0.0778863 | intron-variant | RNFT2 | GRCh38.p7 | 12:116794489 | TGCAATCCCAGCTAC[A/G]CGGGAGGCTGAGGTG | 84900 |
rs12815953 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116849848 | CTTCCTTCCTTCCTT[C/T]TTTTTTTTTTTTTAA | 84900 |
rs12815954 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116849849 | TTCCTTCCTTCCTTT[C/T]TTTTTTTTTTTTAAA | 84900 |
rs12816240 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | RNFT2 | GRCh38.p7 | 12:116746994 | GTGGGTTTTGGTCCA[C/T]GACTCAAGGTTGGTT | 84900 |
rs12816258 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116794676 | agggaggaaggaagg[A/G]agggagggagggagg | 84900 |
rs12816289 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116762735 | tcctgcctcagcctc[C/T]tgagtagctgagatt | 84900 |
rs12818416 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116794672 | aggaagggaggaagg[A/G]agggagggagggagg | 84900 |
rs12822842 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, missense | RNFT2, C12orf49 | GRCh38.p7 | 12:116737910 | CACCATCCCGGCGCG[G/T]ACGTggggcgcggcg | 84900 |
rs12824289 | snp | C/T | | | upstream-variant-2KB, missense, synonymous-codon | RNFT2, C12orf49 | GRCh38.p7 | 12:116737854 | AGGGCGAGCACCCAC[C/T]TCTTCCGCAGAAGCC | 84900 |
rs12829112 | snp | A/G | 0.00479614 | 0.0487346 | intron-variant | RNFT2 | GRCh38.p7 | 12:116845698 | TAGTGGGAATCTGTA[A/G]AAGCTGCAGGGCTTG | 84900 |
rs12829990 | snp | C/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116832899 | ACCCAAGTCGTGttc[C/T]ttttttttttttttt | 84900 |
rs16946969 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | RNFT2 | GRCh38.p7 | 12:116753477 | CAATGTATGCTTTTA[C/T]CACAAATTCTATCTG | 84900 |
rs16946979 | snp | C/T | 0.078151 | 0.181571 | intron-variant | RNFT2 | GRCh38.p7 | 12:116776463 | ACGGGAGCTCAGGGC[C/T]GCAAACCTCTCCCTG | 84900 |
rs16946996 | snp | C/G | 0.18134 | 0.240387 | intron-variant | RNFT2 | GRCh38.p7 | 12:116801345 | ACAAAATGTACCTCC[C/G]TTTCTGTTGCCAGGA | 84900 |
rs16947003 | snp | A/G | 0.180383 | 0.240111 | intron-variant | RNFT2 | GRCh38.p7 | 12:116810934 | GCCCACTGATAACAC[A/G]TCTCAACTTTTAGCT | 84900 |
rs16947036 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | RNFT2 | GRCh38.p7 | 12:116816436 | TGGGACCATAGCACC[A/G]GAGGCGATCGCGGCC | 84900 |
rs16947041 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | RNFT2 | GRCh38.p7 | 12:116828157 | CTTTTCCTTCACCTC[G/T]TGGCTCTGGAACACC | 84900 |
rs16947046 | snp | C/T | 0.208169 | 0.246476 | intron-variant | RNFT2 | GRCh38.p7 | 12:116844913 | TCTGAGCAAGAACCG[C/T]ACTCAGCATAAAACC | 84900 |
rs16947049 | snp | C/T | 0.0454069 | 0.143672 | synonymous-codon, intron-variant | RNFT2 | GRCh38.p7 | 12:116849385 | GCTCTGCCGCTCGGT[C/T]GCCGTGGACACCCTG | 84900 |
rs16947055 | snp | A/G | 0.0807086 | 0.18396 | utr-variant-3-prime, intron-variant | RNFT2 | GRCh38.p7 | 12:116852628 | CAACTGGTTTTTATC[A/G]GAAAGATCATCCTGC | 84900 |
rs17429022 | snp | C/T | 0.137867 | 0.223442 | intron-variant | RNFT2 | GRCh38.p7 | 12:116783055 | TCAATACATGTTGGC[C/T]ACCAGGGTGATGCTT | 84900 |
rs17500871 | snp | A/C | 0.0693013 | 0.172766 | intron-variant | RNFT2 | GRCh38.p7 | 12:116779407 | TCATGCAGAGGATTC[A/C]GGGTGCCTTCTGAGG | 84900 |
rs17501002 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | RNFT2 | GRCh38.p7 | 12:116813358 | CCTCTTAGGGCTGAA[C/T]CATGCTCTTGTTCTC | 84900 |
rs17582582 | snp | G/T | 0.140581 | 0.224783 | intron-variant | RNFT2 | GRCh38.p7 | 12:116796785 | ATTCTAAGCCTCAGC[G/T]ATGGTTTTGGCTGCA | 84900 |
rs17616249 | snp | G/T | 0.0901694 | 0.192235 | intron-variant | RNFT2 | GRCh38.p7 | 12:116774511 | GCTGTTTGTGGAAAC[G/T]ATCAGAGCTGTCAGA | 84900 |
rs17616308 | snp | A/T | 0.0558544 | 0.157504 | intron-variant | RNFT2 | GRCh38.p7 | 12:116801214 | TGCCTGCAGCTGTTA[A/T]TGAAGATGTCCCTTT | 84900 |
rs17850811 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116851698 | GTGAGCCGAGATTGC[A/G]CCACAGCACTCCAAC | 84900 |
rs28392543 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116765781 | AGGGCTTTGAGAATT[A/G]GGTATATAAGCTTGG | 84900 |
rs28441540 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116743042 | GCTATGATTGCACCA[C/T]TGCATTCCAGCCTGG | 84900 |
rs28457152 | snp | A/C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116750851 | ATATTATATATATAT[A/C/T]ATATATATTATATAT | 84900 |
rs28483850 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116750836 | ATATATATAATATAT[A/G]TATTATATATATATA | 84900 |
rs28496917 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116819198 | TGCTGGACAAGGGGT[A/C]TTCGGGGTGAAATGT | 84900 |
rs28519467 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116811385 | TGTATTTTTTTTTTT[C/T]CTTTTTTTGAGACAG | 84900 |
rs28572085 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116811387 | TATTTTTTTTTTTCC[C/T]TTTTTTGAGACAGAG | 84900 |
rs28605918 | snp | C/T | 0.375 | 0.216506 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750842 | ATAATATATATATTA[C/T]ATATATATAATATAT | 84900 |
rs33936190 | in-del | -/A | 0.414553 | 0.188208 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800634 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAATGGT | 84900 |
rs34013122 | in-del | -/A | 0.243919 | 0.249926 | intron-variant | RNFT2 | GRCh38.p7 | 12:116763619 | ATAACAAAAAAAAAA[-/A]TTAGCTGGATGTGGT | 84900 |
rs34043649 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116816447 | ACCAGAGGCGATCGC[-/G]GGCCTCCTCCTCCCC | 84900 |
rs34116756 | in-del | -/T | 0.324145 | 0.238752 | intron-variant | RNFT2 | GRCh38.p7 | 12:116850322 | ACCAGGCCTGGCTAA[-/T]TTTTTTTTTTTTTTA | 84900 |
rs34154674 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116740831 | CCTCCTCTGTGAAAT[-/G]GGGGTGATAGCTTTC | 84900 |
rs34193365 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116803951 | GCCTCACCTAACAGC[-/G]GGATAATCTGGGAAA | 84900 |
rs34195193 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116799345 | TAAATTAGACTCACT[-/G]GGGACAGCCTGCTAA | 84900 |
rs34209604 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116768052 | GAAATAATAATTGCC[-/T]TCTTGGTGGGCACTG | 84900 |
rs34269187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNFT2 | GRCh38.p7 | 12:116796904 | CAGGGGCTGGAAGAA[G/T]GTTAAGTAGTGATTC | 84900 |
rs34273674 | in-del | -/TTT | 0.174932 | 0.238463 | intron-variant | RNFT2 | GRCh38.p7 | 12:116846920 | TTTTTTTTTTTTTTT[-/TTT]GAGATGGAATCTAGC | 84900 |
rs34308260 | in-del | -/TT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116745191 | TCCATTGCACCAGAT[-/TT]TTTTTTTTTTTTTTT | 84900 |
rs34358849 | in-del | -/TG | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116840922 | TTAGGGGTATGTGTC[-/TG]TGTGTGTGTGTGTGT | 84900 |
rs34410160 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | RNFT2 | GRCh38.p7 | 12:116825133 | TTAAGGTCCTGTATC[-/T]GGGGCCTCAGTTCTC | 84900 |
rs34424913 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116818336 | AAAAAAAAAAAAAAA[-/A]TCCGCTTTTTCGTCT | 84900 |
rs34454980 | snp | A/G | 0.239326 | 0.249772 | intron-variant | RNFT2 | GRCh38.p7 | 12:116783043 | CATCATAAGTGCTCA[A/G]TACATGTTGGCTACC | 84900 |
rs34625924 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116817487 | TCTTCCTTGCTGTTA[-/T]TAAAGGTGAGAGCAT | 84900 |
rs34675778 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116848685 | GTGCTTTTCCCCAAG[-/T]ATCTCATCAGGGCTC | 84900 |
rs34709337 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116800254 | TAATCCCTGCACATT[-/G]GGGAGGCCAGGGCGG | 84900 |
rs34769770 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116838964 | GCCTGGAAAGGCAGA[-/G]ATGATTCACATAGGT | 84900 |
rs34830867 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116840210 | AAGAGAATGGTGACT[-/A]CCTGTTGATTTCGTG | 84900 |
rs34850407 | in-del | -/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116769841 | TTTGAGACCAGCCTG[-/C]ACCAACATGGTGAAA | 84900 |
rs34926821 | in-del | -/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116785091 | CCCCCTCTGTTTCTT[-/C]CCCTCTGCCCTCCTC | 84900 |
rs34931867 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116821904 | AGTGGCGCAACCTCA[-/G]GCCCACTGCAGCCTC | 84900 |
rs34948838 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116833957 | GTGAGGTGGCCCCAA[-/G]GCTGGAGGGCCGGCC | 84900 |
rs34964792 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116800863 | AAAATAAAATAAAAA[-/T]CCATTTAACAGATAA | 84900 |
rs34978801 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116759453 | TTTGTCATATTACCA[-/G]GGGATGGTTTTCTGG | 84900 |
rs35004032 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116840762 | GGCAGCTTGTAGGAC[-/T]TTTTTTAAGAGTCAT | 84900 |
rs35105179 | in-del | -/C | | | frameshift-variant, intron-variant | RNFT2 | GRCh38.p7 | 12:116849419 | GCTGGAAGGACGGCG[-/C]CCACGTCCGCACACT | 84900 |
rs35134859 | in-del | -/C | | | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116736669 | ATTATCCTGGGTGCA[-/C]CCTGGGGTGTAACCA | 84900 |
rs35150112 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116740588 | AGAGCTGGAAGGAAG[-/T]TTTTGGTTTGACCAC | 84900 |
rs35163899 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116814359 | GATGGAGATCAAACA[-/G]GGGAGTGTCATTGTT | 84900 |
rs35217100 | in-del | -/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116781771 | TAACATTCACAGGTT[-/C]CCAGGCATTAAGGTG | 84900 |
rs35229705 | in-del | -/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116832897 | TACCCAAGTCGTGTT[-/C]CTTTTTTTTTTTTTT | 84900 |
rs35275810 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116840024 | CTCTGACAGGCTACA[-/G]GGGAGCCAGGGAAAG | 84900 |
rs35310448 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116787621 | TTGAGAGGCTGAAGT[-/G]GGGAGGATCATTGAG | 84900 |
rs35358523 | in-del | -/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116749136 | TTCTTATAACAAATT[-/C]CTGGAGGCTGGAAGG | 84900 |
rs35370485 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116810162 | AGCTCACAGTCCAGT[-/G]GGGGGTGTTGCAGGC | 84900 |
rs35385697 | in-del | -/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116740604 | TTTGGTTTGACCACT[-/C]CCACCCCTCCCATGT | 84900 |
rs35386897 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116750906 | ATATATATATATATA[-/T]TTTTTTTTTTTGAGA | 84900 |
rs35397958 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116754284 | CATCCAGGTCACTGC[-/A]AAGTGCTGTTAATTC | 84900 |
rs35408626 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116749594 | TAACCTCTTCTTACA[-/G]GGGACAGCAGTCACA | 84900 |
rs35412759 | snp | A/G | 0.114036 | 0.209795 | intron-variant | RNFT2 | GRCh38.p7 | 12:116769754 | ATAAATGTAACGGCC[A/G]GGCATGGTGGCTCAT | 84900 |
rs35453575 | in-del | -/T | 0.308166 | 0.243139 | intron-variant | RNFT2 | GRCh38.p7 | 12:116811373 | TGCTCAATGGGTGTA[-/T]TTTTTTTTTTTCCTT | 84900 |
rs35482097 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116793210 | ACATATCCAGATAGC[-/T]TTTTTTTTTTTTTTT | 84900 |
rs35505804 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNFT2 | GRCh38.p7 | 12:116834714 | TTGTATTTTTGAGGT[C/T]CATCCACATTGTAAC | 84900 |
rs35534991 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116787058 | AATCACATCTGCAAA[-/G]GACATGATTATTTTC | 84900 |
rs35547030 | in-del | -/T | 0.27893 | 0.24832 | intron-variant | RNFT2 | GRCh38.p7 | 12:116799579 | TATAAGTTAGCTGTG[-/T]TTTTTTTTTAACAGC | 84900 |
rs35549005 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116829578 | AGGAATCCTCTTCTG[-/A]AGTGACATGTGCCCA | 84900 |
rs35646975 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116763949 | AAAATGTAGAACCAT[-/G]CCCAAATGCCCATCA | 84900 |
rs35683000 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116765489 | AGGGAAGGTTACACT[-/G]GGGAAAGTTATGACC | 84900 |
rs35687933 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116843492 | GTGTGACTGTGTCTC[-/A]AAAAAAAAAAAAAAA | 84900 |
rs35729098 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116780556 | CCAGTCTTCAGCCCC[-/A]AGGACCCCTGGTTTC | 84900 |
rs35779552 | in-del | -/A | 0.457853 | 0.138915 | intron-variant | RNFT2 | GRCh38.p7 | 12:116831198 | TACAAAAAAAAAAAA[-/A]GAGAGAGAGAGAGAT | 84900 |
rs35796456 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116770256 | TGCCCTTTCTGTTTA[-/G]GATATACAGATACCA | 84900 |
rs35804239 | in-del | -/GT/TG | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116840923 | TGTGTGTGTGTGTGT[-/GT/TG]CCTGTCTGGTAGTAG | 84900 |
rs35816260 | snp | A/G | 0.0208361 | 0.0999196 | intron-variant | RNFT2 | GRCh38.p7 | 12:116835913 | TTGTGCAGGGGTCAC[A/G]AGTGATCCTTGGGTA | 84900 |
rs35830752 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116805122 | GGTTAAGACATTGTC[-/T]TTTTTTTTTTTTTTT | 84900 |
rs35844275 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797900 | GGGTGATGGTCATGG[A/G]AAGCGGTGGTAACTC | 84900 |
rs35874913 | snp | A/G | 0.375 | 0.216506 | intron-variant | RNFT2 | GRCh38.p7 | 12:116740267 | CATCTGCTTATAGCT[A/G]CCAACAATGTCCTAA | 84900 |
rs35895349 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116840035 | TACAGGGAGCCAGGG[-/A]AAAGGGCATTTTGAA | 84900 |
rs35911608 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116771461 | TGAGATCCTATCGTT[-/A]AAAAAAAAAAAAAAA | 84900 |
rs35917136 | in-del | -/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116812126 | AGCTGTTGGGATAAG[-/C]ACCTGACCCTGACTT | 84900 |
rs35922781 | in-del | -/TTTTTTTTTTTT | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116846449 | TAATTTTTTTTTTTT[-/TTTTTTTTTTTT]GTAGAGACATATGGG | 84900 |
rs35958280 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116823443 | AATCCCAGCACTTTA[-/G]GAGGCCGAAGTGTGT | 84900 |
rs36004111 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116780500 | ACCCACTGCTCACCT[-/A]CCTGCTGTGCGACCT | 84900 |
rs36033401 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116741781 | GCCTCCTGAGTAGCT[-/G]GGGACTACAGGCATG | 84900 |
rs36045826 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116750908 | TATATATATATATAT[-/A]TTTTTTTTTGAGACA | 84900 |
rs36066877 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116749550 | TCCCAAAGTACAGGG[-/G]ATTACAGGCATGAGC | 84900 |
rs36103586 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116770398 | AGTTTTGTGTAAGTC[-/A]AACTCTGTGGTGTTC | 84900 |
rs36214312 | in-del | -/GAAGTCACCA | 0.116138 | 0.211142 | intron-variant | RNFT2 | GRCh38.p7 | 12:116775321 | GTCCTTGTCCTTACT[-/GAAGTCACCA]GAAGTCACCAGTCTA | 84900 |
rs55824940 | snp | A/T | 0.085491 | 0.188381 | downstream-variant-500B | RNFT2 | GRCh38.p7 | 12:116854128 | CTTACAGTGCCCACT[A/T]CAGGGGCTAACTGGA | 84900 |
rs55846478 | snp | A/C/T | 0.0883596 | 0.190715 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800863 | TAAAATAAAATAAAA[A/C/T]CCATTTAACAGATAA | 84900 |
rs55856437 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116762062 | ACAGAGTGAGACTGT[C/T]TCAAAAAAAAAAAAA | 84900 |
rs55900757 | snp | C/T | 0.461813 | 0.132798 | intron-variant | RNFT2 | GRCh38.p7 | 12:116799134 | TCAGTTCTGTGTGAT[C/T]GTAGGACTTGAGGTC | 84900 |
rs55935763 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | RNFT2 | GRCh38.p7 | 12:116793071 | GGAATCCTCATACCT[C/G]GGCCTTCTAGGAGAA | 84900 |
rs55938203 | in-del | -/A | 0.497151 | 0.037632 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787719 | TGTTGTCTCTAAAAG[-/A]AAAAAAAAAAAAAAG | 84900 |
rs56032141 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116806380 | CTCAAAAAAAAAAAA[A/T]AATATATATATATAT | 84900 |
rs56036824 | snp | C/T | 0.140581 | 0.224783 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797428 | AGCCAGGTTTGGTGG[C/T]GTGTGCCTGTAATCC | 84900 |
rs56052356 | snp | A/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806378 | GTCTCAAAAAAAAAA[A/T]AAAATATATATATAT | 84900 |
rs56064465 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116800818 | GACTCCATCTTAAAA[A/T]AAAATAAAATAAAAT | 84900 |
rs56118843 | in-del | -/CCT | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116835302 | CCCAACCACACTTCT[-/CCT]ACTGAATGTTTTCTA | 84900 |
rs56120013 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RNFT2 | GRCh38.p7 | 12:116763800 | AAAAGGGGGCGGGGG[C/G]GGAAAGAACTAAAAG | 84900 |
rs56174906 | snp | A/G | 0.190519 | 0.242821 | intron-variant | RNFT2 | GRCh38.p7 | 12:116753414 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAAG | 84900 |
rs56185708 | in-del | -/TGTGTGTG/TGTGTGTGTG | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116785275 | GTGTGTGTGTGTGTG[-/TGTGTGTG/TGTGTGTGTG]GCGGGGGGGGGTTGT | 84900 |
rs56225981 | snp | G/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806391 | AAAAAAATATATATA[G/T]ATATATATAGATAGA | 84900 |
rs56234630 | in-del | -/AAAAAAAAAAAAAAAAAAAA/AAAAAAAAAAAAAAAAAAAAA | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116782094 | AAAAAAAAAAAAAAA[lengthTooLong]TGTGGACATCATGCC | 84900 |
rs56299893 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116744475 | GAGCACCCATTTTAC[A/T]AATGCAGAAGCTGAG | 84900 |
rs56333374 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116762846 | TGAACACTTGACCTC[A/C]GGTGATCCGACCACC | 84900 |
rs56359945 | snp | A/C | 0.029116 | 0.117091 | intron-variant | RNFT2 | GRCh38.p7 | 12:116843021 | AAATGCCCCTCTCCC[A/C]CTCAAAGCCTCTTCT | 84900 |
rs56380580 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116742830 | GTGCATACCTATAGT[C/T]TCAGCACTTTGGGAA | 84900 |
rs56674314 | in-del | -/T/TATAT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116832148 | AAAAAAAAAAAAAAA[-/T/TATAT]ATATATATATATATA | 84900 |
rs56687861 | in-del | -/C/T/TT | 0.396727 | 0.202413 | intron-variant | RNFT2 | GRCh38.p7 | 12:116847532 | CTCTTTTTTTTTTTT[-/C/T/TT]GAGGCAGAGTTTTGC | 84900 |
rs56692573 | snp | G/T | 0.264906 | 0.249555 | intron-variant | RNFT2 | GRCh38.p7 | 12:116786548 | GAAGGCATTTGAGGT[G/T]ACTCATCACCTGGCG | 84900 |
rs56705861 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116787264 | GGACCAGGAGATCAT[C/T]TGCCAGATCGGCCAG | 84900 |
rs56708238 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809584 | AAGATGGTCAGTTCC[C/T]GATTCAGACATCCCG | 84900 |
rs56871630 | in-del | -/T/TT | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116745192 | TTTTTTTTTTTTTTT[-/T/TT]GAGATAGAGTCTCAC | 84900 |
rs56877048 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | RNFT2 | GRCh38.p7 | 12:116814185 | TGTCCTAGGCACTTT[A/C]CATTCATCCATTTCT | 84900 |
rs56995727 | in-del | -/TT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116850619 | TTTTTCTTTTCTTTT[-/TT]CTTTTTTTTTTTTTT | 84900 |
rs57008991 | in-del | -/TGTG | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116785272 | GTGTGTGTGTGTGTG[-/TGTG]GCGGGGGGGGGTTGT | 84900 |
rs57033312 | snp | C/T | 0.18134 | 0.240387 | intron-variant | RNFT2 | GRCh38.p7 | 12:116799701 | TTTTTTTGGTAGAGA[C/T]GGGGTTTCACCATGG | 84900 |
rs57175151 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | RNFT2 | GRCh38.p7 | 12:116825941 | GTATAAAAGAGATTC[A/G]TAAACAGGCAAAGCT | 84900 |
rs57196677 | in-del | -/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116754924 | GTGAAGATTTTCTCC[-/C]ACTCTGTGGGTTGTC | 84900 |
rs57277786 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RNFT2 | GRCh38.p7 | 12:116776343 | GGAAAGGATAAGTCA[C/G]ATCTTCATTTGATCA | 84900 |
rs57370760 | snp | C/T | 0.126564 | 0.217402 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797955 | AACTAACATGGCATA[C/T]TGTTGGGCATGGCTT | 84900 |
rs57382425 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116832147 | AAAAAAAAAAAAAAA[-/T]AATATATATATATAT | 84900 |
rs57392634 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNFT2 | GRCh38.p7 | 12:116805324 | TAACAGACAAGGTTC[A/G]CCAGAGAAACAGAAC | 84900 |
rs57634837 | in-del | -/AGATAGATAGAT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116806431 | GATAGATAGATAGAT[-/AGATAGATAGAT]TCATCTAGTTTAATC | 84900 |
rs57652323 | in-del | -/TT | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116776935 | TTTTTTTTTTTTTTT[-/TT]GAGAAGGAGTCTCAC | 84900 |
rs57855440 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116850804 | AGCTAATTTTTTTTT[-/T]GTATTTTTAGTAGAG | 84900 |
rs57921806 | snp | C/G | 0.0887219 | 0.191022 | intron-variant | RNFT2 | GRCh38.p7 | 12:116756539 | GTTTTAATCATAAAG[C/G]GATGCTGGATTTTGT | 84900 |
rs57930179 | in-del | -/AATA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116806382 | AAAAAAAAAAAAAAA[-/AATA]TATATATATATATAT | 84900 |
rs58206736 | snp | A/G | 0.046775 | 0.145601 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787054 | TCCTTAATCACATCT[A/G]CAAAGACATGATTAT | 84900 |
rs58367668 | snp | A/G | 0.239326 | 0.249772 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787035 | TAACCTCCCCATGCC[A/G]ATATCCTTAATCACA | 84900 |
rs58464552 | in-del | -/CG | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116771498 | AAAAAAAAAAAAATA[-/CG]TATATGAGCAATTTT | 84900 |
rs58464832 | in-del | -/ATTTT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116850614 | AGTATTTTTTCTTTT[-/ATTTT]CTTTTCTTTTTTTTT | 84900 |
rs58472915 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RNFT2 | GRCh38.p7 | 12:116764764 | GGGCATGGTGGTGGG[C/T]GCCTGTAATCCCAGC | 84900 |
rs58593739 | snp | A/T | 0.084728 | 0.187577 | utr-variant-3-prime | RNFT2 | GRCh38.p7 | 12:116853348 | AGTCCTTAGAAATGG[A/T]CCTCTTCATGTAAAA | 84900 |
rs58595545 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116832145 | AAAAAAAAAAAAAAA[-/T]AAAATATATATATAT | 84900 |
rs58603950 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | RNFT2 | GRCh38.p7 | 12:116774871 | TTTCTGGGTATGATG[A/T]TATTCCCAGTCTCAG | 84900 |
rs58635030 | in-del | -/CA | 0.084728 | 0.187577 | downstream-variant-500B | RNFT2 | GRCh38.p7 | 12:116854045 | GAAGGCCCCAGATAC[-/CA]GCAAAGCACACGAAA | 84900 |
rs58724135 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | RNFT2 | GRCh38.p7 | 12:116745062 | TATTATCATTATTAT[C/T]ATCCAGAGCCCAGTG | 84900 |
rs58813329 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116850886 | GATCCACCTGCCTCA[A/G]CCTCCCAGAGTGCTG | 84900 |
rs58861983 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNFT2 | GRCh38.p7 | 12:116839912 | AGATTGTTAATTGAA[A/G]CTGGTTGGGCAGACA | 84900 |
rs58951469 | snp | C/T | 0.084728 | 0.187577 | utr-variant-3-prime | RNFT2 | GRCh38.p7 | 12:116852764 | TTCTGATTCCAAACT[C/T]TTTATTACTTTGGGA | 84900 |
rs58963573 | snp | C/G | 0.143284 | 0.226079 | intron-variant | RNFT2 | GRCh38.p7 | 12:116821175 | AACTCTGCCATTTCT[C/G]TCTTCCTTTCTTCTG | 84900 |
rs58975799 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116761581 | TGCGTGCCCGGCACA[A/G]TACTGAGCCCATTGC | 84900 |
rs58984530 | snp | C/T | 0.0613536 | 0.16405 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851645 | CTCAGGAGGCTAAGG[C/T]AGGGAGAACTGCTTG | 84900 |
rs59112507 | in-del | -/T/TAT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116832146 | AAAAAAAAAAAAAAA[-/T/TAT]AAATATATATATATA | 84900 |
rs59185647 | in-del | -/GA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116806396 | ATATATATATATATA[-/GA]TATAGATAGATAGAT | 84900 |
rs59203442 | in-del | -/CA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116750772 | AATATGTGTAAAACA[-/CA]TTATTTTTACTATAT | 84900 |
rs59532955 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116806762 | AAAAAAAAAAAAAAA[-/A]GCTGTTGAATTTGAT | 84900 |
rs59801471 | in-del | -/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116755383 | TTTTTTTTTTTTTTT[-/T]AACACCTATTATGCC | 84900 |
rs59935649 | snp | A/G | 0.18325 | 0.240924 | intron-variant | RNFT2 | GRCh38.p7 | 12:116795302 | AATCCCAGCTACTCC[A/G]GAGGCTGAGTCAGAA | 84900 |
rs59940898 | in-del | -/A | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116775279 | AAAAAAAAAAAAAAA[-/A]GAGAGAGAGAAGAGC | 84900 |
rs60271353 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNFT2 | GRCh38.p7 | 12:116803253 | TCCTCTGGGTGCAAC[C/T]GACACCACCTGCCAC | 84900 |
rs60336521 | in-del | -/T | 0.264906 | 0.249555 | intron-variant | RNFT2 | GRCh38.p7 | 12:116786544 | AAGGAAGGCATTTGA[-/T]GGTTACTCATCACCT | 84900 |
rs60447155 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | RNFT2 | GRCh38.p7 | 12:116846498 | TCTCGCCATGTTGCC[C/G]AGGCTGGTCTCAAAC | 84900 |
rs60469052 | in-del | -/GA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116806394 | AAATATATATATATA[-/GA]TATATAGATAGATAG | 84900 |
rs60500557 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | RNFT2 | GRCh38.p7 | 12:116773214 | TGATCTGCCCGCCTT[A/G]GCCTCCCAAAGTGCT | 84900 |
rs60679444 | snp | C/T | 0.32885 | 0.23724 | intron-variant | RNFT2 | GRCh38.p7 | 12:116798076 | GCTACCTCACTAGGA[C/T]GGGCCCTGGTCCAAT | 84900 |
rs60801685 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | RNFT2 | GRCh38.p7 | 12:116823192 | CACTTATAGCCTAAA[C/G]TGACACCAGTAGTTG | 84900 |
rs60974249 | in-del | -/AA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116802945 | CCAAAAAAAAAAAAA[-/AA]TTAGCCTAGCACGGT | 84900 |
rs61120684 | snp | C/T | 0.206336 | 0.246157 | intron-variant | RNFT2 | GRCh38.p7 | 12:116763970 | ATGCCCATCAACCAA[C/T]GAGTGGGTAAAGAAA | 84900 |
rs61232241 | in-del | -/T/TAAAA/TAAAATAAAA | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800862 | TAAAATAAAATAAAA[-/T/TAAAA/TAAAATAAAA]ACCATTTAACAGATA | 84900 |
rs61274161 | in-del | -/GA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116806398 | ATATATATATATATA[-/GA]TAGATAGATAGATAG | 84900 |
rs61306390 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | RNFT2 | GRCh38.p7 | 12:116783121 | CTGCTGCTACCACCC[A/G]GTAGGAGATACACAC | 84900 |
rs61394295 | in-del | -/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116763795 | AAAAAAAAAGGGGGC[-/G]GGGGGGGAAAGAACT | 84900 |
rs61442995 | snp | C/T | 0.181022 | 0.240296 | intron-variant | RNFT2 | GRCh38.p7 | 12:116817710 | TGTAGCAAGGGGCTT[C/T]TGAACTTCCTAGAAA | 84900 |
rs61443846 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | RNFT2 | GRCh38.p7 | 12:116742900 | TCAGCCTGGGCAAAA[C/T]AGGGAGACCCTATCT | 84900 |
rs61737205 | snp | A/C/T | 0.0183134 | 0.0939231 | missense, synonymous-codon, nc-transcript-variant | RNFT2 | GRCh38.p7 | 12:116833881 | ATACATCATGGGTGA[A/C/T]GACTCCTCCAACAGC | 84900 |
rs61936690 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116758957 | CCCCAAATATGTTTT[A/C]CAAGCTTTCAGAATT | 84900 |
rs61936723 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116778074 | TATTGGCCTGCCTTC[A/C]TAATTTCCTTCCTCC | 84900 |
rs61936724 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116778973 | ACTCCAGGCCAATAT[G/T]GCCATTTAACTCTCA | 84900 |
rs61936725 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116797556 | AAAAAAAAAAAAAGT[A/T]ATTAAGTTAGAGTGA | 84900 |
rs61936726 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | RNFT2 | GRCh38.p7 | 12:116825926 | CAGATGAAAAAATGT[A/G]TATAAAAGAGATTCG | 84900 |
rs62637841 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNFT2 | GRCh38.p7 | 12:116789369 | GTGGATGGGTAAATG[A/G]GAGGAGAGTGAGTAG | 84900 |
rs62637916 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789458 | TGGATGGATGGATGG[A/G]TGGATGGGTGGATGG | 84900 |
rs62637917 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789460 | GATGGATGGATGGAT[A/G]GATGGGTGGATGGGT | 84900 |
rs62647045 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789396 | GTAGATGGATAGATG[A/G]GTGGATGAGTAAATG | 84900 |
rs62647046 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789404 | ATAGATGAGTGGATG[A/G]GTAAATGGTAGGAGA | 84900 |
rs62647047 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789413 | TGGATGAGTAAATGG[G/T]AGGAGAGTGGTGGGT | 84900 |
rs62647048 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789439 | TGGGTGGATGGATGG[G/T]AGATGGATGGATGGA | 84900 |
rs62647049 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789449 | GATGGTAGATGGATG[A/G]ATGGATGGATGGATG | 84900 |
rs62647050 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789465 | ATGGATGGATGGATG[A/G]GTGGATGGGTAAATG | 84900 |
rs62647051 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789473 | ATGGATGGGTGGATG[A/G]GTAAATGGGAGGAGA | 84900 |
rs62647052 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789482 | TGGATGGGTAAATGG[G/T]AGGAGAGTGGATGGG | 84900 |
rs62647053 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789485 | ATGGGTAAATGGGAG[G/T]AGAGTGGATGGGTGG | 84900 |
rs62647054 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116789491 | AAATGGGAGGAGAGT[A/G]GATGGGTGGATGGGT | 84900 |
rs66464081 | in-del | -/A | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116800645 | TCTCAAAAAAAAAAA[-/A]TGGTTTAAAAATGCA | 84900 |
rs66493219 | in-del | -/CCT/CTC | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116835301 | TCCCAACCACACTYC[-/CCT/CTC]TMCTGAATGTTTTCT | 84900 |
rs66541257 | in-del | -/AAAAATATA/TATAT | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806377 | GTCTCAAAAAAAAAA[-/AAAAATATA/TATAT]TATATATATATATAG | 84900 |
rs66581476 | snp | A/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116832147 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 84900 |
rs66920809 | in-del | -/AAA | 0.340108 | 0.233197 | intron-variant | RNFT2 | GRCh38.p7 | 12:116845244 | GCAAGACCCGGTTTC[-/AAA]AAAAAAAAAAAAATA | 84900 |
rs67556946 | in-del | -/A | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116763177 | AGTCTGTGCTTTCAG[-/A]AAAAAAAAAAAAATC | 84900 |
rs67604448 | snp | A/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750906 | TATATATATATATAT[A/T]TTTTTTTTTTGAGAC | 84900 |
rs71095588 | in-del | -/AA | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116743105 | AAAAAAAAAAAAAAA[-/AA]GGTTAAATGAAGCAG | 84900 |
rs71095592 | in-del | -/A | 0.367297 | 0.220775 | intron-variant | RNFT2 | GRCh38.p7 | 12:116762403 | AACAAAAAAAAAAAA[-/A]CAAAGAAAGAAATAG | 84900 |
rs71095596 | in-del | -/GGTGGATGGA/TGGA/TGGATGGA | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116789960 | TGGTGGATGGGTGGG[-/GGTGGATGGA/TGGA/TGGATGGA]TGGATGGATGGATGG | 84900 |
rs71095598 | in-del | -/T/TTT | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116805137 | TTTTTTTTTTTTTTT[-/T/TTT]AGAAGTTTTAGATTT | 84900 |
rs71095599 | in-del | -/ATAGATAGATAG | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806417 | TAGATAGATAGATAG[-/ATAGATAGATAG]ATAGATAGATAGATT | 84900 |
rs71095600 | in-del | -/TCATTCAT | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809217 | CATTCATTCATTCAT[-/TCATTCAT]CACCTGGGAGCAGAG | 84900 |
rs71095601 | in-del | -/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116832922 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 84900 |
rs71099003 | in-del | -/AGAG | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116841959 | TATAAATATATATAT[-/AGAG]AGAGAGAGAGAGAGA | 84900 |
rs71099004 | in-del | -/A | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116843515 | AAAAAAAAAAAAAAA[-/A]CCCCAAGAAACAAAC | 84900 |
rs71099005 | in-del | -/CC/CCTTTTTTTTTTT | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116849847 | CTTCCTTCCTTCCTT[-/CC/CCTTTTTTTTTTT]TTTTTTTTTTTTTTA | 84900 |
rs71099006 | in-del | -/TTTT | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116850169 | TTTTTTTTTTTTTTT[-/TTTT]GAGACAGGGTCTGGG | 84900 |
rs71099008 | in-del | -/CTTTTA/CTTTTTA/CTTTTTT | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116850626 | TTTATTTTCTTTTTT[-/CTTTTA/CTTTTTA/CTTTTTT]TTTTTTTTTTTGTTG | 84900 |
rs71099009 | in-del | -/CCCCTT | 0 | 0 | utr-variant-3-prime, intron-variant | RNFT2 | GRCh38.p7 | 12:116852385 | CAGGACTTTCCCCTT[-/CCCCTT]GGCTTGGCATCCCTG | 84900 |
rs71305654 | multinucleotide-polymorphism | AAA/TAT | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116771483 | AAAAAAAAAAAAAAA[AAA/TAT]ATATATATATATATA | 84900 |
rs71442798 | snp | A/G | 0.266273 | 0.24947 | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116737551 | AAGGTGAGGAAGGTA[A/G]GGAAGGAAGGGAGGC | 84900 |
rs71442799 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116743270 | AACACTCATGAGCTA[A/G]AATTTTTTTTTTTTG | 84900 |
rs71442800 | snp | A/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116841818 | ATAAATATATATATA[A/T]AAATATATATATAAA | 84900 |
rs71442997 | in-del | -/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116768775 | TGCCCTTGTCGCCCA[-/G]GCTGGAGTGCAGTGG | 84900 |
rs71442998 | in-del | -/TG/TGTGTG/TGTGTGTG/TGTGTGTGTGTG | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116785249 | GTGATTACCTACTTC[lengthTooLong]TGTGTGTGTGTGTGT | 84900 |
rs71442999 | in-del | -/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116788220 | GCGTGAGCCACTGCG[-/C]CCAGCCTCTTTTGCT | 84900 |
rs71469777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNFT2 | GRCh38.p7 | 12:116762814 | ATGGGGTTTCACCAC[A/G]TTGGCCAGGCTGGTC | 84900 |
rs71469778 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116772923 | AACCTCCGTCTCCTG[A/G]GTTCAAGCAATTCTC | 84900 |
rs71469779 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116782140 | TATACTAAAACTGGA[A/C]CAATACAGAGATTAG | 84900 |
rs71469780 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116788428 | CTCAAAGAGCCTTCC[C/T]TCTTTCTCATGTCTT | 84900 |
rs71469781 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116790977 | AAAAAATAAAATAAA[A/C]CAATAAAAATAAACC | 84900 |
rs71469782 | snp | G/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806387 | AAAAATATATATATA[G/T]ATAGATAGATAGATA | 84900 |
rs71854403 | in-del | -/GGAT | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116788956 | TAAATGGGAGGAGAG[-/GGAT]GGATGGATGGATGGA | 84900 |
rs72126193 | in-del | -/AC | 0.0872718 | 0.189788 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750769 | CTTAATATGTGTAAA[-/AC]ACATTATTTTTACTA | 84900 |
rs73220422 | snp | C/T | 0.0399222 | 0.135526 | upstream-variant-2KB, missense, synonymous-codon | RNFT2, C12orf49 | GRCh38.p7 | 12:116737803 | ACCTGCTTGAAGGTG[C/T]TGCTGAGGAAGTAGA | 84900 |
rs73220423 | snp | C/T | 0.0988009 | 0.199095 | upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738149 | TTGGTCCCTAAGGAA[C/T]GGCGGCCTCCTATTG | 84900 |
rs73220424 | snp | C/T | 0.0799831 | 0.183287 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116739021 | AAAAGAGAAAGGAGG[C/T]TTCACTGGCGGGTCA | 84900 |
rs73220431 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | RNFT2 | GRCh38.p7 | 12:116746530 | CCTCAATCCAGGGAG[A/G]GAGATTTTAGCTGAA | 84900 |
rs73220455 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787718 | ATGTTGTCTCTAAAA[A/G]AAAAAAAAAAAAAAA | 84900 |
rs73220457 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116788830 | GATGGATGGATAGAT[A/G]GATGGATGGATGGAT | 84900 |
rs73220465 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | RNFT2 | GRCh38.p7 | 12:116810828 | CTTCCATTGGGGTAG[C/G]GGGGACTACCCTGCT | 84900 |
rs73220476 | snp | C/T | 0.167781 | 0.236093 | intron-variant | RNFT2 | GRCh38.p7 | 12:116849307 | CTGCTGATTGCTGTC[C/T]CCGCAGCACGTGTTC | 84900 |
rs73403114 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | RNFT2 | GRCh38.p7 | 12:116778328 | TGAGTGGTTTGGTGT[C/T]GTTCTCATGACAGTG | 84900 |
rs73405110 | snp | A/G | 0.239326 | 0.249772 | intron-variant | RNFT2 | GRCh38.p7 | 12:116790814 | TACAAAGATTTAGCC[A/G]AGCATGGTGGCACTC | 84900 |
rs73405124 | snp | A/G | 0.276267 | 0.248616 | intron-variant | RNFT2 | GRCh38.p7 | 12:116793636 | TCCAAAGCACCCAGC[A/G]CCTTCCTTCTCAGGC | 84900 |
rs73405130 | snp | C/G | 0.130008 | 0.219321 | intron-variant | RNFT2 | GRCh38.p7 | 12:116798031 | CTTGGCCCCATATCT[C/G]AGCCCCATCTCTGGA | 84900 |
rs73405150 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806003 | CCTAGCTAGCTGAAT[C/T]GAGACATTAAACTAA | 84900 |
rs73405184 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | RNFT2 | GRCh38.p7 | 12:116824319 | CTCATTTGTCCATTA[C/T]TCATTCAGCAAATAT | 84900 |
rs73405186 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | RNFT2 | GRCh38.p7 | 12:116824564 | CAAGATGGTAGCAAG[A/C]GCACCAGCCATCACA | 84900 |
rs73405189 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RNFT2 | GRCh38.p7 | 12:116826059 | CTTGATTATGCCTCT[C/T]CTCCCTTCCTCCCCA | 84900 |
rs73405197 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | RNFT2 | GRCh38.p7 | 12:116840616 | CTGACTCCTCCATCC[A/G]GTCATCTATGCTTTG | 84900 |
rs73407205 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | RNFT2 | GRCh38.p7 | 12:116844724 | TGTGAGAGCCTCAGT[G/T]AATGTGTTGAATGAA | 84900 |
rs73407209 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | RNFT2 | GRCh38.p7 | 12:116845910 | CCTTCAGCCTGGAAT[A/G]TTCTATCTCTATCCC | 84900 |
rs73407273 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | RNFT2 | GRCh38.p7 | 12:116848579 | CATCCACCCCAACAA[C/T]CCCAGCCCAGCTATC | 84900 |
rs73407286 | snp | C/G | 0.0901694 | 0.192235 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851024 | CAGCAGGCAAAGCAT[C/G]CAGCATCCTGCTTGG | 84900 |
rs73407288 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | RNFT2 | GRCh38.p7 | 12:116852198 | GCACAACAGGCTGGC[A/G]CCAATGGCATTACAG | 84900 |
rs74238483 | snp | A/G | 0.145305 | 0.227022 | intron-variant | RNFT2 | GRCh38.p7 | 12:116807368 | AGATGATAATACGAC[A/G]GAGTAATAATAAATA | 84900 |
rs74320096 | snp | A/G | 0.135825 | 0.222405 | intron-variant | RNFT2 | GRCh38.p7 | 12:116828011 | GGACCAGAGTCAGCC[A/G]GATGCCAGCAGGCAG | 84900 |
rs74328007 | snp | A/G | 0.145305 | 0.227022 | intron-variant | RNFT2 | GRCh38.p7 | 12:116799326 | TTTTAAAGGGCTTAG[A/G]TGATTAAATTAGACT | 84900 |
rs74331018 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | RNFT2 | GRCh38.p7 | 12:116783947 | ATGTACAAACTCATT[A/G]AGTCATGACCACATC | 84900 |
rs74436787 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | RNFT2 | GRCh38.p7 | 12:116847316 | GCATTTTTTTTGCCA[C/T]CCCTGGGACCAATCA | 84900 |
rs74442896 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RNFT2 | GRCh38.p7 | 12:116746818 | AAGGAACACAGAATG[A/G]GAAGCCCTGGGAGGG | 84900 |
rs74449334 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNFT2 | GRCh38.p7 | 12:116821540 | TTCCTTGTCCTGGCC[A/G]CCCACTTGGGAGCAG | 84900 |
rs74450036 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809231 | TTCATTCATCACCTG[A/G]GAGCAGAGTCGTGGC | 84900 |
rs74483871 | snp | G/T | 0.105569 | 0.204058 | intron-variant | RNFT2 | GRCh38.p7 | 12:116794130 | CGTATCCAAGCATAG[G/T]GTCATGCACCTGCAG | 84900 |
rs74528756 | snp | A/T | 0.157972 | 0.232445 | intron-variant | RNFT2 | GRCh38.p7 | 12:116814683 | GCCGTATGATATTTT[A/T]TTTTTTTTCCGACAG | 84900 |
rs74559863 | snp | A/G | 0.102014 | 0.201495 | intron-variant | RNFT2 | GRCh38.p7 | 12:116804260 | AAGTGCAGTCCCTGG[A/G]CCAGTAGCATGAGCA | 84900 |
rs74567077 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | RNFT2 | GRCh38.p7 | 12:116767130 | ACATCTTCTAGTTAC[C/G/T]GAAAACTAAACAGAA | 84900 |
rs74571812 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | RNFT2 | GRCh38.p7 | 12:116808636 | GTTCCGCCACTAGAG[A/G]AGATGAAAAACAACC | 84900 |
rs74619534 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RNFT2 | GRCh38.p7 | 12:116791786 | TTTTGTGGTAAATAC[A/G]TAGGCAGAGAATTCT | 84900 |
rs74625612 | snp | A/G | 0.114036 | 0.209795 | intron-variant | RNFT2 | GRCh38.p7 | 12:116848574 | TCTCCCATCCACCCC[A/G]ACAACCCCAGCCCAG | 84900 |
rs74625713 | snp | C/T | 0.078151 | 0.181571 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116739573 | GCCTCTGGGAAGAGA[C/T]GACATTTGCCCTGCG | 84900 |
rs74653836 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNFT2 | GRCh38.p7 | 12:116774909 | TGCCCCCATCAAAGC[A/G]GGCTGAGTCAAACTG | 84900 |
rs74668907 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNFT2 | GRCh38.p7 | 12:116742565 | AAGCGCAAGCCACCA[C/T]GCCTGGCCTCAAGGT | 84900 |
rs74680129 | snp | A/G | 0.143959 | 0.226396 | intron-variant | RNFT2 | GRCh38.p7 | 12:116802211 | CACACTCACATAGTA[A/G]AGGCTCTGAGAAGTC | 84900 |
rs74693564 | snp | C/T | 0.157972 | 0.232445 | intron-variant | RNFT2 | GRCh38.p7 | 12:116819214 | TTCGGGGTGAAATGT[C/T]CAAATAAGAGAGCGG | 84900 |
rs74695944 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | RNFT2 | GRCh38.p7 | 12:116770547 | TTTTAAGTATGTATG[C/T]CTTTTTTCTTTGTTT | 84900 |
rs74747450 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | RNFT2 | GRCh38.p7 | 12:116772834 | ATGCAAGGAGCATTT[C/G]TTTATTTATTTTGAG | 84900 |
rs74852953 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNFT2 | GRCh38.p7 | 12:116795029 | CTCTGTCCCAGAAAC[A/G]TACATAGAAATATAT | 84900 |
rs74866454 | snp | A/T | 0.444444 | 0.157135 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750820 | ATATAATATATATAT[A/T]ATATATATAATATAT | 84900 |
rs74881721 | snp | A/C | 0.145642 | 0.227177 | intron-variant | RNFT2 | GRCh38.p7 | 12:116816366 | ATTTTTACTCACAGC[A/C]CAGCAACTCTTTTGG | 84900 |
rs74891123 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116792150 | CACCTCCCAGGTTCA[A/G]GCAATTCTCCTGACT | 84900 |
rs74948197 | snp | A/G/T | 0.0225133 | 0.103744 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851435 | GGGCCCAGCAGACAC[A/G/T]GTCTTCTAAAAGCAC | 84900 |
rs74960353 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RNFT2 | GRCh38.p7 | 12:116770937 | CTCACTAAAACAGAG[A/G]TTGGCAGACTACAGC | 84900 |
rs75005395 | in-del | -/AAGGTAAG | | | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116737545 | AGGAGGAAGGTGAGG[-/AAGGTAAG]GAAGGAAGGGAGGCA | 84900 |
rs75034338 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | RNFT2 | GRCh38.p7 | 12:116843160 | GACTGGTTTAACCCC[A/C]ATTCTGTGCTTCGGG | 84900 |
rs75083621 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RNFT2 | GRCh38.p7 | 12:116849702 | CTTGATGCCCTTCTA[A/G]ATGCATCTTCCTTCT | 84900 |
rs75155644 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851389 | ACTCTTAACCTCCGC[A/T]CTGCTCTGCCCCTCA | 84900 |
rs75194960 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809178 | CTGGGCACAGTTAGA[A/G]CTGAGTTTGTTCATT | 84900 |
rs75203558 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNFT2 | GRCh38.p7 | 12:116794806 | CTGCTTATTTCCCAC[C/T]GCATGGAGTTCGGCT | 84900 |
rs75222084 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116785831 | AGATGGGTGGATCGC[G/T]CGAGTTCATGAGTTC | 84900 |
rs75283087 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | RNFT2 | GRCh38.p7 | 12:116786563 | TACTCATCACCTGGC[A/G]CCTTCTGGGTTCTGT | 84900 |
rs75319040 | snp | A/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116795928 | TTCTTTTTCTTTTTG[A/T]GACAGAGTCTCACTC | 84900 |
rs75319091 | snp | G/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116762596 | TTTTTTTTTTTTTTT[G/T]TGAGATGAAGTCTCA | 84900 |
rs75518948 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116744225 | AGTGAGACTCCTCCT[A/C]AAAAAAAAAAAAAAA | 84900 |
rs75531183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNFT2 | GRCh38.p7 | 12:116745619 | GCCAGGGAAACCACC[A/G]TGTCCCACTGCTGTG | 84900 |
rs75541039 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116827617 | AAGTTTTATTGGAAC[A/C]CAGCCACACCCATTC | 84900 |
rs75566361 | snp | A/G | 0.10237 | 0.201756 | intron-variant | RNFT2 | GRCh38.p7 | 12:116798742 | CAGCTAATTTTTCAT[A/G]TATTTCTTTTTTTGG | 84900 |
rs75579390 | snp | G/T | 0.0861826 | 0.188849 | intron-variant | RNFT2 | GRCh38.p7 | 12:116753124 | TATGGCGTTGTAAGT[G/T]TTTTCTTTTTCTTTT | 84900 |
rs75592131 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | RNFT2 | GRCh38.p7 | 12:116788255 | TATACTCATTAACTC[A/G]CCCCATTCTGCAGCA | 84900 |
rs75606005 | snp | A/G | 0.10237 | 0.201756 | intron-variant | RNFT2 | GRCh38.p7 | 12:116795785 | AGACAGCACTGCAGA[A/G]TAGAAAGAACACAGC | 84900 |
rs75614800 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116769709 | AGTAAGCTAAGGTCA[A/G]TTTATGATTGAAGAA | 84900 |
rs75635710 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | RNFT2 | GRCh38.p7 | 12:116815648 | GTCACCTGGGATAAT[C/T]TCCCCATCTCAGGAG | 84900 |
rs75713326 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116827219 | GGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 84900 |
rs75767702 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNFT2 | GRCh38.p7 | 12:116781627 | TCTGCCTTCATTGTC[A/G]CATCTCCTGATTCTC | 84900 |
rs75810123 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | RNFT2 | GRCh38.p7 | 12:116829913 | TAAACATATCACATG[C/T]TCAGTATAAAAAATC | 84900 |
rs75903102 | snp | G/T | 0.157972 | 0.232445 | intron-variant | RNFT2 | GRCh38.p7 | 12:116816675 | GCTTAGGCAAAATGG[G/T]GAACTTCTCTGAAAC | 84900 |
rs76013059 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | RNFT2 | GRCh38.p7 | 12:116782716 | CTACAACATCCCTGG[A/G]AAGCGGGCACTGTTA | 84900 |
rs76058084 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116753461 | CAGCGGTGAGTTTTT[C/T]CAATGTATGCTTTTA | 84900 |
rs76069216 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | RNFT2 | GRCh38.p7 | 12:116781554 | CTTCCTCCGTCTTCC[A/G]AGTCAGTGATGGCAG | 84900 |
rs76091754 | snp | C/G | 0.444444 | 0.157135 | intron-variant | RNFT2 | GRCh38.p7 | 12:116757276 | TTTTCAAAGAACCAG[C/G]TTTTTGTTTCATTTA | 84900 |
rs76134362 | snp | G/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116768115 | TTTTTTTTTTTTTTT[G/T]GGAGATGGAGTTTCA | 84900 |
rs76156784 | snp | C/G | 0.095934 | 0.196885 | intron-variant | RNFT2 | GRCh38.p7 | 12:116838498 | AATGTATCCACTTAG[C/G]CTGTTAGTATGCAGT | 84900 |
rs76181922 | snp | A/C | 0.0490535 | 0.14873 | intron-variant | RNFT2 | GRCh38.p7 | 12:116801429 | TGTGGAATCGTCGAA[A/C]GAGCACATACTATAC | 84900 |
rs76196473 | snp | A/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116802947 | CAAAAAAAAAAAAAT[A/T]AGCCTAGCACGGTAG | 84900 |
rs76199241 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116811186 | GAGGTGGGAGGATGG[A/C]TTGAGCCCAAGAGTT | 84900 |
rs76206335 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNFT2 | GRCh38.p7 | 12:116752359 | TGAAAGCTGGCATCT[C/T]CCCCACTACCCTGAA | 84900 |
rs76219619 | snp | C/T | 0.10237 | 0.201756 | intron-variant | RNFT2 | GRCh38.p7 | 12:116799099 | GTCTACTTCCAGGCT[C/T]ATTAAGGTTGTTGGC | 84900 |
rs76235447 | snp | A/G | 0.000547695 | 0.0165393 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851798 | GAAGGAAGGAAGGAA[A/G]GAAAGAAAGGTCAGC | 84900 |
rs76262816 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNFT2 | GRCh38.p7 | 12:116818164 | TCTACAAAAAAAGTC[A/T]TTAAAAAATTATCTG | 84900 |
rs76304695 | snp | A/G | 0.046775 | 0.145601 | intron-variant | RNFT2 | GRCh38.p7 | 12:116811874 | AAGAAGGGAGGAAAT[A/G]TTATCCTTACTAGTT | 84900 |
rs76353798 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116797738 | AGCACCGTGACTACT[A/C]CTGCAGAGCAGGGCT | 84900 |
rs76366432 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797266 | ATATTTGGAAATAGG[G/T]TCTATAAAGATGGCC | 84900 |
rs76388367 | snp | A/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116745173 | CCTCCATTGCACCAG[A/T]TTTTTTTTTTTTTTT | 84900 |
rs76411133 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | RNFT2 | GRCh38.p7 | 12:116782252 | GTGGTGGCTCAATGG[C/T]TCAAACCTGTAATCC | 84900 |
rs76435913 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | RNFT2 | GRCh38.p7 | 12:116778421 | GTTCTTATAAAGCCA[A/G]GACGCCCCTGGGGTT | 84900 |
rs76442689 | snp | A/G | 0.102726 | 0.202016 | intron-variant | RNFT2 | GRCh38.p7 | 12:116816669 | CTATAAGCTTAGGCA[A/G]AATGGTGAACTTCTC | 84900 |
rs76489167 | snp | A/T | 0.185472 | 0.241529 | intron-variant | RNFT2 | GRCh38.p7 | 12:116807657 | AGCAGCAGCCACTGC[A/T]CCCTGTGCACCTGCA | 84900 |
rs76508418 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116779167 | TGGCCCTAAGGGAAC[C/T]TTCTGACTCTCTCAA | 84900 |
rs76520510 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | RNFT2 | GRCh38.p7 | 12:116784651 | AGCACCTCCCTCCAC[C/T]CCACTGTTCACATCA | 84900 |
rs76560894 | snp | G/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116786137 | CTTTTTTTTTTTTTT[G/T]TGAGACAGAGTTTCA | 84900 |
rs76575304 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNFT2 | GRCh38.p7 | 12:116747764 | TGGTCTGTGGAGGTG[C/T]CTGCAGGGTGAGAGA | 84900 |
rs76612147 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNFT2 | GRCh38.p7 | 12:116779543 | GGCTCTTTGTCATCA[C/T]CACTTTGTCACACCT | 84900 |
rs76613018 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809656 | CCTCTTTTTCACAGA[C/T]CGGTAGACCCAGAAA | 84900 |
rs76629522 | snp | G/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116832920 | TTTTTTTTTTTTTTT[G/T]TTGAGATGGAGTCTT | 84900 |
rs76644732 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | RNFT2 | GRCh38.p7 | 12:116766275 | GAACAGAAAAAAAAA[A/T]TAAAATAAAAAATTT | 84900 |
rs76690826 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNFT2 | GRCh38.p7 | 12:116853595 | TTAATGTCTCCCAAA[C/G]TACCCTTCAGCCAAT | 84900 |
rs76700650 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116791511 | GATGGGGTTTCGCCA[C/T]GTAGGCCAGCCTGGT | 84900 |
rs76742224 | snp | C/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116757157 | ATATTACAACTGACA[C/T]CACAGAAACACAAAG | 84900 |
rs76771582 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime | RNFT2, C12orf49 | GRCh38.p7 | 12:116738062 | CCTTGGGCGCAGCCC[C/T]ACGTGACCCCGCCCT | 84900 |
rs76788182 | snp | A/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116841459 | CCCTGTCTCAAAAAA[A/T]TAAAATGACTGGGCA | 84900 |
rs76788790 | snp | G/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116805487 | TTGTTGTTGTTGTTG[G/T]TTTTTGACACAGCGT | 84900 |
rs76818059 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | RNFT2 | GRCh38.p7 | 12:116840317 | TAATAGAGACAAAGA[A/C]TCAGGCTCAGAAAAA | 84900 |
rs76821444 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116752198 | CTACTGAAAAAAAAA[A/G]AGAGAGAGAGAAAGC | 84900 |
rs76865895 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | RNFT2 | GRCh38.p7 | 12:116742548 | CTGCTCGCTGGGATT[A/G]TAAGCGCAAGCCACC | 84900 |
rs76884830 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116850627 | TTTCTTTTCTTTTTT[C/T]TTTTTTTTTTGTTGT | 84900 |
rs76889522 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNFT2 | GRCh38.p7 | 12:116817843 | TTCAGTGTCATATTA[C/T]GACAGGCACTGCGAA | 84900 |
rs76928482 | snp | A/C | 0.0490535 | 0.14873 | intron-variant | RNFT2 | GRCh38.p7 | 12:116805418 | AAGTCTGAAATCTGC[A/C]GAACAGGCCAGCAGG | 84900 |
rs76958378 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738986 | ATGCTGCTGCTGACC[C/G]GTTTGTTACCTAATT | 84900 |
rs76963921 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | RNFT2 | GRCh38.p7 | 12:116842322 | TACTTAAGGGAAGGG[G/T]ATGCATGAGGCTATG | 84900 |
rs76964910 | snp | C/G | 0.0471551 | 0.14613 | intron-variant | RNFT2 | GRCh38.p7 | 12:116813037 | CACGATTCATTGCAG[C/G]CATGACCTCCCAGGC | 84900 |
rs77058857 | snp | C/T | 0.102014 | 0.201495 | intron-variant | RNFT2 | GRCh38.p7 | 12:116804478 | CAGCAATATGTAATA[C/T]TCTTTGGTTTATTCA | 84900 |
rs77060641 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RNFT2 | GRCh38.p7 | 12:116844911 | CATCTGAGCAAGAAC[C/T]GTACTCAGCATAAAA | 84900 |
rs77080591 | snp | C/G | 0.185472 | 0.241529 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806741 | GATACAAGAGACCCT[C/G]TCTCAAAAAAAAAAA | 84900 |
rs77170328 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812076 | CAAATGAGGTCATGA[A/G]GTTTAGAACAGAGTT | 84900 |
rs77179606 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116804748 | GGCCACAGTGGGCAG[A/C]TGACCCCTAGGAGTT | 84900 |
rs77197427 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | RNFT2 | GRCh38.p7 | 12:116742030 | GAGAGGCTAATGACA[C/T]TGAAAGATGAGATTT | 84900 |
rs77236042 | snp | A/T | 0.102014 | 0.201495 | intron-variant | RNFT2 | GRCh38.p7 | 12:116798585 | ATTTTTATTTTTTAT[A/T]TTTTTGAGACAGAGT | 84900 |
rs77237550 | snp | C/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116757160 | TGTATTTCTGTGGTG[C/G]CAGTTGTAATATCTC | 84900 |
rs77279671 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNFT2 | GRCh38.p7 | 12:116770263 | TTCTGTTTAGATATA[C/T]AGATACCATTGTGTT | 84900 |
rs77358363 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNFT2 | GRCh38.p7 | 12:116813584 | ATCATGTGATGTTGT[C/G]TTTGCTGGTTTGTCT | 84900 |
rs77385527 | snp | G/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116844218 | CTTGTGTATTATGGG[G/T]TTTTTTTTTGTTTTG | 84900 |
rs77497992 | snp | C/T | 0.102014 | 0.201495 | intron-variant | RNFT2 | GRCh38.p7 | 12:116802404 | TGGAAACCAGCCATG[C/T]CCATTTATGTATGCA | 84900 |
rs77512392 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNFT2 | GRCh38.p7 | 12:116829175 | GGGAATGAAAGTTCA[A/G]ATCATGGATATTCTG | 84900 |
rs77528585 | snp | C/T | 0.116838 | 0.211584 | intron-variant | RNFT2 | GRCh38.p7 | 12:116771740 | TGACTCAGAGTTCTA[C/T]GCAATGTGGTGGGGC | 84900 |
rs77539387 | snp | A/G | 0.375 | 0.216506 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750867 | ATATATATTATATAT[A/G]TATAATATATATATT | 84900 |
rs77571915 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116775263 | GAAACTCCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 84900 |
rs77631989 | snp | G/T | 0.0752113 | 0.178743 | intron-variant | RNFT2 | GRCh38.p7 | 12:116744737 | TCAGGCTGAAATCTC[G/T]GCTGGATGCAGGGGA | 84900 |
rs77637079 | snp | C/T | 0.127254 | 0.217792 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851137 | GCACAGAGCTTGGTG[C/T]GGTAACTTTCCCAGG | 84900 |
rs77655122 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116795410 | GAGACTCCATCTCCA[A/G]AAAAAAAAAAAAAGA | 84900 |
rs77670497 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116811193 | GAGGATGGCTTGAGC[C/T]CAAGAGTTCAAGTCC | 84900 |
rs77743947 | snp | G/T | 0.151668 | 0.229849 | intron-variant | RNFT2 | GRCh38.p7 | 12:116767569 | TATAAAAATTATGTT[G/T]TTTTTTTGTTTGTTT | 84900 |
rs77773258 | snp | G/T | 0.43221 | 0.171171 | intron-variant | RNFT2 | GRCh38.p7 | 12:116806393 | AAAAATATATATATA[G/T]ATATATAGATAGATA | 84900 |
rs77793538 | snp | C/T | 0.000590842 | 0.0171777 | synonymous-codon, intron-variant | RNFT2 | GRCh38.p7 | 12:116849415 | GCGCTGCTGGAAGGA[C/T]GGCGCCACGTCCGCA | 84900 |
rs77800793 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | RNFT2 | GRCh38.p7 | 12:116788767 | TGGGTGAATGGATAT[A/G]TAGGTAGGTAGATAG | 84900 |
rs77833795 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | RNFT2 | GRCh38.p7 | 12:116845787 | TCTGTGTGGACTTCT[C/T]TCCTTTCCCCAATCC | 84900 |
rs77839941 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | RNFT2 | GRCh38.p7 | 12:116807567 | ACTCTAAGACTCTTA[A/T]TCACTGCATGATTCT | 84900 |
rs77895841 | snp | A/C | 0.0517044 | 0.152246 | intron-variant | RNFT2 | GRCh38.p7 | 12:116798239 | TCAAAAAAAAAAAAG[A/C]AGCAGCAGCAGCAGC | 84900 |
rs77917060 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RNFT2 | GRCh38.p7 | 12:116773688 | CAACTACTTGGAAGA[A/G]TCTGTAGAGGGTGTA | 84900 |
rs77952430 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116780345 | TCCACTTCAGATCAT[A/C]AGGCATTGGATTCTC | 84900 |
rs77971218 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNFT2 | GRCh38.p7 | 12:116820615 | TAGCTTGTATCTTTT[C/T]TTTCTCTTTCTCCCA | 84900 |
rs77978738 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787838 | CCCTGTCTGGCATCT[A/T]ACTTACTCATCCCTC | 84900 |
rs77987860 | snp | C/T | 0.142609 | 0.225759 | intron-variant | RNFT2 | GRCh38.p7 | 12:116833002 | TAACTGCAACTCTGC[C/T]TCCCAAGTTCAAGCA | 84900 |
rs77989562 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116791514 | GGGGTTTCGCCATGT[A/C]GGCCAGCCTGGTCTG | 84900 |
rs77993062 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNFT2 | GRCh38.p7 | 12:116807520 | AGAGAAGGTAAGTGA[C/T]TTGCCTGGGGTATGT | 84900 |
rs77994869 | snp | C/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797475 | GAGGCAGGAGACTCA[C/G]TTGAACCCGGGAGGT | 84900 |
rs78026573 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116765916 | TGAATCTTCTGCTGG[A/G]TTGTAAACTCTTAAT | 84900 |
rs78118428 | snp | C/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116785830 | AAGATGGGTGGATCG[C/G]TCGAGTTCATGAGTT | 84900 |
rs78204217 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | RNFT2 | GRCh38.p7 | 12:116826282 | GTCGGAATAGAATCC[A/G]CCTTCCCAACTTGAC | 84900 |
rs78239829 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | RNFT2 | GRCh38.p7 | 12:116824965 | TGAAAAAACCATTTA[A/G]TTCTCACAATTTTGC | 84900 |
rs78256313 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | RNFT2 | GRCh38.p7 | 12:116753862 | GGATTTTTTTTATTT[A/T]TCTCTCTCTTCTGTC | 84900 |
rs78327083 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809395 | CATGTGGCCTGGGGG[C/G]TCCAGCGCTTCTTTG | 84900 |
rs78332370 | in-del | -/AA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116800644 | GTCTCAAAAAAAAAA[-/AA]TGGTTTAAAAATGCA | 84900 |
rs78389334 | snp | A/C | 0.102014 | 0.201495 | intron-variant | RNFT2 | GRCh38.p7 | 12:116802552 | GAAGTTAGTGTAAAG[A/C]TGGGGGCAGACATTG | 84900 |
rs78443129 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | RNFT2 | GRCh38.p7 | 12:116826252 | TGTCCCACCCCTCAT[C/T]TTGGCAGTGAGGAAG | 84900 |
rs78447731 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNFT2 | GRCh38.p7 | 12:116840829 | AATCATAGTGTATTA[C/T]ACCGATATTCAGTAT | 84900 |
rs78452181 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNFT2 | GRCh38.p7 | 12:116760998 | ATCCTCTGACCTCAG[C/T]CTCCTAGGGAGGCCA | 84900 |
rs78708735 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | RNFT2 | GRCh38.p7 | 12:116811759 | AAATCCAGGCCCTGT[C/T]GCAGGGGGCTTGGCA | 84900 |
rs78754402 | snp | C/T | 0.144632 | 0.226711 | intron-variant | RNFT2 | GRCh38.p7 | 12:116813147 | TATTTTTTGTAGAGA[C/T]AGGGTTTTGCCATGT | 84900 |
rs78762453 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800634 | GCAAGACTCTGTCTC[A/C]AAAAAAAAAAATGGT | 84900 |
rs78801484 | snp | C/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812548 | TCTTTTTTTTTTTTT[C/T]CCTTGAGACAGGGTC | 84900 |
rs78807400 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | RNFT2 | GRCh38.p7 | 12:116803709 | ATGAAATCACCATCC[C/T]CCAGGATGTTCTCAT | 84900 |
rs78868537 | snp | A/T | 0.0592355 | 0.161582 | upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738247 | GCGCCGGACCCGGCG[A/T]CGCCAAGAAACCACC | 84900 |
rs78870015 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | RNFT2 | GRCh38.p7 | 12:116788254 | TTATACTCATTAACT[C/T]GCCCCATTCTGCAGC | 84900 |
rs78870614 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | RNFT2 | GRCh38.p7 | 12:116781267 | CTTTCTCACCCTGCT[C/G]TCTGCCCAGGGGGCT | 84900 |
rs78883955 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812550 | TTTTTTTTTTTTTTC[C/T]TTGAGACAGGGTCTC | 84900 |
rs78903267 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | RNFT2 | GRCh38.p7 | 12:116830683 | GCTGAAGTGAAGTAG[C/G]TGGATCACCTGTGGT | 84900 |
rs78907568 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNFT2 | GRCh38.p7 | 12:116843790 | GGATTGTGAGCTCCC[A/G]GAGGGCAGGGACCAG | 84900 |
rs78989967 | snp | C/T | 0.084364 | 0.187256 | intron-variant | RNFT2 | GRCh38.p7 | 12:116742511 | GGCTCAAGCGATCTG[C/T]CCGACTTGGCCGCCC | 84900 |
rs79000863 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | RNFT2 | GRCh38.p7 | 12:116799209 | AAGCCACGCTCCAGT[A/C]CTTGTACACAGTTGC | 84900 |
rs79036659 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNFT2 | GRCh38.p7 | 12:116803532 | ATCCACTGTATTGTT[G/T]CCTGTCTGTATTAAT | 84900 |
rs79045084 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116743247 | AAAAAAAAAAAAACC[A/G]GTTAAAAAACACTCA | 84900 |
rs79052751 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNFT2 | GRCh38.p7 | 12:116824369 | TCCCAAACGCTTTCT[A/G]TTAGTTAGGATTGGA | 84900 |
rs79112353 | in-del | -/AAA | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116782077 | AGCGAGACTCCGTCT[-/AAA]CCAAAAAAAAAAAAA | 84900 |
rs79113899 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116841964 | ATATATATATAGAGA[A/G]AGAGAGAGAGAGAGA | 84900 |
rs79139219 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNFT2 | GRCh38.p7 | 12:116800236 | GCATGGTGGCTCATG[C/T]CTGTAATCCCTGCAC | 84900 |
rs79167145 | snp | C/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116774814 | GAGGGTGGAGGAGGT[C/G]GAGTTTCCCAGAACC | 84900 |
rs79195170 | snp | A/G | 0.143284 | 0.226079 | intron-variant | RNFT2 | GRCh38.p7 | 12:116802958 | AAATTAGCCTAGCAC[A/G]GTAGCATATGCATAT | 84900 |
rs79244509 | snp | G/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116832923 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTTGCT | 84900 |
rs79296690 | snp | G/T | 0.158302 | 0.232576 | intron-variant | RNFT2 | GRCh38.p7 | 12:116819739 | TCTTGCCTTTTTTCC[G/T]TTTTCTTTTGTATTG | 84900 |
rs79315548 | snp | G/T | 0.00670406 | 0.0575072 | utr-variant-3-prime | RNFT2 | GRCh38.p7 | 12:116852729 | GAAATAGAACAGTCT[G/T]CTGGGAGTCAGACCT | 84900 |
rs79316254 | snp | C/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809398 | GTGGCCTGGGGGGTC[C/G]AGCGCTTCTTTGAAG | 84900 |
rs79317584 | snp | A/G | 0.157972 | 0.232445 | intron-variant | RNFT2 | GRCh38.p7 | 12:116819927 | AACAACTAGAAAGGA[A/G]CAGGTGACTTTAATT | 84900 |
rs79321021 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | RNFT2 | GRCh38.p7 | 12:116781577 | GATGGCAGGTTGAGC[A/G]TTCTCTCCTCTCTCC | 84900 |
rs79325423 | snp | C/T | 0.104149 | 0.203046 | intron-variant | RNFT2 | GRCh38.p7 | 12:116796687 | TGTTGGAGGCATCTT[C/T]GCTCCTGGAGGTCAT | 84900 |
rs79368525 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | RNFT2 | GRCh38.p7 | 12:116823041 | AAAATACAACTAGAG[A/G]ACTAGAGAAGGCTCT | 84900 |
rs79442021 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNFT2 | GRCh38.p7 | 12:116788528 | GTGCTCCCACGAGGA[C/T]TCCTACAGCACCCTA | 84900 |
rs79491461 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | RNFT2 | GRCh38.p7 | 12:116771033 | TTTATGAGTTCATCT[A/G]TGCTCCAACAAAGTT | 84900 |
rs79510906 | snp | A/T | 0.0905309 | 0.192535 | intron-variant | RNFT2 | GRCh38.p7 | 12:116791839 | TGAACCTTTTGAGGA[A/T]CTGTCAAACCTTCCC | 84900 |
rs79518302 | snp | A/G | 0.310878 | 0.242475 | intron-variant | RNFT2 | GRCh38.p7 | 12:116838706 | CTTGGTAGCAGGGAC[A/G]ATTTGAACATGATGT | 84900 |
rs79545559 | snp | A/C/T | 0.0302957 | 0.119399 | intron-variant | RNFT2 | GRCh38.p7 | 12:116743874 | TGGTGACTTTGATAC[A/C/T]TGACTTCACCCCTAG | 84900 |
rs79546899 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | RNFT2 | GRCh38.p7 | 12:116798548 | GGATCATAATAGTAC[C/G]TATCTGCATTAGGTT | 84900 |
rs79567557 | snp | C/T | 0.118584 | 0.212673 | intron-variant | RNFT2 | GRCh38.p7 | 12:116780276 | CAGGAACCGGTTTCA[C/T]GGAAGACAGTTTTTC | 84900 |
rs79574670 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116744226 | GTGAGACTCCTCCTC[A/C]AAAAAAAAAAAAAAA | 84900 |
rs79666868 | snp | G/T | 0.185472 | 0.241529 | intron-variant | RNFT2 | GRCh38.p7 | 12:116808021 | TTGCCCAGGCTGGAG[G/T]GCAATGGCACGATCT | 84900 |
rs79770698 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNFT2 | GRCh38.p7 | 12:116821058 | GAGCAATTGGTGTGC[C/T]GTTCCTGGCCCCTGG | 84900 |
rs79787816 | snp | A/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116788846 | GATGGATGGATGGAT[A/G]GATAAATGGGAGGAG | 84900 |
rs79889559 | snp | G/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116801993 | TGCCCAGCTAATTTT[G/T]GTATTTGTAGCAGAG | 84900 |
rs79932938 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | RNFT2 | GRCh38.p7 | 12:116772625 | GTAATTTATTTTTAA[C/T]TGTGAAAATTGGAAA | 84900 |
rs79950669 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116831198 | GACCTCGTCTCTCTA[A/C]AAAAAAAAAAAAGAG | 84900 |
rs80023411 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNFT2 | GRCh38.p7 | 12:116782659 | GGTTACCATGGGTCA[A/G]TGCTATTCCTTGTAC | 84900 |
rs80045288 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | RNFT2 | GRCh38.p7 | 12:116816469 | CTCCTCCCCCTCCTC[A/G]CCAGAAGAGCAGAGA | 84900 |
rs80067286 | snp | A/G | 0.15698 | 0.23205 | intron-variant | RNFT2 | GRCh38.p7 | 12:116817992 | TCAACAAGCACTAGA[A/G]ACAAATAAAAACAAT | 84900 |
rs80075462 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNFT2 | GRCh38.p7 | 12:116831879 | ACACCAGTAATTCCA[A/G]CACTTCAGGAGGCTG | 84900 |
rs80076978 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797700 | GCTTTATTGAAGAGG[C/T]GTTACAGCTCAGGCA | 84900 |
rs80122818 | in-del | -/CTC | 0.197703 | 0.244469 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797736 | ACAGCACCGTGACTA[-/CTC]CTGCAGAGCAGGGCT | 84900 |
rs80133541 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | RNFT2 | GRCh38.p7 | 12:116829632 | GTTGGCTATAAATCT[C/G]TGTCCACATGCCACG | 84900 |
rs80249399 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | RNFT2 | GRCh38.p7 | 12:116744249 | AAAAAAAAAAGAGTT[A/G]TTTATGGATGAAGGA | 84900 |
rs80289192 | snp | C/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116814706 | TCCGACAGAGTCTCA[C/G]TCTGTTGCCCAGACT | 84900 |
rs80294669 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738918 | GAGGATTAAGTTGAG[A/G]TTGCAAATTCTTGAA | 84900 |
rs80314325 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | RNFT2 | GRCh38.p7 | 12:116783980 | TGTGAACAGGGTCCT[A/G]TTATTACCACCATCC | 84900 |
rs80318779 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116843988 | AGGGCAGGGCAGATG[C/T]TGACTAAGCATTTAG | 84900 |
rs111173962 | snp | A/G | 0.264632 | 0.249571 | intron-variant | RNFT2 | GRCh38.p7 | 12:116789106 | ATGGATGGATGGGTA[A/G]ATGGAAGGAGAGTGG | 84900 |
rs111256849 | snp | C/T | 0.404893 | 0.196235 | synonymous-codon, nc-transcript-variant | RNFT2 | GRCh38.p7 | 12:116750102 | CCAGCCCCACCACCA[C/T]TTCCACCATGGCGGC | 84900 |
rs111289254 | snp | G/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116837367 | GTGCCGTGTAAGAGA[G/T]ATTCATGCAGTGTCT | 84900 |
rs111290164 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RNFT2 | GRCh38.p7 | 12:116834410 | AGGCATGAGCCACCA[C/T]GCCCGGCCTCCAGTA | 84900 |
rs111292661 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116839425 | GGGATGGGTGGGTGG[A/G]TGGATGGATGGATGG | 84900 |
rs111292995 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | RNFT2 | GRCh38.p7 | 12:116830046 | GATATCTTTCATCAG[G/T]ATGATTTCTTTTTTA | 84900 |
rs111323331 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RNFT2 | GRCh38.p7 | 12:116761020 | GGGAGGCCATTCTTC[A/G]GTCTATCACCCCTGG | 84900 |
rs111336255 | snp | C/G | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116849947 | CTCCTGGGTTCAAGC[C/G]ATTCTCCTGCCTCAG | 84900 |
rs111354284 | in-del | -/AGAA | 0.0858192 | 0.188533 | intron-variant | RNFT2 | GRCh38.p7 | 12:116822708 | AAGAAGAGGAGAGAT[-/AGAA]AGAGAACTGGCTGGG | 84900 |
rs111373994 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116842572 | TTTATTTATTTATTT[A/G]TTTGTTTGTTTGTTT | 84900 |
rs111391543 | in-del | -/AT | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116747374 | TATATATTTTAAAAC[-/AT]ATTTCCTGGAGCCAA | 84900 |
rs111402191 | snp | G/T | 0.030665 | 0.119967 | intron-variant | RNFT2 | GRCh38.p7 | 12:116749259 | TACTCTCTGTACCTG[G/T]GTCCTAATCTCTTCC | 84900 |
rs111468861 | snp | C/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116791055 | AGTGTTGTACAACCA[C/T]CACCTCTGTCTAGTT | 84900 |
rs111482789 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116742395 | ACCTCTCAGCCTTCC[A/G]AGTAGCTGGGACTAA | 84900 |
rs111502886 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | RNFT2 | GRCh38.p7 | 12:116764888 | CAAGAGCGAAAGTCC[A/G]TCTCAAAAACAAACA | 84900 |
rs111523257 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RNFT2 | GRCh38.p7 | 12:116756285 | AGGTTTTTCAACTCC[A/G]TGGTTAGGTATATTC | 84900 |
rs111534257 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNFT2 | GRCh38.p7 | 12:116770294 | ATAATTGTCTATAGT[A/G]TTCAGTACAGTAACA | 84900 |
rs111539415 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116794022 | TGTAATCCCAGCACT[C/T]TGAGAGTGTGAGGTG | 84900 |
rs111572246 | snp | A/C | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116759389 | CTTCTTGGTTTAGAT[A/C]CATTGCTGGTGAACT | 84900 |
rs111625819 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116813060 | TCCCAGGCTCAAGCC[A/G]TCTTCCTGCCTCAGC | 84900 |
rs111638157 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116843516 | AAAAAAAAAAAAAAA[A/C]CCCAAGAAACAAACA | 84900 |
rs111707873 | snp | A/G | 0.19646 | 0.2442 | intron-variant | RNFT2 | GRCh38.p7 | 12:116822854 | ATAGAAAAATTAGCC[A/G]GCCATGGTGGTGCAC | 84900 |
rs111718517 | snp | C/G | 0.021333 | 0.101051 | intron-variant | RNFT2 | GRCh38.p7 | 12:116796894 | TACCCACACACAGGG[C/G]CTGGAAGAAGGTTAA | 84900 |
rs111751224 | snp | C/T | 0.237882 | 0.249706 | intron-variant | RNFT2 | GRCh38.p7 | 12:116789938 | TGGGAGGAGAGTGGA[C/T]GGATGGATGGTGGAT | 84900 |
rs111755775 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | RNFT2 | GRCh38.p7 | 12:116786362 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 84900 |
rs111778251 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | RNFT2 | GRCh38.p7 | 12:116834270 | CTACAGGCATCCACC[A/G]CTATACCCAGCTAAT | 84900 |
rs111797869 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNFT2 | GRCh38.p7 | 12:116780818 | GCAGGGTTCCAGGTC[A/G]GCACCACGCACTTGA | 84900 |
rs111811486 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116774934 | AAACTGGTGCACAGA[A/G]AGAGAGAGAGAGAGA | 84900 |
rs111811594 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | RNFT2 | GRCh38.p7 | 12:116767813 | TCAAACTCCTGACCT[C/T]GTGATCCACCTGCCT | 84900 |
rs111852606 | snp | A/G | 0.314787 | 0.241459 | intron-variant | RNFT2 | GRCh38.p7 | 12:116769225 | TTAGCTGGGCGTGGT[A/G]GCAGGTGCCTGTAAT | 84900 |
rs111895763 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNFT2 | GRCh38.p7 | 12:116822467 | CGTCACCTGGGGCAG[A/G]TTATCTAACTTTTCT | 84900 |
rs111902006 | snp | A/G | 0.0577344 | 0.159793 | intron-variant, downstream-variant-500B | RNFT2 | GRCh38.p7 | 12:116836523 | AGAATGCCAAATTCC[A/G]TATGGTGTAACATCA | 84900 |
rs111944404 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116818517 | GTGGTGTGAGTGAGC[A/G]GTCTCTAAGCGATGG | 84900 |
rs111946924 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116850332 | GCTAATTTTTTTTTT[C/T]TTTTAATTTTTAGTA | 84900 |
rs111959200 | snp | C/T | 0.133777 | 0.221342 | upstream-variant-2KB, utr-variant-5-prime | RNFT2, C12orf49 | GRCh38.p7 | 12:116738023 | GCCGGCCCCGCCGCC[C/T]GCAGCCCAGTCTGCT | 84900 |
rs111960905 | snp | G/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116811415 | GAGTCTCACTCTGTC[G/T]CCCAGGCTGGAGTGC | 84900 |
rs111961943 | in-del | -/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116768713 | TACTTTTCATTGTCA[-/T]TTTTTTTTTTATTTT | 84900 |
rs111987803 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116760751 | GTGGGTCCTCTCGGG[A/T]TTGCTGGTTTGTCCT | 84900 |
rs112004657 | in-del | -/GATG | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116788827 | GTGGATGGATGGATA[-/GATG]GATGGATGGATGGAT | 84900 |
rs112018008 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116742335 | TGCAGTGGCACGATC[A/T]CGGCTCACTGCAGCC | 84900 |
rs112061843 | snp | C/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116762416 | AACAAAAAAAAAAAA[C/G]AAAGAAAGAAATAGT | 84900 |
rs112085446 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116848779 | CCCAACCCGCCCAAG[C/T]CCTCCCTGTTCCTTC | 84900 |
rs112093335 | in-del | -/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116812535 | AGGCCTGTTCCTATC[-/T]TTTTTTTTTTTTTCC | 84900 |
rs112132121 | snp | A/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116766115 | TGTCTCTAAAAAAAA[A/T]TAAAAATTTTTTTTT | 84900 |
rs112143707 | snp | A/T | 0.444444 | 0.157135 | intron-variant | RNFT2 | GRCh38.p7 | 12:116753579 | GATCTAGAAGCTTTA[A/T]CCCTCTATGAGGTAT | 84900 |
rs112180336 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787383 | CAGAAAATCGAGATG[C/T]TAACAGTAGCGTTCT | 84900 |
rs112186221 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787217 | AATGAAAATCCAACT[C/T]TTCCAACTCCCAAGC | 84900 |
rs112197019 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116835344 | TCAAAAATAGTATCC[A/G]TGTTAAATTGCACAC | 84900 |
rs112216457 | in-del | -/A | 0.216456 | 0.247739 | intron-variant | RNFT2 | GRCh38.p7 | 12:116838022 | TTTTTTAAAAAAAAA[-/A]CATAAGTTATAGTAC | 84900 |
rs112278267 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | RNFT2 | GRCh38.p7 | 12:116798796 | GCCCAGGCTGGGCTC[A/G]AACTCCTAAGCTCAA | 84900 |
rs112303271 | snp | A/G | 0.254944 | 0.249951 | intron-variant | RNFT2 | GRCh38.p7 | 12:116768951 | GGCCAGGCTGGTCTC[A/G]AACTCCTGATCTCAG | 84900 |
rs112321616 | in-del | -/G | 0.0341408 | 0.126114 | intron-variant | RNFT2 | GRCh38.p7 | 12:116767565 | CGATATAAAAATTAT[-/G]GTTTTTTTTTTGTTT | 84900 |
rs112353321 | snp | C/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116767720 | AAGTAGCTGGGATTA[C/T]AGACATGCGCCACCA | 84900 |
rs112355530 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNFT2 | GRCh38.p7 | 12:116760421 | GATTTGCTTCTCCCT[A/G]TGGAGTTTTAGCCCT | 84900 |
rs112371401 | snp | C/G | 0.239037 | 0.24976 | intron-variant | RNFT2 | GRCh38.p7 | 12:116791529 | AGGCCAGCCTGGTCT[C/G]AGACTCCTGACCTCA | 84900 |
rs112383442 | snp | A/G | 0.181659 | 0.240478 | intron-variant | RNFT2 | GRCh38.p7 | 12:116769149 | CAGATCACGAGGTCA[A/G]GAGTTCAAGACCACC | 84900 |
rs112387634 | snp | A/G | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116740833 | CTCCTCTGTGAAATG[A/G]GGTGATAGCTTTCCT | 84900 |
rs112413711 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116819817 | GATTTTTACAAACAT[A/G]TGTAATCACTCAGAT | 84900 |
rs112439132 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116820533 | CTGTGTCCTCACTTC[C/T]CCCACCAGGGGTACC | 84900 |
rs112439556 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | RNFT2, C12orf49 | GRCh38.p7 | 12:116738708 | CAGATGCATCCCGCG[A/T]GCAAAAATTTATTCC | 84900 |
rs112505687 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | RNFT2 | GRCh38.p7 | 12:116826299 | CTTCCCAACTTGACA[C/G]TCCCACCCCCTTTAT | 84900 |
rs112542343 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116795913 | AGTGGTCATTTCTTT[C/T]TCTTTTTCTTTTTGA | 84900 |
rs112570650 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116850322 | ACCAGGCCTGGCTAA[A/T]TTTTTTTTTTTTTTA | 84900 |
rs112573456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNFT2 | GRCh38.p7 | 12:116846418 | TAGCTGGGACGGCAC[A/T]TGCCACCATGCCCAG | 84900 |
rs112592208 | snp | C/T | 0.0879971 | 0.190408 | intron-variant | RNFT2 | GRCh38.p7 | 12:116822934 | CCCAGGAGGCAGAGA[C/T]TGCAGTGAGCCAAGA | 84900 |
rs112604474 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116783777 | GAGGAGCAAGACAGG[C/T]GGAGCCCACAGAGTG | 84900 |
rs112607340 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116820097 | GATATTGTTTGTTTG[C/T]TTGTTTGTTTTTAAA | 84900 |
rs112633758 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RNFT2 | GRCh38.p7 | 12:116774997 | CCATGTGCGGTGGCT[C/T]ACGCCTGTAATCCAA | 84900 |
rs112659326 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNFT2 | GRCh38.p7 | 12:116828506 | CTACCACACTGTATT[A/G]TAGTAGTTTGCTTAG | 84900 |
rs112664083 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | RNFT2 | GRCh38.p7 | 12:116839105 | ACTAGTCACGTCCCT[A/G]GCTATATGGTCTCAT | 84900 |
rs112665314 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116795977 | GCAGTGGTGCAATCT[C/T]GGCTCACTGAAACCT | 84900 |
rs112691782 | snp | C/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116742238 | GTTTGAATCATGTTG[C/G]TGGGCTCTGGGGTAC | 84900 |
rs112700871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNFT2 | GRCh38.p7 | 12:116792815 | CCCCTAATGGCTCAC[A/G]GCACAGATGCTCTTT | 84900 |
rs112750553 | in-del | -/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809689 | CAGAAAGACCTTTTC[-/T]TTTTTTTTTGAGATG | 84900 |
rs112757288 | snp | A/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116848837 | TTTGTTTTTTTGTTT[A/T]TAGACAGATTCTTGC | 84900 |
rs112770923 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | RNFT2 | GRCh38.p7 | 12:116787914 | ACAGACAGACCCTAC[C/T]TCTTTTGCTTCTTTT | 84900 |
rs112795683 | in-del | -/C | 0.039522 | 0.134904 | intron-variant | RNFT2 | GRCh38.p7 | 12:116827504 | GGGATGTGTTAGAAT[-/C]CCCATCGTGACTTAT | 84900 |
rs112798542 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116850321 | CACCAGGCCTGGCTA[A/T]TTTTTTTTTTTTTTT | 84900 |
rs112850108 | in-del | -/T | 0.224709 | 0.248717 | intron-variant | RNFT2 | GRCh38.p7 | 12:116762581 | TTTCTTCTCTACCAA[-/T]TTTTTTTTTTTTTTT | 84900 |
rs112903394 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851613 | GGCGCGGTGGCGGGT[A/G]CCTGTAATCCCAGCT | 84900 |
rs112939314 | snp | C/T | 0.239326 | 0.249772 | intron-variant | RNFT2 | GRCh38.p7 | 12:116786268 | CTGGGATTATAGACA[C/T]GTGCCACCACGCCTG | 84900 |
rs112948240 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116839429 | TGGGTGGGTGGGTGG[A/G]TGGATGGATGGATGG | 84900 |
rs112988020 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNFT2 | GRCh38.p7 | 12:116801804 | TTTCTGTGGGGTTTT[G/T]TTTGTTTGTTTGTTT | 84900 |
rs112992516 | snp | C/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116842750 | AGCTAATTTTTGCAT[C/T]TTTAGTAGGGACGGG | 84900 |
rs113005494 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNFT2 | GRCh38.p7 | 12:116836130 | AGTGCTCCTGAGGGC[A/G]TAGTTCCCAAGGGCG | 84900 |
rs113020050 | snp | A/G | 0.323434 | 0.238972 | intron-variant | RNFT2 | GRCh38.p7 | 12:116834242 | CTTGCCTCAGCCTCC[A/G]GAATAGCTGGGACTA | 84900 |
rs113021396 | snp | A/G | 0.0812036 | 0.184412 | synonymous-codon, nc-transcript-variant | RNFT2 | GRCh38.p7 | 12:116766861 | CCTGGCCTTTCTGGC[A/G]GGGAACACCCTCTAT | 84900 |
rs113036560 | snp | C/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116820678 | TCTCCCTTTCTCTGT[C/T]TCTCAGAGTGGCACA | 84900 |
rs113074925 | snp | C/T | 0.084728 | 0.187577 | intron-variant | RNFT2 | GRCh38.p7 | 12:116850720 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 84900 |
rs113086456 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | RNFT2 | GRCh38.p7 | 12:116811623 | TCAAATAATCTGCCC[G/T]CCTTGGCCTCCCAAA | 84900 |
rs113095132 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116762448 | CATACAAGGTGTTTA[A/G]CACAAGTACTGGGTA | 84900 |
rs113132488 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116822998 | CGAGACTCTGTCTCA[A/G]AAAGCAAAAAACGAA | 84900 |
rs113145402 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116815928 | GCTCCAGACCACCAG[A/G]AAAGGAGATGCCCTC | 84900 |
rs113163617 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNFT2 | GRCh38.p7 | 12:116809987 | GGCCAGAAAGACCTT[C/T]TTATTCTGCTGATTT | 84900 |
rs113186327 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116741157 | GGTGAGGGGCAACCC[A/G]AAACTGGATTGAACA | 84900 |
rs113190899 | in-del | -/TGGA | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116789934 | TGGATGGGAGGAGAG[-/TGGA]TGGATGGATGGTGGA | 84900 |
rs113194697 | snp | C/T | 0.000297937 | 0.0122016 | synonymous-codon, nc-transcript-variant | RNFT2 | GRCh38.p7 | 12:116750306 | CTTTCAGCATAAGCT[C/T]GGTGAGTTCTGGGGG | 84900 |
rs113205467 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNFT2 | GRCh38.p7 | 12:116754339 | TTCCACCATGTATAT[A/G]TGTATATACATATAT | 84900 |
rs113238406 | in-del | -/A/AAA | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116766117 | AAAAAAAAATAAAAA[-/A/AAA]TTTTTTTTTAATTAG | 84900 |
rs113300201 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116786733 | GAAATAACAGAAATT[C/T]GTTCTCTCACAGTTC | 84900 |
rs113307712 | snp | C/T | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116781670 | TCCTCTTATAAGGAC[C/T]CTGTGATGACACTGG | 84900 |
rs113326826 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNFT2 | GRCh38.p7 | 12:116848619 | CTGTTCCTCCCGCAC[A/G]TCAAACACAGTCCAG | 84900 |
rs113327017 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | RNFT2 | GRCh38.p7 | 12:116829741 | CGTGCCACCATACCC[A/G]GCTATTTTTTTGTAT | 84900 |
rs113432788 | snp | C/T | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116852330 | CCCTTCCCCCTGCCC[C/T]GCCGTAGATTCAGGA | 84900 |
rs113442296 | snp | C/T | 0.5 | 0 | synonymous-codon, downstream-variant-500B | RNFT2 | GRCh38.p7 | 12:116836249 | CGCCATCTGTCAGGC[C/T]GAGTTCCGAGAGCCT | 84900 |
rs113489046 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RNFT2 | GRCh38.p7 | 12:116821032 | GAACGCGTCATAACT[A/G]CCTACAAGAGGAGCA | 84900 |
rs113531694 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116769912 | TGGTGGCAGGATCCT[A/G]TAATCCCAGCTACTT | 84900 |
rs113573555 | snp | A/C | 0.0696718 | 0.173152 | intron-variant | RNFT2 | GRCh38.p7 | 12:116768857 | TGCCTCAGCCTCCCA[A/C]ATAGCTGGGATTACA | 84900 |
rs113591947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNFT2 | GRCh38.p7 | 12:116849724 | CTTCCTTCTCCACTC[C/T]AAGTCAAGGACCTGG | 84900 |
rs113623886 | in-del | -/AG | 0 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116752197 | TCTACTGAAAAAAAA[-/AG]AGAGAGAGAGAAAGC | 84900 |
rs113683019 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116818005 | GAGACAAATAAAAAC[A/C]ATTCATGGAGAATTC | 84900 |
rs113722045 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116830723 | GAGACCAGCCTGGCC[A/G]ACATGGTGAAACCCC | 84900 |
rs113761307 | in-del | -/AGAGAG | 0.0517044 | 0.152246 | intron-variant | RNFT2 | GRCh38.p7 | 12:116774935 | AACTGGTGCACAGAA[-/AGAGAG]AGAGAGAGAGAGAGA | 84900 |
rs113804773 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RNFT2 | GRCh38.p7 | 12:116832458 | ATCATTTGTTTATCC[A/G]TTCTTCCATTGATGG | 84900 |
rs113886167 | snp | A/C | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116756523 | TGCCATTTTGCTGAG[A/C]GTTTTAATCATAAAG | 84900 |
rs113916208 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNFT2 | GRCh38.p7 | 12:116764340 | CCTGTTCACCAAAAA[C/T]CTATGGAAATAATTT | 84900 |
rs113918104 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | RNFT2 | GRCh38.p7 | 12:116763046 | ATGATTGCACCACTG[C/T]ACTCTAGCCTGGGCA | 84900 |
rs113983803 | snp | A/G | 0.5 | 0 | intron-variant | RNFT2 | GRCh38.p7 | 12:116831209 | TCTACAAAAAAAAAA[A/G]AGAGAGAGAGAGAGA | 84900 |
rs114061237 | snp | C/T | 0.102014 | 0.201495 | intron-variant | RNFT2 | GRCh38.p7 | 12:116802110 | AAAGGTGTGAGCCAC[C/T]GCACCCAGCCTAATA | 84900 |
rs114064259 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797809 | GCCATATTTATACCT[A/C]CTTTTAATTACATGT | 84900 |
rs114090490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT2 | GRCh38.p7 | 12:116761397 | CGGTAATCCGCACAC[C/T]TTGGCCTCCAAAAGT | 84900 |
rs114097274 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNFT2 | GRCh38.p7 | 12:116784634 | TCTAGATCTCAGAGT[A/G]TAGCACCTCCCTCCA | 84900 |
rs114098968 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RNFT2 | GRCh38.p7 | 12:116804926 | GATCCACGATTACAC[C/T]ACTGCACTCCATCCT | 84900 |
rs114104096 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RNFT2 | GRCh38.p7 | 12:116834625 | TGTCTCTATGAATAT[A/C]CTTATTATGAATGTT | 84900 |
rs114104771 | snp | C/T | 0.095934 | 0.196885 | intron-variant | RNFT2 | GRCh38.p7 | 12:116828131 | AAGATGGCGCTCAGA[C/T]CAGTGACCATCTTTT | 84900 |
rs114149041 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNFT2 | GRCh38.p7 | 12:116839336 | ATGGACAGAAGGAAG[A/G]ATGGATGGGATGGTT | 84900 |
rs114184082 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | RNFT2 | GRCh38.p7 | 12:116780593 | AGCCAAAATCCTAGG[C/T]TGTTGAGGTTTTCTT | 84900 |
rs114263645 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNFT2 | GRCh38.p7 | 12:116847496 | ACGGTGGAACCCATT[A/G]GTCTTTCCAATCTCC | 84900 |
rs114374110 | snp | A/T | 0.0379877 | 0.132479 | intron-variant, nc-transcript-variant | RNFT2 | GRCh38.p7 | 12:116825032 | TTGTCTCTCCTCCCC[A/T]TGATATCTGCTGGGG | 84900 |
rs114382338 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNFT2 | GRCh38.p7 | 12:116741359 | AGATGTCTTAGTCCA[C/T]ACAGGCTGCTATCAC | 84900 |
rs114443504 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | RNFT2 | GRCh38.p7 | 12:116756284 | GAGGTTTTTCAACTC[C/T]GTGGTTAGGTATATT | 84900 |
rs114455559 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RNFT2 | GRCh38.p7 | 12:116777369 | TCCCCCTCTTGGGGG[A/G]TGTTGGAGAGCAGTG | 84900 |
rs114456148 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RNFT2 | GRCh38.p7 | 12:116795740 | AGCGGGCCCTTCCCT[A/G]AGAACTCTCTACAAG | 84900 |
rs114460273 | snp | C/T | 0.102726 | 0.202016 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797048 | TGCACAGGACAGCCC[C/T]CTACTGCAACCCAGA | 84900 |
rs114466287 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNFT2 | GRCh38.p7 | 12:116838440 | TTACTGGGTCAGAAG[A/G]CACACAGTTTTGACA | 84900 |
rs114587107 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | RNFT2 | GRCh38.p7 | 12:116764686 | CACCTGAGTTCAGCA[A/G]TTCGAGACCAGCTTG | 84900 |
rs114631515 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | RNFT2 | GRCh38.p7 | 12:116794041 | GAGTGTGAGGTGGGA[A/G]GATCACTTGAGCCTA | 84900 |
rs114660826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT2 | GRCh38.p7 | 12:116791162 | CTCCTGGCAACTGCC[A/C]ATCTGCTTTTCATCT | 84900 |
rs114689015 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | RNFT2 | GRCh38.p7 | 12:116770633 | GTGTGATCACACTCA[C/T]TGAAACCTTGACCTC | 84900 |
rs114747821 | snp | C/T | 0.10237 | 0.201756 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797297 | AGGCTCTGTGGGTCA[C/T]TCCTGTAATCCCAGC | 84900 |
rs114750191 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNFT2 | GRCh38.p7 | 12:116760846 | AATCTAGTCCTGCCT[C/T]CCATCCGCCATGATC | 84900 |
rs114754591 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNFT2 | GRCh38.p7 | 12:116794853 | CTCACCAATTTCACT[G/T]ATGTTATTCAGGACC | 84900 |
rs114759046 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RNFT2 | GRCh38.p7 | 12:116835567 | ATGTAGTATCAGCCA[C/T]TGGGGCATACTGATT | 84900 |
rs114786349 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RNFT2 | GRCh38.p7 | 12:116750441 | CTTCAGGATGTGGGA[A/T]TCTGAGTCAGACCTG | 84900 |
rs114791221 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNFT2 | GRCh38.p7 | 12:116767963 | TAACCACATTTCAAG[G/T]GTTCAAAATGGTTAG | 84900 |
rs114885879 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNFT2 | GRCh38.p7 | 12:116824655 | AGTTTCTACATGATG[C/T]TTATAATTGTGTTCA | 84900 |
rs114886188 | snp | A/C/T | 0.0271762 | 0.113356 | intron-variant | RNFT2 | GRCh38.p7 | 12:116810388 | ACAGTTCGGGGTGTG[A/C/T]GTTTTTCCAGATAAC | 84900 |
rs114902422 | snp | A/T | 0.0596104 | 0.162024 | upstream-variant-2KB, intron-variant | RNFT2, C12orf49 | GRCh38.p7 | 12:116737279 | CGGCGGCGCCGCTGC[A/T]GAAGTCGGGAGGTCG | 84900 |
rs114956193 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RNFT2 | GRCh38.p7 | 12:116846412 | CCCAAGTAGCTGGGA[C/T]GGCACATGCCACCAT | 84900 |
rs114965132 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNFT2 | GRCh38.p7 | 12:116765487 | CACAGGGAAGGTTAC[A/G]CTGGGAAAGTTATGA | 84900 |
rs114966619 | snp | A/G | | | utr-variant-3-prime | RNFT2 | GRCh38.p7 | 12:116853609 | AGTACCCTTCAGCCA[A/G]TAAATACCATCTGTT | 84900 |
rs115038428 | snp | A/T | 0.0490535 | 0.14873 | intron-variant | RNFT2 | GRCh38.p7 | 12:116802872 | GGCCGAGCCAGGAGG[A/T]TCACTTGAATCCAGG | 84900 |
rs115039812 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RNFT2 | GRCh38.p7 | 12:116834187 | TCGGTAGCGCAGTCT[C/T]GGCTCACTGCAACCT | 84900 |
rs115072934 | snp | A/G | 0.101658 | 0.201233 | intron-variant | RNFT2 | GRCh38.p7 | 12:116794708 | AAGGGAAGGGAGGAA[A/G]GAAAGAAAGAAATGA | 84900 |
rs115076336 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RNFT2 | GRCh38.p7 | 12:116774824 | GAGGTGGAGTTTCCC[A/T]GAACCTTGGATGAAT | 84900 |
rs115079194 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RNFT2 | GRCh38.p7 | 12:116847494 | GAACGGTGGAACCCA[C/T]TGGTCTTTCCAATCT | 84900 |
rs115130857 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | RNFT2 | GRCh38.p7 | 12:116853438 | TAGGTGCATCAGCTT[C/T]GGAAGAGAAGAATGA | 84900 |
rs115148685 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | RNFT2 | GRCh38.p7 | 12:116780168 | CAACCCATAACCCCA[A/C]TCTTTGGGCCTGTTT | 84900 |
rs115167772 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | RNFT2 | GRCh38.p7 | 12:116808228 | CCTTGGCCTCCTAAA[A/G]TGCTCGTAAGCCACC | 84900 |
rs115189856 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime | RNFT2 | GRCh38.p7 | 12:116852883 | CTAGTGAATACCCCA[A/G]TGGTTTCTCCAATTA | 84900 |
rs115201325 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNFT2 | GRCh38.p7 | 12:116785851 | TTCATGAGTTCGAGA[C/T]AAGCCTGGGCAGCAT | 84900 |
rs115202548 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | RNFT2 | GRCh38.p7 | 12:116836358 | CCATGGGCAGTCCTC[A/G]GGTCTCTGGCATGGG | 84900 |
rs115248006 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | RNFT2 | GRCh38.p7 | 12:116828010 | GGGACCAGAGTCAGC[C/T]AGATGCCAGCAGGCA | 84900 |
rs115265020 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | RNFT2 | GRCh38.p7 | 12:116829893 | GACTCATTTCCCCTC[C/T]AATTTAAACATATCA | 84900 |
rs115339357 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | RNFT2 | GRCh38.p7 | 12:116770644 | CTCACTGAAACCTTG[A/G]CCTCCCAGCCTCAAG | 84900 |
rs115390806 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RNFT2 | GRCh38.p7 | 12:116742596 | GCTCTTTAGTTTGGT[A/G]TCTGGCCCTAGATGA | 84900 |
rs115470858 | snp | A/C | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116762403 | CACTCCATCTCAAAA[A/C]AAAAAAAAAAAACAA | 84900 |
rs115533050 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797053 | AGGACAGCCCTCTAC[A/T]GCAACCCAGAGTTAT | 84900 |
rs115599601 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | RNFT2 | GRCh38.p7 | 12:116810831 | CCATTGGGGTAGGGG[A/G]GACTACCCTGCTTCC | 84900 |
rs115608307 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNFT2 | GRCh38.p7 | 12:116846707 | TTGCATGAAACTCTT[C/T]TATTCTTCATCCAGA | 84900 |
rs115623312 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNFT2 | GRCh38.p7 | 12:116801481 | AAGTTCTAGCTCCTT[C/T]TGCCTCTGAGACCTT | 84900 |
rs115624445 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNFT2 | GRCh38.p7 | 12:116848018 | CAGCCCCCGCAACAG[A/G]CCCCAGTATGTTGTT | 84900 |
rs115741476 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNFT2 | GRCh38.p7 | 12:116833498 | CAGAGGGTGACCCAC[C/T]CTCCAGCCCTCTGCC | 84900 |
rs115783561 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNFT2 | GRCh38.p7 | 12:116851173 | CCAGCCAGCATGGGC[A/G]GGCCAAGTTTCCAAC | 84900 |
rs115849936 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | RNFT2 | GRCh38.p7 | 12:116785504 | ACTTTGTTGCCCAGG[C/T]TAGTCTTGAACTCCT | 84900 |
rs115852052 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | RNFT2 | GRCh38.p7 | 12:116789228 | GATGGGTAAATGGGA[A/G]GAGAGTAGATGGATG | 84900 |
rs115898422 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNFT2 | GRCh38.p7 | 12:116796125 | TTTTGGCCAGGGTAG[C/T]CTTGAACTCCCGACC | 84900 |
rs115900469 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | RNFT2 | GRCh38.p7 | 12:116756520 | GTATGCCATTTTGCT[A/G]AGAGTTTTAATCATA | 84900 |
rs115900725 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | RNFT2 | GRCh38.p7 | 12:116821546 | GTCCTGGCCGCCCAC[C/T]TGGGAGCAGGACTTG | 84900 |
rs115916374 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNFT2 | GRCh38.p7 | 12:116785130 | CTCGGCCTCTTGCAC[A/G]TGCCCTTCAGACCCC | 84900 |
rs115918051 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNFT2 | GRCh38.p7 | 12:116761930 | ATCCAGGCCGGTCGC[A/G]GTGGCTCACGCCTGT | 84900 |
rs115957192 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNFT2 | GRCh38.p7 | 12:116814688 | ATGATATTTTTTTTT[C/T]TTTCCGACAGAGTCT | 84900 |
rs116008648 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | RNFT2 | GRCh38.p7 | 12:116814083 | CCCAGCCCTCCCCGT[G/T]TCATTCTCCAGGAGT | 84900 |
rs116024945 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RNFT2 | GRCh38.p7 | 12:116749253 | ATGGTCTACTCTCTG[C/T]ACCTGTGTCCTAATC | 84900 |
rs116060860 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNFT2 | GRCh38.p7 | 12:116797530 | ACTGCACTCCAGCCT[A/G]TCTATCTCAAAAAAA | 84900 |
rs116186503 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | RNFT2 | GRCh38.p7 | 12:116783839 | ACGGATCATTTTTCT[G/T]CCTGTTCTAGTTAGG | 84900 |
rs116237247 | snp | A/G | 0.144296 | 0.226554 | intron-variant | RNFT2 | GRCh38.p7 | 12:116808234 | CCTCCTAAAGTGCTC[A/G]TAAGCCACCACACCT | 84900 |
rs116240456 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNFT2 | GRCh38.p7 | 12:116775462 | TCTTAGCCTTGGAGG[C/T]GACACTTACCACTGA | 84900 |
rs116243410 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | RNFT2 | GRCh38.p7 | 12:116813024 | GCAGTGGCACGATCA[C/T]GATTCATTGCAGCCA | 84900 |
rs116268432 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNFT2 | GRCh38.p7 | 12:116785567 | AAAGTACTTGTGTAA[C/T]TATTACATTCATTCC | 84900 |
rs116269828 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNFT2 | GRCh38.p7 | 12:116790799 | CTGTCTCCACCAAAA[C/T]ACAAAGATTTAGCCG | 84900 |
rs116298732 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | RNFT2 | GRCh38.p7 | 12:116845728 | GCTGACCCCTGGGTC[C/T]TGCCCTCCAGACCAT | 84900 |
rs116306354 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RNFT2 | GRCh38.p7 | 12:116758570 | TAATGGGTGAATTCT[C/T]TTAGCATTTGTTTGT | 84900 |
rs116325980 | snp | A/G | 0.046775 | 0.145601 | intron-variant | RNFT2 | GRCh38.p7 | 12:116814950 | TATGTTAGCCAGGCC[A/G]GTCACAAACTCCTGA | 84900 |
rs116353608 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNFT2 | GRCh38.p7 | 12:116833387 | GTCGCCTGTGATGCT[C/T]GAGTCAGCCCTCTAA | 84900 |
rs116385338 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | RNFT2 | GRCh38.p7 | 12:116767567 | GATATAAAAATTATG[G/T]TTTTTTTTTGTTTGT | 84900 |
rs116387939 | snp | A/C | 0.030278 | 0.119257 | intron-variant | RNFT2 | GRCh38.p7 | 12:116761106 | TACACCTAGCCCAGT[A/C]CCTTTACGCCGCAGA | 84900 |
rs116394982 | snp | A/T | | | intron-variant | RNFT2 | GRCh38.p7 | 12:116838118 | GATTGCTCCTTATCC[A/T]ATTTTATAGCTGCAT | 84900 |
rs116435200 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | RNFT2 | GRCh38.p7 | 12:116836640 | TAAAATGGACATAAT[A/G]GTGGCCAGGCACAGT | 84900 |
rs116478425 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNFT2 | GRCh38.p7 | 12:116769611 | GAAAATATTTCTGTA[C/T]AGCTGTACAATCTGT | 84900 |
rs116518347 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RNFT2 | GRCh38.p7 | 12:116838913 | TATGACCAGGCCAGG[A/C]ACACATTTTAGTCTT | 84900 |
rs116534378 | snp | A/G | 0.0908922 | 0.192833 | intron-variant | RNFT2 | GRCh38.p7 | 12:116756385 | ATTCTCTACTTGGTC[A/G]CCGTTGGTGTATAAA | 84900 |