SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs479929 | snp | G/T | 0 | 0 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460592 | CCTATTACCTCATTT[G/T]GGCGTTGTTTCTGGG | 494470 |
rs480879 | snp | A/C | 0 | 0 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460707 | TTTCGTCCGAACTAT[A/C]AGGGTGTGTGATTGC | 494470 |
rs494056 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448061 | CACCGAAAAGTCAGG[G/T]TATAGGAGGTTGAGA | 494470 |
rs494117 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448040 | GAGGTTGAGAACACA[G/T]GGGAGCTACGTCATA | 494470 |
rs498358 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442307 | caaagtcatgatcta[A/C]atttccgccttaaga | 494470 |
rs503368 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448292 | GGAGCCAGGACACAA[G/T]AAGGCCAGGGCACAA | 494470 |
rs503402 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448284 | GACACAATAAGGCCA[G/T]GGCACAAGAAGGCCA | 494470 |
rs512934 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443316 | aaaataaaataagat[A/T]aaataaagtggtatg | 494470 |
rs513845 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443233 | caaaaaacagacaca[A/C]attttaaaagaaaaa | 494470 |
rs513874 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443219 | aaattttaaaagaaa[A/G]acaacaaaatgacaa | 494470 |
rs516205 | snp | C/G | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461431 | gggcagatcacttga[C/G]atcaggagtttgaga | 494470 |
rs525531 | snp | C/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46450994 | TGAGAGGCCTTCCAT[C/G]TTCCCTCCTGGCCAC | 494470 |
rs530304 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443222 | cacaaattttaaaag[A/G]aaaacaacaaaatga | 494470 |
rs534006 | snp | C/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46453074 | TTGACACCACCAGCA[C/T]ATGGGTTAGGGAAAA | 494470 |
rs535750 | snp | G/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46445678 | tctccctgctcatgg[G/T]ctggaatgtgccttc | 494470 |
rs564978 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441768 | cccgagtagctggga[C/G]tacaggcgcccgcca | 494470 |
rs580082 | snp | G/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46443075 | acagagattgtcaac[G/T]gcaaaacaattgcca | 494470 |
rs693140 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442662 | tataaatgtctctta[C/G]atcaagttagtcgac | 494470 |
rs747575 | snp | C/G | 0.431769 | 0.17164 | intron-variant | RNF165 | GRCh38.p7 | 18:46345361 | CAGGTTGTCATCTGG[C/G]CTTCTCTCCCACCTC | 494470 |
rs753463 | snp | A/T | 0.484771 | 0.0859212 | intron-variant | RNF165 | GRCh38.p7 | 18:46438205 | TGTGGGATATTCCTG[A/T]GACCCCTTTAGACAC | 494470 |
rs753464 | snp | A/G | 0.124144 | 0.21601 | intron-variant | RNF165 | GRCh38.p7 | 18:46438296 | GCTAATTTCTCTTTG[A/G]GTCAGGTCCTGGTCA | 494470 |
rs920781 | snp | G/T | 0.448066 | 0.152544 | intron-variant | RNF165 | GRCh38.p7 | 18:46340784 | AGGTGCCTAGGATGT[G/T]CTAGACAGTTGCCCC | 494470 |
rs948596 | snp | A/T | 0.450231 | 0.149691 | intron-variant | RNF165 | GRCh38.p7 | 18:46346484 | TCGGCCCCCAAGAAG[A/T]CCCAGCAAACACAGC | 494470 |
rs1197784 | snp | C/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46446701 | TTTCTTTTTTTTTTT[C/T]ttttccttttttttt | 494470 |
rs1197949 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439857 | gcgacagagcgagac[G/T]ccgtctcaaaaaaac | 494470 |
rs1206885 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451773 | ctgttgtccaggcta[A/G]aatgcagtggtgcaa | 494470 |
rs1376080 | snp | A/G | 0.429688 | 0.173817 | intron-variant | RNF165 | GRCh38.p7 | 18:46450081 | ATTAATAAAGTGACA[A/G]CTAACCTTCAtggca | 494470 |
rs1470324 | snp | A/G | 0.499683 | 0.0125759 | intron-variant | RNF165 | GRCh38.p7 | 18:46378210 | AGCAAGTTTGAGGTC[A/G]TGGTGTCCAAAAGCA | 494470 |
rs1580009 | snp | A/C | 0.494855 | 0.0504572 | intron-variant | RNF165 | GRCh38.p7 | 18:46449691 | agaatgagtgccaag[A/C]gaatggggaggtccc | 494470 |
rs1668049 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445934 | aaaacagcctggatt[C/T]ttcaacaaatacatt | 494470 |
rs1788264 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445987 | gatttaaggggttgc[A/T]tttttgtgttgtcat | 494470 |
rs1788265 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446070 | ggcttgagtaaattc[A/G]ggttcaactcttatt | 494470 |
rs1893974 | snp | C/G/T | 0.139903 | 0.224452 | | | GRCh38.p7 | 18:46346840 | CTGACTGCCCAAGGG[C/G/T]CTGCTTTGCACTCCC | 494470 |
rs1964444 | snp | C/T | 0.493881 | 0.054972 | intron-variant | RNF165 | GRCh38.p7 | 18:46364356 | TAATGTTGTTAACTT[C/T]TGTGAATTTTTGACC | 494470 |
rs2000707 | snp | C/T | 0.317451 | 0.240729 | intron-variant | RNF165 | GRCh38.p7 | 18:46342682 | TCCCCTTCCTGAGGC[C/T]TTGAGCCCCAAGATG | 494470 |
rs2008211 | snp | C/T | 0.353371 | 0.227628 | intron-variant | RNF165 | GRCh38.p7 | 18:46341124 | CTCAGAGCACAACTC[C/T]AGGAGTTAAGCAGCA | 494470 |
rs2044221 | snp | A/G | 0.367091 | 0.220884 | intron-variant | RNF165 | GRCh38.p7 | 18:46379022 | GGCCTGGAGTAGGGA[A/G]GGAGCGGGGCACCAG | 494470 |
rs2053957 | snp | A/G | 0.464629 | 0.128197 | intron-variant | RNF165 | GRCh38.p7 | 18:46385481 | CAGTAGAGCCACGCT[A/G]GAAAAGCTCCTGGGT | 494470 |
rs2167198 | snp | A/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46438739 | CTTGGAGCCAGTTGG[A/T]TGCAAACTTAGAAAT | 494470 |
rs2364833 | snp | G/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333875 | GGNCTGACCCCTCCC[G/T]CGCGCCCCGCAGCGG | 494470 |
rs2364834 | snp | A/G | 0.203882 | 0.245709 | intron-variant | RNF165 | GRCh38.p7 | 18:46359327 | GAACGTGACAAAGGG[A/G]GTGTGCAGGCAGCTG | 494470 |
rs2364835 | snp | C/T | 0.497776 | 0.0332724 | intron-variant | RNF165 | GRCh38.p7 | 18:46360102 | CAGAATACCCTGAGA[C/T]GCATCACAAGTCCAT | 494470 |
rs2364836 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46384771 | ctgtaatcccagtgn[A/C/T]tttgggagaccgaag | 494470 |
rs2365331 | snp | G/T | 0.219947 | 0.248187 | intron-variant | RNF165 | GRCh38.p7 | 18:46402519 | TCTACATGTGTGTGT[G/T]TTTTTTTCTTTTCGA | 494470 |
rs2365332 | snp | A/G | 0.469346 | 0.119947 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461187 | ATGACAGACGTCCCA[A/G]TGACCTTGAGCAAGT | 494470 |
rs2365333 | snp | A/G | 0.463343 | 0.130326 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461432 | GGCAGATCACTTGAG[A/G]TCAGGAGTTTGAGAC | 494470 |
rs2365334 | snp | C/T | 0.463343 | 0.130326 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461519 | GCGTGGTGGTAGGCG[C/T]CTGTAATCCCAGCTA | 494470 |
rs2365335 | snp | C/G | 0.473266 | 0.112482 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461709 | AGGAGAAAAGGAGAG[C/G]AAAGAAGAAGAGAAG | 494470 |
rs2601041 | snp | G/T | | | | | GRCh38.p7 | 18:46389925 | gtagagacagggttt[G/T]gccatgttgcccagg | 494470 |
rs2601042 | snp | A/C | | | | | GRCh38.p7 | 18:46404980 | gctccgtttggctcc[A/C]aagtctctgttgttt | 494470 |
rs2601043 | snp | A/C | | | | | GRCh38.p7 | 18:46405048 | TGGCAAGACCCCACC[A/C]ATTTTTTTTTTGGTA | 494470 |
rs2601044 | snp | A/C | 0 | 0 | | | GRCh38.p7 | 18:46429716 | TTACAAATTCTTACC[A/C]AACTCTCTATCACAT | 494470 |
rs2852085 | snp | G/T | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389786 | caggctgcagtgcag[G/T]ggtgcaatcttggct | 494470 |
rs2852086 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389854 | ccacctcagcctccc[G/T]ggtagttgggactat | 494470 |
rs2852087 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389900 | tacccagctaagttt[G/T]gtattttttgtagag | 494470 |
rs2852088 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405045 | ATATGGCAAGACCCC[A/C]CCCATTTTTTTTTTG | 494470 |
rs2886191 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344329 | AGTGGAAGGGAAGGG[A/G]TNGGAGGCGCTCTCC | 494470 |
rs2886344 | snp | A/G | 0.420892 | 0.182472 | intron-variant | RNF165 | GRCh38.p7 | 18:46417717 | caatagaagtataac[A/G]taaggccgggagcgg | 494470 |
rs3220798 | microsatellite | (CA)20/21/22/23/24/25 | 0.5576 | 0.26408 | intron-variant | RNF165 | GRCh38.p7 | 18:46348901 | TATGCTTCTAGAAAT[(CA)20/21/22/23/24/25]GAAAGAGAGAGAGAG | 494470 |
rs3844039 | snp | A/G | 0.147321 | 0.227941 | intron-variant | RNF165 | GRCh38.p7 | 18:46424995 | ACAGGACAGCCGGCC[A/G]CAGGGCTGGAGAGGC | 494470 |
rs3850524 | snp | A/G | 0.497959 | 0.0318836 | intron-variant | RNF165 | GRCh38.p7 | 18:46364223 | CAGTGGCTCATGGCT[A/G]TAATCCCAGCACTTT | 494470 |
rs3850525 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | RNF165 | GRCh38.p7 | 18:46385431 | TGCAACACCTTCCTC[C/T]TCAGAATCCCTCCCT | 494470 |
rs3850526 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391469 | GGTTGCCGCTATTCC[A/C]CCCTCAGTGTCCTCA | 494470 |
rs3850527 | snp | G/T | 0.279991 | 0.248195 | intron-variant | RNF165 | GRCh38.p7 | 18:46425379 | CCGGGGCTACCCCAG[G/T]GATGATGGCCTTCTG | 494470 |
rs3861807 | snp | A/G | 0.490063 | 0.0697833 | intron-variant | RNF165 | GRCh38.p7 | 18:46419460 | CACTTCCTGTCTCTG[A/G]ACTTCAGCTTTCCAA | 494470 |
rs3861808 | snp | C/G | 0.4862 | 0.0819127 | intron-variant | RNF165 | GRCh38.p7 | 18:46422357 | ATGAAATCCGAATTT[C/G]TCCCAGGCTAGAAAA | 494470 |
rs3861809 | snp | A/G | 0.461037 | 0.134028 | intron-variant | RNF165 | GRCh38.p7 | 18:46428057 | AGCCCTCCCGCAGCC[A/G]TCCACACTGGTCTAC | 494470 |
rs3889358 | snp | G/T | 0.0629771 | 0.165899 | intron-variant | RNF165 | GRCh38.p7 | 18:46364857 | CAGCCGCCTGCTGAG[G/T]CCCCAAGCCTCCTGC | 494470 |
rs3889748 | snp | A/G | 0.146314 | 0.227484 | intron-variant | RNF165 | GRCh38.p7 | 18:46396786 | GCCCTGAGCTGTCCC[A/G]ACATAGGCGTGGTGC | 494470 |
rs3889942 | snp | C/T | 0.238749 | 0.249747 | intron-variant | RNF165 | GRCh38.p7 | 18:46426440 | GTGACCCACAAATGC[C/T]TGGGGACTGCTGGCT | 494470 |
rs3894151 | snp | A/G | 0.485049 | 0.0851591 | intron-variant | RNF165 | GRCh38.p7 | 18:46379740 | CTGAAGTCACATGTC[A/G]CTTTAGATTCAGAAA | 494470 |
rs3897684 | snp | A/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46364441 | AGTCGTAGAACACGC[A/T]TTCTAAAGTAACTGG | 494470 |
rs3902741 | snp | A/G | 0.108402 | 0.206034 | intron-variant | RNF165 | GRCh38.p7 | 18:46420892 | AGTAAATTAAAAGCA[A/G]AAAAGCAAATCTCCA | 494470 |
rs3911129 | snp | A/T | 0.472522 | 0.113946 | intron-variant | RNF165 | GRCh38.p7 | 18:46415599 | TCTCAATAAAGGGCC[A/T]AGTGCACCAGGGAGG | 494470 |
rs3911130 | snp | A/C | 0.381503 | 0.21262 | intron-variant | RNF165 | GRCh38.p7 | 18:46411566 | TCCGTGAGGCAGAAC[A/C]TCAGCTGTCCAGCTC | 494470 |
rs3911131 | snp | A/C | 0.495407 | 0.0477027 | intron-variant | RNF165 | GRCh38.p7 | 18:46411393 | AGCATACGTCCTATT[A/C]AGGATAGTCACATAG | 494470 |
rs3916035 | snp | A/C | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46422161 | TCAGAGATGAAGAAA[A/C]CGAAAGTGGGCCATC | 494470 |
rs3930378 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390129 | TATGCTCCTCTCCCT[C/T]TTCCTGACCTCCCCA | 494470 |
rs4020476 | in-del | -/GA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364745 | GCTCACATACTGATG[-/GA]NGNGGNTGGCCTTTT | 494470 |
rs4020477 | in-del | -/GA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364747 | CACATACTGATGGAN[-/GA]GGNTGGCCTTTTCTG | 494470 |
rs4101620 | snp | C/T | 0.251578 | 0.249995 | intron-variant | RNF165 | GRCh38.p7 | 18:46415508 | GACAGATCCTTGTTC[C/T]GTCGCCCAGGCTGGA | 494470 |
rs4286190 | snp | A/G | 0.194278 | 0.243711 | intron-variant | RNF165 | GRCh38.p7 | 18:46421998 | ATAGATAGAGAGGGA[A/G]GAAAGCAGACCCATG | 494470 |
rs4290554 | snp | A/G | 0.101658 | 0.201233 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460596 | TTACCTCATTTTGGC[A/G]TTGTTTCTGGGAGTG | 494470 |
rs4580283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374641 | CTTTGTGCTCTAATT[C/G]TTTGGTTTTTAAACT | 494470 |
rs4602126 | snp | C/T | 0.473634 | 0.111748 | intron-variant | RNF165 | GRCh38.p7 | 18:46368619 | ACAGCTCTATGGAGT[C/T]GAGTCTTAATCAGTT | 494470 |
rs4890325 | snp | A/G | 0.269267 | 0.249256 | intron-variant | RNF165 | GRCh38.p7 | 18:46413901 | CATGGATCCTTCCAG[A/G]AATCATCTGCATGTT | 494470 |
rs4890326 | snp | C/G | 0.491783 | 0.0635686 | intron-variant | RNF165 | GRCh38.p7 | 18:46427389 | CTCCTAATGAGGCTC[C/G]AGAGAAACCTGAAGG | 494470 |
rs4890327 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46428876 | acattataattctgt[C/T]ggacagtgctgGGTG | 494470 |
rs4890328 | snp | C/T | 0.492435 | 0.0610346 | intron-variant | RNF165 | GRCh38.p7 | 18:46452393 | caagcaattctccca[C/T]gtcagcctcccaagc | 494470 |
rs4890643 | snp | G/T | 0.331874 | 0.236213 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333162 | GAATTTGCAGGAGCC[G/T]CAGAGCCTGATGTTA | 494470 |
rs4890644 | snp | C/T | 0.454423 | 0.143914 | intron-variant | RNF165 | GRCh38.p7 | 18:46374408 | TGTCCCCATTAAACA[C/T]GAACTCCCCATTCTC | 494470 |
rs4890645 | snp | C/T | 0.47934 | 0.0995154 | intron-variant | RNF165 | GRCh38.p7 | 18:46380870 | CAGCCTTCCTTCCCA[C/T]GTCTCAGCACTGCAG | 494470 |
rs4890646 | snp | C/G | 0.479904 | 0.0982045 | intron-variant | RNF165 | GRCh38.p7 | 18:46381201 | GGCATTGGGATAAGG[C/G]CAGGCACTGCCTTTG | 494470 |
rs4890647 | snp | C/T | 0.357024 | 0.225933 | intron-variant | RNF165 | GRCh38.p7 | 18:46381315 | CCACAAGAGCAGGTT[C/T]AGCCGCAAGAAACAG | 494470 |
rs4890648 | snp | G/T | 0.480064 | 0.0978296 | intron-variant | RNF165 | GRCh38.p7 | 18:46403991 | GGATTCTACTGCCCT[G/T]TGTGATTAACAATTC | 494470 |
rs4890649 | snp | A/T | 0.479502 | 0.0991411 | intron-variant | RNF165 | GRCh38.p7 | 18:46403992 | GATTCTACTGCCCTG[A/T]GTGATTAACAATTCC | 494470 |
rs4890650 | snp | A/G | 0.489318 | 0.0722982 | intron-variant | RNF165 | GRCh38.p7 | 18:46417980 | ctgcactccagcctg[A/G]gcaacagagcaagac | 494470 |
rs4890651 | snp | C/T | 0.460365 | 0.13508 | intron-variant | RNF165 | GRCh38.p7 | 18:46419301 | TTGAGCCATCCTCCG[C/T]AGCCAGCCCTAGGCC | 494470 |
rs4890652 | snp | A/T | 0.124837 | 0.216412 | intron-variant | RNF165 | GRCh38.p7 | 18:46426973 | CATGGACCCAGATAT[A/T]CTATCCTGGGAGTTT | 494470 |
rs5824623 | in-del | -/G | 0.490007 | 0.0699769 | intron-variant | RNF165 | GRCh38.p7 | 18:46346443 | GCTCCCTTGGGTTTA[-/G]GGGCCTCCTCCCAGG | 494470 |
rs5824624 | in-del | -/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46374630 | TTATGCCTTCTCTTT[-/G]TGCTCTAATTCTTTG | 494470 |
rs5824625 | in-del | -/A | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46381831 | GCGAGACCCTGTCTC[-/A]AAAAAAAAAAAGATG | 494470 |
rs6507697 | snp | C/T | 0.434687 | 0.168495 | intron-variant | RNF165 | GRCh38.p7 | 18:46368322 | GTTGGTTTAAGCACT[C/T]ACTCTTCCCCCATTG | 494470 |
rs6507698 | snp | C/G | 0.434831 | 0.168337 | intron-variant | RNF165 | GRCh38.p7 | 18:46368324 | TGGTTTAAGCACTTA[C/G]TCTTCCCCCATTGCC | 494470 |
rs6507699 | snp | C/T | 0.350546 | 0.22889 | intron-variant | RNF165 | GRCh38.p7 | 18:46368384 | TCATCACCCTAAACC[C/T]CCAGAACCACTGGGT | 494470 |
rs6507700 | snp | A/G | 0.456803 | 0.140473 | intron-variant | RNF165 | GRCh38.p7 | 18:46382916 | CACCACCATGAGCTC[A/G]TGTAGTCCCATCCCC | 494470 |
rs6507701 | snp | C/T | 0.384976 | 0.210431 | intron-variant | RNF165 | GRCh38.p7 | 18:46382954 | ATGAAGACAACGTCA[C/T]ACTCTTCTTGGCATG | 494470 |
rs7229614 | snp | A/T | 0.297382 | 0.245469 | intron-variant | RNF165 | GRCh38.p7 | 18:46385932 | CATAAAATAAGGGGA[A/T]GGGGCTAGATGACCT | 494470 |
rs7229863 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | RNF165 | GRCh38.p7 | 18:46452761 | GTCAAGCCAAGGACC[A/G]TCTTCACTCCCTCAT | 494470 |
rs7230249 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46419539 | GAGCAGGCACAATCT[A/C]GGCCTGAGGGGCCTT | 494470 |
rs7231421 | snp | C/T | 0.221141 | 0.248329 | intron-variant | RNF165 | GRCh38.p7 | 18:46368580 | TTGGACCTTCTGAGG[C/T]AATTCAATTCTGTTC | 494470 |
rs7231582 | snp | C/T | 0.21875 | 0.248039 | intron-variant | RNF165 | GRCh38.p7 | 18:46368645 | CAGTTGCACAAGGCA[C/T]CATGAAGTGCTTACT | 494470 |
rs7232401 | snp | A/C | 0.110519 | 0.207473 | intron-variant | RNF165 | GRCh38.p7 | 18:46347599 | GTGAGTTTAATCCTC[A/C]TCTGGATTAAACGAG | 494470 |
rs7232751 | snp | C/T | 0.204189 | 0.245767 | intron-variant | RNF165 | GRCh38.p7 | 18:46368648 | TTGCACAAGGCACCA[C/T]GAAGTGCTTACTGTG | 494470 |
rs7232954 | snp | C/T | 0.496245 | 0.0431677 | intron-variant | RNF165 | GRCh38.p7 | 18:46435680 | GACAGGGATAGAAAA[C/T]ATTTCCCAGGCTCAG | 494470 |
rs7235217 | snp | A/G | 0.480539 | 0.0967035 | intron-variant | RNF165 | GRCh38.p7 | 18:46404462 | TCTCATTAAAACTCA[A/G]TGAAGTACTGACCAG | 494470 |
rs7235605 | snp | A/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46453455 | ACCAATGCTAAGAAT[A/T]AAAAGGGGAAATGGA | 494470 |
rs7236110 | snp | A/T | 0.356169 | 0.226336 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390122 | CTGCAAATATGCTCC[A/T]CTCCCTCTTCCTGAC | 494470 |
rs7236880 | snp | C/T | 0.101658 | 0.201233 | intron-variant | RNF165 | GRCh38.p7 | 18:46374907 | CCCTTGAGTCTGACA[C/T]TTGGTCTTGAGGGCC | 494470 |
rs7237941 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46353840 | CCTGGAGTTGGGAGA[G/T]GGAGTAGCGGGGCCT | 494470 |
rs7238416 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | RNF165 | GRCh38.p7 | 18:46401684 | TGCTTCAGGCTGCTC[A/G]TTAAGTGAACACAAA | 494470 |
rs7239205 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNF165 | GRCh38.p7 | 18:46445664 | gctctgcttagttct[C/T]tccctgctcatggtc | 494470 |
rs7239901 | snp | A/G | 0.485528 | 0.0838238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440011 | atttttgtattttta[A/G]tagagacagggtttc | 494470 |
rs7240808 | snp | A/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46405858 | ATTTTCTAGAATCAC[A/T]GGCAGGGAAGCCATC | 494470 |
rs7240896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46449135 | acaaaagagtattat[C/G]ctgattttaaagatt | 494470 |
rs7242055 | snp | G/T | 0.331874 | 0.236213 | intron-variant | RNF165 | GRCh38.p7 | 18:46375738 | CCCATGACAGGCAAG[G/T]TGGAGGAGATATTTT | 494470 |
rs7243450 | snp | C/T | 0.364817 | 0.222075 | intron-variant | RNF165 | GRCh38.p7 | 18:46379062 | GCCAGCATCTGTTCC[C/T]CAGAGTGTGTGGGTG | 494470 |
rs7243484 | snp | A/G | 0.382473 | 0.212016 | intron-variant | RNF165 | GRCh38.p7 | 18:46411148 | AATTTTGAGAGTTGA[A/G]TGAAGGGAGAGAGCC | 494470 |
rs7504568 | snp | G/T | 0.191461 | 0.24305 | intron-variant | RNF165 | GRCh38.p7 | 18:46424763 | GGAGAAGTCCATGGG[G/T]CTGTCCAGGTCTGAC | 494470 |
rs7506443 | snp | A/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46449021 | AAGCACCATCTCTTA[A/G]GAATAaagaagcaag | 494470 |
rs8084078 | snp | A/G | 0.146985 | 0.227789 | intron-variant | RNF165 | GRCh38.p7 | 18:46424180 | CTTGGAGGGCTCCCA[A/G]GGGAGTTAACATCTG | 494470 |
rs8084469 | snp | A/G | 0.109814 | 0.206997 | intron-variant | RNF165 | GRCh38.p7 | 18:46424202 | TAACATCTGCCCAGG[A/G]TAGTCAGGGTTGGAC | 494470 |
rs8084936 | snp | A/C | 0.336635 | 0.234509 | intron-variant | RNF165 | GRCh38.p7 | 18:46334475 | GCTTCCCCCCACCCC[A/C]TTTTAGGGGGACCCC | 494470 |
rs8085030 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46410164 | TCACATGACCTCAGG[A/G]CCCTGCTCTGGTCAG | 494470 |
rs8085058 | snp | C/T | 0.464203 | 0.128908 | intron-variant | RNF165 | GRCh38.p7 | 18:46393955 | CTGGTGGGGATCCTG[C/T]GGGATTCTGGAGGGA | 494470 |
rs8085800 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | RNF165 | GRCh38.p7 | 18:46380079 | GCTGTCGGGTTAAAC[G/T]TTTTAGAAACTGCCC | 494470 |
rs8085844 | snp | A/G | 0.114036 | 0.209795 | intron-variant | RNF165 | GRCh38.p7 | 18:46350831 | TACGGCCAATATTAT[A/G]TCTCTGACATAGAGA | 494470 |
rs8086767 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | RNF165 | GRCh38.p7 | 18:46368065 | ggattagaatcttgg[A/G]ttgggCTTGAGACTC | 494470 |
rs8088481 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | RNF165 | GRCh38.p7 | 18:46338625 | AATATCTTTTTTTTT[C/T]CCATAATTACACTGG | 494470 |
rs8089300 | snp | C/G | 0.495252 | 0.0484902 | intron-variant | RNF165 | GRCh38.p7 | 18:46365002 | CTCCCTCTGTGACAG[C/G]AGAAGAGTGAGGGGT | 494470 |
rs8091164 | snp | A/T | 0.0733688 | 0.176922 | intron-variant | RNF165 | GRCh38.p7 | 18:46374141 | CACACACGAGAAGAC[A/T]GGGGCCCAGGCAGCT | 494470 |
rs8091625 | snp | A/C | 0.472522 | 0.113946 | intron-variant | RNF165 | GRCh38.p7 | 18:46383721 | caccgcgcccggcta[A/C]ttttttgtattttta | 494470 |
rs8091740 | snp | C/T | 0.391769 | 0.205917 | intron-variant | RNF165 | GRCh38.p7 | 18:46383715 | agccaccaccgcgcc[C/T]ggctaattttttgta | 494470 |
rs8092525 | snp | A/G | 0.21695 | 0.247806 | intron-variant | RNF165 | GRCh38.p7 | 18:46362444 | GGGAGGAGTGTGTGC[A/G]CGCCCCAAGGGGTTT | 494470 |
rs8092672 | snp | C/T | 0.499759 | 0.0109798 | intron-variant | RNF165 | GRCh38.p7 | 18:46383655 | TGCCTCCAGGGTTCA[C/T]GCCATTCTCCTGCCT | 494470 |
rs8093368 | snp | G/T | 0.316968 | 0.240864 | intron-variant | RNF165 | GRCh38.p7 | 18:46341336 | GGGGGTGGGACAGGC[G/T]TGGGGGGTAGGGAGG | 494470 |
rs8093834 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46378484 | TTTTGCACCGCTTTC[G/T]GTAAGTCACCACCCA | 494470 |
rs8094043 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | RNF165 | GRCh38.p7 | 18:46366188 | tcccagctactcggg[A/G]ggctgaggcaggaga | 494470 |
rs8094224 | snp | A/G | 0.431916 | 0.171483 | intron-variant | RNF165 | GRCh38.p7 | 18:46445719 | ctagggaggttgcag[A/G]gctcacctcatgtgt | 494470 |
rs8094363 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RNF165 | GRCh38.p7 | 18:46445798 | aaacagagatttcat[A/G]tattctgttcagctt | 494470 |
rs8094423 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | RNF165 | GRCh38.p7 | 18:46366218 | actcgcttgaacccg[G/T]gaggtggaggttgaa | 494470 |
rs8094448 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | RNF165 | GRCh38.p7 | 18:46366351 | TCTTGTGATATAGGC[C/T]TAAGCCCTCTGGCAG | 494470 |
rs8096386 | snp | A/G | 0.490175 | 0.0693959 | intron-variant | RNF165 | GRCh38.p7 | 18:46442434 | ATTTAGAAGTTTATT[A/G]TTTAATTTTTGAAAA | 494470 |
rs8096701 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF165 | GRCh38.p7 | 18:46362947 | aatcagacagacccc[A/G]gggctcttgTGTGGA | 494470 |
rs8097148 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RNF165 | GRCh38.p7 | 18:46370746 | GGGTGGCAAGACCCA[A/G]TGGACAGTTGGGTTG | 494470 |
rs8097171 | snp | A/C | 0.246485 | 0.249975 | intron-variant | RNF165 | GRCh38.p7 | 18:46370824 | AGGCCAAGATCCTAC[A/C]AGCTGTTGGAACTCA | 494470 |
rs8098242 | snp | C/T | 0.369142 | 0.219784 | intron-variant | RNF165 | GRCh38.p7 | 18:46351000 | ATAAATCATGGCAGA[C/T]GCCAGCAGCGCTGAG | 494470 |
rs8098249 | snp | C/T | 0.496999 | 0.0386216 | intron-variant | RNF165 | GRCh38.p7 | 18:46351009 | GGCAGACGCCAGCAG[C/T]GCTGAGACCAGAGGG | 494470 |
rs8098272 | snp | A/G | 0.203575 | 0.245652 | intron-variant | RNF165 | GRCh38.p7 | 18:46358085 | ATCTTCAAAGACCCT[A/G]TTTCCAAATAAGGTC | 494470 |
rs8099095 | snp | C/T | 0.491987 | 0.0627894 | intron-variant | RNF165 | GRCh38.p7 | 18:46351614 | TCCGCTCATGAGGGG[C/T]ACATCAGGGGCTTTA | 494470 |
rs8099685 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397586 | tgtgtggtcatgctg[A/G]ggtgtgagggtgtgt | 494470 |
rs9635947 | snp | A/G | 0.319376 | 0.240181 | intron-variant | RNF165 | GRCh38.p7 | 18:46410941 | CTCCTGGGCACCAGT[A/G]TGTGTCAGGTGCTGG | 494470 |
rs9646520 | snp | A/T | 0.0603597 | 0.1629 | intron-variant | RNF165 | GRCh38.p7 | 18:46409374 | AATGAGCTCAAGGGA[A/T]CCTTTGAGGTTTGGC | 494470 |
rs9646545 | snp | A/G | 0.487746 | 0.0773096 | intron-variant | RNF165 | GRCh38.p7 | 18:46380236 | CCAGTCTCCTCTCCT[A/G]TGGCATCTGGCACAG | 494470 |
rs9946773 | snp | C/G | 0.210301 | 0.246828 | intron-variant | RNF165 | GRCh38.p7 | 18:46412134 | GCCCTGGGAATCAAA[C/G]CACAGCCCCCTCCCC | 494470 |
rs9947220 | snp | C/T | 0.382473 | 0.212016 | intron-variant | RNF165 | GRCh38.p7 | 18:46410816 | GCATCGTTTCTTCAA[C/T]TGTCCAGGCTCATGA | 494470 |
rs9947248 | snp | A/T | 0.186105 | 0.241697 | intron-variant | RNF165 | GRCh38.p7 | 18:46373488 | GCCTGCCTGGGTGCA[A/T]CCTGGGGAGCAGGTC | 494470 |
rs9949033 | snp | C/G | 0.408188 | 0.193589 | intron-variant | RNF165 | GRCh38.p7 | 18:46425312 | GGCTCTGGTCAGCTG[C/G]CAGGCCTGCAACAGG | 494470 |
rs9949861 | snp | A/C | 0.354019 | 0.227333 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390153 | CTCCCCACCCCAACC[A/C]CTGTGGGATGAGCCA | 494470 |
rs9950147 | snp | C/T | 0.251578 | 0.249995 | intron-variant | RNF165 | GRCh38.p7 | 18:46413259 | AGTTTTATAAAGCAG[C/T]GTCGCTCAAGCCCAG | 494470 |
rs9950561 | snp | A/G | 0.195837 | 0.244062 | intron-variant | RNF165 | GRCh38.p7 | 18:46360793 | TGTGGAATCCTACCT[A/G]GGTAGCACCAGGCAG | 494470 |
rs9950789 | snp | C/T | 0.474453 | 0.110094 | intron-variant | RNF165 | GRCh38.p7 | 18:46383824 | CCAAAGTGCTGGGAT[C/T]ACAGGCGTGAGCCAC | 494470 |
rs9951141 | snp | A/T | 0.483053 | 0.0904792 | intron-variant | RNF165 | GRCh38.p7 | 18:46348180 | GTGAGTCTTAAAGGA[A/T]CTGGTTGCCCAGGAA | 494470 |
rs9951417 | snp | A/G | 0.386123 | 0.209692 | intron-variant | RNF165 | GRCh38.p7 | 18:46408669 | GTTAATTAGAGCATC[A/G]TCTTGGTCAGAATTT | 494470 |
rs9951686 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | RNF165 | GRCh38.p7 | 18:46378802 | AGTTCTGGAGAGGAG[C/G]GCTGCTATGGATGGT | 494470 |
rs9952113 | snp | C/T | 0.368733 | 0.220005 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332801 | TAGATTCTTTCCAGC[C/T]CCACATACTGTGATT | 494470 |
rs9954074 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF165 | GRCh38.p7 | 18:46378981 | AAGGGACCTCACTGT[C/T]CCCAGGGCTCACCTG | 494470 |
rs9954097 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNF165 | GRCh38.p7 | 18:46379087 | TGGGTGTTGGGGGCA[A/G]TGAAGGAAAGGGAAG | 494470 |
rs9954165 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46379060 | CAGCCAGCATCTGTT[A/C]CTCAGAGTGTGTGGG | 494470 |
rs9954663 | snp | C/G | 0.194278 | 0.243711 | intron-variant | RNF165 | GRCh38.p7 | 18:46372194 | AAGTTCAGAGGCACT[C/G]AAGGGTCCTCCCTGG | 494470 |
rs9956758 | snp | A/C | 0.43598 | 0.167067 | intron-variant | RNF165 | GRCh38.p7 | 18:46355251 | AGCCACCGGGCCCGG[A/C]CTGTTTTAATATTTT | 494470 |
rs9957217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46355589 | GCCTATCTGAGGACC[A/G]CCTATTTTTCCAGAC | 494470 |
rs9957532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410360 | GCTGTGCCTGCAACT[A/G]TCATCATTCCAGCTT | 494470 |
rs9958049 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46380544 | AACTCTGACCCAGGC[A/G]CTTGCGTTTCCTCAG | 494470 |
rs9958239 | snp | A/G | 0.206029 | 0.246103 | intron-variant | RNF165 | GRCh38.p7 | 18:46431471 | tgcagagctcttcct[A/G]ggaccaatgattttc | 494470 |
rs9958625 | snp | G/T | 0.330714 | 0.236612 | intron-variant | RNF165 | GRCh38.p7 | 18:46334824 | TGTATTCATTTTTTG[G/T]TCATTAGTACCGATG | 494470 |
rs9961494 | snp | A/G | 0.182296 | 0.240658 | intron-variant | RNF165 | GRCh38.p7 | 18:46432447 | TATTCTCTGGGAATT[A/G]GGGCTCCATATGGAT | 494470 |
rs9962113 | snp | A/G | 0.496681 | 0.0405994 | intron-variant | RNF165 | GRCh38.p7 | 18:46369350 | TAAGGCTGAGCAGAG[A/G]GTGTTGTAGAATCCT | 494470 |
rs9962451 | snp | A/G | 0.409212 | 0.192748 | intron-variant | RNF165 | GRCh38.p7 | 18:46399736 | GAGGCAGAGGAGGAC[A/G]GTGTCCGGCCCGAGG | 494470 |
rs9963982 | snp | A/T | 0.395087 | 0.203592 | intron-variant | RNF165 | GRCh38.p7 | 18:46404956 | TGATACATGCAGAAG[A/T]CATATTCAGCTCCGT | 494470 |
rs9964835 | snp | A/T | 0.462144 | 0.132269 | intron-variant | RNF165 | GRCh38.p7 | 18:46345683 | CAATTTGGGGAAAAC[A/T]TGAAGTTTATATTAA | 494470 |
rs9965681 | snp | A/G | 0.479744 | 0.0985793 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458480 | CAATAAGACCGGGGT[A/G]AGGGGGACAGGATAC | 494470 |
rs9965822 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363305 | TTGGCTGCAGAGGAA[G/T]CAAAGGCCAGGTCTT | 494470 |
rs9965884 | snp | C/G | 0.0513262 | 0.151752 | intron-variant | RNF165 | GRCh38.p7 | 18:46430786 | gatccttcttcaaga[C/G]cttcctgttgttgca | 494470 |
rs9966500 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | RNF165 | GRCh38.p7 | 18:46402020 | GGTTGGACTGAACTT[C/T]CCCTTGGAGCCATCT | 494470 |
rs9966539 | snp | C/T | 0.210301 | 0.246828 | intron-variant | RNF165 | GRCh38.p7 | 18:46411179 | AGGGTAGAAAGGAAA[C/T]GACAGCCCCTTGGGG | 494470 |
rs9966774 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | RNF165 | GRCh38.p7 | 18:46411500 | TCCCCTTTGCTATCG[A/T]ttgattcatttcaac | 494470 |
rs9966943 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNF165 | GRCh38.p7 | 18:46381462 | GCTCTCAGGGACATC[C/T]GTTGAGTCCCTGTTT | 494470 |
rs9967509 | snp | C/T | 0.434687 | 0.168495 | intron-variant | RNF165 | GRCh38.p7 | 18:46345990 | TGGAACTCGGTTTCT[C/T]GACTCTGAGGGCTGG | 494470 |
rs10083921 | snp | C/T | 0.186737 | 0.241863 | intron-variant | RNF165 | GRCh38.p7 | 18:46373116 | TAGTAAATAGAGGGC[C/T]CTCTCATCCCTCTCA | 494470 |
rs10163727 | snp | C/T | 0.243919 | 0.249926 | intron-variant | RNF165 | GRCh38.p7 | 18:46362104 | ACTCATATGGGAGTG[C/T]AATGGGGTGCCCAAG | 494470 |
rs10438967 | snp | C/T | 0.499 | 0.0223418 | intron-variant | RNF165 | GRCh38.p7 | 18:46357304 | GCACTGCTCTAGCCA[C/T]GGCCTAGACTGTAGT | 494470 |
rs10541103 | in-del | -/AAAAAAAAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441872 | ATCTCAAAAAAAAAA[-/AAAAAAAAA]GAGGCCGGGCGCGGT | 494470 |
rs10555028 | in-del | -/AAT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375564 | AATAATAATAATAAT[-/AAT]AATAATAATAACTTG | 494470 |
rs10612548 | in-del | -/CCCA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355747 | CCCTCTATCTCTCCA[-/CCCA]TCATGTGCACACATG | 494470 |
rs10707136 | in-del | -/G | 0.315758 | 0.241197 | intron-variant | RNF165 | GRCh38.p7 | 18:46341320 | GGCTGAGGTCAGGGA[-/G]GGGGGTGGGACAGGC | 494470 |
rs10717970 | in-del | -/T | 0.438666 | 0.164028 | intron-variant | RNF165 | GRCh38.p7 | 18:46445903 | TACTTCTCCATATCC[-/T]TTTTTTTTTTTCTCC | 494470 |
rs10853542 | snp | C/T | 0.119281 | 0.213102 | intron-variant | RNF165 | GRCh38.p7 | 18:46446271 | CCCTTATTCATTTAT[C/T]AGCTGAAAAACTTTT | 494470 |
rs11082523 | snp | A/G | 0.466412 | 0.125164 | intron-variant | RNF165 | GRCh38.p7 | 18:46343888 | GCTAAACCTGGAAGC[A/G]CAGACACAGGGCTCC | 494470 |
rs11082524 | snp | G/T | 0.146985 | 0.227789 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391146 | TCGCCTCCATAAACA[G/T]GGTTCGCCACTTCGC | 494470 |
rs11082525 | snp | C/T | 0.0618563 | 0.164627 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439282 | CATTGCAGGGCAATG[C/T]GTAGCCAAACCCAGG | 494470 |
rs11082526 | snp | A/C | 0.206642 | 0.246211 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460910 | CACTTGGCACCCCCC[A/C]GCCCCCACCACAACC | 494470 |
rs11306231 | in-del | -/A | 0.403334 | 0.197456 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336385 | CTCACCCCCCCCAAC[-/A]AAAAAAAATCCAACA | 494470 |
rs11369500 | in-del | -/A | 0.352721 | 0.227922 | intron-variant | RNF165 | GRCh38.p7 | 18:46341206 | TCTGAAGGCCTCTGG[-/A]AGAGTTTGGACTGGC | 494470 |
rs11413245 | in-del | -/A/AA | 0.477345 | 0.103991 | intron-variant | RNF165 | GRCh38.p7 | 18:46442162 | CAAAAAAAAAAAAAA[-/A/AA]GAAAAAGAAAATAGC | 494470 |
rs11659512 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | RNF165 | GRCh38.p7 | 18:46394174 | GGGTCCCCTGCCGAG[A/G]GACAGAATTTACACA | 494470 |
rs11659712 | snp | A/C | 0 | 0 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389215 | TTCACCTCTGAAGGA[A/C]CCAAGAAAGTTAAGT | 494470 |
rs11659834 | snp | A/C | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46412366 | CCCAGAGGGTTACCA[A/C]TAAGCCTGCAGGCAA | 494470 |
rs11660340 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460060 | GGCCAGGACCCCCTT[C/T]GGCACCCAGTTGCCC | 494470 |
rs11660808 | snp | A/G | 0.352287 | 0.228117 | intron-variant | RNF165 | GRCh38.p7 | 18:46383694 | cgagtagctgggact[A/G]caggcagccaccacc | 494470 |
rs11661206 | snp | G/T | 0.453209 | 0.145623 | intron-variant | RNF165 | GRCh38.p7 | 18:46348821 | TCCCTGGTAAGTCCT[G/T]CAACCAAGAGAGCCC | 494470 |
rs11661226 | snp | C/G | 0.375 | 0.216506 | intron-variant | RNF165 | GRCh38.p7 | 18:46341608 | GAGTTGAGACTTCTA[C/G]TCCTTTACATACAGA | 494470 |
rs11661320 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366294 | cagaactctggctca[A/C]aaaaaaaaaaaaaaa | 494470 |
rs11661527 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | RNF165 | GRCh38.p7 | 18:46396884 | TTGGGTGGATTTTCC[A/G]CTAATTGTCCAACTG | 494470 |
rs11663834 | snp | G/T | 0.470811 | 0.117228 | intron-variant | RNF165 | GRCh38.p7 | 18:46365041 | TCTGGGAGTTCCCTT[G/T]CTTCTAATGCCCTAT | 494470 |
rs11663963 | snp | A/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46365489 | GACTTTCTCATTTTG[A/T]GATCTTGAAtttttt | 494470 |
rs11664652 | snp | C/T | 0.444444 | 0.157135 | intron-variant | RNF165 | GRCh38.p7 | 18:46348909 | CTCTTTCTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 494470 |
rs11665153 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442228 | tttatttcactgatt[G/T]atttcactgatttct | 494470 |
rs11665226 | snp | A/C | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46363836 | GAATTCATAGGGGCC[A/C]CCGTTGAGGGTGTGA | 494470 |
rs11872683 | snp | A/G | 0.479984 | 0.0980171 | intron-variant | RNF165 | GRCh38.p7 | 18:46382021 | CCCCACAGCAGTGCC[A/G]GGAGATGGAACTTTG | 494470 |
rs11873913 | snp | C/T | 0.186737 | 0.241863 | intron-variant | RNF165 | GRCh38.p7 | 18:46436175 | AGTTCACTGAATATT[C/T]AGAGGTAAAAGGCAT | 494470 |
rs11874510 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | RNF165 | GRCh38.p7 | 18:46442267 | ttttattatttcctc[C/G]cttctacttatttgg | 494470 |
rs11874989 | snp | C/T | 0.375797 | 0.216044 | intron-variant | RNF165 | GRCh38.p7 | 18:46367253 | ATCCTGGCTGTCATA[C/T]CTGGCTTTCCAGGTA | 494470 |
rs11877737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442348 | tctaatataagcata[C/T]aaaactgaatttttc | 494470 |
rs11877799 | snp | C/T | 0.11963 | 0.213316 | intron-variant | RNF165 | GRCh38.p7 | 18:46442541 | attctaatcctttta[C/T]atttattgagacttg | 494470 |
rs12172855 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46355875 | GCCCTGCCATGTTGG[A/G]TATGTGACTGCCGTG | 494470 |
rs12373204 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNF165 | GRCh38.p7 | 18:46364201 | gatctgcaagcctca[A/G]cctcccaaagtgctg | 494470 |
rs12454111 | snp | G/T | 0.362104 | 0.223456 | intron-variant | RNF165 | GRCh38.p7 | 18:46367702 | CCAAACTGGCCTCGG[G/T]GTCCCCACCAGTAGC | 494470 |
rs12454466 | snp | A/G | 0.451109 | 0.148509 | intron-variant | RNF165 | GRCh38.p7 | 18:46447230 | GTCTTTCCATTACTC[A/G]GTGCCTCTGGCTTGC | 494470 |
rs12456260 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | RNF165 | GRCh38.p7 | 18:46340728 | ATGAAACCTACCTGA[C/T]AGGCTATGTCTAAGC | 494470 |
rs12456872 | snp | G/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46452071 | atcatactctaacgg[G/T]ggatacatgacatta | 494470 |
rs12457799 | snp | C/T | 0.342134 | 0.232404 | intron-variant | RNF165 | GRCh38.p7 | 18:46392099 | CATACACACACACCA[C/T]GCATACACACACTGT | 494470 |
rs12458834 | snp | C/G | 0.479984 | 0.0980171 | intron-variant | RNF165 | GRCh38.p7 | 18:46381448 | ATTGCTCACCCAGTG[C/G]TCTCAGGGACATCCG | 494470 |
rs12604347 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF165 | GRCh38.p7 | 18:46424565 | GCTCTAGGACCCTGG[C/T]GGCGGTACAACACTG | 494470 |
rs12604630 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF165 | GRCh38.p7 | 18:46352707 | ACAGCACtgcacaag[C/T]cacccccactcacac | 494470 |
rs12604983 | snp | G/T | 0.472335 | 0.114312 | intron-variant | RNF165 | GRCh38.p7 | 18:46416465 | CAATACAGGGACTTT[G/T]CTCTTTAAGCATTCA | 494470 |
rs12605122 | snp | C/G | 0.377187 | 0.215229 | intron-variant | RNF165 | GRCh38.p7 | 18:46360010 | AATGGGAGGAAGAAG[C/G]ATATTGGGAGACATC | 494470 |
rs12606026 | snp | A/C | 0.273049 | 0.248935 | intron-variant | RNF165 | GRCh38.p7 | 18:46409892 | TCTTTTGTACTTACC[A/C]GCCATAGAGCACATT | 494470 |
rs12606614 | snp | G/T | 0.31503 | 0.241394 | intron-variant | RNF165 | GRCh38.p7 | 18:46373188 | CTAGGCCCTGCCAGG[G/T]TGTCATCTCCTTCAT | 494470 |
rs12607113 | snp | A/G | 0.465263 | 0.127129 | intron-variant | RNF165 | GRCh38.p7 | 18:46416906 | gcctaagccagtcac[A/G]tggccatgcccagag | 494470 |
rs12607371 | snp | C/T | 0.266819 | 0.249434 | intron-variant | RNF165 | GRCh38.p7 | 18:46392011 | CCACACATATGCACA[C/T]AACACACACACCTTA | 494470 |
rs12607419 | snp | A/C | 0.361053 | 0.22398 | intron-variant | RNF165 | GRCh38.p7 | 18:46422305 | TCCCAAGCACCCTGC[A/C]TCTGAATGACTCACA | 494470 |
rs12607460 | snp | G/T | 0.376989 | 0.215346 | intron-variant | RNF165 | GRCh38.p7 | 18:46420632 | GGTGGATCACCTGAG[G/T]TCAGGAGTTCGAGAC | 494470 |
rs12607488 | snp | C/G | 0.362732 | 0.22314 | intron-variant | RNF165 | GRCh38.p7 | 18:46422458 | GAGAGGAGGCTCCCT[C/G]GGGGCCATGTTGAGT | 494470 |
rs12607970 | snp | G/T | 0.271162 | 0.249103 | intron-variant | RNF165 | GRCh38.p7 | 18:46396922 | TCAGTCACATCCAGC[G/T]GTGCCTGGGCAGCCT | 494470 |
rs12608433 | snp | G/T | 0.282632 | 0.247861 | intron-variant | RNF165 | GRCh38.p7 | 18:46397120 | CCAGGCTTGGTGTTG[G/T]CTGGGAGGGCCCTGC | 494470 |
rs12953606 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455844 | agtctcaaaaacaaa[A/C]caaaacaaacaaaaa | 494470 |
rs12953609 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455853 | aacaaaacaaaacaa[A/C]caaaaaaagaaACTT | 494470 |
rs12956271 | snp | C/G | 0.333261 | 0.235728 | intron-variant | RNF165 | GRCh38.p7 | 18:46394855 | TTTTATTACAGGCTA[C/G]TTCTTTGAAAATAGA | 494470 |
rs12956369 | snp | A/G | 0.231482 | 0.249313 | intron-variant | RNF165 | GRCh38.p7 | 18:46403373 | GCTCTCCCTGCCCCC[A/G]GAGAGAGCCCTCCCT | 494470 |
rs12957205 | snp | A/G | 0.283684 | 0.24772 | intron-variant | RNF165 | GRCh38.p7 | 18:46428078 | CGGGAGGGCTTGGAG[A/G]GGGTCTGTGGGAAAC | 494470 |
rs12957997 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338468 | CTGCTTCATCTACGG[C/G]CCTAGGGCCTCTCTT | 494470 |
rs12958001 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338481 | GGCCCTAGGGCCTCT[C/T]TTAAGAGAAAGACAG | 494470 |
rs12958258 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338488 | GGGCCTCTCTTAAGA[A/G]AAAGACAGCTAAGAT | 494470 |
rs12958723 | snp | C/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46391884 | aacccatatacacag[C/G]atgcacacatactac | 494470 |
rs12959457 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391635 | CTGAGCTGTTCTGCT[A/T]GGTTTGGTGACATAT | 494470 |
rs12959629 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391742 | TCACCCTTCCCAAGA[G/T]CTGTGCcacaaacac | 494470 |
rs12962139 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | RNF165 | GRCh38.p7 | 18:46448288 | CTTCTTGTGCCCTGG[A/C/G]CTTCTTGTGTCCTGG | 494470 |
rs12962350 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441200 | gtcttgctatgttgc[A/C]taggctgatcctcta | 494470 |
rs12963221 | snp | A/G | 0.257732 | 0.24988 | intron-variant | RNF165 | GRCh38.p7 | 18:46407972 | GGAAGCCTTCCTGGG[A/G]GAGGTGGCATAGCAG | 494470 |
rs12965332 | snp | C/G | 0.238171 | 0.24972 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387635 | AGAAGTCCAGAGCTG[C/G]GCATACAGACCCGTG | 494470 |
rs12966506 | snp | A/G | 0.48955 | 0.071525 | intron-variant | RNF165 | GRCh38.p7 | 18:46433007 | CTCCATCAGGTACAC[A/G]CACACAGCCTTCACC | 494470 |
rs12968253 | snp | C/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46393364 | CCAGGCCCTGCCTGA[C/T]AGGCAGACACCTTCC | 494470 |
rs12968582 | snp | C/T | 0.448708 | 0.151707 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458594 | GGTAAAAGTAACAGG[C/T]GGGCAGATTTTGGCT | 494470 |
rs12968635 | snp | C/T | 0.462582 | 0.131564 | intron-variant | RNF165 | GRCh38.p7 | 18:46384515 | TTCCTTGAATATTTC[C/T]CATGGATACACACCC | 494470 |
rs12969932 | snp | A/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333590 | CCCTTGTGCCCGCAG[A/T]CAGGCTCTACACGTG | 494470 |
rs12970465 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446671 | gcgagactccatctc[A/C]aaaaaaaaaaaaaaa | 494470 |
rs13381678 | snp | C/T | 0.190519 | 0.242821 | intron-variant | RNF165 | GRCh38.p7 | 18:46374083 | TTGTCATCCCTGTCC[C/T]CCACCTCCCCTCCCC | 494470 |
rs16978542 | snp | G/T | 0.0584853 | 0.160693 | intron-variant | RNF165 | GRCh38.p7 | 18:46341595 | TGGCAACGTCTGGGA[G/T]TTGAGACTTCTAGTC | 494470 |
rs16978543 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | RNF165 | GRCh38.p7 | 18:46342319 | GACCAAGGCAAGAAT[A/G]AGAAAGGAATACCTG | 494470 |
rs16978544 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | RNF165 | GRCh38.p7 | 18:46342514 | CATGGTGGACCAGAA[A/T]CTCTCCAGAGTGGGA | 494470 |
rs16978545 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | RNF165 | GRCh38.p7 | 18:46347857 | GATAGTGAGGCTCAG[A/G]TTTGATCATGGATTT | 494470 |
rs16978546 | snp | C/G | 0.110167 | 0.207236 | intron-variant | RNF165 | GRCh38.p7 | 18:46348073 | AACAGACAGACGCAG[C/G]AACAGCATGGCCCTA | 494470 |
rs16978547 | snp | C/T | 0.21845 | 0.248001 | intron-variant | RNF165 | GRCh38.p7 | 18:46358344 | CCTAGTGTGAGGAAG[C/T]GAACGAGTGAAGGAC | 494470 |
rs16978548 | snp | C/T | 0.25214 | 0.249991 | intron-variant | RNF165 | GRCh38.p7 | 18:46366874 | CAGCAAACAAAACAG[C/T]CTTGGAGAGCAAAAA | 494470 |
rs16978549 | snp | A/G | 0.495521 | 0.0471118 | intron-variant | RNF165 | GRCh38.p7 | 18:46369017 | GTTATTTAATCATGT[A/G]GTTTAAGTGTTACTC | 494470 |
rs16978550 | snp | G/T | 0.021333 | 0.101051 | intron-variant | RNF165 | GRCh38.p7 | 18:46376425 | CTAGTTTTGAACTTT[G/T]TTCCTGGCAGGTGGA | 494470 |
rs16978551 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | RNF165 | GRCh38.p7 | 18:46377451 | CTGTGTGGAGCATCC[A/C]GAGAACCCACAGGAA | 494470 |
rs16978552 | snp | C/T | 0.264358 | 0.249587 | intron-variant | RNF165 | GRCh38.p7 | 18:46378188 | ATTTATCAATTTATA[C/T]TGGGGAAGCAAGTTT | 494470 |
rs16978553 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | RNF165 | GRCh38.p7 | 18:46378548 | CCAGAGGTGTCAGAT[A/G]ATCCCTCCATTTGAT | 494470 |
rs16978554 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | RNF165 | GRCh38.p7 | 18:46379969 | TAAATGGAACTGGAA[C/T]GTCAGAGAAGAGATG | 494470 |
rs16978555 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RNF165 | GRCh38.p7 | 18:46394954 | TGTGGGGCTTTGCTC[C/T]GAATGTGCTATAATG | 494470 |
rs16978556 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RNF165 | GRCh38.p7 | 18:46395635 | AGTCCGGGATTTTAC[C/T]ATAATTCCTGCTGCA | 494470 |
rs16978558 | snp | C/T | 0.241627 | 0.24986 | intron-variant | RNF165 | GRCh38.p7 | 18:46400113 | CTTGGCTTCATTTCT[C/T]CTGGCGGGTGTCCTG | 494470 |
rs16978559 | snp | C/T | 0.228547 | 0.249078 | intron-variant | RNF165 | GRCh38.p7 | 18:46402268 | TGAGCAGGTATTATA[C/T]ACTATGTGCTAGAAT | 494470 |
rs16978560 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | RNF165 | GRCh38.p7 | 18:46404080 | TTTGTCAAGGTGTTT[C/T]TACATTCCCATGGAA | 494470 |
rs16978561 | snp | C/T | 0.157642 | 0.232314 | intron-variant | RNF165 | GRCh38.p7 | 18:46405741 | GCCATCCAGGATGGG[C/T]TGAATATGATGTCTA | 494470 |
rs16978562 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | RNF165 | GRCh38.p7 | 18:46429216 | TGCAGTCAGGCAGAA[A/G]TTCTTTGGATTTTCA | 494470 |
rs16978563 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNF165 | GRCh38.p7 | 18:46454431 | GCCATGACAATTATA[C/T]GGGACTATGGATGTA | 494470 |
rs16978564 | snp | C/T | 0.0252325 | 0.109451 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457135 | CGCTATTACCGAATT[C/T]GCACCAAATATTTCT | 494470 |
rs17760907 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | RNF165 | GRCh38.p7 | 18:46408492 | TTCCAGGTCTAACCC[A/G]TTAAAACCCACCAGC | 494470 |
rs17766830 | snp | C/T | 0.323197 | 0.239044 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460697 | GCAAACTTTATTTCG[C/T]CCGAACTATCAGGGT | 494470 |
rs28367364 | snp | C/T | 0.212425 | 0.24716 | intron-variant | RNF165 | GRCh38.p7 | 18:46405952 | AGGCATGTGCACACA[C/T]GTGTACACCCTACAC | 494470 |
rs28463123 | snp | A/C/T | 0.0861826 | 0.188849 | intron-variant | RNF165 | GRCh38.p7 | 18:46385020 | CTCTGTTCCCTCCCC[A/C/T]TCAAAGATTTCCAGA | 494470 |
rs28488658 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | RNF165 | GRCh38.p7 | 18:46392003 | CACACATACCACACA[C/T]ATGCACACAACACAC | 494470 |
rs28546352 | snp | C/G | 0.205417 | 0.245993 | intron-variant | RNF165 | GRCh38.p7 | 18:46370381 | AGCAGGGAAATCAGT[C/G]TGCAGAGCTTGTGTC | 494470 |
rs28591220 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | RNF165 | GRCh38.p7 | 18:46453858 | GGGCTGGGCACACTG[A/G]CTCATGCACTCTGGG | 494470 |
rs28592287 | snp | C/T | 0.106278 | 0.204558 | intron-variant | RNF165 | GRCh38.p7 | 18:46418868 | TCAGCACCTCCGTGG[C/T]TTTCCATTCTCTCTG | 494470 |
rs28625493 | snp | C/T | 0.0894459 | 0.191631 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388372 | TTCAACTTTATAATG[C/T]TTCCATGCACTTCTT | 494470 |
rs28642302 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | RNF165 | GRCh38.p7 | 18:46402990 | AGCCTTTCTGAGCCA[C/T]GTCTGTGGCTCCTGT | 494470 |
rs28657556 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335883 | TTTTTTTCTTCATTG[C/T]GTAGCTCAGTGAATG | 494470 |
rs28688425 | snp | A/G | 0.210301 | 0.246828 | intron-variant | RNF165 | GRCh38.p7 | 18:46405565 | GAGAGAGAGGGCGAA[A/G]GAGACAGCGCAAGAG | 494470 |
rs28689134 | snp | A/C | 0.0995161 | 0.199636 | intron-variant | RNF165 | GRCh38.p7 | 18:46405145 | ATGTCTATGGTGTAC[A/C]GTGTGGCATACTGGT | 494470 |
rs28700072 | snp | A/G | 0.089084 | 0.191327 | intron-variant | RNF165 | GRCh38.p7 | 18:46384735 | AAAATGGCCCATCAT[A/G]GCCAAGCACAGTGGC | 494470 |
rs28703931 | snp | C/T | 0.212425 | 0.24716 | intron-variant | RNF165 | GRCh38.p7 | 18:46406242 | TTGCATTGAACCCCC[C/T]TCTCAACCTCCCCAG | 494470 |
rs28708509 | snp | C/T | 0.210301 | 0.246828 | intron-variant | RNF165 | GRCh38.p7 | 18:46405263 | AGCTCTGAGGGCTCC[C/T]CAGAAATAGTAGAGT | 494470 |
rs33913588 | in-del | -/A | 0.430434 | 0.173042 | intron-variant | RNF165 | GRCh38.p7 | 18:46439705 | ATAAACTTTTTTATT[-/A]AAAAAAACCCTTTTT | 494470 |
rs34000306 | in-del | -/TTTC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334813 | ATGTGTGTTTTGTAT[-/TTTC]TCATTTTTTGTTCAT | 494470 |
rs34013022 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444454 | GTCTTTTTCTGATGG[G/T]GTGCTTCATTTTGGA | 494470 |
rs34026934 | snp | C/T | 0.318896 | 0.240319 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391400 | AGGCGAGGCCTAGTA[C/T]GGGGCTGGGCTCACT | 494470 |
rs34046291 | snp | A/T | 0.243633 | 0.249919 | intron-variant | RNF165 | GRCh38.p7 | 18:46415547 | AATAAAAAAAATAAA[A/T]AAATAAATAAAAATA | 494470 |
rs34058917 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342723 | TTGCATTTTTTCTTA[A/G]AAATTCTTGAAGCCT | 494470 |
rs34139708 | snp | A/G | 0.229136 | 0.249128 | intron-variant | RNF165 | GRCh38.p7 | 18:46397201 | TTAGGTAGATGTCAT[A/G]CCTCTCTCTCTTCCC | 494470 |
rs34158553 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344816 | GGTGTGTGTGTCCCC[A/T]ACCTCTGTGCTGAGG | 494470 |
rs34223668 | snp | C/G | 0.375 | 0.216506 | intron-variant | RNF165 | GRCh38.p7 | 18:46420963 | ACTCATGACCTAAGA[C/G]GAACTCTACATGGTT | 494470 |
rs34226090 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422728 | ATCTCCTGGTGGGCC[-/A]AAAAGGGCCCTGGAA | 494470 |
rs34229367 | snp | C/T | 0.472052 | 0.11486 | intron-variant | RNF165 | GRCh38.p7 | 18:46416227 | TCTAGGAAGTCAAAG[C/T]TCAACTATAAACTCT | 494470 |
rs34271155 | snp | A/G | 0.281577 | 0.247998 | intron-variant | RNF165 | GRCh38.p7 | 18:46415617 | CCCTTTATTGAGAAC[A/G]TGTTTTGGTGGTGCT | 494470 |
rs34311565 | snp | A/C | 0.270621 | 0.249148 | intron-variant | RNF165 | GRCh38.p7 | 18:46395410 | GGCAGCATTCCTGGC[A/C]CCTCCCCACTAGATG | 494470 |
rs34358447 | in-del | -/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457932 | GCTAGGTTTGGGAGG[-/C]CCCTCAGCTTGGTTT | 494470 |
rs34430605 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375319 | CACTTTGGGAGGCCG[-/A]AAGTGGGTGGGTCAC | 494470 |
rs34463229 | in-del | -/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460488 | ACTTGTAGATATCGT[-/G]GGGTTCTTATTTAAT | 494470 |
rs34472213 | snp | A/C | 0.229136 | 0.249128 | intron-variant | RNF165 | GRCh38.p7 | 18:46403172 | GTCTGTGCTTCCAGG[A/C]CATTGGAATCTTGTG | 494470 |
rs34493341 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344776 | GGACTTGGGCCCAAA[-/T]GAACTGGTCCTCGCA | 494470 |
rs34521340 | in-del | -/GT | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46335045 | TGTGTGTGTGTGTGT[-/GT]CTGTATGTGTGTGTG | 494470 |
rs34543105 | snp | A/G | 0.4021 | 0.198407 | intron-variant | RNF165 | GRCh38.p7 | 18:46402509 | AACTGGGCTTTCTAC[A/G]TGTGTGTGTTTTTTT | 494470 |
rs34554777 | in-del | -/A | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457939 | TGGGAGGCCCCTCAG[-/A]CTTGGTTTGGGAGTG | 494470 |
rs34611350 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46343103 | AAAATGCCATAGGTT[C/T]TAGGCCGCTTGGTGC | 494470 |
rs34650515 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357758 | TGTGGCTGCTGTGAC[-/A]AAAATAGCACACGCT | 494470 |
rs34656919 | snp | A/G | 0.228253 | 0.249052 | intron-variant | RNF165 | GRCh38.p7 | 18:46402620 | ATCCTCCCATCAGCA[A/G]CCTCCCAAGTTGCTG | 494470 |
rs34661771 | in-del | -/TAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375554 | GTGAGACTCTGTCTC[-/TAA]TAATAATAATAATAA | 494470 |
rs34725545 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370369 | CCAAAATTAGAAGCA[-/G]GGGAAATCAGTGTGC | 494470 |
rs34775648 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344817 | TGTGTGTGTCCCCAA[-/G]CCTCTGTGCTGAGGA | 494470 |
rs34807673 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412525 | ACTGAGTGCAGCCCA[-/G]GGTAGTGGGAGGAGA | 494470 |
rs34811585 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453656 | ATAAAGAAGAAAAAC[A/C]CCTTAAAAATTTAAA | 494470 |
rs34836612 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345545 | TGCACAGGTGCACCT[-/G]GGGGAGCATCTGGCT | 494470 |
rs34849876 | multinucleotide-polymorphism | AA/GG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344774 | GGGGGACTTGGGCCC[AA/GG]AGAACTGGTCCTCGC | 494470 |
rs34863608 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414855 | GCCATTTCACCCCTA[-/G]GAAACATTTTCATTT | 494470 |
rs34875920 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338872 | CTGGGCTGACTGACT[-/C]CCCCGGCTCACCCTG | 494470 |
rs34909923 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364444 | CGTAGAACACGCATT[A/C]TAAAGTAACTGGAAA | 494470 |
rs34913649 | in-del | -/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389568 | GTCAGGGGCAACCGT[-/G]GGGGGTGGATTATTA | 494470 |
rs34921335 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403384 | CCCGGAGAGAGCCCT[-/C]CCCTGCCCCCCGTCT | 494470 |
rs34953839 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378047 | TCTTGGCAACTGCTG[-/A]AGTTGCAGACATTGA | 494470 |
rs34956061 | in-del | -/A | 0.262435 | 0.249691 | intron-variant | RNF165 | GRCh38.p7 | 18:46418000 | CAGAGCAAGACTCTT[-/A]AAAAAAAAAAGTATA | 494470 |
rs34960770 | snp | C/G | 0.219349 | 0.248114 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391175 | GCAATTCATCACTTA[C/G]AGTTTACAGGTCACA | 494470 |
rs34961062 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405505 | AGTGGTGGGTGGGAG[-/T]TGGCTGTTGGCGATG | 494470 |
rs34996956 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370042 | TCTTGCTGCCTGTGG[-/C]CCCCCTCAATGTGAA | 494470 |
rs35017625 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377128 | CTCCAATCAGCACAT[-/G]GGCCTGACCTTGGAT | 494470 |
rs35025356 | snp | G/T | 0.24134 | 0.24985 | intron-variant | RNF165 | GRCh38.p7 | 18:46400932 | CTTTGACTGGGCAGG[G/T]GGAAGTGGTGGGAGA | 494470 |
rs35044751 | snp | C/T | 0.228253 | 0.249052 | intron-variant | RNF165 | GRCh38.p7 | 18:46402626 | CCATCAGCAACCTCC[C/T]AAGTTGCTGGGACCA | 494470 |
rs35078704 | snp | G/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460488 | AACTTGTAGATATCG[G/T]GGGTTCTTATTTAAT | 494470 |
rs35081404 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370472 | TAGGGGGACCCTGCT[-/C]CCCCAGTCAGGGTCT | 494470 |
rs35085822 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408697 | TTGAAGGGTTGCTGG[-/C]AACAGTCCGAGGTCA | 494470 |
rs35094317 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344789 | AAGAACTGGTCCTCG[-/T]CATGGCCCAGAGGTG | 494470 |
rs35178576 | snp | A/G | 0.472429 | 0.114129 | intron-variant | RNF165 | GRCh38.p7 | 18:46415117 | GGAGTCCCTGTGTCA[A/G]TCCAGAGTGTCCCCT | 494470 |
rs35294254 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408565 | TTATCAGCCTGCTGC[-/G]GGGGAGGAAGAGAGC | 494470 |
rs35308870 | snp | A/G | 0.372391 | 0.217992 | intron-variant | RNF165 | GRCh38.p7 | 18:46420023 | TGAGCAGTGATGGTT[A/G]GGAATCTAATTTTAC | 494470 |
rs35398939 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394146 | AAGTGACTAGGGATG[-/T]ATGAGACAGATGGGG | 494470 |
rs35412526 | in-del | -/CCAC | 0.496874 | 0.0394129 | intron-variant | RNF165 | GRCh38.p7 | 18:46355744 | CTCCCCTCTATCTCT[-/CCAC]CCATCATGTGCACAC | 494470 |
rs35423080 | in-del | -/TGTG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348901 | CTCTCTCTCTCTTTC[-/TGTG]TGTGTGTGTGTGTGT | 494470 |
rs35449079 | in-del | -/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460053 | TCCACCTGGCCAGGA[-/C]CCCCTTCGGCACCCA | 494470 |
rs35467767 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364489 | GGGCTCCCCAGAGAA[-/C]CCTTCGTGATGCCGA | 494470 |
rs35518422 | in-del | -/A | 0.49645 | 0.0419827 | intron-variant | RNF165 | GRCh38.p7 | 18:46364406 | TGGTCTAAGAAACTT[-/A]AAAAAAAAAAAAGCT | 494470 |
rs35572825 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344833 | CCTCTGTGCTGAGGA[C/G]AGAGACAGCGGAGGT | 494470 |
rs35576376 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421477 | AGGCTCTGCCTTCAT[-/G]GGAGTGTACAGTCTT | 494470 |
rs35594949 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359045 | TTGGGCAAGTCACTT[-/C]CCCCCTCCCAGGACT | 494470 |
rs35623061 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445341 | CTCAAAAGGCTCTTC[-/T]TGGGGTCTCTATTGT | 494470 |
rs35626129 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379116 | GGCTTGGGGGCCTCG[-/T]TTTTCCCTGCTGGGA | 494470 |
rs35691656 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338732 | TCAGCCCAGAACAAG[-/C]CCTTGCTAAATGAGG | 494470 |
rs35704459 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362669 | AGCCAGTGAAACCTT[-/G]GGGAACTTGCTTCAG | 494470 |
rs35807611 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376602 | TGACTTGGAAAGAAA[-/T]TTTCTTTTGGGGCCT | 494470 |
rs35861789 | in-del | -/C | | | frameshift-variant | RNF165 | GRCh38.p7 | 18:46456612 | CGAGTGGACATTGAG[-/C]ACACAACTGGGAGCC | 494470 |
rs35897092 | snp | A/G | 0.307423 | 0.243316 | intron-variant | RNF165 | GRCh38.p7 | 18:46416046 | GCTGCTGGCATTTTC[A/G]TGGCTAATTAACATG | 494470 |
rs35899854 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375065 | TTTGCCGGAGGATTT[-/G]GGGGTTTCTCCCCAC | 494470 |
rs35927866 | snp | A/C | 0.105924 | 0.204309 | intron-variant | RNF165 | GRCh38.p7 | 18:46392954 | CACCATGGAAACCCA[A/C]GACACACCACCCTGG | 494470 |
rs35939778 | snp | G/T | 0.256897 | 0.249905 | intron-variant | RNF165 | GRCh38.p7 | 18:46399975 | GGCAAGTGGCTCAGG[G/T]TTAGTGAGGTGCAAG | 494470 |
rs36020946 | snp | C/T | 0.243633 | 0.249919 | intron-variant | RNF165 | GRCh38.p7 | 18:46396284 | GTGAAGAGGAGGGAA[C/T]GGAGGCCATTTTTGT | 494470 |
rs36071668 | multinucleotide-polymorphism | GT/TA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403991 | GGATTCTACTGCCCT[GT/TA]GTGATTAACAATTCC | 494470 |
rs36170052 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441891 | AAAAGAGGCCGGGCG[-/C]CGGTGGCTCACGCCT | 494470 |
rs55693400 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459411 | CTGTGCGCCCACCCA[A/G]CTATTGAAAAGGACT | 494470 |
rs55701724 | snp | A/G | 0.0383715 | 0.133092 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389235 | GAAAGTTAAGTGCAC[A/G]AGCATTTAGGAAAGG | 494470 |
rs55715634 | in-del | -/A | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46454138 | AAAAAAAAAAAAAAA[-/A]GTAAAAGGGAAGGTT | 494470 |
rs55761820 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46382609 | CTCAGTTAGCCTTGC[A/T]TGACTTAAGTTTCCC | 494470 |
rs55781361 | in-del | -/TAATAATAATAA | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46375587 | TAATAATAATAATAA[-/TAATAATAATAA]CTTGTCCTGGCTTCC | 494470 |
rs55889589 | snp | A/G | 0.0908922 | 0.192833 | intron-variant | RNF165 | GRCh38.p7 | 18:46421563 | CCATACACTTTGTTG[A/G]TTTAGATGGGGAAAG | 494470 |
rs55929958 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RNF165 | GRCh38.p7 | 18:46346793 | AACACACCTCTGCTT[A/G]TTCAGGCCTGGGACA | 494470 |
rs55949821 | snp | C/G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422027 | TGGCAGCCCTGGGGG[C/G/T]TAAGCCAAGCAATAG | 494470 |
rs56018116 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | RNF165 | GRCh38.p7 | 18:46348974 | GCATACCTTGAACTT[G/T]GTTGCATGGAGCACA | 494470 |
rs56104239 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391741 | CTCACCCTTCCCAAG[A/C]TCTGTGCCACAAACA | 494470 |
rs56126321 | snp | A/G | 0.368119 | 0.220336 | intron-variant | RNF165 | GRCh38.p7 | 18:46419942 | CCACTGACGTCCACC[A/G]TCTCTTTTTCTCTCA | 494470 |
rs56146941 | snp | C/T | 0.368938 | 0.219895 | intron-variant | RNF165 | GRCh38.p7 | 18:46386639 | GTGCTCATTTCATTC[C/T]AACCATGTAGATAGC | 494470 |
rs56203809 | snp | C/T | 0.0566069 | 0.158427 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388322 | GAAGTTGGCAGGAAA[C/T]AAAACAAAACAAAAC | 494470 |
rs56267717 | snp | A/T | 0.361053 | 0.22398 | intron-variant | RNF165 | GRCh38.p7 | 18:46421608 | GATCATGCCCAGAAT[A/T]TTGTCCCATTATGCA | 494470 |
rs56272051 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381145 | GAGTGAGACGGCAAC[G/T]CTGTTCTGAAGCGAG | 494470 |
rs56312029 | in-del | -/T | 0.402806 | 0.197864 | intron-variant | RNF165 | GRCh38.p7 | 18:46403037 | GAACACGAGACTCAC[-/T]TTCCTTTCAGCTGCT | 494470 |
rs56350939 | in-del | -/AAAAAAAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366312 | AAAAAAAAAAAAAAA[-/AAAAAAAA]TAGAGAGAGAGATAA | 494470 |
rs56377789 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368056 | CAGAACCATGGATTA[G/T]AATCTTGGGTTGGGC | 494470 |
rs56404401 | in-del | -/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46392571 | AGTGGACACGGCTCA[-/G]GAGGAGAGGCTCTGG | 494470 |
rs57020165 | snp | C/T | 0.0566069 | 0.158427 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387739 | GACGGGAGAAGCTTC[C/T]AGTCTTCATCATCGA | 494470 |
rs57027858 | snp | C/T | 0.281313 | 0.248031 | intron-variant | RNF165 | GRCh38.p7 | 18:46394317 | CCAGCTCACTGGTCA[C/T]ATCCTTTGCCCAAGA | 494470 |
rs57030664 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334729 | GTGAGAGAGAGAGAG[A/C]GCGCGCGCGCGAGAG | 494470 |
rs57032280 | in-del | -/TTCA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421396 | TCATTCATTCATTCA[-/TTCA]GTGAGTTCTTACTGT | 494470 |
rs57157539 | in-del | -/TTCA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421393 | TCATTCATTCATTCA[-/TTCA]GTGAGTTCTTACTGT | 494470 |
rs57214592 | snp | C/T | 0.399253 | 0.200558 | intron-variant | RNF165 | GRCh38.p7 | 18:46369575 | TTGCAGGGCGGGATT[C/T]CCTATTCCCACTCCC | 494470 |
rs57235512 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373355 | CATCTTGACAGTCAT[C/T]TGGAAGGCGGCTGGC | 494470 |
rs57399080 | snp | C/T | 0.238749 | 0.249747 | intron-variant | RNF165 | GRCh38.p7 | 18:46402557 | TCTCTCTGTCACCCA[C/T]GCTGGAGTGCGTGAC | 494470 |
rs57418419 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446418 | GCTCATGCCTGTAAT[C/T]TCAGCACTTTGGGAT | 494470 |
rs57479072 | in-del | -/CCCATCCA | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46386592 | CCATCCACCCATCCA[-/CCCATCCA]TCCATCATTCCATCC | 494470 |
rs58016810 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | RNF165 | GRCh38.p7 | 18:46360837 | ACCTAAACACTGTTC[A/G]GCCTTGGGGTGTTCA | 494470 |
rs58048630 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | RNF165 | GRCh38.p7 | 18:46412060 | GGTGCTATTTTTAAA[C/T]GCCCTCTCTTCCCCA | 494470 |
rs58057012 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377701 | TCGCATGAGGGCAAA[A/G]GCATGAGAGATCAAT | 494470 |
rs58223751 | snp | A/G | 0.229136 | 0.249128 | intron-variant | RNF165 | GRCh38.p7 | 18:46398769 | ATATCCCAAATACTC[A/G]GGCTCCTCCCTCATG | 494470 |
rs58282229 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RNF165 | GRCh38.p7 | 18:46410805 | ACTCACTTTAAGCAT[C/T]GTTTCTTCAATTGTC | 494470 |
rs58470864 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46418450 | TTTAATTAATTTTAA[A/C]AGTTACTAATTTTTT | 494470 |
rs58796895 | snp | A/G | 0.0566069 | 0.158427 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387893 | GCCAGTCCAGCTCTT[A/G]GGACTGGGGCAGTCA | 494470 |
rs58798217 | in-del | -/TG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397576 | GTGTGTGTGTGTGTG[-/TG]GTCATGCTGGGGTGT | 494470 |
rs58843633 | snp | C/T | 0.281313 | 0.248031 | intron-variant | RNF165 | GRCh38.p7 | 18:46394323 | CACTGGTCATATCCT[C/T]TGCCCAAGACAGAGA | 494470 |
rs58951440 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | RNF165 | GRCh38.p7 | 18:46368350 | TTGCCTCCCTTTCTG[C/T]CTCCACCCCCTGCTC | 494470 |
rs59002413 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335683 | AGGGCCAGCGCTTTA[A/G]TGCGCCCCAGGGGCC | 494470 |
rs59086564 | in-del | -/C | 0.180702 | 0.240204 | intron-variant | RNF165 | GRCh38.p7 | 18:46386537 | TATCTTATGTCTTGA[-/C]CCCCCCATCAATCCA | 494470 |
rs59158010 | snp | C/G | 0.0603597 | 0.1629 | intron-variant | RNF165 | GRCh38.p7 | 18:46407816 | ATGAGATCCACCCAT[C/G]TGAAAAGTTGGGTGA | 494470 |
rs59160393 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | RNF165 | GRCh38.p7 | 18:46453303 | TAAGCTATTGGAGAA[G/T]AACATAGAAGGAAAT | 494470 |
rs59357832 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46362723 | ACAACCACATCAGGT[C/T]GAATGGCACTTAAGT | 494470 |
rs59470064 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46392405 | CCCCAGGCTAAGGCC[C/T]TCAGGGCCCTCAGGG | 494470 |
rs59486389 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390270 | ATCACCCCATCTTTC[C/T]AGGTGGTGAAGAAGC | 494470 |
rs59488762 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338701 | TTCAGCCATTTGTCA[A/T]TTACACCTATTCAAT | 494470 |
rs59545505 | snp | A/G | 0.191147 | 0.242974 | intron-variant | RNF165 | GRCh38.p7 | 18:46422239 | ACTCTCAGTTCTGCC[A/G]TTCAAGGTTCCCCAC | 494470 |
rs59573475 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | RNF165 | GRCh38.p7 | 18:46355733 | CAGAGCTGTGGCTCC[C/G]CTCTATCTCTCCACC | 494470 |
rs59579825 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46379546 | CTGGCCAACAGCACC[A/G]CCCTCATTTGTTTCT | 494470 |
rs59633174 | snp | C/G | 0.103082 | 0.202275 | intron-variant | RNF165 | GRCh38.p7 | 18:46367635 | CCCACATTGCCTAAA[C/G]CTTCTGACATGGAAC | 494470 |
rs59656467 | in-del | -/AAAAAA | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461647 | AACAAAACTCAGTCC[-/AAAAAA]AAAAAAAAAAAAAAA | 494470 |
rs59685383 | in-del | -/AGAGAGAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334721 | GTGTGTGTGTGAGAG[-/AGAGAGAG]AGCGCGCGCGCGAGA | 494470 |
rs59722077 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386562 | AATCCATCCATCCAT[C/T]CATCCATTCACCCAC | 494470 |
rs59853366 | snp | G/T | 0.0547245 | 0.156101 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388785 | ATTTCCCGAGTGAGG[G/T]GTAAACGTAGAGAAC | 494470 |
rs60099048 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | RNF165 | GRCh38.p7 | 18:46395624 | TATGGCCCCAAAGTC[C/T]GGGATTTTACCATAA | 494470 |
rs60120179 | in-del | -/TCTA/TCTT | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46334814 | TGTGTGTTTTGTATT[-/TCTA/TCTT]CATTTTTTGGTCATT | 494470 |
rs60121328 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | RNF165 | GRCh38.p7 | 18:46420192 | ACCAGCTCCTTAAAA[C/T]GTAACCACTCCTGAG | 494470 |
rs60238338 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446504 | GGTGAAACCCCATCT[C/T]TACTAAAACTACAAA | 494470 |
rs60275227 | snp | A/T | 0.334642 | 0.235236 | intron-variant | RNF165 | GRCh38.p7 | 18:46368601 | AATTCTGTTCTTTTC[A/T]GGACAGCTCTATGGA | 494470 |
rs60350327 | snp | A/G | 0.089084 | 0.191327 | intron-variant | RNF165 | GRCh38.p7 | 18:46412835 | TGTGGGCCAGGGGCC[A/G]CCATATCTTGTTATA | 494470 |
rs60412216 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF165 | GRCh38.p7 | 18:46356771 | TCTGCTCCTTCCACC[A/G]TGTCACCTCTTCTCC | 494470 |
rs60431087 | snp | C/T | 0.399253 | 0.200558 | intron-variant | RNF165 | GRCh38.p7 | 18:46369633 | GGCCTGGAGACAGCT[C/T]CTTGCTGGAGGTGGG | 494470 |
rs60571036 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | RNF165 | GRCh38.p7 | 18:46348381 | TTGCCTATTGGCCAG[C/T]GTTGCTGGTGGTTGA | 494470 |
rs60614021 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF165 | GRCh38.p7 | 18:46365089 | GATATTCCTGCTTTA[C/T]CACCATTCCCTGCGT | 494470 |
rs60656282 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413850 | TGCCCCAGCTGCCCA[G/T]GTTCTCTCCTCATGG | 494470 |
rs60662788 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383572 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC | 494470 |
rs60703536 | snp | A/G | 0.48955 | 0.071525 | intron-variant | RNF165 | GRCh38.p7 | 18:46400956 | TGGGAGATGGGATAC[A/G]GGGAACATGAAGATG | 494470 |
rs60888146 | in-del | -/TGTGTGTG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348941 | GTGTGTGTGTGTGTG[-/TGTGTGTG]ATTTCTAGAAGCATA | 494470 |
rs61134885 | in-del | -/T | 0.234692 | 0.249531 | intron-variant | RNF165 | GRCh38.p7 | 18:46402331 | TCCCTCTAAATCTGA[-/T]TTTTCTCAATCCAGC | 494470 |
rs61160449 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430243 | CAGATAATTCTAGAT[G/T]GGAAATCACCCTTCC | 494470 |
rs61257154 | snp | C/G | 0.26518 | 0.249539 | intron-variant | RNF165 | GRCh38.p7 | 18:46418341 | CAGCCTGAGTGACAG[C/G]GCAAGACACTGTCTC | 494470 |
rs61261998 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336191 | ACATTACACTAGGCA[A/G]AAATTCAAAAATGAT | 494470 |
rs61430362 | in-del | -/TG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369378 | CCTGGTGTGTGTGTG[-/TG]CTGGGGTGGCAGGGG | 494470 |
rs61617924 | snp | C/G | 0.039522 | 0.134904 | intron-variant | RNF165 | GRCh38.p7 | 18:46428170 | AATCCCAGCACGTTG[C/G]GAGGCCGAGGCTGGC | 494470 |
rs61732298 | snp | C/G | 0.42 | 0.183303 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435340 | CCTCCATCCCAGCTT[C/G]GACTTCGGCCAACTG | 494470 |
rs61744490 | snp | G/T | 0.0331099 | 0.124333 | missense | RNF165 | GRCh38.p7 | 18:46456066 | GTCTATGCTGGAAGA[G/T]GGAGAAGATGTGAGG | 494470 |
rs62095677 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334717 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGCG | 494470 |
rs62095678 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335378 | ATTTTCCCCTCTTCT[A/C]CCCACCTCCACTCCA | 494470 |
rs62095679 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | RNF165 | GRCh38.p7 | 18:46340710 | CAATGACTGATGACT[G/T]CCATGAAACCTACCT | 494470 |
rs62095680 | snp | G/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46341962 | GGGGAACGGGAGGGA[G/T]CCCGACCCAGTAGCG | 494470 |
rs62095681 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | RNF165 | GRCh38.p7 | 18:46349895 | CATCCCTCTATGGGC[A/C]CCATGCAATATGCAT | 494470 |
rs62095682 | snp | C/T | 0.424037 | 0.179474 | intron-variant | RNF165 | GRCh38.p7 | 18:46352329 | TAGCCTCAGTTTGCA[C/T]TGGCTATATTGGGTA | 494470 |
rs62095683 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | RNF165 | GRCh38.p7 | 18:46357323 | CTAGACTGTAGTGAA[A/C]AGAGCCCAGGTGGTC | 494470 |
rs62095706 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | RNF165 | GRCh38.p7 | 18:46362020 | AGGCATTTACAGATG[A/G]CAAGCAAAATGGAGC | 494470 |
rs62095707 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | RNF165 | GRCh38.p7 | 18:46362642 | ATTTCCAGACATATG[A/G]TTTCTTGGCCTTAGC | 494470 |
rs62095708 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | RNF165 | GRCh38.p7 | 18:46362672 | CCAGTGAAACCTTGG[G/T]AACTTGCTTCAGTGA | 494470 |
rs62095709 | snp | C/G | 0.126219 | 0.217206 | intron-variant | RNF165 | GRCh38.p7 | 18:46362720 | GCGACAACCACATCA[C/G]GTTGAATGGCACTTA | 494470 |
rs62095710 | snp | A/C/T | 0.0729998 | 0.176553 | intron-variant | RNF165 | GRCh38.p7 | 18:46363838 | ATTCATAGGGGCCAC[A/C/T]GTTGAGGGTGTGACC | 494470 |
rs62095711 | snp | C/T | 0.336017 | 0.234736 | intron-variant | RNF165 | GRCh38.p7 | 18:46366898 | GCAAAAATCCAAGTC[C/T]AGCAAAAGGTCTTCT | 494470 |
rs62095712 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | RNF165 | GRCh38.p7 | 18:46368055 | CCAGAACCATGGATT[A/G]GAATCTTGGGTTGGG | 494470 |
rs62095713 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | RNF165 | GRCh38.p7 | 18:46368161 | TGGACCTCCATGAGA[C/T]TTTGTGCTTGAGGAA | 494470 |
rs62095715 | snp | C/T | 0.305186 | 0.243833 | intron-variant | RNF165 | GRCh38.p7 | 18:46369568 | TTTAGGTTTGCAGGG[C/T]GGGATTCCCTATTCC | 494470 |
rs62095718 | snp | A/T | 0.421526 | 0.181876 | intron-variant | RNF165 | GRCh38.p7 | 18:46372517 | CCTTAGTAAGCCCCC[A/T]TCCAGCTCACCCCAC | 494470 |
rs62095719 | snp | A/G | 0.256061 | 0.249927 | intron-variant | RNF165 | GRCh38.p7 | 18:46377858 | GCATGTGATGCTCAG[A/G]TAACCATGTCTAGAG | 494470 |
rs62095720 | snp | C/T | 0.165853 | 0.235413 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387752 | TCTAGTCTTCATCAT[C/T]GAGGACTGCTGAAAT | 494470 |
rs62095721 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387964 | GCAGCATCAGAATTC[C/T]TCTGAACAATCCCCA | 494470 |
rs62095722 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390293 | GAAGAAGCCTCACAG[C/T]CATCCCCAACATCTC | 494470 |
rs62095723 | snp | A/G | 0.127599 | 0.217986 | intron-variant | RNF165 | GRCh38.p7 | 18:46392100 | ATACACACACACCAC[A/G]CATACACACACTGTG | 494470 |
rs62095724 | snp | C/T | 0.127254 | 0.217792 | intron-variant | RNF165 | GRCh38.p7 | 18:46393375 | CTGACAGGCAGACAC[C/T]TTCCCGCTGACCACC | 494470 |
rs62095726 | snp | A/G | 0.204189 | 0.245767 | intron-variant | RNF165 | GRCh38.p7 | 18:46402902 | CTGAACCTTCCTGGT[A/G]TCTCAGGACACTAGA | 494470 |
rs62095727 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46404815 | AACAACCCCCCCACC[A/C]AAACAAACAAACAAA | 494470 |
rs62095754 | snp | A/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46432725 | CACTTTGGGAGGCCG[A/T]GGCGGGTGGATCACG | 494470 |
rs66548443 | in-del | -/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46376689 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 494470 |
rs66958251 | in-del | -/TTACCCTGATGGGACACATAAG | 0.0166325 | 0.0896639 | intron-variant | RNF165 | GRCh38.p7 | 18:46406890 | TCTAGCCCAGAATCC[-/TTACCCTGATGGGACACATAAG]GATAGGGTAGGGAAA | 494470 |
rs67258513 | in-del | -/T | 0.375 | 0.216506 | intron-variant | RNF165 | GRCh38.p7 | 18:46383572 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC | 494470 |
rs67448701 | in-del | -/TT | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46366318 | TTATCTCTCTCTCTA[-/TT]TTTTTTTTTTTTTTT | 494470 |
rs71160802 | in-del | -/CACACA | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46348943 | TATGCTTCTAGAAAT[-/CACACA]CACACACACACACAC | 494470 |
rs71264818 | in-del | -/T | 0.5 | 0 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461667 | CTCCCTCTTTCCCTC[-/T]TTTTTTTTTTTTTTT | 494470 |
rs71264819 | in-del | -/AGAAA | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46365390 | TCTGTTCATTAGTGG[-/AGAAA]AGAAAAGGCTCTTCC | 494470 |
rs71364530 | snp | C/T | 0.375 | 0.216506 | intron-variant | RNF165 | GRCh38.p7 | 18:46347439 | GCTCCAATGGGTCAT[C/T]GTGCCGCCCCTGGAA | 494470 |
rs71364531 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46403400 | CCCTGCCCCCCGTCT[C/T]CCTCTAGGTTGACAT | 494470 |
rs71364532 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46406060 | CATGTACACACTCCT[C/T]CCACATACACACTCA | 494470 |
rs71364533 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46414205 | CATAGTGAGTGACTG[A/C]TTAAGACGGGACCTG | 494470 |
rs71364534 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46415886 | CAGAGTTCACGAGGG[A/G]CCTGGAGTGCCAGGT | 494470 |
rs71364535 | snp | C/T | 0.304937 | 0.243889 | intron-variant | RNF165 | GRCh38.p7 | 18:46421029 | CCCTCCTTCCCTGGC[C/T]AGGAATGGCAGGATG | 494470 |
rs71364536 | snp | C/T | 0.375797 | 0.216044 | intron-variant | RNF165 | GRCh38.p7 | 18:46421974 | CATACTCCATTGGAC[C/T]GGGAACCAATAGATA | 494470 |
rs71364537 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46424861 | GACTTCTTGGTAGTG[A/G]TGCCTTCCTCACTGG | 494470 |
rs71364538 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46427351 | ATGGTAGAAACCTCC[A/C]CAGGCTGGGGCGGTT | 494470 |
rs71364539 | snp | G/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46430900 | TCCTCGAGTTCATTG[G/T]TTAAAAATTATTCTT | 494470 |
rs71364540 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46453638 | ACACAAGTGAAAAAG[A/C]CAATAAAGAAGAAAA | 494470 |
rs72068481 | in-del | -/GT | 0.252973 | 0.249982 | intron-variant | RNF165 | GRCh38.p7 | 18:46397560 | TGCTGGGGTGTGAGG[-/GT]GTGTGTGTGTGTGTG | 494470 |
rs72423266 | in-del | -/TCAT | 0.206105 | 0.246116 | intron-variant | RNF165 | GRCh38.p7 | 18:46421366 | CTCACCTGTTCGTGA[-/TCAT]TCATTCATTCATTCA | 494470 |
rs72907355 | snp | C/T | 0.303688 | 0.244167 | intron-variant | RNF165 | GRCh38.p7 | 18:46356868 | TACATTCAGGGAAAA[C/T]GGAAACTCCAGAGGT | 494470 |
rs72907358 | snp | G/T | 0.304688 | 0.243945 | intron-variant | RNF165 | GRCh38.p7 | 18:46356869 | ACATTCAGGGAAAAC[G/T]GAAACTCCAGAGGTT | 494470 |
rs72907368 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | RNF165 | GRCh38.p7 | 18:46363546 | CTCTGGATCCCTGAT[C/T]CACCCCTGCAAACCT | 494470 |
rs72907383 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370711 | ACCATCTCTGTCCTC[A/G]TTCTCTTGAGCCACT | 494470 |
rs72907387 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF165 | GRCh38.p7 | 18:46379358 | AACAAATCAATCTCA[C/T]GAGACTAAGCGCTGG | 494470 |
rs72909307 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | RNF165 | GRCh38.p7 | 18:46393486 | GGGGCTGGGAGGCTT[C/T]CTTCTCTTTCTGCCA | 494470 |
rs72909308 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46398313 | ACAGTGAGGCCGCAG[A/G]GCAGGAAGAAGGAAG | 494470 |
rs72909325 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46449264 | GGGTGAGGGAAAGGC[A/G]AGTGAGGCAGGCCAT | 494470 |
rs72909329 | snp | A/G | 0.0138799 | 0.0821421 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458087 | CCCATTTCCGGTCCT[A/G]CTACCTCACCTAGAT | 494470 |
rs73427187 | snp | A/C | 0.0711525 | 0.174681 | intron-variant | RNF165 | GRCh38.p7 | 18:46351148 | TTCTTTGCTGGGAGG[A/C]GGCCCTGGAAGATCA | 494470 |
rs73427188 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | RNF165 | GRCh38.p7 | 18:46351279 | TGAGTGGAGCTCGGG[A/G]CTTCCCTCCAGTCTG | 494470 |
rs73427193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353935 | AAGGGTTTTATTGGA[A/G]GCCTGGAAAGGACCC | 494470 |
rs73427194 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | RNF165 | GRCh38.p7 | 18:46355651 | CTTCTCTTCTTGCTC[C/T]TCCAGCAGCCACAAT | 494470 |
rs73427195 | snp | A/T | 0.0704125 | 0.17392 | intron-variant | RNF165 | GRCh38.p7 | 18:46358252 | ATGTTTTGCGCAGGC[A/T]GGGGTGGACAGGGCA | 494470 |
rs73429107 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | RNF165 | GRCh38.p7 | 18:46366512 | CAGACAATTTGGTGA[A/G]GAGGCATGGAGAATT | 494470 |
rs73429119 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | RNF165 | GRCh38.p7 | 18:46372499 | GAACCCCATGTGGGG[C/T]CACCTTAGTAAGCCC | 494470 |
rs73429129 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | RNF165 | GRCh38.p7 | 18:46413282 | AAGCCCAGCCCTATC[C/T]AGAAGTGGACCATGT | 494470 |
rs73429130 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | RNF165 | GRCh38.p7 | 18:46417498 | GAAAGCACTTTGCCT[G/T]GATATCTGCCAGTTC | 494470 |
rs73429141 | snp | A/G | 0.0107246 | 0.0724382 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459569 | CCACCAGAGGGGAGA[A/G]GGAAGCTGCTTACTT | 494470 |
rs73953817 | snp | A/G | 0.178144 | 0.239451 | intron-variant | RNF165 | GRCh38.p7 | 18:46334783 | CTTTTTTTGAGGTAT[A/G]TGTGTGTTTTGTGTT | 494470 |
rs73953818 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337479 | GAAACGTACTGTGGT[C/T]GTGTAGCCCGGGCCA | 494470 |
rs73953819 | snp | A/C/G | 0.016652 | 0.0898765 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337883 | ATAGATGTCTGGAGC[A/C/G]ATAGGAGGGGCCAGT | 494470 |
rs73953823 | snp | C/G | 0.0858192 | 0.188533 | intron-variant | RNF165 | GRCh38.p7 | 18:46345010 | CCCTAAGGGCTGGGT[C/G]AGGAGGGAAGCTGAG | 494470 |
rs73953824 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | RNF165 | GRCh38.p7 | 18:46345099 | GGGCAGGGGTGCCTG[A/G]GATGCAGGGGTGCCT | 494470 |
rs73953826 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF165 | GRCh38.p7 | 18:46345810 | TCCAGGCTGTGCCCC[A/G]ACTCCCGGGGTGGCT | 494470 |
rs73953829 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | RNF165 | GRCh38.p7 | 18:46362907 | TAAAGGGGAAGAAAA[A/G]TCACCGGGAGGGATA | 494470 |
rs73953830 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46363609 | GTACAGCCCCATCAC[A/G]GGCCCAGGGGAGGGG | 494470 |
rs73953831 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | RNF165 | GRCh38.p7 | 18:46364598 | TGCCTGGATTTTAGG[A/C]TTGGCTTATAGCTGG | 494470 |
rs73953832 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | RNF165 | GRCh38.p7 | 18:46365046 | GAGTTCCCTTTCTTC[C/T]AATGCCCTATAAGTC | 494470 |
rs73953835 | snp | A/C | 0.0770498 | 0.180522 | intron-variant | RNF165 | GRCh38.p7 | 18:46385985 | GATGCTCTGGCCCCA[A/C]GAACCCCTTGTCTCC | 494470 |
rs73953836 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RNF165 | GRCh38.p7 | 18:46386163 | GTTAGCTACCTACAT[A/G]CCAGGGTTTCTCTTC | 494470 |
rs73953837 | snp | C/T | 0.0551013 | 0.156571 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391722 | AGTCAGCATCCTCTG[C/T]TCACTCACCCTTCCC | 494470 |
rs73953838 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | RNF165 | GRCh38.p7 | 18:46392292 | CCCAAAGACACCTGG[A/T]TGCCCCCCGCTCCCT | 494470 |
rs73953839 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | RNF165 | GRCh38.p7 | 18:46392453 | GCTGACCACATTTGG[C/T]GGGAATGGACAAGAA | 494470 |
rs73953840 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | RNF165 | GRCh38.p7 | 18:46392835 | CCCAGGAGGACAACA[A/C]GCCTGGGTGGAGTTG | 494470 |
rs73953841 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | RNF165 | GRCh38.p7 | 18:46392941 | GAAACCCAAGAAACA[A/C]CATGGAAACCCAAGA | 494470 |
rs73953842 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | RNF165 | GRCh38.p7 | 18:46392968 | AAGACACACCACCCT[A/G]GAAGGGAAATCGGCA | 494470 |
rs73953843 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | RNF165 | GRCh38.p7 | 18:46392970 | GACACACCACCCTGG[A/G]AGGGAAATCGGCAAC | 494470 |
rs73953845 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | RNF165 | GRCh38.p7 | 18:46408333 | CCTTGTCCTGTCATC[G/T]CTTGGTCCCACCTCC | 494470 |
rs73953846 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RNF165 | GRCh38.p7 | 18:46412636 | TCCTCCCTACTCCAG[C/T]AGCTGGCTGTTAAAT | 494470 |
rs73953847 | snp | C/T | 0.242775 | 0.249896 | intron-variant | RNF165 | GRCh38.p7 | 18:46416679 | GGAAGTCCTTTTGGT[C/T]TTCTTGGGCTCACTC | 494470 |
rs73953849 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | RNF165 | GRCh38.p7 | 18:46437011 | GGAGCAGCACAGGTG[C/T]TGGCCCTGTCCTCAG | 494470 |
rs73953850 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | RNF165 | GRCh38.p7 | 18:46437763 | CTGAGTTCTTTTCAC[A/T]CTCCTTCTTGGACTC | 494470 |
rs73953851 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46438399 | CCCACCTAGGGCAGA[C/T]CATCCCACCCATTTG | 494470 |
rs73953852 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RNF165 | GRCh38.p7 | 18:46455383 | AGGGAAACTGTGCAC[A/G]GTCATAGCTTTGCAA | 494470 |
rs74321425 | snp | A/G | 0.210301 | 0.246828 | intron-variant | RNF165 | GRCh38.p7 | 18:46415145 | CCTCCCCAGGCCTAC[A/G]TGACCTCTGCCAGAG | 494470 |
rs74327679 | snp | C/T | 0.100944 | 0.200705 | intron-variant | RNF165 | GRCh38.p7 | 18:46350289 | CATCTGCAGGCCAGC[C/T]GCAGAGCCTGGGCCT | 494470 |
rs74334972 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46446668 | AGAGCGAGACTCCAT[A/C]TCAAAAAAAAAAAAA | 494470 |
rs74358173 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | RNF165 | GRCh38.p7 | 18:46373625 | GAGGCTGAGAGCTGA[C/G]TGCTGCCACACTGGC | 494470 |
rs74372021 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46409192 | AATGTTGATGCCTCA[A/G]AAGAAAGGATAGTCT | 494470 |
rs74418733 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RNF165 | GRCh38.p7 | 18:46452524 | ATCTCAAGTGATCCA[C/T]CCACCTTGGCCTCCA | 494470 |
rs74466310 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46396587 | ATTTGTTTTCTTGAA[C/T]TCAATTCAGTGGTCT | 494470 |
rs74466705 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46382877 | CCATCCCTCCTGGAC[C/T]GTCAGAGCCTCGGGA | 494470 |
rs74479057 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | RNF165 | GRCh38.p7 | 18:46377688 | GGTGTCATTAATTTC[G/T]CATGAGGGCAAAGGC | 494470 |
rs74502394 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | RNF165 | GRCh38.p7 | 18:46385298 | TCCTGGGAGATGAAA[A/G]TGGTGGCTTGTGAGG | 494470 |
rs74559334 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46346217 | GGGAGGCCAGGAGAC[A/G]GAGAGAACCCCACCA | 494470 |
rs74572970 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46381817 | ATCTGGGTGACAGAG[A/C]GAGACCCTGTCTCAA | 494470 |
rs74590773 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | RNF165 | GRCh38.p7 | 18:46430331 | GAAAAATCTCAAGCT[A/G]TTCTGATTTCTGACC | 494470 |
rs74595541 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46396798 | TGTCGGGACAGCTCA[C/G]GGCATCCAAGGACGG | 494470 |
rs74744131 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | RNF165 | GRCh38.p7 | 18:46358925 | TCTCAGTCACACCCC[C/T]GGACTCTTGTCCCCA | 494470 |
rs74785247 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46446673 | GAGACTCCATCTCAA[A/C]AAAAAAAAAAAAAAA | 494470 |
rs74807254 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF165 | GRCh38.p7 | 18:46386190 | CTTCCTCTGGCTGCC[C/T]CATTTCTTACACTGG | 494470 |
rs74821754 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46423150 | ATGCAAGCCCTAAAG[A/C]CTTTCCTTTGGGGGA | 494470 |
rs74841759 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46369130 | TGAATCTAGACCTCT[A/C]TGATCTAAAAGGCCA | 494470 |
rs74864372 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | RNF165 | GRCh38.p7 | 18:46385866 | TGAGGTATCTGGGGC[C/T]GGAAGAGTTGCTTTT | 494470 |
rs74876717 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | RNF165 | GRCh38.p7 | 18:46435674 | GAGGGGGACAGGGAT[A/G]GAAAACATTTCCCAG | 494470 |
rs74882204 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46433637 | GGGGCTACAGGCTCC[C/T]AGACTCCTGGCTTCT | 494470 |
rs74913230 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402052 | TCACGGTTTATGAGG[C/G]AGTCACTCCACTGTT | 494470 |
rs74946075 | snp | A/T | 0.0611083 | 0.163768 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388570 | AGGAAGCACACGGGG[A/T]TGGCACTGAACCAAG | 494470 |
rs74950965 | snp | A/T | 0.0543475 | 0.155628 | intron-variant | RNF165 | GRCh38.p7 | 18:46442611 | TATAAGTATTTTTAA[A/T]AAGTGTATATTCTAC | 494470 |
rs74960313 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | RNF165 | GRCh38.p7 | 18:46421894 | GGCCCTGGGGAAGCA[C/T]CACAAAGCTGCTCTT | 494470 |
rs74967846 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46406638 | GACTCTACCTGGCCC[A/G]GGTGCCCTCAGTGTG | 494470 |
rs74984040 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | RNF165 | GRCh38.p7 | 18:46375001 | TTGGGCCCCAGCCAG[A/G]CCCCAGGCCCTTGTA | 494470 |
rs74986120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46357640 | GTGGGGCACTGGGCT[C/T]GAGGCCTGGGGCACA | 494470 |
rs74997066 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | RNF165 | GRCh38.p7 | 18:46403143 | AGGCCTGTGATATTT[C/T]ACCTTGTTGGTTCGT | 494470 |
rs75019044 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | RNF165 | GRCh38.p7 | 18:46450941 | TGCTCTAAAGCTGTA[A/C]TAACTTCCCAGGGTC | 494470 |
rs75099049 | snp | C/T | 0.0356815 | 0.128715 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459262 | TGACAAAGTGGGCAA[C/T]ACTAGAAACTTCCCT | 494470 |
rs75118365 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46416380 | TCCCTCCCTCCATCC[A/G]TAAGCATCCGCCAAG | 494470 |
rs75122889 | snp | A/C | 0.0182019 | 0.0936463 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460634 | TTGCATGCATTGGTA[A/C]GATGACAAACAACTA | 494470 |
rs75140478 | snp | C/T | 0.0626037 | 0.165477 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458720 | TTCTCCCAGCACTAA[C/T]ATCCTGGTGTTCTAT | 494470 |
rs75160545 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RNF165 | GRCh38.p7 | 18:46420580 | CCAGATGCGGTGGCT[C/T]ACGCCTGTAATCTCA | 494470 |
rs75186827 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | RNF165 | GRCh38.p7 | 18:46348607 | GTATCTGGGAGACCT[C/T]CTGGAAGACACAGGG | 494470 |
rs75188192 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332270 | GACTTGCCTCTGGCC[A/G]TCTTCATCCCTGAGT | 494470 |
rs75207832 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386599 | ACCCATCCATCCATC[A/C]TTCCATCCGGCAGAT | 494470 |
rs75209553 | snp | G/T | | | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447587 | TGTGGATGCTGGCTT[G/T]AGTCCTGCTCAGTTC | 494470 |
rs75243927 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392934 | AGCTCCAGAAACCCA[A/T]GAAACACCATGGAAA | 494470 |
rs75271447 | snp | A/G | 0.11963 | 0.213316 | intron-variant | RNF165 | GRCh38.p7 | 18:46446217 | TATTTCTTTAGGGGA[A/G]GCAAAATGATGACAA | 494470 |
rs75283669 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348898 | ACTCTCTCTCTCTCT[C/T]TCTGTGTGTGTGTGT | 494470 |
rs75337494 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46354475 | CGCCCAAACCCAGTA[A/G]TGCTGCTGACAAGAT | 494470 |
rs75355886 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | RNF165 | GRCh38.p7 | 18:46392422 | CAGGGCCCTCAGGGC[C/G]CTCTTTTGGTGGCTT | 494470 |
rs75381931 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46393224 | TAACTTTGCCAAGAG[A/G]TTATGACCACTGGTT | 494470 |
rs75497634 | snp | C/T | 0.115788 | 0.21092 | intron-variant | RNF165 | GRCh38.p7 | 18:46442677 | GATCAAGTTAGTCGA[C/T]AGTATTGTTCAGGTC | 494470 |
rs75513789 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | RNF165 | GRCh38.p7 | 18:46369984 | ACACACGCACCCTAG[A/T]CTTGGGAATGATTCT | 494470 |
rs75526563 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46355274 | AATATTTTTTTTTAA[C/T]ATGGCAGCTCACACC | 494470 |
rs75562487 | snp | A/G | 0.444444 | 0.157135 | intron-variant | RNF165 | GRCh38.p7 | 18:46376047 | AGTGTGCACAGCTCA[A/G]AACAGGGCCGGGCCC | 494470 |
rs75566991 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | RNF165 | GRCh38.p7 | 18:46367842 | CAATTCGGATTTCTC[A/G]GCTCTGCTTCTGGAT | 494470 |
rs75581183 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46338250 | ACCCTCTTCTATGTG[A/C]ATATTTAAATTTTTA | 494470 |
rs75584069 | snp | A/G | 0.216349 | 0.247725 | intron-variant | RNF165 | GRCh38.p7 | 18:46347143 | TTCCCCGAGGAGGAA[A/G]AGCTGTAGCTCTGCT | 494470 |
rs75669385 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46433882 | GAAATTTGACTAGGG[A/G]ACTCCTCATGTCCCC | 494470 |
rs75693328 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | RNF165 | GRCh38.p7 | 18:46347809 | TTCTTATCTGTAAAA[C/T]GGGAATAATTACAGC | 494470 |
rs75724261 | snp | C/G | 0.127254 | 0.217792 | intron-variant | RNF165 | GRCh38.p7 | 18:46348900 | TCTCTCTCTCTCTTT[C/G]TGTGTGTGTGTGTGT | 494470 |
rs75786747 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46437295 | GGCCAGCCTAGTGGC[A/G]CCGAGGGGTTTTGTG | 494470 |
rs75820445 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46340587 | CACGAATGGCAGAAC[A/G]TCCTGACTGCTGAGA | 494470 |
rs75826803 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46362328 | CGGTTTACTGTCTCA[A/G]GGCCTGCTAGGTGAG | 494470 |
rs75827603 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389746 | TTTCCTTTTTTTTTT[C/T]CAGACAAGGTCTCAC | 494470 |
rs75843623 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF165 | GRCh38.p7 | 18:46394308 | AGTTGCGTCCCAGCT[C/T]ACTGGTCATATCCTT | 494470 |
rs75876421 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383189 | AAGGGAGATGCCGTC[A/G]GGCCCCTCCCACCCA | 494470 |
rs75883924 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | RNF165 | GRCh38.p7 | 18:46365333 | AGGGTCGAGTCCAGG[A/C]GGTCTTTTTTGGGAT | 494470 |
rs75960501 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RNF165 | GRCh38.p7 | 18:46364563 | CTCTAACTGGAAAAG[C/G]CTTCACACCTACTGC | 494470 |
rs75975024 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386593 | CCATCCACCCATCCA[C/T]CCATCATTCCATCCG | 494470 |
rs76009246 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46395240 | AGGGGTCCTTGAGCC[C/G]ACGTCTCCAGGGGAC | 494470 |
rs76076946 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46381601 | TTTGGGAGGCTGAGG[C/T]GGGAGGATTGCTACA | 494470 |
rs76095029 | snp | A/G | 0.0119091 | 0.0762411 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457635 | AATGTGTTCCTGGGA[A/G]CCGAGAGACCCATGG | 494470 |
rs76095283 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | RNF165 | GRCh38.p7 | 18:46346705 | AAAGTACGAGACACC[C/T]GAAATCCTGGGAAGT | 494470 |
rs76095974 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | RNF165 | GRCh38.p7 | 18:46382707 | GCAGGTGTGATTTCC[A/T]CTGTGTGCAGGGAAA | 494470 |
rs76130012 | snp | C/G | 0.0618563 | 0.164627 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459110 | GGGTGGTCTAGGAAG[C/G]TCACTCCTCTCTTAG | 494470 |
rs76204487 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46362548 | CAAACCCTGAAGAAC[A/G]GCATAGAAGCCACCC | 494470 |
rs76249069 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | RNF165 | GRCh38.p7 | 18:46406279 | GCCACTGTCACGGGA[C/T]TGGATGCCCCGGGCA | 494470 |
rs76273042 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388121 | CTTACTGAAGGTTAC[A/G]TGTTTATTTGGGATT | 494470 |
rs76279000 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46352695 | AAAGAGCATGACACA[A/G]CACTGCACAAGCCAC | 494470 |
rs76324870 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNF165 | GRCh38.p7 | 18:46438334 | TTAGGGTTCGAGGAA[C/T]CACATCCCCTGTTGG | 494470 |
rs76326930 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | RNF165 | GRCh38.p7 | 18:46410104 | AGGAGTAGTGGGTGG[A/G]AGGTCTTGGTGATCA | 494470 |
rs76342737 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | RNF165 | GRCh38.p7 | 18:46413523 | CTGCGACCTGGACTA[C/T]GGGATAGCAAGTTGT | 494470 |
rs76389655 | snp | C/T | 0.0879971 | 0.190408 | intron-variant | RNF165 | GRCh38.p7 | 18:46396811 | CAGGGCATCCAAGGA[C/T]GGGCGTGGTGGGGCC | 494470 |
rs76405673 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | RNF165 | GRCh38.p7 | 18:46443204 | AACAACAAAATGACA[C/T]CAACAACAAAACAGA | 494470 |
rs76453780 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46363246 | TCTCTGGGCTTTGAA[A/C/T]GGGACCCTGAAGATG | 494470 |
rs76503078 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46442162 | AGCGAAACTCCGTCT[A/C]AAAAAAAAAAAAAAG | 494470 |
rs76522751 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46402781 | ACTGGGATTGCAGGC[A/G]TGAGCCACCACGCCT | 494470 |
rs76547094 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46397075 | GTCAGGAGTCCGTGA[C/G]GTTGGCTTCCCCTGG | 494470 |
rs76559423 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46341320 | GGCTGAGGTCAGGGA[A/G]GGGGGTGGGACAGGC | 494470 |
rs76577438 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46403955 | CTTGGGTGACCCCAT[C/T]ATAGAAGCTCATTCT | 494470 |
rs76583241 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46437567 | CAAGGTCGTCCACCC[C/G]CTGAGGTTACCCTGG | 494470 |
rs76646421 | snp | C/G | 0.0607341 | 0.163335 | intron-variant | RNF165 | GRCh38.p7 | 18:46411279 | AAGTAGCTTTGGGTT[C/G]GGTGAGTTTGCTGAA | 494470 |
rs76680662 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | RNF165 | GRCh38.p7 | 18:46414434 | GACCACAGCTGCTCT[C/T]TGTGTGTGCACACAC | 494470 |
rs76732127 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46384468 | AATATATCTGGTGGC[A/G]ACTTTCTTTCCTCCC | 494470 |
rs76799414 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459726 | GGGTCTGTGCTTCTG[C/T]TCCCGGCACTGGTCA | 494470 |
rs76807745 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | RNF165 | GRCh38.p7 | 18:46408837 | TTAGATAGTCTGTGA[C/T]GAGCCTTCATCCCAG | 494470 |
rs76808114 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | RNF165 | GRCh38.p7 | 18:46363897 | GCCCTGACTCTGCTT[C/T]CTGACCTTGCTTTTC | 494470 |
rs76834088 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46378877 | TCCTATGAAGCACCC[C/T]GCTATGGTCCTGTCT | 494470 |
rs76862870 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | RNF165 | GRCh38.p7 | 18:46421968 | CCTTGGCATACTCCA[C/T]TGGACTGGGAACCAA | 494470 |
rs76900748 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332898 | ATGTAGGGAATGTCC[C/T]CTGTCTTTCTGCCCG | 494470 |
rs76904486 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | RNF165 | GRCh38.p7 | 18:46420152 | CCGGCTGCTGTCTGA[A/C]ATCCCACCATTAGAA | 494470 |
rs76966045 | snp | A/G | 0.119281 | 0.213102 | intron-variant | RNF165 | GRCh38.p7 | 18:46442638 | CTACTCTTATTGGAT[A/G]GAGTATTCTATAAAT | 494470 |
rs76981973 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | RNF165 | GRCh38.p7 | 18:46445306 | ACTCTAGATCTTCCC[G/T]AATAAGACTCATAAA | 494470 |
rs76991679 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46381086 | GCGCCTCAGTTTTTC[C/T]ATCTGTAAAATAGGG | 494470 |
rs76994083 | snp | C/T | 0.120674 | 0.21395 | intron-variant | RNF165 | GRCh38.p7 | 18:46441336 | ATGATTCTCCTGCCT[C/T]AGCTTCCCATGTAGC | 494470 |
rs77245507 | snp | A/G/T | 0.035324 | 0.128276 | intron-variant | RNF165 | GRCh38.p7 | 18:46432113 | CCATGTTTAGCAGCA[A/G/T]GTTTTCTGTAAATCT | 494470 |
rs77266390 | snp | C/T | 0.0629771 | 0.165899 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391717 | TCTCCAGTCAGCATC[C/T]TCTGTTCACTCACCC | 494470 |
rs77278839 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | RNF165 | GRCh38.p7 | 18:46421783 | CCATGGGCAAGTAGG[G/T]TTCCTTAGGATGCAA | 494470 |
rs77281773 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | RNF165 | GRCh38.p7 | 18:46413388 | AACCCACAGCCTTGT[A/G]GGGCTTTCCTTGAGC | 494470 |
rs77361740 | snp | G/T | 0.277778 | 0.248452 | intron-variant | RNF165 | GRCh38.p7 | 18:46342898 | CTATTTGTTGTTTTT[G/T]GGGGGGGAGTGGAGC | 494470 |
rs77396414 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46387554 | TGTGGAAGTCCCTGT[A/G]CTTCCCGGCACCACC | 494470 |
rs77406360 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46428888 | TGTTGGACAGTGCTG[A/G]GTGAGAGTCTTGACA | 494470 |
rs77476875 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | RNF165 | GRCh38.p7 | 18:46412806 | ACCACGTTTCATGCT[C/T]CAGATGGCACACCTG | 494470 |
rs77495796 | snp | A/G | 0.0640965 | 0.167152 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459414 | TGCGCCCACCCAGCT[A/G]TTGAAAAGGACTTTC | 494470 |
rs77537725 | snp | G/T | 0.0111196 | 0.0737302 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458248 | TTCCTGAACCCCAAA[G/T]GGAGCAGAGAGATAA | 494470 |
rs77542123 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RNF165 | GRCh38.p7 | 18:46408512 | AACCCACCAGCAGAG[A/G]GCCATGAGGAACTTA | 494470 |
rs77579463 | snp | A/G/T | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46422606 | ATGCTTCTTCCCCCC[A/G/T]ACCGAGGTCCAGCTC | 494470 |
rs77584956 | snp | C/G | 0.0659589 | 0.169201 | intron-variant | RNF165 | GRCh38.p7 | 18:46419885 | TCTTCCCCTGCTCTC[C/G]TCTAACCTTCTTTCT | 494470 |
rs77587032 | snp | C/T | 0.193653 | 0.243567 | intron-variant | RNF165 | GRCh38.p7 | 18:46340039 | CGACAGGTCCTTGAC[C/T]CTGATTCAGGGTGTG | 494470 |
rs77620160 | snp | C/G | 0.0618563 | 0.164627 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459471 | GGGCTGGGGGCACAC[C/G]TGCTGGGTGAGACAG | 494470 |
rs77636588 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46430103 | TTATTTTGTTGTTCC[C/T]CTTTCTTGGTTTGTG | 494470 |
rs77688543 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386600 | CCCATCCATCCATCA[A/T]TCCATCCGGCAGATA | 494470 |
rs77740466 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | RNF165 | GRCh38.p7 | 18:46421572 | TTGTTGGTTTAGATG[A/G]GGAAAGTATCTTCTT | 494470 |
rs77785229 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46430771 | TCTTGTTTTCTCATT[G/T]ATCCTTCTTCAAGAG | 494470 |
rs77793444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349292 | GTGCCAGCAGGTTTG[C/T]TGCGGGTGAGGGTCC | 494470 |
rs77822874 | snp | C/T | 0.126219 | 0.217206 | intron-variant | RNF165 | GRCh38.p7 | 18:46348743 | ACATATTCCAACAAT[C/T]TGGAAATACTACACA | 494470 |
rs77826603 | snp | C/T | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390260 | CACTGTCTAAATCAC[C/T]CCATCTTTCCAGGTG | 494470 |
rs77836822 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | RNF165 | GRCh38.p7 | 18:46374055 | GCATGAGCAGGGCCA[G/T]GCTGGGGCATTCTTG | 494470 |
rs77873919 | snp | C/G | 0.0626037 | 0.165477 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458243 | CAATTTTCCTGAACC[C/G]CAAAGGGAGCAGAGA | 494470 |
rs77910750 | snp | C/G | 0.251014 | 0.249998 | intron-variant | RNF165 | GRCh38.p7 | 18:46415212 | GAGCCCCAAGGCAGT[C/G]ACCTTACCAGTAAGT | 494470 |
rs77946228 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | RNF165 | GRCh38.p7 | 18:46382605 | CAGGCTCAGTTAGCC[C/T]TGCATGACTTAAGTT | 494470 |
rs77951385 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | RNF165 | GRCh38.p7 | 18:46348423 | CAAGAATAAAGTGCA[A/C]AGAACCTCTGTGTGT | 494470 |
rs77955066 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RNF165 | GRCh38.p7 | 18:46415616 | GCCCTTTATTGAGAA[C/T]GTGTTTTGGTGGTGC | 494470 |
rs78007193 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | RNF165 | GRCh38.p7 | 18:46445250 | AGGCTTGCTTTTAGG[A/T]CTTCTTCCAGCAGGA | 494470 |
rs78010865 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46343195 | TCAGGTGTGACAACT[C/T]TCACTCCTCTCTGCC | 494470 |
rs78012338 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | RNF165 | GRCh38.p7 | 18:46403230 | CCTGGCAAAATGTCC[A/T]TCTCTCCCAGACTCG | 494470 |
rs78060271 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | RNF165 | GRCh38.p7 | 18:46339683 | TCTTTCTGAACAAGA[G/T]AACTTCTCTCTTGAA | 494470 |
rs78094922 | snp | G/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46444653 | ATTTTTTTTTTTTTT[G/T]GTAGACGTGATATCC | 494470 |
rs78136128 | snp | A/G | 0.0298908 | 0.118541 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461839 | GAGTTAGGTGGACAC[A/G]TATAGGACGTGCCCT | 494470 |
rs78139156 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | RNF165 | GRCh38.p7 | 18:46393541 | CCCCCGCCACCACCC[A/C]ACCCCATCTACATAG | 494470 |
rs78168931 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46392699 | CACGGTCCTGTGCCT[C/T]GTCAGTCTCTCCCCT | 494470 |
rs78269855 | snp | A/G | 0.119281 | 0.213102 | intron-variant | RNF165 | GRCh38.p7 | 18:46442979 | TTTCTTCCAGTTAGC[A/G]CTTACGGGGTATATC | 494470 |
rs78301552 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | RNF165 | GRCh38.p7 | 18:46368515 | TCACCTTGATCAAAG[C/G]TTGGCCTGGGTTTTG | 494470 |
rs78310305 | snp | C/T | 0.251859 | 0.249993 | intron-variant | RNF165 | GRCh38.p7 | 18:46414453 | GTGTGCACACACACA[C/T]GTGCAGACATACATG | 494470 |
rs78354614 | snp | C/G | 0.0607341 | 0.163335 | intron-variant | RNF165 | GRCh38.p7 | 18:46451687 | GTATGAACTTGTAGT[C/G]CTAGTTACTAGGGAG | 494470 |
rs78444364 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46348333 | TGCAGGGAAGCTAAG[G/T]CTTTGTTGGCCCTCC | 494470 |
rs78448136 | snp | C/G | 0.119281 | 0.213102 | intron-variant | RNF165 | GRCh38.p7 | 18:46443058 | AATGGACAGCATATA[C/G]TTGGCAATTGTTTTG | 494470 |
rs78517143 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402050 | TCTCACGGTTTATGA[G/T]GCAGTCACTCCACTG | 494470 |
rs78519827 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383188 | AAAGGGAGATGCCGT[C/G]AGGCCCCTCCCACCC | 494470 |
rs78534405 | snp | A/C | 0 | 0 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389165 | CATCAGGTAGTGAGG[A/C]CCACAAGGAAACAGG | 494470 |
rs78547810 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383191 | GGGAGATGCCGTCAG[A/G]CCCCTCCCACCCAGG | 494470 |
rs78566630 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | RNF165 | GRCh38.p7 | 18:46404722 | CGCGCCGCCACACTC[C/T]AGCCTGGGGCACAGA | 494470 |
rs78613829 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | RNF165 | GRCh38.p7 | 18:46386207 | ATTTCTTACACTGGC[A/G]AGGGAGCTGAATGAA | 494470 |
rs78635775 | snp | G/T | 0.0629771 | 0.165899 | intron-variant | RNF165 | GRCh38.p7 | 18:46404975 | ATTCAGCTCCGTTTG[G/T]CTCCAAAGTCTCTGT | 494470 |
rs78635935 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46354578 | TCCAGGGTCTCTGCC[C/T]GATCCTCTCTAGAGT | 494470 |
rs78637469 | snp | C/T | 0.133777 | 0.221342 | intron-variant | RNF165 | GRCh38.p7 | 18:46347637 | ATGTAATGTACCCAC[C/T]GTGAGTGGCTCCTGG | 494470 |
rs78716241 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46421819 | CCTCCCATCAGTGTT[C/T]TGAGAGCAGGAATTC | 494470 |
rs78745492 | snp | G/T | 0.212728 | 0.247206 | intron-variant | RNF165 | GRCh38.p7 | 18:46404488 | ACCAGGCGTGGTGGC[G/T]CACACCTGTAATCCC | 494470 |
rs78747278 | snp | C/G/T | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46351207 | GACACTAAATTAGAA[C/G/T]CATCTGGAAGCTTGT | 494470 |
rs78770859 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | RNF165 | GRCh38.p7 | 18:46416501 | ACATTCAGAACATTG[A/G]GAGCACAACTCAAAA | 494470 |
rs78774078 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | RNF165 | GRCh38.p7 | 18:46373492 | GCCTGGGTGCATCCT[G/T]GGGAGCAGGTCACTG | 494470 |
rs78776541 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | RNF165 | GRCh38.p7 | 18:46394902 | GCAGAATAACTCTGC[A/G]AACCTGGAACATTTG | 494470 |
rs78816227 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | RNF165 | GRCh38.p7 | 18:46415136 | AGAGTGTCCCCTCCC[C/G]AGGCCTACATGACCT | 494470 |
rs78817772 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | RNF165 | GRCh38.p7 | 18:46370848 | GAACTCAGGGGGCGT[A/G]AGGTCAGCATGAGCT | 494470 |
rs78818319 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | RNF165 | GRCh38.p7 | 18:46352036 | TTCCTGCCCTGGTGG[C/T]CTGGCAGACCCTGTC | 494470 |
rs78931753 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | RNF165 | GRCh38.p7 | 18:46399411 | TAGGCTGGGCCAGGC[C/T]ATGGGGCCTCCAGGG | 494470 |
rs78943891 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | RNF165 | GRCh38.p7 | 18:46360335 | GGAACACAGAGGGTG[A/C]TCCCCTGCAACAGTG | 494470 |
rs78974895 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46441292 | CCACTGTGCCCAGAC[A/G]CAGGCTGGTCTTACA | 494470 |
rs79006465 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | RNF165 | GRCh38.p7 | 18:46409334 | TCCGGTGAGATTGAC[A/G]TGATCTTCTGAGAAA | 494470 |
rs79074033 | snp | A/C | 0.0513262 | 0.151752 | intron-variant | RNF165 | GRCh38.p7 | 18:46416611 | CCTTAAAACAACAAC[A/C]TTTTATGCAGCTCAC | 494470 |
rs79120202 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46385301 | TGGGAGATGAAAGTG[A/G]TGGCTTGTGAGGACA | 494470 |
rs79121450 | snp | A/C/G/T | 0.00571518 | 0.0531541 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334301 | CCACGTCGGCTATCT[A/C/G/T]GTGCTTCCAGTGTTT | 494470 |
rs79135368 | snp | A/G | 0.121369 | 0.214369 | intron-variant | RNF165 | GRCh38.p7 | 18:46400349 | TGTGTTCCCCGGAAC[A/G]GGGATTGGACACCTG | 494470 |
rs79175238 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | RNF165 | GRCh38.p7 | 18:46408192 | AAGCAAGGAATTGTG[A/G]GGGCTGATAAAGAGG | 494470 |
rs79221032 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374629 | TTTATGCCTTCTCTT[-/T]GTGCTCTAATTCTTT | 494470 |
rs79255873 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | RNF165 | GRCh38.p7 | 18:46393355 | TGCATCTGGCCAGGC[C/T]CTGCCTGACAGGCAG | 494470 |
rs79258079 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | RNF165 | GRCh38.p7 | 18:46367917 | AACCACTTTCCTCCA[C/T]GATTCTGATGCCCAG | 494470 |
rs79263747 | snp | G/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46373203 | GTGTCATCTCCTTCA[G/T]GGGCCTCCAGGGCAT | 494470 |
rs79280864 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383187 | AAAAGGGAGATGCCG[A/T]CAGGCCCCTCCCACC | 494470 |
rs79300137 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | RNF165 | GRCh38.p7 | 18:46382097 | GTAGAGCCAGGTTGG[C/T]TTTGGGGGCTGGGCT | 494470 |
rs79300377 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | RNF165 | GRCh38.p7 | 18:46364728 | CTCTCTCTGCCCATC[C/T]GTGCTCACATACTGA | 494470 |
rs79336828 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNF165 | GRCh38.p7 | 18:46421285 | AATTCCATGCAGTTT[C/T]AAAATGCTGAGAGGC | 494470 |
rs79378929 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | RNF165 | GRCh38.p7 | 18:46430416 | CTCATTGTTTGGACA[A/C]TTCACAGGGAGATGT | 494470 |
rs79383830 | snp | A/T | 0.116138 | 0.211142 | intron-variant | RNF165 | GRCh38.p7 | 18:46441492 | TGGAATCTGTAATAA[A/T]GCTCCCTCTTTCATT | 494470 |
rs79391102 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46399272 | TCCAGGGCAGTGCTC[C/T]GGCAGCTTGGGCAAA | 494470 |
rs79424607 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | RNF165 | GRCh38.p7 | 18:46434473 | CGTGGCTTAATAGAA[A/G]GCAGCTGTGTTCTTA | 494470 |
rs79425753 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391134 | AAATGGCACCAATCG[C/T]CTCCATAAACAGGGT | 494470 |
rs79434156 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | RNF165 | GRCh38.p7 | 18:46399476 | CCTCCTGTGAGGAGC[C/T]GGTTTTATGGGATTT | 494470 |
rs79470099 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | RNF165 | GRCh38.p7 | 18:46394171 | ATGGGGTCCCCTGCC[A/G]AGGGACAGAATTTAC | 494470 |
rs79486622 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370395 | TGTGCAGAGCTTGTG[A/T]CTTCAACCAATTCTT | 494470 |
rs79508756 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46408520 | AGCAGAGGGCCATGA[A/G]GAACTTACCCGTAGT | 494470 |
rs79515264 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | RNF165 | GRCh38.p7 | 18:46363463 | GAGACAGTGCCCGTT[C/T]CTGGCTTCTCTAGGG | 494470 |
rs79603473 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46434335 | AAATATTTATTAATT[C/G]TCTTAAAAATAACAA | 494470 |
rs79704808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46373080 | TGTGTCAAAAGGTAG[A/G]CTAGAAACTCCAAAG | 494470 |
rs79720501 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNF165 | GRCh38.p7 | 18:46427599 | TGCCATTCTCTTTCC[C/T]GTTCCGTTTCAAACC | 494470 |
rs79749503 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RNF165 | GRCh38.p7 | 18:46343096 | TGCACTCAAAATGCC[A/G]TAGGTTCTAGGCCGC | 494470 |
rs79785829 | snp | C/T | 0.224709 | 0.248717 | intron-variant | RNF165 | GRCh38.p7 | 18:46414906 | AATGGGGAGCGTGCA[C/T]TTCCACCCAGGGCTG | 494470 |
rs79800788 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46396209 | CACATTCAAAGATGG[G/T]GAAATAGACTCTACC | 494470 |
rs79807947 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425380 | CCCGGGGCTACCCCA[G/T]GATGATGGCCTTCTG | 494470 |
rs79870671 | snp | A/C | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388841 | TGGGTGTGGGTGAAA[A/C]TTTCACACCCCACTT | 494470 |
rs79892972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46380282 | GGCTGGGGCCTGGAA[A/G]GGCGTCTTGGAAGAT | 494470 |
rs79901892 | snp | C/T | 0.0611083 | 0.163768 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461302 | ATGTGACACAGATCC[C/T]GTGGGAAACCACTGT | 494470 |
rs79909160 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334719 | GTGTGTGTGTGTGAG[A/T]GAGAGAGAGAGCGCG | 494470 |
rs79927208 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RNF165 | GRCh38.p7 | 18:46401788 | AGGCCTTGGAGAGGA[C/T]CTCCTTCTATGGTTT | 494470 |
rs79933342 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46346096 | TGCATGACTGGGTGA[A/G]GCTTGAGGACAGCTT | 494470 |
rs79957671 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46449892 | ATGGACTCTGCCACC[A/C]AACTGCCTGGGTTTG | 494470 |
rs79962213 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | RNF165 | GRCh38.p7 | 18:46352506 | TAAAGGTGGCTTAAA[C/G]GGATAGCAACTCTCA | 494470 |
rs79963152 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | RNF165 | GRCh38.p7 | 18:46380064 | CCATCCATGAGCTCT[C/G]CTGTCGGGTTAAACT | 494470 |
rs79963577 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392933 | CAGCTCCAGAAACCC[A/G]AGAAACACCATGGAA | 494470 |
rs80011616 | snp | A/G | 0.152001 | 0.229992 | intron-variant | RNF165 | GRCh38.p7 | 18:46404184 | GATTCTTGATTTCTC[A/G]AAAACTGCTCAATGT | 494470 |
rs80021114 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46378311 | CCCATACTACAGATG[A/G]GAAAACCGAGGCTGG | 494470 |
rs80033350 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | RNF165 | GRCh38.p7 | 18:46382653 | TCCTCTGTCTATTGT[C/T]CATCTCCTCTGATGT | 494470 |
rs80078409 | snp | C/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46353465 | TGTGGGAGTGAAAAT[C/T]TGTGTAGCTTTTAGC | 494470 |
rs80080586 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46338227 | GCCATGATCTGGAAT[C/T]TTAAAGTACCCTCTT | 494470 |
rs80141748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46452125 | TGGTGCAACACAGAG[A/C]AAACCCTAATGTAAA | 494470 |
rs80161699 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | RNF165 | GRCh38.p7 | 18:46391886 | CCCATATACACAGCA[C/T]GCACACATACTACAC | 494470 |
rs80190808 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392937 | TCCAGAAACCCAAGA[A/G]ACACCATGGAAACCC | 494470 |
rs80199220 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | RNF165 | GRCh38.p7 | 18:46408242 | TTCAGGGGAAGGTCC[A/G]CAGAAGGTGTCTTAG | 494470 |
rs80203161 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46402315 | TTTAGTTAAAACCTC[C/T]TTCCCTCTAAATCTG | 494470 |
rs80222434 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46344006 | TCCTCCTGCTGTCCT[G/T]TCCTTGAAACATGCC | 494470 |
rs80226076 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46372287 | TGTGGTGGTAAGTTG[C/T]TGCACTCATCCAGCC | 494470 |
rs80226491 | snp | G/T | 0.24019 | 0.249807 | intron-variant | RNF165 | GRCh38.p7 | 18:46397491 | GCTGAGGTGTGAGGG[G/T]GTGTGTGTGTGTGTG | 494470 |
rs80230338 | snp | C/G | 0.0248432 | 0.108648 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460993 | CTCAGCCCACCCAGC[C/G]GGTATCCTCTGAGGA | 494470 |
rs80234498 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46387494 | GGACTAGGGGAGAAA[C/T]TTGTCCCAACTTTAG | 494470 |
rs80236794 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46442163 | GCGAAACTCCGTCTC[A/C]AAAAAAAAAAAAAGA | 494470 |
rs80261922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343947 | TCTGGTGCTGCTGCT[C/T]TTGTTGGGCCACTGA | 494470 |
rs80270431 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | RNF165 | GRCh38.p7 | 18:46338770 | GACACTGAGGAAATG[A/C]GTTGATTAAAGAAAT | 494470 |
rs80280255 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46381780 | AGGCTACAGTGAGCT[A/G]GGATTCTACCACTGC | 494470 |
rs80298772 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46381831 | GCGAGACCCTGTCTC[A/C]AAAAAAAAAAGATGC | 494470 |
rs80327030 | snp | C/G | 0.0170251 | 0.090679 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388408 | CATTTGATCCTGGGA[C/G]CCTTCAGTGACCTAG | 494470 |
rs111164056 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46397696 | TGTGTGGTTATGCTG[A/G]GGTGTGAGGGTGTGT | 494470 |
rs111174320 | snp | G/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46397901 | GCTGAGGTGTGAGGG[G/T]GTGTGTGCATGTGGT | 494470 |
rs111174321 | snp | G/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46397982 | TGTGTGTGGTCATGC[G/T]GAGGTGTGAGGGTGT | 494470 |
rs111260223 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | RNF165 | GRCh38.p7 | 18:46447262 | CGATTTAGATTCTTC[C/T]TTCAGCATTTCTCTC | 494470 |
rs111315613 | snp | A/G | 0.444444 | 0.157135 | intron-variant | RNF165 | GRCh38.p7 | 18:46359197 | CACATGGCAATTTCT[A/G]CATGATGCCAGGCCC | 494470 |
rs111318826 | in-del | -/T | 0.0410537 | 0.137264 | intron-variant | RNF165 | GRCh38.p7 | 18:46338616 | AACCCTTAAAATATC[-/T]TTTTTTTTTCCATAA | 494470 |
rs111321933 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46362500 | ATTTCATCCTGGAAG[A/C]CCTCTCTGTCACTCA | 494470 |
rs111340156 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | RNF165 | GRCh38.p7 | 18:46456220 | AATGTGCTTCATGGT[C/T]GCCCTGGGAAGGTGG | 494470 |
rs111358566 | snp | C/T | 0.000773987 | 0.0196569 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46450356 | CTTGCTCTCCAGGGA[C/T]TAAATCCCAGCAGAC | 494470 |
rs111397317 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RNF165 | GRCh38.p7 | 18:46355827 | CCTTGCATGGCACCC[C/T]TGTGCCTGGAGGACC | 494470 |
rs111405092 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RNF165 | GRCh38.p7 | 18:46377462 | ATCCCGAGAACCCAC[A/G]GGAAGGTGCTTCATA | 494470 |
rs111409382 | snp | C/G | 0.0872718 | 0.189788 | intron-variant | RNF165 | GRCh38.p7 | 18:46365531 | GTTTTTGAGACCAAG[C/G]CTTGCTCTGTCGCCC | 494470 |
rs111435109 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | RNF165 | GRCh38.p7 | 18:46422037 | GGGGGCTAAGCCAAG[A/C]AATAGGCCTCTTGGG | 494470 |
rs111504308 | in-del | -/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46352706 | ACAGCACTGCACAAG[-/T]CCACCCCCACTCACA | 494470 |
rs111535399 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46350897 | CATCAGATGGGCCCA[C/T]TACCTGGGAGGAGAA | 494470 |
rs111550236 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46448412 | TGGTTCTGCTGAGGG[C/G]AGTAGGAGTGGGCAC | 494470 |
rs111580063 | snp | A/C | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46339752 | TTTAATAATAATTTT[A/C]CGCAAACCAGCAAAT | 494470 |
rs111592638 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374630 | TTATGCCTTCTCTTT[G/T]TGCTCTAATTCTTTG | 494470 |
rs111612159 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | RNF165 | GRCh38.p7 | 18:46353661 | ACGGGGCCCTGGAGA[C/T]GCATGCTGCTGGTAG | 494470 |
rs111618956 | in-del | -/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46424178 | TCTTGGAGGGCTCCC[-/T]AAGGGAGTTAACATC | 494470 |
rs111662158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46432924 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 494470 |
rs111676896 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RNF165 | GRCh38.p7 | 18:46351217 | TAGAATCATCTGGAA[A/G]CTTGTTAAAATACAG | 494470 |
rs111678098 | snp | G/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46410976 | GCATGGGTGGCAGAT[G/T]CCCAAGGCTCTGTCT | 494470 |
rs111702336 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46398701 | TCTAGCCCCACAGGC[C/T]CTGTAAGACCAGTGC | 494470 |
rs111711717 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | RNF165 | GRCh38.p7 | 18:46407912 | CACAGAGATTGGTGG[C/T]GTCTTCAGGATTTCA | 494470 |
rs111797085 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF165 | GRCh38.p7 | 18:46372745 | TGTTACCTGTGGCCA[A/G]GCTGTTTTATCCATA | 494470 |
rs111798602 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46370314 | CTGAAGCCTTGAAGG[A/G]ATAATCATCTTGTCC | 494470 |
rs111850759 | in-del | -/GGGT/GT/GTGT/GTGTGT | 0.378514 | 0.286291 | intron-variant | RNF165 | GRCh38.p7 | 18:46397489 | TGCTGAGGTGTGAGG[-/GGGT/GT/GTGT/GTGTGT]GTGTGTGTGTGTGTG | 494470 |
rs111858752 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383565 | GTTTTTTTTTTTTTT[C/T]TTTTTTTGAGACGGA | 494470 |
rs111862585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406259 | CTCAACCTCCCCAGA[C/G]AGTGGCCACTGTCAC | 494470 |
rs111874940 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | RNF165 | GRCh38.p7 | 18:46441274 | TGGGATTACAGGTGT[A/G]AGCCACTGTGCCCAG | 494470 |
rs111941131 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46370607 | TTGCCACCCTTCTCA[C/T]GTCTGATCTTAAACG | 494470 |
rs111975023 | snp | C/T | 0.118235 | 0.212457 | intron-variant | RNF165 | GRCh38.p7 | 18:46441760 | AGGTGCAGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 494470 |
rs112015192 | snp | C/G/T | 0.030278 | 0.119257 | intron-variant | RNF165 | GRCh38.p7 | 18:46445643 | TCAAATCATTAAGAT[C/G/T]GTCATGCTCTGCTTA | 494470 |
rs112035412 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF165 | GRCh38.p7 | 18:46372739 | AGCTTCTGTTACCTG[C/T]GGCCAGGCTGTTTTA | 494470 |
rs112052764 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46447530 | TGGCTAAATCACACC[A/G]CCCTATGGTTCACTG | 494470 |
rs112105428 | snp | A/G | 0.124491 | 0.216211 | intron-variant | RNF165 | GRCh38.p7 | 18:46454769 | GAGAGGGACAGAATG[A/G]GTAATTTTCTTCTTA | 494470 |
rs112132213 | snp | C/G | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333823 | TCTCCGGCCCGCGGG[C/G]GGCCAGGGACCCGCG | 494470 |
rs112132593 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46438501 | GGACTTTGCTTTGGT[A/T]GAATTCCTTGAACAT | 494470 |
rs112141684 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46445744 | ATGTGTTGTCCTTCT[A/G]TTGATAACAGTCTGC | 494470 |
rs112157618 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | RNF165 | GRCh38.p7 | 18:46344335 | AGGGAAGGGGTGGAG[A/G]CGCTCTCCATGTCTT | 494470 |
rs112196743 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | RNF165 | GRCh38.p7 | 18:46350644 | CGTTCCTCCTGCCAC[C/G]CTCGGTGGTGGCACT | 494470 |
rs112209517 | snp | A/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46432405 | TTTTTTCCTTAAAAG[A/T]GTATGCAAAACAACT | 494470 |
rs112215257 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46437559 | GTCCAGCCCAAGGTC[A/G]TCCACCCCCTGAGGT | 494470 |
rs112215358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391487 | CTCAGTGTCCTCATC[C/T]GTCATGTGTGTTGAA | 494470 |
rs112290447 | snp | C/T | 0.0640965 | 0.167152 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459619 | CCCTCCTCCTTCCCC[C/T]ACAGATGGGGACAGG | 494470 |
rs112296445 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429542 | TTTCTGTTCTAATAT[A/G]GCTTATTATTTGTTT | 494470 |
rs112310000 | snp | A/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46412387 | CTGCAGGCAAACATG[A/T]CCCTGCCAGTCTGCT | 494470 |
rs112317174 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | RNF165 | GRCh38.p7 | 18:46448722 | CTTGTGGCTGCAGAG[G/T]GCCGAATCATGGGTC | 494470 |
rs112350767 | in-del | -/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46444638 | CAACTAATTTAAACA[-/T]TTTTTTTTTTTTTTT | 494470 |
rs112384083 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46395186 | TCCAGTACCACGTTT[A/G]CTATTAGTACTTTCC | 494470 |
rs112385668 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | RNF165 | GRCh38.p7 | 18:46383761 | GGGTTTCACCGTGTT[A/G]GCCAGGATGGTCTTG | 494470 |
rs112463311 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362302 | GGTTTCTAACTGAGA[A/C/G]TCTTAGGCCTCGGTT | 494470 |
rs112471349 | snp | G/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46399262 | ACTCTGGACGTCCAG[G/T]GCAGTGCTCCGGCAG | 494470 |
rs112484237 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46454720 | CTTCAGATTTTTCTC[C/T]TTGCAAAATGATCTT | 494470 |
rs112561635 | snp | C/T | 0.0640965 | 0.167152 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459607 | AGACCCTGAAGCCCC[C/T]CCTCCTTCCCCCACA | 494470 |
rs112562198 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF165 | GRCh38.p7 | 18:46383388 | TGTAAGGAAAAATAC[A/G]TATATATAAAATATG | 494470 |
rs112575185 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46398125 | TGTGAGATCATGCTG[A/G]GGTGGGAAGGTGTGT | 494470 |
rs112576698 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46383842 | AGGCGTGAGCCACCG[C/T]GCCCGGCCACCATGT | 494470 |
rs112578496 | snp | G/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46398238 | TGTGGTGTGTGTGTG[G/T]GGTCATGCGGAGGTG | 494470 |
rs112610036 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46378212 | CAAGTTTGAGGTCGT[A/G]GTGTCCAAAAGCAAG | 494470 |
rs112651349 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46407055 | ACTCGACTTTTGCCT[C/T]GGCCTCTACCACCTC | 494470 |
rs112653197 | snp | C/G/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46345116 | ATGCAGGGGTGCCTG[C/G/T]GATGCAGGGCTGCTG | 494470 |
rs112747244 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46436822 | TTTAATTGCAATTTG[A/G]ATTGAATTCTGTCCC | 494470 |
rs112748522 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46403739 | AAGAATTAGCCAGGC[A/G]TGGTGGCGGTCACTT | 494470 |
rs112772851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445521 | CTCAAGGGAATCTCC[A/G]TGCAGATTTCTGGAG | 494470 |
rs112820280 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46362517 | CTCTCTGTCACTCAG[A/G]GGTTTTCTGTCCCTG | 494470 |
rs112822492 | snp | A/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46363714 | CTCACCGTTATAATG[A/T]GCTGGCCTTGTAGTC | 494470 |
rs112823157 | snp | G/T | 0.157642 | 0.232314 | intron-variant | RNF165 | GRCh38.p7 | 18:46353244 | ACAGTAGACACTGAA[G/T]GAAAGCTGCACATCC | 494470 |
rs112825972 | snp | G/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46412201 | TCAGATCTCAAATTG[G/T]GCAACTGCCCACAAA | 494470 |
rs112833294 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46338600 | ATTGAGTTGAAAAAA[A/G]AACCCTTAAAATATC | 494470 |
rs112840669 | snp | A/G | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391416 | GGGGCTGGGCTCACT[A/G]TATGCTCTCAGATCA | 494470 |
rs112960761 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | RNF165 | GRCh38.p7 | 18:46419492 | GTACCCAAGTCACTC[C/T]CCTGAGAGCCTGCCG | 494470 |
rs112985106 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | RNF165 | GRCh38.p7 | 18:46452488 | TTTCACCATGTTGCC[C/T]AGGCTGGTCTTGAAC | 494470 |
rs112993525 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46381937 | CTTGCTCTCTGGCAC[A/G]GGCTTTGGCTTAAGC | 494470 |
rs113047095 | in-del | -/CA | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46414481 | ATGTACACACACACA[-/CA]TCACAGGTGCCACAA | 494470 |
rs113099524 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46410806 | CTCACTTTAAGCATC[A/G]TTTCTTCAATTGTCC | 494470 |
rs113102042 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF165 | GRCh38.p7 | 18:46432936 | GGCGACAGAGCGAGA[C/T]TCCGTCTCAAAAAAT | 494470 |
rs113186246 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | RNF165 | GRCh38.p7 | 18:46429894 | AGTGTTGGGATTATG[G/T]ATGTGAGCCACTGTG | 494470 |
rs113202392 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | RNF165 | GRCh38.p7 | 18:46445615 | GCCTCCTGGAAATAA[G/T]ATCTCTGAATCCTCA | 494470 |
rs113238964 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336438 | AAAGTTTACTTTCAC[A/G]GCAAACATGCCCACA | 494470 |
rs113271376 | snp | C/G/T | 0.5 | 0 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457703 | GTCACAAAGAGGCAA[C/G/T]GTAGCCACTGCCTCC | 494470 |
rs113324664 | in-del | -/C | 0.0205511 | 0.0992634 | intron-variant | RNF165 | GRCh38.p7 | 18:46404804 | ACACACACACAACAA[-/C]CCCCCCCACCAAAAC | 494470 |
rs113327669 | in-del | -/C | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460904 | TTGCTACACTTGGCA[-/C]CCCCCCCGCCCCCAC | 494470 |
rs113366835 | snp | C/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46381194 | TCAGCCAGGCATTGG[C/G]ATAAGGCCAGGCACT | 494470 |
rs113428938 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46378837 | AGCTGCACAACGGAG[C/G/T]GGGTGCAGGATAGAG | 494470 |
rs113431014 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46398153 | TGTGTGTGGCCATGC[A/G]GAGGTGTGAGGGTGT | 494470 |
rs113452881 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46345192 | ACTGGAAGGAAGTTT[A/G]CGCCCGCTGGAACCT | 494470 |
rs113514370 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46369330 | TTACTGGAGAAGCAG[A/G]GGGATAAGGCTGAGC | 494470 |
rs113515778 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46367699 | CTACCAAACTGGCCT[C/T]GGTGTCCCCACCAGT | 494470 |
rs113548194 | snp | C/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46420377 | AGGAATAAAGCTACT[C/G]TCTGTCCTGTCCACC | 494470 |
rs113549943 | snp | C/T | 0.116838 | 0.211584 | intron-variant | RNF165 | GRCh38.p7 | 18:46441267 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACTG | 494470 |
rs113603041 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46350544 | CCCCCAACCCCAAGA[A/G]CCCCTGCAGCAGTTA | 494470 |
rs113605551 | snp | C/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46374793 | AGAGACCCTACACCC[C/G]AAGCCTGGCATTCCT | 494470 |
rs113613903 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408291 | TGAAGGGGCTACTGA[A/G]AAGATGGGCATCTGC | 494470 |
rs113629436 | snp | A/G | 0.108755 | 0.206276 | intron-variant | RNF165 | GRCh38.p7 | 18:46346184 | AGTGTGCCAGGCCTA[A/G]GAACCAGAGCCTGAG | 494470 |
rs113633179 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46366447 | GCCCCTGCAGAGGAC[C/T]TCTCATTCTCCCAAA | 494470 |
rs113660185 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | RNF165 | GRCh38.p7 | 18:46342820 | AATCAAAGGAAAAAA[A/T]ACCTCATAGGAGTCC | 494470 |
rs113671329 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | RNF165 | GRCh38.p7 | 18:46454975 | CATCTGAATTTGAGA[C/T]TTTACATAATGGTAA | 494470 |
rs113701012 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46414095 | TCTCATCTGAATCCA[C/T]GGCCTTCTGGAGGTA | 494470 |
rs113754831 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | RNF165 | GRCh38.p7 | 18:46383614 | GATTGGAGTACAGTG[A/G]TGCGATCTCAGCTCA | 494470 |
rs113758229 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46382000 | GGGTGAGATGCTCTG[C/T]AGGAGCCCCACAGCA | 494470 |
rs113787875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431315 | GCTCTCTGTTCATGC[C/G]AAAGAGTAGGTCACT | 494470 |
rs113789920 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46393277 | AGTTTGCGGAAAACT[C/T]TGTGGGGTGACTGTT | 494470 |
rs113790981 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46435166 | AGTGCTTGCTAGACT[A/G]TGGGTGCTAAGTGGG | 494470 |
rs113875246 | snp | G/T | 0.135825 | 0.222405 | intron-variant | RNF165 | GRCh38.p7 | 18:46397453 | GCTGAGGTGTGAGGG[G/T]GTGTGTGTGTGTGTG | 494470 |
rs113896990 | snp | C/T | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46398147 | AAGGTGTGTGTGTGG[C/T]CATGCAGAGGTGTGA | 494470 |
rs113914892 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF165 | GRCh38.p7 | 18:46425189 | ACACCTGAGAGCTGG[C/T]CTGAGGAGGCGGGAA | 494470 |
rs113917773 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369301 | GGCTGAGGCAGGGTG[A/G]CCTGAGCTGGGATTT | 494470 |
rs113964736 | snp | A/G | 0.5 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46381938 | TTGCTCTCTGGCACG[A/G]GCTTTGGCTTAAGCA | 494470 |
rs113992392 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46369797 | GTAAGACTTTGCATG[C/T]GCATTTCAAGAGATT | 494470 |
rs114047240 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46453946 | AGAGAGATTCTGTCT[A/C]TACAATAAAAAGAAA | 494470 |
rs114056267 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46340814 | CTTCCCTTCACAACT[A/G]TAGGTGTTTGCTAGC | 494470 |
rs114057500 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357641 | TGGGGCACTGGGCTC[A/C/G]AGGCCTGGGGCACAG | 494470 |
rs114123329 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | RNF165 | GRCh38.p7 | 18:46364134 | TGTGTTTTTAATAGA[A/C]CTGGGATTTCTCCAT | 494470 |
rs114139310 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF165 | GRCh38.p7 | 18:46423896 | CTTCCTCCTTTCCCT[C/T]GTTCCTCCTTCTTCA | 494470 |
rs114147213 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | RNF165 | GRCh38.p7 | 18:46345859 | TGGGTCCATCCAGGG[G/T]TGAGTGAGAGTAATT | 494470 |
rs114165845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344481 | CCACCTCCTAGAACA[C/T]CTGCTTCTACTCCTC | 494470 |
rs114168264 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46411502 | CCCTTTGCTATCGAT[C/T]GATTCATTTCAACAT | 494470 |
rs114168327 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | RNF165 | GRCh38.p7 | 18:46381344 | AGTGACCCATGCCAA[A/G]AGAATTTGGAGCTTC | 494470 |
rs114168352 | snp | A/G | 0.496778 | 0.0400063 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333896 | CCCGCAGCGGGCCGC[A/G]GCGATTGGCCGCCGG | 494470 |
rs114170557 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46395127 | TCCCATTTTATGGAG[A/C/T]TATGGGGTGGAGGGA | 494470 |
rs114189794 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46364518 | GACAGACAAGGTGAC[C/T]ACCAGACATATCATT | 494470 |
rs114215008 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RNF165 | GRCh38.p7 | 18:46385375 | AAGGACTTGCATGTG[C/T]CTGTGCATGTGTGTG | 494470 |
rs114246990 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46364061 | CAAGCAGTTCTCATG[A/C]GTCAGCCTCCTGAGT | 494470 |
rs114276298 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | RNF165 | GRCh38.p7 | 18:46448250 | TATCAACACCCCATG[A/C]CCTGACTCCCTTGTG | 494470 |
rs114296015 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RNF165 | GRCh38.p7 | 18:46391861 | TGCACAATACACCCC[C/T]CATATGCAACCCATA | 494470 |
rs114318720 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RNF165 | GRCh38.p7 | 18:46414579 | CCACAGACACATGCT[C/T]GCACATGCCCATATC | 494470 |
rs114338345 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46378969 | ATATGTCAAATGAAG[A/G]GACCTCACTGTCCCC | 494470 |
rs114340281 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46443580 | CAAATCTTGCCTGCT[C/G]TCTGTTCTTGTAAAT | 494470 |
rs114354530 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46393451 | CGCTGTTTCCTCTTC[C/T]GGCCCAGGGCTTTAG | 494470 |
rs114358173 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | RNF165 | GRCh38.p7 | 18:46360154 | CTCCAGCTCACTCCT[C/G]CAAACAGAGCTGTCC | 494470 |
rs114404673 | snp | A/C/G | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46456144 | GTGACCAATCACTGC[A/C/G]CCGTGTGTCTGGGAG | 494470 |
rs114412081 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46414918 | GCACTTCCACCCAGG[A/G]CTGCAGGAGGATGTG | 494470 |
rs114453084 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46344679 | GGGAAGGGACCATAC[C/T]TGCCCCCTCTGCCTG | 494470 |
rs114457934 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | RNF165 | GRCh38.p7 | 18:46345359 | TTGAGGTGGGAGAGA[A/C]GGCCAGATGACAACC | 494470 |
rs114482866 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF165 | GRCh38.p7 | 18:46411259 | GGTTTAATAGGGTCA[C/T]TGGCAAGTAGCTTTG | 494470 |
rs114501525 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46379439 | TTACCCTCACACCCA[C/G]CTTCCCTCCCCGAGT | 494470 |
rs114516897 | snp | A/G | 0.084728 | 0.187577 | intron-variant | RNF165 | GRCh38.p7 | 18:46383454 | TGCTAAATTAGACAC[A/G]AGACTAGTTAATATC | 494470 |
rs114523634 | snp | C/T | 0.0236746 | 0.106192 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387860 | TACAGGGACAGCCAG[C/T]GCAGGGCAACGCAGG | 494470 |
rs114537678 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF165 | GRCh38.p7 | 18:46347503 | AGCTGGGGGCTTCGT[A/G]TCCTCCCTCTGAAGC | 494470 |
rs114591675 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46354419 | GGGGGTCCTCATGCA[C/T]GAAGTGCAGGATTGG | 494470 |
rs114597396 | snp | A/T | 0.021333 | 0.101051 | intron-variant | RNF165 | GRCh38.p7 | 18:46372823 | CTTTATTCTAACCAC[A/T]CTGCGGTGCTATTAT | 494470 |
rs114608796 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46341040 | AGTGTGTGTTGATGG[C/T]GGGGCGGAGGCACAT | 494470 |
rs114624114 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46454251 | GAATAATGATGGCAA[A/G]AAAATAGTAGAAAGT | 494470 |
rs114648926 | snp | A/C | 0.0607341 | 0.163335 | intron-variant | RNF165 | GRCh38.p7 | 18:46410848 | AGTGGTCAGCAAGTC[A/C]TCCTTAAACTCTACA | 494470 |
rs114653238 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46374239 | CAATTATTTAATTAA[C/T]GAATTTTTATGGTGG | 494470 |
rs114716867 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RNF165 | GRCh38.p7 | 18:46339807 | AAAAGACCACCAAAA[A/G]TGTTGAGGCCCTAAT | 494470 |
rs114729428 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46385198 | GGGTGGTGTGATGTC[A/C]TGGGCCAGGGGAATC | 494470 |
rs114738609 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46404989 | GGCTCCAAAGTCTCT[A/G]TTGTTTCCACTGGAC | 494470 |
rs114768013 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RNF165 | GRCh38.p7 | 18:46338924 | CCTGCCTGACCACAG[C/T]GCTTCCTTGCCTTCT | 494470 |
rs114804859 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46451001 | GGAGGGAAGATGGAA[A/G]GCCTCTCATTAGTAA | 494470 |
rs114870027 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RNF165 | GRCh38.p7 | 18:46346493 | GCTGGGACTTCTTGG[A/G]GGCCGAGGGGATGGG | 494470 |
rs114870096 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46347509 | GGGCTTCGTGTCCTC[C/T]CTCTGAAGCGGGCAA | 494470 |
rs114875176 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46414703 | ACATGCACATACACA[C/T]AGCCTTGAGACTCCA | 494470 |
rs114892591 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46357169 | GAAAAATATAAACAA[C/T]ATGAAGGACTCCTCG | 494470 |
rs114967306 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | RNF165 | GRCh38.p7 | 18:46401764 | AGTCATGGGACTTTA[A/C]AGTTGAGGAGGCCTT | 494470 |
rs114970623 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46343722 | GAGCTTCTATTCCTA[C/T]CACCTTTTTGCTTTT | 494470 |
rs115005276 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386573 | CCATCCATCCATTCA[C/T]CCACCCATCCACCCA | 494470 |
rs115010787 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | RNF165 | GRCh38.p7 | 18:46381818 | TCTGGGTGACAGAGC[A/G]AGACCCTGTCTCAAA | 494470 |
rs115011335 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | RNF165 | GRCh38.p7 | 18:46416073 | CATGTCATGGGGGTG[A/G]AGAGGAAGAAAAACT | 494470 |
rs115014641 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | RNF165 | GRCh38.p7 | 18:46412519 | CCTCATACTGAGTGC[A/T]GCCCAGGGTAGTGGG | 494470 |
rs115040584 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RNF165 | GRCh38.p7 | 18:46344698 | CCCCTCTGCCTGTGA[C/T]GTTTGGGACTTCTGA | 494470 |
rs115046258 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46395096 | TATGCCTGAAGTCAA[C/T]GCTGACTAGCTGGAC | 494470 |
rs115065421 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46382191 | TGGTAACACCCATCC[C/T]TCCTGGACGGTCTGT | 494470 |
rs115118095 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348212 | GGGTGGGGTGAGGGC[A/G]TTGTGGGCCAAGGGG | 494470 |
rs115130027 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46341916 | TTGCCTCCACTACTT[C/T]GCAAAAGGCCATCCC | 494470 |
rs115154207 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | RNF165 | GRCh38.p7 | 18:46392220 | CCAACTCATCCCCAT[C/T]CTGTTCCCCTCTCAC | 494470 |
rs115182217 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF165 | GRCh38.p7 | 18:46399957 | ACCCTGCAAGGTGAT[C/T]AGGGCAAGTGGCTCA | 494470 |
rs115185145 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46443858 | CTCTTTATTCCTTTG[C/T]AGAGAGCTAAGTTTC | 494470 |
rs115199325 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46360046 | GTCTCTACCATAGTC[A/G]TCATGTCCAGTGTTT | 494470 |
rs115229515 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46349353 | CCTTGCATGGCAGAT[C/G]GTGAGAGGGACTCCT | 494470 |
rs115258158 | snp | A/G/T | 0.0287284 | 0.116357 | intron-variant | RNF165 | GRCh38.p7 | 18:46360756 | CTTGCCCTCTAATAC[A/G/T]CCTGGGCACACGAGG | 494470 |
rs115263539 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RNF165 | GRCh38.p7 | 18:46439710 | CTTTTTTATTAAAAA[A/G]AACCCTTTTTATTAT | 494470 |
rs115322145 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390997 | CTTGAAAACAGCAAA[C/T]GAAATGGAAATTCTG | 494470 |
rs115335748 | snp | G/T | 0.0244538 | 0.107838 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387819 | CAGCCTCTTGAAGCA[G/T]AAGCTGACCTTAGGG | 494470 |
rs115385848 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | RNF165 | GRCh38.p7 | 18:46428839 | GTGACTACTAGGAAA[C/T]GTAAAATTCCCTGTG | 494470 |
rs115468765 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | RNF165 | GRCh38.p7 | 18:46398279 | TGTGCATGTGGTGTG[C/T]GTGTGAGTGTGTGTG | 494470 |
rs115522263 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF165 | GRCh38.p7 | 18:46391947 | TGCACACAACACACA[C/T]GCACATGACACAATA | 494470 |
rs115526545 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46355425 | TCCTTCTGCCTCATT[C/T]TCTAGGCTCTGGTGA | 494470 |
rs115530058 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46374687 | CAATGGAATCCTCCC[C/T]CATCTTTTCCCCCTT | 494470 |
rs115600079 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | RNF165 | GRCh38.p7 | 18:46384398 | TCTTATTGCAGAGAT[C/G]CTCTTCTTCAGAGAT | 494470 |
rs115603394 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RNF165 | GRCh38.p7 | 18:46448107 | ATCCTGGCTCCCCTG[C/T]GCTCCGGATTCCATA | 494470 |
rs115639615 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | RNF165 | GRCh38.p7 | 18:46355929 | TGATGATGATGATGA[A/T]GCAGATGGGCCTCTG | 494470 |
rs115645969 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | RNF165 | GRCh38.p7 | 18:46352473 | TGTAAGTTTGGCTGT[C/G]GTAACAGAGATCCAA | 494470 |
rs115698107 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | RNF165 | GRCh38.p7 | 18:46399962 | GCAAGGTGATCAGGG[A/C]AAGTGGCTCAGGTTT | 494470 |
rs115702894 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46444531 | GTGCAGTGGTGGCAT[C/T]ACAGCTCATTGTAGC | 494470 |
rs115705660 | snp | A/G | 0.0107246 | 0.0724382 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458891 | GTATCACAGCGTCCA[A/G]CTCAGTAGCTCCAGT | 494470 |
rs115735841 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46402691 | TTTTTTGTAGACACA[A/G]GGTTTTGCCATGTTG | 494470 |
rs115766797 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF165 | GRCh38.p7 | 18:46436296 | TGTGTGTGTGCGTGT[A/G]AGTATATACATTGTG | 494470 |
rs115855087 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | RNF165 | GRCh38.p7 | 18:46376959 | AGGCGTAAGCCACAG[C/G]GCCCGGCCAAGAATC | 494470 |
rs115867482 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | RNF165 | GRCh38.p7 | 18:46413870 | TCTCCTCATGGGGAG[C/G]CTTGTTGTTATGTCT | 494470 |
rs115874272 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | RNF165 | GRCh38.p7 | 18:46341955 | GGAGCAGGGGGAACG[A/G]GAGGGAGCCCGACCC | 494470 |
rs115913626 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RNF165 | GRCh38.p7 | 18:46396356 | TCCTGGAAGCTCGTG[A/G]CCCATCAGTGAGAGA | 494470 |
rs115941879 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | RNF165 | GRCh38.p7 | 18:46379304 | TCCACTTTGACAAAC[A/T]CAAAACCCTCTCCTT | 494470 |
rs115942088 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF165 | GRCh38.p7 | 18:46373651 | CTGGCTCCTCGGGCT[C/T]CAGGGACAGCCCACC | 494470 |
rs115943261 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF165 | GRCh38.p7 | 18:46400707 | ACTCAGACAGCCTGT[C/T]GGGAAGCCTCTGTTG | 494470 |
rs115975854 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | RNF165 | GRCh38.p7 | 18:46366011 | TAAGAGATAACTCTT[A/G]GCTGGGCGCGGTGGC | 494470 |
rs115990555 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46362003 | ATCCCTGAGGATTTC[A/C]AAGGCATTTACAGAT | 494470 |
rs116011557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351378 | GTTCCAAGCAAAGGC[A/G]TCCCTTCCGTGGATA | 494470 |
rs116044171 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF165 | GRCh38.p7 | 18:46355564 | ACCAGCGGTCCCAGC[C/T]CCCATCTGTGCCTAT | 494470 |
rs116049974 | snp | A/G | 0.039522 | 0.134904 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456858 | CCATCCGCCTGGCTG[A/G]GCAGGAGAGAGGGAG | 494470 |
rs116051098 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46422337 | AGGGTGCATTACCTA[G/T]TTGCATGAAATCCGA | 494470 |
rs116104360 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46405589 | GCAAGAGGAAAAATG[C/G]TAAGAAGGTTCCTGG | 494470 |
rs116106348 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RNF165 | GRCh38.p7 | 18:46442301 | CTAGCTTCTTAAGGC[A/G]GAAATTTAGATCATG | 494470 |
rs116113911 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46422546 | TGGGCGCAGCCCCAC[C/T]GGCTTGCTCCCTGAG | 494470 |
rs116121700 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RNF165 | GRCh38.p7 | 18:46376905 | TGATTTCTGATCTCG[C/T]GATCTGCCCGCCTCG | 494470 |
rs116145556 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF165 | GRCh38.p7 | 18:46451036 | GGAGAGCTGGGTATC[C/T]GTGTGTGCATGTGGA | 494470 |
rs116156464 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46345329 | TTCCCCGGGCAGGTG[C/T]GGTGGGAGTGTTGAT | 494470 |
rs116161681 | snp | A/G | 0.0333238 | 0.124705 | intron-variant | RNF165 | GRCh38.p7 | 18:46407891 | AGAACCTGGCATACT[A/G]AGAAGCACAGAGATT | 494470 |
rs116175686 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | RNF165 | GRCh38.p7 | 18:46371132 | CATTTATAAAACCAT[C/T]GGATCTCATGAGTCT | 494470 |
rs116283654 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46373734 | CTCCAGGATCTCTGC[A/G]GGTGTGGGGGGAATT | 494470 |
rs116283944 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RNF165 | GRCh38.p7 | 18:46400836 | CCCCCTTGGTCTTCT[A/G]TTAGAATGAAAATCC | 494470 |
rs116314555 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46362424 | TGAGGGGAGAGTGTG[C/T]TGAGGGGAGGAGTGT | 494470 |
rs116315426 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | RNF165 | GRCh38.p7 | 18:46398454 | CCTAGCCCCTTACCC[A/C]CAAGGTGCCTGCTGG | 494470 |
rs116366231 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | RNF165 | GRCh38.p7 | 18:46361531 | GTGCCCGGCCACACG[G/T]TTCCCCTCCACAGTT | 494470 |
rs116380338 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458890 | AGTATCACAGCGTCC[A/G]ACTCAGTAGCTCCAG | 494470 |