SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs116400156 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF165 | GRCh38.p7 | 18:46342237 | GGGGAACCTAGGTGA[C/T]TGGACACTCGACTAT | 494470 |
rs116435583 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46358556 | CCTCAGCCTCCCTCT[A/G]TGACCTTCCTCAACT | 494470 |
rs116467799 | snp | A/C/G | 0.0189856 | 0.0955633 | intron-variant | RNF165 | GRCh38.p7 | 18:46403212 | GTGTGCCAGAGTCTG[A/C/G]CACCTGGCAAAATGT | 494470 |
rs116471496 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RNF165 | GRCh38.p7 | 18:46453751 | TATAGAAAATACTGA[A/G]TCAAAATAGAAAAAT | 494470 |
rs116494215 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46352881 | GTTGGTCATCTCTGC[C/T]TCAGTTGGTGCTTAG | 494470 |
rs116495091 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412125 | CATCTCACAGCCCTG[A/G]GAATCAAAGCACAGC | 494470 |
rs116506365 | snp | A/T | 0.0168055 | 0.0901129 | intron-variant | RNF165 | GRCh38.p7 | 18:46448595 | AAATGGAAATGAAGA[A/T]GCCTGCCTCGCCCAT | 494470 |
rs116577175 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | RNF165 | GRCh38.p7 | 18:46338970 | ACTCTCCTCTCCCCC[C/G]ATGGCTGCCCTCTCT | 494470 |
rs116617214 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | RNF165 | GRCh38.p7 | 18:46410150 | TTCCACTTCTAAGGT[C/T]ACATGACCTCAGGGC | 494470 |
rs116650875 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | RNF165 | GRCh38.p7 | 18:46452987 | CAACGGGATGATGCA[C/T]TTGAACAGCTTGGCA | 494470 |
rs116684218 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF165 | GRCh38.p7 | 18:46341586 | AGGGGATTGTGGCAA[C/T]GTCTGGGAGTTGAGA | 494470 |
rs116748060 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | RNF165 | GRCh38.p7 | 18:46416422 | CATCCAGCCCTGTCC[A/T]GAGGGTGCTCTGGGT | 494470 |
rs116796983 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46416032 | GCCTTCCTGACTTTG[C/T]TGCTGGCATTTTCAT | 494470 |
rs116840055 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46414550 | ACCTGCACATGAACA[C/T]GTTCACACAAATCCC | 494470 |
rs116962884 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | RNF165 | GRCh38.p7 | 18:46380550 | GACCCAGGCGCTTGC[A/G]TTTCCTCAGGTCCTA | 494470 |
rs116964387 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46437083 | TTAAACCAGTCTGCA[C/T]TCCTGACCACTACCT | 494470 |
rs117003531 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | RNF165 | GRCh38.p7 | 18:46439074 | GCAGTCCTTCCTGCC[C/T]GTAGCAGCTGGACCT | 494470 |
rs117043606 | snp | A/G | 0.114036 | 0.209795 | intron-variant | RNF165 | GRCh38.p7 | 18:46383843 | GGCGTGAGCCACCGC[A/G]CCCGGCCACCATGTT | 494470 |
rs117108283 | snp | A/G | 0.0437281 | 0.141251 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439420 | GCCTCCTGCCATCTC[A/G]CTCCTGTAGGATCTG | 494470 |
rs117149340 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46400776 | CAGTAGCCCCGTCAC[C/T]GTGCTCCTAATGGCA | 494470 |
rs117170568 | snp | A/T | 0.0599851 | 0.162463 | intron-variant | RNF165 | GRCh38.p7 | 18:46454160 | GGGAAGGTTAATGAA[A/T]CGAGAAGATATATAG | 494470 |
rs117252985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423567 | CTCTGGGCATACCAC[A/G]TGGAGACGTGTATGG | 494470 |
rs117285965 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | RNF165 | GRCh38.p7 | 18:46375641 | CCTTGAATGAATTGC[G/T]CCGTTATATGAGCTG | 494470 |
rs117286345 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332896 | CAATGTAGGGAATGT[C/T]CTCTGTCTTTCTGCC | 494470 |
rs117288289 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RNF165 | GRCh38.p7 | 18:46373812 | TGCCTAGGCCAGACC[A/G]TGCAGCCAGAGAAAG | 494470 |
rs117352526 | snp | C/T | 0.0648419 | 0.167978 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460252 | TAAGCCCCCCGCCTG[C/T]AGGCGGGACAAACAC | 494470 |
rs117358197 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46421737 | GGCCCTTTGCTGCTT[C/G]TTGGAAGCTTGCTGC | 494470 |
rs117383265 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | RNF165 | GRCh38.p7 | 18:46419639 | AGCGGAGTGGGCAGC[G/T]CACAGCTGGACCAGG | 494470 |
rs117455626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376919 | GCGATCTGCCCGCCT[C/T]GGCATCTCAAAGTGC | 494470 |
rs117482031 | snp | A/G | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390008 | GCTTGGACTATAGGC[A/G]TGAGCCACCATGAAA | 494470 |
rs117541970 | snp | A/G | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390695 | GGTGTGGAATATCAG[A/G]CTAAGGAGATACAAA | 494470 |
rs117578696 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46350409 | GGGCTTCCTGGAGGC[G/T]TTGAGTCTTCAGCTG | 494470 |
rs117594963 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RNF165 | GRCh38.p7 | 18:46455570 | GGCCGGGCAAGGTGG[C/T]TCACATCTATAATCC | 494470 |
rs117669813 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RNF165 | GRCh38.p7 | 18:46423464 | TAGGGGAACTCAGGA[A/G]AGAGAGAGGGATGGG | 494470 |
rs117743342 | snp | A/C | 0.0648419 | 0.167978 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460253 | AAGCCCCCCGCCTGT[A/C]GGCGGGACAAACACT | 494470 |
rs117750034 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | RNF165 | GRCh38.p7 | 18:46350280 | GTGTGTCCACATCTG[C/T]AGGCCAGCCGCAGAG | 494470 |
rs117791286 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | RNF165 | GRCh38.p7 | 18:46369968 | ACACGCACACATGCA[A/C]ACACACGCACCCTAG | 494470 |
rs117799339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46398357 | GGAGCGACACCAGGC[A/G]AGCAGGTGTTGGATG | 494470 |
rs117800764 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46378476 | TGATGGGCTTTTGCA[C/G]CGCTTTCTGTAAGTC | 494470 |
rs117816477 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46426062 | CTATCTAATCACCTC[C/T]CAAAGGCCCTGCCTC | 494470 |
rs117850089 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46400387 | CCCAGTGCATAGATA[A/T]GGCTTTAAGAGCTCT | 494470 |
rs117860160 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46372802 | GCGCCAAAATCCATA[C/T]GTTTCCTTTATTCTA | 494470 |
rs117880461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432333 | TAAATGATAATGTTA[C/T]AACACATTATTTAAC | 494470 |
rs117887409 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46386806 | AACATTTTGTTTTCA[C/G]TTCTCATCACTTCCT | 494470 |
rs117897336 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | RNF165 | GRCh38.p7 | 18:46383608 | CACCCAGATTGGAGT[A/G]CAGTGGTGCGATCTC | 494470 |
rs117911495 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46394400 | GACGGGGTTCACTCT[A/C]GGAGATGACACAGCT | 494470 |
rs117950407 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46412095 | CAGATCTCAGCTCAG[C/T]GGGAGACAACGGCTC | 494470 |
rs117993275 | snp | C/T | 0.0126979 | 0.078662 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333562 | TTGCGGCTGCTTGTT[C/T]GCATTCCAGCTTCCC | 494470 |
rs118032702 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417416 | ACCACTCAAGCCTCC[A/C/T]GAAGTTTCTCAAAAT | 494470 |
rs118143938 | snp | A/G | 0.030665 | 0.119967 | intron-variant | RNF165 | GRCh38.p7 | 18:46368715 | CACACTGAAAGTTTA[A/G]CGTAGTGGTCAGGGT | 494470 |
rs137890331 | snp | A/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332386 | CCTGGGTTCTGCCCT[A/T]GCCACTGGGAATATG | 494470 |
rs137901861 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388672 | CAAGACATGAAGAAG[G/T]GGCTTGGGGCTGGGC | 494470 |
rs137929179 | snp | A/G | 1.98762e-05 | 0.00315241 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334313 | TCTCGTGCTTCCAGT[A/G]TTTGGCTCTGTGCGA | 494470 |
rs137947145 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46424430 | CGTGGCAGCCATTTA[C/T]TTGGAAGAGGGATTT | 494470 |
rs137951410 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46456370 | CTGATCTGAAAGCGC[C/T]TCCTGGCGGAGGCTT | 494470 |
rs137968536 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46353178 | TATAGTAGAATGTTA[C/G]ATCTAAAAATGAGAT | 494470 |
rs137968556 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46392656 | GCCAAGGCTGGGGGA[A/C/T]ACTGGGCCAGCCTCG | 494470 |
rs137969413 | snp | C/T | 0.000477716 | 0.0154476 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46450382 | CAGACACACCTCCGC[C/T]GTACGGGAGAGCTAT | 494470 |
rs138012294 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46344489 | TAGAACACCTGCTTC[A/T]ACTCCTCAAATTCCC | 494470 |
rs138033662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46384171 | ACCACTGCCCCGGCC[A/G]TGCTTCCAGCCCAAC | 494470 |
rs138053235 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46419181 | TGCTACTCTCCCCTG[C/T]CTGGTATTTTACTAC | 494470 |
rs138067870 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | RNF165 | GRCh38.p7 | 18:46448670 | TCTTGGGCCTAGCCT[G/T]CCTATCCAGTTCTGC | 494470 |
rs138069505 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46374414 | CATTAAACACGAACT[A/C]CCCATTCTCCTCCCG | 494470 |
rs138090722 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46407802 | TTATAGTTGGAGTGA[G/T]GAGATCCACCCATGT | 494470 |
rs138121187 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445703 | GCCTTCATGCAAAAA[-/A]CTAGGGAGGTTGCAG | 494470 |
rs138128489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46454850 | AGGTGGGCTGATTTC[A/G]CTCACGACTAGATTT | 494470 |
rs138132159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356983 | GGGACAAGTGGCTTT[G/T]TCCAACTCCCACACC | 494470 |
rs138140175 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46380394 | CCAGAGGAACTTGCT[G/T]AAGGTTTCTTTGAGA | 494470 |
rs138180534 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439663 | AGGTAAAACTTGGAG[A/G]TAGTGGATGTTACCT | 494470 |
rs138193572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46433042 | TGGGTTAAGGATGAC[C/T]ACATGCCTCTAACAG | 494470 |
rs138224085 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF165 | GRCh38.p7 | 18:46406317 | GAGCTGCAGCAGAGC[A/G]ACAGCCAGGCAGCCC | 494470 |
rs138287361 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46340611 | GCTGAGATAAAAGAG[C/G]TTGGAGCAGTCCAGG | 494470 |
rs138330552 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | RNF165 | GRCh38.p7 | 18:46444379 | CCCCTCTTTTTGGGT[A/C]TTTACTTACCCATGT | 494470 |
rs138346987 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF165 | GRCh38.p7 | 18:46344000 | GCTGCTTCCTCCTGC[C/T]GTCCTTTCCTTGAAA | 494470 |
rs138397674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393064 | GCACACAGCTACTTA[A/G]TGGCAGGATGAGTCC | 494470 |
rs138411887 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46362314 | AGACTCTTAGGCCTC[A/G]GTTTACTGTCTCAGG | 494470 |
rs138413525 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46399193 | GTGAGGACAGTGAAT[C/T]CTTCGAGGAGAAGGT | 494470 |
rs138442855 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46395816 | TCCAGAGCTTTCTGG[G/T]GCCAGGTGGTGATGG | 494470 |
rs138527410 | snp | A/C | 0.00676609 | 0.0577691 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459844 | CCTCCTCCTGCTCAA[A/C]TCAAGGGACTCAGAC | 494470 |
rs138584539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352289 | CAGACTCTTTCCCCA[C/T]CTAGAATCTACACTT | 494470 |
rs138598135 | snp | C/G/T | 0.000675208 | 0.0183618 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46456570 | CGTGGACCAGTGGCT[C/G/T]GCCATGAGCAAGAAA | 494470 |
rs138606867 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388294 | AAAGACTTGGAAAGG[C/T]TGCAAACCTGGAGAA | 494470 |
rs138610151 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458886 | AATGAGTATCACAGC[A/G]TCCAACTCAGTAGCT | 494470 |
rs138629324 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46404217 | TTAGGGTCACACCTG[C/T]GAGTTCTTTCCTGGT | 494470 |
rs138650235 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46444820 | AGTCACTAATCTTTT[C/G]TTTTGTAGTATCTAA | 494470 |
rs138651098 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RNF165 | GRCh38.p7 | 18:46357244 | TACCCAGGTCTCTTC[C/T]CCAGTGGTAACAGTG | 494470 |
rs138662716 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46378171 | GTCCCCTGCACCAAA[C/G]CATTTATCAATTTAT | 494470 |
rs138696533 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46360768 | TACGCCTGGGCACAC[A/C/G]AGGCGGGTATGTGGA | 494470 |
rs138702654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423697 | CCAACTTGGCCATGA[C/T]TACTCTAGAGCCCTC | 494470 |
rs138703338 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386570 | CATCCATCCATCCAT[C/T]CACCCACCCATCCAC | 494470 |
rs138704166 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | RNF165 | GRCh38.p7 | 18:46348311 | GGGAGCTGGGGGACT[A/G]ATGGCATGCAGGGAA | 494470 |
rs138704920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46412035 | GGGAGCAGAGGTATT[C/T]GAGTCAGTTGGTGCT | 494470 |
rs138712044 | in-del | -/TG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436277 | GTGGGTATATATGTA[-/TG]TGTGTGTGTGTGCGT | 494470 |
rs138724973 | snp | A/C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419762 | GACGGACAGGCCTCT[A/C/G]CTGCTTGTTAGGCAT | 494470 |
rs138733891 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | RNF165 | GRCh38.p7 | 18:46382101 | AGCCAGGTTGGCTTT[C/G]GGGGCTGGGCTCTTA | 494470 |
rs138736798 | in-del | -/A | 0.0295267 | 0.117862 | intron-variant | RNF165 | GRCh38.p7 | 18:46367025 | TACTTAGTTTCCAAG[-/A]AAAAATCACCAAGCA | 494470 |
rs138739761 | in-del | -/CTTTT | 0.0167096 | 0.0898644 | intron-variant | RNF165 | GRCh38.p7 | 18:46365383 | AGTCTCTGGAAGAGC[-/CTTTT]CTTTTCTCCACTAAT | 494470 |
rs138741244 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399231 | GGGTCACACAGGCGG[G/T]GGGGGTGGGACTGGT | 494470 |
rs138766536 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46399727 | AGGAACTGAGAGGCA[A/G]AGGAGGACAGTGTCC | 494470 |
rs138905429 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46367365 | TGAGCACAAATTGGA[A/G]GATTGCATTTATGTT | 494470 |
rs138998035 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF165 | GRCh38.p7 | 18:46395333 | TTTACTTTGTCACTA[C/T]TGACATTTTGGGCAG | 494470 |
rs139017583 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46432347 | ATAACACATTATTTA[A/G]CTATTACTTAAATTA | 494470 |
rs139017902 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RNF165 | GRCh38.p7 | 18:46393445 | AGGGTGCGCTGTTTC[C/T]TCTTCTGGCCCAGGG | 494470 |
rs139031609 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46372950 | CCTCCTAATGCCACC[A/G]TCATCAGCCTCACTC | 494470 |
rs139076129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46433885 | ATTTGACTAGGGAAC[C/T]CCTCATGTCCCCTCC | 494470 |
rs139081730 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46401771 | GGACTTTAAAGTTGA[G/T]GAGGCCTTGGAGAGG | 494470 |
rs139094382 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46412739 | ACTCTTAGAAAATGA[C/G]AAGGCCGCCTCGGGC | 494470 |
rs139102089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46377288 | AGATTGACAGTTCAT[A/G]TCATCCCTCTTTCTC | 494470 |
rs139102163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46335622 | TGATGTCTTCCCTTG[A/G]CCGACCAGGGCTCCT | 494470 |
rs139147821 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | RNF165 | GRCh38.p7 | 18:46438341 | TCGAGGAACCACATC[A/C]CCTGTTGGGGTAGCC | 494470 |
rs139168954 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46368914 | TAGTGTTTAGAACAG[G/T]GCATGGCACACAGTA | 494470 |
rs139202971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46375912 | CAGGTTCAGTCCCTG[C/T]CTTTGATGAGACTGT | 494470 |
rs139277814 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46426413 | TGTCCTCCTATCCAC[C/T]CACTATCCAGCAGCC | 494470 |
rs139316583 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RNF165 | GRCh38.p7 | 18:46420016 | TGCCCCATGAGCAGT[A/G]ATGGTTGGGAATCTA | 494470 |
rs139331895 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46341966 | AACGGGAGGGAGCCC[A/G]ACCCAGTAGCGTATT | 494470 |
rs139380694 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46421573 | TGTTGGTTTAGATGG[A/G]GAAAGTATCTTCTTG | 494470 |
rs139411150 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386895 | GATTTCTAGTACCTT[C/T]GGCATCATGGGCAGT | 494470 |
rs139494770 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46386178 | GCCAGGGTTTCTCTT[C/T]CTCTGGCTGCCTCAT | 494470 |
rs139498752 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46345158 | CCACGGAACCAGAGG[G/T]ATAGGGCAGCAAGGG | 494470 |
rs139504743 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46436896 | GGAGTACTCAGGGCC[C/T]TTGCATATGGCTGAG | 494470 |
rs139517164 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46383052 | CTTGGCCAGATCATG[A/G]CATCCATCTCATGCC | 494470 |
rs139521483 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46449678 | GATGGTTTTACAAGG[G/T]ACCTCCCCATTCGCT | 494470 |
rs139593094 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46393650 | CCAGTTCTTCTCAAA[C/T]CTTGATGTATCTTCC | 494470 |
rs139600716 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46341477 | GACCATGAAGACAAA[C/T]GGGGAACATGGGAGG | 494470 |
rs139609664 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46430813 | TGCATGGATCCAACA[C/T]CTTATTTTCCTGAGG | 494470 |
rs139629856 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390167 | CCCTGTGGGATGAGC[C/T]AGGCTGGCAAGTCAG | 494470 |
rs139714120 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | RNF165 | GRCh38.p7 | 18:46430997 | TTGCTGCACCCATCA[A/G]TCCATCATCTACATT | 494470 |
rs139716920 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46393951 | CTGCCTGGTGGGGAT[A/C]CTGTGGGATTCTGGA | 494470 |
rs139724171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358094 | GACCCTGTTTCCAAA[G/T]AAGGTCACACTCACA | 494470 |
rs139734280 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46396896 | TCCGCTAATTGTCCA[A/G]CTGGCTCAGTTCAGT | 494470 |
rs139748098 | in-del | -/AT | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46339571 | TCAACCACCTGACAC[-/AT]GTCTGTTTTAGCACC | 494470 |
rs139779598 | snp | A/G | 0.0115949 | 0.0752539 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46435352 | CTTCGACTTCGGCCA[A/G]CTGCAGACACCTCAG | 494470 |
rs139849171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408027 | TTGGACATCATGGAT[A/G]GGGTGGCAGGGATTG | 494470 |
rs139852042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46371326 | ATTCCCCTGGCCAAC[A/G]AGATGGCCCACTGCA | 494470 |
rs139872431 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46405096 | CCTTTTATCTAGGAC[C/T]TGATTCATAAAATGG | 494470 |
rs139878081 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46355372 | TGGTTCTCTCTCAGG[A/G]CCTCGGGCTCCTCAC | 494470 |
rs139903101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336250 | ATTATCCTGATTAAA[C/T]CATTACCATCCTCAT | 494470 |
rs139907326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400459 | CCTGTCACCTCTTCA[A/G]CTCAGATCCAGTGGG | 494470 |
rs139917883 | snp | A/G | 0.0186134 | 0.0948125 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389459 | TCATTTTGTAGGCAC[A/G]GAAGTATATGTAGGA | 494470 |
rs139928495 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460127 | CTGCAAATGTTCCCA[G/T]CCTCCGTGCAAGTAT | 494470 |
rs139936190 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46375146 | ACCCTCCCAACTCCC[C/G]CCGCCCTCAGAGGCC | 494470 |
rs139966902 | snp | A/T | 3.30066e-05 | 0.00406229 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435357 | ACTTCGGCCAACTGC[A/T]GACACCTCAGCCCAG | 494470 |
rs140062140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46425626 | CTTGCTGCCTTCCAC[A/G]GTCCCTGGCATCTGA | 494470 |
rs140080341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46358827 | GTCATCACTGTGTCC[C/T]GGTGCCTAGAGGAGG | 494470 |
rs140082769 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46422016 | AAGCAGACCCATGGC[A/T]GCCCTGGGGGCTAAG | 494470 |
rs140134527 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RNF165 | GRCh38.p7 | 18:46452343 | GGAGTGCAGTGGCAC[A/G]ATCTTGACTCACTGC | 494470 |
rs140151158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350387 | TTGGATGCCATGTGG[C/T]CTGGGAGGGCTTCCT | 494470 |
rs140168998 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46412987 | GAGGGATGCTTGCAC[G/T]TCAAACAACACAGCC | 494470 |
rs140200209 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409858 | GTTCTCCTATTGATG[G/T]ACATTTCGTTGTTTC | 494470 |
rs140205305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360970 | CAAGTGGACGTCCAC[A/G]GAACACTGCACTTGA | 494470 |
rs140208753 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46437470 | TCTGTTGCATCCCCT[A/C]TCCCCTTTAGAGAAC | 494470 |
rs140255216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46371727 | CCCAGCTTCAGGTGC[A/G]CTTTCTTCCCAGTGA | 494470 |
rs140290495 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332295 | CTGAGTTCTCTGGGG[G/T]CAGCCAGAGTTTAGG | 494470 |
rs140322324 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | RNF165 | GRCh38.p7 | 18:46353739 | CCCATGCTGCTGCCT[C/T]GGATCCTTGATCTGA | 494470 |
rs140340427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46416788 | GTTAGCCTGGGCTTG[C/T]TCTTATGGTAGAGGC | 494470 |
rs140382456 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | RNF165 | GRCh38.p7 | 18:46383836 | GATCACAGGCGTGAG[C/G]CACCGCGCCCGGCCA | 494470 |
rs140392802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46454105 | GCAAGAGGGCAAGGC[C/T]GTCTCAAAAAAAAAA | 494470 |
rs140397394 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF165 | GRCh38.p7 | 18:46356788 | GTCACCTCTTCTCCC[C/T]GCAGCTTCCTGCCTC | 494470 |
rs140401397 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46419039 | GGAGAATTTTTGGCT[C/G]TAGTGGGAACGCTAT | 494470 |
rs140412829 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449037 | GAATAAAGAAGCAAG[-/C]ATTTATTGAGCACTT | 494470 |
rs140458173 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458081 | TGCAGCCCCATTTCC[A/G]GTCCTGCTACCTCAC | 494470 |
rs140489747 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46403647 | CTTTGGGAGGCCGAG[A/G]CGGGTGGATAATTTG | 494470 |
rs140508084 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46414865 | CCCTAGGAAACATTT[G/T]CATTTTGTGTCATCA | 494470 |
rs140574018 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46368337 | TACTCTTCCCCCATT[G/T]CCTCCCTTTCTGCCT | 494470 |
rs140588718 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46376290 | GTGTCAAGAATCTCT[A/G]TGAGGTAAATGTTAG | 494470 |
rs140616528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46351520 | TGCACCTGCAGAGCC[A/G]CCCTGCCATTGTCCT | 494470 |
rs140653943 | in-del | -/CTG | 0.0663309 | 0.169604 | intron-variant | RNF165 | GRCh38.p7 | 18:46431630 | GACTTTCACTTAATC[-/CTG]CTGTGTTTGTTAGCA | 494470 |
rs140659550 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46428485 | TCACCAGTAAGCAGT[G/T]GTCACTGCTCCACTC | 494470 |
rs140700959 | snp | A/G | 0.0123036 | 0.0774623 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332562 | CACCCACTGGGCTGG[A/G]TGCCCCTCCAAGGCT | 494470 |
rs140707584 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | RNF165 | GRCh38.p7 | 18:46442378 | CTTTAAGGACTACAA[A/T]CTTTCTAGTTAGCAT | 494470 |
rs140728386 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46438009 | ATGGTGCTGGCACTC[A/G]TAGGGCCAGATTCTG | 494470 |
rs140735320 | snp | A/C/T | 0.000206288 | 0.0101541 | intron-variant, missense, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433468 | CTGCAGCAGCAGCTC[A/C/T]TGGAAGCCCAGCACC | 494470 |
rs140740755 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46338895 | TCACCCTGCTCCTCG[A/C]TGGCGGGTGCACCCC | 494470 |
rs140749698 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46370305 | ATGAGAAAACTGAAG[C/G]CTTGAAGGGATAATC | 494470 |
rs140749944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46365549 | TGCTCTGTCGCCCAG[C/T]CTGGAGTGCAATGGT | 494470 |
rs140779573 | snp | A/G | 1.65419e-05 | 0.00287588 | missense, intron-variant | RNF165 | GRCh38.p7 | 18:46450744 | TGGGTAATGTGACTC[A/G]GGGAGCTGTACAGAA | 494470 |
rs140804138 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46423264 | TGTCCTTGGCATTTC[C/T]TTAGTCTAGGGAGGA | 494470 |
rs140850362 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46402195 | TGAAAGCATCTATAC[A/C]CTGTTGGTTAACTCT | 494470 |
rs140892229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388134 | ACATGTTTATTTGGG[A/T]TTACAGCTGGGAGGT | 494470 |
rs140967870 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46455573 | CGGGCAAGGTGGCTC[A/G]CATCTATAATCCCAG | 494470 |
rs140970564 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414737 | GGGCAAACACAGCAC[A/G]TGGAATCCTGGTCCT | 494470 |
rs140975273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46347804 | CAGTGTTCTTATCTG[C/T]AAAATGGGAATAATT | 494470 |
rs140983543 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46438062 | GCAACCAGACCACAC[A/C]ATGTTCAAGAACATT | 494470 |
rs140994237 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF165 | GRCh38.p7 | 18:46383773 | GTTGGCCAGGATGGT[C/T]TTGATCTGACCTCGT | 494470 |
rs141032818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417632 | TGCTTCATTTTTTCC[A/T]TAGCTCTGTCATCAT | 494470 |
rs141082865 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46343084 | GCTGGCTTCGCATGC[A/C]CTCAAAATGCCATAG | 494470 |
rs141085474 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46405686 | GCAGGGCCCGGTAAA[G/T]GGACTTGATTTGGAT | 494470 |
rs141091578 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46351865 | TGCAGCCTCAGCAAA[A/C]GGTAAATCTATTGGT | 494470 |
rs141095606 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46414880 | TCATTTTGTGTCATC[A/G]CAGCCTTGTGAATGG | 494470 |
rs141139057 | snp | A/G | 0.0126979 | 0.078662 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458595 | GTAAAAGTAACAGGC[A/G]GGCAGATTTTGGCTT | 494470 |
rs141195505 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46349295 | CCAGCAGGTTTGTTG[C/T]GGGTGAGGGTCCACT | 494470 |
rs141209531 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46427310 | TTCACTTCCCAGTGC[A/G]TCTGCTGGAGGGCAC | 494470 |
rs141215701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388553 | GCCATGATCAAGGGC[A/G]CAGGAAGCACACGGG | 494470 |
rs141217175 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46385259 | TCCTGGGCCTCAAAT[A/C]TAATTGCACAGAGAT | 494470 |
rs141248647 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46423815 | ATTGGAGGATTCCAT[A/G]AAGAACTATGCTTCT | 494470 |
rs141261962 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46356222 | AATCCGTGACCAGCC[A/G]ACCCTGTTCCAGGTG | 494470 |
rs141263969 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46418590 | GGACAGAACTAGATT[A/G]CAGTTCCACAATGGC | 494470 |
rs141341080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407419 | TTGTGACATATTGTC[A/G]TCATCATCATTATTA | 494470 |
rs141359063 | snp | C/T | 1.8285e-05 | 0.00302361 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433329 | AGGCCTCAGCGCCCA[C/T]ATGGCCCCGGCCCAC | 494470 |
rs141376288 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46448350 | CGCAGCTCCTATTCA[C/T]ACTCTGGCTTTATGG | 494470 |
rs141391872 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46396841 | CCTGTCTCTGGAAAC[G/T]CTTCCCAGGTTCTTG | 494470 |
rs141402633 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46369215 | TAGAAGCAACGTGTG[C/G]TTGTTTCCAGATACC | 494470 |
rs141410887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431876 | CATTGTGCAGCAAGA[C/T]TTGTCCATTCCTTCT | 494470 |
rs141547111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369434 | GAAGCTGATTGACTC[A/G]GGAAGAAGAGGTGAG | 494470 |
rs141624248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412043 | AGGTATTCGAGTCAG[C/T]TGGTGCTATTTTTAA | 494470 |
rs141635412 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RNF165 | GRCh38.p7 | 18:46447390 | CCTTTCCTTCTCTGA[A/G]TCTCTGTTTCCTTCC | 494470 |
rs141666682 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377383 | TGATGTGTGTCTTTC[A/G]GTGAGGCCAAGAGAA | 494470 |
rs141671652 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46443892 | CTGGTGTTATTTTTC[C/T]TTAGTTTGAAGAACT | 494470 |
rs141678281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382891 | CCGTCAGAGCCTCGG[G/T]ACTGCCAAACACCAC | 494470 |
rs141693227 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46378174 | CCCTGCACCAAACCA[C/T]TTATCAATTTATATT | 494470 |
rs141695121 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46415686 | ATTCCCAACCTGGGC[C/T]AAGTGATGCTGAGCA | 494470 |
rs141697066 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46416538 | CCCCACCTCAATAAA[C/T]GACAACGCCATTTGT | 494470 |
rs141777993 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46377962 | TGGATGGTGGTGGAC[C/T]GCACAACAGAGGTGG | 494470 |
rs141782214 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNF165 | GRCh38.p7 | 18:46444589 | TCAACCTCAGCCTCC[C/T]GAGTAGCTTGGACCA | 494470 |
rs141795164 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNF165 | GRCh38.p7 | 18:46343231 | GCAGCCCCTTCCATC[A/G]AGAGGCCCAAATAAG | 494470 |
rs141821436 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46430605 | ATGTGCAATTTCTGA[C/T]GGGTTCCTTCAACGT | 494470 |
rs141863911 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46340765 | AAGATACCTGGCACG[A/C/T]GGCAGGTGCCTAGGA | 494470 |
rs141868332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382187 | TTGTTGGTAACACCC[A/G]TCCCTCCTGGACGGT | 494470 |
rs141921388 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46399464 | CTCGGCACGTGACCT[C/T]CTGTGAGGAGCCGGT | 494470 |
rs141924238 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425436 | CAGGTGCCCTGTGGG[A/G]CCTTTCAGGCTGCCT | 494470 |
rs141960726 | in-del | -/G | | | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388959 | CTTAACTCTGTGGCT[-/G]GTTTATTGGATTTCT | 494470 |
rs141972308 | snp | C/G | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333373 | TGAGCTTTGTGCTCT[C/G]CAAGAGCAACGACGC | 494470 |
rs142019524 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389271 | AAACTGAAAGATAGA[G/T]ATTCAATGGGTAAAT | 494470 |
rs142037160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429902 | GATTATGGATGTGAG[A/C]CACTGTGCAGTAATA | 494470 |
rs142040260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395012 | GAGACAGCTTCTTTC[A/G]GACCAAGAATCTGCC | 494470 |
rs142040909 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46342569 | GGTGGAGAGTCCTTT[C/T]ACCCTCAGATGCCGT | 494470 |
rs142064272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445922 | TTTTTTTTCTCCAAT[A/G]TATTTGTTGAAGAAT | 494470 |
rs142068939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425989 | TGGAAGCAGCAAGCC[A/G]GCTCTTTGGGGCCTC | 494470 |
rs142080962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46392671 | CACTGGGCCAGCCTC[A/G]GGCTGAGGGTGACAC | 494470 |
rs142101495 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432494 | AGGCTTCAGTGAAAT[G/T]CTGAGCTTGGCTAGG | 494470 |
rs142101797 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46393463 | TTCTGGCCCAGGGCT[C/T]TAGAAATGGGGCTGG | 494470 |
rs142117147 | in-del | -/T/TAAAT | 0.112125 | 0.211569 | intron-variant | RNF165 | GRCh38.p7 | 18:46432970 | AAATAAATAAATAAA[-/T/TAAAT]AAATAAAGATAACAC | 494470 |
rs142141763 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337469 | TTACCCTGCTGAAAC[A/G]TACTGTGGTCGTGTA | 494470 |
rs142148312 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46401035 | GCTGGGGAGGCCAGA[A/C]CCCCTCCCCATAAGT | 494470 |
rs142182318 | in-del | -/AGA | 0.0225045 | 0.103662 | intron-variant | RNF165 | GRCh38.p7 | 18:46371489 | TTCTCTGGTTAAGGG[-/AGA]AGAAGTTAAAGGAGA | 494470 |
rs142209872 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46359725 | AGTGGCAAAGACCCA[C/G]GCTCCTTCTACTTAT | 494470 |
rs142239161 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391415 | CGGGGCTGGGCTCAC[C/T]GTATGCTCTCAGATC | 494470 |
rs142256256 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386569 | CCATCCATCCATCCA[C/T]TCACCCACCCATCCA | 494470 |
rs142270041 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46395446 | AGCATCCCTGGCTTG[G/T]TTGTTGAGAACTACT | 494470 |
rs142334527 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46351157 | GGGAGGAGGCCCTGG[A/G]AGATCACCCTGCCAA | 494470 |
rs142361436 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | RNF165 | GRCh38.p7 | 18:46362634 | GCTTTGCTATTTCCA[C/G]ACATATGGTTTCTTG | 494470 |
rs142371048 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457793 | CTTGGCCACAGTGCT[C/G]TCAGCCAGCACTAAG | 494470 |
rs142406670 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46414758 | TCCTGGTCCTCAGGT[C/T]CTCCTTTGCCCCAGT | 494470 |
rs142418299 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46410218 | TGCTTAGCCAAGCTT[C/G]GCTTCTTGCACCTCA | 494470 |
rs142454924 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46408728 | CATCCTTAGAACACA[C/T]CAGCCATTAGGGAAT | 494470 |
rs142456452 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46406494 | TTGGAGTGGAACACA[A/G]GTGGGAACTGGGAGA | 494470 |
rs142470259 | snp | A/G | 0.000280054 | 0.01183 | missense | RNF165 | GRCh38.p7 | 18:46450299 | TCTACCCAACAGGTC[A/G]TCCATGAAATCCGAA | 494470 |
rs142487936 | in-del | -/C | 0.0267878 | 0.112589 | intron-variant | RNF165 | GRCh38.p7 | 18:46395282 | CTCCATGGCTGCTTA[-/C]CATAGTGCCAGGGAC | 494470 |
rs142488603 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46375931 | TGATGAGACTGTACA[A/C]TTTTGGGTGAGTGAC | 494470 |
rs142491733 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46445641 | CCTCAAATCATTAAG[A/G]TCGTCATGCTCTGCT | 494470 |
rs142500465 | in-del | -/GT | 0.397994 | 0.201489 | intron-variant | RNF165 | GRCh38.p7 | 18:46369367 | TGTTGTAGAATCCTG[-/GT]GTGTGTGTGTGCTGG | 494470 |
rs142512314 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397596 | TGCTGGGGTGTGAGG[-/GT]GTGTGTGTGTGTGTG | 494470 |
rs142513807 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46344823 | GTGTCCCCAACCTCT[A/G]TGCTGAGGAGAGAGA | 494470 |
rs142520312 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46407817 | TGAGATCCACCCATG[C/T]GAAAAGTTGGGTGAC | 494470 |
rs142585802 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46376871 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGGATGG | 494470 |
rs142596532 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46370961 | ACTGCTAATAAAGAC[A/G]TACGCGACACTGGGT | 494470 |
rs142598953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436222 | AGGGGAAAAAAATCT[A/G]TCTATCTAATCTATC | 494470 |
rs142649029 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46379918 | CTTGGCCCACTGGGA[C/T]GTTGCTGCCAGTGGC | 494470 |
rs142682026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411423 | TCTGAGTCAGCTGAT[G/T]AATTTTCACTCTTGC | 494470 |
rs142718161 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46359368 | CAGCTGGGATTTCAG[C/G]TGGTTCCAGGGTCAG | 494470 |
rs142733758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46422691 | GCCAAAAGGAGGGTA[C/G]ATGTTGCAGGGAATT | 494470 |
rs142868332 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46383760 | GGGGTTTCACCGTGT[A/T]GGCCAGGATGGTCTT | 494470 |
rs142883681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46370434 | TCTAGTTCTCATGAG[C/T]TGAGGTGGATGGAGG | 494470 |
rs142887578 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RNF165 | GRCh38.p7 | 18:46418271 | CTGAGATGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 494470 |
rs142893195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46434193 | GGATAGTCAGTGGAT[C/T]TCAAACTTTTTGGTC | 494470 |
rs142909969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46362418 | AGTGGTTGAGGGGAG[A/G]GTGTGTTGAGGGGAG | 494470 |
rs142950733 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46373607 | TAGATCCCCAGTGAC[A/G]TTGAGGCTGAGAGCT | 494470 |
rs142968200 | in-del | -/T | 0.0501905 | 0.150254 | intron-variant | RNF165 | GRCh38.p7 | 18:46402517 | TTCTACATGTGTGTG[-/T]TTTTTTTTTCTTTTC | 494470 |
rs142974059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379392 | CTTTTCAGGGCTCAT[A/G]TCTTATTCTTCCAGA | 494470 |
rs143012344 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46431659 | AGCATGGTGCTGCAC[C/T]CCTGCCCTCTCCTGC | 494470 |
rs143078710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46366731 | ACGGAAGCTTTCTCT[A/G]ACCTTCCTAGTCCTG | 494470 |
rs143084762 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46429280 | ATCAGTGACATGCAC[A/G]TAATATACAAGGCTG | 494470 |
rs143087644 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46340091 | CTCCACAACTGTCAC[A/G]CAAATCTGCAAGACA | 494470 |
rs143096599 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46395054 | AGTGTCATACAGGTA[C/G]CCCCTCTCCTCGCTG | 494470 |
rs143126572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405346 | AGGGAAGCTCTGCAG[A/G]TCCACAGGGCTGGCA | 494470 |
rs143127422 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46335756 | CCCAGCTGTCCCCAG[C/T]CCCGCGCCTCTCCCC | 494470 |
rs143136562 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46384413 | GCTCTTCTTCAGAGA[A/T]CTGCCCCTAGCTGGG | 494470 |
rs143172116 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46402433 | TTGATGTAAATATAT[C/G]TCAATATTGCATGGA | 494470 |
rs143184623 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46356305 | TTGCATTCTAGTGGG[A/G]AAGGCAGACAGCAAA | 494470 |
rs143219960 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46344031 | CATGCCTGGGTGTGC[C/T]GCTGTGTGCAGCTGA | 494470 |
rs143232835 | in-del | -/TCAT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421365 | CTCACCTGTTCGTGA[-/TCAT]TCATTCATTCATTCA | 494470 |
rs143237774 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46382020 | GCCCCACAGCAGTGC[C/T]GGGAGATGGAACTTT | 494470 |
rs143245734 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46448035 | TTCCATATGACCTAG[C/G]TCCCCTGTGTTCTCA | 494470 |
rs143256507 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46375148 | CCTCCCAACTCCCCC[C/T]GCCCTCAGAGGCCCC | 494470 |
rs143297095 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46408339 | CCTGTCATCTCTTGG[C/T]CCCACCTCCCTTCTA | 494470 |
rs143297175 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46371388 | CACAGCCCAGGCCAG[C/T]GAGGAGGCTCTGACA | 494470 |
rs143312902 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46456437 | GCCGGGCAGTTCCCC[A/G]GGAGTCCTAGGTGTG | 494470 |
rs143325318 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46339587 | TGTCTGTTTTAGCAC[C/G]TTGACTTCAGGATTT | 494470 |
rs143325527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46402904 | GAACCTTCCTGGTGT[C/T]TCAGGACACTAGACA | 494470 |
rs143348386 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46443439 | TACAACAGCATACTT[C/T]CATTACCCCTTTGCA | 494470 |
rs143368096 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388813 | AACTCAGAGGTGTGT[A/T]TTTGTGGAGAGGTGG | 494470 |
rs143378503 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459230 | TGGTGTCCCAGGTTC[C/T]AGTCTGGGCTCTTCA | 494470 |
rs143431740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398173 | TGTGAGGGTGTGTGT[A/G]CATGTGGTGTATGTG | 494470 |
rs143449385 | in-del | -/GA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440274 | GCATTTTGAGAGACT[-/GA]GAGAGAGAGAGAGAG | 494470 |
rs143497045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46357034 | GAGCTTGCAAAATCC[A/G]CATTCCCAGGCCCTA | 494470 |
rs143516232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46365103 | ATCACCATTCCCTGC[A/G]TCTCTGCCATGTCCT | 494470 |
rs143523328 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458910 | AGTAGCTCCAGTGTA[C/T]GAAAATGTCTCCAGG | 494470 |
rs143539302 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF165 | GRCh38.p7 | 18:46353586 | AAACCCTTAATCCCA[C/T]TCCATCCCTCTACAA | 494470 |
rs143552665 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46422221 | TTATGTAGTGTACCC[A/C]AGACTCTCAGTTCTG | 494470 |
rs143553492 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46352544 | CTAGAGTGGTGCTCA[A/G]TATCAAGGACTCAGG | 494470 |
rs143591064 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46418714 | ATAAGTCAAATTCTG[A/G]ATCAAATACAATTAT | 494470 |
rs143641997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46377484 | TGCTTCATAGGAGGG[A/G]CAGCAAGTGGCTGGA | 494470 |
rs143652528 | in-del | -/GGGGGGGG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405510 | TGGGTGGGAGTGGCT[-/GGGGGGGG]GTTGGCGATGTGGAA | 494470 |
rs143662504 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46411016 | GGAAGTTGCTGAGAT[A/G]AGCCTCCCAAAGTGA | 494470 |
rs143685046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389973 | AGCTCAACTGACCTG[C/T]TACCTTGGCCTCCCA | 494470 |
rs143720085 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400491 | ACCCTCAGTCTGTAA[C/T]GGGCAGTTCGTAAGA | 494470 |
rs143726148 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387647 | CTGGGCATACAGACC[C/T]GTGGAGGGTGCAAGG | 494470 |
rs143750732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438030 | CCAGATTCTGGGAAG[A/C]ACTTAGGGTCTGTAC | 494470 |
rs143785893 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368208 | CTAAGCTTATTGGAA[A/G]TTCACTAAATGCATT | 494470 |
rs143785987 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46403747 | GCCAGGCGTGGTGGC[A/C/G]GTCACTTGTAATCCC | 494470 |
rs143832738 | snp | A/C | 0.00636936 | 0.0560724 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333008 | TTTTCACAGAAGGTC[A/C]GCTGAGCATGCAAGA | 494470 |
rs143876858 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389002 | TGACTCTCGGTTCAC[A/G]AGGAATTCTACCAGA | 494470 |
rs143880449 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46412939 | GACCCTCAAAATCCC[C/G]CAGAATTCCTGAGGC | 494470 |
rs143906012 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46372684 | GAGACGCAGGAGGAG[A/G]GAGCTGAGCCTTCTC | 494470 |
rs143922034 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46370131 | CTACCAATCTGGGTC[A/C]CCACTTCCTTCCCTG | 494470 |
rs143993638 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46437586 | AGGTTACCCTGGCCT[G/T]TTTTCCTACTTTGGG | 494470 |
rs144013691 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46374875 | GATTTGATTGACTTG[A/G]GTCATGAGTGAGAAG | 494470 |
rs144032694 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46341976 | AGCCCGACCCAGTAG[C/T]GTATTGGGAGAGGAG | 494470 |
rs144036424 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433195 | TGCCTTCCAGGTGCC[C/T]CCTTTCAAAGGTCTC | 494470 |
rs144041738 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | RNF165 | GRCh38.p7 | 18:46404607 | AAAATACCAAAATTA[G/T]CAGGGCATGGTGGCG | 494470 |
rs144092656 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46417181 | CTTTCACCTTCCCCC[A/G]ATTGCCACCCTAGTC | 494470 |
rs144131300 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459877 | TTTCTTGACTGAGAC[A/G]CATGAGTGCCTTCTG | 494470 |
rs144144603 | in-del | -/TG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397372 | ACAGGGAAGGGTGCC[-/TG]TGTGTGTGTGTGGTC | 494470 |
rs144184972 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390302 | TCACAGCCATCCCCA[A/G]CATCTCCAGACCCTG | 494470 |
rs144189033 | snp | C/T | 0.0298908 | 0.118541 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461434 | CAGATCACTTGAGAT[C/T]AGGAGTTTGAGACCA | 494470 |
rs144206328 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458260 | AAAGGGAGCAGAGAG[A/G]TAAGAGGACAGAAGA | 494470 |
rs144224194 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | RNF165 | GRCh38.p7 | 18:46433845 | CACGATCCTCACAGT[A/G]GACTCCTGCATGGTG | 494470 |
rs144286535 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46358383 | CAGGAATGTACACAG[C/T]ACACCCAGCCATAGG | 494470 |
rs144312072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46396325 | TCATAGTGCTCATCT[A/G]GTCTTCTGGCTCAGT | 494470 |
rs144324990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355990 | GCTGCTGGGCCAAGC[C/T]ACCCGTCTGGTCCTT | 494470 |
rs144327072 | snp | A/G/T | 0.0174175 | 0.0916809 | intron-variant | RNF165 | GRCh38.p7 | 18:46393806 | TGGCAGGTCATGAGC[A/G/T]CTGGTCTTGCTCTGC | 494470 |
rs144351963 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457719 | GTAGCCACTGCCTCC[C/T]TATGCAAAAAATTAA | 494470 |
rs144356836 | in-del | -/C | 0.191775 | 0.243125 | intron-variant | RNF165 | GRCh38.p7 | 18:46372260 | GTATTCTGGAGAGAG[-/C]CCAGTTTGAGATGTG | 494470 |
rs144365816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363824 | AGGTGGTCACATGAA[C/T]TCATAGGGGCCACCG | 494470 |
rs144378115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426547 | CAGGGCTATCCTCAG[C/T]CCTGGACCCACCTCA | 494470 |
rs144411951 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF165 | GRCh38.p7 | 18:46393312 | GCTCTTGTTCTGGGC[C/T]GGTGGAGAGCAGTCT | 494470 |
rs144431142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46345395 | TGGCACAGTCCCATC[C/T]TGAAGGTCCCTGACA | 494470 |
rs144432683 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46408482 | AGCCTTCAAATTCCA[C/G]GTCTAACCCATTAAA | 494470 |
rs144443040 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46357854 | GTCCGCGGGGCCAGC[C/T]GTCTCCTCTGAAGGC | 494470 |
rs144454435 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46450651 | CCATATCCTGTGTGC[A/G]TGTGGGCATTTATAC | 494470 |
rs144540564 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46404271 | TGGAAGATGTAGGTG[A/G]TATGAGTATGCTGGA | 494470 |
rs144550050 | snp | A/G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430834 | TTTCCTGAGGGTATG[A/G/T]ATTATATTGTTTTGA | 494470 |
rs144581408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46369096 | AGTTTACACAACTAA[C/T]AAATGGTAGGCCAGG | 494470 |
rs144693150 | in-del | -/CCAATGCCAT | 0.0322114 | 0.122752 | intron-variant | RNF165 | GRCh38.p7 | 18:46420991 | GTTTGCAAAAGCCAC[-/CCAATGCCAT]CCACAGTGCAGACCC | 494470 |
rs144707107 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46430222 | TTGATTAATGGTTTG[G/T]CTGGGCAGATAATTC | 494470 |
rs144709326 | snp | A/G | 0.0103295 | 0.0711199 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461357 | AGAGAAGAAAGAGGG[A/G]GAAAAGGCAGGGCAT | 494470 |
rs144752845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367869 | GGATATTCATTGCAG[C/T]TGGTGTGGGATGGTG | 494470 |
rs144791192 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46380052 | CTCAAAGTTTCCCCA[C/T]CCATGAGCTCTGCTG | 494470 |
rs144796140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455680 | TGTCTCTACAAAAAT[A/G]CAAAAATTAGCCAGG | 494470 |
rs144797330 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46447364 | TCTAGCTCCTTCAGA[C/G]CTTTCAGAGTCCTTT | 494470 |
rs144866137 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46424823 | CAGAGACCTTACACC[A/G]GGTGACTCTGCCTGG | 494470 |
rs144921735 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | RNF165 | GRCh38.p7 | 18:46415442 | GAGGCAGAAGAATGG[C/T]GTGGACCTGGGAGGT | 494470 |
rs144924323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46368995 | GTACTTACTTAGATT[A/G]TCTGATGTTATTTAA | 494470 |
rs144927297 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46431295 | AAACGACCGATCACT[C/G]TTAGGCTCTCTGTTC | 494470 |
rs144949403 | in-del | -/C | 0.0193772 | 0.0965046 | intron-variant | RNF165 | GRCh38.p7 | 18:46427373 | GGGGCGGTTGGTGCT[-/C]CTCCTAATGAGGCTC | 494470 |
rs144951856 | snp | C/T | 0.116138 | 0.211142 | intron-variant | RNF165 | GRCh38.p7 | 18:46383786 | GTCTTGATCTGACCT[C/T]GTGATCCGCCCACCT | 494470 |
rs144961250 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46451190 | ATTCTATGTCCAATC[A/T]CACATGTGAACAAAT | 494470 |
rs144978269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349922 | GCATTTACACATTCA[C/T]CCACAGTTCACATAC | 494470 |
rs145047116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46426494 | AGGTGGGCGTCAGGC[A/G]AGCCCAGCACCTGTG | 494470 |
rs145097545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429862 | TCCTCTTGCCTTACC[C/T]TCCTAAGTAATCCCA | 494470 |
rs145112290 | in-del | -/CCACCCAT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386573 | CATCCATCCATTCAC[-/CCACCCAT]CCACCCATCCACCCA | 494470 |
rs145159709 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | RNF165 | GRCh38.p7 | 18:46371824 | GCAGGTGGAATTTAC[C/G]TGTGTCCAAGGCCCT | 494470 |
rs145179393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369318 | CTGAGCTGGGATTTA[C/T]TGGAGAAGCAGGGGG | 494470 |
rs145188116 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46432336 | ATGATAATGTTATAA[A/C]ACATTATTTAACTAT | 494470 |
rs145198195 | snp | C/G/T | 0.00478364 | 0.0487146 | intron-variant | RNF165 | GRCh38.p7 | 18:46394807 | CTGCAGGATCCAAAG[C/G/T]CTTCCTGAATAAACA | 494470 |
rs145199111 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332380 | GTGAACCCTGGGTTC[A/T]GCCCTTGCCACTGGG | 494470 |
rs145207264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390600 | TAACCCTTCTCAAAG[C/T]GATAGAAATAAGCCG | 494470 |
rs145234061 | snp | C/T | 0.000329473 | 0.0128307 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46450379 | CAGCAGACACACCTC[C/T]GCCGTACGGGAGAGC | 494470 |
rs145240230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431134 | CACTTATGAGTGAGA[C/G]CATGCGGTGTTTGGT | 494470 |
rs145286830 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454108 | AGAGGGCAAGGCCGT[C/T]TCAAAAAAAAAAAAA | 494470 |
rs145311225 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46396970 | TTTGCAAGCCCAATC[A/G]CTCTGGAAGGGTGGC | 494470 |
rs145326818 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46350746 | AAAGAGATCATATGA[C/T]ACTAATGTCACTGTT | 494470 |
rs145343399 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46442824 | ACTTATTTTGACTTA[C/T]ATATATTAGGATATT | 494470 |
rs145349619 | snp | A/G | 4.94173e-05 | 0.00497053 | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447652 | ACCTAGCCACTCCTC[A/G]AATGCACCACTTTCC | 494470 |
rs145360700 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46387082 | AGGCTGAGGAGAGTG[C/T]GCCAGGCCAGGGAAG | 494470 |
rs145410560 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425478 | CCTCTTTCAGCCCCC[-/T]TTTTCCTTGGAGGAC | 494470 |
rs145421417 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46382714 | TGATTTCCTCTGTGT[G/T]CAGGGAAAGAAAGAC | 494470 |
rs145433124 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46448602 | AATGAAGATGCCTGC[C/G]TCGCCCATCTCACAG | 494470 |
rs145510023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46346696 | CACTCATATAAAGTA[C/T]GAGACACCCGAAATC | 494470 |
rs145524280 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457718 | CGTAGCCACTGCCTC[C/T]CTATGCAAAAAATTA | 494470 |
rs145524449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46410017 | GATCTTGCCAAATCA[C/T]TCTCCTTAGAGGTTG | 494470 |
rs145555838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46348668 | GGCAGCATTTTCCAC[A/G]GTGTCCAAGCAAGCA | 494470 |
rs145591665 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46394131 | CTTTTCACTTGGATG[C/G]AAGTGACTAGGGATG | 494470 |
rs145606009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46454756 | CAGCCTGTCTCTGGA[A/G]AGGGACAGAATGAGT | 494470 |
rs145621212 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46351666 | CTGATGTTGATCTTT[C/G]AGTTACTTTTTTATG | 494470 |
rs145639991 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46388052 | CCATTCCCCATCTAG[A/G]TGAACACCCTTATTT | 494470 |
rs145681727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350466 | TAGAGCATGAGAGAA[G/T]GGAGCGCTGAGGTAT | 494470 |
rs145699860 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46413416 | AGCTTTATAGTCAGT[A/T]CTGAGTGGGATAGGT | 494470 |
rs145716707 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46359035 | AGACACAAAGCTTGG[G/T]CAAGTCACTTCCCCC | 494470 |
rs145726052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46453923 | TTTGAGACCAGCCTG[A/G]CCATCATAGAGAGAT | 494470 |
rs145774630 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46395616 | TGAGTCTGTATGGCC[A/C]CAAAGTCCGGGATTT | 494470 |
rs145807794 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46405754 | GGTTGAATATGATGT[C/G]TATGTGAGCCATCCA | 494470 |
rs145841192 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46371959 | ATTAAATACTGACTC[C/T]TAACGTACTAGACTT | 494470 |
rs145868105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46360365 | GCAGGTGCTCCCCAC[A/G]ATGGTGCTCAAAATT | 494470 |
rs145895663 | in-del | -/TG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397667 | ATGCTGGGGCAGAAT[-/TG]TGTGTGTGTGTGTGT | 494470 |
rs145900190 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46357243 | CTACCCAGGTCTCTT[C/G]CCCAGTGGTAACAGT | 494470 |
rs145907401 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF165 | GRCh38.p7 | 18:46419750 | GAGGTAACTGGAGAC[A/G]GACAGGCCTCTGCTG | 494470 |
rs145954652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46449338 | TTTTGCTCAGCATGG[A/G]GGTTTTTTTTGCATT | 494470 |
rs145956033 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46404746 | GCACAGAGCGAGACT[C/T]CATCTCAAAACACAC | 494470 |
rs145972697 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46423323 | GCACTGTGCCTGAGC[A/G]GTTGTGCTCACCTCA | 494470 |
rs145991989 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46349126 | TGACTGCCTGAATTA[C/G]TTCCCACCATAGTCT | 494470 |
rs146003255 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNF165 | GRCh38.p7 | 18:46345017 | GGCTGGGTCAGGAGG[A/G]AAGCTGAGCTTGGGA | 494470 |
rs146005045 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46408000 | CAGCTGAGCTTTGAA[G/T]TCTGAGTCAGTTTGG | 494470 |
rs146070197 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373024 | TCTGTGCATGTGCGA[-/GT]GTGTGTGTGTGTACG | 494470 |
rs146078253 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46421897 | CCTGGGGAAGCATCA[C/T]AAAGCTGCTCTTGGC | 494470 |
rs146126586 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46362443 | GGGGAGGAGTGTGTG[C/T]GCGCCCCAAGGGGTT | 494470 |
rs146128089 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46425513 | AGTGCCTCTCAGCCC[C/T]GGAGTCTTGAGGATG | 494470 |
rs146226782 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46375307 | CCTGTCATCCCAGCA[A/C]TTTGGGAGGCCGAAG | 494470 |
rs146233748 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46341666 | CAACAATAAAAATTC[C/T]TCATACTCACATGAC | 494470 |
rs146245859 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | RNF165 | GRCh38.p7 | 18:46378440 | TTCCCCCTGACCACC[A/G]TGGAGGGGCAGCGTG | 494470 |
rs146249498 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46445194 | AGAGTGTTAGGCTTC[A/G]TTCTGGTAAGGAGCA | 494470 |
rs146282354 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF165 | GRCh38.p7 | 18:46344441 | CTCAGGGGCCCCCTC[C/T]GGGCTGCCTGTGCCC | 494470 |
rs146299150 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46426398 | CCCTATGGGTTCTTC[A/T]GTCCTCCTATCCACC | 494470 |
rs146318650 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389976 | TCAACTGACCTGCTA[C/T]CTTGGCCTCCCAAAG | 494470 |
rs146369745 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | RNF165 | GRCh38.p7 | 18:46393513 | GCCAGAGCTTCATAC[C/G]CTGTCTGGACGCCCC | 494470 |
rs146406507 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | RNF165 | GRCh38.p7 | 18:46362101 | CCCACTCATATGGGA[A/G]TGTAATGGGGTGCCC | 494470 |
rs146415573 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46338369 | AGGGCCAGCAGCGGA[C/T]CTGTTACTGTAGGAA | 494470 |
rs146421004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402171 | TGAGTTCTGACATGT[A/G]TATACCTATGAAAGC | 494470 |
rs146430794 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46442300 | TCTAGCTTCTTAAGG[C/T]GGAAATTTAGATCAT | 494470 |
rs146508542 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458461 | AGTCTCAATGCCCTC[A/G]TATCAATAAGACCGG | 494470 |
rs146543370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46356212 | TGCAAATGTCAATCC[A/G]TGACCAGCCGACCCT | 494470 |
rs146543634 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46418282 | GGATCGCTTGAGCCC[A/G]GGAGACAGAAGCTGC | 494470 |
rs146553582 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46351806 | AGGCAGTGTCCCACC[A/G]TGGCGGCAGGGCCTG | 494470 |
rs146554311 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46414872 | AAACATTTTCATTTT[A/G]TGTCATCACAGCCTT | 494470 |
rs146592144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46358703 | GACAGGTTCCAGACC[C/T]CCAGGAACACCCCTT | 494470 |
rs146624787 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RNF165 | GRCh38.p7 | 18:46402567 | ACCCACGCTGGAGTG[C/T]GTGACTCACTGCAGG | 494470 |
rs146627031 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431828 | TCCTGCCTTCCAAAG[-/T]TAGCCACTGCCTCCA | 494470 |
rs146641522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372932 | TCCCTTCTTTTCCCA[C/T]AGCCTCCTAATGCCA | 494470 |
rs146660114 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46371494 | CTGGTTAAGGGAGAA[G/T]TTAAAGGAGATTGGA | 494470 |
rs146671527 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46369104 | CAACTAATAAATGGT[A/G]GGCCAGGATTTGAAT | 494470 |
rs146728223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337882 | AATAGATGTCTGGAG[C/T]GATAGGAGGGGCCAG | 494470 |
rs146743839 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46418768 | GAAAAGAGCTATCAA[A/C]TGGCTATATCCATGC | 494470 |
rs146782071 | snp | C/G | 0.0236746 | 0.106192 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387728 | TCAAACGCTGGGACG[C/G]GAGAAGCTTCTAGTC | 494470 |
rs146793834 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46422452 | AGAGGGGAGAGGAGG[A/C]TCCCTGGGGGCCATG | 494470 |
rs146867582 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46437935 | TTGTCCTTTCCCCTC[C/T]GGGCAACCTTGCCTC | 494470 |
rs146872731 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46450340 | CCCTCAGCTTCACTT[C/T]CTTGCTCTCCAGGGA | 494470 |
rs146924555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46424084 | TTGGAGATAAAATTC[A/G]TACACAAACAAAATG | 494470 |
rs146968714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388596 | CCAAGCTGCCCTCAA[C/T]TGGGATCTGGGGAGC | 494470 |
rs146968776 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46427800 | CCAGTGTGAAGAGAC[A/T]GCTCAAGGTAGCCAC | 494470 |
rs146977516 | in-del | -/G | 0.0799831 | 0.183287 | intron-variant | RNF165 | GRCh38.p7 | 18:46360197 | GTGTGGTTCATTCAA[-/G]GGCTTCCTCCTCTCC | 494470 |
rs146983737 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46392456 | GACCACATTTGGCGG[C/G]AATGGACAAGAACTC | 494470 |
rs147030742 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444134 | ATTGTTCTTACCTAC[A/T]TTCTTCTATGTTGAA | 494470 |
rs147061104 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46343781 | AGGACTCAGTAGGCA[C/T]GTGAACTTCCACTGG | 494470 |
rs147071511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340138 | TCTATGGATCTAAAC[A/G]GCTTTGTAAAAATTC | 494470 |
rs147072677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46403738 | TAAGAATTAGCCAGG[C/T]GTGGTGGCGGTCACT | 494470 |
rs147072951 | snp | C/T | 0.000461323 | 0.0151805 | intron-variant | RNF165 | GRCh38.p7 | 18:46447708 | GTAAGTGAAAGAAGA[C/T]GGACTCCCTTGCGCC | 494470 |
rs147088833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406177 | CCATGTGCACCCCCA[A/G]TACGCCTGCATCCAG | 494470 |
rs147132073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46353628 | TGGGAGGACTCTGAA[A/G]GTCAGAGAGTGGGAG | 494470 |
rs147142406 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46349969 | CGCATTCATTTACAC[A/G]TACGTATCTGTATTA | 494470 |
rs147145856 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459402 | GCGGCAGAGCTGTGC[A/G]CCCACCCAGCTATTG | 494470 |
rs147231231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46400877 | TCAGGATCAGGTCTC[A/G]TGCAGACATTTACCA | 494470 |
rs147239923 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46370238 | CACATGATATCCTTA[C/T]GATCATCTCTATAGG | 494470 |
rs147247740 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46368285 | GCTTGGGACGTGGAG[C/G]CCTAAATAAAGAATA | 494470 |
rs147249737 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46404018 | ATTCCCTCTTTCCCC[C/G]CTTTCTCTTTTTAAG | 494470 |
rs147313766 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46417376 | TGTCTCCCCAGCCCC[C/T]AAGATCAGTATCACC | 494470 |
rs147347474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46385713 | AGCTTCTGTGCCCCT[C/T]CCCAGCCTCTTGCTC | 494470 |
rs147355916 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46419935 | TGTATTTCCACTGAC[A/G]TCCACCGTCTCTTTT | 494470 |
rs147419528 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435057 | AGACCTCTGCACAGC[A/G]GGCAGCCCGGAGACA | 494470 |
rs147422001 | snp | A/G | 0.000612975 | 0.017496 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433455 | CCAGCAATACCTCCT[A/G]CAGCAGCAGCTCCTG | 494470 |
rs147451042 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46400155 | CCAGCTCTAGGCCTT[A/G]TTTCTAAGGCTGGGC | 494470 |
rs147460930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46396883 | GTTGGGTGGATTTTC[C/T]GCTAATTGTCCAACT | 494470 |
rs147461849 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439222 | CAGACTCCCCTGAAG[C/G]CTGATGGCTTTGTTG | 494470 |
rs147492240 | snp | C/T | 3.30071e-05 | 0.00406232 | intron-variant, stop-gained | RNF165 | GRCh38.p7 | 18:46435356 | GACTTCGGCCAACTG[C/T]AGACACCTCAGCCCA | 494470 |
rs147524309 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457371 | GGCTTTTGTTTTTCT[C/T]ATGTTTACAGTGCAC | 494470 |
rs147547666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386733 | TTCTCTTTCTGGGAC[A/G]TGGTGCTGTCTTTAT | 494470 |
rs147610064 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46359591 | GAGAGCCATGGACTC[C/T]ACCTGAAAGCCCATG | 494470 |
rs147620220 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46394862 | ACAGGCTAGTTCTTT[A/G]AAAATAGATGCCCTG | 494470 |
rs147653440 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46363014 | TAGAGTTAAAACCAG[A/T]CCAACCTCTGCTGCT | 494470 |
rs147688667 | in-del | -/TTTC | 0.426507 | 0.177046 | intron-variant | RNF165 | GRCh38.p7 | 18:46334812 | TATGTGTGTTTTGTA[-/TTTC]ATTCATTTTTTGTTC | 494470 |
rs147695537 | in-del | -/C | 0.0295035 | 0.117819 | intron-variant | RNF165 | GRCh38.p7 | 18:46427642 | CCAGCCTCAAACCCG[-/C]CAGCCCCTTCGAGCC | 494470 |
rs147717339 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46414512 | ACATGCATGTACATG[C/G]ACATATCCATGAATA | 494470 |
rs147717436 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | RNF165 | GRCh38.p7 | 18:46376759 | CACTGCAACATCCGC[A/C]TCCCAGGTTCAAGCG | 494470 |
rs147726931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410123 | TCTTGGTGATCAAGC[A/G]ATCAATACATCTTCC | 494470 |
rs147733271 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46379602 | CCCACAGGGCAAAGT[C/T]GCTCTTTGAAGCCAC | 494470 |
rs147820349 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46368620 | CAGCTCTATGGAGTC[A/G/T]AGTCTTAATCAGTTG | 494470 |
rs147822430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430899 | TTCCTCGAGTTCATT[A/G]TTTAAAAATTATTCT | 494470 |
rs147830792 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | RNF165 | GRCh38.p7 | 18:46427166 | TGGAGATGGTGGAGG[C/G]AAGAAGCACAGCCTC | 494470 |
rs147927993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451919 | ATGGCTGTGTACTGT[A/G]TGTTTCCAAATATAT | 494470 |
rs147937917 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46447377 | GACCTTTCAGAGTCC[C/T]TTCCTTCTCTGAGTC | 494470 |
rs147969868 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46346151 | GGGATGGCATTTCAA[C/T]ATGGTGGCAGATCCT | 494470 |
rs147979025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365291 | GTCAGTGGTCCCCAC[C/G]CTACACTCCCCAACT | 494470 |
rs147998401 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46416047 | CTGCTGGCATTTTCA[A/T]GGCTAATTAACATGT | 494470 |
rs148008545 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458932 | GTCTCCAGGGCTAAA[C/G]GCTGGAGATCTCACC | 494470 |
rs148052163 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46411407 | TGAATAGGACGTATG[C/T]TCTGAGTCAGCTGAT | 494470 |
rs148095012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46377660 | GAACCAAATGTATGG[A/G]AGGTCAGAGGAGGGT | 494470 |
rs148138182 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333330 | ACCTCAGTGAATGAG[C/T]GAATTTCAATTCAGC | 494470 |
rs148145779 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372298 | GTTGTTGCACTCATC[C/T]AGCCACCCACTTGCT | 494470 |
rs148148661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438051 | GGGTCTGTACAGCAA[C/T]CAGACCACACCATGT | 494470 |
rs148157148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389159 | AGTCACCATCAGGTA[A/G]TGAGGACCACAAGGA | 494470 |
rs148168303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425267 | CATCCTACTCTCCCA[A/G]GATCCCACATCCCTG | 494470 |
rs148211351 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46385068 | CTTTCAGTTGGCAAA[A/C]CTTTTGACATCTCCA | 494470 |
rs148213260 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | RNF165 | GRCh38.p7 | 18:46455725 | CCTGTAATCCCAGCT[A/T]CTCGGAGGCTGAGGT | 494470 |
rs148234302 | snp | A/C/G | 0.000130971 | 0.00809143 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433278 | GCAGCAGCTCGCTCC[A/C/G]GACTTCCCGCTGGCC | 494470 |
rs148303886 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46344032 | ATGCCTGGGTGTGCC[A/G]CTGTGTGCAGCTGAG | 494470 |
rs148308150 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46407065 | TGCCTCGGCCTCTAC[C/T]ACCTCTTGGAGGGAA | 494470 |
rs148357733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403157 | TCACCTTGTTGGTTC[A/G]TCTGTGCTTCCAGGC | 494470 |
rs148412164 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46345577 | GGGGGTGGACTAGAC[A/G]TGTGCGCAGCAGAGA | 494470 |
rs148413274 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46408662 | GGCTGGAGTTAATTA[C/G]AGCATCATCTTGGTC | 494470 |
rs148466655 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46404297 | CTGGATGGCTCGCTT[C/T]CTCTCTTAAGCTAAT | 494470 |
rs148483287 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46370890 | TGGGAATCAGGTACA[A/C]GAAAAGGAGGATGGG | 494470 |
rs148507204 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46367933 | GATTCTGATGCCCAG[C/T]TACGGTTGAGAATCA | 494470 |
rs148527629 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46418177 | AACATAGTGAGACCC[C/T]TATCTCTACAAAAAA | 494470 |
rs148536171 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46430446 | TCTTTCGGGTGGGTT[A/C]TTTCCCCCATCCATT | 494470 |
rs148623477 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46445668 | TGCTTAGTTCTCTCC[C/G]TGCTCATGGTCTGGA | 494470 |
rs148639450 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46342555 | GCATTGGAACCCAGG[A/G]TGGAGAGTCCTTTCA | 494470 |
rs148663360 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337444 | AATGTACAGCGCTCG[A/G]TTAGAGATGTTACCC | 494470 |
rs148675068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440328 | ATTTTTTGCAGTATA[C/T]TGTTATAATTGTTCT | 494470 |
rs148691370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46400974 | GAACATGAAGATGCT[A/G]GAGGCAGAGATGACC | 494470 |
rs148694257 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46426516 | GCACCTGTGGGTTCC[C/T]CCTGTCCCAGCTGTG | 494470 |
rs148706524 | in-del | -/CC | 0.0433465 | 0.140692 | intron-variant | RNF165 | GRCh38.p7 | 18:46342339 | AGGAATACCTGCTTT[-/CC]CGCCATAGCTGGTGG | 494470 |
rs148734178 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46362446 | GAGGAGTGTGTGCGC[A/G]CCCCAAGGGGTTTGG | 494470 |
rs148735942 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46387371 | ACCACTCTGAAGTAA[A/G]GAAAGCAGCTTTTCC | 494470 |
rs148739457 | snp | C/T | 0.0325976 | 0.123435 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457766 | AGACAGCATAGGTGA[C/T]GGCTGCTTGGTCTTG | 494470 |
rs148745292 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46396676 | TTTTGTTCACTTCTC[A/G/T]GCCTGGCTGTCGGGA | 494470 |
rs148788447 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46357935 | AGTCACAGTCCTTGG[A/G]GCTCCCTGGCTTGTA | 494470 |
rs148791982 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46451185 | AAATAATTCTATGTC[A/C]AATCTCACATGTGAA | 494470 |
rs148844986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364329 | CACTTTTTACCAACC[A/G]AAGTTTGCTTGGGTC | 494470 |
rs148848388 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458899 | GCGTCCAACTCAGTA[A/G]CTCCAGTGTATGAAA | 494470 |
rs148895086 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46359240 | TGGGCCAGGTGGGCT[C/G]TTCCCTGCCTGTGGG | 494470 |
rs148898858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422535 | CTCCCTCCACCTGGG[C/T]GCAGCCCCACCGGCT | 494470 |
rs148917361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410819 | TCGTTTCTTCAATTG[C/T]CCAGGCTCATGAAAG | 494470 |
rs148919119 | in-del | -/AAAC | 0.223225 | 0.248562 | intron-variant | RNF165 | GRCh38.p7 | 18:46404816 | ACAACCCCCCCACCA[-/AAAC]AAACAAACAAACAAC | 494470 |
rs148992980 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46405882 | AGCCATCCCCTGTAT[C/T]AACCTTCCTGCAGGA | 494470 |
rs149009362 | snp | A/C/G | 0.00319074 | 0.0398324 | intron-variant | RNF165 | GRCh38.p7 | 18:46371992 | TCCCATGTCACTTCC[A/C/G]AGAGCTGACTGTAGG | 494470 |
rs149062294 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46369073 | TGAGAAATTAATCTA[C/T]GTGTTTAAGTTTACA | 494470 |
rs149063726 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46431412 | ATACAGTGGCCAGTT[A/G]GGGACCCAGTGATTT | 494470 |
rs149106650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391242 | CTCGCTTAGTCTTGA[A/G]GTGGGAGGCTGGGGT | 494470 |
rs149127504 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448017 | GCTCCCCTGTGCCCC[A/C/G]GCTTCCATATGACCT | 494470 |
rs149150021 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46380842 | TTCCTGCAGGTCCCC[A/G]TCACACTCGCCCCAG | 494470 |
rs149179740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442897 | TTATGAAACATCCTT[C/T]CTTATCCTTGGTAAT | 494470 |
rs149180110 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | RNF165 | GRCh38.p7 | 18:46447654 | CTAGCCACTCCTCGA[A/G]TGCACCACTTTCCCA | 494470 |
rs149200670 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNF165 | GRCh38.p7 | 18:46350888 | CTCTTTCATCATCAG[A/G]TGGGCCCATTACCTG | 494470 |
rs149221572 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNF165 | GRCh38.p7 | 18:46339012 | CTTTGTTCTCGTGCT[C/T]TTCCCAGCCTGGATG | 494470 |
rs149221776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402607 | CCAGGCTTAAGTGAT[C/T]CTCCCATCAGCAACC | 494470 |
rs149234451 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46383288 | TCAAAATGTGAAAAA[G/T]ACAATTTTTCTACAA | 494470 |
rs149236752 | snp | A/G | 0.00403048 | 0.0447101 | intron-variant | RNF165 | GRCh38.p7 | 18:46450280 | TGCTCTATCCAAGGC[A/G]TTTTCTACCCAACAG | 494470 |
rs149257034 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46357490 | GCCTGATTTTGGTGG[A/G]CTGTGCTGGCAGAGG | 494470 |
rs149288316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444866 | ACCCAGTGAATTTCC[C/T]ATTTCAGACATTGCA | 494470 |
rs149290110 | snp | C/G | 9.89071e-05 | 0.00703163 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456638 | GAGCCGACAGCTGAG[C/G]GAGGAATTAGCCAGT | 494470 |
rs149310570 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46352542 | GCCTAGAGTGGTGCT[C/T]AATATCAAGGACTCA | 494470 |
rs149328143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341622 | AGTCCTTTACATACA[A/G]ATTCCTGGTTGGGGT | 494470 |
rs149331801 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404268 | TGTTGGAAGATGTAG[A/G]TGGTATGAGTATGCT | 494470 |
rs149372368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367703 | CAAACTGGCCTCGGT[C/G]TCCCCACCAGTAGCC | 494470 |
rs149429101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424542 | CCATCTCAGGTCTGC[C/T]CTGTCCAGCTCTAGG | 494470 |
rs149446778 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46412750 | ATGACAAGGCCGCCT[C/T]GGGCAGGTACGGAGA | 494470 |
rs149498288 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46384182 | GGCCGTGCTTCCAGC[C/G]CAACCTCATCTACTG | 494470 |
rs149521241 | snp | C/T | 7.82304e-05 | 0.00625373 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334322 | TCCAGTGTTTGGCTC[C/T]GTGCGAAACAGAGGT | 494470 |
rs149532788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336612 | AGTTTGCCAGCTTAA[A/C]TCTGTTCTTTTTAGT | 494470 |
rs149544146 | snp | C/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46439804 | CAGCTATGACATCAA[C/T]TCATGGCCAGTTTTG | 494470 |
rs149586675 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46395908 | CCCAGTAGTTCTTCC[A/G/T]ATCTCATTTAGGCTC | 494470 |
rs149595438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46433702 | TCTGTAGGAAGTAGC[C/T]ATTGTTTCAGAGGCA | 494470 |
rs149702126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46437225 | CTTGTTTTGTTCCCA[C/G]TTCCCAAGTAGGATG | 494470 |
rs149704592 | in-del | -/T | 0.0278988 | 0.114765 | intron-variant | RNF165 | GRCh38.p7 | 18:46456123 | CCCCTCTCTTATAGG[-/T]TATTGGTGACCAATC | 494470 |
rs149745196 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46394064 | CTTCCTGTTGCCCTC[A/G]GGTACCGGAAATCCT | 494470 |
rs149761601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358967 | GTCCCCTACCCCTTT[G/T]TCCATGCCACTGTGT | 494470 |
rs149765860 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | RNF165 | GRCh38.p7 | 18:46453607 | ATAAAATGTGGAAAA[A/T]ACCCTTAAAAATTAT | 494470 |
rs149812205 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46355377 | CTCTCTCAGGGCCTC[A/G]GGCTCCTCACTGGTT | 494470 |
rs149816586 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF165 | GRCh38.p7 | 18:46417772 | ACTTTGAGAGGCCGA[A/G]GCAGGTGGATCACCT | 494470 |
rs149825091 | snp | A/C | 0.0138799 | 0.0821421 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460384 | AAAATGAAAAAAAAA[A/C]CACAAAAAACAAAAA | 494470 |
rs149860463 | snp | C/G/T | 0.00597598 | 0.0543831 | intron-variant | RNF165 | GRCh38.p7 | 18:46405753 | GGGTTGAATATGATG[C/G/T]CTATGTGAGCCATCC | 494470 |
rs149904125 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368981 | TGCCAGGCACTATGG[C/T]ACTTACTTAGATTGT | 494470 |
rs149914123 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46401985 | AATTCAGAAAACCTC[C/T]CCTCACTGCTCTCAC | 494470 |
rs149954948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362707 | AGAATAATGCCCTGC[A/G]ACAACCACATCAGGT | 494470 |
rs150003945 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46417319 | ACCCTCCTCAGAGTC[A/G]AAGGCAACATCCTGT | 494470 |
rs150009353 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF165 | GRCh38.p7 | 18:46421884 | ATCAAAGCCTGGCCC[C/T]GGGGAAGCATCACAA | 494470 |
rs150024742 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RNF165 | GRCh38.p7 | 18:46387023 | ATTCTCTTCTAATTC[A/G]TTCCTCACACAGTTC | 494470 |
rs150027581 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404787 | ACACACACACACACA[C/T]ACACACACACACAAC | 494470 |
rs150047491 | snp | C/T | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, synonymous-codon | RNF165 | GRCh38.p7 | 18:46447614 | GTTCCAGGTGCGGCC[C/T]ATCCCTCAGCACTAT | 494470 |
rs150071422 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46442535 | TGTGTAATTCTAATC[A/C]TTTTATATTTATTGA | 494470 |
rs150133707 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388252 | TACCACCTCTAACTC[A/G]AAGATTCACCACTCA | 494470 |
rs150135240 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458830 | ACAAGACACATCCAA[C/T]GCTGCAAAAATGGTG | 494470 |
rs150176797 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46352262 | TGGGAAGGCAGCCAG[C/T]ATGGACTCCATCAGA | 494470 |
rs150179435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46444751 | ATGCTGGGATTAGAG[A/G]CATGAGCCACTGTGC | 494470 |
rs150225847 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46348099 | CCCTAAGGTATGTGC[G/T]GGGTGTTCTCTTAGC | 494470 |
rs150230274 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46410330 | TGTGTTCCAGGTGCT[C/T]AATGTCTTACTGGTG | 494470 |
rs150232279 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RNF165 | GRCh38.p7 | 18:46438101 | AAAATAAAGTTCAGC[A/G]TGATGTTTAGATACA | 494470 |
rs150246711 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333675 | TCAGGGTCGTGTGCA[C/G]TAAGGGCGCTCGTGC | 494470 |
rs150246967 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46399597 | AATGATGGGAGGGTG[A/G]GCTGGCAATGAGTGT | 494470 |
rs150290082 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46361463 | GGCACATGATCCAGT[A/G]TCCAAAAAAAGGCAG | 494470 |
rs150299861 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | RNF165 | GRCh38.p7 | 18:46395292 | GCTTACCATAGTGCC[A/G]GGGACTGGCCCAGAG | 494470 |
rs150342596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419044 | ATTTTTGGCTCTAGT[A/G]GGAACGCTATTACTG | 494470 |
rs150396035 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46414871 | GAAACATTTTCATTT[C/T]GTGTCATCACAGCCT | 494470 |
rs150437784 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46380349 | ACTTGGGGAGTGTGC[A/G]CAGGGGACATCCAGC | 494470 |
rs150459974 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46432885 | GGGAGGCGGAGCTTG[C/T]AGTGAGCCGAGATCG | 494470 |
rs150482583 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46338968 | CAACTCTCCTCTCCC[A/C]CCATGGCTGCCCTCT | 494470 |
rs150505552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416666 | TTGGGCTCAGCTGGG[A/G]AGTCCTTTTGGTCTT | 494470 |
rs150548671 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382949 | ATTTTATGAAGACAA[C/T]GTCATACTCTTCTTG | 494470 |
rs150568679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436608 | CAGGAATGATTCCAG[A/G]GAATAGTTCCAGTCA | 494470 |
rs150599141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46378156 | AATGCTCCAAGGTAC[A/G]TCCCCTGCACCAAAC | 494470 |
rs150611459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393857 | ACCTGGGTTCAAATC[C/T]TGCCTCTGCCACTTC | 494470 |
rs150615602 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340925 | GAGGGAGGAGGAGGA[A/G]GAGGAGAGAGCACCC | 494470 |
rs150620163 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46430727 | ATTTCATTTCACCTC[A/G]TACATTTCTAATTTC | 494470 |
rs150661072 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389357 | AAAACATCACTGTAA[A/G]TTCTAAACACACTGG | 494470 |
rs150664073 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460012 | GCTTGGTTGGGTGCA[A/G]GCAGAGGGTGAGCAG | 494470 |
rs150703142 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46353982 | ACCCCCTCATTTTAC[A/G]GGGACTTGGCCAAGA | 494470 |
rs150715053 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46456282 | GGTACGGACGCGAGG[A/T]TGAAAAGTGTAGGAG | 494470 |
rs150756231 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | RNF165 | GRCh38.p7 | 18:46349592 | CCCAGTGGCATTTTT[C/G]CTGGCCAGCCAGGGG | 494470 |
rs150757332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412459 | GCTCTGAAAACAGAG[A/C]AGAAAGCAGCCACCC | 494470 |
rs150810946 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46407612 | ATCCCTTCTAATGCA[C/G]AGGGTATTTCCAGAC | 494470 |
rs150872336 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46357985 | CGCCTCTGTTGTCAC[A/C]GTGTCTCAGTGTCTC | 494470 |
rs150935066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376261 | GGGCCTGACATTAGT[C/T]GGGTACTTTCTCTGT | 494470 |
rs150982814 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46423163 | AGCCTTTCCTTTGGG[G/T]GATGTCCAAAGGCCC | 494470 |
rs150988378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370964 | GCTAATAAAGACGTA[C/T]GCGACACTGGGTAAT | 494470 |
rs150999776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388116 | AGTGGCTTACTGAAG[A/G]TTACATGTTTATTTG | 494470 |
rs151093954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46347105 | ATCAGGAGGGCCTCC[C/T]GGAGGAGGCAGGACT | 494470 |
rs151106398 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46446437 | GCACTTTGGGATACC[A/G]AGGTGGGTGGATCAC | 494470 |
rs151140656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395128 | CCCATTTTATGGAGC[C/T]ATGGGGTGGAGGGAT | 494470 |
rs151148332 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46405464 | AGGGACAGGAGGGCT[A/G]CAGACACAGCTGAGG | 494470 |
rs151150740 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46431782 | CTTACACAGATTGCA[A/G]TCAGTCTCCCTGTTC | 494470 |
rs151193891 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391763 | CCACAAACACACACA[C/T]GCACACACACACTAT | 494470 |
rs151201427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46401575 | CCAAGACTGCACCTG[A/G]GTCACAGAGCAGAGC | 494470 |
rs151210122 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46356567 | GCAGGCACGGAATGC[A/G]TACTTCTTGCCTCCA | 494470 |
rs151246846 | snp | C/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457895 | GTCCCTCAGAGATGG[C/G]CCTGGCTCTGAGGTC | 494470 |
rs151264264 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46414763 | GTCCTCAGGTCCTCC[A/T]TTGCCCCAGTGCGGA | 494470 |
rs151271634 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348237 | GTGGGCCAAGGGGCT[-/G]GGGGGGGTGAGGGGA | 494470 |
rs151286178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351343 | AGATGGGCTGGAGCA[G/T]TTCCCTCCAGGTGCC | 494470 |
rs151313862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46409363 | AAGAGGGAAGGAATG[A/G]GCTCAAGGGATCCTT | 494470 |
rs180673236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394281 | AGCGAGAGCCCTGGC[C/T]TGGGAATCTCTAGTT | 494470 |
rs180678268 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46438616 | TTGAGCCCAGGCAAG[G/T]GTGTGAAACCCTGAT | 494470 |
rs180688398 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46368359 | TTTCTGCCTCCACCC[C/G]CTGCTCATATCATCA | 494470 |
rs180689871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381187 | GTTTTTGTCAGCCAG[G/T]CATTGGGATAAGGCC | 494470 |
rs180690663 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46402442 | ATATATCTCAATATT[G/T]CATGGAACATGCTTA | 494470 |
rs180691062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422132 | GAATGGCCTTTGAAG[C/G]TGGGTTCTGGGCAGA | 494470 |
rs180697338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385650 | GATCTAGAAGTGTCA[C/G]CTGTCCCCCTTTGGA | 494470 |
rs180701503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46349799 | AGTAACCCACAGCTA[C/T]ATTTGACACGCTGCA | 494470 |
rs180716421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372498 | TGAACCCCATGTGGG[A/G]CCACCTTAGTAAGCC | 494470 |
rs180725436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356358 | ATCAGAGGTGACATG[C/T]GCCATGGTGCAAAAT | 494470 |
rs180729827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46338950 | CTTCTTTGTGGCTTC[A/G]TGCAACTCTCCTCTC | 494470 |
rs180839582 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446361 | AAGGCTCTTTTCATT[C/T]ATTTACTAGTTTTCA | 494470 |
rs180865627 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456814 | GAGGGGGTTGGGGAG[A/G]ACCCACCTCTCCAGA | 494470 |
rs180873860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414212 | AGTGACTGATTAAGA[C/T]GGGACCTGAACACAA | 494470 |
rs180897613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430774 | TGTTTTCTCATTGAT[C/T]CTTCTTCAAGAGCTT | 494470 |
rs180986545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46435213 | ACCCTCAGGCTGCCC[C/T]GGTTTCTCAGAGCTC | 494470 |
rs180994102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46442674 | TTAGATCAAGTTAGT[C/T]GACAGTATTGTTCAG | 494470 |
rs180998687 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46417021 | CCATTTTTGCAAACT[A/G]TCAGCCACACCAATC | 494470 |
rs181010770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409321 | TAGAACAAACAAGTC[C/T]GGTGAGATTGACGTG | 494470 |
rs181011056 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RNF165 | GRCh38.p7 | 18:46428238 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 494470 |
rs181023251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46377286 | TGAGATTGACAGTTC[A/T]TGTCATCCCTCTTTC | 494470 |
rs181027307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46450096 | CTGTCACTTTATTAA[A/T]TCTGTTATTCCTTCT | 494470 |
rs181028887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46398796 | CATGGCTCAGTGCTC[C/T]TGGTGGGGTGTGGTT | 494470 |
rs181036090 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46344025 | TTGAAACATGCCTGG[A/G]TGTGCCGCTGTGTGC | 494470 |
rs181037119 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391218 | ATGGGTTCATTTCAC[A/G]TGAGTGATCTCGCTT | 494470 |
rs181049908 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46383615 | ATTGGAGTACAGTGG[C/T]GCGATCTCAGCTCAC | 494470 |
rs181049968 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46370518 | GACTTTTCTGTCCTT[A/G]GCTGTAGGGAAAACA | 494470 |
rs181053579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362960 | CCGGGGCTCTTGTGT[A/G]GAGTCCACAGAGATC | 494470 |
rs181057686 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46353310 | TTCTCATCTGAGAGA[C/G/T]GGGGATGTCATCGTG | 494470 |
rs181192307 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46368136 | CTGCTCTAGACCTTA[C/T]CTGCTTCCTTGGACC | 494470 |
rs181219984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349197 | TTGGACTGCAGTAAC[A/G]AAATGCCATAGACTG | 494470 |
rs181235127 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439283 | ATTGCAGGGCAATGC[A/G]TAGCCAAACCCAGGC | 494470 |
rs181240614 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458049 | TTCCTTCTCCTTTGA[A/G/T]GGGGGAGAGAGAACA | 494470 |
rs181245314 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423564 | CCTCTCTGGGCATAC[A/C]ACGTGGAGACGTGTA | 494470 |
rs181251114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46387213 | GTTCTCAAACTTCAA[C/T]GTCCAGCTGAGGCAT | 494470 |
rs181255904 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46403746 | AGCCAGGCGTGGTGG[C/T]GGTCACTTGTAATCC | 494470 |
rs181334332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430391 | AAGGCTTCAGAACCA[C/T]CTCTTTGCTCTCATT | 494470 |
rs181346223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46394019 | AAGCAGGTGCAGCTC[A/G]CCTTAGGTAACCCCA | 494470 |
rs181367047 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46408862 | TCCCAGTGGTACTGT[C/T]ATCTGTTTTCTGAGT | 494470 |
rs181373508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427750 | GTGGGGATCCAGATA[C/G]AGCAAAGACACGAAG | 494470 |
rs181374866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390549 | GAACTCATATTTAAA[A/G]CTTGTGGAGTTCCAG | 494470 |
rs181384107 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46376872 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGATGGT | 494470 |
rs181424875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445644 | CAAATCATTAAGATC[A/G]TCATGCTCTGCTTAG | 494470 |
rs181479060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46413803 | CCTATGGTGCAAAAG[A/G]ATGTACATACAGAGA | 494470 |
rs181481645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46380307 | GAAGATGGTGCCCAC[A/G]GGGGCTGTTGGCCTT | 494470 |
rs181498674 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46362412 | TACCCCAGTGGTTGA[A/G]GGGAGAGTGTGTTGA | 494470 |
rs181551145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441805 | AGGCAGGAGAATGGC[A/G]TGAACCGGGAGGCGG | 494470 |
rs181552264 | snp | C/T | 0.00438332 | 0.0466095 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461441 | CTTGAGATCAGGAGT[C/T]TGAGACCAGCCTGGC | 494470 |
rs181641479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46343563 | AATAGTCCTGGCTTC[A/G]TGGCCTCTCTGCCAG | 494470 |
rs181666651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373066 | CACACATTGGAGGAT[A/G]TGTCAAAAGGTAGGC | 494470 |
rs181684425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46393184 | TTAAAAGCAACACCA[A/G]GAAAGGGCATTGTGA | 494470 |
rs181684702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356975 | TCAGGTGGGGGACAA[A/G]TGGCTTTGTCCAACT | 494470 |
rs181686298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46339205 | GACTTAGAAAGCCTC[C/T]AATCCAACCTCAACA | 494470 |
rs181690924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379843 | CTGTCCTGAGAGGGT[G/T]CCCCTTGCTAAACTC | 494470 |
rs181691124 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451537 | TAGTGACTCACACCT[A/G]TAATCTCAGTGCTTT | 494470 |
rs181808976 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46375975 | GCTTCCATTTTCTTG[A/T]CTACGAAGTGGATGA | 494470 |
rs181810595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46361837 | CACTGACCTTAGCTT[C/T]CTGCACTAGCAAATG | 494470 |
rs181824601 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46342901 | TTTGTTGTTTTTTGG[C/G]GGGGAGTGGAGCTGT | 494470 |
rs181859206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46439010 | CTGGGTCTTCTGACA[A/G]CTGCTGCTGTTCAGG | 494470 |
rs181863787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435816 | ACAGAGAAGTGCCAG[A/G]GCATGCCAGCAAGGC | 494470 |
rs181867428 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46402867 | GCTGTATAGAATCAG[C/G]TCTCAGTACCTCTAG | 494470 |
rs181903083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46348746 | TATTCCAACAATTTG[C/G]AAATACTACACACTA | 494470 |
rs181951774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46450611 | CTATGTGAATGCTTC[C/T]TGCTCATGTCTTCCA | 494470 |
rs181955157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390143 | TCTTCCTGACCTCCC[C/G]ACCCCAACCCCTGTG | 494470 |
rs181964205 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46435525 | TTCTCAGGCCCCAGC[A/G]TTTGCCTCTGCTCCC | 494470 |
rs181974092 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RNF165 | GRCh38.p7 | 18:46417919 | TGAGGTGGGAGAATC[A/G]CTTGAACCTGGGAGG | 494470 |
rs182006813 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332412 | ATATGGTAGCTGTCT[A/G]GGTAAAGCCAGGCTG | 494470 |
rs182114293 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422937 | CTGCAGCTATTACCT[A/G]ACCCAGAGTTTCCTC | 494470 |
rs182138134 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46386657 | CCATGTAGATAGCTA[C/T]AGAGTAGTGAACAAA | 494470 |
rs182168068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415569 | ATAAAAATAAAAAAG[G/T]TGCTGAAGGAGCCCC | 494470 |
rs182179523 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458616 | ATTTTGGCTTGAGGA[A/G]GAGCTTCTAGCACGA | 494470 |
rs182179999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46367244 | CCGCCTCCCATCCTG[A/G]CTGTCATACCTGGCT | 494470 |
rs182182460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46396271 | CAAGGGAGCAGAAGT[A/G]AAGAGGAGGGAATGG | 494470 |
rs182182552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46439781 | TGAATTCACACATAT[A/G]TGTTATCCAGCTATG | 494470 |
rs182187497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399574 | CTTTGATGGGAAAAC[A/G]GTGAGGCAATGATGG | 494470 |
rs182189040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382742 | GACAGGCTCATGGAG[G/T]GTCCCTCTGGGTGAA | 494470 |
rs182190960 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369678 | CTATCTCATTTAGTT[C/G]TGCTTTGCTTTGAGT | 494470 |
rs182203820 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46427325 | GTCTGCTGGAGGGCA[A/C]AGGTTGTAGGATGGT | 494470 |
rs182210613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370885 | GCCAATGGGAATCAG[A/G]TACACGAAAAGGAGG | 494470 |
rs182283010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419192 | CCTGCCTGGTATTTT[A/G]CTACAGACGGCACTG | 494470 |
rs182286735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353436 | AAGGGTCTGTGACCT[C/T]TTGACAGGGTTGCTG | 494470 |
rs182295753 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383856 | GCGCCCGGCCACCAT[C/G]TTGGTTTTCTAATGA | 494470 |
rs182297375 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46400167 | CTTGTTTCTAAGGCT[A/G]GGCTGGATATTCCCG | 494470 |
rs182310736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371394 | CCAGGCCAGCGAGGA[A/G]GCTCTGACAATGCAA | 494470 |
rs182311469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354594 | GATCCTCTCTAGAGT[C/T]TTCAAAGACTGTACC | 494470 |
rs182357613 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46358888 | GCTTTTGACTTAAAG[A/T]CCACAGTGAGAGGAG | 494470 |
rs182424791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46452710 | TAAAAGCTTGACAAA[C/G]ATTAAGAATCTTAGA | 494470 |
rs182434737 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46436724 | ACACTCTCCATTAAA[A/T]TGAACAATTCCATAA | 494470 |
rs182450383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441119 | GCCTCCCAAGTAGCT[A/G]GGACTACAGGTGTGC | 494470 |
rs182462628 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46383654 | CTGCCTCCAGGGTTC[A/G]TGCCATTCTCCTGCC | 494470 |
rs182482606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46408120 | GTAGCTCAGATAGGT[C/T]GGGGCAGTGGATTGG | 494470 |
rs182523149 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46447924 | AGATCAACAGCTCCC[C/T]TCTCTTCCCAGCTTC | 494470 |
rs182539264 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF165 | GRCh38.p7 | 18:46424600 | CAAACATCTTCCTGG[C/T]GCTTTCTACTTTCTA | 494470 |
rs182571175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46387520 | TTTAGTGCCAAATTC[A/C]CCTCCAGGCTGTGCA | 494470 |
rs182589702 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46351351 | TGGAGCAGTTCCCTC[C/T]AGGTGCCCCTAGTTC | 494470 |
rs182595630 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46373579 | GCACAGTGCCTGGAC[A/G]CTGAGGGCTTTATAG | 494470 |
rs182610090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373811 | GTGCCTAGGCCAGAC[C/T]GTGCAGCCAGAGAAA | 494470 |
rs182612640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357883 | GCACCAGGGAAGATT[C/T]CTTCCTCATCTCTCC | 494470 |
rs182619491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46339930 | CTGCAGTAGCACATT[A/G]GATGATTTAATGGTT | 494470 |
rs182726157 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371250 | ATTACAATTCAAGAC[A/C/G]AGATTTGCATGGGGA | 494470 |
rs182730344 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353797 | AGAGATAACCAGATA[A/C]AGACAGCCCATGTCA | 494470 |
rs182736391 | snp | C/T | 0.0178098 | 0.0926698 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333809 | CTTCACGCGCGCCCT[C/T]TCCGGCCCGCGGGCG | 494470 |
rs182811737 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392575 | GGACACGGCTCAGAG[A/G]AGAGGCTCTGGGGAG | 494470 |
rs182828489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404704 | GTTGTAGTGAGCCGA[A/G]ACCGCGCCGCCACAC | 494470 |
rs182830870 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46444162 | GAATGGGTCTTTTGT[C/T]CTTTCACTATTTTTA | 494470 |
rs182947671 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366068 | GAGGCCAAGGAGGGC[G/T]GATCACCTGAGGTCA | 494470 |
rs182993659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46429072 | GAGTGAAGGGAAGGG[A/G]GTCCGGTGCCGCTTG | 494470 |
rs183000958 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46443735 | ACTATTTATGATCCT[C/T]TACAGAAGAAGTTTG | 494470 |
rs183003421 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46335676 | GGGTCGCAGGGCCAG[C/T]GCTTTAGTGCGCCCC | 494470 |
rs183004695 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410269 | CTTGGCTTTTCTGCT[C/T]TCCAGCTATCCCTAA | 494470 |
rs183041690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431958 | TCCTCCATCTGCTTT[C/G]TTTTTCTTCCAAAAA | 494470 |
rs183047945 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46395888 | CTCGCCATTCTATGG[C/G]AAAGCCCAGTAGTTC | 494470 |
rs183071209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369153 | AAAGGCCATGTTTTT[A/G]TTTTCCCCTGTGTGT | 494470 |
rs183106126 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46339753 | TTAATAATAATTTTC[C/T]GCAAACCAGCAAATA | 494470 |
rs183120675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431247 | CATTTTTAAAAATTT[C/G]GTAGGTTCTCTTTCT | 494470 |
rs183123599 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388848 | GGGTGAAAATTTCAC[A/C]CCCCACTTAGGGGCA | 494470 |
rs183133470 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446648 | TGCACTCCAGCCTGT[A/G]TGACAGAGCGAGACT | 494470 |
rs183141134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414912 | GAGCGTGCACTTCCA[C/G]CCAGGGCTGCAGGAG | 494470 |
rs183142826 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374773 | CTGGCTGAACTGGGG[A/G]GGCTAGAGACCCTAC | 494470 |
rs183143944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46359883 | TTCCTAGAAATTGCA[C/T]GTGACATTTTCACTT | 494470 |
rs183148259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395358 | GGGCAGGATGATTCT[A/T]TGTTGCAGGGGCTGT | 494470 |
rs183150961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429659 | TCCTGGTCATAATAA[C/T]TGCCTCACTTTCTTT | 494470 |
rs183157794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340575 | CCAAAATGTCCACAC[A/G]AATGGCAGAACGTCC | 494470 |
rs183262728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46436907 | GGCCCTTGCATATGG[C/T]TGAGTGATTGGAACA | 494470 |
rs183264264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46454986 | GAGACTTTACATAAT[A/G]GTAAACTACATAATG | 494470 |
rs183290121 | snp | A/G | 0.000395407 | 0.0140551 | intron-variant | RNF165 | GRCh38.p7 | 18:46447706 | TGGTAAGTGAAAGAA[A/G]ACGGACTCCCTTGCG | 494470 |
rs183313859 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46415474 | GAGCTTGCAGTGAGC[C/T]GAGATCGTGCCACTG | 494470 |
rs183315397 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46382142 | CATGAGGGTTTCAAA[C/T]ATGGCAAGGTCTGGT | 494470 |
rs183411842 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46418569 | ATTTGGTAACCATAC[A/G]GGACAGGACAGAACT | 494470 |
rs183419408 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391575 | GGGCAGGCCCTGCTC[A/G]AGCAGGGTAGTTTGC | 494470 |
rs183428073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46364503 | ACCCTTCGTGATGCC[A/G]ACAGACAAGGTGACT | 494470 |
rs183443300 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46409447 | TTTAGCCGAGGACAG[A/G]GCAGGAGGAAATGAA | 494470 |
rs183447534 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378094 | AAGTTGGCCCTGAGA[C/T]TTGCATTTGAGCTAA | 494470 |
rs183459526 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363435 | CCGGCCATCAGGGGC[A/G/T]TGTGCCTGCCTGGAG | 494470 |
rs183464061 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46345143 | GCTGGCTGCCACCTG[C/T]CACGGAACCAGAGGG | 494470 |
rs183467660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345809 | GTCCAGGCTGTGCCC[C/T]GACTCCCGGGGTGGC | 494470 |
rs183554837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405850 | GAGGCACTATTTTCT[A/G]GAATCACAGGCAGGG | 494470 |
rs183587344 | snp | A/G/T | 0.00358923 | 0.042236 | intron-variant | RNF165 | GRCh38.p7 | 18:46350435 | AGCTGGGATGGAAGC[A/G/T]TGAGGTCCATGTCAG | 494470 |
rs183620041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46351724 | GTTCTCAGTTACATC[A/G]CCTGGAAACAGAGGC | 494470 |
rs183662832 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46399743 | AGGAGGACAGTGTCC[A/G]GCCCGAGGCCCTGCC | 494470 |
rs183665544 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378700 | CCATAAATACACATT[A/C/G]TACTTAAGGTGTGGT | 494470 |
rs183719840 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46440047 | GTTGGCCAGGATGGT[C/G]TCGATCTCTTGACCT | 494470 |
rs183737845 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46346884 | ATATTTCAGCTTAAT[G/T]GTGTAAGCAGTTACT | 494470 |
rs183812126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368767 | CAAACCCCAGCTCTG[A/C]CATTCACTTGCTGTG | 494470 |
rs183918324 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46400318 | CAGTGATGACAGGAA[A/C]CTGATTGTTCATTTC | 494470 |
rs183929274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428646 | GGCGAATTGACATGT[A/G]TGGCAAGTACAAAAT | 494470 |
rs183935230 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46371468 | ATCTCAGAGAGACTC[A/T]GTGAGATTCTCTGGT | 494470 |
rs183942050 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459004 | TAGTTACTGATAGCC[A/G]CAGGAAGTTGAGACT | 494470 |
rs183942432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424978 | CCGGCTCTTGAGGCT[A/G]AGCCTCTCCAGCCCT | 494470 |
rs183954510 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336169 | TTCCTCTTAAAACGG[G/T]TGTGGAACATTACAC | 494470 |
rs184006441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46456431 | TCCATAGCCGGGCAG[C/T]TCCCCAGGAGTCCTA | 494470 |
rs184020780 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF165 | GRCh38.p7 | 18:46437929 | CTCCGATTGTCCTTT[C/T]CCCTCCGGGCAACCT | 494470 |
rs184039056 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46421907 | CATCACAAAGCTGCT[C/G]TTGGCTGTAAAGGAT | 494470 |
rs184044885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385485 | AGGAGCTTTTCTAGC[A/G]TGGCTCTACTGACTC | 494470 |
rs184048712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402060 | TATGAGGCAGTCACT[C/G]CACTGTTTTGTGAGG | 494470 |
rs184051645 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46372337 | TGAGGCAAGTCACTT[C/G]GCTCTTCCTGCCTCG | 494470 |
rs184077814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46443018 | CCTTTTACTTGTAAC[C/T]TAGTATCTACATATT | 494470 |
rs184090290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420912 | TTTAATTTACTTGAG[C/T]CTTTGTTAAAAATAT | 494470 |
rs184090629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384358 | ACATGTATGTGTGTG[G/T]GGGGGATTCTTGATA | 494470 |
rs184108215 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46355077 | GCCTTAGCCTCCGGA[C/G]TAGCTAGGACTACGG | 494470 |
rs184183892 | snp | G/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46440232 | GGTTTCAGTTACCCA[G/T]GTAAACCACGGTCTG | 494470 |
rs184191600 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46407383 | GGCCCTTTCTTGCTT[G/T]CTCACATGTTTTCTC | 494470 |
rs184198427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425450 | GGCCTTTCAGGCTGC[C/G]TGTTCTTCCCCTCTT | 494470 |
rs184198521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389384 | CTGGATAAAGTCCCA[C/T]TGGACAGACTCACAC | 494470 |
rs184202765 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46370420 | ATTCTTTACACAGGT[C/G]TAGTTCTCATGAGCT | 494470 |
rs184209069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353006 | CCTCCATGGCTTCAC[C/T]CAAATAGGCAAAGAC | 494470 |
rs184213002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374898 | GTGAGAAGCCCCTTG[A/G]GTCTGACATTTGGTC | 494470 |
rs184220540 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460274 | GACAAACACTCCCTG[C/T]GTGGGGCTGTAGCAA | 494470 |
rs184248241 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46426873 | TTAACTTGAAGGAGT[A/G]ACTCTAACAGGGAAA | 494470 |
rs184261202 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46430145 | TTGAGAAGGAGTGTT[A/G]AGAAGGTTAATTTTT | 494470 |
rs184270525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445464 | TTGTTCAACCTACTA[A/G]AATTTCACCCCATGT | 494470 |
rs184273509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412149 | GCACAGCCCCCTCCC[C/T]TCAAGGTTTAAGTCC | 494470 |
rs184308905 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389575 | GGCAACCGTGGGGGT[A/G]GATTATTACGCTTTC | 494470 |
rs184321929 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361450 | ACTGAGTATGGCAGG[C/T]ACATGATCCAGTGTC | 494470 |
rs184334412 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459680 | CCCACTTCTTTAGCC[A/G]GGCAGCTGTTTGGGG | 494470 |
rs184406201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440590 | CTATGTATCTCGAGA[G/T]ATAATGATTCTGCTT | 494470 |
rs184419423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407933 | CAGGATTTCACAGTG[A/G]CAAAGATCCAGAGAG | 494470 |
rs184430140 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46375643 | TTGAATGAATTGCGC[C/T]GTTATATGAGCTGCC | 494470 |
rs184447817 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46342612 | CTGGCTGGCTTGCTG[C/G]AGGAACTCCAGGGAG | 494470 |
rs184505938 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46384566 | CACCCCTGCCATATG[A/G]ACACACACATAATGC | 494470 |
rs184505976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372046 | GATGTCCTGAAGATG[A/C]GGCCCACAGTTCCTT | 494470 |
rs184519352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46355244 | AAGCATGAGCCACCG[A/G]GCCCGGCCTGTTTTA | 494470 |
rs184521438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337007 | TGTTTAATTGTACAA[C/T]GTCAAGAGCATCTTT | 494470 |
rs184563673 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46449604 | GAGATAATTGAATCA[G/T]GTGGGGGCAGTTTCC | 494470 |
rs184579832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390149 | TGACCTCCCCACCCC[A/G]ACCCCTGTGGGATGA | 494470 |
rs184581883 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46433135 | GGGCACAAGGGTCAG[C/T]GTGGCGGCCGCTCGT | 494470 |
rs184583966 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46408553 | AACAGAGTTAAGGTT[A/T]TCAGCCTGCTGCGGG | 494470 |
rs184588091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376083 | CATCACAGCAAGCCT[C/T]AGCTGCTCTGAGTGT | 494470 |
rs184590658 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337730 | CCCCCTTGCTTTTCT[A/T]TCCCCACCCTCACCC | 494470 |
rs184592568 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46365580 | GCGATCTTGGCTCAC[A/T]GCAACTTCTGCCTCC | 494470 |
rs184594456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416234 | AGTCAAAGCTCAACT[A/C]TAAACTCTTGAGACA | 494470 |
rs184602142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46361858 | CTAGCAAATGAGGAG[G/T]TTAGGTGATATGCTC | 494470 |
rs184646360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411303 | TGCTGAAAGATAATT[A/G]TGGTGGCATTGGCTG | 494470 |
rs184712417 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46411979 | CCCTGGGCTAAAAGC[C/G]TCTTGTCAGCAGAGT | 494470 |
rs184722483 | snp | A/C | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46429819 | GCTATGTTGTCCAGG[A/C]TGGTCTTGAACCCCT | 494470 |
rs184738996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46379246 | AATCTCTTTTGGGGT[A/G]CATCTAGTCCACAGG | 494470 |
rs184745413 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46367045 | ATCACCAAGCAAAAT[A/C]ACGCTATGGACCTCA | 494470 |
rs184751716 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | RNF165 | GRCh38.p7 | 18:46348234 | GCCAAGGGGCTGGGG[C/G]GGGTGAGGGGAGGGG | 494470 |
rs184770382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398636 | GCTGACACCATGGGT[C/T]GGTGGGTCTGAATTG | 494470 |
rs184832520 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46341744 | ATTCACATGTGTCTT[C/T]ACTGGCTTAGGTCAC | 494470 |
rs184908443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46383304 | ACAATTTTTCTACAA[A/G]TATCTAGTGATTTAT | 494470 |
rs184929241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360857 | TGGGGTGTTCAGCAG[C/T]GGAACTCCTGGGGAG | 494470 |
rs184973013 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46434665 | CTCCCAAGGATGCTC[A/G/T]GAGCACACTTTCAGA | 494470 |
rs185065816 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46449905 | CCCAACTGCCTGGGT[A/C/T]TGAAATCCTGGTTCT | 494470 |
rs185069181 | snp | A/G/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457320 | GGAGGCGGGAGGGGG[A/G/T]GGTTCTCGTTTTATT | 494470 |
rs185074258 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46416956 | ACTCTGCCTTTAATG[A/G]GAGGAGCTTGTATGG | 494470 |
rs185108201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421621 | ATATTGTCCCATTAT[C/G]CACAGAGGTTTTCTT | 494470 |
rs185112246 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455903 | GGGAAGAGCAGGCTG[G/T]GGGTGAAAACCACCA | 494470 |
rs185114194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393423 | AGGCCTGAGGGCAGA[C/T]GCCAGAAGGGTGCGC | 494470 |
rs185130588 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46367305 | TGAGGTTTCCATTTG[C/T]TTTAAAAGTCAACAG | 494470 |
rs185218127 | snp | A/T | 0.00049518 | 0.0157272 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46435361 | CGGCCAACTGCAGAC[A/T]CCTCAGCCCAGGTAT | 494470 |
rs185227376 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46379981 | GAACGTCAGAGAAGA[A/G]ATGAGGCTCCAAAGG | 494470 |
rs185233544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46437558 | TGTCCAGCCCAAGGT[C/T]GTCCACCCCCTGAGG | 494470 |
rs185245117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46401019 | GCCTTGAACTGGAAA[C/T]GCTGGGGAGGCCAGA | 494470 |
rs185246031 | snp | A/G/T | 0.00637159 | 0.0561118 | intron-variant | RNF165 | GRCh38.p7 | 18:46383618 | GGAGTACAGTGGTGC[A/G/T]ATCTCAGCTCACTGC | 494470 |
rs185247423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46348789 | GGAGAGTCGGTGTGC[A/G]TATTAGCAAATTAAA | 494470 |
rs185257352 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344353 | CTCTCCATGTCTTCC[C/T]CCTTCTCCCCCCGCC | 494470 |
rs185261749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46370608 | TGCCACCCTTCTCAC[A/G]TCTGATCTTAAACGT | 494470 |
rs185265597 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353333 | TCATCGTGACCTCCT[C/T]CATGGATTGTTGGGG | 494470 |
rs185286530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439565 | GCACACTGCAAGAAA[C/T]GACTGCTTGCAGCAT | 494470 |
rs185287514 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46352699 | AGCATGACACAGCAC[A/T]GCACAAGCCACCCCC | 494470 |
rs185290735 | snp | G/T | 0.00716266 | 0.059414 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458349 | TGGAAGACACCAGAT[G/T]AGCTGGAATTCTGCC | 494470 |
rs185298584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46403813 | AACCTGGAAGGTGGA[A/G]GTTGCAGTGAGCTGA | 494470 |
rs185306104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424059 | CGAAAACACTCACTT[A/C]GCAACTTTATTGGAG | 494470 |
rs185306310 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46387485 | AATATTCCAGGACTA[A/G/T]GGGAGAAACTTGTCC | 494470 |
rs185384308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370210 | ATACTGGACCAGGCT[C/T]ATCTAAGGGGTTCAC | 494470 |
rs185405892 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46441361 | TGTAGCTGGGATTAC[A/G]GGTGTGTGCCACTGC | 494470 |
rs185446289 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46382989 | AATACTCACTCCCCC[C/G]ACCCCCTGGGTCTGG | 494470 |
rs185475472 | snp | G/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333983 | GCTGTCCCCCGCGGT[G/T]CCGGCGAGGCCGCGC | 494470 |
rs185515385 | snp | G/T | 0.0023933 | 0.0345097 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461267 | TGGGAGATCTTTAGG[G/T]TCCCTTAGATTCAAG | 494470 |
rs185546015 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46427364 | CCCCAGGCTGGGGCG[A/G]TTGGTGCTCCTCCTA | 494470 |
rs185582095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46397164 | TCTTTCTGCACTCCA[A/G]CTTGGAGGAGGAGGG | 494470 |
rs185584871 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368224 | TTCACTAAATGCATT[A/C]ATCCTGGAAGTGTAG | 494470 |
rs185588840 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46349387 | GGGCCTCTTTTATAA[C/T]GGCACTAATTCCATT | 494470 |
rs185639282 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | RNF165 | GRCh38.p7 | 18:46441940 | GAGGCCGAGACGGGC[A/G]GATCACGAGGTCAGG | 494470 |
rs185643515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409153 | GCCATTATTACAACT[C/G]CAGGCCTTCAAGATC | 494470 |
rs185652385 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46371276 | GGGGACACAGCCAAA[A/C]CCTATCAGGAGGTCA | 494470 |
rs185652629 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46383846 | GTGAGCCACCGCGCC[C/T]GGCCACCATGTTGGT | 494470 |
rs185654705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427977 | TGGGAGCACAAACTC[G/T]CCAGTGGGAACATGA | 494470 |
rs185666877 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46354045 | ATCTCAGTCTCCACT[C/G]TCACTCTAAACCAGG | 494470 |
rs185668922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390661 | TAGTCCATCAGCCCC[C/G]ATTCAGCAGCATTTA | 494470 |
rs185736944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438721 | GAGGGGCTGACCTAG[A/T]GGATTTCTAAGTTTG | 494470 |
rs185786546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386736 | TCTTTCTGGGACATG[G/T]TGCTGTCTTTATAGG | 494470 |
rs185793474 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402945 | TAGTCTCAACACCAT[A/G]GGTTTAATTAATGAT | 494470 |
rs185803834 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46373309 | TCCTCAGAGCTTGCC[C/G]AGTGCTTTCTAAGAT | 494470 |
rs185808856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357064 | ACACCAGATCTACCT[C/T]TCTGAGGTAGGAATC | 494470 |
rs185820459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46339303 | TCAATCTTAACCAAT[G/T]CCAGGATTTCATTTT | 494470 |
rs185863232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422245 | AGTTCTGCCGTTCAA[G/T]GTTCCCCACAATTTC | 494470 |
rs185874387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391338 | TGGGCTCTCTGTTGG[C/T]CAAATGGGACGACAT | 494470 |
rs185879848 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46362982 | ACAGAGATCTTTCCA[A/C]GCCCACAGAAAAAGT | 494470 |
rs185880467 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46445111 | TTTTTTATTGAATGA[G/T]GAACATCATTTATGA | 494470 |
rs185995394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409333 | GTCCGGTGAGATTGA[C/T]GTGATCTTCTGAGAA | 494470 |
rs186006258 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46377335 | GTATTTATGGGAACT[C/T]GCTATATGCCAGGAA | 494470 |
rs186047980 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46428302 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 494470 |
rs186153091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343342 | CAAACTTCCACTGTG[A/T]TCTTGAACAGGTTAG | 494470 |
rs186155595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46446951 | TCTAGTTATGACAAG[A/G]TGTTTCCATCTTATC | 494470 |
rs186161868 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNF165 | GRCh38.p7 | 18:46442748 | GAATTATAAAGGAGG[A/G]TGGATGTCTAGAACT | 494470 |
rs186173870 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46431490 | CCAATGATTTTCTTT[A/G]GAGAAGCATCCCCCA | 494470 |
rs186181540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445689 | ATGGTCTGGAATGTG[A/C]CTTCATGCAAAAAAC | 494470 |
rs186210213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414028 | GTCCTTAATACCAGG[C/T]CTCATTTGTGTAGGG | 494470 |
rs186216039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380355 | GGAGTGTGCGCAGGG[G/T]ACATCCAGCAGGCTG | 494470 |
rs186218503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358349 | TGTGAGGAAGTGAAC[C/G]AGTGAAGGACAGCAG | 494470 |
rs186288579 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46443020 | TTTTACTTGTAACCT[A/G]GTATCTACATATTTA | 494470 |
rs186292527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46450996 | GGCCAGGAGGGAAGA[C/T]GGAAGGCCTCTCATT | 494470 |
rs186295636 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46428764 | CATTTTGGATATGAT[A/G]AATTACAGAAACATA | 494470 |
rs186350877 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46430436 | CAGGGAGATGTCTTT[C/T]GGGTGGGTTCTTTCC | 494470 |
rs186352204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46377032 | CAGCCCCTACCTCAG[A/G]GAGTGGTCAGGCACC | 494470 |
rs186357056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373592 | ACGCTGAGGGCTTTA[C/T]AGATCCCCAGTGACG | 494470 |
rs186359831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394071 | TTGCCCTCGGGTACC[G/T]GAAATCCTGCCACAC | 494470 |
rs186369693 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46343778 | TTTAGGACTCAGTAG[A/G]CACGTGAACTTCCAC | 494470 |
rs186374940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46339763 | TTTTCCGCAAACCAG[C/G]AAATACTATTAGTTA | 494470 |
rs186446600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349954 | GTTATAACAGCAGCA[C/T]GCATTCATTTACACG | 494470 |
rs186512100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46436416 | AATTCTTTATGCTGT[C/T]CTTGCAACTTTTAGG | 494470 |
rs186517294 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399825 | CCCTGCTCTTATTCT[C/T]CTCCTTCAGGTCTGG | 494470 |
rs186558090 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46362574 | CACCCAAATAGATAG[G/T]GGCACAGCCAAGCCT | 494470 |
rs186560342 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46446483 | CAAGACCAGCCTGGA[A/C]AACATGGTGAAACCC | 494470 |
rs186564576 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414677 | ACATACACAGATGCA[C/G]GCTCACAGACACATG | 494470 |
rs186571425 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46371421 | GCAACCTCATCCCAG[C/G]GATGACCCAGGCCCT | 494470 |
rs186571750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430823 | CAACATCTTATTTTC[C/T]TGAGGGTATGGATTA | 494470 |
rs186587583 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46394349 | AGAGAGAGCTCCCTC[C/T]TTCTAGCTTGCCAGG | 494470 |
rs186595181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381293 | AGTCAGGTTCTGCCA[C/T]GTGGGGCCACAAGAG | 494470 |
rs186595551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368495 | TGGGTCTGCGTGTGC[C/T]CAGGTCACCTTGATC | 494470 |
rs186651410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422952 | GACCCAGAGTTTCCT[C/T]TTCCCTGCTCATGCC | 494470 |
rs186654431 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46395436 | AGATGCTAGTAGCAT[C/T]CCTGGCTTGGTTGTT | 494470 |
rs186701315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451909 | TTAGCCCAAAATGGC[C/T]GTGTACTGTATGTTT | 494470 |
rs186712918 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46436774 | CCAACTTCTGCCCAG[C/G]CTTTTCCAATTAGCA | 494470 |
rs186716699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418700 | TATTTGATGATTGAA[G/T]AAGTCAAATTCTGAA | 494470 |
rs186719045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46452912 | GTCCACCTCCCCCTT[C/T]TAAAATGTGAAATGG | 494470 |
rs186726631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46419300 | ATTGAGCCATCCTCC[A/G]TAGCCAGCCCTAGGC | 494470 |
rs186732241 | snp | A/C/T | 0.00796322 | 0.0626896 | intron-variant | RNF165 | GRCh38.p7 | 18:46366020 | ACTCTTGGCTGGGCG[A/C/T]GGTGGCTCACACCTG | 494470 |
rs186733724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383918 | CTCAGTAGTCAGTCC[A/G]ATGAAGTTATATCTT | 494470 |
rs186738058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347348 | TCCATCCTCCCTGCC[A/T]TCCCCTGGCCCTGGC | 494470 |
rs186738081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400237 | ATACCCTCCTCTGAG[C/T]CTTTCACCCTGGCCA | 494470 |
rs186843436 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457776 | GGTGATGGCTGCTTG[C/G]TCTTGGCCACAGTGC | 494470 |
rs186858137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46382238 | TGAGGACAGGTCCCA[C/T]GGAGGCAGGGGTTGC | 494470 |
rs186866225 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46369240 | GATACCCAGGAGCCA[A/G]TTGAAGGGTGGTTCA | 494470 |
rs186866393 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46351602 | AGGACAGAAATATCC[A/G/T]CTCATGAGGGGCACA | 494470 |
rs186870968 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46381866 | GAATAAAACTCCAAA[G/T]GTGGGGTTTCAGGCA | 494470 |
rs187027318 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46418427 | CTACATCCAAAATAT[G/T]ATCAGTATTTAATTA | 494470 |
rs187031387 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF165 | GRCh38.p7 | 18:46383755 | CAGACGGGGTTTCAC[C/T]GTGTTGGCCAGGATG | 494470 |
rs187052922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46439187 | CATACTCTCATGAGC[A/G]TAACCCAGGTAACAG | 494470 |
rs187058638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353575 | ATGTTACCTAAAAAC[C/T]CTTAATCCCACTCCA | 494470 |
rs187064195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415130 | CAGTCCAGAGTGTCC[C/T]CTCCCCAGGCCTACA | 494470 |
rs187140585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440370 | GGTTATTGTTAGCCT[C/G]TTACTGTGCCTAATT | 494470 |
rs187143671 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46407493 | ATCACCCGACAGGAC[A/T]GTGTTAGCCTGTTGA | 494470 |
rs187175289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425867 | CAGAAATGCACTAAT[C/T]ACAGTTCTGGAGGCT | 494470 |
rs187196149 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | RNF165 | GRCh38.p7 | 18:46372507 | TGTGGGGCCACCTTA[G/T]TAAGCCCCCTTCCAG | 494470 |
rs187209021 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46339157 | AGATTTTGTTTGTTT[C/T]GTTTTCTTCTTTTTA | 494470 |
rs187216802 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46435661 | TCCTGCAGTGGGGGA[A/G]GGGGACAGGGATAGA | 494470 |
rs187224112 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46399653 | CTCTTACTGCTGGGG[C/T]CACCAGCGCTCTAGG | 494470 |
rs187245146 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46370905 | CGAAAAGGAGGATGG[A/G]CACATTGTGGGAGAG | 494470 |
rs187258327 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333275 | ATGAGTGGCCCTGGG[C/T]TTTCTGGGCAGTGTG | 494470 |
rs187283252 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46421734 | ACTGGCCCTTTGCTG[C/T]TTGTTGGAAGCTTGC | 494470 |
rs187289005 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RNF165 | GRCh38.p7 | 18:46429377 | GCAAAATCCCTCAAC[C/T]GCAGTGCGCTTTTAA | 494470 |
rs187301630 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46444049 | GTTTACAGTTTTTTT[C/T]CCCTTCAGCAGTGCA | 494470 |
rs187406293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385877 | GGGCTGGAAGAGTTG[C/T]TTTTACTAATACATG | 494470 |
rs187413843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46356523 | GCCCTGCAGATCCCA[A/G]GGGTTGATTCTTGCC | 494470 |
rs187440990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46360213 | GGCTTCCTCCTCTCC[C/T]GCATGGGGCCCTCAG | 494470 |
rs187444363 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46340764 | CAAGATACCTGGCAC[A/G]CGGCAGGTGCCTAGG | 494470 |
rs187532013 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452445 | CCACCACACCCAGCT[A/C]ATTTTTATATTTTTA | 494470 |
rs187537170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46335804 | CTTGGCCCCCTTAGG[C/T]CTGTTTGAACCGCAG | 494470 |
rs187579402 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46425277 | TCCCAGGATCCCACA[A/T]CCCTGGAGCAGGCAG | 494470 |
rs187584384 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388991 | TAATAGCTTATTGAC[A/T]CTCGGTTCACGAGGA | 494470 |
rs187587912 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46406119 | ACTCCTACACTCCCC[A/T]CATAGACACACACTT | 494470 |
rs187601525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374858 | GCCTGGAGAGAGGGG[C/T]CGATTTGATTGACTT | 494470 |
rs187644548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46429752 | AATTCCTTCAAATAC[C/T]ATTTTTTAAAATACT | 494470 |
rs187705115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410083 | TGCTGTTTTACTTAT[A/G]TGGTGAGGAGTAGTG | 494470 |
rs187714598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391648 | CTTGGTTTGGTGACA[C/T]ATTAAAATGTTTGCA | 494470 |
rs187725705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378539 | GGAGAAAGCCCAGAG[A/G]TGTCAGATGATCCCT | 494470 |
rs187744878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363652 | GCAGCTGTCAAGTCA[C/T]AGCCCTGCCCATGGG | 494470 |
rs187785774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354616 | GACTGTACCTTCCCT[G/T]CCAGCCACAGCATCA | 494470 |
rs187786624 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46415504 | GTACTCCAGCCTGGG[C/T]GACAGAACAAGGATC | 494470 |
rs187794938 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389415 | TGTTTTAGGAAACAA[A/T]GAGTGTCAGGTCATC | 494470 |
rs187801516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46361368 | TATAGAAATCATTAC[A/T]TATGTCTGTGTATAT | 494470 |
rs187869887 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46432939 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAATAAA | 494470 |
rs187876167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448761 | TTTGGGGGCCTTTGG[C/G]CTCCTGACATTGCAA | 494470 |
rs187883986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415836 | AGGTAAAGTGATATG[A/C]TGATATGACTGGGAT | 494470 |
rs187898777 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46382789 | GGCCAAGCCTAGGTT[C/G]TTAAATTAGAGACTA | 494470 |
rs187903186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396557 | ATAATAGTTGGTAAA[G/T]GTGAAATTATTTCAA | 494470 |
rs187905917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46444728 | TCCTCCTGCCTTGGC[C/T]TCCCAAAATGCTGGG | 494470 |
rs187913959 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46369726 | GGTAACTCATAAACC[A/G]GGGGGTCCTTATTCC | 494470 |
rs187935732 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF165 | GRCh38.p7 | 18:46411703 | GTTCCAAAGGGGTGA[A/G]GCCCTACTGAAGGAA | 494470 |
rs187942893 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46379170 | GATTTTATCCTGTCA[C/T]ACAAGAGTTGCTGGA | 494470 |
rs187972534 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46447754 | GTGGTCTGAGGCCTG[C/T]GGTCCCCTGTGCCCT | 494470 |
rs188072087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432101 | GTACTGAATCTGCCA[C/T]GTTTAGCAGCAAGTT | 494470 |
rs188078117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46395944 | GGCTCACTCAGACAC[A/G]TGTGGCTTGCTGCTC | 494470 |
rs188079829 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46437726 | AATAACTTGATCCTG[A/T]CCTTAAGCCGCAACC | 494470 |
rs188080581 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46374975 | TCCCTCCTAAATGTC[C/T]TCTTCAGGTCTTGGG | 494470 |
rs188082772 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340128 | CCTTAGTTTCTCTAT[G/T]GATCTAAACAGCTTT | 494470 |
rs188118746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46410567 | ATTGCTGTCAATTTC[A/G]TCCCAGGAAGATGCT | 494470 |
rs188135172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378979 | TGAAGGGACCTCACT[C/G]TCCCCAGGGCTCACC | 494470 |
rs188152276 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46346689 | GAGTTCTCACTCATA[A/T]AAAGTACGAGACACC | 494470 |
rs188166383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435524 | GTTCTCAGGCCCCAG[C/T]GTTTGCCTCTGCTCC | 494470 |
rs188182691 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNF165 | GRCh38.p7 | 18:46417764 | ATCCCAGCACTTTGA[A/G]AGGCCGAGGCAGGTG | 494470 |
rs188291880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368861 | GACAATGTCTACCTG[A/G]TAGAGTGGTTGGGAG | 494470 |
rs188296449 | snp | A/C | 0.00146796 | 0.0270522 | intron-variant | RNF165 | GRCh38.p7 | 18:46456515 | TCTCCCTCCTCTCTT[A/C]CAGACGCCTACCCTG | 494470 |
rs188310864 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394198 | TTACACAGGGCAAAA[A/G]CAAGGGCCTGAAGGG | 494470 |
rs188315000 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46438427 | TTGAGGGACAAGGTG[C/T]CTCTTGCTTTTCCAG | 494470 |
rs188324696 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46402194 | ATGAAAGCATCTATA[A/C]CCTGTTGGTTAACTC | 494470 |
rs188333534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46422077 | ACTGGAGCAAAAGAG[A/G]TTAAACTGATACACC | 494470 |
rs188337330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385491 | TTTTCTAGCGTGGCT[C/T]TACTGACTCTAGTGG | 494470 |
rs188378481 | snp | A/T | 0.00689924 | 0.0583268 | intron-variant | RNF165 | GRCh38.p7 | 18:46455932 | CAGCCACCAGCTGAG[A/T]CTGCCCCAGGTAATG | 494470 |
rs188437436 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46364904 | CTGGAACTTCAGGGT[A/G]GAAAACAGCCCTGAC | 494470 |
rs188437872 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459388 | AACACATCTTCAAGG[C/T]GGCAGAGCTGTGCGC | 494470 |
rs188490628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353007 | CTCCATGGCTTCACC[C/T]AAATAGGCAAAGACA | 494470 |
rs188494506 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | RNF165 | GRCh38.p7 | 18:46442342 | TTCTTTTCTAATATA[A/G]GCATATAAAACTGAA | 494470 |
rs188587738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421221 | AAAGCTAGTCTTTCT[A/G]CCTTGCACTTTATCT | 494470 |
rs188601880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384374 | GGGGGATTCTTGATA[C/T]TTCTTCCTTCTTATT | 494470 |
rs188610127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46355132 | TTTTTGTTTTTTTTT[C/T]AGTAGAGACAGGGTT | 494470 |
rs188653307 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398663 | ATTGCAGGGGTCCAC[A/G]CTGCTGAACTGAGAG | 494470 |
rs188671836 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46370453 | GGTGGATGGAGGAGG[A/G]GGTTTAGGGGGACCC | 494470 |
rs188674581 | snp | A/C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383577 | TTTTTTTTTTTGAGA[A/C/T]GGAGTCTCACTCTGT | 494470 |
rs188712593 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46440050 | GGCCAGGATGGTCTC[C/G]ATCTCTTGACCTCGT | 494470 |
rs188768896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455114 | TTCATGATTGCTTTA[C/T]GATAGTGCCTATCTT | 494470 |
rs188812426 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46401613 | CACACAAATGAAACT[G/T]GGTCTCACTCCCTCC | 494470 |
rs188820435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372062 | GGCCCACAGTTCCTT[C/T]AGGGTAGAAGAAAGG | 494470 |
rs188826536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355484 | AGCCTTGGAAAGGAC[A/G]GAAGTGCCCCAGTCT | 494470 |
rs188838545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337281 | ATTAAACAGGGGTAG[C/T]GTGTTCTGCTGTGCT | 494470 |
rs188857656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400650 | CATCTGTTCAGGAAG[A/T]TCCCGGGTGTGTCAG | 494470 |
rs188886288 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RNF165 | GRCh38.p7 | 18:46371487 | AGATTCTCTGGTTAA[A/G]GGAGAAGTTAAAGGA | 494470 |
rs188902015 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336389 | CCCCCCCCAACAAAA[A/C]AAAATCCAACAACAC | 494470 |
rs188926028 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46439803 | CCAGCTATGACATCA[A/G]CTCATGGCCAGTTTT | 494470 |
rs188928320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46405141 | CAACATGTCTATGGT[A/G]TACAGTGTGGCATAC | 494470 |
rs188939531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46351827 | GCAGGGCCTGGCTAC[A/G]TCAATCCACTGCGCA | 494470 |
rs188945431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374133 | AAACTTCTCACACAC[A/G]AGAAGACTGGGGCCC | 494470 |
rs188955841 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46441503 | ATAAAGCTCCCTCTT[C/T]CATTCCTCATATGAG | 494470 |
rs188964525 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF165 | GRCh38.p7 | 18:46449803 | TCAATTAAACCTCCT[C/T]TTTTTTAAGTTACCC | 494470 |
rs188966397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408664 | CTGGAGTTAATTAGA[A/G]CATCATCTTGGTCAG | 494470 |
rs188970871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427466 | AGGCAGGCAGCTGCA[C/T]GTTCATGGCAGTGGG | 494470 |
rs188976850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390194 | TCAGGTGGGAACTGG[A/G]CCGATTCCTGCTGGG | 494470 |
rs188988523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376584 | TTGCAAGATTATGCC[C/T]CTGTGACTTGGAAAG | 494470 |
rs189002289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362170 | AGTCAAGGGGCAGTC[A/G]CTGTCCCCTCCAAGG | 494470 |
rs189005535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46343461 | GCATAGGAAACAAGT[C/T]GAGAAGCCAGCCAAA | 494470 |
rs189051746 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46437294 | GGGCCAGCCTAGTGG[C/T]GCCGAGGGGTTTTGT | 494470 |
rs189061072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440786 | CATTTAATCTACATG[G/T]TCCTGGATTCAAATT | 494470 |
rs189137502 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339158 | GATTTTGTTTGTTTC[A/G]TTTTCTTCTTTTTAA | 494470 |
rs189139425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46367065 | TATGGACCTCATAAA[A/G]CAAACACAACAGGAA | 494470 |
rs189141509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379808 | TCTGTTTCAGGGCCC[A/G]TTCAAGAGATGCCTA | 494470 |
rs189155815 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46348358 | CCCTCCTGGTCAACA[C/T]GGCAGCTTTGCCTAT | 494470 |
rs189192502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430710 | TCCAATTGCCCTGTT[A/G]AATTTCATTTCACCT | 494470 |
rs189194989 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46424822 | ACAGAGACCTTACAC[C/T]GGGTGACTCTGCCTG | 494470 |
rs189198905 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458961 | CCAGTGGGGAAAGTA[C/T]ATCTGAGTCAGGATT | 494470 |
rs189228843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46387525 | TGCCAAATTCCCCTC[C/T]AGGCTGTGCAAAATG | 494470 |
rs189236207 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372477 | AGGGCATCATTGTCA[C/T]CTCAATGAACCCCAT | 494470 |
rs189242523 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358939 | CCGGACTCTTGTCCC[C/T]ACAGAGCCCCAGGTC | 494470 |
rs189252203 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337993 | ATTTCATCTTAGTTT[C/T]CAAGATACATGGGCA | 494470 |
rs189295268 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46445193 | GAGAGTGTTAGGCTT[C/T]GTTCTGGTAAGGAGC | 494470 |
rs189305215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412010 | AATTGGATCTGACTT[A/G]CAGCAGGCAGGGAGC | 494470 |
rs189309765 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46430019 | CCTCCTGCTCCCCTG[A/T]GGAATGGCTGCAGAG | 494470 |
rs189337186 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460767 | TGGATACATTCCATA[C/T]GAAATGCAAACCTTT | 494470 |
rs189461331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46361778 | GCAGGTCACCACCCA[C/T]TGTTGCTGGCTGTGT | 494470 |
rs189462027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445874 | ATCACCAGTAGAAGC[A/G]GAAATTCCTTTAATA | 494470 |
rs189475954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342774 | GTTTCATGGAGATGA[C/T]AGAATCACATTCTGG | 494470 |
rs189527176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46450050 | ATTAGTCACGTTAAG[G/T]GCTTAGAACAGTGCC | 494470 |
rs189533328 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46416981 | GTATGGGAGGGTAAG[A/C]ATACAAGGAGGGGAG | 494470 |
rs189536466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356309 | ATTCTAGTGGGGAAG[G/T]CAGACAGCAAACAAG | 494470 |
rs189562528 | snp | A/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46436790 | CTTTTCCAATTAGCA[A/G]ATTCAAATTAGGAAG | 494470 |
rs189565829 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46453748 | AAATATAGAAAATAC[A/T]GAGTCAAAATAGAAA | 494470 |
rs189568181 | snp | A/C/G | 0.0341408 | 0.126114 | intron-variant | RNF165 | GRCh38.p7 | 18:46383624 | CAGTGGTGCGATCTC[A/C/G]GCTCACTGCAAGCTC | 494470 |
rs189570265 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46399457 | ACTGGGCCTCGGCAC[A/G]TGACCTCCTGTGAGG | 494470 |
rs189685429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342286 | CCATGGCCTGCATAC[A/G]GCAAGGAGCCTCATC | 494470 |
rs189703547 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46412929 | CCCTGACTAGGACCC[A/T]CAAAATCCCCCAGAA | 494470 |
rs189707947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380124 | GAGTGCAGGGGCCTC[A/G]AACCTCTGCCTTCTT | 494470 |
rs189722890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424508 | AAATGCTGGGTGTCA[C/T]ATCACAGCTCTGATG | 494470 |
rs189734685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349047 | ACTGGCCAGAAGCAA[C/T]TCCCTTATACTGTGG | 494470 |
rs189745891 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377852 | TATTTAGCATGTGAT[A/G]CTCAGGTAACCATGT | 494470 |
rs189819946 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46434840 | GAGGAAGGCTTTGAC[C/T]TGTGCCATGAAAGCT | 494470 |
rs189895365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381157 | AACGCTGTTCTGAAG[C/T]GAGGAGGCATTGCTG | 494470 |
rs189902297 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46368287 | TTGGGACGTGGAGGC[A/C]TAAATAAAGAATAAA | 494470 |
rs189903918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349446 | CACTTCTCGAAGACC[C/T]CATCTTTTAACACCA | 494470 |
rs189906023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439578 | AACGACTGCTTGCAG[C/T]ATATTTTCTCTAATA | 494470 |
rs189906390 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458438 | CCCCTCACCTCCATT[C/T]ATAACCCAGTCTCAA | 494470 |
rs189963450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46393853 | ACAGACCTGGGTTCA[A/G]ATCTTGCCTCTGCCA | 494470 |
rs189971324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367778 | ATGTTAGGTTAGAGG[C/T]ATGGCTCTCAAGCCT | 494470 |
rs190009555 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461333 | GCTGTGCTGTCTCAC[A/C]TTCTGAGGAGAGAAG | 494470 |
rs190030199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46433667 | TCTCCCTGGCCTGGC[C/T]GGCAGTCACCAAGTG | 494470 |
rs190037081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418948 | GTTAATGTGTTGCCC[C/T]CTTTTGGGCATTTGC | 494470 |
rs190040488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46397191 | AGGGTTGGCCTTAGG[C/T]AGATGTCATGCCTCT | 494470 |
rs190046678 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46428064 | AGTGTGGACGGCTGC[A/G]GGAGGGCTTGGAGGG | 494470 |
rs190056204 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46400079 | GCACTGGGACCCCCA[A/C]GGTACCTCTTACCCA | 494470 |
rs190063020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383847 | TGAGCCACCGCGCCC[A/G]GCCACCATGTTGGTT | 494470 |
rs190065123 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371353 | TGCAAGGAGGGTCAC[A/G]GGGTCTGATAAGGAG | 494470 |
rs190065849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370217 | ACCAGGCTCATCTAA[A/G]GGGTTCACATGATAT | 494470 |
rs190071073 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46354178 | TCCAGCGAAGGCCCA[A/G]GGAAGGGCATGTATG | 494470 |
rs190083220 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46334641 | CCTAATACCTAGCCC[G/T]GTATGATCGAAAGGA | 494470 |
rs190136092 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46430214 | TCTCATACTTGATTA[A/G]TGGTTTGGCTGGGCA | 494470 |
rs190214965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373394 | TACAGGAGGGACTGG[A/G]CAAGAGTCACCCAGC | 494470 |
rs190216890 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357118 | TTCAAGTATGAACTC[A/G]TTGTTTTATCATTAA | 494470 |
rs190225187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46339434 | CATGTTTTAGCAATG[A/T]ATGCAGTGTATTTAA | 494470 |
rs190301000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416533 | TGAGTCCCCACCTCA[A/G]TAAACGACAACGCCA | 494470 |
rs190301395 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46383123 | GCCTAGCCTAGGCCG[C/G]GGTAGGTGCTGGTTG | 494470 |
rs190316667 | snp | A/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457463 | TGGCCTCTGAGGGTT[A/C]AGCGGAGGTGAGGAA | 494470 |
rs190321163 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352748 | AAACTGGGTCACGTA[A/G]CCACCCTTAGCTGTA | 494470 |
rs190337440 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46422609 | CTTCTTCCCCCCGAC[C/G]GAGGTCCAGCTCTCT | 494470 |
rs190366594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439239 | TGATGGCTTTGTTGG[C/G]TTTTTCCCTCAGAAA | 494470 |
rs190369049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46386017 | GAAGGGAGTTGCTTC[C/T]AACCATCTGGGCCTC | 494470 |
rs190384140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46356928 | CCCCGGCTGGAAAGG[C/T]GTGATCTGTGCCCTG | 494470 |
rs190384613 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423498 | AAGAGGTGGTACCAC[A/C]AGGACCATGGCATGT | 494470 |
rs190392539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46386869 | GCCATTTTGGGAGTC[C/T]CCCACTTTCTGATTT | 494470 |
rs190394729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403552 | GACTACTTATTGAAT[C/G]CTTCCGTATGCAATG | 494470 |
rs190510445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408031 | ACATCATGGATGGGG[A/T]GGCAGGGATTGGGGA | 494470 |
rs190514974 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46353434 | GCAAGGGTCTGTGAC[C/T]TCTTGACAGGGTTGC | 494470 |
rs190518999 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375841 | TGCTTACATCAAACA[A/G]CTGGAGGTTGATCAG | 494470 |
rs190557161 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333604 | GTCAGGCTCTACACG[C/T]GCGCCAGCCTCCGAG | 494470 |
rs190597394 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46438808 | CTGTTCCAGGGATTC[A/G]GGCTGATAATGGCTT | 494470 |
rs190619043 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372674 | TTGGGGGGCAGAGAC[A/G/T]CAGGAGGAGGGAGCT | 494470 |
rs190637394 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46442816 | TTTGCTTCACTTATT[C/T]TGACTTATATATATT | 494470 |
rs190637997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391764 | CACAAACACACACAC[A/G]CACACACACACTATA | 494470 |
rs190652414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378614 | GGCCAGCAGGCAGGG[A/C]CACTGTTTATCAAAT | 494470 |
rs190656238 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46363982 | AGAGAGAGTCTCTCT[C/T]TGCCCCCCAGGCTAG | 494470 |
rs190665767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409438 | CTTCGTTAGTTTAGC[C/T]GAGGACAGGGCAGGA | 494470 |
rs190740776 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46427079 | GAGGAGAGGCCCCAG[C/G]GGGCAAGGTGGATGT | 494470 |
rs190759547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370812 | GAGAGATTTGGGAGG[C/T]CAAGATCCTACAAGC | 494470 |
rs190767778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389655 | GGACTTGGGCCCACC[C/T]GGGAGCTGTCTTAGG | 494470 |
rs190786807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404396 | GCAGGTATTAAGCAC[A/C]TTTTTCGTGTGGGAC | 494470 |
rs190810009 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373696 | GTGTAAATGGCACTT[C/T]ACAACTCTTAGGACA | 494470 |
rs190818605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46443535 | CATTTTTGCTTTAAA[C/T]CAGTGGTTGGCAAAT | 494470 |
rs190826403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46339888 | CCTCCTGCCCCACCC[A/T]GTCCTTCCCATCTTT | 494470 |
rs190828935 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46410224 | GCCAAGCTTGGCTTC[C/T]TGCACCTCAGCTCTG | 494470 |
rs190832975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429031 | GGCAGTCTCCTTCCC[C/T]TTGTCCTGTGTGATG | 494470 |
rs190907060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46428633 | GGAATGAGGCTAGGG[C/T]GAATTGACATGTGTG | 494470 |
rs190959136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46431180 | TGGTTTGCTGAGAAT[A/G]ATGGTTTCCAGTTTC | 494470 |
rs190968510 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46446531 | CAAAAGTTATCCGGG[A/C]GTGGTGTGGCATGCC | 494470 |
rs190974236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414830 | AGTGGCCGTGTTAGA[C/T]TCATTGGGAGCCATT | 494470 |
rs190980253 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46374725 | GTCTCATACGGAGGT[C/T]TAGTAAATACAGCAC | 494470 |
rs190998277 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394661 | TAACAAACTAATGAC[C/T]CTGGCGAGGTTACTT | 494470 |
rs191006634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46381745 | TTGAGGTGGGAGGAT[C/T]GCTTGAGCCCAGGAT | 494470 |
rs191009114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368725 | GTTTAGCGTAGTGGT[A/C]AGGGTTAGAGCAAGA | 494470 |
rs191053111 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46387492 | CAGGACTAGGGGAGA[A/C]ACTTGTCCCAACTTT | 494470 |
rs191059594 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358577 | TTCCTCAACTCCTGC[A/T]GCTCTGGCCTTCAGG | 494470 |
rs191083478 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46452080 | TAACGGTGGATACAT[G/T]ACATTATGCATTTGT | 494470 |
rs191125601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46392429 | CTCAGGGCCCTCTTT[C/T]GGTGGCTTGCTGACC | 494470 |
rs191135036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363118 | GTGCTGAACATAATA[A/G]GTGCTCAATAAGTAC | 494470 |
rs191139524 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46400274 | TAGGCCTGGGGGACT[C/T]TCTTTACTTGGGCTT | 494470 |
rs191141004 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420483 | GGCTTTCTGAACTGG[G/T]TCCCCTCCTTTTGGC | 494470 |
rs191143451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344548 | CCACCCCCAGCGTGG[A/G]GACACTGGCCTTCCT | 494470 |
rs191144805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379214 | TGGCAAGTCACTCAG[C/T]CAAGGAAAACCTCTT | 494470 |
rs191148810 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366565 | TTAGTAAATGGCAGT[C/G]CCTAGCAATGCAGAA | 494470 |
rs191152785 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | RNF165 | GRCh38.p7 | 18:46347583 | CATTCTTACCTGCCA[A/G]GTGAGTTTAATCCTC | 494470 |
rs191154715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390766 | CTGGGCTCAGGTTCC[A/C]GTTGCACCACTTCTG | 494470 |
rs191288009 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46369631 | TTGGCCTGGAGACAG[C/T]TCCTTGCTGGAGGTG | 494470 |
rs191289227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351191 | GCTTCCCACTGGAGT[A/C]GACACTAAATTAGAA | 494470 |
rs191289938 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46382681 | TGTCCACCACAGCCC[C/T]GTGAAGTTAGGCAGG | 494470 |
rs191303695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351641 | TTTATAGGCATCATC[G/T]CTTTGTCCTCTGATG | 494470 |
rs191338270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436659 | CTAGGTGCAGGAAGT[C/T]GTGGCTTTCACATGT | 494470 |
rs191374263 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46409242 | CAAAGGAGAAAAAAG[C/G]GGAACAGCAATATGA | 494470 |
rs191391310 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46377042 | CTCAGGGAGTGGTCA[A/G]GCACCTAGGAGGAGG | 494470 |
rs191411056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343982 | GACATTCCCCCGGAT[G/T]CTGCTGCTTCCTCCT | 494470 |
rs191419858 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446972 | CCATCTTATCTTGCT[A/C]ATTTTCTCTCCAGAT | 494470 |
rs191450053 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | RNF165 | GRCh38.p7 | 18:46415337 | CACCCTGGCTAACAC[G/T]GTGAAACCCCATCTC | 494470 |
rs191456355 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46415539 | TCAAAAAAAATAAAA[A/T]AAATAAAAAAATAAA | 494470 |
rs191468292 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46396018 | AGACTTGGCGTTGTT[C/G]TGTGTGGTCTCTCAT | 494470 |
rs191556937 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460163 | ACTCTTTACGCCTAA[C/T]GAACAAGCACAGTTT | 494470 |
rs191583424 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440539 | ATATTTGGAAACAAA[G/T]CCAGGCATCATATTA | 494470 |
rs191588251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435757 | ATTCCGAGGAACTGG[A/G]TTGTCAGGAAGGCTT | 494470 |
rs191593004 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46399742 | GAGGAGGACAGTGTC[C/T]GGCCCGAGGCCCTGC | 494470 |
rs191617398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345755 | ATAAACCTTTGAATG[A/C]AAATACAGAATTTGG | 494470 |
rs191621792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371143 | CCATCGGATCTCATG[A/G]GTCTTATTCACCATC | 494470 |
rs191681572 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457798 | CCACAGTGCTCTCAG[A/C]CAGCACTAAGGGCTG | 494470 |
rs191686547 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46431736 | CACTGCCTTGCATGA[C/G]AAAGGGGAGGAGCCC | 494470 |
rs191696078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46384994 | GTCACCTTTGTGCCC[A/G]TAGACAGTATCTCTG | 494470 |
rs191699215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46401661 | GCCCTCTTGAACAAA[C/T]TTCAGCATGCTTCAG | 494470 |
rs191700564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46395876 | CACTTATTATTGCTC[A/G]CCATTCTATGGGAAA | 494470 |
rs191703313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444073 | CAGTGCATAGGTGCC[A/G]TTCCTTTGTCTTCTG | 494470 |
rs191713397 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46372301 | GTTGCACTCATCCAG[C/T]CACCCACTTGCTGTG | 494470 |
rs191715089 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355683 | TCTAAGTGCCCCTGG[C/T]TGCCCCTGAACTCAG | 494470 |
rs191722829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337533 | GTTCTGTTGCCCTTC[C/T]GAAGCATGGTGGGCC | 494470 |
rs191725026 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369026 | TCATGTAGTTTAAGT[A/G]TTACTCTACAGAGAT | 494470 |
rs191844925 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437830 | GTGGACTATACCCCA[A/C]TCTGTCACAGCTGCA | 494470 |
rs191859363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421892 | CTGGCCCTGGGGAAG[C/G]ATCACAAAGCTGCTC | 494470 |
rs191894133 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46418480 | TACATTATTTTGTTT[A/G]CACTAAGTCTCTGAT | 494470 |
rs191896003 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458987 | GGATTTTGGGGGAAA[A/G]CTAGTTACTGATAGC | 494470 |
rs191912546 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46383840 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCACCAT | 494470 |
rs191918855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388774 | AAGCAATTTCCATTT[C/T]CCGAGTGAGGGGTAA | 494470 |
rs191921348 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46353590 | CCTTAATCCCACTCC[A/G]TCCCTCTACAAATGG | 494470 |
rs191966346 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459655 | ATGGGGTGCTCAGAA[C/T]CCTGCAGCTCCCACT | 494470 |
rs191986160 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46440134 | CGCCCAGATCTCATG[A/G]CCAGTTTTACTCATC | 494470 |
rs192000134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425308 | AGCTGGCTCTGGTCA[C/G]CTGGCAGGCCTGCAA | 494470 |
rs192006076 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388995 | AGCTTATTGACTCTC[A/G]GTTCACGAGGAATTC | 494470 |
rs192012582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352915 | CCACACGTCAGGTCT[C/T]ACATTGATCCTGGGT | 494470 |
rs192014507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407098 | GAGTACTATAAATTG[C/T]ATCCTACCACACAAA | 494470 |
rs192019364 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46374859 | CCTGGAGAGAGGGGC[C/T]GATTTGATTGACTTG | 494470 |
rs192034971 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360637 | AAAGACCCCTGCATT[A/G]GTAAATCAGTCAGCT | 494470 |
rs192043693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341526 | GAATTGAGTTTAGTG[C/T]ACAGATAAGCACATA | 494470 |
rs192079490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46451251 | CAAACCTGACTGAGC[A/G]TCAGGATCACCTGGG | 494470 |
rs192151346 | snp | A/C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444810 | TGTGTCTTAAAGTCA[A/C/T]TAATCTTTTCTTTTG | 494470 |
rs192167641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355168 | ATGTTGGCCAGGTTG[A/G]TCTGGAACTCCTGAC | 494470 |
rs192171769 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336865 | TTAGTTGGAGGCAAA[A/C]AATGTTAAACATATG | 494470 |
rs192179426 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46411935 | CCATGGAGCCCAGCT[C/G]CCTGGAGTGGGGTCG | 494470 |
rs192187195 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46439814 | ATCAACTCATGGCCA[C/G]TTTTGTTTTTGTTTT | 494470 |
rs192193106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384355 | TGTACATGTATGTGT[G/T]TGGGGGGGATTCTTG | 494470 |
rs192215439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354855 | CCTATAAGTAAATCT[A/G]TTGACTCTTTAAAGA | 494470 |
rs192220143 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46405750 | GATGGGTTGAATATG[A/G]TGTCTATGTGAGCCA | 494470 |
rs192238685 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46430060 | AGCTGTGTGCTTGGG[A/T]AGCTTTCCACCTCTG | 494470 |
rs192245446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445305 | TACTCTAGATCTTCC[C/T]GAATAAGACTCATAA | 494470 |
rs192249749 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46412096 | AGATCTCAGCTCAGC[A/G]GGAGACAACGGCTCA | 494470 |
rs192266577 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46350254 | TATCTAGGAAAACAC[C/T]ATGCGTATGCGTGTG | 494470 |
rs192324221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342543 | GAAATGAACAGGGCA[C/T]TGGAACCCAGGGTGG | 494470 |
rs192415941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46397136 | CTGGGAGGGCCCTGC[C/T]GGAGGCGTCCCCTCT | 494470 |
rs192438846 | snp | A/G | 0.0123036 | 0.0774623 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332323 | AGGGTGGGAAAGAGA[A/G]CTCAGGCCTGAGAGA | 494470 |
rs192482425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46359068 | CCAGGACTCAGTTGT[C/T]CTCCCCGTAAAAGGA | 494470 |
rs192489023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46407616 | CTTCTAATGCAGAGG[A/G]TATTTCCAGACCTGA | 494470 |
rs192490350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46340272 | GGGCTTATCTTGGAA[C/T]GACTCAGATTTTCAG | 494470 |
rs192509839 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF165 | GRCh38.p7 | 18:46432867 | GGAAAGTGGCGTGAA[C/T]CCGGGAGGCGGAGCT | 494470 |
rs192515466 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46375326 | GGGAGGCCGAAGTGG[C/G]TGGGTCACTTGAGCC | 494470 |
rs192549751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429806 | GAGATGGGGTCTTGC[A/T]ATGTTGTCCAGGCTG | 494470 |
rs192592632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46432940 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAATAAAT | 494470 |
rs192605447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371453 | ACTGGATTCTCAGTC[A/T]TCTCAGAGAGACTCA | 494470 |
rs192629947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429462 | ACCAAAGATTAGATT[C/T]CTATTTGTCTATTTT | 494470 |
rs192630904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336053 | TAGCCATGGGGGTGA[C/G]GGGGAGTGGGTGTGT | 494470 |
rs192665730 | snp | A/C | 0.0555427 | 0.157119 | intron-variant | RNF165 | GRCh38.p7 | 18:46365383 | AAGTCTCTGGAAGAG[A/C]CTTTTCTCCACTAAT | 494470 |
rs192749332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46456163 | TGTGTCTGGGAGTTG[A/G]GGTGCTTGTTTGCTT | 494470 |
rs192791654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426049 | GGTTTTATCCCCACT[A/G]TCTAATCACCTCCCA | 494470 |
rs192799793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447819 | GCTCCCCTGTGCCCC[A/G]GCTTCCACATGACCC | 494470 |
rs192806425 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46449875 | ACCAAAAGGTGAAGG[A/G]AATGGACTCTGCCAC | 494470 |
rs192807223 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389572 | AGGGGCAACCGTGGG[A/G]GTGGATTATTACGCT | 494470 |
rs192814361 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361441 | TAATATTTAACTGAG[A/T]ATGGCAGGCACATGA | 494470 |
rs192821192 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46416749 | GTTTATTTGTATATC[A/T]CATGGTCTGTCATTC | 494470 |
rs192828271 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383300 | AAATACAATTTTTCT[A/G]CAAATATCTAGTGAT | 494470 |
rs192880196 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46378982 | AGGGACCTCACTGTC[C/T]CCAGGGCTCACCTGC | 494470 |
rs192891408 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346850 | AGCAGGCCCTTGGGC[A/T]GTCAGGGAAGGGCTG | 494470 |
rs192988273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46437552 | AGCCCATGTCCAGCC[C/G]AAGGTCGTCCACCCC | 494470 |
rs192991214 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46400894 | GCAGACATTTACCAC[C/T]TACCCCCTTCAGGTG | 494470 |
rs192999294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371674 | AAATGAGAGCTGAAA[C/T]AATGGTTTGAGAACC | 494470 |
rs193021132 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46433929 | CCTGATTCTAACACC[C/T]AAGCACCCTAAAGAA | 494470 |
rs193026337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398490 | ACAGGAAGCTGACAC[A/G]GGTGAGACAATTGGC | 494470 |
rs193037249 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46370271 | GGGGAGGGGAAACAT[C/T]GTTATTCCCATTTTA | 494470 |
rs193070008 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46369964 | GCACACACGCACACA[C/T]GCACACACACGCACC | 494470 |
rs193111973 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461091 | CATTACAAGAGGAAC[A/G]TCAGAGAGCCAAAAA | 494470 |
rs193195509 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46421613 | TGCCCAGAATATTGT[C/T]CCATTATGCACAGAG | 494470 |
rs193196466 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455650 | AAGACCAGCCTGACC[A/C]ACATGGTGAAACCCT | 494470 |
rs193203585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384377 | GGATTCTTGATACTT[A/C]TTCCTTCTTATTGCA | 494470 |
rs193233073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382958 | AGACAACGTCATACT[A/C]TTCTTGGCATGTATT | 494470 |
rs193238207 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46352231 | GATGAACTCCAGCTG[A/G]TCAAAGCCCAGAAAA | 494470 |
rs199555498 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431073 | GACAGGCCCCGGTGT[A/G]TGATGTTCCCCTCTC | 494470 |
rs199635104 | in-del | -/TA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398274 | TGTGTGTGCATGTGG[-/TA]TGTGTGTGTGAGTGT | 494470 |
rs199673750 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436660 | TAGGTGCAGGAAGTC[A/G]TGGCTTTCACATGTT | 494470 |
rs199676315 | in-del | -/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336394 | CCCAACAAAAAAAAA[-/T]CCAACAACACAAATT | 494470 |
rs199742248 | snp | C/G | 3.67836e-05 | 0.00428841 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433322 | CGCAGCCAGGCCTCA[C/G]CGCCCACATGGCCCC | 494470 |
rs199767180 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368237 | TTCATCCTGGAAGTG[G/T]AGGTTAGGCCTACCT | 494470 |
rs199794004 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344197 | CAGCACCAGCCTGCA[C/G]GTGGAGAGGGGGTGG | 494470 |
rs199794398 | in-del | -/TA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403990 | GGATTCTACTGCCCT[-/TA]GTGTGATTAACAATT | 494470 |
rs199795234 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454249 | ATGAATAATGATGGC[-/A]AAAAAATAGTAGAAA | 494470 |
rs199838983 | in-del | -/AGAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366321 | AAAAAAAAAAAAAAT[-/AGAG]AGAGAGATAATTCTT | 494470 |
rs199872331 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | RNF165 | GRCh38.p7 | 18:46379896 | TGGCTGTCCTGCCCC[-/T]GGCCTCCTTGGCCCA | 494470 |
rs199880040 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420855 | CATCTTAAAAAAAAA[A/G]AGAAAGAAAGTTATT | 494470 |
rs199890824 | in-del | -/AC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414470 | TGCAGACATACATGT[-/AC]ACACACACACATCAC | 494470 |
rs199901843 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334819 | TGTTTTGTATTCATT[C/T]TTTGTTCATTAGTAC | 494470 |
rs199956364 | snp | A/C | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336385 | CTCACCCCCCCCAAC[A/C]AAAAAAAATCCAACA | 494470 |
rs199965613 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408705 | GTTGCTGGAACAGTC[C/T]GAGGTCACATCCTTA | 494470 |
rs200027522 | snp | C/T | 4.94564e-05 | 0.0049725 | intron-variant | RNF165 | GRCh38.p7 | 18:46447726 | ACTCCCTTGCGCCTA[C/T]TGAGTGCCAGTGGTG | 494470 |
rs200037510 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF165 | GRCh38.p7 | 18:46391948 | GCACACAACACACAC[A/G]CACATGACACAATAC | 494470 |
rs200098539 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343415 | CACATCTTATGGCTT[A/C]TGCCTTACTGGACTC | 494470 |
rs200107296 | snp | C/T | 1.64882e-05 | 0.00287121 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46435334 | CCACCGCCTCCATCC[C/T]AGCTTCGACTTCGGC | 494470 |
rs200124034 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446643 | ACCACTGCACTCCAG[C/T]CTGTGTGACAGAGCG | 494470 |
rs200132930 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384793 | AGACCGAAGTGGGAG[C/G]ATTGCTTGAGGCCAG | 494470 |
rs200169625 | in-del | -/TAATAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375554 | GTGAGACTCTGTCTC[-/TAATAA]TAATAATAATAATAA | 494470 |
rs200171862 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398087 | ATGCTGACGTGTGAG[G/T]GTGTGTGCGCATGTG | 494470 |
rs200235065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46453421 | TCACTTCAACAGGCA[A/C]GAGGAAATTGTGAAG | 494470 |
rs200298066 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443248 | TTGTGTCTGTTTTTT[A/C]CCTTCTTTTGGATCA | 494470 |
rs200299590 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375800 | TTTTGAGTGTCCCTC[C/T]AATCCCACCTGGCAA | 494470 |
rs200332139 | snp | A/C | 2.27306e-05 | 0.00337117 | missense | RNF165 | GRCh38.p7 | 18:46456072 | GCTGGAAGATGGAGA[A/C]GATGTGAGGTAGGAG | 494470 |
rs200338216 | in-del | -/C | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389747 | TTCCTTTTTTTTTTT[-/C]CAGACAAGGTCTCAC | 494470 |
rs200363897 | in-del | -/T | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337806 | TTCTTTTTACTTTAC[-/T]TTTTTTTTTTTGTGG | 494470 |
rs200399979 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437171 | TGCTAGGAGGCCCTG[-/C]CCTAGAGGCCCGCCT | 494470 |
rs200419680 | in-del | -/C | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336373 | CTACCTTCTCCCTCA[-/C]CCCCCCCCAACAAAA | 494470 |
rs200429780 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46366207 | TGAGGCAGGAGACTC[A/G]CTTGAACCCGGGAGG | 494470 |
rs200433746 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367168 | CGGATGAAGAGTTTT[A/G]GGGGTTTTCCAAGAG | 494470 |
rs200491826 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364659 | GAGGCTGGAGGCACC[A/C]CAGCCTCTCCTTTGG | 494470 |
rs200528656 | in-del | -/ATAC | 0.0240643 | 0.107019 | intron-variant | RNF165 | GRCh38.p7 | 18:46392040 | TACACACCACACATA[-/ATAC]ATACAACACACACAC | 494470 |
rs200572329 | snp | G/T | 0.24449 | 0.249939 | intron-variant | RNF165 | GRCh38.p7 | 18:46397645 | GGGTGTGTGTGTGTG[G/T]GGGGTCATGCTGGGG | 494470 |
rs200622427 | in-del | -/GAGGTGTGAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397441 | GTGTGTGGTCATGCT[-/GAGGTGTGAG]GGGGTGTGTGTGTGT | 494470 |
rs200626691 | snp | C/T | 0.00124828 | 0.0249516 | intron-variant | RNF165 | GRCh38.p7 | 18:46435261 | GGGTAGCCCCTGACA[C/T]GAGGGCTCTCCATCC | 494470 |
rs200707418 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335045 | CAAGATGCTTGGGCG[C/T]GTGTGTGTGTGTGTG | 494470 |
rs200752643 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347990 | GCAGATGCTCACGTA[A/G]CACTTACTCTGTGCC | 494470 |
rs200760233 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392573 | GTGGACACGGCTCAG[C/T]GGAGAGGCTCTGGGG | 494470 |
rs200783050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435263 | GTAGCCCCTGACACG[A/T]GGGCTCTCCATCCCT | 494470 |
rs200800563 | in-del | -/C | 0.0205511 | 0.0992634 | intron-variant | RNF165 | GRCh38.p7 | 18:46353538 | GCTCCCCGTCCGCTA[-/C]CCCCACTGTCACTGG | 494470 |
rs200811742 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358758 | ACCAGCTTCTCACCC[C/T]TTCCTTCTCACATGC | 494470 |
rs200818701 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431074 | ACAGGCCCCGGTGTG[A/T]GATGTTCCCCTCTCT | 494470 |
rs200861552 | in-del | -/T | 0.0260105 | 0.111035 | intron-variant | RNF165 | GRCh38.p7 | 18:46429769 | TTTTTTAAAATACTC[-/T]TTTTTTTTCCTTTCT | 494470 |
rs200868401 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334815 | TGTGTGTTTTGTATT[C/T]ATTTTTTGTTCATTA | 494470 |
rs200912102 | snp | C/T | 9.88321e-05 | 0.00702896 | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447627 | CCCATCCCTCAGCAC[C/T]ATCAGCATTACCTAG | 494470 |
rs200923302 | snp | C/G | 1.6717e-05 | 0.00289106 | intron-variant | RNF165 | GRCh38.p7 | 18:46450696 | TGTGCACATTTTTCT[C/G]TTTCCAGGAGCTGCT | 494470 |
rs200938104 | in-del | -/AAAAAAAAAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366293 | GCAGAACTCTGGCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 494470 |
rs200946251 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374544 | TCTGGTTTATTTCAT[C/T]CAGGAGAACGTCTTC | 494470 |
rs200974688 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378983 | GGGACCTCACTGTCC[C/T]CAGGGCTCACCTGCT | 494470 |
rs201001299 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444654 | TTTTTTTTTTTTTTT[A/C]TAGACGTGATATCCC | 494470 |
rs201077019 | in-del | -/C | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336384 | CCTCACCCCCCCCAA[-/C]AAAAAAAAATCCAAC | 494470 |
rs201079005 | in-del | -/A | 0.0170251 | 0.090679 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388271 | ATTCACCACTCATAC[-/A]GTATGCAAAAGACTT | 494470 |
rs201118231 | snp | C/T | 0.000247115 | 0.0111129 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46450298 | TTCTACCCAACAGGT[C/T]GTCCATGAAATCCGA | 494470 |
rs201136557 | in-del | -/CGTATG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397865 | TGTGTGCATGTGGTG[-/CGTATG]TGTGTGTGTGATCAT | 494470 |
rs201156569 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442177 | CAAAAAAAAAAAAAA[C/T]AAAAAGAAAATAGCC | 494470 |
rs201166445 | snp | C/T | 0.000399281 | 0.0141238 | missense | RNF165 | GRCh38.p7 | 18:46450332 | TACCCTTACCCTCAG[C/T]TTCACTTCCTTGCTC | 494470 |
rs201261734 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341207 | TCTGAAGGCCTCTGG[A/G]GAGTTTGGACTGGCT | 494470 |
rs201313675 | snp | A/G | 0.000385971 | 0.0138866 | intron-variant | RNF165 | GRCh38.p7 | 18:46433524 | GGTGCTGCCTGGGGC[A/G]GAGGTGGGGACCCGG | 494470 |
rs201370214 | snp | C/G | 8.24232e-05 | 0.0064191 | intron-variant | RNF165 | GRCh38.p7 | 18:46447723 | CGGACTCCCTTGCGC[C/G]TATTGAGTGCCAGTG | 494470 |
rs201387063 | in-del | -/ATA | 0.0744748 | 0.178019 | intron-variant | RNF165 | GRCh38.p7 | 18:46363112 | GGCCCAGTGCTGAAC[-/ATA]ATAAGTGCTCAATAA | 494470 |
rs201391889 | in-del | -/GC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369379 | CTGGTGTGTGTGTGT[-/GC]TGGGGTGGCAGGGGG | 494470 |
rs201435044 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408113 | CCTGGAAGTAGCTCA[A/G]ATAGGTCGGGGCAGT | 494470 |
rs201512855 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377504 | AAGTGGCTGGAGGGG[C/T]TTTTCCTGGAGGAAG | 494470 |
rs201627920 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46444041 | TTTCTAAGTTTACAG[-/T]TTTTTTTTCCCTTCA | 494470 |
rs201653308 | in-del | -/T | 0.0368353 | 0.130617 | intron-variant | RNF165 | GRCh38.p7 | 18:46355262 | CGGCCTGTTTTAATA[-/T]TTTTTTTTTAACATG | 494470 |
rs201675119 | snp | A/G/T | 0.000297473 | 0.0121925 | intron-variant | RNF165 | GRCh38.p7 | 18:46435284 | CTCCATCCCTTCTGG[A/G/T]GCAGGCGGAGTCAGG | 494470 |
rs201678647 | snp | A/C | 4.94336e-05 | 0.00497135 | intron-variant | RNF165 | GRCh38.p7 | 18:46447705 | ATGGTAAGTGAAAGA[A/C]GACGGACTCCCTTGC | 494470 |
rs201682950 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334816 | GTGTGTTTTGTATTC[A/C]TTTTTTGTTCATTAG | 494470 |
rs201684282 | snp | G/T | 0.000543465 | 0.0164753 | missense | RNF165 | GRCh38.p7 | 18:46447665 | TCGAATGCACCACTT[G/T]CCCAGAAACTCCTCC | 494470 |
rs201746422 | snp | C/T | 3.62365e-05 | 0.0042564 | intron-variant | RNF165 | GRCh38.p7 | 18:46456105 | CGCCATTTTGATTCC[C/T]TCTCCCCTCTCTTAT | 494470 |
rs201763931 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341206 | TTCTGAAGGCCTCTG[A/G]AGAGTTTGGACTGGC | 494470 |
rs201776077 | snp | C/G | 0.000280017 | 0.0118292 | missense | RNF165 | GRCh38.p7 | 18:46450341 | CCTCAGCTTCACTTC[C/G]TTGCTCTCCAGGGAC | 494470 |
rs201779712 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429729 | CCAAACTCTCTATCA[C/T]ATTATAAAATTCCTT | 494470 |
rs201802166 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF165 | GRCh38.p7 | 18:46397894 | TGATCATGCTGAGGT[A/G]TGAGGGGGTGTGTGC | 494470 |
rs201837799 | snp | A/C | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336384 | CCTCACCCCCCCCAA[A/C]AAAAAAAAATCCAAC | 494470 |
rs201845856 | in-del | -/TCTGTGTGTG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348899 | CTCTCTCTCTCTCTT[-/TCTGTGTGTG]TGTGTGTGTGTGTGT | 494470 |
rs201853208 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420211 | ACCACTCCTGAGAAA[-/A]GCCATGGTCCAAGCT | 494470 |
rs201902618 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408959 | GCTGCCCGCAGGACC[A/G]TCTTCTATTTAAAGT | 494470 |
rs201908142 | in-del | -/GTT | 0.0376037 | 0.131863 | intron-variant | RNF165 | GRCh38.p7 | 18:46396301 | GAGGCCATTTTTGTA[-/GTT]GTTGTCTCATAGTGC | 494470 |
rs201993683 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367023 | TATACTTAGTTTCCA[-/A]GAAAAAATCACCAAG | 494470 |
rs202016863 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403040 | ACACGAGACTCACTT[C/T]CTTTCAGCTGCTCTC | 494470 |
rs202033258 | in-del | -/A | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390573 | TTCCAGCTTTGTGTG[-/A]AAAAAAAATACTAAC | 494470 |
rs202038363 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460910 | ACTTGGCACCCCCCC[-/A]GCCCCCACCACAACC | 494470 |
rs202118615 | snp | A/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391758 | CTGTGCCACAAACAC[A/T]CACACGCACACACAC | 494470 |
rs202192735 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371484 | TGAGATTCTCTGGTT[-/A]AAGGGAGAAGTTAAA | 494470 |
rs202223407 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348913 | TTCTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 494470 |
rs367545424 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420856 | TCTTAAAAAAAAAAA[-/A]GAAAGAAAGTTATTG | 494470 |
rs367562138 | snp | C/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459951 | TGCAGCAGCTGTGCC[C/G]CCGCGGGTCCACCGA | 494470 |
rs367566166 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443181 | CTCTTTCTTTTCTCT[C/T]TCTTCCATCTGTTTT | 494470 |
rs367571101 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398274 | GTGTGTGTGCATGTG[A/G]TGTGTGTGTGAGTGT | 494470 |
rs367578282 | in-del | -/CACACACACACACA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404800 | ATACACACACACACA[-/CACACACACACACA]ACAACCCCCCCACCA | 494470 |
rs367591870 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424275 | GCAGAGAATGGCTGT[C/T]GAGGGCCCAGAGGCA | 494470 |
rs367636030 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352973 | GCATTAGTGGCACTG[C/T]GGGTGGGACTAGCAT | 494470 |
rs367639711 | in-del | -/TT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363672 | CTGCCCATGGGAGAC[-/TT]ATGGGCTGCTTGAGG | 494470 |
rs367644804 | snp | C/T | 1.65449e-05 | 0.00287614 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46435376 | ACCTCAGCCCAGGTA[C/T]TTGGCTGAGGGCACT | 494470 |
rs367815001 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432567 | AGGGTCAGTGGGCTT[A/G/T]CATAGGAGTCTAATT | 494470 |
rs367821188 | in-del | -/TGT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396306 | CATTTTTGTAGTTGT[-/TGT]CTCATAGTGCTCATC | 494470 |
rs367862482 | snp | A/G | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333681 | TCGTGTGCACTAAGG[A/G]CGCTCGTGCCCGTCT | 494470 |
rs367878282 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376599 | CCTGTGACTTGGAAA[G/T]AAATTTCTTTTGGGG | 494470 |
rs367889879 | snp | G/T | 1.65255e-05 | 0.00287445 | intron-variant | RNF165 | GRCh38.p7 | 18:46435285 | TCCATCCCTTCTGGT[G/T]CAGGCGGAGTCAGGA | 494470 |
rs367903084 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352906 | GCTTAGAACCCACAC[A/G]TCAGGTCTTACATTG | 494470 |
rs367925021 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363823 | GAGGTGGTCACATGA[A/G]TTCATAGGGGCCACC | 494470 |
rs367957872 | in-del | -/CTCT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348894 | CAGAACTCTCTCTCT[-/CTCT]TTCTGTGTGTGTGTG | 494470 |
rs367961667 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455207 | GTTTGTAAGAGTTGA[-/T]TGTCTTCACGTAGTT | 494470 |
rs367963577 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456271 | TGTGATGCCCGGGTA[C/G]GGACGCGAGGATGAA | 494470 |
rs367973413 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340472 | GGATACAGAAGAAAT[A/G]GAGACCTGAGTGCCT | 494470 |
rs367976520 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46400709 | TCAGACAGCCTGTCG[A/G]GAAGCCTCTGTTGTC | 494470 |
rs368002873 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384116 | TCAACACAGAGATGG[C/T]GAAGACAGAGTTGGT | 494470 |
rs368022090 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446071 | GCTTGAGTAGATTCA[C/G]GTTCAACTCTTATTT | 494470 |
rs368025351 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428221 | CAAGACCATTCTGGC[C/T]AACATGGTGAAACCC | 494470 |
rs368047928 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367333 | CAGTTCAGTGATTTT[C/G]AGGATAATCTAGGGT | 494470 |
rs368059387 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448187 | CCTGGCCCCCTTATA[A/T]CCTGGCTCCCCTGTG | 494470 |
rs368060028 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46395457 | CTTGGTTGTTGAGAA[A/C]TACTTCTGTGCATAT | 494470 |
rs368065578 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422521 | CCTCTGGACTACATC[G/T]CCCTCCACCTGGGCG | 494470 |
rs368066656 | snp | A/G | 3.29571e-05 | 0.00405924 | missense | RNF165 | GRCh38.p7 | 18:46450387 | ACACCTCCGCCGTAC[A/G]GGAGAGCTATGAGGT | 494470 |
rs368078766 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452729 | AAGAATCTTAGAGCA[A/G]GACTGTCCTCATCAT | 494470 |
rs368101901 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397810 | TGAGGGTGTGTGTGC[A/C]TGTGGTGTGTGTGTG | 494470 |
rs368104798 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438100 | GAAAATAAAGTTCAG[C/T]GTGATGTTTAGATAC | 494470 |
rs368132685 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373636 | CTGAGTGCTGCCACA[C/G]TGGCTCCTCGGGCTC | 494470 |
rs368182539 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397815 | GTGTGTGTGCATGTG[-/GT]GTGTGTGTGTGGTCA | 494470 |
rs368319756 | snp | A/G | 0.000169736 | 0.00921082 | intron-variant | RNF165 | GRCh38.p7 | 18:46456091 | GTGAGGTAGGAGACC[A/G]CCATTTTGATTCCCT | 494470 |
rs368347322 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341787 | CTTTCTTACAATATG[A/T]ACTCCTCCCGGAGTT | 494470 |
rs368348355 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400681 | CGTGCCTCTCAGTGC[A/G]GTGGGCTCAGACTCA | 494470 |
rs368406686 | in-del | -/AAAAAC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428419 | TCTCAAAACAAAAAG[-/AAAAAC]AAAAACAAAAACAAA | 494470 |
rs368429163 | snp | C/T | 1.65441e-05 | 0.00287607 | synonymous-codon, intron-variant | RNF165 | GRCh38.p7 | 18:46450718 | GGAGCTGCTGCAGCT[C/T]GAGGACAGGTTGGGT | 494470 |
rs368466522 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46409168 | GCAGGCCTTCAAGAT[C/T]AGGAAAAGAATGTTG | 494470 |
rs368468233 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345129 | GCGATGCAGGGCTGC[-/C]TGGCTGCCACCTGCC | 494470 |
rs368470050 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442877 | ATGAATTGACCCCTT[G/T]ATCATTATGAAACAT | 494470 |
rs368485963 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357559 | ATCCCAGGTGATTGT[A/G]AAGGAACCACTGGGG | 494470 |
rs368489272 | snp | C/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333040 | CACCGCCTCAGTCGT[C/T]CTCCTGGCAACAAAG | 494470 |
rs368516936 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46411499 | GTCCCCTTTGCTATC[A/G]ATTGATTCATTTCAA | 494470 |
rs368522956 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423758 | AGATCTTCATCTGTA[C/G]AATGAAGGCTGTGTG | 494470 |
rs368531850 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46383404 | TATATATAAAATATG[C/T]ATACACACACACATG | 494470 |
rs368533891 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422111 | AGTACATAAGGAACC[C/T]GGAAAGAATGGCCTT | 494470 |
rs368560170 | snp | A/C/G | 3.29485e-05 | 0.00405874 | missense | RNF165 | GRCh38.p7 | 18:46450312 | TCGTCCATGAAATCC[A/C/G]AAACTACCCTTACCC | 494470 |
rs368565509 | snp | A/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457512 | GGTGAAGGGAGAGTT[A/C]ATCTAGGCGGGGCTC | 494470 |
rs368609746 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46365411 | AATGAACAGATGTAC[C/T]TATGTCTTCACAAGA | 494470 |
rs368611561 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345886 | AATTCTTCAGGGTCA[C/T]CCCAAGGCCTCATCT | 494470 |
rs368632887 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RNF165 | GRCh38.p7 | 18:46404823 | CCCCACCAAAACAAA[C/T]AAACAAACAACTCAA | 494470 |
rs368668220 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454631 | AGAGTTTAGGACCAG[A/G]GGCCAGAGAAGGGAG | 494470 |
rs368668559 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46427737 | CCAAGCCAGGTGCGT[A/G]GGGATCCAGATACAG | 494470 |
rs368681755 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369504 | AAGTGAAGGGAGTCA[A/G]GGAACGAGAAATGCC | 494470 |
rs368739988 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46401158 | GCCCTGGGTCCCCAG[A/G]GGCCTACTTGGTCCT | 494470 |
rs368761835 | in-del | -/GG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446695 | AAAAAAAAAAAAAAA[-/GG]AAAAGAAAAAAAAAA | 494470 |
rs368769087 | snp | A/C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398684 | GAACTGAGAGCACAC[A/C/G]GTCTAGCCCCACAGG | 494470 |
rs368890757 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448012 | TGCTGGCTCCCCTGT[G/T]CCCCGGCTTCCATAT | 494470 |
rs368895567 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383833 | TGGGATCACAGGCGT[A/G]AGCCACCGCGCCCGG | 494470 |
rs368963577 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360292 | GGGCACAGAGGCGGG[A/G]TATCATGTGTTTGTG | 494470 |
rs368966486 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383550 | ATGTTGGTTTTCTCT[G/T]TTTTTTTTTTTTTTT | 494470 |
rs369060420 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386821 | CTTCTCATCACTTCC[C/T]CCTTCCTTCTTCCCA | 494470 |
rs369064885 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399588 | CGGTGAGGCAATGAT[A/G]GGAGGGTGGGCTGGC | 494470 |
rs369069625 | snp | A/G | 1.64868e-05 | 0.00287109 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456641 | CCGACAGCTGAGGGA[A/G]GAATTAGCCAGTGGA | 494470 |
rs369075214 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459405 | GCAGAGCTGTGCGCC[C/T]ACCCAGCTATTGAAA | 494470 |
rs369102562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46392300 | CACCTGGATGCCCCC[C/T]GCTCCCTGAATGCTT | 494470 |
rs369112473 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454486 | AAGGGAAAACTTATT[A/G]CAGAAGCCTAGCAGG | 494470 |
rs369162094 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450491 | TCTGCTGGTGAGTAG[C/G]GTATGGGTGTCAGGA | 494470 |
rs369165543 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369992 | ACCCTAGACTTGGGA[A/G]TGATTCTGGTGTGGA | 494470 |
rs369175492 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457620 | CAGCTACTGGTACCC[A/G]ATGTGTTCCTGGGAG | 494470 |
rs369187139 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432584 | ATAGGAGTCTAATTC[A/G]AAAGGCCAAGCTTTA | 494470 |
rs369192275 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439702 | TAGATAAACTTTTTT[A/T]TTAAAAAAAACCCTT | 494470 |
rs369214969 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407859 | TACATCATCACAAAT[G/T]TCACAAAGCTGCTTG | 494470 |
rs369252255 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337894 | GAGCGATAGGAGGGG[A/C]CAGTTGTCCTGTTAC | 494470 |
rs369302096 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348558 | CTACTGCTGGGAGGG[A/T]GGGAAACTTCAGAGA | 494470 |
rs369302504 | in-del | -/AGG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410419 | TTAAGGTGGAGGAGG[-/AGG]CAGCCAGCCAGCTGT | 494470 |
rs369302827 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46428573 | CCTATAGAGTTGCAC[G/T]GTCCAAAATGGAAGT | 494470 |
rs369311882 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375149 | CTCCCAACTCCCCCC[A/G]CCCTCAGAGGCCCCA | 494470 |
rs369380073 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409566 | GAGGCTGTGGGCTCC[C/T]GGCCACATCTAACCA | 494470 |
rs369384886 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447848 | CCAGCTCACCTGTGT[A/G]TCAATCCCCCATGCC | 494470 |
rs369390382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46448725 | GTGGCTGCAGAGTGC[C/T]GAATCATGGGTCAGG | 494470 |
rs369423181 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46365508 | CTTGAATTTTTTTTT[G/T]TTGTTTTGTTTTTGA | 494470 |
rs369426854 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46415654 | GAAAGACGGGCTTGG[A/T]ATCAAACAGGCTCCA | 494470 |
rs369428647 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344171 | AGGAAAGGAAGCGGC[A/G]GCTGCTGACTCAGCA | 494470 |
rs369429340 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379807 | ATCTGTTTCAGGGCC[C/G]GTTCAAGAGATGCCT | 494470 |
rs369435050 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428825 | TTTACTTTTAAAAGG[C/T]GACTACTAGGAAATG | 494470 |
rs369435946 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439933 | CTTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 494470 |
rs369440360 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379406 | TATCTTATTCTTCCA[A/G]ATTCTAAAGGCCTCT | 494470 |
rs369441478 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46441051 | CCAGGCTGGAGTGCA[C/G]CTTGGCTCACTGCAG | 494470 |
rs369457485 | snp | A/C/T | 8.3015e-05 | 0.00644216 | intron-variant | RNF165 | GRCh38.p7 | 18:46456488 | TCCCTCAGCTCTTGC[A/C/T]GGGCCTCTGACTCTC | 494470 |
rs369481064 | in-del | -/GAAA | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46347452 | ATCGTGCCGCCCCTG[-/GAAA]GAGAGTCACGTGGAG | 494470 |
rs369490199 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46444219 | AGGAATTAGATTATT[A/G]TGTCCCTTGGAGTGG | 494470 |
rs369526531 | in-del | -/CAGGTGGGC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359238 | GTGGGCCAGGTGGGC[-/CAGGTGGGC]TGTTCCCTGCCTGTG | 494470 |
rs369639582 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344950 | CCTCCCCTCTGGTGG[C/G]CTCATGTCCCTCAGG | 494470 |
rs369686305 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422073 | TGAGACTGGAGCAAA[A/G]GAGGTTAAACTGATA | 494470 |
rs369692386 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457780 | ATGGCTGCTTGGTCT[C/T]GGCCACAGTGCTCTC | 494470 |
rs369698897 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354047 | CTCAGTCTCCACTCT[C/T]ACTCTAAACCAGGAA | 494470 |
rs369706608 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384209 | ACTGGGCCAACCCCT[C/T]CCTCCATCTAGAATT | 494470 |
rs369764562 | in-del | -/ACAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404830 | AAAACAAACAAACAA[-/ACAA]CTCAATGAAGTAGGG | 494470 |
rs369811723 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460395 | AAAAACACAAAAAAC[A/G]AAAAACATGGCACGT | 494470 |
rs369818378 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445555 | TCCTTCTATGTAGCT[G/T]CCTCTTCTCTCCAAA | 494470 |
rs369878472 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359853 | GGATGGGAGTGCCTT[A/G]TGAAACTAAGGCACT | 494470 |
rs369884430 | snp | C/G | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337189 | CAAATAGCCTCCCCA[C/G]ACTGCCATTTGGCAA | 494470 |
rs369887577 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454067 | GCAGTGAGCCGTGAT[G/T]ATACCACTGCACTCC | 494470 |
rs369894404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374351 | TGCTATTATCTTCAC[A/C]ATCCATCTCCAGAAC | 494470 |
rs369895835 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419085 | CTTTCTGATGTCCCC[A/G]AGTTCACCCCAGAAG | 494470 |
rs369895982 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455339 | TAAAGGGTGTTGAGG[A/G]GGAGTGGATGGTGTG | 494470 |
rs369916347 | snp | C/T | 0.0009801 | 0.0221154 | intron-variant | RNF165 | GRCh38.p7 | 18:46433513 | CACCCCAGGTTGGTG[C/T]TGCCTGGGGCGGAGG | 494470 |
rs369920599 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354728 | TTTAATTGCCTCTTA[A/C]AAATCTTTTAGTGGT | 494470 |
rs369944041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343978 | GCGGGACATTCCCCC[A/G]GATGCTGCTGCTTCC | 494470 |
rs369957334 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342013 | GGGAGTAGGGACTGA[A/G]GACAAGGACAGGGGC | 494470 |
rs369998988 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408022 | TCAGTTTGGACATCA[A/C/T]GGATGGGGTGGCAGG | 494470 |
rs370004261 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364438 | TAAAGTCGTAGAACA[C/T]GCATTCTAAAGTAAC | 494470 |
rs370005247 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420582 | AGATGCGGTGGCTCA[C/T]GCCTGTAATCTCAGC | 494470 |
rs370005806 | snp | C/T | 6.58903e-05 | 0.00573941 | utr-variant-5-prime, synonymous-codon | RNF165 | GRCh38.p7 | 18:46447596 | TGGCTTGAGTCCTGC[C/T]CAGTTCCAGGTGCGG | 494470 |
rs370038524 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439712 | TTTTTATTAAAAAAA[A/C]CCCTTTTTATTATAG | 494470 |
rs370047718 | snp | C/T | 9.32705e-05 | 0.00682836 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46456075 | GGAAGATGGAGAAGA[C/T]GTGAGGTAGGAGACC | 494470 |
rs370053321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438188 | CCCTGTGGCTTTAGG[A/T]CTGTGGGATATTCCT | 494470 |
rs370065883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376063 | AACAGGGCCGGGCCC[A/G]GGGTCATCACAGCAA | 494470 |
rs370080761 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348831 | GTCCTGCAACCAAGA[C/G]AGCCCTTTGGTTTTG | 494470 |
rs370088617 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433974 | GGCTGGTTCCAGGAA[A/C]GGCTGGTTCCCACCC | 494470 |
rs370102274 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417328 | AGAGTCAAAGGCAAC[A/T]TCCTGTAATGACCAG | 494470 |
rs370103128 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383298 | AAAAATACAATTTTT[C/T]TACAAATATCTAGTG | 494470 |
rs370114270 | snp | A/C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384439 | CTGGGGCTTGGGAGG[A/C/T]CCCTCTTTCTTAAAA | 494470 |
rs370116659 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363063 | AATGGCATGAGTTTT[C/G]CCTGATTTGTTCACT | 494470 |
rs370122516 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414351 | CCAAACCAGGGCTCT[C/G]TGTAGGTGCTGCTTA | 494470 |
rs370124425 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415990 | GTGCTGCACCAGCTG[G/T]CCACTCAGGGCTGGG | 494470 |
rs370193700 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405826 | TAAGGTTTGGGGTTA[C/G]TGCTGTGAGAGGCAC | 494470 |
rs370229462 | snp | A/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459039 | CCCCATTCTCTCCAA[A/T]GGCTGGGTGAAAACC | 494470 |
rs370250841 | in-del | -/GTGTGTGTGTGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334706 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGA]GAGAGAGAGAGAGCG | 494470 |
rs370289226 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340398 | CACTCACTTGTTTGT[C/T]CATTTAGTTAATGAG | 494470 |
rs370306474 | snp | C/T | 1.69092e-05 | 0.00290763 | intron-variant | RNF165 | GRCh38.p7 | 18:46435415 | AGTCTTCAGGGCCCC[C/T]GGGGGAGGAAGGGAG | 494470 |
rs370339011 | snp | A/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457325 | CGGGAGGGGGGGGTT[A/C]TCGTTTTATTTTTGT | 494470 |
rs370351416 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447743 | GAGTGCCAGTGGTGG[G/T]CTGAGGCCTGCGGTC | 494470 |
rs370424150 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446151 | ACTACTGTCTGGTTG[C/T]TGCTTCTTTTGTGAT | 494470 |
rs370436278 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452901 | GGCCCCTCCCTGTCC[A/G]CCTCCCCCTTTTAAA | 494470 |
rs370437270 | in-del | -/TG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397686 | GTGTGTGTGTGTGTG[-/TG]GTTATGCTGGGGTGT | 494470 |
rs370451728 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394935 | TAACATGAACTTTCA[C/T]GTATGTGGGGCTTTG | 494470 |
rs370476889 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456265 | TAGATGTGTGATGCC[C/T]GGGTACGGACGCGAG | 494470 |
rs370521018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338277 | TTTAGGACTTGCAAT[A/G]TAAGTTTTGCATTGA | 494470 |
rs370553051 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454139 | AAAAAAAAAAAAAAA[-/GT]AAAAGGGAAGGTTAA | 494470 |
rs370567973 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384607 | CCCAAACCTACTCAG[A/T]TTCCCTGGAGAAGCA | 494470 |
rs370585676 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456323 | TGTTCGGTCTGAATG[A/C]GTCTAAGACAAAGTT | 494470 |
rs370645873 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372581 | CACCATGTGAGGACA[C/G]GTGACCATGGTCACA | 494470 |
rs370646416 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438708 | CACCTGTGAATATGA[C/G]GGGCTGACCTAGTGG | 494470 |
rs370647277 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46397826 | TGTGGTGTGTGTGTG[G/T]GGTCATGCTGGGGTA | 494470 |
rs370661164 | snp | A/C/G | 9.9345e-05 | 0.00704725 | intron-variant | RNF165 | GRCh38.p7 | 18:46435275 | ACGAGGGCTCTCCAT[A/C/G]CCTTCTGGTGCAGGC | 494470 |
rs370665476 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346727 | CTGGGAAGTGTTTAG[A/G]AAAGATGGCCATTTC | 494470 |
rs370692136 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369433 | GGAAGCTGATTGACT[C/T]GGGAAGAAGAGGTGA | 494470 |
rs370698040 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46378763 | AAGAGGGTGGGGCTT[G/T]GCATCACGAAGCATC | 494470 |
rs370790761 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400206 | GCTGGTCACCCCTCT[C/T]ATGGGCTCTGCTCCT | 494470 |
rs370797942 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414748 | GCACGTGGAATCCTG[A/G]TCCTCAGGTCCTCCT | 494470 |
rs370802376 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426948 | CAGACATCACTGATC[A/G]TTGATTTGTCATGGA | 494470 |
rs370824975 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395913 | TAGTTCTTCCGATCT[C/T]ATTTAGGCTCATTGG | 494470 |
rs370830171 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431313 | AGGCTCTCTGTTCAT[A/G]CCAAAGAGTAGGTCA | 494470 |
rs370843688 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422690 | GGCCAAAAGGAGGGT[A/C]GATGTTGCAGGGAAT | 494470 |
rs370852285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447336 | TAAAGAAATTTCATA[C/G]AGCCTGGATTGCTCT | 494470 |
rs370884401 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451240 | GCAGAGGTTTTCAAA[C/T]CTGACTGAGCGTCAG | 494470 |
rs370960869 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361635 | GTACTATCATTCAAT[A/G]TACATGATTATGGCA | 494470 |
rs370961316 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375690 | CATCCTGGGAGTTCT[C/T]TTGTTCCCAGCAATT | 494470 |
rs370993860 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447826 | TGTGCCCCGGCTTCC[A/T]CATGACCCAGCTCAC | 494470 |
rs371014363 | snp | A/G | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332582 | CCTCCAAGGCTCCCC[A/G]TTTGCCCAGCTTCCC | 494470 |
rs371015933 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46427464 | CGAGGCAGGCAGCTG[A/C]ACGTTCATGGCAGTG | 494470 |
rs371017125 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459401 | GGCGGCAGAGCTGTG[C/T]GCCCACCCAGCTATT | 494470 |
rs371022075 | multinucleotide-polymorphism | CC/TT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378981 | AAGGGACCTCACTGT[CC/TT]CCAGGGCTCACCTGC | 494470 |
rs371024050 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46387127 | GGTCTCACAGCAGTG[-/A]CACTCTGACATAGCT | 494470 |
rs371025772 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46338902 | GCTCCTCGCTGGCGG[A/G]TGCACCCCTGCCTGA | 494470 |
rs371034406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372749 | ACCTGTGGCCAGGCT[A/G]TTTTATCCATACTTG | 494470 |
rs371060190 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357839 | GGCTGCAATCAAGCT[C/G]TCCGCGGGGCCAGCC | 494470 |
rs371068800 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403620 | CAGTGGCTCACAACT[A/G]TAATCCCAGCACTTT | 494470 |
rs371110137 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345687 | TTGGGGAAAACATGA[A/C]GTTTATATTAAACTA | 494470 |
rs371137771 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410690 | AGCCTCCCTGACAAA[A/C/G]AAACAAGTGGAAATC | 494470 |
rs371138093 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385610 | TGCACAGACAGAAAA[C/T]CTTAATACAAGCCCC | 494470 |
rs371141635 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422268 | ACAATTTCCCCACAC[C/G]CTCATTTTTCCTGTA | 494470 |
rs371257940 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364702 | CTTCTTGGGACATTC[C/T]TGTCCTGAGGCTCTC | 494470 |
rs371261387 | snp | A/G | 4.25469e-05 | 0.00461212 | intron-variant | RNF165 | GRCh38.p7 | 18:46433149 | GTGTGGCGGCCGCTC[A/G]TGCTGGTCGTCATGG | 494470 |
rs371286215 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448014 | CTGGCTCCCCTGTGC[C/T]CCGGCTTCCATATGA | 494470 |
rs371298776 | snp | A/G | 4.94279e-05 | 0.00497107 | missense | RNF165 | GRCh38.p7 | 18:46450380 | AGCAGACACACCTCC[A/G]CCGTACGGGAGAGCT | 494470 |
rs371313444 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF165 | GRCh38.p7 | 18:46360710 | GCCCTGCCCCTGGCC[C/T]GCCTTCACCACCTCC | 494470 |
rs371323142 | in-del | -/ATT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444469 | TGTGCTTCATTTTGG[-/ATT]ATTATTATTATTATT | 494470 |
rs371324401 | snp | A/T | 0.00026065 | 0.011413 | intron-variant | RNF165 | GRCh38.p7 | 18:46450654 | TATCCTGTGTGCATG[A/T]GGGCATTTATACATG | 494470 |
rs371336075 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452578 | AGCCACCATGCCTGG[A/C]CTGTTTTTGCTTAAT | 494470 |
rs371342520 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355747 | CCCTCTATCTCTCCA[C/T]CCATCATGTGCACAC | 494470 |
rs371369679 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417731 | CATAAGGCCGGGAGC[A/G]GTGGCTCACGCCTGT | 494470 |
rs371375870 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432683 | ACTTCCCCGGCCAGG[A/C]GCGGTGGCTCACGCC | 494470 |
rs371376182 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432604 | GCCAAGCTTTAGGAA[C/G]CTTAAAACTTTTAAA | 494470 |
rs371391301 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406005 | CTCCCCTCAGACACT[C/T]GCATACATACCCCTG | 494470 |
rs371447990 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46407413 | CTTTCTTTGTGACAT[A/G/T]TTGTCGTCATCATCA | 494470 |
rs371451123 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46373839 | AAAGGCAGAGCTGGG[A/G]CTCGCTAGCCCTCAG | 494470 |
rs371470459 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424481 | TGTTTCTCCCTGGTT[C/T]CAGCCCACTTCAAAT | 494470 |
rs371477338 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459979 | CGAGGACGCCAATCA[A/G]TCAACCCAACACCAC | 494470 |
rs371492985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409399 | TTTGGCCCATCTGCA[A/G]GTAAACGGTGGTGGT | 494470 |
rs371505230 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439703 | AGATAAACTTTTTTA[A/T]TAAAAAAAACCCTTT | 494470 |
rs371512212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46365375 | GTCTCTAGAAGTCTC[C/T]GGAAGAGCCTTTTCT | 494470 |
rs371522760 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366820 | ACGTGTGGACTACCT[G/T]CCATAAGTCAGACGC | 494470 |
rs371550635 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447169 | TGTTTTCTCAAAGTG[C/G]TAAAAATATAGCCTC | 494470 |
rs371563468 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457517 | AGGGAGAGTTCATCT[A/G]GGCGGGGCTCCCCAG | 494470 |
rs371593721 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366494 | TCATTTTATGATGAG[G/T]CCCAGACAATTTGGT | 494470 |
rs371593826 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385890 | TGCTTTTACTAATAC[A/T]TGCCAAGAAGACTGT | 494470 |
rs371609061 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413163 | ATTGCAAGCTGGGAA[C/G]CCTGCCAGGTCCTCT | 494470 |
rs371638228 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417386 | GCCCCCAAGATCAGT[A/G]TCACCTAAACTCCTA | 494470 |
rs371651727 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46452068 | GGTATCATACTCTAA[A/C/T]GGTGGATACATGACA | 494470 |
rs371756867 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448336 | AGCTCCCCTCTCTTC[C/G]CAGCTCCTATTCACA | 494470 |
rs371763097 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353320 | AGAGACGGGGATGTC[A/T]TCGTGACCTCCTCCA | 494470 |
rs371775649 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384135 | GACAGAGTTGGTACA[C/G]CAGGGCTTTTACTGT | 494470 |
rs371840479 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382159 | TGGCAAGGTCTGGTA[C/T]CTGAACACTTGGTTG | 494470 |
rs371853366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46359493 | GCATCTTAGAGGCCA[A/G]GGCTCATGGCTTGTC | 494470 |
rs371871840 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46387214 | TTCTCAAACTTCAAC[A/G]TCCAGCTGAGGCATG | 494470 |
rs371879510 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452804 | TGCATTGGTCGAGAG[C/T]ACTCTTAGAGTTAGA | 494470 |
rs371901845 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389193 | AGGGAAACATCCACT[A/G]TATTTATTCACCTCT | 494470 |
rs371902205 | snp | C/T | 3.30573e-05 | 0.00406541 | intron-variant | RNF165 | GRCh38.p7 | 18:46447513 | AGGTCCCTTCTCTAA[C/T]CTGGCTAAATCACAC | 494470 |
rs371943650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371073 | GAGGAGCAAAGGCAC[A/G]TCTTACATGGTGGCA | 494470 |
rs371997138 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428834 | AAAAGGTGACTACTA[A/G]GAAATGTAAAATTCC | 494470 |
rs372002528 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457396 | GTGCACGGAGTGTGG[A/G]AGGGGGTCTAGGAGA | 494470 |
rs372040721 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428282 | GGTGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 494470 |
rs372053162 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421512 | CCACATATGCCTTCC[A/T]CAAAATGCCTTGTTA | 494470 |
rs372064022 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351062 | GACCCCAGAGCTCAC[A/G]TGTGGCAGAGGGGCT | 494470 |
rs372072039 | snp | G/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332583 | CTCCAAGGCTCCCCG[G/T]TTGCCCAGCTTCCCG | 494470 |
rs372207133 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425793 | CCTGGGAGGCCCCCC[-/C]GTCTTAGTCTGTTTT | 494470 |
rs372224282 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381104 | CTGTAAAATAGGGAC[A/G]AGGCTATCTCTCTGC | 494470 |
rs372265834 | in-del | -/AT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398011 | GTGTGTGCATGTGGT[-/AT]GTGTGTGTGGTCATG | 494470 |
rs372272853 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420923 | TGAGTCTTTGTTAAA[A/G]ATATAATAGTAGGAG | 494470 |
rs372351593 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336061 | GGGGTGAGGGGGAGT[A/G]GGTGTGTGAGGAAGA | 494470 |
rs372403229 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433650 | CCTAGACTCCTGGCT[C/T]CTCTCCCTGGCCTGG | 494470 |
rs372446203 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392372 | TGCAGATTGTCCTGG[C/T]GTCCACTCTGTAAGC | 494470 |
rs372446901 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392687 | GGCTGAGGGTGACAC[G/T]GTCCTGTGCCTTGTC | 494470 |
rs372454610 | snp | C/G | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439417 | CATGCCTCCTGCCAT[C/G]TCGCTCCTGTAGGAT | 494470 |
rs372465390 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429804 | TTGAGATGGGGTCTT[C/G]CTATGTTGTCCAGGC | 494470 |
rs372491456 | snp | A/T | 3.31895e-05 | 0.00407353 | intron-variant | RNF165 | GRCh38.p7 | 18:46456485 | GTGTCCCTCAGCTCT[A/T]GCCGGGCCTCTGACT | 494470 |
rs372518540 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422276 | CCCACACCCTCATTT[C/T]TCCTGTATCACTTTC | 494470 |
rs372520252 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415682 | CCAGATTCCCAACCT[G/T]GGCCAAGTGATGCTG | 494470 |
rs372541949 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353787 | GCCCTCCAGAAGAGA[C/T]AACCAGATACAGACA | 494470 |
rs372555123 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386064 | CCAAAAATAAAGTAT[A/T]GGGGTTCACCCTCAG | 494470 |
rs372582008 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441354 | CTTCCCATGTAGCTG[C/G]GATTACAGGTGTGTG | 494470 |
rs372612905 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399985 | TCAGGTTTAGTGAGG[G/T]GCAAGCTGGGGCCAC | 494470 |
rs372629298 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426444 | AGCAGTCCCCAGGCA[C/T]TTGTGGGTCACCTAT | 494470 |
rs372647629 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46369333 | CTGGAGAAGCAGGGG[C/G]ATAAGGCTGAGCAGA | 494470 |
rs372650054 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46338087 | TTCTTAACTAGCAAT[C/T]TTGTAGCATTTCAGA | 494470 |
rs372651610 | in-del | C/GGATGCAGGGGTGCCTGG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345116 | ATGCAGGGGTGCCTG[C/GGATGCAGGGGTGCCTGG]GATGCAGGGCTGCTG | 494470 |
rs372677788 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350882 | TATAAGCTCTTTCAT[C/G]ATCAGATGGGCCCAT | 494470 |
rs372678464 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341797 | ATATGAACTCCTCCC[A/G]GAGTTGTACCAATCA | 494470 |
rs372683313 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374984 | AATGTCCTCTTCAGG[C/T]CTTGGGCCCCAGCCA | 494470 |
rs372697216 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378409 | TCAGCCTGGGGCATG[A/T]CCTCCAGCACATTCA | 494470 |
rs372704836 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46399347 | GGGCATCAAAGGATG[C/T]TGGGGTGCTGGCCCC | 494470 |
rs372718605 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46456009 | GGGCAAGAAGGATGA[A/G]GGGGAGGAGTCAGAC | 494470 |
rs372797614 | in-del | -/TACA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392045 | ACCACACATAATACA[-/TACA]ACACACACACCACAC | 494470 |
rs372802300 | snp | A/G | 4.94425e-05 | 0.0049718 | intron-variant | RNF165 | GRCh38.p7 | 18:46447709 | TAAGTGAAAGAAGAC[A/G]GACTCCCTTGCGCCT | 494470 |
rs372944466 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379720 | ACCCTGGGGAGCTAA[C/T]GTACTTTCTGAATCT | 494470 |
rs372953147 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357170 | AAAAATATAAACAAT[A/T]TGAAGGACTCCTCGC | 494470 |
rs372983604 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344365 | TCCCCCTTCTCCCCC[A/C]GCCCCCAGCTAGCTT | 494470 |
rs373012048 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382752 | TGGAGTGTCCCTCTG[A/G]GTGAAGAGGCAGCAG | 494470 |
rs373027766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46432723 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 494470 |
rs373033635 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360906 | TTTGGCCCAGAGGCC[A/G]GGCGTCAGCCCCACA | 494470 |
rs373058688 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430085 | CCTCTGTCAGGTGCA[A/G]CCTTATTTTGTTGTT | 494470 |
rs373099841 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46412680 | AGGATGTGGTCAGGC[C/T]GGAAGGGAATTGCTG | 494470 |
rs373122230 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360404 | GGCCCTGCTGGACAA[G/T]CAGTTTTACTGCCTC | 494470 |
rs373130146 | snp | A/G | 1.6486e-05 | 0.00287102 | intron-variant | RNF165 | GRCh38.p7 | 18:46447725 | GACTCCCTTGCGCCT[A/G]TTGAGTGCCAGTGGT | 494470 |
rs373141345 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455280 | AATGAAACCTGCTGG[G/T]CCTGAAAGTGGAGGG | 494470 |
rs373143559 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422214 | AGTTAGCTTATGTAG[C/T]GTACCCCAGACTCTC | 494470 |
rs373184896 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384514 | TTTCCTTGAATATTT[A/C]TCATGGATACACACC | 494470 |
rs373204000 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386565 | CCATCCATCCATCCA[C/T]CCATTCACCCACCCA | 494470 |
rs373226454 | in-del | -/GTGTGTGTGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334708 | TGTGTGTGTGTGTGT[-/GTGTGTGTGA]GAGAGAGAGAGAGCG | 494470 |
rs373236527 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381227 | CTTTGTCTTCTGTGG[C/T]CAAAGCCTGATTTCC | 494470 |
rs373237938 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419575 | TCTAGCTGGAGTGAC[C/T]GGGTCAAAGGGCTGC | 494470 |
rs373249863 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457621 | AGCTACTGGTACCCA[A/C/G]TGTGTTCCTGGGAGC | 494470 |
rs373317084 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46417417 | CCACTCAAGCCTCCC[A/G]AAGTTTCTCAAAATT | 494470 |
rs373336549 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389656 | GACTTGGGCCCACCC[A/G]GGAGCTGTCTTAGGC | 494470 |
rs373345644 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369071 | CCTGAGAAATTAATC[C/T]ATGTGTTTAAGTTTA | 494470 |
rs373357278 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406194 | ACGCCTGCATCCAGA[A/G]TCGTCACAAACTTCC | 494470 |
rs373361535 | snp | C/T | 1.65004e-05 | 0.00287227 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456661 | TAGCCAGTGGACACC[C/T]CATTTCCTTCACCAG | 494470 |
rs373364590 | snp | A/G | 0.000107941 | 0.00734566 | intron-variant | RNF165 | GRCh38.p7 | 18:46435446 | GAAGGGAGGGAGGAG[A/G]GAGGTCTTGCCAGAT | 494470 |
rs373500305 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348879 | AAAACTATCTGACCA[C/T]AGAACTCTCTCTCTC | 494470 |
rs373510549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383101 | CTGGGCCAGGAGCAG[G/T]CCAAGGGCCTAGCCT | 494470 |
rs373514667 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450928 | TGCTCTGGTTAGATG[C/T]TCTAAAGCTGTAATA | 494470 |
rs373518188 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338769 | AGACACTGAGGAAAT[G/T]AGTTGATTAAAGAAA | 494470 |
rs373522131 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413304 | GGACCATGTGGTGAC[A/G]TCCCAGGGACCCTGG | 494470 |
rs373558925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411622 | TTCCTGTCCCCAGCT[A/G]TGACGAGAGCCCATC | 494470 |
rs373562508 | snp | C/G | 0.000248725 | 0.011149 | intron-variant | RNF165 | GRCh38.p7 | 18:46456129 | CTCTTATAGGTATTG[C/G]TGACCAATCACTGCA | 494470 |
rs373612102 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375319 | GCACTTTGGGAGGCC[A/G]AAGTGGGTGGGTCAC | 494470 |
rs373630699 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417520 | TGCCAGTTCAGTCCT[C/T]ACCTTCTTCAGCTCT | 494470 |
rs373661138 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404480 | AAGTACTGACCAGGC[A/G]TGGTGGCTCACACCT | 494470 |
rs373668684 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354387 | GGGCCCATGCACACA[C/G]TCAGGCTGTAATGAT | 494470 |
rs373674046 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452082 | ACGGTGGATACATGA[C/T]ATTATGCATTTGTCA | 494470 |
rs373683020 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384320 | AGTGTCCAGTCTTCC[C/T]GAGGACATGCAGGCT | 494470 |
rs373697169 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450505 | GGGTATGGGTGTCAG[A/G]AAGCTTCAGGGTTAA | 494470 |
rs373701448 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376519 | GATCCCCTGATGGGA[A/C]CTCAGACCACACCTA | 494470 |
rs373708010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425444 | CTGTGGGGCCTTTCA[A/G]GCTGCCTGTTCTTCC | 494470 |
rs373713876 | in-del | -/GGAAAAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446695 | AAAAAAAAAAAAAAA[-/GGAAAAG]AAAAAAAAAAAGAAA | 494470 |
rs373718811 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358057 | CAGTATGACCTCATC[C/T]GAACTTGATCACATC | 494470 |
rs373719197 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373345 | TCCTGCCCTTCATCT[C/T]GACAGTCATCTGGAA | 494470 |
rs373725588 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345126 | GCCTGCGATGCAGGG[C/G]TGCTGGCTGCCACCT | 494470 |
rs373752526 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340689 | CTGCTTTGAGCATCC[C/T]CTGAACAATGACTGA | 494470 |
rs373785029 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455829 | AACACAGCAAGAATC[A/C]GTCTCAAAAACAAAA | 494470 |
rs373826647 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348225 | GCGTTGTGGGCCAAG[A/G]GGCTGGGGGGGGTGA | 494470 |
rs373829878 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456112 | TTGATTCCCTCTCCC[C/T]TCTCTTATAGGTATT | 494470 |
rs373926109 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384815 | TGAGGCCAGGAGTTC[A/G]AGACCAGCCTGGGCA | 494470 |
rs373935385 | snp | C/T | 0.000157988 | 0.00888645 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334244 | GGGCCCGCGCGCAGC[C/T]GCCGCCGCCGCCGCC | 494470 |
rs373939301 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452723 | AACATTAAGAATCTT[A/G]GAGCAGGACTGTCCT | 494470 |
rs373942142 | snp | A/G | 0.000164758 | 0.0090748 | missense | RNF165 | GRCh38.p7 | 18:46450383 | AGACACACCTCCGCC[A/G]TACGGGAGAGCTATG | 494470 |
rs374042915 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433722 | TTTCAGAGGCATCCA[C/G]TTCAGGCAGTGAGCA | 494470 |
rs374090419 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380660 | GGAGCTGGGAGCAGG[A/G]AGCAGGGACTTCTGA | 494470 |
rs374093607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417833 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 494470 |
rs374184808 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46419869 | ATCCTTTTGTTATCT[C/T]TCTTCCCCTGCTCTC | 494470 |
rs374224448 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385368 | TGGAAGGAAGGACTT[A/G]CATGTGCCTGTGCAT | 494470 |
rs374235564 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341078 | CCTACAGGGAGCACC[A/G]GGATCATTGTCCTGT | 494470 |
rs374246432 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374718 | CAACAGAGTCTCATA[C/T]GGAGGTCTAGTAAAT | 494470 |
rs374249250 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456398 | CTTCATGGTTTCCCA[C/T]CTCAGCCACAGCCTC | 494470 |
rs374315346 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380286 | GGGGCCTGGAAGGGC[A/G]TCTTGGAAGATGGTG | 494470 |
rs374338192 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441494 | GAATCTGTAATAAAG[C/G]TCCCTCTTTCATTCC | 494470 |
rs374343418 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363247 | CTCTGGGCTTTGAAC[A/G]GGACCCTGAAGATGA | 494470 |
rs374377068 | in-del | -/CGCACACA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369956 | ACACACACGCACACA[-/CGCACACA]TGCACACACACGCAC | 494470 |
rs374439832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46437712 | TCTTGCCCATGCCTA[A/G]TAACTTGATCCTGAC | 494470 |
rs374443660 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46370629 | TCTTAAACGTACCAG[A/G]TGTGGGTGAGGCCTC | 494470 |
rs374465689 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420078 | AGCAGATATCCACTC[A/G]CTGATGTGATCTGAT | 494470 |
rs374477199 | in-del | -/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46381841 | TTATTCCTAAGCATC[-/T]TTTTTTTTTTTGAGA | 494470 |
rs374543182 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459046 | CTCTCCAATGGCTGG[A/G]TGAAAACCAAGAATT | 494470 |
rs374577971 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348905 | CTCTCTCTTTCTGTG[C/T]GTGTGTGTGTGTGTG | 494470 |
rs374594077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46339264 | CACTCTCATATTTGC[C/G]CTAGAGAACAGTGGC | 494470 |
rs374604135 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF165 | GRCh38.p7 | 18:46361768 | AGGAGCTGCTGCAGG[C/T]CACCACCCATTGTTG | 494470 |
rs374654989 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337500 | GCCCGGGCCATCTGC[C/T]CATTGTACGCTGCTT | 494470 |
rs374696361 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453435 | ACGAGGAAATTGTGA[A/C]GAGAACCAATGCTAA | 494470 |
rs374714937 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431050 | CCTCCTCTTGCCCCC[A/C]ACCCCTGGACAGGCC | 494470 |
rs374718980 | snp | A/G | 1.64833e-05 | 0.00287078 | stop-lost | RNF165 | GRCh38.p7 | 18:46456636 | GGGAGCCGACAGCTG[A/G]GGGAGGAATTAGCCA | 494470 |
rs374750107 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355571 | GTCCCAGCTCCCATC[G/T]GTGCCTATCTGAGGA | 494470 |
rs374767284 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402181 | CATGTATATACCTAT[A/G]AAAGCATCTATACCC | 494470 |
rs374858571 | in-del | -/TAATAATAATAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375554 | GTGAGACTCTGTCTC[-/TAATAATAATAA]TAATAATAATAATAA | 494470 |
rs374863861 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46397974 | GGGGTGTGTGTGTGT[A/G]GTCATGCGGAGGTGT | 494470 |
rs374867512 | snp | C/T | 1.72794e-05 | 0.00293928 | intron-variant | RNF165 | GRCh38.p7 | 18:46450668 | GTGGGCATTTATACA[C/T]GCTGAGCACACATGT | 494470 |
rs374875638 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46428500 | GTCACTGCTCCACTC[-/T]TATCAGTTAGGAAAC | 494470 |
rs374879908 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348427 | AATAAAGTGCACAGA[A/T]CCTCTGTGTGTCCTG | 494470 |
rs374893671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382426 | GTGGTTTTCAGAGAT[C/G]AGTTGTTTACCATTT | 494470 |
rs374925345 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456737 | GCCATTTGACGTAGA[A/G]GAAAAGCCTGCAAGC | 494470 |
rs374968260 | snp | A/G | 1.64885e-05 | 0.00287123 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435335 | CACCGCCTCCATCCC[A/G]GCTTCGACTTCGGCC | 494470 |
rs374977282 | in-del | -/AAAAAAAAA | 0.362104 | 0.223456 | intron-variant | RNF165 | GRCh38.p7 | 18:46441862 | GCGAGACTCCATCTC[-/AAAAAAAAA]AAAAAAAAAAGAGGC | 494470 |
rs375039548 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46454391 | TTAAGCAGGCAGATC[A/T]TCATGACTCTATTCA | 494470 |
rs375083291 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46409543 | GTATTAGGATTGGGG[C/G]AAGCTAAGAGGCTGT | 494470 |
rs375087255 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46374167 | CAGCTTGAACGAGTC[C/T]GAGAAACTCAGGGGT | 494470 |
rs375110583 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412105 | CTCAGCGGGAGACAA[C/T]GGCTCATCTCACAGC | 494470 |
rs375120066 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425057 | TGGAGAGGGAGTCTC[A/G]GGCCTTCCCCTCCTT | 494470 |
rs375142438 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355235 | TGAGATTACAAGCAT[A/G]AGCCACCGGGCCCGG | 494470 |
rs375177198 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443245 | AATTTGTGTCTGTTT[C/T]TTGCCTTCTTTTGGA | 494470 |
rs375195130 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46416862 | TGGGCTCAGAATTGG[A/C]ATGATGTCACTTCTG | 494470 |
rs375262874 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357389 | ACTGAGAGTAAGCAA[A/G]TGATCCACAAGTCAA | 494470 |
rs375264868 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398990 | GCTCCTGGGTGTGGC[C/T]GCCAGAGATCCTGAT | 494470 |
rs375269287 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460257 | CCCCCGCCTGTAGGC[A/G]GGACAAACACTCCCT | 494470 |
rs375271244 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425208 | AGGAGGCGGGAACTC[A/G]GGCTTCCGGGGAACC | 494470 |
rs375347547 | in-del | -/CAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341014 | ACAGAAAGTACGTAG[-/CAG]GAGGGAAGAGTGTGT | 494470 |
rs375363042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46346763 | TCCCACCACACACCC[C/T]ACTTCCCCCATGCAA | 494470 |
rs375439529 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46427660 | GCCCCTTCGAGCCAC[A/G]GAGCTTCCCTCACTC | 494470 |
rs375460122 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414147 | TCATTTTGCAGGTCA[A/G]GAAGCTGAGGCTCAG | 494470 |
rs375631311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370330 | ATAATCATCTTGTCC[A/G]AGATAAGACTAATAA | 494470 |
rs375632479 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369459 | GGTGAGACAGGCCAG[C/T]TTCCGGGGAATGTTG | 494470 |
rs375648395 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341691 | CATGACTTGTCCCCC[C/G]CAGACTCTCTGTTGA | 494470 |
rs375653875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363902 | GACTCTGCTTCCTGA[C/T]CTTGCTTTTCTTTTT | 494470 |
rs375657785 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46339769 | GCAAACCAGCAAATA[C/G]TATTAGTTACTCAAA | 494470 |
rs375665429 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347500 | GGGAGCTGGGGGCTT[C/T]GTGTCCTCCCTCTGA | 494470 |
rs375684899 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381144 | GGAGTGAGACGGCAA[C/T]GCTGTTCTGAAGCGA | 494470 |
rs375687478 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433745 | AGTGAGCACTGTCCT[A/G]ATCTGACAGGGGCTC | 494470 |
rs375704358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46451666 | AAAGTTAAAAAGTTC[A/G]TGGTGGTATGAACTT | 494470 |
rs375707901 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384363 | TATGTGTGTGGGGGG[A/G]ATTCTTGATACTTCT | 494470 |
rs375719437 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415909 | TGCCAGGTGGGAGGA[A/G]AGGTAAGCAGGGAGG | 494470 |
rs375761374 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449435 | CTTTAAATTTTGTGC[C/T]CCCACCTTGGTGCTG | 494470 |
rs375769962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46354553 | AGACTTGAGAGCTGG[C/T]TAGAATATCTCCAGG | 494470 |
rs375795910 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401367 | ATCAAATGTCAGTCA[A/G]GGACATTTTTTCTTA | 494470 |
rs375801398 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441961 | CGAGGTCAGGGGATC[A/G]AGACCATCCTGGCTG | 494470 |
rs375818785 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335078 | TGTGTCTGTATGTGT[C/G]TGTGCATGTGTGCGA | 494470 |
rs375846060 | snp | A/G/T | 4.62217e-05 | 0.00480719 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433190 | GTCCTTGCCTTCCAG[A/G/T]TGCCCCCTTTCAAAG | 494470 |
rs375852087 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46347695 | CTATATGGCTATCTG[C/T]TAGGGAGTTGCCATG | 494470 |
rs375879385 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454409 | ATGACTCTATTCATA[C/T]TCTAAAGCCATGACA | 494470 |
rs375891196 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447828 | TGCCCCGGCTTCCAC[A/T]TGACCCAGCTCACCT | 494470 |
rs375904132 | in-del | -/AA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364417 | ACTTAAAAAAAAAAA[-/AA]GCTCTAAAGTCGTAG | 494470 |
rs375924331 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374775 | GCTGAACTGGGGGGG[-/G]CTAGAGACCCTACAC | 494470 |
rs375982028 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342072 | AAGAGGGGTTTTTTC[A/G]CAATTCAAAGCTCTC | 494470 |
rs375989344 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460904 | TTGCTACACTTGGCA[C/T]CCCCCCGCCCCCACC | 494470 |
rs375989399 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332382 | GAACCCTGGGTTCTG[A/C]CCTTGCCACTGGGAA | 494470 |
rs376014941 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461600 | CAGTGAGCTGGGAGC[A/G]TGCACCACTGCACTC | 494470 |
rs376018016 | snp | C/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460243 | GAAATCCCCTAAGCC[C/G]CCCGCCTGTAGGCGG | 494470 |
rs376072622 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423915 | CCTCCTTCTTCACTG[-/T]CCTCTCTCCATGTCC | 494470 |
rs376074305 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444659 | TTTTTTTTTTGTAGA[C/T]GTGATATCCCACTAT | 494470 |
rs376127055 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368800 | ACCTTGGGGAAATCA[C/T]TGAACATCTTTGAAC | 494470 |
rs376157220 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440064 | CGATCTCTTGACCTC[A/G]TGATATACCCGCCTC | 494470 |
rs376177684 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409901 | CTTACCAGCCATAGA[A/G]CACATTTTGTTTGTG | 494470 |
rs376178362 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344835 | TCTGTGCTGAGGAGA[C/G]AGACAGCGGAGGTAG | 494470 |
rs376184957 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46365412 | ATGAACAGATGTACC[A/T]ATGTCTTCACAAGAA | 494470 |
rs376214389 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386447 | AGCAGAGGCAGAGGG[-/G]TTAATATCAATTTTT | 494470 |
rs376261136 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430268 | CCTTCCCCCTCAATA[A/C]CTTGAAGGTAGCTGC | 494470 |
rs376312117 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361149 | TTAACCCCTTGACAC[C/T]ATACTGAGTCTTTTC | 494470 |
rs376315223 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46338876 | GGCTGACTGACTCCC[C/T]GGCTCACCCTGCTCC | 494470 |
rs376329134 | snp | A/G | 1.64895e-05 | 0.00287132 | intron-variant | RNF165 | GRCh38.p7 | 18:46447735 | CGCCTATTGAGTGCC[A/G]GTGGTGGTCTGAGGC | 494470 |
rs376329166 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46366231 | CGGGAGGTGGAGGTT[A/G]AAGTGAGCCAAGATC | 494470 |
rs376336573 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380549 | TGACCCAGGCGCTTG[C/T]GTTTCCTCAGGTCCT | 494470 |
rs376337421 | snp | A/C/G/T | 0.000306014 | 0.0123665 | intron-variant | RNF165 | GRCh38.p7 | 18:46456090 | TGTGAGGTAGGAGAC[A/C/G/T]GCCATTTTGATTCCC | 494470 |
rs376340012 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394555 | TCAGCATTCAGTTCA[C/T]CTCTGCTCACATAGC | 494470 |
rs376345891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389869 | TGGTAGTTGGGACTA[C/T]AGGCACGTGCCACCA | 494470 |
rs376346794 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410210 | GCCCCAAATGCTTAG[C/G]CAAGCTTGGCTTCTT | 494470 |
rs376369779 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428399 | GGTGACAGAGCGAGA[A/C]TCCATCTCAAAACAA | 494470 |
rs376390177 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353396 | TGCAATGTCTGGGCC[A/G]TGAGTCAGGCTGCTA | 494470 |
rs376401197 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374632 | ATGCCTTCTCTTTGT[C/G]CTCTAATTCTTTGGT | 494470 |
rs376428480 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441310 | GGCTGGTCTTACATG[C/T]CTAGGCCCAAATGAT | 494470 |
rs376432962 | snp | A/G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424672 | CTATTTGAGGCCCCT[A/G/T]CCAGCAAAGAGATTT | 494470 |
rs376439046 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460651 | ATGACAAACAACTAC[A/G]AATACAAAAAAAAAA | 494470 |
rs376449145 | in-del | -/AAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371494 | TGGTTAAGGGAGAAG[-/AAG]TTAAAGGAGATTGGA | 494470 |
rs376465588 | snp | A/C/G/T | 3.3215e-05 | 0.00407512 | intron-variant | RNF165 | GRCh38.p7 | 18:46435266 | GCCCCTGACACGAGG[A/C/G/T]CTCTCCATCCCTTCT | 494470 |
rs376468613 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375805 | AGTGTCCCTCCAATC[C/T]CACCTGGCAACCATG | 494470 |
rs376474631 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337893 | GGAGCGATAGGAGGG[A/G]CCAGTTGTCCTGTTA | 494470 |
rs376481869 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46420103 | TCTGATTTCAGGGGC[A/G]TGTGGAGGTCAACTC | 494470 |
rs376482139 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455839 | GAATCAGTCTCAAAA[A/G]CAAAACAAAACAAAC | 494470 |
rs376491918 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374500 | GGCCCCTCATGTCAG[C/T]GGAATCACACAGTGC | 494470 |
rs376507147 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388750 | AGAAGGTGGGCTCAG[A/G]ATAAATCAAAGCAAT | 494470 |
rs376510168 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414960 | GGGCTGAGCTAAGCC[A/G/T]CAGTCCTGCTGGGCC | 494470 |
rs376518353 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46369226 | TGTGGTTGTTTCCAG[A/T]TACCCAGGAGCCAAT | 494470 |
rs376518452 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383186 | AAAAAGGGAGATGCC[A/G]TCAGGCCCCTCCCAC | 494470 |
rs376563639 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46453878 | TGCACTCTGGGAGGC[A/G]GTGGCAGGAGGATAG | 494470 |
rs376594134 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418864 | TCATTCAGCACCTCC[A/G]TGGTTTTCCATTCTC | 494470 |
rs376628764 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46369949 | TCCACACACACACAC[A/G]CACACACGCACACAT | 494470 |
rs376644984 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457538 | GGCTCCCCAGGCCCA[A/G]GGCTCAACTTCATGG | 494470 |
rs376650506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46439932 | GCTTCCCAGGTTCAA[A/G]CGATTCTCCTGCCTC | 494470 |
rs376656864 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457493 | AGGCAGCAGAGCTCC[A/C]GCAGGTGAAGGGAGA | 494470 |
rs376672483 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439705 | ATAAACTTTTTTATT[A/T]AAAAAAACCCTTTTT | 494470 |
rs376717714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394237 | CCTGCCTTGATTTCA[C/T]CATGGCAGAGGAATC | 494470 |
rs376755615 | in-del | -/TAGA | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389205 | CTGTATTTATTCACC[-/TAGA]TCTGAAGGAACCAAG | 494470 |
rs376763965 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352126 | ATTGGCCCTGGACAG[C/G]CTTTGCAGGGCTCTG | 494470 |
rs376796461 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406510 | GTGGGAACTGGGAGA[A/G]TTTCTAGAGTGCCTC | 494470 |
rs376823068 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353539 | GCTCCCCGTCCGCTA[C/T]CCCACTGTCACTGGT | 494470 |
rs376842032 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437065 | CTTGTCTTTCTTAAT[A/C]ATTTAAACCAGTCTG | 494470 |
rs376904474 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397902 | CTGAGGTGTGAGGGG[-/G]TGTGTGCATGTGGTG | 494470 |
rs376945849 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433816 | GCAGGGTCGGGGACG[G/T]GTAACTGGTGGTCCA | 494470 |
rs376949896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383102 | TGGGCCAGGAGCAGG[C/T]CAAGGGCCTAGCCTA | 494470 |
rs377002782 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425745 | CCAGTGTGTCCTCTT[G/T]GTGTCCTGGCCCTAT | 494470 |
rs377093868 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395925 | TCTCATTTAGGCTCA[C/T]TGGGGCTCACTCAGA | 494470 |
rs377094202 | snp | A/C | 0.0337553 | 0.125452 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336590 | TCTTCTTGTAAAACT[A/C]TTAGAGAGTTTGCCA | 494470 |
rs377096526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375091 | CCCACAAACCTCACC[C/G]AGGCAGGCTTTATCT | 494470 |
rs377113893 | in-del | -/ACAC | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46406038 | TGTGTGTACACCCTT[-/ACAC]ACCCATGTACACACT | 494470 |
rs377148160 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460917 | CACCCCCCCGCCCCC[A/G]CCACAACCCTGCCTC | 494470 |
rs377151244 | in-del | -/CA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369936 | GAGCTGCTGGCCCTC[-/CA]CACACACACACGCAC | 494470 |
rs377168427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421212 | TAATTCTTCAAAGCT[A/G]GTCTTTCTACCTTGC | 494470 |
rs377180615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341959 | CAGGGGGAACGGGAG[A/G]GAGCCCGACCCAGTA | 494470 |
rs377187291 | multinucleotide-polymorphism | GTG/TTT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402519 | TCTACATGTGTGTGT[GTG/TTT]TTTTTCTTTTCGAGA | 494470 |
rs377189495 | snp | A/G | 6.59076e-05 | 0.00574016 | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447564 | CTGTTTCCCTGCAGG[A/G]ATCTCAGTGTGGATG | 494470 |
rs377198385 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385027 | CCCTCCCCCTCAAAG[A/G]TTTCCAGAGTGGTGT | 494470 |
rs377220866 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383745 | ATTTTTAATACAGAC[A/G]GGGTTTCACCGTGTT | 494470 |
rs377230326 | snp | A/G | 0.00013188 | 0.00811929 | intron-variant | RNF165 | GRCh38.p7 | 18:46447721 | GACGGACTCCCTTGC[A/G]CCTATTGAGTGCCAG | 494470 |
rs377310743 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46366609 | TTCACAGCCCAGTGG[C/T]CCTTAAAGATGAGAG | 494470 |
rs377311679 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347127 | GGCAGGACTGGAGCT[C/G]TTCCCCGAGGAGGAA | 494470 |
rs377315937 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | RNF165 | GRCh38.p7 | 18:46456084 | AGAAGATGTGAGGTA[A/G]GAGACCGCCATTTTG | 494470 |
rs377406778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455559 | AAGAACTTTATGGCC[A/G]GGCAAGGTGGCTCAC | 494470 |
rs377463375 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455476 | ACAGCAAAAATGATG[C/T]CCACTTGACCTCTTC | 494470 |
rs377485719 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46431654 | TTGTTAGCATGGTGC[C/T]GCACCCCTGCCCTCT | 494470 |
rs377490239 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397019 | TCAGTGCTGGCTGTG[C/T]GAGCGTGGCCCAGAT | 494470 |
rs377496896 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454837 | ATGTGAACATGAAAG[G/T]TGGGCTGATTTCGCT | 494470 |
rs377511340 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441479 | TCATTTTAACATCTG[C/G]AATCTGTAATAAAGC | 494470 |
rs377517228 | snp | C/T | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461640 | TGATAAGAACAAAAC[C/T]CAGTCCAAAAAAAAA | 494470 |
rs377547191 | snp | A/G | | | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387628 | ACTTGGAAGAAGTCC[A/G]GAGCTGGGCATACAG | 494470 |
rs377551880 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452836 | CCAATTTTGACTCTC[A/G]GTTCTACCCCTTATA | 494470 |
rs377556089 | snp | C/G | 0.000153988 | 0.00877328 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456684 | TTCACCAGGTCCCCC[C/G]ACGGCCATAGCCCTT | 494470 |
rs377558726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46450985 | GTGCCAGGTGTGGCC[A/G]GGAGGGAAGATGGAA | 494470 |
rs377591210 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364490 | GGCTCCCCAGAGAAC[C/G]CTTCGTGATGCCGAC | 494470 |
rs377622584 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357730 | TTGCCTCCGATGAGG[G/T]GTCTGTTGGCTTCTG | 494470 |
rs377625317 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440257 | GGTCTGAAGATATTA[A/C]AGCATTTTGAGAGAC | 494470 |
rs377626555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46374132 | GAAACTTCTCACACA[C/T]GAGAAGACTGGGGCC | 494470 |
rs377678542 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447392 | TTTCCTTCTCTGAGT[C/T]TCTGTTTCCTTCCCT | 494470 |
rs386387577 | in-del | -/TCATTCAT/TTCA | 0.0112469 | 0.0741414 | intron-variant | RNF165 | GRCh38.p7 | 18:46421373 | TTCGTGATCATTCAT[-/TCATTCAT/TTCA]TCATTCATTCATTCA | 494470 |
rs386802879 | in-del | GTG/TT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341336 | GGGGGTGGGACAGGC[GTG/TT]GGGGGTAGGGAGGAG | 494470 |
rs386802880 | multinucleotide-polymorphism | GTG/TTC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348898 | ACTCTCTCTCTCTCT[GTG/TTC]TGTGTGTGTGTGTGT | 494470 |
rs386802881 | multinucleotide-polymorphism | CG/TT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356868 | TACATTCAGGGAAAA[CG/TT]GAAACTCCAGAGGTT | 494470 |
rs386802882 | multinucleotide-polymorphism | CAG/TAC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368322 | GTTGGTTTAAGCACT[CAG/TAC]TCTTCCCCCATTGCC | 494470 |
rs386802883 | multinucleotide-polymorphism | ACC/CCT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379060 | CAGCCAGCATCTGTT[ACC/CCT]CAGAGTGTGTGGGTG | 494470 |
rs386802884 | multinucleotide-polymorphism | AAA/GAC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382874 | CACCCATCCCTCCTG[AAA/GAC]CGTCAGAGCCTCGGG | 494470 |
rs386802885 | multinucleotide-polymorphism | AGG/GGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392968 | AAGACACACCACCCT[AGG/GGA]AGGGAAATCGGCAAC | 494470 |
rs386802887 | in-del | AAG/TTTAAGTCCTTCC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412156 | CCCCTCCCCTCAAGG[AAG/TTTAAGTCCTTCC]AACCCCATTCTTCAA | 494470 |
rs386802888 | multinucleotide-polymorphism | ATCA/TCGG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440711 | TCTGTTATACTTTGT[ATCA/TCGG]ATCAAGATCCGAATA | 494470 |
rs386802889 | multinucleotide-polymorphism | AA/GC | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457620 | CAGCTACTGGTACCC[AA/GC]TGTGTTCCTGGGAGC | 494470 |
rs397808885 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403039 | ACACGAGACTCACTT[-/T]CCTTTCAGCTGCTCT | 494470 |
rs397814720 | in-del | -/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336393 | ATTTGTGTTGTTGGA[-/T]TTTTTTTTGTTGGGG | 494470 |
rs397828862 | in-del | -/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46392572 | GTGGACACGGCTCAG[-/G]AGGAGAGGCTCTGGG | 494470 |
rs397937405 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442176 | CAAAAAAAAAAAAAA[-/A]GAAAAAGAAAATAGC | 494470 |
rs397940090 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335067 | TGTGTGTGTGTGTGT[-/GT]CTGTATGTGTGTGTG | 494470 |
rs397945214 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402335 | TCTAAATCTGATTTT[-/T]CTCAATCCAGCTCCA | 494470 |
rs397949008 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386543 | ATGTCTTGACCCCCC[-/C]ATCAATCCATCCATC | 494470 |
rs398059210 | in-del | -/TGTG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348945 | GTGTGTGTGTGTGTG[-/TGTG]ATTTCTAGAAGCATA | 494470 |
rs398120428 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341207 | CTGAAGGCCTCTGGA[-/A]GAGTTTGGACTGGCT | 494470 |
rs398120429 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346446 | CCCTTGGGTTTAGGG[-/G]CCTCCTCCCAGGCAG | 494470 |
rs527245563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46417769 | AGCACTTTGAGAGGC[C/T]GAGGCAGGTGGATCA | 494470 |
rs527246610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338677 | TTTTTTCCCAGAGTG[C/G]AACCCAAATTCAGCC | 494470 |
rs527249775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344704 | TGCCTGTGACGTTTG[G/T]GACTTCTGACCAGAC | 494470 |
rs527265408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383979 | TCTGTCAGACAATGC[C/T]GTAACATGACTTTAA | 494470 |
rs527275405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378884 | AAGCACCCCGCTATG[C/G]TCCTGTCTAACCCAC | 494470 |
rs527347500 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46373768 | ATCTGAATCTTACAC[A/G/T]TGGGGAAGCTGAGTT | 494470 |
rs527347535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379799 | TACAAGGGATCTGTT[C/T]CAGGGCCCGTTCAAG | 494470 |
rs527349954 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363421 | TTTTTTGCAGTTCTC[C/T]GGCCATCAGGGGCAT | 494470 |
rs527359293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412288 | GTCAAGGGCTGGTTT[A/G]GGCTGGTTGCCCAGT | 494470 |
rs527384326 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451481 | GGCACATCCAGATAA[A/T]GGAATATTATTCTGC | 494470 |
rs527408895 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46452250 | GTTGGGAGTATAGGG[C/T]ATATGGGAAAACACT | 494470 |
rs527409450 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46374203 | AGGAAGCCTTTTTTT[C/T]CCACCAAAATAGTTT | 494470 |
rs527425846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412783 | CTGCTAACAGCCAAC[A/G]CGGAGTGACCACGTT | 494470 |
rs527435175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46406684 | TTGACCACAGAGGGA[C/T]CACATGTGGGCTCAC | 494470 |
rs527449265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400492 | CCCTCAGTCTGTAAC[A/G]GGCAGTTCGTAAGAC | 494470 |
rs527453078 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447997 | CCTGGCCCCCTTATA[G/T]GCTGGCTCCCCTGTG | 494470 |
rs527499149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400946 | GTGGAAGTGGTGGGA[A/G]ATGGGATACGGGGAA | 494470 |
rs527521497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349817 | TTGACACGCTGCACA[A/C]GATCCACCCAGCACC | 494470 |
rs527531444 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46396532 | TGCCTGGCACACAGT[-/A]GCTTTTCAGATAATA | 494470 |
rs527539213 | in-del | -/TG | 0.0244538 | 0.107838 | intron-variant | RNF165 | GRCh38.p7 | 18:46397666 | ATGCTGGGGCAGAAT[-/TG]TGTGTGTGTGTGTGT | 494470 |
rs527564702 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401387 | ATTTTTTCTTATGCA[A/G]TTTTTCAAATCTCTC | 494470 |
rs527581539 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46437865 | TGCCTAGGTGGAGGT[C/G]TCTAAGTACCTGGGA | 494470 |
rs527593464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357735 | TCCGATGAGGGGTCT[C/G]TTGGCTTCTGTGGCT | 494470 |
rs527610963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46395483 | CATATATCATCACAC[A/G]TAATCCTCATGGCAG | 494470 |
rs527656006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358187 | ATGAGTCATGCAGGC[C/T]TCATGAGCTGGACCC | 494470 |
rs527657826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351546 | GTCCTCCCTCAGCAG[C/G]CCAGCCCCTTCCTGC | 494470 |
rs527660870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46424627 | TCTACTTAGCCTCCC[C/T]GTGAATAAGATGAGA | 494470 |
rs527670893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396096 | TTAGAGACACAGAGA[C/G]CAAGAGAAATATGCA | 494470 |
rs527687119 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390761 | CTGGGCTGGGCTCAG[G/T]TTCCAGTTGCACCAC | 494470 |
rs527738086 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332311 | CAGCCAGAGTTTAGG[A/G]TGGGAAAGAGAGCTC | 494470 |
rs527767318 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399380 | CCCTCCATCATGTGT[C/T]CCCCGCCCCCCATTT | 494470 |
rs527768114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352041 | GCCCTGGTGGCCTGG[C/T]AGACCCTGTCACTCC | 494470 |
rs527769649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46425119 | CCTCCCTGTTCTGCC[C/T]CAACACTGGGGAAGA | 494470 |
rs527776349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345615 | CTTGACTCCTAGGGC[A/G]AAACAGGGCTTGGGC | 494470 |
rs527783888 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445196 | AGTGTTAGGCTTCGT[C/T]CTGGTAAGGAGCACT | 494470 |
rs527830530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425515 | TGCCTCTCAGCCCTG[G/T]AGTCTTGAGGATGAA | 494470 |
rs527837927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46413672 | TGGGAGATGAGAAAG[A/G]GCAGGAGAGCAGCGC | 494470 |
rs527839283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419559 | TGAGGGGCCTTTTGG[A/G]TCTAGCTGGAGTGAC | 494470 |
rs527851007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46346841 | GGAGTGCAAAGCAGG[C/G]CCTTGGGCAGTCAGG | 494470 |
rs527854351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340661 | CTTGACCTGGAAGGG[A/T]GATCTTAGGCCACTG | 494470 |
rs527856637 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460061 | GCCAGGACCCCCTTC[A/G]GCACCCAGTTGCCCT | 494470 |
rs527865480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385469 | GTCCAGGTTGAAACC[C/T]AGGAGCTTTTCTAGC | 494470 |
rs527893890 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460662 | CTACGAATACAAAAA[A/C]AAAATTTAAATAAAA | 494470 |
rs527923246 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430717 | GCCCTGTTGAATTTC[A/G]TTTCACCTCGTACAT | 494470 |
rs527925564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381148 | TGAGACGGCAACGCT[A/G]TTCTGAAGCGAGGAG | 494470 |
rs527933587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374904 | AGCCCCTTGAGTCTG[A/G]CATTTGGTCTTGAGG | 494470 |
rs527933637 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395466 | TGAGAACTACTTCTG[C/T]GCATATATCATCACA | 494470 |
rs527946119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375318 | AGCACTTTGGGAGGC[C/T]GAAGTGGGTGGGTCA | 494470 |
rs527950371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370115 | CACTTTCCAGGCTCA[G/T]CTACCAATCTGGGTC | 494470 |
rs527978505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46454246 | ATCATGAATAATGAT[A/G]GCAAAAAAATAGTAG | 494470 |
rs528003428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455072 | ATGAAAAACAGTACA[A/C]GGGAAGTCAACAAGT | 494470 |
rs528016861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46446485 | AGACCAGCCTGGACA[A/G]CATGGTGAAACCCCA | 494470 |
rs528061584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354333 | GGACACACCTCCCAG[A/C]ATTAGAGTGATTAAC | 494470 |
rs528066343 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398692 | AGCACACGGTCTAGC[A/C/T]CCACAGGCTCTGTAA | 494470 |
rs528100460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46387098 | GCCAGGCCAGGGAAG[C/G]AGTGATTTTTGGTGG | 494470 |
rs528126503 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443694 | CTGTGACAGAGACTG[C/T]ACGGCTTTTGAAGCC | 494470 |
rs528164406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428063 | CAGTGTGGACGGCTG[C/T]GGGAGGGCTTGGAGG | 494470 |
rs528172194 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432711 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCGAG | 494470 |
rs528174627 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46354961 | TTTTAATATATACAT[A/G]TTTTTTGAGACTGAG | 494470 |
rs528183398 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46348382 | TGCCTATTGGCCAGC[A/G]TTGCTGGTGGTTGAT | 494470 |
rs528185977 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430805 | CCTGTTGTTGCATGG[A/G]TCCAACATCTTATTT | 494470 |
rs528235245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422112 | GTACATAAGGAACCC[A/G]GAAAGAATGGCCTTT | 494470 |
rs528237710 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46415796 | TGGATGGTTGTAGGG[C/T]TGAATTTGGGAAAAG | 494470 |
rs528242358 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RNF165 | GRCh38.p7 | 18:46343164 | CCAGCCATGTGGGGA[A/G]GAGGTAGTGAGTGGA | 494470 |
rs528290035 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456886 | GAGCTGGCGGTGCCC[A/G]GCGCAAGGGCGGGAA | 494470 |
rs528323294 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384529 | CTCATGGATACACAC[C/T]CCATGATACACACAC | 494470 |
rs528326044 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343618 | CAAGCCTGAGTACTC[C/T]GCGACTTCACTGCCT | 494470 |
rs528335233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383363 | ATGATGCACCTGGTT[C/T]GAAAGGGGATGTAAG | 494470 |
rs528343839 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46377554 | TGAAGGGCAGCAGAG[A/C]AGTATTTTGTTAGAT | 494470 |
rs528345496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372351 | TCGCTCTTCCTGCCT[C/T]GGTCCCACCATTGCT | 494470 |
rs528349726 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369180 | GTGTATGCTCTGTGG[A/G]CAAGAAAGCTTGTTG | 494470 |
rs528350709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416320 | GGGTGACACAGAAAC[C/G]TGGCTCATGATAAGG | 494470 |
rs528355939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378377 | CACCAGGGACAGAAT[C/T]CAGGCTCCTGGTCTT | 494470 |
rs528365912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410529 | AAGGCTCACCCTTAA[A/C]AAGCTGAACAAGCCT | 494470 |
rs528418917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410967 | GCTGGCTGTGCATGG[A/G]TGGCAGATGCCCAAG | 494470 |
rs528503425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405426 | CAGTGGGAACAGTGA[A/G]GTGCTACAGCAGTGG | 494470 |
rs528511179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367912 | CTTTGAACCACTTTC[C/T]TCCATGATTCTGATG | 494470 |
rs528515654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395065 | GGTACCCCCTCTCCT[C/T]GCTGGAACTCAAGCT | 494470 |
rs528516069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442915 | TATCCTTGGTAATAT[C/T]CCTTGGTTCAAAGTC | 494470 |
rs528552973 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349946 | CACATACAGTTATAA[C/G]AGCAGCACGCATTCA | 494470 |
rs528570211 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408600 | CATGGGAACTGTGGG[G/T]CATCCTAAAGGGGGC | 494470 |
rs528572568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355932 | TGATGATGATGATGC[A/G]GATGGGCCTCTGTAG | 494470 |
rs528576216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436139 | TTGGATCAGAACCCT[G/T]GAAAACTTAAAAAGA | 494470 |
rs528608207 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428550 | CTGTGTACGGAGTTG[A/G]CTTTTTTCCTATAGA | 494470 |
rs528618024 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346826 | TTTAGGGGTCTTAGG[A/G]GAGTGCAAAGCAGGC | 494470 |
rs528626015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399943 | CATCTTCACATGAAA[A/C]CCTGCAAGGTGATCA | 494470 |
rs528632281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46356492 | AGCCCTGAGCCTGAG[A/G]GCAGAGAGAGAGGGA | 494470 |
rs528651506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429223 | AGGCAGAAATTCTTT[C/G]GATTTTCATTTCTTT | 494470 |
rs528687767 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46394284 | GAGAGCCCTGGCCTG[G/T]GAATCTCTAGTTGCG | 494470 |
rs528688068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388908 | AAAGAAAAAAAAAGA[C/T]ACGAAACATTGAAGC | 494470 |
rs528722936 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335776 | CGCCTCTCCCCAGAA[C/T]CTAAAAGGCAAGCTT | 494470 |
rs528736023 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381105 | TGTAAAATAGGGACA[A/G]GGCTATCTCTCTGCC | 494470 |
rs528741624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356891 | CCAGAGGTTAAAAGG[C/T]TTCCTCTGGAACCAG | 494470 |
rs528754828 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389458 | TTCATTTTGTAGGCA[A/C]GGAAGTATATGTAGG | 494470 |
rs528755636 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410227 | AAGCTTGGCTTCTTG[A/C]ACCTCAGCTCTGCTG | 494470 |
rs528760120 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455582 | TGGCTCACATCTATA[A/G]TCCCAGCACTTTGGG | 494470 |
rs528766001 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46423030 | AACCCTGCTGTCCAT[A/C]ATCAGAGTCCAGTTT | 494470 |
rs528771584 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46449994 | TCAGTAAAATGGGGA[C/G]AGTAATAGCACCCAC | 494470 |
rs528783509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423706 | CCATGACTACTCTAG[A/T]GCCCTCAGACATGCC | 494470 |
rs528800589 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377152 | CTTGGATTATTTAAA[C/T]TGCAAATATATTCAT | 494470 |
rs528812933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344476 | ACCACCCACCTCCTA[C/G]AACACCTGCTTCTAC | 494470 |
rs528841131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416985 | GGGAGGGTAAGCATA[A/C]AAGGAGGGGAGAAAT | 494470 |
rs528995011 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46378461 | GGGCAGCGTGAGAAG[C/T]GATGGGCTTTTGCAC | 494470 |
rs529006911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343830 | TAGGTGGGAAGGGAG[C/T]AGTAATTGCCCCTGC | 494470 |
rs529010910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411096 | CAGGCACCCCTTAAT[C/G]ACAGCTCTTTTTGTT | 494470 |
rs529068017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383709 | ACAGGCAGCCACCAC[C/T]GCGCCCGGCTAATTT | 494470 |
rs529070728 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457777 | GTGATGGCTGCTTGG[A/T]CTTGGCCACAGTGCT | 494470 |
rs529072018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411531 | ATACATTTGGTAAGT[C/T]CCTACTATGTGCCAG | 494470 |
rs529105162 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458259 | CAAAGGGAGCAGAGA[A/G]ATAAGAGGACAGAAG | 494470 |
rs529132815 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365373 | CTGTCTCTAGAAGTC[A/T]CTGGAAGAGCCTTTT | 494470 |
rs529144133 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384389 | CTTCTTCCTTCTTAT[G/T]GCAGAGATGCTCTTC | 494470 |
rs529144489 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405507 | GTGGTGGGTGGGAGT[G/T]GCTGTTGGCGATGTG | 494470 |
rs529148115 | in-del | -/GA | 0.0520825 | 0.152737 | intron-variant | RNF165 | GRCh38.p7 | 18:46440273 | GCATTTTGAGAGACT[-/GA]GAGAGAGAGAGAGAG | 494470 |
rs529194926 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383716 | GCCACCACCGCGCCC[A/G]GCTAATTTTTTGTAT | 494470 |
rs529205129 | snp | A/G/T | 0.00319098 | 0.0398384 | intron-variant | RNF165 | GRCh38.p7 | 18:46442985 | CCAGTTAGCACTTAC[A/G/T]GGGTATATCTCTTTC | 494470 |
rs529226936 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452232 | TAGTAATAGAAACTC[G/T]GTGTTGGGAGTATAG | 494470 |
rs529267245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399973 | AGGGCAAGTGGCTCA[C/G]GTTTAGTGAGGTGCA | 494470 |
rs529281993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436276 | TGTGGGTATATATGT[A/G]TGTGTGTGTGTGTGC | 494470 |
rs529305857 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46443733 | TTACTATTTATGATC[A/C]TTTACAGAAGAAGTT | 494470 |
rs529307116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362854 | CTTAGAGGTGTGTTC[A/G]CTCAGTCCTTCCACT | 494470 |
rs529341428 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436823 | TTAATTGCAATTTGG[A/T]TTGAATTCTGTCCCT | 494470 |
rs529345272 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376817 | CTGGGACTACAGGCA[C/T]GCACCACCATGCCTG | 494470 |
rs529353486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430002 | CCTCCCAGAGTCCCC[A/G]CCCTCCTGCTCCCCT | 494470 |
rs529358333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394936 | AACATGAACTTTCAC[A/G]TATGTGGGGCTTTGC | 494470 |
rs529387300 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425382 | AAGGCCATCATCCCT[-/G]GGGTAGCCCCGGGTG | 494470 |
rs529388777 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46363520 | CCACAAATCAGGATG[C/T]ACCCTGTGGTCTCTG | 494470 |
rs529398510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46350951 | CAGTGTGCTGAGTCC[C/T]TCTGCCCCTGGCGTG | 494470 |
rs529405242 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454985 | TGAGACTTTACATAA[C/T]GGTAAACTACATAAT | 494470 |
rs529437390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423845 | TTTACTAGCTAATAA[C/G]TTCATCCTTACCTGT | 494470 |
rs529488986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389485 | TAGGAGTGAGAGGGA[C/T]CCCTGGCTCAAGGCC | 494470 |
rs529508944 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361385 | ATGTCTGTGTATATA[C/T]CTGTGTCGATCTGCT | 494470 |
rs529533069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344913 | TCATCTTGGACACCA[C/G]GGTGGTGGGCTGTGG | 494470 |
rs529544021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417820 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 494470 |
rs529555798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384069 | CAGACAGAGGCAGTC[A/G]GGGTGAAACTGTGGG | 494470 |
rs529581754 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406165 | CAGACACTCACCCCA[C/T]GTGCACCCCCAATAC | 494470 |
rs529607380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379821 | CCGTTCAAGAGATGC[C/T]TAGAGGCTGTCCTGA | 494470 |
rs529613507 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444795 | GATTATTTTTATTGT[C/T]GTGTCTTAAAGTCAC | 494470 |
rs529675432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439314 | CATGTGGGATCCAGG[C/T]TCAGTAGCAGCAGGC | 494470 |
rs529688105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402558 | CTCTCTGTCACCCAC[A/G]CTGGAGTGCGTGACT | 494470 |
rs529713616 | in-del | -/GGGAGGAA | 1.69661e-05 | 0.00291252 | intron-variant | RNF165 | GRCh38.p7 | 18:46435417 | CTTCAGGGCCCCTGG[-/GGGAGGAA]GGGAGGAAGGGAGGA | 494470 |
rs529719663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396826 | CGGGCGTGGTGGGGC[C/G]CTGTCTCTGGAAACT | 494470 |
rs529729696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365164 | GGTGGGAAAGTAGAG[G/T]TGCTCTTTGGAACTT | 494470 |
rs529735820 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46432140 | ATCTTTCTGAAATGC[C/T]GGGTCTACTTCTTGG | 494470 |
rs529737771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46439870 | GGAGTCTCGCTCTGT[C/T]GCCAGGCTGGAATGA | 494470 |
rs529751370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432750 | ATCACGAGGTCAAGA[A/G]ATCGAGACCACGGTG | 494470 |
rs529773210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441969 | GGGGATCGAGACCAT[C/T]CTGGCTGACACGGTG | 494470 |
rs529810506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353531 | GCTAGTTTGCTCCCC[A/G]TCCGCTACCCCACTG | 494470 |
rs529812272 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46433065 | TCTAACAGTGATGAC[G/T]CTGCTGTGTCCTAAT | 494470 |
rs529916946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386918 | TGGGCAGTGTTTGGG[G/T]GGCGGAGGAGCAGCT | 494470 |
rs529917746 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461546 | GCTACTCGGGAGGCT[A/G]AGGCAGGAGAATGGC | 494470 |
rs529933587 | snp | C/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46427314 | CTTCCCAGTGCGTCT[C/G]CTGGAGGGCACAGGT | 494470 |
rs529966362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46348232 | GGGCCAAGGGGCTGG[C/G]GGGGGTGAGGGGAGG | 494470 |
rs529972253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381957 | TTGGCTTAAGCACCC[A/G]CAGGGCCTCCCTTCT | 494470 |
rs529988728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420329 | GAAAGGGGCATCAGA[C/T]GAAACAATTCTCCCA | 494470 |
rs529993098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421076 | GTCTGAAATTGCTTC[C/T]TCTTCTGTTAGTTGA | 494470 |
rs530009461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342384 | TGCTAGGCTCTTTGT[C/T]CACAGTGGAAAAGGA | 494470 |
rs530027817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382506 | TAAAAATCAATACAT[A/T]CATCTAGTGTCAGTC | 494470 |
rs530032155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341952 | ATGGGAGCAGGGGGA[A/T]CGGGAGGGAGCCCGA | 494470 |
rs530047306 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46335112 | TGCGCGCGCGCCTCG[A/G]AGAGTCAGACCTGCG | 494470 |
rs530067312 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387614 | GAAAAACATTCCCCA[C/T]TTGGAAGAAGTCCAG | 494470 |
rs530074340 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46415432 | TCGGGAGGCTGAGGC[A/C]GAAGAATGGCGTGGA | 494470 |
rs530091322 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46364127 | TAATTTTTGTGTTTT[C/T]AATAGAACTGGGATT | 494470 |
rs530096284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371563 | CAAACAAGATCTTTA[C/T]GAAGCTTGGATGATA | 494470 |
rs530127281 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456802 | GTCGAGGGAGAGGAG[A/G]GGGTTGGGGAGGACC | 494470 |
rs530138717 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46415664 | CTTGGAATCAAACAG[C/G]CTCCAGATTCCCAAC | 494470 |
rs530151599 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46350524 | GGCAAGCATGGTCAG[A/G]AGCGCCCCCAACCCC | 494470 |
rs530158017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46372202 | AGGCACTGAAGGGTC[C/T]TCCCTGGGGCCCTCC | 494470 |
rs530165771 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371373 | CTGATAAGGAGGAAG[A/C]ACAGCCCAGGCCAGC | 494470 |
rs530203541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448217 | GCCCTGGCTTCCACA[A/T]GACCCAGCTCCTCTG | 494470 |
rs530225892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404309 | CTTCCTCTCTTAAGC[C/T]AATGAATTATTCCCA | 494470 |
rs530234546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46366665 | TTCTGAGAAGTTTTA[C/T]ACTTGGGAGCAAGGT | 494470 |
rs530239880 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46398765 | CCAGATATCCCAAAT[A/T]CTCGGGCTCCTCCCT | 494470 |
rs530246849 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403804 | AATTGCTTGAACCTG[C/G/T]AAGGTGGAGGTTGCA | 494470 |
rs530251929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410271 | TGGCTTTTCTGCTTT[C/T]CAGCTATCCCTAATA | 494470 |
rs530264617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441520 | ATTCCTCATATGAGT[A/C]ATTTGTATGTTCTCT | 494470 |
rs530297835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393328 | GGTGGAGAGCAGTCT[C/T]GAGGTGTGGGGTGCA | 494470 |
rs530324602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46361442 | AATATTTAACTGAGT[A/G]TGGCAGGCACATGAT | 494470 |
rs530372057 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46442191 | AGAAAAAGAAAATAG[A/C]CTTTGATCCCATTAC | 494470 |
rs530414992 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355588 | TGCCTATCTGAGGAC[C/T]GCCTATTTTTCCAGA | 494470 |
rs530424918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428132 | AGGCCAAGGGGAGGC[C/T]GGGCGCAGTGGCTCA | 494470 |
rs530425239 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46425474 | CCTCTTTCAGCCCCC[-/T]TTTTCCTTGGAGGAC | 494470 |
rs530426900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435120 | TTCATCTGGGAAGCT[C/T]CCTTGGAGTTTGTCA | 494470 |
rs530432517 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46362276 | TCCTTCAGGGGTTTT[G/T]CAAGAAAGCTGGTTT | 494470 |
rs530434936 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46398062 | GTACCTGTGGTGTGT[C/G]TGTGTGGTCATGCTG | 494470 |
rs530454506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46440585 | TTTCACTATGTATCT[C/T]GAGAGATAATGATTC | 494470 |
rs530455021 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46432838 | TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 494470 |
rs530457184 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445566 | AGCTGCCTCTTCTCT[C/T]CAAATCATGGTACCA | 494470 |
rs530483357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366357 | GATATAGGCCTAAGC[C/T]CTCTGGCAGATTAGG | 494470 |
rs530488396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46392603 | GAGCCCTTGTCCGGG[A/G]TGATGGGTCAGTTCA | 494470 |
rs530488911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46359926 | ACAGATTTTAGTCAC[A/G]GGATCACACTTAGCT | 494470 |
rs530498147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360517 | GGCCCAGGTTGCTTG[C/T]GTCCTTTTCTGAAAG | 494470 |
rs530514079 | snp | C/T | 1.87271e-05 | 0.00305994 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433262 | TGGGCCCCCCGCAGC[C/T]GCAGCAGCTCGCTCC | 494470 |
rs530529721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46392014 | CACATATGCACACAA[A/C]ACACACACCTTACAC | 494470 |
rs530551624 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362745 | CACTTAAGTACACAT[A/G]CTCAAAGTGCTTGAC | 494470 |
rs530557594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46354095 | TCACCAGGCTCCCCA[A/G]TTCTCTCCTCTTCCT | 494470 |
rs530586493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46427963 | AGCAGCCAGGGAGAT[A/G]GGAGCACAAACTCTC | 494470 |
rs530630015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342435 | CCAAGCTTCGAGGGG[G/T]TCTAGACCCCCAACC | 494470 |
rs530694004 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46421649 | CTTCTGTAATTGTAT[C/T]CTGTCTCTAACCAAA | 494470 |
rs530697421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421152 | TGCTGGACCTGCAAC[C/T]GGGCCCCTATACTCA | 494470 |
rs530765500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46387506 | AAACTTGTCCCAACT[C/T]TAGTGCCAAATTCCC | 494470 |
rs530773524 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369427 | CAGGGAGGAAGCTGA[C/T]TGACTCGGGAAGAAG | 494470 |
rs530776282 | snp | A/C/G | 0.00159649 | 0.0282165 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336376 | ACCTTCTCCCTCACC[A/C/G]CCCCCAACAAAAAAA | 494470 |
rs530783380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376773 | CCTCCCAGGTTCAAG[A/C]GATTCTCTTGCCTCA | 494470 |
rs530784692 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456833 | CACCTCTCCAGAATG[G/T]CGACTGTCCCCATCC | 494470 |
rs530798126 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46347979 | TAAGGGCAGTAGCAG[A/T]TGCTCACGTAGCACT | 494470 |
rs530821037 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457617 | CCTCAGCTACTGGTA[C/T]CCAATGTGTTCCTGG | 494470 |
rs530822948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448770 | CTTTGGGCTCCTGAC[A/G]TTGCAAGCTGCATGG | 494470 |
rs530849044 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46344627 | ACCTCGGCATCCACA[-/G]TGGGCTCATTCCCTG | 494470 |
rs530882923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46335235 | GCCAGGCCTTTGCCC[C/G]GGGCAGCGGTTGACA | 494470 |
rs530901167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367281 | GTATAGGGTAGACCA[C/G]ATGACCTCTGAGGTT | 494470 |
rs530907520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46449747 | GCTTTCCACCATGGC[C/T]GTAGGTTTCCTGAGG | 494470 |
rs530952337 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46404373 | AGAAGGATGACAGGA[A/C]GACATGAGCAGGTAT | 494470 |
rs530958189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410858 | AAGTCCTCCTTAAAC[C/T]CTACACATGCCTTTG | 494470 |
rs530974423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362331 | TTTACTGTCTCAGGG[C/G]CTGCTAGGTGAGTGT | 494470 |
rs530987688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441692 | AGGAGATCCAGACCA[C/T]CCTGGCTATCATGGT | 494470 |
rs530995029 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386921 | GCAGTGTTTGGGTGG[C/T]GGAGGAGCAGCTACT | 494470 |
rs531023251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372735 | AAAAAGCTTCTGTTA[C/T]CTGTGGCCAGGCTGT | 494470 |
rs531041049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435214 | CCCTCAGGCTGCCCC[A/G]GTTTCTCAGAGCTCT | 494470 |
rs531049454 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46342704 | CCCAAGATGAGGGCA[A/C/T]GTTTTGCATTTTTTC | 494470 |
rs531065125 | in-del | -/TG | 0.116838 | 0.211584 | intron-variant | RNF165 | GRCh38.p7 | 18:46440713 | GTTATACTTTGTATC[-/TG]AATCAAGATCCGAAT | 494470 |
rs531086495 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429156 | CCTGACTTATGGAAA[C/T]CCTTGTGGGAATTAA | 494470 |
rs531087691 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460325 | GTTTCATCTCCTGCG[C/T]GCGTAGAGCAAATGC | 494470 |
rs531125361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399282 | TGCTCCGGCAGCTTG[G/T]GCAAAAGGACAAAGC | 494470 |
rs531184862 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422213 | TAGTTAGCTTATGTA[A/G]TGTACCCCAGACTCT | 494470 |
rs531209109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394218 | GGCCTGAAGGGACAA[A/G]GTGCCTGCCTTGATT | 494470 |
rs531215496 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459939 | CGTCCTAGCAGCTGC[A/G]GCAGCTGTGCCGCCG | 494470 |
rs531227877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435834 | ATGCCAGCAAGGCAG[A/T]GCTGGGTGGGGTGGC | 494470 |
rs531237181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429171 | TCCTTGTGGGAATTA[A/C]AGTTCTAGATAATTC | 494470 |
rs531247175 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46420776 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 494470 |
rs531247767 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402118 | TTGAGGTATAGCTGA[C/T]GCTAAATAAACTGCA | 494470 |
rs531267414 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379450 | CCCACCTTCCCTCCC[C/G]GAGTCCATTTTACAG | 494470 |
rs531293789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412830 | ACACCTGTGGGCCAG[A/G]GGCCACCATATCTTG | 494470 |
rs531296420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369395 | CTGGGGTGGCAGGGG[A/G]GTGGGAGAGGACAGG | 494470 |
rs531297418 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46374771 | CTCTGGCTGAACTGG[C/G]GGGGCTAGAGACCCT | 494470 |
rs531300623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46453351 | CCAGGAGCAGCACCT[G/T]TGTCCCGGACCAGGG | 494470 |
rs531301184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340061 | CAGGGTGTGACTTTG[C/G]TTCCCTCAATCCTAC | 494470 |
rs531308074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46364108 | AGGGACCACCATGTC[C/T]GGCTAATTTTTGTGT | 494470 |
rs531308096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46369948 | CTCCACACACACACA[C/T]GCACACACGCACACA | 494470 |
rs531341916 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46400983 | GATGCTGGAGGCAGA[A/G]ATGACCTCCCGCAAA | 494470 |
rs531358457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46406831 | GCAGGTGGCTGGGAG[C/T]GGATGGTGAGGGCAG | 494470 |
rs531366371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46374312 | TGCCACAGTTTAGTG[A/G]TATTAGCAGCATTCA | 494470 |
rs531367838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364619 | TTATAGCTGGATTTT[A/G]TTTTCTTCAGATGTG | 494470 |
rs531470201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46407485 | CTAATCCTATCACCC[A/G]ACAGGACAGTGTTAG | 494470 |
rs531478586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46396765 | CCTTCATGGTGCTGG[C/T]CATGTGCACCACGCC | 494470 |
rs531501367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439206 | CCCAGGTAACAGGGA[C/T]CAGACTCCCCTGAAG | 494470 |
rs531577756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385277 | ATTGCACAGAGATGA[A/G]AGCTCTCCTGGGAGA | 494470 |
rs531581615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352749 | AACTGGGTCACGTAA[A/C]CACCCTTAGCTGTAA | 494470 |
rs531584157 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354555 | ACTTGAGAGCTGGTT[A/G]GAATATCTCCAGGGT | 494470 |
rs531595240 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46347521 | CTCCCTCTGAAGCGG[G/T]CAACCCTCTTGGGGC | 494470 |
rs531615062 | snp | G/T | | | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447579 | GATCTCAGTGTGGAT[G/T]CTGGCTTGAGTCCTG | 494470 |
rs531631793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46431410 | TTATACAGTGGCCAG[C/T]TGGGGACCCAGTGAT | 494470 |
rs531632809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358304 | CCTCCCTGTCTGAGA[A/G]AATCCAGGTACATGG | 494470 |
rs531645936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425205 | CTGAGGAGGCGGGAA[C/T]TCGGGCTTCCGGGGA | 494470 |
rs531709106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425586 | CAGGACCTCCAGCTC[A/G]GGAGTCAGTCTTCCC | 494470 |
rs531730420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381816 | AATCTGGGTGACAGA[A/G]CGAGACCCTGTCTCA | 494470 |
rs531732038 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430068 | GCTTGGGAAGCTTTC[C/T]ACCTCTGTCAGGTGC | 494470 |
rs531757745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420125 | GGTCAACTCCCATGG[C/T]GCCTCCACTCACCGG | 494470 |
rs531781379 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461378 | GGCAGGGCATGGTGG[C/T]TCACGCCTGTAATCC | 494470 |
rs531787743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381190 | TTTGTCAGCCAGGCA[A/T]TGGGATAAGGCCAGG | 494470 |
rs531820882 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460812 | TGATCTAGTGAAAAA[C/T]TCCAATATAGTGACT | 494470 |
rs531828027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46346887 | TTTCAGCTTAATTGT[A/G]TAAGCAGTTACTGAG | 494470 |
rs531841449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375893 | GGCTGGGGAAATAGC[A/G]AAACAGGTTCAGTCC | 494470 |
rs531850301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375342 | TGGGTCACTTGAGCC[C/T]AGGAGTTCAACACCA | 494470 |
rs531871155 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394957 | GGGGCTTTGCTCCGA[A/C]TGTGCTATAATGTCC | 494470 |
rs531881615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46414695 | TCACAGACACATGCA[C/T]ATACACACAGCCTTG | 494470 |
rs531904866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341817 | TGTACCAATCAGTAT[C/T]CCGAAATCTGAGTTG | 494470 |
rs531916287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403220 | GAGTCTGGCACCTGG[A/C]AAAATGTCCATCTCT | 494470 |
rs531942648 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444203 | TTTATTACTATTTTT[C/T]AGGAATTAGATTATT | 494470 |
rs531950642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455122 | TGCTTTACGATAGTG[C/T]CTATCTTAAGTGAAC | 494470 |
rs531955229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46453394 | TACCGAGGATGCACG[C/T]CTCACCTGCTGTCAC | 494470 |
rs531969127 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332269 | AGACTTGCCTCTGGC[C/T]GTCTTCATCCCTGAG | 494470 |
rs531983272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415303 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATGGA | 494470 |
rs532031668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371010 | GGTTTAACTGACTCA[C/T]AGTTCCACATGGCTA | 494470 |
rs532044196 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416415 | CAGATTGCATCCAGC[C/G]CTGTCCTGAGGGTGC | 494470 |
rs532046012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365946 | CCTGAGAAGGAAAAG[A/T]CACATCTTGTGAACA | 494470 |
rs532062307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438683 | ACTGTCCTTCTGCAG[A/G]CCTCAGATGCACCTG | 494470 |
rs532076301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447982 | CTGACTCCCCTGTGC[C/T]CTGGCCCCCTTATAT | 494470 |
rs532082583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407556 | GGTCTTGTTTAGTGT[G/T]TTTTTGTTTTGTTTT | 494470 |
rs532083485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365093 | TTCCTGCTTTATCAC[A/C]ATTCCCTGCGTCTCT | 494470 |
rs532101195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370418 | CAATTCTTTACACAG[G/T]TCTAGTTCTCATGAG | 494470 |
rs532131467 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418542 | TGTGAATTTGAACTA[A/G]CCATATTTCACATTT | 494470 |
rs532161294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46401991 | GAAAACCTCTCCTCA[A/C]TGCTCTCACAAGTGG | 494470 |
rs532212685 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353991 | TTTTACGGGGACTTG[A/G]CCAAGATCATTCAGC | 494470 |
rs532231711 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403467 | GTATCCATTACCTAG[A/G]CTACATTTATTATTT | 494470 |
rs532233732 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395851 | AAGGAGTTGAGTAGA[C/G]AACCACAATCACTTA | 494470 |
rs532247904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439255 | TTTTTCCCTCAGAAA[A/G]ATCTCAGATGACATT | 494470 |
rs532280417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46391938 | CGTACACCATGCACA[C/T]AACACACACGCACAT | 494470 |
rs532294874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432693 | CCAGGCGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 494470 |
rs532335610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46396787 | CACCACGCCTATGTC[A/G]GGACAGCTCAGGGCA | 494470 |
rs532348418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391558 | CTCCTGAGGCCTCTA[C/T]GGGGCAGGCCCTGCT | 494470 |
rs532357508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381264 | ACTTGCTGTCCCCTC[C/T]GTGGTCTCTGAGGAG | 494470 |
rs532407356 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | RNF165 | GRCh38.p7 | 18:46368060 | ACCATGGATTAGAAT[C/G]TTGGGTTGGGCTTGA | 494470 |
rs532416229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352816 | GCCCAGCTGAATTTA[C/G]GGGTTGCATTACCGT | 494470 |
rs532426108 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429421 | ATTTCTTTCCTGAAA[A/G]ACATAAATTACCAAG | 494470 |
rs532450463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419765 | GGACAGGCCTCTGCT[C/G]CTTGTTAGGCATATG | 494470 |
rs532470934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347104 | AATCAGGAGGGCCTC[C/T]CGGAGGAGGCAGGAC | 494470 |
rs532485754 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46376631 | CTCAGTTCAGTTTAT[C/T]TGAAGTTAGTTCAGC | 494470 |
rs532511602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420156 | CTGCTGTCTGAAATC[C/G]CACCATTAGAACTTC | 494470 |
rs532516862 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46379909 | CCTGGCCTCCTTGGC[A/C]CACTGGGACGTTGCT | 494470 |
rs532519940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341410 | GCAGGATTGAGTCTA[C/T]GTGGAAGGGGCTGAG | 494470 |
rs532523720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403327 | CAGCCCAAGGCTAAG[C/T]ACAGAAGCCTGTGCT | 494470 |
rs532548304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409441 | CGTTAGTTTAGCCGA[C/G]GACAGGGCAGGAGGA | 494470 |
rs532559895 | snp | C/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46341896 | GTGGGCAAGTACCAG[C/G]AGCTTTGCCTCCACT | 494470 |
rs532570961 | snp | C/T | 2.93768e-05 | 0.00383243 | intron-variant | RNF165 | GRCh38.p7 | 18:46456095 | GGTAGGAGACCGCCA[C/T]TTTGATTCCCTCTCC | 494470 |
rs532590701 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425948 | GCCTCCTCATAGATG[G/T]TTCCTTCCCTCTGTG | 494470 |
rs532627991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455417 | ATCGATTCATTAGGA[A/T]CCCAATTTCTTTCTA | 494470 |
rs532656082 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390338 | CTTCCTGCCCGCTGG[A/G]TGTTGGTGCAGGAAT | 494470 |
rs532660527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371074 | AGGAGCAAAGGCACG[A/T]CTTACATGGTGGCAG | 494470 |
rs532682251 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46408893 | CATCACACAGGACTT[C/T]CTGCAAGTTGTGGCT | 494470 |
rs532690926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415371 | TAAAAATACAAAAAA[A/T]TTTTTATATTTATAG | 494470 |
rs532694065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398098 | TGAGGGTGTGTGCGC[A/T]TGTGGTGTGTGTGTG | 494470 |
rs532739411 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46334835 | TTTGTTCATTAGTAC[C/T]GATGGCTGGCTAGCT | 494470 |
rs532744996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46383586 | TTGAGACGGAGTCTC[A/G]CTCTGTCACCCAGAT | 494470 |
rs532752756 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365071 | TAAGTCTCTGGTTCT[C/T]CTGATATTCCTGCTT | 494470 |
rs532802183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383753 | TACAGACGGGGTTTC[A/T]CCGTGTTGGCCAGGA | 494470 |
rs532804820 | snp | A/T | 0.116838 | 0.211584 | intron-variant | RNF165 | GRCh38.p7 | 18:46440715 | TTATACTTTGTATCA[A/T]TCAAGATCCGAATAA | 494470 |
rs532812704 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363612 | CAGCCCCATCACGGG[A/C]CCAGGGGAGGGGACA | 494470 |
rs532836576 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340766 | AGATACCTGGCACGC[A/G]GCAGGTGCCTAGGAT | 494470 |
rs532866277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416978 | CTTGTATGGGAGGGT[A/G]AGCATACAAGGAGGG | 494470 |
rs532877461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379147 | GCCCCCAGGCCCCCC[A/G]ACCCTCTGATTTTAT | 494470 |
rs532902600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373290 | GAGTGTAACACTGCA[C/T]ATTTCCTCAGAGCTT | 494470 |
rs532915635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350434 | CAGCTGGGATGGAAG[C/T]GTGAGGTCCATGTCA | 494470 |
rs532922494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422749 | GGCCCTGGAAGTACT[A/C]CAGGTCACACCCCCG | 494470 |
rs532929079 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46343911 | AGGGCTCCTTGACCC[C/G]GAGCTCAAGGCTGGC | 494470 |
rs532970158 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46344363 | CTTCCCCCTTCTCCC[C/T]CCGCCCCCAGCTAGC | 494470 |
rs532975440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406034 | TGTGTGTGTGTACAC[C/T]CTTACACACCCATGT | 494470 |
rs532994190 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383668 | CATGCCATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 494470 |
rs533010402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368487 | CTTCCCTGTGGGTCT[C/G]CGTGTGCCCAGGTCA | 494470 |
rs533072234 | snp | C/T | 3.31016e-05 | 0.00406813 | intron-variant | RNF165 | GRCh38.p7 | 18:46450246 | TGCATGCTGGGCTCA[C/T]GGAGAAACCTTGAAT | 494470 |
rs533108175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338403 | GAGGGTCTGTGCCCT[C/T]TGCAGGCTGTGAGCC | 494470 |
rs533144779 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343697 | CACTGTGCTTTCCTC[A/G]TGATGAGAAGAGCTT | 494470 |
rs533155130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400886 | GGTCTCGTGCAGACA[C/T]TTACCACTTACCCCC | 494470 |
rs533161132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395021 | TCTTTCGGACCAAGA[A/T]TCTGCCAGAAACTCA | 494470 |
rs533173070 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46451286 | TTTTAAAGCCACAGA[A/G]TCACAGGTTTTATCC | 494470 |
rs533178336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373740 | GATCTCTGCAGGTGT[G/T]GGGGGAATTGTTATC | 494470 |
rs533220244 | in-del | -/GGT | 0.0225178 | 0.103691 | intron-variant | RNF165 | GRCh38.p7 | 18:46375275 | TACTTGTCCTGGCCG[-/GGT]GGCACAGTGGCTCAC | 494470 |
rs533266854 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425164 | GTAGCTGAGCACAGC[A/G]GGAAACCTGACACCT | 494470 |
rs533311393 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376173 | TGGCTTGTTAACAGC[C/T]TTGGCAGCAAAACGG | 494470 |
rs533318778 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46425000 | TCCAGCCCTGTGGCC[A/G]GCTGTCCTGTCTTCT | 494470 |
rs533318811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46418575 | TAACCATACAGGACA[A/G]GACAGAACTAGATTG | 494470 |
rs533329970 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46363927 | CTTTTTCTTTTCTTT[A/T]TTTTTCTTTTTTCTT | 494470 |
rs533331994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357014 | TGTCATTTGGGCTAC[C/T]TGAGGAGCTTGCAAA | 494470 |
rs533372127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46346016 | GCTGGTGGACGTTTT[G/T]TGTTTTGACTCAATG | 494470 |
rs533397891 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426113 | GTTAGGATTTGAACA[C/T]ATGACTTTGGGGTGA | 494470 |
rs533408388 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459493 | GTGAGACAGTGGGCC[C/T]TCGTCCCCTCCCCCC | 494470 |
rs533411958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46374397 | AATGAAAACTCTGTC[C/T]CCATTAAACACGAAC | 494470 |
rs533426692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418947 | AGTTAATGTGTTGCC[C/T]TCTTTTGGGCATTTG | 494470 |
rs533429175 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390162 | CCAACCCCTGTGGGA[C/T]GAGCCAGGCTGGCAA | 494470 |
rs533442292 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421265 | TTCTCCCTCTGACAC[C/T]ATCAAATTCCATGCA | 494470 |
rs533458003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430657 | TCCCCATTTCTCTGT[C/G]TTCTCATTCCGGTTT | 494470 |
rs533508811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351426 | AAGATCAAGAGCTGG[A/C]AAATAATAGACCTGG | 494470 |
rs533521392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46450221 | CTGAGTGGGTTACAG[A/G]TGGAGAAGTTGCATG | 494470 |
rs533532763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372975 | TCACTCAGGGAGGGG[A/G]ACCCTCCTGCTGGGA | 494470 |
rs533541341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384463 | CTTAAAATATATCTG[A/G]TGGCGACTTTCTTTC | 494470 |
rs533561586 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46399690 | AGACTATAGCAATGG[G/T]AGGCATCTCATTTCA | 494470 |
rs533579571 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358462 | AAAATGAGGCCACGG[C/T]AATTTTGAAGCCTGA | 494470 |
rs533591824 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377454 | TGTGGAGCATCCCGA[G/T]AACCCACAGGAAGGT | 494470 |
rs533592412 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46373398 | GGAGGGACTGGGCAA[A/G]AGTCACCCAGCAAGT | 494470 |
rs533593024 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371964 | ATACTGACTCCTAAC[A/G]TACTAGACTTGGTCC | 494470 |
rs533681211 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379141 | CTGGGAGCCCCCAGG[C/G]CCCCCAACCCTCTGA | 494470 |
rs533682474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400097 | TACCTCTTACCCATC[G/T]CTTGGCTTCATTTCT | 494470 |
rs533696499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394477 | CTGGGGATGTGCAGT[C/T]CTGTGGGTCACGAGT | 494470 |
rs533700090 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396529 | AGGTGCCTGGCACAC[A/G]GTAGCTTTTCAGATA | 494470 |
rs533720317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46413547 | AAGTTGTTTACTTTC[C/T]TTGAGTCTCAGTTTA | 494470 |
rs533728299 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46411838 | GCCTGGGGCTGAGCC[A/G]TGTATGTGTGATCTT | 494470 |
rs533750010 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458387 | TTTGTGCCCCACCCC[C/G]CACTGTTCCCTCATT | 494470 |
rs533774121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442639 | TACTCTTATTGGATA[C/G]AGTATTCTATAAATG | 494470 |
rs533782938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429694 | TGTTTTGTTTTCCAT[A/G]GCATTTTTACAAATT | 494470 |
rs533787787 | snp | A/G | 1.95383e-05 | 0.0031255 | intron-variant | RNF165 | GRCh38.p7 | 18:46450850 | GAATGGGGCAGGGGG[A/G]TTGTCTAATTGACTC | 494470 |
rs533823692 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407375 | TGGGGATTGGCCCTT[C/T]CTTGCTTGCTCACAT | 494470 |
rs533838316 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332482 | CTTCTCCCATTCTTT[A/C]TTCTTCAAGTCTCAA | 494470 |
rs533844128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423286 | TAGGGAGGAGGCCTG[A/G]GGCTATTGGCCAAGG | 494470 |
rs533859720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46344597 | TTCCCCAGGGGACCT[C/T]GGCCTCCACAGGGGA | 494470 |
rs533862792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46443098 | ATCTCTGTCTGTTAA[C/T]TGGGGTGTCTAGACC | 494470 |
rs533875442 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46383831 | GCTGGGATCACAGGC[A/G]TGAGCCACCGCGCCC | 494470 |
rs533897295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436419 | TCTTTATGCTGTTCT[C/T]GCAACTTTTAGGTCA | 494470 |
rs533906141 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440861 | TATTGGTTTATAGGG[-/T]TTTTTTTTTTCCTTG | 494470 |
rs534007916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379988 | AGAGAAGAGATGAGG[C/T]TCCAAAGGCAGAGGC | 494470 |
rs534011353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356778 | CTTCCACCGTGTCAC[A/C]TCTTCTCCCCGCAGC | 494470 |
rs534012327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412592 | CTGCCTGGTTGGTCA[A/G]TTTCTTCTCACTTGT | 494470 |
rs534015253 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46418702 | TTTGATGATTGAATA[A/C]GTCAAATTCTGAATC | 494470 |
rs534059202 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46350630 | AAGCTCTCTGCTGGC[A/G]TTCCTCCTGCCACGC | 494470 |
rs534061772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340163 | AAATTCCCGGCTTAA[C/T]ATTGTATGAATGTGA | 494470 |
rs534070064 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442651 | ATAGAGTATTCTATA[A/T]ATGTCTCTTAGATCA | 494470 |
rs534072668 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46413005 | AAACAACACAGCCCC[A/C]TCTCCGAGAAGCTGG | 494470 |
rs534075680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357117 | TTTCAAGTATGAACT[C/T]GTTGTTTTATCATTA | 494470 |
rs534091622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46430129 | TTGTGTTAGTACCTT[C/T]TTGAGAAGGAGTGTT | 494470 |
rs534149902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46345048 | GGCAGCTCCTGCCTC[A/G]CTCCTTCTGGCCAAG | 494470 |
rs534157164 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373477 | TGGAAGGACTGGCCT[G/T]CCTGGGTGCATCCTG | 494470 |
rs534243312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46438773 | TTAGTTCATTTCCCA[A/G]GTGACAGGCTCATCA | 494470 |
rs534243550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46357957 | TGGCTTGTAGCCGCA[C/T]CACTCCAGTCTCCGC | 494470 |
rs534249712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364825 | CCACTGGATATCTCT[A/G]GGCTCCTGCTCTCTG | 494470 |
rs534257454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46374062 | CAGGGCCAGGCTGGG[A/G]CATTCTTGTCATCCC | 494470 |
rs534268128 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459547 | ATATTAGGGACTGGG[A/G]AGGGGACCACCAGAG | 494470 |
rs534292348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420660 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCAT | 494470 |
rs534293356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46339674 | CACAGTTCTTCTTTC[C/T]GAACAAGAGAACTTC | 494470 |
rs534319456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386346 | TGGCTTACCAGGTAC[A/C]ATCAAATATATAGTC | 494470 |
rs534352282 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46405873 | AGGCAGGGAAGCCAT[A/C]CCCTGTATCAACCTT | 494470 |
rs534361900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407173 | TCTATTTGAGGCACT[G/T]GGATCAGTGGCCAGG | 494470 |
rs534373793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374423 | CGAACTCCCCATTCT[C/T]CTCCCGCCAGCCCCT | 494470 |
rs534403848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421206 | TGTCTGTAATTCTTC[A/G]AAGCTAGTCTTTCTA | 494470 |
rs534403990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415208 | ACGTGAGCCCCAAGG[C/G]AGTGACCTTACCAGT | 494470 |
rs534416858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415529 | AGGATCTGTCTCAAA[A/G]AAAATAAAAAAAATA | 494470 |
rs534423747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46401351 | TTCTCCCATCACCAA[C/T]ATCAAATGTCAGTCA | 494470 |
rs534434121 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349968 | ACGCATTCATTTACA[C/T]GTACGTATCTGTATT | 494470 |
rs534467774 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424373 | GGGAGGGGGATTTGG[C/G]CAGGGAATGGAATGC | 494470 |
rs534480512 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46335379 | TTTTCCCCTCTTCTC[C/T]CCACCTCCACTCCAC | 494470 |
rs534485519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409982 | GCAGTAGACAGGATT[G/T]GAGCATTTGTGATTT | 494470 |
rs534510770 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46448399 | CTGGACTGGAAGCTG[A/G]TTCTGCTGAGGGGAG | 494470 |
rs534525149 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46404395 | AGCAGGTATTAAGCA[-/C]CTTTTTCGTGTGGGA | 494470 |
rs534530378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395887 | GCTCGCCATTCTATG[G/T]GAAAGCCCAGTAGTT | 494470 |
rs534559627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371771 | ACCAAGGACCAAAGA[G/T]ACTAGTGACTGGGTC | 494470 |
rs534565664 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46441129 | TAGCTGGGACTACAG[C/G]TGTGCACCACTGTGC | 494470 |
rs534570509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46366834 | TGCCATAAGTCAGAC[A/G]CTGTGCTAGGTACTA | 494470 |
rs534595688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46449084 | TGTTCTAAGCAGTTC[A/G]TGTAAATTATCCCAT | 494470 |
rs534628788 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46441801 | GCTGAGGCAGGAGAA[G/T]GGCGTGAACCGGGAG | 494470 |
rs534651721 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461882 | GGGCAGTCATTTGGC[A/G]AGTGAGCTGAAATCC | 494470 |
rs534681316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376195 | GCAAAACGGTCACCT[A/G]CCCTTCCTGTTCACT | 494470 |
rs534690665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455728 | GTAATCCCAGCTACT[C/T]GGAGGCTGAGGTGGG | 494470 |
rs534728945 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429768 | TTTTTTAAAATACTC[-/T]TTTTTTTTTCCTTTC | 494470 |
rs534788242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355298 | TCACACCCAAGAACT[C/G]AGGATGAACATATCT | 494470 |
rs534841195 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365498 | TTTTGTGATCTTGAA[-/T]TTTTTTTTTGTTGTT | 494470 |
rs534861264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343409 | AATGGGCACATCTTA[C/T]GGCTTGTGCCTTACT | 494470 |
rs534862124 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449402 | CGTTAATCTTTATTA[C/T]TGAGGCTTTTGGTGG | 494470 |
rs534911458 | snp | A/C | | | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387644 | GAGCTGGGCATACAG[A/C]CCCGTGGAGGGTGCA | 494470 |
rs534916537 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant | RNF165 | GRCh38.p7 | 18:46334697 | GTGTGTGTGTGTGTG[-/T]GTGTGTGTGTGTGTG | 494470 |
rs534936650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367410 | GGAAACAATTTGTCC[A/G]TAGTAGTGACCTGAA | 494470 |
rs534958745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398400 | TGTGTCAAGTGCCCC[A/G]AGCCTTCATCAGGGC | 494470 |
rs534962060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404403 | TTAAGCACCTTTTTC[A/G]TGTGGGACATGCAAT | 494470 |
rs534971150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398873 | ATCTCAAATGAGACA[C/T]GTCGACAACATCTAG | 494470 |
rs535019895 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452739 | GAGCAGGACTGTCCT[C/T]ATCATTGTCAAGCCA | 494470 |
rs535021496 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369277 | CAGCATCCATCATCA[A/G]GATGGGCTGGCTGAG | 494470 |
rs535037787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46393434 | CAGACGCCAGAAGGG[C/T]GCGCTGTTTCCTCTT | 494470 |
rs535057161 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46415543 | AAAAAATAAAAAAAA[A/T]AAAAAAATAAATAAA | 494470 |
rs535083880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382689 | ACAGCCCCGTGAAGT[C/T]AGGCAGGTGTGATTT | 494470 |
rs535112598 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364168 | GGCCAGGCTGGTCTC[A/G]AACTCCTGATTTCAA | 494470 |
rs535165132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46415907 | AGTGCCAGGTGGGAG[A/G]AGAGGTAAGCAGGGA | 494470 |
rs535175890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349955 | TTATAACAGCAGCAC[A/G]CATTCATTTACACGT | 494470 |
rs535188579 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46335556 | ACGTCTGCTTAAATC[C/T]CTGCTGGCTCAGGCC | 494470 |
rs535221817 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46410612 | CTTGGTTATGACCTG[G/T]AGCCATGCCCAGAAA | 494470 |
rs535246372 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357627 | ATCATCTCTTTCTGT[G/T]GGGCACTGGGCTCGA | 494470 |
rs535256193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404471 | AACTCAGTGAAGTAC[G/T]GACCAGGCGTGGTGG | 494470 |
rs535277503 | in-del | -/GGCGG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341043 | GTGTGTTGATGGCGG[-/GGCGG]AGGCACATGTGCAGG | 494470 |
rs535297828 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46441892 | AAAAGAGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 494470 |
rs535311980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399020 | TTCTGTGAGTTACCA[C/T]GACACCCGGGAGTCT | 494470 |
rs535322762 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336475 | TCAAGGGCTGAGGGG[C/T]GAGTTGGTCTGTGGG | 494470 |
rs535325822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337142 | TAAAAGAATAAGGCC[A/C]CTACTTTGAGGGCCC | 494470 |
rs535326621 | in-del | -/TCAT | 0.281553 | 0.248001 | intron-variant | RNF165 | GRCh38.p7 | 18:46421369 | CCTGTTCGTGATCAT[-/TCAT]TCATTCATTCATTCA | 494470 |
rs535377684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428269 | CAAAAATTAGCTGGG[C/T]GTGGTGGCAGGCGCC | 494470 |
rs535409734 | in-del | -/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337553 | ATGGTGGGCCCAGCC[-/T]TTTTTTTTTGTATCG | 494470 |
rs535474459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383023 | CTCATGCACCCCCTA[A/G]CCTGCTGGGCCAGCT | 494470 |
rs535483364 | in-del | -/GTGTGAGTGTGC | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46385388 | TGCCTGTGCATGTGT[-/GTGTGAGTGTGC]GTGTGCATATGTGTG | 494470 |
rs535487172 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46456426 | CTCCCTCCATAGCCG[C/G]GCAGTTCCCCAGGAG | 494470 |
rs535489925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428818 | GTTTCTTTTTACTTT[C/T]AAAAGGTGACTACTA | 494470 |
rs535494684 | in-del | -/GTGTGTGTGT | 0.00785585 | 0.0621789 | intron-variant | RNF165 | GRCh38.p7 | 18:46335046 | AAGATGCTTGGGCGC[-/GTGTGTGTGT]GTGTGTGTGTGTCTG | 494470 |
rs535515937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448502 | TAAGATCAGGCAGAG[C/T]AGACCTTGCACTTCA | 494470 |
rs535524716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46343220 | TCTGCCCACCAGCAG[C/T]CCCTTCCATCGAGAG | 494470 |
rs535531822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350067 | CTCACCACTCACATA[C/T]ATGTACACACATGCA | 494470 |
rs535548813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429384 | CCCTCAACCGCAGTG[C/T]GCTTTTAACTCTTCT | 494470 |
rs535551017 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46344553 | CCCAGCGTGGAGACA[A/C/G]TGGCCTTCCTTAAGC | 494470 |
rs535559913 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46372441 | TATAGTGCCCAGGGC[A/G]GCCTGAAAATAGTGA | 494470 |
rs535563572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336642 | TTTCCATTGTAGTAG[C/T]GTAGGATGTAGGCCA | 494470 |
rs535567262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350508 | GAGGGGTGTCAAGAG[G/T]GGCAAGCATGGTCAG | 494470 |
rs535584206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404005 | TGTGTGATTAACAAT[A/T]CCCTCTTTCCCCCCT | 494470 |
rs535603558 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46344490 | AGAACACCTGCTTCT[A/T]CTCCTCAAATTCCCT | 494470 |
rs535627120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337954 | CCCCTACCTTTGGCC[A/G]CCTGTGTACTCAGTA | 494470 |
rs535653652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378685 | GGGAGTGGCATGAAC[C/T]CATAAATACACATTC | 494470 |
rs535658509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405093 | ACCCCTTTTATCTAG[G/T]ACCTGATTCATAAAA | 494470 |
rs535671663 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382888 | GGACCGTCAGAGCCT[C/T]GGGACTGCCAAACAC | 494470 |
rs535674015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367594 | CTGTCTCAGTGAAGA[A/G]GTGGACTGTAACTTG | 494470 |
rs535731864 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458949 | CTGGAGATCTCACCA[A/G]TGGGGAAAGTACATC | 494470 |
rs535744096 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446527 | ACTACAAAAGTTATC[C/T]GGGCGTGGTGTGGCA | 494470 |
rs535757954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46450957 | TAACTTCCCAGGGTC[A/G]TGTTACTTTTCTGTG | 494470 |
rs535758487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368587 | TTCTGAGGCAATTCA[A/G]TTCTGTTCTTTTCAG | 494470 |
rs535761018 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363882 | TTCAGTGGGTCTGAG[A/G]CCCTGACTCTGCTTC | 494470 |
rs535806738 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421475 | CCTAGGCTCTGCCTT[C/T]ATGGAGTGTACAGTC | 494470 |
rs535854884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388512 | GCAGCAAGACACACA[C/G]AACTCTGTTTTTGTG | 494470 |
rs535876997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431563 | GCTTAGGTAACAGTG[C/T]TTTTGGCACCAAGTA | 494470 |
rs535904193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358445 | GGGACTGGGAATCAC[A/G]TAAAATGAGGCCACG | 494470 |
rs535945336 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457893 | CAGTCCCTCAGAGAT[A/G]GCCCTGGCTCTGAGG | 494470 |
rs535952357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352876 | ACTCAGTTGGTCATC[A/T]CTGCCTCAGTTGGTG | 494470 |
rs535956419 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436513 | GAATTATCTTAAAGA[C/T]TGATGTGCCGTTGTG | 494470 |
rs535976113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425872 | ATGCACTAATCACAG[A/T]TCTGGAGGCTGGGCA | 494470 |
rs535995616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347134 | CTGGAGCTGTTCCCC[A/G]AGGAGGAAGAGCTGT | 494470 |
rs536018153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417198 | TTGCCACCCTAGTCC[A/G]AGAAACCATCATCTC | 494470 |
rs536083560 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460965 | TTTCCTCCTCCCTCG[A/C]TCCTCCCACAACCTC | 494470 |
rs536099125 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46446671 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 494470 |
rs536113922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375637 | AGCTCCTTGAATGAA[C/T]TGCGCCGTTATATGA | 494470 |
rs536141648 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46411932 | GCACCATGGAGCCCA[C/G]CTCCCTGGAGTGGGG | 494470 |
rs536147487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341478 | ACCATGAAGACAAAC[A/G]GGGAACATGGGAGGA | 494470 |
rs536151557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436559 | TTGTCAGGCTTAGTC[C/T]AGGGTTGCTTTGGGA | 494470 |
rs536229297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376004 | GATAATAGCTCAGAG[A/G]GTGGCCTGAGGGTGA | 494470 |
rs536246626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390653 | AGGACAGTTAGTCCA[G/T]CAGCCCCCATTCAGC | 494470 |
rs536248001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396477 | TGAACTCCATGACAG[C/T]ATGGGCCTTATTCAT | 494470 |
rs536271941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46403372 | AGCTCTCCCTGCCCC[C/T]GGAGAGAGCCCTCCC | 494470 |
rs536275100 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335116 | CGCGCGCCTCGGAGA[A/G]TCAGACCTGCGCTGC | 494470 |
rs536295294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371133 | ATTTATAAAACCATC[A/G]GATCTCATGAGTCTT | 494470 |
rs536304488 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346216 | GGGGAGGCCAGGAGA[C/T]GGAGAGAACCCCACC | 494470 |
rs536340906 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46425319 | GTCAGCTGGCAGGCC[C/T]GCAACAGGGACCCTG | 494470 |
rs536348201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372044 | GAGATGTCCTGAAGA[A/T]GAGGCCCACAGTTCC | 494470 |
rs536398725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340972 | GTGATTTTGGCCAAG[C/G]CCAGTGGCTCTGCTG | 494470 |
rs536426805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414166 | GCTGAGGCTCAGAGA[A/G]GCCAGGCTGCTTGCC | 494470 |
rs536427147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46380850 | GGTCCCCATCACACT[C/T]GCCCCAGCCTTCCTT | 494470 |
rs536440032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46392214 | TTGCCTCCAACTCAT[C/T]CCCATCCTGTTCCCC | 494470 |
rs536450530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386488 | GGCCTGGTAAGGACT[A/G]GGGCCAGAACTAGAA | 494470 |
rs536452517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46392793 | GGCCTGTGTGAGGAA[C/T]ACGCATGCAGTGGCA | 494470 |
rs536526609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46454669 | ATCCGGGCCTTGCCC[C/T]ACGGTCATTCTCTAG | 494470 |
rs536538341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427572 | AAAACCCAGAGCCTA[C/T]TTGGCCCCACTTGCC | 494470 |
rs536539305 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332520 | AGAAGTCACTTTCCC[A/G]GAGTCAGCCTCAACT | 494470 |
rs536552058 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46383841 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCACCATG | 494470 |
rs536607295 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46352940 | CTGGGTGGAGCTCCT[C/G]CTTTGTCTACCCTTC | 494470 |
rs536616486 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46447182 | TGGTAAAAATATAGC[A/C]TCAGCTCCCTCCTCC | 494470 |
rs536616583 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333908 | CGCAGCGATTGGCCG[C/T]CGGCCCCCTTCCAGC | 494470 |
rs536671504 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46396969 | CTTTGCAAGCCCAAT[C/T]GCTCTGGAAGGGTGG | 494470 |
rs536712283 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458160 | TCTTCTGAGAACCTT[A/G]TGGGGTGTCGGGATG | 494470 |
rs536740401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426694 | TGTCTTACCATTGAT[A/G]TGTTTATTTAATGTG | 494470 |
rs536762911 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432931 | GCCTGGGCGACAGAG[A/C]GAGACTCCGTCTCAA | 494470 |
rs536767930 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344267 | GACACCTGTCTCAAG[A/G]AAGGGCAGGAAGCGT | 494470 |
rs536786578 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46347871 | GATTTGATCATGGAT[G/T]TGTTCAGCTCATCTA | 494470 |
rs536808450 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461753 | AGCTGAGAATTTGAG[C/T]TTGCTCAGAGTTGAC | 494470 |
rs536863188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46334396 | GCAGGCACCGGGGCG[G/T]GGGCGGGCGCCGCGG | 494470 |
rs536864117 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453906 | TAGATTGAGCCCAGG[A/G]GTTTGAGACCAGCCT | 494470 |
rs536880288 | snp | G/T | 0.00262502 | 0.0361333 | intron-variant | RNF165 | GRCh38.p7 | 18:46433549 | ACCCGGATGGGGTCG[G/T]GTGAGGGGGCAGGGC | 494470 |
rs536884058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353659 | TGACGGGGCCCTGGA[A/G]ACGCATGCTGCTGGT | 494470 |
rs536893274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455677 | CCCTGTCTCTACAAA[A/T]ATACAAAAATTAGCC | 494470 |
rs536903610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371239 | ACGTGAGGATTATTA[C/T]AATTCAAGACGAGAT | 494470 |
rs536922097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46348052 | AAAATACTGAACCTC[A/G]TGGGAAACAGACAGA | 494470 |
rs536932904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447778 | GTGCCCTGGCTGCTA[C/T]ATGGCCTGGCTCCCC | 494470 |
rs536942976 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434369 | ATTCATGTTAACACC[A/G]ATAATATATTTTTAT | 494470 |
rs536944300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354439 | TGCAGGATTGGAGAA[C/T]ACATGATCAGGGCCC | 494470 |
rs536948019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420718 | GGTGTGGTGGTGTGT[G/T]CCTGTAATCCCAGTT | 494470 |
rs536955197 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46408238 | CTGATTCAGGGGAAG[A/G]TCCGCAGAAGGTGTC | 494470 |
rs537001500 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409846 | CCAATAATGCATGTT[C/T]TCCTATTGATGGACA | 494470 |
rs537020050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448272 | TCCCTTGTGCCCTGG[A/C]CTTCTTGTGCCCTGG | 494470 |
rs537044889 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46385849 | GTTTCAGCTGAGCCT[A/G]GTGAGGTATCTGGGG | 494470 |
rs537064347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398340 | GAAGCAGGTAGGGAG[A/G]GGGAGCGACACCAGG | 494470 |
rs537075418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46360299 | GAGGCGGGGTATCAT[A/G]TGTTTGTGGCCAGCC | 494470 |
rs537095052 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457598 | AAACCAGGGAGGGCT[C/T]GGCCCTCAGCTACTG | 494470 |
rs537101576 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46433572 | GGCAGGGCCAGGGCG[A/T]GGGCAGGGCCAGGAC | 494470 |
rs537122106 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414125 | AGAGATGGCAATATC[A/G]TTATGCTCATTTTGC | 494470 |
rs537146131 | snp | G/T | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389385 | TGGATAAAGTCCCAC[G/T]GGACAGACTCACACT | 494470 |
rs537150628 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46414849 | TTGGGAGCCATTTCA[C/G]CCCTAGGAAACATTT | 494470 |
rs537159319 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411406 | CTGAATAGGACGTAT[A/G]CTCTGAGTCAGCTGA | 494470 |
rs537172295 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384877 | AATAAAACAAAATTA[A/T]ATATAAAATAGAATA | 494470 |
rs537172721 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461070 | CCAGAATTGGAGCCC[C/T]CCAGACATTACAAGA | 494470 |
rs537186576 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46392811 | GCATGCAGTGGCACC[A/G]CTCCTGCACCCAGGA | 494470 |
rs537207258 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46348605 | TGGTATCTGGGAGAC[C/T]TCCTGGAAGACACAG | 494470 |
rs537225053 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333292 | TTCTGGGCAGTGTGT[C/G]TCTGTGTAGACTGTT | 494470 |
rs537227143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375665 | TGAGCTGCCACATCC[G/T]GGGTTTATGCATCCT | 494470 |
rs537246834 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46387342 | CTCCATGATTCCAGT[A/G]CAGAGCTTGGGGAAC | 494470 |
rs537341266 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383050 | AGCTTGGCCAGATCA[C/T]GGCATCCATCTCATG | 494470 |
rs537362516 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426770 | AAAATATTATTTAGC[C/T]CATAATGGGTCTTTC | 494470 |
rs537379864 | snp | C/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459500 | AGTGGGCCCTCGTCC[C/G]CTCCCCCCTCCCAAT | 494470 |
rs537381376 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46403382 | GCCCCCGGAGAGAGC[C/T]CTCCCTGCCCCCCGT | 494470 |
rs537393782 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46403927 | TTGCACTCTGGTATT[C/G]TTCATCTACCAACTT | 494470 |
rs537406173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400128 | CCTGGCGGGTGTCCT[G/T]CTCCTCCAGCTCCAG | 494470 |
rs537418167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451674 | AAAGTTCATGGTGGT[A/G]TGAACTTGTAGTCCT | 494470 |
rs537475027 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368975 | TCTATGTGCCAGGCA[C/G]TATGGTACTTACTTA | 494470 |
rs537475545 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375333 | CGAAGTGGGTGGGTC[A/G]CTTGAGCCCAGGAGT | 494470 |
rs537488825 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400618 | GCAGTCAGAACTCCC[C/T]CATTCTCACAGGTCT | 494470 |
rs537569726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46434423 | TTTAGTGAGAAGAAT[A/G]ACTTTTTAAAACATA | 494470 |
rs537607756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357855 | TCCGCGGGGCCAGCC[A/G]TCTCCTCTGAAGGCA | 494470 |
rs537616543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355170 | GTTGGCCAGGTTGGT[C/G]TGGAACTCCTGACCT | 494470 |
rs537639034 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46393380 | AGGCAGACACCTTCC[C/T]GCTGACCACCAGCTC | 494470 |
rs537639830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389871 | GTAGTTGGGACTATA[C/G]GCACGTGCCACCATA | 494470 |
rs537652354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384208 | TACTGGGCCAACCCC[C/T]CCCTCCATCTAGAAT | 494470 |
rs537652436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390345 | CCCGCTGGGTGTTGG[C/T]GCAGGAATGGGGCAT | 494470 |
rs537672097 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46428166 | CTGTAATCCCAGCAC[G/T]TTGGGAGGCCGAGGC | 494470 |
rs537676210 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF165 | GRCh38.p7 | 18:46385130 | TTCTCAGAGATCCTG[C/T]TTACCACACTGGTGC | 494470 |
rs537712028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384617 | CTCAGATTCCCTGGA[A/G]AAGCAGCAAAGCCTC | 494470 |
rs537724936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351629 | CACATCAGGGGCTTT[A/C]TAGGCATCATCTCTT | 494470 |
rs537727381 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406016 | CACTCGCATACATAC[A/C]CCTGTGTGTGTGTAC | 494470 |
rs537767576 | in-del | -/CT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416942 | GGGTGGGAAAGTAGA[-/CT]CTGCCTTTAATGGGA | 494470 |
rs537776957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343312 | AAACTATTCTGAGAC[C/G]TAGATTCTGGTCCAC | 494470 |
rs537803499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406214 | CACAAACTTCCACTC[C/T]CAATAGCTCTTGTTG | 494470 |
rs537895836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380614 | AGTTGCTGAGCTGGT[C/T]GCTGGGAGGCTGGAG | 494470 |
rs537897444 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351499 | GGTTTGCTAAGGCTG[C/T]CTCCTTGCACCTGCA | 494470 |
rs537905275 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357845 | AATCAAGCTGTCCGC[A/G]GGGCCAGCCGTCTCC | 494470 |
rs537925919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407289 | CTACCCAGTCTTTTG[C/G]GGTAAGATTCTTCTT | 494470 |
rs537936038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363729 | AGCTGGCCTTGTAGT[C/T]CCAGCTGACTATAAG | 494470 |
rs537942198 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440433 | ACAGTATAGGAAGAA[A/G]CATAGTATATATAGG | 494470 |
rs537946214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357183 | ATATGAAGGACTCCT[C/T]GCTGAATAGTAAGTT | 494470 |
rs537980876 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46395133 | TTTATGGAGCTATGG[G/T]GTGGAGGGATTAAAA | 494470 |
rs538002281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351192 | CTTCCCACTGGAGTC[A/G]ACACTAAATTAGAAT | 494470 |
rs538010863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402230 | GCACATCTATTAATT[A/C]ATTGATTAGGTCAGC | 494470 |
rs538062739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46446658 | CCTGTGTGACAGAGC[A/G]AGACTCCATCTCAAA | 494470 |
rs538102843 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423240 | GGCCTGCTCTACAGA[C/G]GCAGGGCTTGTCCTT | 494470 |
rs538103583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46431696 | TCAACCCCCACTCCT[A/G]TTGGAGCCTCTCTGG | 494470 |
rs538107318 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349518 | ACACAAACATTCAAG[A/T]CATAGCACCTACTCT | 494470 |
rs538110825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439526 | GCTGTGTCCTAATTA[C/T]CAGGGACCACTTCAA | 494470 |
rs538146818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418725 | TCTGAATCAAATACA[A/G]TTATGTGGAAAGATA | 494470 |
rs538159636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46359130 | TCCCATGAGAGGAAG[A/T]CGTTAGAAGCTAGAA | 494470 |
rs538163725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432335 | AATGATAATGTTATA[A/C]CACATTATTTAACTA | 494470 |
rs538176998 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371963 | AATACTGACTCCTAA[C/T]GTACTAGACTTGGTC | 494470 |
rs538178726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345725 | AACTCTTCTACCTCT[A/G]TTTGCAAATTTTACA | 494470 |
rs538192699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396872 | GCATGACGTGGGTTG[A/G]GTGGATTTTCCGCTA | 494470 |
rs538204450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46413019 | CCTCTCCGAGAAGCT[A/G]GAGGAGTTCCAGGAG | 494470 |
rs538209305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395163 | AGATGGAAGTTGAAC[C/T]AGTTATTTCCAGTAC | 494470 |
rs538212738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340242 | ATATTTCCAAGAGAA[C/T]TGGGGGAAAGGGGAG | 494470 |
rs538217683 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461034 | GCACTAGAGGCCACT[A/G]TCTCCACCTGGCCTC | 494470 |
rs538222288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445159 | ACTGTTAAGTAGTTA[C/T]GTTTGTTTTATTCAT | 494470 |
rs538276391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374461 | TTTATTCCACTTTCT[C/G]TCTCTGTGAATTTGA | 494470 |
rs538292496 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46393910 | CTTCTGAATATTAGT[C/T]GATGTGAGGCTTACA | 494470 |
rs538296291 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428592 | CAAAATGGAAGTCAC[A/T]CACCTCCAGTGGCTC | 494470 |
rs538325959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46453812 | GAAAGCAACATATAA[A/T]ATTAACATCAATAAC | 494470 |
rs538326052 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391477 | CTATTCCACCCTCAG[C/T]GTCCTCATCCGTCAT | 494470 |
rs538338994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357895 | ATTCCTTCCTCATCT[C/G]TCCTCTCTTCTGGGG | 494470 |
rs538362834 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394481 | GGATGTGCAGTTCTG[C/T]GGGTCACGAGTCTCC | 494470 |
rs538365933 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46387088 | AGGAGAGTGCGCCAG[G/T]CCAGGGAAGCAGTGA | 494470 |
rs538459440 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46380150 | TTCTTCTCCATCTTC[A/G]TGTCTCTGCCTTGGT | 494470 |
rs538474162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438992 | TGGACTTGGGACAAG[A/G]ACCTGGGTCTTCTGA | 494470 |
rs538520139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358575 | CCTTCCTCAACTCCT[A/G]CAGCTCTGGCCTTCA | 494470 |
rs538520808 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46380803 | TAGTGCTCCCCCAAC[A/C]CCCGGGGCTAGGACC | 494470 |
rs538527071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365292 | TCAGTGGTCCCCACC[C/T]TACACTCCCCAACTC | 494470 |
rs538552410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46346372 | TTCACAGTACTGTGC[A/G]AACATCACTACTTTC | 494470 |
rs538559639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440119 | AGGCGTGAGCCACCA[C/T]GCCCAGATCTCATGG | 494470 |
rs538600846 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374258 | TTTTTATGGTGGGGA[A/T]ATATACATATTGTAT | 494470 |
rs538615497 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391389 | CTGGGAATCAGAGGC[A/G]AGGCCTAGTACGGGG | 494470 |
rs538621578 | snp | C/G | 0.0023933 | 0.0345097 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460908 | TACACTTGGCACCCC[C/G]CCGCCCCCACCACAA | 494470 |
rs538653342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395777 | TGCCCAATGCAAGGG[C/T]CTCAACCTAAGAATT | 494470 |
rs538656836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46454530 | TATATAGGGCACAGC[A/G]AGGCAGAGAGCAGAA | 494470 |
rs538666028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438037 | CTGGGAAGAACTTAG[A/G]GTCTGTACAGCAACC | 494470 |
rs538694745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375427 | GGTATGGTGGTACAC[A/G]CCTGTAATCCTAGCT | 494470 |
rs538697842 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352385 | TCATGTGGACCAGAG[C/T]TCCCAAATCTGATAA | 494470 |
rs538716141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370646 | GTGGGTGAGGCCTCC[C/T]CAGAATGCCCCATGC | 494470 |
rs538732835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351685 | TACTTTTTTATGAAA[C/T]CCCACTGAAAGATAA | 494470 |
rs538753224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424825 | GAGACCTTACACCGG[G/T]TGACTCTGCCTGGCT | 494470 |
rs538761676 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373555 | AAAGTGATGTGGTAA[C/T]GAGAGACAGCACAGT | 494470 |
rs538772306 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349049 | TGGCCAGAAGCAACT[C/T]CCTTATACTGTGGAG | 494470 |
rs538778384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365337 | TCGAGTCCAGGAGGT[C/T]TTTTTTGGGATGACC | 494470 |
rs538783359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345807 | CAGTCCAGGCTGTGC[C/T]CCGACTCCCGGGGTG | 494470 |
rs538824915 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46384764 | GCTCATGCCTGTAAT[C/T]CCAGTGCTTTGGGAG | 494470 |
rs538863662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418766 | CAGAAAAGAGCTATC[A/C]ACTGGCTATATCCAT | 494470 |
rs538864047 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RNF165 | GRCh38.p7 | 18:46397532 | GGTGTGAGGTGGTGT[A/G]TGTGTGGGGTCATGC | 494470 |
rs538923799 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46419271 | TTTGGGAATATGTCC[A/C]GTTCAAGGAAATCAT | 494470 |
rs538928248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414069 | TTTTCAAGGCACCAT[C/T]CCCCAGCAGTTCTCA | 494470 |
rs538929655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340305 | TGATTTAAGAACCAA[A/G]AGCAAACCCTTATAA | 494470 |
rs538945909 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46352637 | GGTTCACACCTTTAT[C/T]CACTTTCCAAGCATC | 494470 |
rs538958335 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RNF165 | GRCh38.p7 | 18:46340540 | CTTAGGAAACCAGAT[A/G]CTGTCTAAGATGTTC | 494470 |
rs538973815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426910 | GGTTGTCTATTAATG[C/G]GGTATTTGGGATGTC | 494470 |
rs538983280 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361628 | CTTCTCAGTACTATC[A/T]TTCAATATACATGAT | 494470 |
rs538989533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407880 | AAGCTGCTTGGAGAA[A/C]CTGGCATACTGAGAA | 494470 |
rs539006605 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332463 | TGTCCATTGTCTTAC[C/G]TCACTTCTCCCATTC | 494470 |
rs539028576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410737 | AACACACCCCATGAC[C/T]AGGAGGGCCACTCAT | 494470 |
rs539035644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46446041 | TATTCTCTGGACCTT[G/T]GCACCAAGATTAAGG | 494470 |
rs539041120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46377967 | GGTGGTGGACTGCAC[A/G]ACAGAGGTGGTGCAG | 494470 |
rs539041515 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333028 | AGCATGCAAGAACAC[A/C]GCCTCAGTCGTCCTC | 494470 |
rs539050886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46346458 | AGGGCCTCCTCCCAG[C/G]CAGGTTAAGGGCTGT | 494470 |
rs539119303 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420521 | AATGCTAACGTGGTC[C/T]AGGTAGCCACCCTAG | 494470 |
rs539123461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46446933 | TTTGATAGTTCTCTT[C/G]TTTCTAGTTATGACA | 494470 |
rs539123972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404559 | GGGAGGTCGAGACCA[C/G]CCTGACTAACATGGT | 494470 |
rs539140082 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453247 | TAATTAAGGGTGTCA[C/T]CTACAGGGGAAAATG | 494470 |
rs539187769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405136 | ATTTTCAACATGTCT[A/G]TGGTGTACAGTGTGG | 494470 |
rs539255180 | in-del | -/GCCAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415154 | GCCTACATGACCTCT[-/GCCAG]AGTTTGACTGACACT | 494470 |
rs539256940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432412 | CTTAAAAGTGTATGC[A/C]AAACAACTTCTGGTT | 494470 |
rs539261476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400005 | GCTGGGGCCACACCC[A/C]AGGTGTTCTGATCTT | 494470 |
rs539273146 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46440079 | GTGATATACCCGCCT[C/T]GGACTCTCAAAGTGC | 494470 |
rs539279093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394035 | CCTTAGGTAACCCCA[A/G]CCTTCCCTGTTAGCT | 494470 |
rs539283186 | snp | C/G/T | 1.65228e-05 | 0.00287422 | intron-variant | RNF165 | GRCh38.p7 | 18:46435286 | CCATCCCTTCTGGTG[C/G/T]AGGCGGAGTCAGGAG | 494470 |
rs539286094 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46409848 | AATAATGCATGTTCT[-/C]CTATTGATGGACATT | 494470 |
rs539316671 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46426097 | ATCCATCACCTTGGC[A/G]GTTAGGATTTGAACA | 494470 |
rs539334636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360094 | TCTAGGTCCAGAATA[A/C]CCTGAGACGCATCAC | 494470 |
rs539337082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46347446 | TGGGTCATCGTGCCG[C/T]CCCTGGAAAGAGAGT | 494470 |
rs539345577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356133 | AGTATTAATTAAGCC[C/T]TCACTCTGTGATATG | 494470 |
rs539346812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353593 | TAATCCCACTCCATC[C/T]CTCTACAAATGGAAG | 494470 |
rs539351502 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46385889 | TTGCTTTTACTAATA[C/T]ATGCCAAGAAGACTG | 494470 |
rs539372133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46350229 | ATATTTCAACAGGAG[A/G]TGCAGGCCTTATCTA | 494470 |
rs539397116 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377788 | TGATAAACAAAGGTT[C/G]AAAGCACTCTGGGCA | 494470 |
rs539399516 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457278 | TCTGTTTACGGTGAA[A/G]AAGGATTTTGTTTTT | 494470 |
rs539414671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336875 | GCAAAAAATGTTAAA[C/T]ATATGTATTAAAAAA | 494470 |
rs539487898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46449349 | ATGGAGGTTTTTTTT[A/G]CATTTATTTGACTTT | 494470 |
rs539493450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46367687 | TGGCAAGTTACTCTA[C/T]CAAACTGGCCTCGGT | 494470 |
rs539525645 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458527 | GAAATTCCATACAGT[A/G]AAGGAAATTTGAGTC | 494470 |
rs539535083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423939 | CATGTCCTTCCCTCT[C/T]TCTTTTCCTCTTTTA | 494470 |
rs539554715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411965 | GATGATGCCAGGCTC[C/T]CTGGGCTAAAAGCCT | 494470 |
rs539555295 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46367972 | CAGTGAGTCTCCAAG[A/T]GTGGTGCCCTAGGCA | 494470 |
rs539577022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338824 | CATTTTGGAGCTGCT[C/G]CTCTTTTGGCCGATG | 494470 |
rs539646935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451701 | TCCTAGTTACTAGGG[A/C]GGCTGAGGCAAGATA | 494470 |
rs539672427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46436408 | TATACAGGAATTCTT[C/T]ATGCTGTTCTTGCAA | 494470 |
rs539724691 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46356690 | CTGAAGGTTGAGAGG[A/G]TGCCTGGGGCTTAGC | 494470 |
rs539729102 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453269 | GGGAAAATGATCATT[C/T]TCTGGAGAGAGAGAG | 494470 |
rs539732397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444356 | TTTTTCTGTCATCTA[A/C]CTTCCATCCCCTCTT | 494470 |
rs539735195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429508 | GCTTATGTTATTCAT[A/G]TTGTGGAAGAAATGT | 494470 |
rs539765087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46363806 | ACTTTCTGAGCAGAA[C/T]TGAGGTGGTCACATG | 494470 |
rs539768732 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46437471 | CTGTTGCATCCCCTA[A/T]CCCCTTTAGAGAACC | 494470 |
rs539773658 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417697 | TTGGATAGGCCAGTG[C/T]TGTCCAATAGAAGTA | 494470 |
rs539783869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407057 | TCGACTTTTGCCTCG[G/T]CCTCTACCACCTCTT | 494470 |
rs539794752 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445514 | GTAAAGACTCAAGGG[A/G]ATCTCCGTGCAGATT | 494470 |
rs539801294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46399228 | TTAGGGTCACACAGG[C/T]GGTGGGGGTGGGACT | 494470 |
rs539819395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389079 | CTATTGGAGGGGGAA[G/T]ACAGGCTTAGGGACC | 494470 |
rs539834263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46361417 | TACATATGCAGCATA[C/T]ATGTACATTAATATT | 494470 |
rs539854358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383798 | CCTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 494470 |
rs539860085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393620 | AGACCACTAAGGTCT[A/T]AGGTCACCCCACCCC | 494470 |
rs539882808 | snp | A/G | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332632 | GGAACAAGCTCTATG[A/G]TGATTGCCCGTTGGC | 494470 |
rs539945443 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344336 | GGGAAGGGGTGGAGG[C/T]GCTCTCCATGTCTTC | 494470 |
rs539980032 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443752 | ACAGAAGAAGTTTGC[C/T]AATCTCTGCTTTAAA | 494470 |
rs539984077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388130 | GGTTACATGTTTATT[G/T]GGGATTACAGCTGGG | 494470 |
rs539991234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412558 | AGGGAGGCCGATGTC[C/T]AGTCATGTGCTGATG | 494470 |
rs540004679 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373997 | ATGGTAAACCCAGGC[C/G]CCTCATGTTTCTAAT | 494470 |
rs540065128 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355309 | AACTGAGGATGAACA[C/T]ATCTGAGGGGAGCAG | 494470 |
rs540072294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373931 | TTTCCCAGAAGCAGA[C/T]GGACAGTTGCTCCGA | 494470 |
rs540109865 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388220 | GCTAAGTAAGTTGGA[-/G]GAAATCCTGTATGTA | 494470 |
rs540149727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417461 | ACCACAGGGCCTTTG[C/T]GTGTGCAGTTCTGTC | 494470 |
rs540157368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353811 | ACAGACAGCCCATGT[C/T]AAGGACCCAGAGACC | 494470 |
rs540202403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442118 | CAGTGAGTCGAGATC[A/G]CGCCACTGCGCTCCA | 494470 |
rs540237501 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415121 | TCCCTGTGTCAGTCC[A/G]GAGTGTCCCCTCCCC | 494470 |
rs540270901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362175 | AGGGGCAGTCGCTGT[C/G]CCCTCCAAGGTCAAT | 494470 |
rs540306076 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372759 | AGGCTGTTTTATCCA[C/T]ACTTGTTAAACCCTG | 494470 |
rs540333667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349762 | GGAGTTTCTTGCCTA[A/T]CTAGTTGGGCACCCC | 494470 |
rs540344411 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46429015 | TTCCCTCTGTCACAC[C/T]GGCAGTCTCCTTCCC | 494470 |
rs540357425 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46369391 | TGTGCTGGGGTGGCA[-/G]GGGGGTGGGAGAGGA | 494470 |
rs540366126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46392686 | GGGCTGAGGGTGACA[C/T]GGTCCTGTGCCTTGT | 494470 |
rs540394946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444462 | CTGATGGTGTGCTTC[A/G]TTTTGGATTATTATT | 494470 |
rs540431074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46400755 | AGCCTAAATTGTGTC[A/G]GCTTTCAGTAGCCCC | 494470 |
rs540441165 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441998 | TGAAACCCCGTCTCT[A/G]CTAAAAATACAAAAA | 494470 |
rs540472160 | in-del | -/AGC | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46341012 | GAACAGAAAGTACGT[-/AGC]AGGAGGGAAGAGTGT | 494470 |
rs540489039 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350912 | TTACCTGGGAGGAGA[A/T]GAGGGCCGGGTTTAA | 494470 |
rs540497906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344112 | GTTGGCCTCCCCTGA[C/T]GACACTGTATCCCTT | 494470 |
rs540507032 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425427 | TAGAGATGTCAGGTG[C/T]CCTGTGGGGCCTTTC | 494470 |
rs540510359 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46356015 | GTCCTTGGCAGCATT[C/T]CCGTGGCCCTCAGCC | 494470 |
rs540548507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351289 | TCGGGACTTCCCTCC[A/G]GTCTGAAGTTTGAGG | 494470 |
rs540577367 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332809 | TTCCAGCTCCACATA[C/T]TGTGATTTTTACCAT | 494470 |
rs540664607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451182 | AGAAAATAATTCTAT[A/G]TCCAATCTCACATGT | 494470 |
rs540712049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455026 | ATGGCTTCTACATAA[C/T]GGTAAACTATTTTCA | 494470 |
rs540752015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408588 | AAGAGAGCACATCAT[A/G]GGAACTGTGGGGCAT | 494470 |
rs540755706 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415875 | AGGGACTGAAGCAGA[A/G]TTCACGAGGGACCTG | 494470 |
rs540782370 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407359 | CTGCCCATGGATAGC[A/G]TGGGGATTGGCCCTT | 494470 |
rs540793136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447836 | CTTCCACATGACCCA[A/G]CTCACCTGTGTATCA | 494470 |
rs540808515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363495 | CTCAGGGCTCTTTCA[C/T]TTGAGACATCCACAA | 494470 |
rs540811720 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46439825 | GCCAGTTTTGTTTTT[G/T]TTTTGTTTGTGTGTT | 494470 |
rs540813237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403091 | CCTTAGGCAGCCCCA[A/G]GCAGAGGTTTTGCAT | 494470 |
rs540849217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395242 | GGGTCCTTGAGCCCA[C/T]GTCTCCAGGGGACTG | 494470 |
rs540875071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46359660 | TATTTCTGTCACATG[C/T]TCAGGAAGAGGTCTG | 494470 |
rs540885262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360337 | AACACAGAGGGTGCT[A/C]CCCTGCAACAGTGCA | 494470 |
rs540943288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424355 | GTGAGAGAGAGCAAG[G/T]CTGGGAGGGGGATTT | 494470 |
rs540957203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390112 | TCCCTGCCTTCTGCA[A/T]ATATGCTCCTCTCCC | 494470 |
rs540972467 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377047 | GGAGTGGTCAGGCAC[A/C]TAGGAGGAGGCAGCA | 494470 |
rs540995034 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422304 | TTCCCAAGCACCCTG[C/T]CTCTGAATGACTCAC | 494470 |
rs541022681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375282 | TCCTGGCCGGGCACA[A/G]TGGCTCACACCTGTC | 494470 |
rs541022788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46381564 | TGGCCTGGGCAGTGG[C/T]TCACACCTGTAGTGC | 494470 |
rs541030045 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360120 | ATCACAAGTCCATGC[A/G]ATGGCCCCATTGAAG | 494470 |
rs541034897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375702 | TCTCTTGTTCCCAGC[A/T]ATTTTATGTTAAGGT | 494470 |
rs541087286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382359 | AGCTTCAGATTTACT[A/G]CATAGCTCAGAGCCC | 494470 |
rs541098071 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439996 | CCCTACACCCAGCTA[A/G]TTTTTGTATTTTTAG | 494470 |
rs541107519 | snp | G/T | 0.14933 | 0.228835 | intron-variant | RNF165 | GRCh38.p7 | 18:46348229 | TGTGGGCCAAGGGGC[G/T]GGGGGGGGTGAGGGG | 494470 |
rs541144577 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46342335 | AGAAAGGAATACCTG[C/G]TTTCCCGCCATAGCT | 494470 |
rs541161368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376695 | TTTTTTTTTTGAGAT[A/G]GAGTCTTGCTCTGAT | 494470 |
rs541186889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362823 | AGAAGCACAACATAC[A/G]AGAGCCAAGAGGAAT | 494470 |
rs541221554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46377196 | AAAAGGTATATAATG[G/T]ACCCCTTTTAAATTC | 494470 |
rs541222079 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456655 | AGGAATTAGCCAGTG[A/G]ACACCCCATTTCCTT | 494470 |
rs541237624 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46372130 | GCTGGTGGCTGGAGG[C/T]TGGCTGCAGGGCCTT | 494470 |
rs541239087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46391946 | ATGCACACAACACAC[A/G]CGCACATGACACAAT | 494470 |
rs541298912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372620 | TCTGGGTTCCAATGA[C/G]AGAGGCTGGCCTAAG | 494470 |
rs541302253 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376025 | CTGAGGGTGAGATGA[A/G]GCAGTGAGTGTGCAC | 494470 |
rs541305500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448718 | CCTTCTTGTGGCTGC[A/T]GAGTGCCGAATCATG | 494470 |
rs541306449 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424991 | CTGAGCCTCTCCAGC[C/G]CTGTGGCCGGCTGTC | 494470 |
rs541313902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46397949 | GGGGTGCGAGGGTGT[A/G]TGTGCATGTGGGGTG | 494470 |
rs541335891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367123 | TCCTACCGGCTGCCC[A/G]TCTGCTGGGGGATGT | 494470 |
rs541365137 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454596 | AGTATTCCCCAGACT[A/C]AACCAGACTCAGGAT | 494470 |
rs541396171 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422023 | CCCATGGCAGCCCTG[G/T]GGGCTAAGCCAAGCA | 494470 |
rs541452108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427761 | GATACAGCAAAGACA[C/T]GAAGCCCAGCCTGGT | 494470 |
rs541505213 | snp | C/G | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333633 | AGCGCACGTCCCCGA[C/G]TGACCCGTGCGCGGT | 494470 |
rs541527974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440563 | CATATTATTTCATCT[A/G]TAAATATTTCACTAT | 494470 |
rs541532525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415387 | TTTTTATATTTATAG[A/G]CAGTGGTGGGCGCCT | 494470 |
rs541536709 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46421575 | TTGGTTTAGATGGGG[A/G]AAGTATCTTCTTGGA | 494470 |
rs541545011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415645 | GCTGAGAGTGAAAGA[C/T]GGGCTTGGAATCAAA | 494470 |
rs541555240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46334897 | CAGCCCCCACCCTCT[C/T]GTGGGCACTTGCACG | 494470 |
rs541575238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46360400 | GGTAGGCCCTGCTGG[A/G]CAAGCAGTTTTACTG | 494470 |
rs541587058 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420407 | CGTATTCACAGGGCC[A/G]GGCTTGTGTAAGCAT | 494470 |
rs541609705 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46398002 | TGTGAGGGTGTGTGT[A/G]CATGTGGTATGTGTG | 494470 |
rs541623822 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446625 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 494470 |
rs541654262 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457316 | TTTGGGAGGCGGGAG[A/G]GGGGGGTTCTCGTTT | 494470 |
rs541663862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427317 | CCCAGTGCGTCTGCT[A/G]GAGGGCACAGGTTGT | 494470 |
rs541738549 | snp | C/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333233 | ACATGGCTGGGTGTA[C/T]CTGTCTCAGATCAGG | 494470 |
rs541775095 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46421620 | AATATTGTCCCATTA[G/T]GCACAGAGGTTTTCT | 494470 |
rs541782774 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400510 | CAGTTCGTAAGACTG[G/T]GTGACCTGCCACCAT | 494470 |
rs541783652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342955 | TACATTCTCTATTTC[C/T]TATTTTACATTAATG | 494470 |
rs541783714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349466 | TTTTAACACCATCAT[C/T]TTGGGGGTTAAGATT | 494470 |
rs541805247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455816 | CTCCAGCCTGGGCAA[C/T]ACAGCAAGAATCAGT | 494470 |
rs541846443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382917 | ACCACCATGAGCTCA[A/T]GTAGTCCCATCCCCT | 494470 |
rs541847522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365583 | ATCTTGGCTCACTGC[A/G]ACTTCTGCCTCCTGG | 494470 |
rs541886637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371352 | CTGCAAGGAGGGTCA[C/T]GGGGTCTGATAAGGA | 494470 |
rs541889758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372239 | TGCTATCAGGTTGGC[A/G]GCATAGTATTCTGGA | 494470 |
rs541897135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366269 | TGCACTCCAGCCTGG[A/G]CAACAAGAGCAGAAC | 494470 |
rs541921787 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46345486 | CCTTCTCAGCTGGTG[C/T]CTCTCAGCCATCTCC | 494470 |
rs541943214 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457467 | CTCTGAGGGTTCAGC[G/T]GAGGTGAGGAAGGCA | 494470 |
rs541956684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336258 | GATTAAATCATTACC[A/G]TCCTCATTAATACCA | 494470 |
rs541962340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366918 | AAAGGTCTTCTGTGT[C/T]TTGCTGGAAGGAACA | 494470 |
rs542018155 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46449694 | ACCTCCCCATTCGCT[C/T]GGCACTCATTCTCTC | 494470 |
rs542033493 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46361118 | TTTTCCTGATGCCCA[C/G]TGTAAAAAAATTTTT | 494470 |
rs542055722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373007 | ACTGGAAGCTCTGTG[A/T]GTCTGTGCATGTGCG | 494470 |
rs542060729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386945 | AGCTACTCCTTTTGG[C/T]GGGGGACACTGACAT | 494470 |
rs542083146 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341722 | TGCCTGAAACCCTTG[C/T]GATGTTATTCACATG | 494470 |
rs542096658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46354753 | AGTGGTTCATAAAGC[A/G]ATGGTCCACTGTGCA | 494470 |
rs542145427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399256 | ACTGGTACTCTGGAC[A/G]TCCAGGGCAGTGCTC | 494470 |
rs542196467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393766 | CAGTAAGTAGAAAGA[C/T]GGTGGACTCACCTTT | 494470 |
rs542209031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383265 | CAAGATGGCATCAAG[C/T]CAAAATTTCAAAATG | 494470 |
rs542211598 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414731 | CCAGAAGGGCAAACA[C/T]AGCACGTGGAATCCT | 494470 |
rs542233893 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387991 | CCCACAGGCTGGGGA[C/T]TTCCAAGATTCAAGC | 494470 |
rs542236936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422005 | GAGAGGGAGGAAAGC[A/G]GACCCATGGCAGCCC | 494470 |
rs542246670 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459435 | AAGGACTTTCTGTGG[G/T]CACACACTCTGTTTC | 494470 |
rs542281627 | in-del | -/G | 0.0345262 | 0.126772 | intron-variant | RNF165 | GRCh38.p7 | 18:46341336 | GGGGGTGGGACAGGC[-/G]TGGGGGGTAGGGAGG | 494470 |
rs542290392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424962 | GAGCCAGCGCTGAAC[C/T]CCGGCTCTTGAGGCT | 494470 |
rs542300093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416112 | TTGATTTGTCTATTT[G/T]CCAGCACATCTGGGA | 494470 |
rs542314399 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378570 | CCATTTGATGTATGG[A/T]CCAATTGTTCCAGTT | 494470 |
rs542336302 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459773 | TGGAGAAGAGGCAGG[A/G]TCAGGCCTCAGCATC | 494470 |
rs542345179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337435 | CCAGTTGACAATGTA[C/T]AGCGCTCGGTTAGAG | 494470 |
rs542346019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410837 | AGGCTCATGAAAGTG[C/G]TCAGCAAGTCCTCCT | 494470 |
rs542350058 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347050 | GCAGGGAGATATCTT[A/G]GCGCACGGGATGGGG | 494470 |
rs542372491 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46340435 | TTGAATACTTACTTG[G/T]GGCCAAACACTGCGC | 494470 |
rs542377982 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443315 | TCATACCACTTTATT[A/T]TATCTTATTTTATTT | 494470 |
rs542413723 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416459 | TGGAGACAATACAGG[C/G]ACTTTTCTCTTTAAG | 494470 |
rs542413821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46411325 | CATTGGCTGGAGAAA[A/G]GAAAGAGATTTCCTA | 494470 |
rs542452956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369867 | ATCAGGGTAGAGCCC[A/G]GGGCCCGTTGGGCCC | 494470 |
rs542465484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370325 | AAGGGATAATCATCT[C/T]GTCCAAGATAAGACT | 494470 |
rs542524276 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395812 | TACTTCCAGAGCTTT[C/T]TGGGGCCAGGTGGTG | 494470 |
rs542525027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362706 | AAGAATAATGCCCTG[C/T]GACAACCACATCAGG | 494470 |
rs542539809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46446211 | ATCCTTTATTTCTTT[A/T]GGGGAAGCAAAATGA | 494470 |
rs542561305 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46396157 | AACAGTCACTTCCAC[A/C]TTCTTCTATTGGCCA | 494470 |
rs542572856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417876 | GGGCTTGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 494470 |
rs542573414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396756 | CACCAGCAGCCTTCA[C/T]GGTGCTGGCCATGTG | 494470 |
rs542603746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402400 | TACATTTTAATTTCA[A/G]ATAAAATGAACATAT | 494470 |
rs542614545 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345892 | TCAGGGTCACCCCAA[A/G]GCCTCATCTTCCCAG | 494470 |
rs542655711 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352685 | GAAAGGTTAGAAAGA[C/G]CATGACACAGCACTG | 494470 |
rs542681498 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46358805 | GGGCAGAGTGACACA[A/C/T]GCCTTGGTCATCACT | 494470 |
rs542682860 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46339981 | GTTCTGTGCTGGATC[C/G]AAGGGCAGCAGGGAC | 494470 |
rs542739119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418788 | TATATCCATGCTCTG[A/G]GCTGTGAGGGCAGGA | 494470 |
rs542741764 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46391820 | AACCACAACACACAT[A/G]TAACACATGTACAGA | 494470 |
rs542753257 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360322 | GGCCAGCCATGGAGG[A/T]ACACAGAGGGTGCTC | 494470 |
rs542775547 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46426286 | CAGATGAGTGTCCCA[G/T]GCAAGGCAGTGAGCC | 494470 |
rs542805095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385954 | AGATGACCTCATGGC[A/G]GTGTGTGGTGGTTCT | 494470 |
rs542817696 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46428220 | TCAAGACCATTCTGG[C/T]CAACATGGTGAAACC | 494470 |
rs542857378 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46381746 | TGAGGTGGGAGGATC[A/G]CTTGAGCCCAGGATA | 494470 |
rs542886029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420071 | GAAAGCAAGCAGATA[A/T]CCACTCACTGATGTG | 494470 |
rs542893263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46401770 | GGGACTTTAAAGTTG[A/G]GGAGGCCTTGGAGAG | 494470 |
rs542902319 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445213 | TGGTAAGGAGCACTT[A/G]CAGTTCAGTTTCATC | 494470 |
rs542910929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438402 | ACCTAGGGCAGACCA[C/T]CCCACCCATTTGAGG | 494470 |
rs542925481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415295 | GGAGGCCGAGGTGGG[C/T]GGATCACGAGGTCAG | 494470 |
rs542928569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341711 | CTCTCTGTTGATGCC[C/T]GAAACCCTTGTGATG | 494470 |
rs542943030 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366216 | AGACTCGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 494470 |
rs542978347 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410102 | TGAGGAGTAGTGGGT[A/G]GGAGGTCTTGGTGAT | 494470 |
rs543011721 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459950 | CTGCAGCAGCTGTGC[C/T]GCCGCGGGTCCACCG | 494470 |
rs543025162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46439183 | GGCTCATACTCTCAT[A/G]AGCGTAACCCAGGTA | 494470 |
rs543053241 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46381006 | CTCCAGAGTAGGAAC[A/G]CATGCCTCATGTCCT | 494470 |
rs543062926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425526 | CCTGGAGTCTTGAGG[A/G]TGAAACTCCACTTTC | 494470 |
rs543072444 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342397 | GTCCACAGTGGAAAA[C/G]GATCTTTCCAGCTAA | 494470 |
rs543080253 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459065 | AAACCAAGAATTCAT[C/G/T]GGAAGATGGCTTTGG | 494470 |
rs543086207 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460323 | GTGTTTCATCTCCTG[C/T]GCGCGTAGAGCAAAT | 494470 |
rs543086723 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46431837 | TCCAAAGTAGCCACT[A/G]CCTCCAATTCCTGAC | 494470 |
rs543101217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432504 | GAAATTCTGAGCTTG[A/G]CTAGGCTGGACTAAC | 494470 |
rs543109870 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342924 | GGAGCTGTAAACACA[A/G]TATATGTATACTTTT | 494470 |
rs543111687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341010 | AAGAACAGAAAGTAC[A/G]TAGCAGGAGGGAAGA | 494470 |
rs543114915 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375258 | TTTCCCTTTCATCAA[A/C]AATACTTGTCCTGGC | 494470 |
rs543120069 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366904 | ATCCAAGTCCAGCAA[A/G]AGGTCTTCTGTGTCT | 494470 |
rs543124264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419627 | TATTAAGCAATGAGC[A/G]GAGTGGGCAGCGCAC | 494470 |
rs543137806 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46454062 | AGCCTGCAGTGAGCC[A/G]TGATTATACCACTGC | 494470 |
rs543140240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414262 | AGATGTGTCTTCTTC[C/T]TTAAGGGAAACTGCT | 494470 |
rs543161585 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385908 | CCAAGAAGACTGTAA[C/T]GCTGTCTTCATAAAA | 494470 |
rs543167565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46353084 | CCACCGGCCTGTGGC[A/G]ATTGGATGTGATTAC | 494470 |
rs543183001 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390183 | AGGCTGGCAAGTCAG[C/G]TGGGAACTGGGCCGA | 494470 |
rs543190431 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332608 | TTCCCGTGCTGCCCA[G/T]TTCTGCATGGAACAA | 494470 |
rs543193268 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46370375 | ATTAGAAGCAGGGAA[A/G]TCAGTGTGCAGAGCT | 494470 |
rs543244271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341136 | CTCTAGGAGTTAAGC[A/G]GCACGAGGTCTGGAG | 494470 |
rs543254694 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46365085 | TCCTGATATTCCTGC[A/T]TTATCACCATTCCCT | 494470 |
rs543262810 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46447248 | GCCTCTGGCTTGCTC[A/G]ATTTAGATTCTTCTT | 494470 |
rs543312325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375833 | ATGGACTCTGCTTAC[A/G]TCAAACAACTGGAGG | 494470 |
rs543318243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342117 | ATTTCCTCCTTGGCA[C/T]AGCCCATGAGGAGTT | 494470 |
rs543337080 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340555 | ACTGTCTAAGATGTT[C/T]TGGGCCAAAATGTCC | 494470 |
rs543368252 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46359560 | GAGAGCCAAGAGAAT[A/G]TAAGAACTGAGGCCT | 494470 |
rs543375735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384167 | CAAGACCACTGCCCC[A/G]GCCGTGCTTCCAGCC | 494470 |
rs543396158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380346 | GCGACTTGGGGAGTG[C/T]GCGCAGGGGACATCC | 494470 |
rs543398138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46455792 | GTGAGCCAAGATCAC[A/G]CTATTGCACTCCAGC | 494470 |
rs543408604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374802 | ACACCCCAAGCCTGG[C/T]ATTCCTGGAGACACT | 494470 |
rs543429695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46432651 | AAAAAGGATGCTTAT[A/G]TATTCATTAAAGATA | 494470 |
rs543430629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385400 | TGTGTGTGAGTGTGC[A/G]TGTGCATATGTGTGC | 494470 |
rs543431081 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46413441 | ATAGGTGAGCGCTCC[C/G]TGGGTTTGGAGTCCT | 494470 |
rs543499337 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46378480 | GGGCTTTTGCACCGC[C/T]TTCTGTAAGTCACCA | 494470 |
rs543565343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46446325 | AAATATTTGATTACC[C/T]GGAAATACAGTAAGA | 494470 |
rs543605399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408518 | CCAGCAGAGGGCCAT[A/G]AGGAACTTACCCGTA | 494470 |
rs543624288 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379310 | TTGACAAACACAAAA[C/T]CCTCTCCTTAAACTT | 494470 |
rs543644478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370850 | ACTCAGGGGGCGTGA[A/G]GTCAGCATGAGCTTT | 494470 |
rs543649950 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454831 | GTGAAGATGTGAACA[C/T]GAAAGGTGGGCTGAT | 494470 |
rs543663801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376534 | CCTCAGACCACACCT[A/G]TGCTCTGGACTATTC | 494470 |
rs543679411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396768 | TCATGGTGCTGGCCA[C/T]GTGCACCACGCCTAT | 494470 |
rs543686053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415304 | GGTGGGCGGATCACG[A/T]GGTCAGGAGATGGAG | 494470 |
rs543710592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403682 | CAGGAGTTCGAGACC[A/G]GTCTGGCCAACATGA | 494470 |
rs543750495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46409406 | CATCTGCAGGTAAAC[A/G]GTGGTGGTGATGCAC | 494470 |
rs543770711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46427809 | AGAGACAGCTCAAGG[C/T]AGCCACTGCCAGGTG | 494470 |
rs543817816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388776 | GCAATTTCCATTTCC[C/T]GAGTGAGGGGTAAAC | 494470 |
rs543848781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420138 | GGCGCCTCCACTCAC[C/T]GGCTGCTGTCTGAAA | 494470 |
rs543875595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426380 | CTCCCTTTCCTTTCC[C/T]TCCCCTATGGGTTCT | 494470 |
rs543891327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353740 | CCATGCTGCTGCCTC[G/T]GATCCTTGATCTGAG | 494470 |
rs543928027 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389347 | GCTGATAAATAAAAC[A/G/T]TCACTGTAAGTTCTA | 494470 |
rs543952968 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339911 | CCATCTTTAAATAAG[C/T]ATCCTGCAGTAGCAC | 494470 |
rs543955035 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46341855 | TTTTATCAAACTTTG[C/T]CTTTCTTGAAAAGAC | 494470 |
rs543962002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356835 | CTTATTCAGGCATGG[C/T]GCAAGAGACAGAGGC | 494470 |
rs543991678 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46342257 | CACTCGACTATGGCC[C/T]CCTGCACTGCCTGCC | 494470 |
rs544027522 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443214 | TGTTGTTGTCATTTT[G/T]TTGTTTTTCTTTTAA | 494470 |
rs544044965 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46392162 | CATGCACACCACACA[C/T]GTGTACCACACACAT | 494470 |
rs544068651 | snp | C/T | 2.7682e-05 | 0.00372025 | intron-variant | RNF165 | GRCh38.p7 | 18:46455936 | CACCAGCTGAGTCTG[C/T]CCCAGGTAATGAATA | 494470 |
rs544108444 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425303 | GGCAGAGCTGGCTCT[A/G]GTCAGCTGGCAGGCC | 494470 |
rs544124839 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362786 | TTTCTGCACTTCCCT[C/G]TAGTCCTCTTCCTTA | 494470 |
rs544140546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379465 | CGAGTCCATTTTACA[G/T]ATGAGGGAATAAGTC | 494470 |
rs544151502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46456440 | GGGCAGTTCCCCAGG[A/T]GTCCTAGGTGTGTGT | 494470 |
rs544166204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406530 | TAGAGTGCCTCTCAT[C/G]TGTCTCATGCAGCTG | 494470 |
rs544170328 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434935 | GAGCCTGTAGGAGGC[A/G]AGTCTGTGTGTCTTG | 494470 |
rs544183928 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372631 | ATGAGAGAGGCTGGC[C/T]TAAGGGGTTGGGGGT | 494470 |
rs544256701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374110 | CCCCACCAGGGGTCC[C/T]CTTATGGAAACTTCT | 494470 |
rs544266077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429111 | GCAGCCCCCGGACTC[A/T]CCAAAGCCAGAATCT | 494470 |
rs544278200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429797 | TCTTTTATTGAGATG[A/G]GGTCTTGCTATGTTG | 494470 |
rs544289645 | snp | C/G | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461729 | AAGAAGAGAAGAATA[C/G]AGAGAGTGAGCTGAG | 494470 |
rs544309170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350392 | TGCCATGTGGCCTGG[A/G]AGGGCTTCCTGGAGG | 494470 |
rs544331795 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412324 | AGAAGCAGACCCACA[G/T]CCTTGGTTTCTTGGT | 494470 |
rs544332053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46437736 | TCCTGACCTTAAGCC[A/G]CAACCCAGGGCCTGA | 494470 |
rs544345844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46344328 | GAGTGGGAGGGAAGG[A/G]GTGGAGGCGCTCTCC | 494470 |
rs544362285 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46371207 | ATCAATTATCTCCAC[A/C]TGGCCCTGCCCTTGA | 494470 |
rs544363864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445450 | ACCTTGGATGCTCTT[C/T]GTTCAACCTACTAAA | 494470 |
rs544381733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344617 | TCCACAGGGGACCTC[A/G]GCATCCACAGTGGGC | 494470 |
rs544425409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417561 | GTTATCTTCTCAGTG[A/C]AGGTTCTCTTGGCAG | 494470 |
rs544459997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373666 | CCAGGGACAGCCCAC[C/G]AGAGGCTCACAGGTG | 494470 |
rs544490757 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373813 | GCCTAGGCCAGACCG[C/T]GCAGCCAGAGAAAGG | 494470 |
rs544513861 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350758 | TGATACTAATGTCAC[C/T]GTTCTGCTTTATAAA | 494470 |
rs544522362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425393 | CCCTGGGGTAGCCCC[A/G]GGTGGGTGGCAGGCC | 494470 |
rs544524378 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46346877 | GCTGGGCATATTTCA[A/C/G]CTTAATTGTGTAAGC | 494470 |
rs544526659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345959 | CAGAGCTGGCTCTTG[A/G]AGCTCTAGTCAGGAT | 494470 |
rs544540386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451208 | CATGTGAACAAATGG[C/G]AAAGCAAGGCATCCA | 494470 |
rs544545385 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418342 | AGCCTGAGTGACAGG[A/G]CAAGACACTGTCTCC | 494470 |
rs544569896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351899 | TGTTGGGATGGGATA[C/T]CAAGAATGTGAGGTG | 494470 |
rs544577299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46452059 | AAAGTATTTGGTATC[A/G]TACTCTAACGGTGGA | 494470 |
rs544597733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46368716 | ACACTGAAAGTTTAG[C/T]GTAGTGGTCAGGGTT | 494470 |
rs544604098 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46397630 | CATGCTGAGGTGTGA[-/G]GGTGTGTGTGTGTGT | 494470 |
rs544619119 | in-del | -/AG | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461675 | AAAAAAAAGAGGGAA[-/AG]AGGGAGAAAGGATTG | 494470 |
rs544642169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444610 | GCTTGGACCAGAGGA[C/T]ACACCACCATACCCA | 494470 |
rs544714796 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46424908 | CCTGCTTTTCAAAAG[G/T]CTGGCTTTCTTTGCT | 494470 |
rs544739357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384302 | TCACCTGGTGCTCCC[C/T]GTAGTGTCCAGTCTT | 494470 |
rs544771723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351245 | CAGATGACCTAGCCC[A/T]ACAGAGTCACCACCT | 494470 |
rs544795501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345193 | CTGGAAGGAAGTTTG[C/T]GCCCGCTGGAACCTG | 494470 |
rs544802624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46379705 | CCAGTTCATTCAGCC[A/G]CCCTGGGGAGCTAAT | 494470 |
rs544819390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46351352 | GGAGCAGTTCCCTCC[A/G]GGTGCCCCTAGTTCC | 494470 |
rs544906963 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439862 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCAGGC | 494470 |
rs544936308 | snp | A/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460346 | GAGCAAATGCTAGAG[A/C]GATTTCAGCTGATAG | 494470 |
rs544939138 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46396529 | AGGTGCCTGGCACAC[-/A]GTAGCTTTTCAGATA | 494470 |
rs544947671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385029 | CTCCCCCTCAAAGAT[C/T]TCCAGAGTGGTGTGC | 494470 |
rs544952365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46453033 | ACTAAGTGCCCAGGA[A/G]TGGTGAGCTGCTGAT | 494470 |
rs544964709 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361076 | AACTTGCCCAAGATC[A/T]CGCTGCTAACTGGGC | 494470 |
rs544966734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46413216 | TAAGGCAGCCTGCCC[C/T]GACCCGTTCCAAGGG | 494470 |
rs544970042 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46424044 | GCATGGTACCTCCTC[C/T]GAAAACACTCACTTC | 494470 |
rs544971538 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46401732 | TGAGGTTCAGGCTTC[C/T]CCACGGAGCTTCCTG | 494470 |
rs544978830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407368 | GATAGCATGGGGATT[A/G]GCCCTTTCTTGCTTG | 494470 |
rs544986827 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389793 | CAGTGCAGTGGTGCA[A/G]TCTTGGCTCACTGCA | 494470 |
rs545031935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350833 | CGGCCAATATTATAT[C/G]TCTGACATAGAGATT | 494470 |
rs545058073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423612 | ATGTGCTGGAAGGCC[A/G]TGACACTGATGTGGC | 494470 |
rs545059934 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372349 | CTTCGCTCTTCCTGC[C/T]TCGGTCCCACCATTG | 494470 |
rs545068247 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46344683 | AGGGACCATACCTGC[C/T]CCCTCTGCCTGTGAC | 494470 |
rs545078697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46396012 | CCAGGCAGACTTGGC[A/G]TTGTTCTGTGTGGTC | 494470 |
rs545122093 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46425027 | TTCTTTCTCCCTGCC[A/C]CTCCCTGGTGCCTTT | 494470 |
rs545141140 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46339006 | GGCCCTCTTTGTTCT[C/G/T]GTGCTCTTCCCAGCC | 494470 |
rs545147083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350375 | ACAAAGCTCTGTTTG[C/G]ATGCCATGTGGCCTG | 494470 |
rs545192557 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357703 | GTCACCCTCCAGTTA[A/G]GGAGGCAGGAATTGC | 494470 |
rs545196437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431753 | AAGGGGAGGAGCCCT[A/G]GGCAGAATTGCTCCT | 494470 |
rs545229493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391349 | TTGGCCAAATGGGAC[A/G]ACATTACAGCTCTTT | 494470 |
rs545294548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385452 | AGGTGTTGCACAAGG[A/G]TGTCCAGGTTGAAAC | 494470 |
rs545313138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46341046 | TGTTGATGGCGGGGC[A/G]GAGGCACATGTGCAG | 494470 |
rs545319329 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370583 | GTCCCAGGTGGCAGT[C/T]ATCGCTATTTGCCAC | 494470 |
rs545323483 | snp | C/T | 0.030278 | 0.119257 | intron-variant | RNF165 | GRCh38.p7 | 18:46349204 | GCAGTAACAAAATGC[C/T]ATAGACTGGGTGGCT | 494470 |
rs545366669 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46344400 | AGCTCCAGCCTTCCT[C/G]CCCCATGCCACCCCC | 494470 |
rs545386461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445532 | CTCCGTGCAGATTTC[A/T]GGAGCCCTCCTTCTA | 494470 |
rs545399422 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444299 | GAATTTATAGTTTTT[A/G]TTAAATTTGGAAATA | 494470 |
rs545433123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438340 | TTCGAGGAACCACAT[C/T]CCCTGTTGGGGTAGC | 494470 |
rs545478447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46358120 | TCACAGGTACTGGGG[A/G]TTAGGACATCAACCT | 494470 |
rs545480488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46439041 | CTGTGGTGTGCATGG[A/G]GTCTGTGAGAGTGAC | 494470 |
rs545481744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441302 | CAGACGCAGGCTGGT[C/G]TTACATGCCTAGGCC | 494470 |
rs545505532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352014 | GCCTTCAGAATGCAA[C/T]GGAGTCTTCCTGCCC | 494470 |
rs545528417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390729 | AATGTGGGAAGGCGG[C/T]GGCTCGGAATCCTAT | 494470 |
rs545535129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399059 | ACATGGTCCCAGGAG[A/T]TCAGGAGAAACTGTC | 494470 |
rs545537905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46358705 | CAGGTTCCAGACCCC[C/T]AGGAACACCCCTTCC | 494470 |
rs545540411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385110 | CCAGCCAACTCTGGC[A/G]TATATTCTCAGAGAT | 494470 |
rs545573496 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400673 | TGTGTCAGCGTGCCT[C/T]TCAGTGCAGTGGGCT | 494470 |
rs545624463 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46346032 | TGTTTTGACTCAATG[A/C]CATTTGTAAGTGGCA | 494470 |
rs545628348 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382876 | CCCATCCCTCCTGGA[A/C]CGTCAGAGCCTCGGG | 494470 |
rs545645555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422068 | GTTGATGAGACTGGA[A/G]CAAAAGAGGTTAAAC | 494470 |
rs545691319 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413277 | CGCTCAAGCCCAGCC[C/T]TATCCAGAAGTGGAC | 494470 |
rs545691972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414481 | ATGTACACACACACA[C/T]ATCACAGGTGCCACA | 494470 |
rs545711142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343676 | TTGCCCCTGCCTGCT[C/G]TAAAGCACTGTGCTT | 494470 |
rs545748382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381073 | ATGCCACACTACTGC[A/G]CCTCAGTTTTTCTAT | 494470 |
rs545750219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46344030 | ACATGCCTGGGTGTG[C/T]CGCTGTGTGCAGCTG | 494470 |
rs545799334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366379 | CAGATTAGGGAGAGA[A/C]AGCTGGGAACAGCTG | 494470 |
rs545856366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367032 | TTTCCAAGAAAAAAT[C/T]ACCAAGCAAAATAAC | 494470 |
rs545868884 | snp | A/C/G | 0.000115317 | 0.00759253 | missense | RNF165 | GRCh38.p7 | 18:46450366 | AGGGACTAAATCCCA[A/C/G]CAGACACACCTCCGC | 494470 |
rs545869767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441965 | GTCAGGGGATCGAGA[C/T]CATCCTGGCTGACAC | 494470 |
rs545870362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46361311 | TCCCTGTAGCCTTGC[C/T]CTTCTGAAAAAGAAC | 494470 |
rs545887281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46338105 | GTAGCATTTCAGACT[C/T]GCCTAAAAACCCATT | 494470 |
rs545889670 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376187 | CCTTGGCAGCAAAAC[A/G]GTCACCTGCCCTTCC | 494470 |
rs545901684 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374168 | AGCTTGAACGAGTCC[A/G]AGAAACTCAGGGGTC | 494470 |
rs545943285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393524 | ATACCCTGTCTGGAC[A/G]CCCCCCGCCACCACC | 494470 |
rs545982633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46394298 | GGGAATCTCTAGTTG[C/T]GTCCCAGCTCACTGG | 494470 |
rs545988081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46443379 | AGCATATCACACTCT[A/G]CCCTAAAATAGAATT | 494470 |
rs546045360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363324 | AGGCCAGGTCTTCTA[C/T]CCTGCAGAAGAGACA | 494470 |
rs546045400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356377 | ATGGTGCAAAATAGC[A/G]CAGGGTCAAAGGGTG | 494470 |
rs546061146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349632 | GTGGTCACAGTTCTG[G/T]AGTGGGCTCTTGGCC | 494470 |
rs546087270 | in-del | -/A | 0.00162042 | 0.028418 | intron-variant | RNF165 | GRCh38.p7 | 18:46367025 | ACTTAGTTTCCAAGA[-/A]AAAAATCACCAAGCA | 494470 |
rs546127407 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402544 | TTTCGAGAGAATCTC[C/T]CTCTGTCACCCACGC | 494470 |
rs546130049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436038 | AGATATCTTTGTTGT[C/G]CTGAGATGCAGGGTC | 494470 |
rs546143814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393313 | CTCTTGTTCTGGGCC[A/G]GTGGAGAGCAGTCTC | 494470 |
rs546155837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383326 | GTGATTTATTTAAGT[C/T]GCTAATGAGGGAACC | 494470 |
rs546160550 | in-del | -/AGGG | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439481 | CTCAAGGGTGCTTTT[-/AGGG]AGGGCCTAGCTGCAC | 494470 |
rs546206143 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46416738 | GGTCTAGGACAGTTT[A/T]TTTGTATATCACATG | 494470 |
rs546218327 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458108 | TCACCTAGATGTTGT[A/G]AGGATTCATATTCTC | 494470 |
rs546229387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378736 | GGCCACCATGTCTAG[C/G]GCAGAGGGTGCAAGA | 494470 |
rs546268997 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412551 | GGAGATCAGGGAGGC[C/T]GATGTCCAGTCATGT | 494470 |
rs546293748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396863 | AGGTTCTTGGCATGA[C/T]GTGGGTTGGGTGGAT | 494470 |
rs546305284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46348387 | ATTGGCCAGCGTTGC[C/T]GGTGGTTGATTGTCT | 494470 |
rs546325506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46405413 | TAGACCAGACAGACA[A/G]TGGGAACAGTGAGGT | 494470 |
rs546384896 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46399827 | CTGCTCTTATTCTTC[C/T]CCTTCAGGTCTGGCT | 494470 |
rs546386470 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438210 | GATATTCCTGTGACC[C/G]CTTTAGACACTTAGC | 494470 |
rs546426838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416360 | AAGAAGTCATCATCC[A/G]TCCTTCCCTCCCTCC | 494470 |
rs546427144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336608 | AGAGAGTTTGCCAGC[G/T]TAAATCTGTTCTTTT | 494470 |
rs546432088 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46453938 | GCCATCATAGAGAGA[G/T]TCTGTCTCTACAATA | 494470 |
rs546465760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337578 | GTATCGTGTGCATGA[C/T]GACATTGTTACACAC | 494470 |
rs546474990 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456916 | AGGAGGGGCCCAGGC[C/T]GCGGAGAACCCAGGT | 494470 |
rs546506214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415177 | TTGACTGACACTCAT[C/T]GAAATGTGAATACCC | 494470 |
rs546514085 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46410562 | TGACAATTGCTGTCA[A/G]TTTCGTCCCAGGAAG | 494470 |
rs546516687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46394824 | TTCCTGAATAAACAA[A/G]GGAAGGTTGCAGGTA | 494470 |
rs546540918 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442032 | GCCGGGCATGGTGGC[A/G]CGCGCCTGTAGTCCC | 494470 |
rs546542713 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46367511 | ACATTCTTTGAGGCA[C/G]GGTAGAATTGGTTAT | 494470 |
rs546550099 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441406 | GTAGTTTGTCTTTCA[A/G]TAAATTTTCTCATTT | 494470 |
rs546575233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404435 | CACTCCATCTTCATT[C/G]TATCATTTCACTCTC | 494470 |
rs546601331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46434119 | AGGTCTGGAGTAGTT[A/G]TGGGGCCCTGGGTAA | 494470 |
rs546631150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421761 | TTGCTGCTTAATTGT[C/G]TCATACCCATGGGCA | 494470 |
rs546633496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442930 | CCCTTGGTTCAAAGT[C/T]TACCTTGTCTGATGT | 494470 |
rs546639728 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46355953 | GCCTCTGTAGTGGGC[A/G]GAGGCATGGCTGAGG | 494470 |
rs546666878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355014 | GAGTGCAGTGGTACA[A/G]TCTCAGCTCACTGCA | 494470 |
rs546702742 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383019 | GAACCTCATGCACCC[A/C]CTAGCCTGCTGGGCC | 494470 |
rs546707403 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395694 | GCTCCAAGGAGCCCA[A/G]GATCTCAGCTGGTGT | 494470 |
rs546731787 | in-del | -/A | 0.393619 | 0.204631 | intron-variant | RNF165 | GRCh38.p7 | 18:46381830 | GCGAGACCCTGTCTC[-/A]AAAAAAAAAAAGATG | 494470 |
rs546745087 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46428720 | TAAAAAGCTCAATAA[C/T]TTTTTACATAGAATA | 494470 |
rs546766270 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393523 | CATACCCTGTCTGGA[C/T]GCCCCCCGCCACCAC | 494470 |
rs546809178 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46377560 | GCAGCAGAGCAGTAT[G/T]TTGTTAGATGAAGGA | 494470 |
rs546815049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350471 | CATGAGAGAAGGGAG[C/T]GCTGAGGTATGGGGG | 494470 |
rs546818395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388442 | CTGCTCAATCCTGTG[G/T]AACAATTTGTTCCTG | 494470 |
rs546819401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372367 | GGTCCCACCATTGCT[C/G]AGCTGAGAGCAGTAA | 494470 |
rs546880933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372789 | GTGCATTTCGAGAGC[G/T]CCAAAATCCATACGT | 494470 |
rs546883376 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46405000 | CTCTGTTGTTTCCAC[C/T]GGACCACAGAGCTTA | 494470 |
rs546896810 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458412 | CTCATTTGCACTGCT[C/G]TGTAAGCCTCCCCCT | 494470 |
rs546935223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46423739 | CCCAGATTTCCTGGC[C/T]TCCAGATCTTCATCT | 494470 |
rs546944839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399353 | CAAAGGATGCTGGGG[G/T]GCTGGCCCCTTCCCT | 494470 |
rs546962035 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382360 | GCTTCAGATTTACTA[C/T]ATAGCTCAGAGCCCT | 494470 |
rs546997032 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46438702 | CAGATGCACCTGTGA[A/G]TATGAGGGGCTGACC | 494470 |
rs547006684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383980 | CTGTCAGACAATGCT[A/G]TAACATGACTTTAAA | 494470 |
rs547032058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46446453 | AGGTGGGTGGATCAC[C/T]TGAAGTCAGGAGTTC | 494470 |
rs547062639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358386 | GAATGTACACAGCAC[A/G]CCCAGCCATAGGACA | 494470 |
rs547086483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46364742 | CCGTGCTCACATACT[A/G]ATGGAGGGTGGCCTT | 494470 |
rs547169175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388911 | GAAAAAAAAAGACAC[A/G]AAACATTGAAGCAAT | 494470 |
rs547172528 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429360 | TGCCCTCCACACCAG[A/C]GGCAAAATCCCTCAA | 494470 |
rs547175635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352382 | ATTTCATGTGGACCA[A/G]AGCTCCCAAATCTGA | 494470 |
rs547217322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46423098 | TTCCAGTACCCAGGA[A/G]TTTCCTTCAACCTTT | 494470 |
rs547237074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352829 | TAGGGGTTGCATTAC[C/T]GTAGAAGGAGAGAAC | 494470 |
rs547273766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338710 | TTGTCAATTACACCT[A/G]TTCAATTTCAGCCCA | 494470 |
rs547276469 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419637 | TGAGCGGAGTGGGCA[C/G]CGCACAGCTGGACCA | 494470 |
rs547281273 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46359002 | CAGGAGAGCTAGGCT[C/G/T]GAGTCCTGACACTGA | 494470 |
rs547292510 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385658 | AGTGTCAGCTGTCCC[C/G/T]CTTTGGAGCATGAAC | 494470 |
rs547302014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378888 | ACCCCGCTATGGTCC[C/T]GTCTAACCCACCTTC | 494470 |
rs547320116 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46425839 | AGGCCATAGGCTGGG[A/G]GCTTATGAACAACAG | 494470 |
rs547339708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46411869 | TACACCTCCCTGGTC[C/T]CTTTCTCCTGAACCT | 494470 |
rs547363952 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403209 | AGAGTGTGCCAGAGT[C/G]TGGCACCTGGCAAAA | 494470 |
rs547377870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341442 | GGCAGGAGGTCTTTG[A/G]GGTGCTTTGGAGAGT | 494470 |
rs547378881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375447 | TAATCCTAGCTACTC[A/T]GGAGGCTGAGGCAAG | 494470 |
rs547379088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381872 | AACTCCAAAGGTGGG[A/G]TTTCAGGCACCACCG | 494470 |
rs547391237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46375979 | CCATTTTCTTGTCTA[C/T]GAAGTGGATGATAAT | 494470 |
rs547410713 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407646 | AGACTCCAGCCGTGG[C/T]TTGCGTGGGAAAAAT | 494470 |
rs547440936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431535 | CTGTGGAGGGTGCAG[A/G]GGAGGGGCACACGCT | 494470 |
rs547470280 | snp | A/G | 0.00478085 | 0.0486577 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461464 | AGCCTGGCCAACATG[A/G]TGAAACCCTGTCTCT | 494470 |
rs547498078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396383 | GAGAGAGAAGTGAAG[A/C]GTTAGTGGGTTCAGG | 494470 |
rs547512054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391136 | ATGGCACCAATCGCC[C/T]CCATAAACAGGGTTC | 494470 |
rs547552271 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46349818 | TGACACGCTGCACAC[A/G]ATCCACCCAGCACCT | 494470 |
rs547556121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46397632 | TGCTGAGGTGTGAGG[A/G]TGTGTGTGTGTGTGG | 494470 |
rs547570499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409043 | AGTGGAGATAATAAC[A/G]GTAGCTACACCATGG | 494470 |
rs547583009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403345 | AGAAGCCTGTGCTGT[A/G]CTCCTAGAGAAAGCT | 494470 |
rs547583927 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46430768 | TTTTCTTGTTTTCTC[A/T]TTGATCCTTCTTCAA | 494470 |
rs547610456 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371123 | AGGAACTCCCATTTA[G/T]AAAACCATCGGATCT | 494470 |
rs547620502 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436368 | TGCAGTAAAATGGTG[A/G]CATTTGGGGAATCTG | 494470 |
rs547671450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419792 | TATGGGATCTGGCAG[C/T]TCCAAGAAGCCTATA | 494470 |
rs547700424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386040 | TGGGCCTCTTTCTCA[A/G]CTGTTTTGCCAAAAA | 494470 |
rs547740441 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431748 | TGAGAAAGGGGAGGA[G/T]CCCTGGGCAGAATTG | 494470 |
rs547786420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432153 | GCCGGGTCTACTTCT[C/T]GGCCTCATTAAAGGC | 494470 |
rs547786463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46439913 | TTGGTTCACTGTAAA[C/G]TCTGCTTCCCAGGTT | 494470 |
rs547792677 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399309 | AAGCTTGGACGTGGG[C/T]TGCGCTTGCATGGGG | 494470 |
rs547794257 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420845 | GCAGGACTCCATCTT[-/A]AAAAAAAAAAAGAAA | 494470 |
rs547809382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341912 | AGCTTTGCCTCCACT[A/G]CTTTGCAAAAGGCCA | 494470 |
rs547827131 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377918 | TCACCAAACATCCAA[C/G]AAGAAGTTCTGGGGC | 494470 |
rs547843429 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403015 | TCCTGTTGAGCTTGT[C/T]GCTCTCAGAACACGA | 494470 |
rs547846771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432787 | CGTCTCTACTAAAAA[C/T]ACAAAAAATTAGCCG | 494470 |
rs547848373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415052 | AAATGGGCAGGGGAG[A/G]GAGCAGAAGCCAAGT | 494470 |
rs547850283 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333124 | CAGGGCACATGTGAC[A/T]CGGTGGCTGCGCCTC | 494470 |
rs547853290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46365268 | CTCTTCAGAAACCCA[C/T]GCCCCCTGTCAGTGG | 494470 |
rs547853496 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438046 | ACTTAGGGTCTGTAC[A/C]GCAACCAGACCACAC | 494470 |
rs547856154 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335815 | TAGGCCTGTTTGAAC[C/T]GCAGTTTTTTGTGTG | 494470 |
rs547888796 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333856 | GGGCTCCACGCTTCC[A/C]GTGGGGCTGACCCCT | 494470 |
rs547895722 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46353535 | GTTTGCTCCCCGTCC[A/G]CTACCCCACTGTCAC | 494470 |
rs547916659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46359074 | CTCAGTTGTCCTCCC[C/T]GTAAAAGGAGAGGCA | 494470 |
rs547917096 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332975 | AGCCTGATTGTAGGC[A/G]TAGGGTTGCCTTGGG | 494470 |
rs547926474 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443971 | AACTTTTTGAAAAAG[C/T]CTTTATTTCACTGTC | 494470 |
rs547927243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46448112 | GGCTCCCCTGCGCTC[C/T]GGATTCCATATGACC | 494470 |
rs547985558 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374921 | ATTTGGTCTTGAGGG[C/T]CTCCCCAGTCACTGC | 494470 |
rs548004093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46440118 | CAGGCGTGAGCCACC[A/G]CGCCCAGATCTCATG | 494470 |
rs548018092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46440724 | GTATCAATCAAGATC[C/T]GAATAAGTTTTACAC | 494470 |
rs548019084 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46357993 | TTGTCACAGTGTCTC[A/G]GTGTCTCCACATGGC | 494470 |
rs548084675 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46360736 | CCTCCTTCCTGCAGG[C/T]CCCCCTTGCCCTCTA | 494470 |
rs548091453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455627 | AGATCACCTGAGCTC[A/T]GGAGTTCAAGACCAG | 494470 |
rs548098498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381958 | TGGCTTAAGCACCCG[C/T]AGGGCCTCCCTTCTC | 494470 |
rs548121262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46377137 | AGCACATGGCCTGAC[C/T]TTGGATTATTTAAAT | 494470 |
rs548126767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420345 | GAAACAATTCTCCCA[A/G]GAGAAATGGGAGGCA | 494470 |
rs548172794 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46341953 | TGGGAGCAGGGGGAA[C/T]GGGAGGGAGCCCGAC | 494470 |
rs548174353 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46456181 | TGCTTGTTTGCTTGT[A/G]CACGTATGTGCCAAG | 494470 |
rs548182422 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46371581 | AGCTTGGATGATATC[C/T]TGGGCATGAAGCCCC | 494470 |
rs548212030 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333977 | GTCCCCGCTGTCCCC[A/C]GCGGTTCCGGCGAGG | 494470 |
rs548214285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46376014 | CAGAGGGTGGCCTGA[A/G]GGTGAGATGAGGCAG | 494470 |
rs548245147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366717 | AATGTAGCTCTGCCA[C/T]GGAAGCTTTCTCTGA | 494470 |
rs548282223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391656 | GGTGACATATTAAAA[C/T]GTTTGCACACCACTT | 494470 |
rs548328630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448237 | CAGCTCCTCTGTATA[C/T]CAACACCCCATGCCC | 494470 |
rs548344104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385718 | CTGTGCCCCTCCCCA[A/G]CCTCTTGCTCCAAGC | 494470 |
rs548348133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46392795 | CCTGTGTGAGGAACA[C/T]GCATGCAGTGGCACC | 494470 |
rs548354674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386170 | ACCTACATGCCAGGG[G/T]TTCTCTTCCTCTGGC | 494470 |
rs548418594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421090 | CTTCTTCTGTTAGTT[G/T]ATTGTGATGCACACT | 494470 |
rs548420896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441019 | TAATTTTTAGATACA[A/G]GGTCTTGCTCTGTCA | 494470 |
rs548473679 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46360767 | ATACGCCTGGGCACA[A/C/G]GAGGCGGGTATGTGG | 494470 |
rs548488939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342405 | TGGAAAAGGATCTTT[C/T]CAGCTAATGGCCTGC | 494470 |
rs548489074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382542 | TTTTCTCACTGCTTA[C/T]TTTACTTACTACTGA | 494470 |
rs548516619 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46409161 | TACAACTGCAGGCCT[C/T]CAAGATCAGGAAAAG | 494470 |
rs548519980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387667 | AGGGTGCAAGGGCCC[C/G]TGAATGGGAACAGAC | 494470 |
rs548523363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46335140 | GCGCTGCTGTGCCCT[C/T]CTTGGGTCCGGCTGG | 494470 |
rs548541611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354458 | TGATCAGGGCCCATA[G/T]GCGCCCAAACCCAGT | 494470 |
rs548551345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46376756 | AGCCACTGCAACATC[C/T]GCCTCCCAGGTTCAA | 494470 |
rs548558280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373400 | AGGGACTGGGCAAGA[A/G]TCACCCAGCAAGTCG | 494470 |
rs548616677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355777 | CATGCCCCCTCAAGA[C/T]CTTCTCCAAACCCAG | 494470 |
rs548630070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409694 | TTTCTGCCACTCAGT[A/C]CTCACTCTGGGTCTT | 494470 |
rs548647442 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382227 | TCCCCTCCTGCTGAG[A/G]ACAGGTCCCATGGAG | 494470 |
rs548666049 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343109 | CCATAGGTTCTAGGC[C/T]GCTTGGTGCTGCTCT | 494470 |
rs548684408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448726 | TGGCTGCAGAGTGCC[A/G]AATCATGGGTCAGGC | 494470 |
rs548695115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379245 | TAATCTCTTTTGGGG[C/T]GCATCTAGTCCACAG | 494470 |
rs548701759 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404328 | GAATTATTCCCAAGT[A/T]ATTTTGATGGATGTG | 494470 |
rs548721341 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369412 | TGGGAGAGGACAGGG[C/T]AGGGAGGAAGCTGAT | 494470 |
rs548725751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46398768 | GATATCCCAAATACT[C/T]GGGCTCCTCCCTCAT | 494470 |
rs548743044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46339186 | TAAATTTTCATTTAC[A/G]GGAGACTTAGAAAGC | 494470 |
rs548754023 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46441616 | TGATCAGGCCAGGCG[C/T]GGTGGCTCATGCCTG | 494470 |
rs548790945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46433554 | GATGGGGTCGGGTGA[C/G]GGGGCAGGGCCAGGG | 494470 |
rs548809366 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415333 | AGACCACCCTGGCTA[A/C]CACGGTGAAACCCCA | 494470 |
rs548816730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406696 | GGATCACATGTGGGC[C/T]CACAGTGTACAGGTT | 494470 |
rs548817851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355156 | CAGGGTTTCACCATG[A/T]TGGCCAGGTTGGTCT | 494470 |
rs548826708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46452255 | GAGTATAGGGTATAT[C/G]GGAAAACACTGTACT | 494470 |
rs548851652 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46395605 | GGACTCAAACCTGAG[C/T]CTGTATGGCCCCAAA | 494470 |
rs548863283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444846 | TCTAATTTACTGTTA[C/T]TCTAACCCAGTGAAT | 494470 |
rs548864413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46428133 | GGCCAAGGGGAGGCC[A/G]GGCGCAGTGGCTCAC | 494470 |
rs548947208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46364103 | TAGGCAGGGACCACC[A/G]TGTCCGGCTAATTTT | 494470 |
rs548957473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357814 | TCTCTGACAGTGCTG[A/G]AGGCTAGAAGGCTGC | 494470 |
rs548997714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451485 | CATCCAGATAATGGA[A/T]TATTATTCTGCAATA | 494470 |
rs549035560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412314 | CCAGTTGGCCAGAAG[A/C]AGACCCACAGCCTTG | 494470 |
rs549059901 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46406181 | GTGCACCCCCAATAC[A/G]CCTGCATCCAGAGTC | 494470 |
rs549082420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444093 | TTTGTCTTCTGGCTT[A/G]CTTTGTTGTTGATGG | 494470 |
rs549093904 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455177 | ACAATATAAATAGTT[C/T]ATAACAATGGCTACA | 494470 |
rs549137248 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46363716 | CACCGTTATAATGAG[A/C]TGGCCTTGTAGTCCC | 494470 |
rs549151158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425167 | GCTGAGCACAGCGGG[A/C]AACCTGACACCTGAG | 494470 |
rs549191099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46437290 | GCGGGGGCCAGCCTA[C/G]TGGCGCCGAGGGGTT | 494470 |
rs549205208 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46437873 | TGGAGGTCTCTAAGT[A/T]CCTGGGACCTGTGGG | 494470 |
rs549234779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340664 | GACCTGGAAGGGTGA[A/T]CTTAGGCCACTGCTT | 494470 |
rs549239926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46357120 | CAAGTATGAACTCGT[C/T]GTTTTATCATTAAAG | 494470 |
rs549259650 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425512 | CAGTGCCTCTCAGCC[C/G]TGGAGTCTTGAGGAT | 494470 |
rs549316501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46452426 | CTGGGATTACAAGCA[C/T]GTGCCACCACACCCA | 494470 |
rs549336631 | snp | A/C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365198 | CTGGCTGAAGGGGAG[A/C/G]GGGTATGGATGGCAG | 494470 |
rs549337736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424669 | AAGCTATTTGAGGCC[C/G]CTGCCAGCAAAGAGA | 494470 |
rs549345730 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46422598 | TTACTGCCATGCTTC[C/T]TCCCCCCGACCGAGG | 494470 |
rs549374943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369396 | TGGGGTGGCAGGGGG[A/G]TGGGAGAGGACAGGG | 494470 |
rs549379428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46431339 | GGTCACTAAAGCTGT[C/T]TAGAATGTCTGTGTG | 494470 |
rs549400884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418706 | ATGATTGAATAAGTC[A/G]AATTCTGAATCAAAT | 494470 |
rs549401728 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46453379 | GGGAGTGTTTACTCC[C/T]ACCGAGGATGCACGC | 494470 |
rs549423063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402559 | TCTCTGTCACCCACG[C/G]TGGAGTGCGTGACTC | 494470 |
rs549424511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46352183 | CTCCCCTCCTCCTTG[A/G]GGGCCTTGGGTCCTA | 494470 |
rs549444047 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46340170 | CGGCTTAACATTGTA[A/T]GAATGTGAATTAGTA | 494470 |
rs549451099 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46449334 | GATATTTTGCTCAGC[A/C]TGGAGGTTTTTTTTG | 494470 |
rs549510748 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460073 | TTCGGCACCCAGTTG[C/T]CCTTGGCCACCACCT | 494470 |
rs549544589 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46364693 | TTCACATGGCTTCTT[A/C/G]GGACATTCCTGTCCT | 494470 |
rs549588901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445830 | CTAGTGGTTTAAAGT[A/G]GAAAGGTAAACTTAA | 494470 |
rs549619854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364841 | GGCTCCTGCTCTCTG[C/G]GCAGGAGGCTTGGGG | 494470 |
rs549644777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363705 | GCTAAGATTCTCACC[A/G]TTATAATGAGCTGGC | 494470 |
rs549698307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438592 | TGCCATGTGAGGCAG[C/T]GCAATGGATTGAGCC | 494470 |
rs549703245 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46335240 | GCCTTTGCCCCGGGC[A/G]GCGGTTGACAAAGCA | 494470 |
rs549712295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385294 | GCTCTCCTGGGAGAT[G/T]AAAGTGGTGGCTTGT | 494470 |
rs549724626 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46385500 | GTGGCTCTACTGACT[C/G]TAGTGGACAGAGAAC | 494470 |
rs549724695 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350528 | AGCATGGTCAGGAGC[A/G]CCCCCAACCCCAAGA | 494470 |
rs549726471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380643 | AGAATCTCCTATGAC[C/T]GGGAGCTGGGAGCAG | 494470 |
rs549785479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444933 | ATATCTCCTCTTCTA[C/T]ATATTTTACTCTTCT | 494470 |
rs549791224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390841 | AATGGGGATATTAAT[A/G]CCTCATGGGGTGTGA | 494470 |
rs549794161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46413833 | AAAAACACTCCTCCC[C/T]CTGCCCCAGCTGCCC | 494470 |
rs549832724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406889 | CTCTAGCCCAGAATC[C/T]TTACCCTGATGGGAC | 494470 |
rs549891929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46407489 | TCCTATCACCCGACA[A/G]GACAGTGTTAGCCTG | 494470 |
rs549894106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400993 | GCAGAGATGACCTCC[C/T]GCAAAGCTAAGCCTT | 494470 |
rs549904564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46401881 | TTCACACTGGGAGGG[A/G]CCATCAGCTTGCATC | 494470 |
rs549911022 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365886 | ACTGAGGAATGACTG[C/T]AGGGGAGGTAGAAAC | 494470 |
rs549918112 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403395 | GCCCTCCCTGCCCCC[C/T]GTCTCCCTCTAGGTT | 494470 |
rs549930427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357881 | AGGCACCAGGGAAGA[G/T]TCCTTCCTCATCTCT | 494470 |
rs549932219 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460850 | GCACATATATAAATA[C/T]AATTTGCACTTGTCA | 494470 |
rs549946524 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46419716 | GGCAGGGGCAGCCAA[G/T]GGGCTGATGGAGCCC | 494470 |
rs549954762 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346430 | AACAGAAACTAAGAG[C/T]TCCCTTGGGTTTAGG | 494470 |
rs549990618 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46370966 | TAATAAAGACGTACG[C/T]GACACTGGGTAATTT | 494470 |
rs549992930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402612 | CTTAAGTGATCCTCC[C/G]ATCAGCAACCTCCCA | 494470 |
rs550008267 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422409 | ACTCAGAAGATACAG[A/G]AAACAAGATTCTGAG | 494470 |
rs550028128 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332980 | GATTGTAGGCGTAGG[A/G]TTGCCTTGGGAGTTT | 494470 |
rs550042548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375347 | CACTTGAGCCCAGGA[A/G]TTCAACACCAGTCTG | 494470 |
rs550063221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431983 | CAAAAATTTGTTGAC[A/G]TCTGTTGCCTGCTGA | 494470 |
rs550065144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425223 | GGGCTTCCGGGGAAC[C/T]CCAGAGAAGCCTGGG | 494470 |
rs550066584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352760 | GTAACCACCCTTAGC[C/T]GTAAAGGAAGCTGGG | 494470 |
rs550092877 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382655 | CTCTGTCTATTGTCC[A/G]TCTCCTCTGATGTCC | 494470 |
rs550105814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46346342 | GTGTACTACAATTCA[C/G]TGGCATTACGTACAT | 494470 |
rs550137897 | snp | C/G | 0.0158469 | 0.0875917 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460240 | AAAGAAATCCCCTAA[C/G]CCCCCCGCCTGTAGG | 494470 |
rs550176087 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46383463 | AGACACAAGACTAGT[A/T]AATATCTAGCAGGAC | 494470 |
rs550212368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46397471 | GTGTGTGTGTGTGTG[A/G]TCATGCTGAGGTGTG | 494470 |
rs550225338 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362865 | GTTCACTCAGTCCTT[C/T]CACTTTCAGATATGG | 494470 |
rs550267849 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46383024 | TCATGCACCCCCTAG[C/T]CTGCTGGGCCAGCTT | 494470 |
rs550274536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411118 | CTTTTTGTTGGCATT[C/T]CCTTAGCACCTGATA | 494470 |
rs550279612 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | RNF165 | GRCh38.p7 | 18:46341338 | GGGTGGGACAGGCGT[G/T]GGGGGTAGGGAGGAG | 494470 |
rs550306494 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333680 | GTCGTGTGCACTAAG[A/G]GCGCTCGTGCCCGTC | 494470 |
rs550342354 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421277 | CACCATCAAATTCCA[C/T]GCAGTTTTAAAATGC | 494470 |
rs550344265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451706 | GTTACTAGGGAGGCT[A/G]AGGCAAGATAATTAC | 494470 |
rs550348441 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46455337 | TGTAAAGGGTGTTGA[C/G]GGGGAGTGGATGGTG | 494470 |
rs550348889 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46415983 | ACACCCAGTGCTGCA[A/C]CAGCTGGCCACTCAG | 494470 |
rs550354272 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386677 | TAGTGAACAAAACAG[G/T]ATCTTTTCCCTGTCC | 494470 |
rs550357672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371039 | TAGGGAGGCCTCACA[A/G]TCATTACAGAAAGCA | 494470 |
rs550366923 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357503 | GGGCTGTGCTGGCAG[A/G]GGTGGAGGTGGGATG | 494470 |
rs550387588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336670 | CCATTTCAGAATAGA[C/T]GTAGAGAAATAACCA | 494470 |
rs550403753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365311 | ACTCCCCAACTCAGG[G/T]TTACGCAGGGTCGAG | 494470 |
rs550448265 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405573 | GGGCGAAGGAGACAG[A/C/T]GCAAGAGGAAAAATG | 494470 |
rs550465297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338358 | CACCCCTATCCAGGG[C/G]CAGCAGCGGACCTGT | 494470 |
rs550491908 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46378813 | GGAGCGCTGCTATGG[A/G]TGGTGGGGAGCTGCA | 494470 |
rs550501591 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46434373 | ATGTTAACACCAATA[A/G]TATATTTTTATGAAA | 494470 |
rs550504834 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360820 | GCAGGGTCACAGGGC[C/G]CACCTAAACACTGTT | 494470 |
rs550506319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46373249 | GCTCTTGGACTGGCA[C/T]GGCTAATGCCCAGCC | 494470 |
rs550506602 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46440313 | CATATTCACATAACA[-/T]TTTTTTGCAGTATAT | 494470 |
rs550530505 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410817 | CATCGTTTCTTCAAT[C/T]GTCCAGGCTCATGAA | 494470 |
rs550561207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429386 | CTCAACCGCAGTGCG[C/T]TTTTAACTCTTCTTC | 494470 |
rs550569424 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408850 | GATGAGCCTTCATCC[A/C]AGTGGTACTGTTATC | 494470 |
rs550569588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362448 | GGAGTGTGTGCGCGC[C/G]CCAAGGGGTTTGGCT | 494470 |
rs550574506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428627 | GCACTTGGAATGAGG[C/T]TAGGGCGAATTGACA | 494470 |
rs550580685 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436311 | AAGTATATACATTGT[G/T]GGGGAGAGAGAAAGG | 494470 |
rs550607362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416456 | GCATGGAGACAATAC[A/G]GGGACTTTTCTCTTT | 494470 |
rs550630646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350510 | GGGGTGTCAAGAGGG[A/G]CAAGCATGGTCAGGA | 494470 |
rs550642224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343221 | CTGCCCACCAGCAGC[C/G]CCTTCCATCGAGAGG | 494470 |
rs550663875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46400343 | CATTTCTGTGTTCCC[C/T]GGAACAGGGATTGGA | 494470 |
rs550674584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337841 | GATATGGTGACTTTA[A/G]TCTCATTTAGTCCAT | 494470 |
rs550681155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46343869 | TAGCCCACCCAGGGC[A/G]TGGGCTAAACCTGGA | 494470 |
rs550733224 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379260 | TGCATCTAGTCCACA[-/G]GTTTTTAAGCTTATT | 494470 |
rs550736998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423885 | AAGAACTCTTTCTTC[C/T]TCCTTTCCCTCGTTC | 494470 |
rs550745212 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426896 | CAGGGAAAATTGCAG[C/G]TTGTCTATTAATGGG | 494470 |
rs550752562 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46356982 | GGGGACAAGTGGCTT[G/T]GTCCAACTCCCACAC | 494470 |
rs550762227 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345684 | AATTTGGGGAAAACA[A/T]GAAGTTTATATTAAA | 494470 |
rs550786804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372828 | TTCTAACCACACTGC[A/G]GTGCTATTATGTAAG | 494470 |
rs550792939 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458266 | AGCAGAGAGATAAGA[C/G]GACAGAAGAATGGAG | 494470 |
rs550793307 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46450044 | AATTCAATTAGTCAC[A/G/T]TTAAGTGCTTAGAAC | 494470 |
rs550799314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46367936 | TCTGATGCCCAGTTA[C/T]GGTTGAGAATCATCT | 494470 |
rs550800458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424438 | CCATTTATTTGGAAG[A/G]GGGATTTCGAAGGTC | 494470 |
rs550803982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350969 | TGCCCCTGGCGTGTG[G/T]GCAGGAGGTGCAGCC | 494470 |
rs550808477 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46344967 | TCATGTCCCTCAGGA[C/T]GGAGGGGGACATCAG | 494470 |
rs550813156 | in-del | -/C | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461202 | TGACCTTGAGCAAGT[-/C]CCCTTGGCCCCTGAG | 494470 |
rs550829787 | snp | C/G | 0.00304564 | 0.0389043 | intron-variant | RNF165 | GRCh38.p7 | 18:46447728 | TCCCTTGCGCCTATT[C/G]AGTGCCAGTGGTGGT | 494470 |
rs550831445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46450512 | GGTGTCAGGAAGCTT[C/T]AGGGTTAAGAGTAAG | 494470 |
rs550838328 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386946 | GCTACTCCTTTTGGC[A/G]GGGGACACTGACATT | 494470 |
rs550875740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46451681 | ATGGTGGTATGAACT[C/T]GTAGTCCTAGTTACT | 494470 |
rs550877770 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459487 | TGCTGGGTGAGACAG[C/T]GGGCCCTCGTCCCCT | 494470 |
rs550883854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340078 | TCCCTCAATCCTACT[C/T]CACAACTGTCACACA | 494470 |
rs550898686 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347992 | AGATGCTCACGTAGC[A/G]CTTACTCTGTGCCAG | 494470 |
rs550907341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384940 | AGCCCAGAGCCAGGG[C/G]ACACACACAGCTGGT | 494470 |
rs550982236 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46378840 | TGCACAACGGAGGGG[C/G]TGCAGGATAGAGAGG | 494470 |
rs550993769 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354736 | CCTCTTAAAAATCTT[G/T]TAGTGGTTCATAAAG | 494470 |
rs550995491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356601 | CAGGGACTAACTACT[C/T]ACTCTGAACACACAG | 494470 |
rs551131400 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46400015 | CACCCCAGGTGTTCT[C/G]ATCTTCAGCCTCTGG | 494470 |
rs551154509 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46402328 | TCCTTCCCTCTAAAT[C/G]TGATTTTCTCAATCC | 494470 |
rs551156606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384072 | ACAGAGGCAGTCGGG[G/T]TGAAACTGTGGGATT | 494470 |
rs551184878 | in-del | -/TGGGATG | 0.0225045 | 0.103662 | intron-variant | RNF165 | GRCh38.p7 | 18:46375278 | TTGTCCTGGCCGGGC[-/TGGGATG]ACAGTGGCTCACACC | 494470 |
rs551194662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417832 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 494470 |
rs551211025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46412468 | ACAGAGCAGAAAGCA[A/G]CCACCCTCCTGCCAA | 494470 |
rs551218270 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46385787 | AAAAATCAGTGTTTG[C/T]CTTTATATTGGAAAA | 494470 |
rs551244252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400433 | GCTGTTGGGAGAGTG[A/C]CATTATGGCCCCTGT | 494470 |
rs551257618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406058 | CCCATGTACACACTC[C/T]TCCCACATACACACT | 494470 |
rs551280254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373755 | GGGGGGAATTGTTAT[C/G]TGAATCTTACACGTG | 494470 |
rs551292728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373843 | GCAGAGCTGGGGCTC[A/G]CTAGCCCTCAGATCC | 494470 |
rs551298527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368851 | AATGCATGATGACAA[C/T]GTCTACCTGATAGAG | 494470 |
rs551314246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406221 | TTCCACTCCCAATAG[C/T]TCTTGTTGCATTGAA | 494470 |
rs551386224 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345569 | TCTGGCTGGGGGGTG[A/G]ACTAGACGTGTGCGC | 494470 |
rs551386981 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458355 | ACACCAGATTAGCTG[C/G]AATTCTGCCACCTTC | 494470 |
rs551410088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423957 | TTTTCCTCTTTTATC[C/G]AGTATCTCATTATCC | 494470 |
rs551452146 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46411830 | GAATCACAGCCTGGG[A/G]CTGAGCCGTGTATGT | 494470 |
rs551453740 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428772 | ATATGATGAATTACA[A/G]AAACATATATTATTA | 494470 |
rs551481136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338466 | AGCTGCTTCATCTAC[A/G]GCCCTAGGGCCTCTC | 494470 |
rs551516304 | snp | C/G | 1.65985e-05 | 0.00288079 | synonymous-codon, intron-variant | RNF165 | GRCh38.p7 | 18:46450763 | AGCTGTACAGAACAC[C/G]ATTGAGAGGTTCACC | 494470 |
rs551531645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430677 | CATTCCGGTTTCTGA[C/G]AGTCCCCAGCTTTGT | 494470 |
rs551544604 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46432715 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG | 494470 |
rs551554200 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46368489 | TCCCTGTGGGTCTGC[A/G]TGTGCCCAGGTCACC | 494470 |
rs551554998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451344 | GCTAAGAACTAGGAA[G/T]CTAGGATAAGATTAG | 494470 |
rs551600874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340142 | TGGATCTAAACAGCT[G/T]TGTAAAAATTCCCGG | 494470 |
rs551642899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444021 | CTAGGTATATATTTC[C/T]ATATATTTCTAAGTT | 494470 |
rs551665742 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343621 | GCCTGAGTACTCCGC[A/G]ACTTCACTGCCTATC | 494470 |
rs551700064 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455771 | ACCCAGGAGGTGGAA[A/G/T]TTGCAGTGAGCCAAG | 494470 |
rs551715956 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460016 | GGTTGGGTGCAAGCA[A/G]AGGGTGAGCAGGGGC | 494470 |
rs551780828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351041 | TGGGAGCTGCCCTAG[C/T]GGGCAGACCCCAGAG | 494470 |
rs551781478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46413588 | ACCTGGGGAGAGAAG[A/G]TGAGCTGACATTTGG | 494470 |
rs551793640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46407592 | GTTTTTGAAGTTGGA[A/G]GCTAATCCCTTCTAA | 494470 |
rs551802853 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46426864 | GATTATTTTTTAACT[C/T]GAAGGAGTAACTCTA | 494470 |
rs551845185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46357685 | GCCTCCAGATGCCTG[A/G]GAGTCACCCTCCAGT | 494470 |
rs551856315 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395884 | ATTGCTCGCCATTCT[A/G]TGGGAAAGCCCAGTA | 494470 |
rs551858479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46392081 | AATATATACAACACA[C/T]AACATACACACACAC | 494470 |
rs551875752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421167 | TGGGCCCCTATACTC[A/G]TTGCAAAGAATTCCC | 494470 |
rs551935276 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440193 | ATTACAGTAGTCTCC[A/T]TTACCTGTGGTTTCG | 494470 |
rs551942879 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459496 | AGACAGTGGGCCCTC[A/G]TCCCCTCCCCCCTCC | 494470 |
rs551954331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347965 | AATAATAATAACCAT[A/C]AGGGCAGTAGCAGAT | 494470 |
rs551981645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46452615 | TAAACTAGAACTGCT[C/G]TACAAAATAACATTT | 494470 |
rs551982361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46456356 | GGCTTTGTTTCAGGC[G/T]GATCTGAAAGCGCTT | 494470 |
rs551994183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421694 | TTCCCTTACTCCTGG[C/T]CCATGATGGCAACTG | 494470 |
rs551996259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342500 | AGACAGGGAGGGTGC[A/G]TGGTGGACCAGAAAC | 494470 |
rs552017967 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46425787 | CTCCTCCCTGGGAGG[-/C]CCCCCCGTCTTAGTC | 494470 |
rs552025416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380393 | CCCAGAGGAACTTGC[C/T]TAAGGTTTCTTTGAG | 494470 |
rs552104446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448772 | TTGGGCTCCTGACAT[G/T]GCAAGCTGCATGGAA | 494470 |
rs552117008 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RNF165 | GRCh38.p7 | 18:46398080 | TGTGGTCATGCTGAC[A/G]TGTGAGGGTGTGTGC | 494470 |
rs552122066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46415505 | TACTCCAGCCTGGGC[A/G]ACAGAACAAGGATCT | 494470 |
rs552122506 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349188 | TTAGCACATTTGGAC[C/T]GCAGTAACAAAATGC | 494470 |
rs552122875 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372807 | AAAATCCATACGTTT[C/T]CTTTATTCTAACCAC | 494470 |
rs552130988 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46344681 | AAGGGACCATACCTG[-/C]CCCCCTCTGCCTGTG | 494470 |
rs552183715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409773 | GGCGTCTTGCTTTCT[G/T]GGCTTCAAGGCATCC | 494470 |
rs552226268 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46371726 | TCCCAGCTTCAGGTG[C/T]GCTTTCTTCCCAGTG | 494470 |
rs552230795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442322 | TTAGATCATGACTTT[A/G]GGTTTTCTTTTCTAA | 494470 |
rs552231289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427443 | TCATGGCAGGAGGGG[C/T]TGCTGCGAGGCAGGC | 494470 |
rs552231725 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377702 | CGCATGAGGGCAAAG[C/G]CATGAGAGATCAATA | 494470 |
rs552243809 | in-del | -/TCATTCAT | 0.0226296 | 0.103936 | intron-variant | RNF165 | GRCh38.p7 | 18:46421366 | CTCACCTGTTCGTGA[-/TCATTCAT]TCATTCATTCATTCA | 494470 |
rs552246493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360533 | GTCCTTTTCTGAAAG[A/G]CATTTCCATGGCAAC | 494470 |
rs552259831 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351355 | GCAGTTCCCTCCAGG[A/T]GCCCCTAGTTCCAAG | 494470 |
rs552299785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441699 | CCAGACCATCCTGGC[C/T]ATCATGGTGAAACCC | 494470 |
rs552342481 | in-del | -/AGAGAGGTTTCTTGCC | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46437691 | ACATCCCAAACCCCT[-/AGAGAGGTTTCTTGCC]CTCTTTCTTGCCCAT | 494470 |
rs552358428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382606 | AGGCTCAGTTAGCCT[C/T]GCATGACTTAAGTTT | 494470 |
rs552359240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367861 | CTGCTTCTGGATATT[C/T]ATTGCAGTTGGTGTG | 494470 |
rs552363359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46434424 | TTAGTGAGAAGAATG[A/T]CTTTTTAAAACATAT | 494470 |
rs552397984 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46393384 | AGACACCTTCCCGCT[A/G]ACCACCAGCTCTCTG | 494470 |
rs552401766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415720 | CTTTCTAACCCTTGA[A/G]CCTCAGTTTCTTCAT | 494470 |
rs552458900 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456841 | CAGAATGGCGACTGT[A/C]CCCATCCGCCTGGCT | 494470 |
rs552461200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410473 | GCTGTGAGACTGAGG[A/G]GCAAACTCACCATCC | 494470 |
rs552461980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46413600 | AAGGTGAGCTGACAT[C/T]TGGGAAGAGGAGTGG | 494470 |
rs552507997 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380123 | GGAGTGCAGGGGCCT[C/T]GAACCTCTGCCTTCT | 494470 |
rs552535945 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46420689 | ATCTCTACTAAAAAT[A/G]CAAAAATTAGCCAGG | 494470 |
rs552556221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429175 | TGTGGGAATTAAAGT[A/T]CTAGATAATTCTTTT | 494470 |
rs552570394 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368084 | GGCTTGAGACTCCAC[A/G]TGGGTAATTGTGATG | 494470 |
rs552610385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415535 | TGTCTCAAAAAAAAT[A/T]AAAAAAATAAAAAAA | 494470 |
rs552614350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46334561 | CGAATTTGGGTCCCT[G/T]CCTCCCCAGCCCCAT | 494470 |
rs552618675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416509 | AACATTGAGAGCACA[A/G]CTCAAAATTGAGTCC | 494470 |
rs552633834 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46404381 | GACAGGAAGACATGA[C/G]CAGGTATTAAGCACC | 494470 |
rs552653197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46335432 | AAAAAATTCCCACCT[C/G]CCAAGCAAATCCGAG | 494470 |
rs552697223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404969 | AGACATATTCAGCTC[C/T]GTTTGGCTCCAAAGT | 494470 |
rs552698841 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46398824 | GTTACTGTCCTTTGA[A/C]CTGCTGGCTTCTGCC | 494470 |
rs552707910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393835 | GCTGGGCTCTGGAGT[C/T]TGACAGACCTGGGTT | 494470 |
rs552709352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399307 | CAAAGCTTGGACGTG[G/T]GCTGCGCTTGCATGG | 494470 |
rs552723943 | snp | A/C | 3.33511e-05 | 0.00408344 | intron-variant | RNF165 | GRCh38.p7 | 18:46435259 | CTGGGTAGCCCCTGA[A/C]ACGAGGGCTCTCCAT | 494470 |
rs552766807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441185 | TTTTGTAGAGACAGA[A/G]TCTTGCTATGTTGCC | 494470 |
rs552782045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355877 | CCTGCCATGTTGGGT[A/T]TGTGACTGCCGTGGA | 494470 |
rs552783889 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46428638 | GAGGCTAGGGCGAAT[G/T]GACATGTGTGGCAAG | 494470 |
rs552802709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447863 | ATCAATCCCCCATGC[A/C]CTGACTCCCTTGTGC | 494470 |
rs552816849 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388341 | ACAAAACAAAACAAA[A/T]ACCTTGTTTAACTTT | 494470 |
rs552817081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403500 | ATCCACAGACATTTC[A/G]TAACAGTCTTCAATT | 494470 |
rs552818779 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46393040 | AAGGGCCTGGGGACT[G/T]GCTCACAGGCACACA | 494470 |
rs552866458 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46422335 | AAAGGGTGCATTACC[C/T]AGTTGCATGAAATCC | 494470 |
rs552868483 | snp | A/G | 1.69049e-05 | 0.00290726 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433432 | TCCTTCCTACCTCAG[A/G]CCCTGCACCAGCAAT | 494470 |
rs552877979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46433679 | GGCCGGCAGTCACCA[A/G]GTGGGTCTCTGTAGG | 494470 |
rs552880596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366245 | TGAAGTGAGCCAAGA[G/T]CACGCCAGTGCACTC | 494470 |
rs552922237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347982 | GGGCAGTAGCAGATG[C/G]TCACGTAGCACTTAC | 494470 |
rs552934793 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414646 | TCATGATCATGCCAC[A/G]TACCACACAATACAC | 494470 |
rs552943203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46434611 | TATTATTAGGAAAAT[G/T]GTTTTGACCTCTTGA | 494470 |
rs552959168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342004 | GAGAGGGCAGGGAGT[A/G]GGGACTGAGGACAAG | 494470 |
rs552981936 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357650 | GGGCTCGAGGCCTGG[A/G]GCACAGAGGACAGCA | 494470 |
rs553004801 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460162 | AACTCTTTACGCCTA[A/G]TGAACAAGCACAGTT | 494470 |
rs553022249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376201 | CGGTCACCTGCCCTT[C/T]CTGTTCACTTTTAGT | 494470 |
rs553023283 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46349388 | GGCCTCTTTTATAAC[A/G]GCACTAATTCCATTC | 494470 |
rs553026309 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389592 | ATTATTACGCTTTCC[C/T]CAGCCCATCCCTCAT | 494470 |
rs553031871 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411740 | ATATGGGTCAGATAC[G/T]TGGGGCTGCTCACCC | 494470 |
rs553041105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46456415 | TCAGCCACAGCCTCC[C/T]TCCATAGCCGGGCAG | 494470 |
rs553056088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46387412 | GCAGGCCTTTGGGAG[G/T]GAATCCAGTACAAAA | 494470 |
rs553064641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46344281 | GGAAGGGCAGGAAGC[A/G]TTGGAACAGCTGCTG | 494470 |
rs553068297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46361929 | TCTACTTCATGCCCC[A/G]TTTCCCCACTTACAG | 494470 |
rs553086739 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46427782 | CCAGCCTGGTGGGGG[C/T]GGCCAGTGTGAAGAG | 494470 |
rs553113215 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409243 | AAAGGAGAAAAAAGG[A/G]GAACAGCAATATGAG | 494470 |
rs553134281 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46376906 | GATTTCTGATCTCGC[A/G]ATCTGCCCGCCTCGG | 494470 |
rs553151814 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406486 | GGATGTCCTTGGAGT[A/G]GAACACAGGTGGGAA | 494470 |
rs553155181 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436036 | ACAGATATCTTTGTT[G/T]TCCTGAGATGCAGGG | 494470 |
rs553164037 | snp | G/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46378577 | ATGTATGGTCCAATT[G/T]TTCCAGTTTCATTTA | 494470 |
rs553168300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372644 | GCCTAAGGGGTTGGG[G/T]GTCTCCTGTTAGAAT | 494470 |
rs553198266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360895 | TGTGGAGGAGCTTTG[A/G]CCCAGAGGCCAGGCG | 494470 |
rs553225750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46412785 | GCTAACAGCCAACGC[A/G]GAGTGACCACGTTTC | 494470 |
rs553270835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422387 | AGTCAGTGTGGGCCA[C/T]TGAGAGACTCAGAAG | 494470 |
rs553272030 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436880 | TCAATTCAGCACACA[C/G]GGAGTACTCAGGGCC | 494470 |
rs553314355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398907 | TCGTCTAGGATGCAC[A/T]TGTAGGGCAGTGGTT | 494470 |
rs553350327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357260 | CCAGTGGTAACAGTG[A/G]TCAGTACCCAGCATT | 494470 |
rs553375855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337942 | GCCTAGAGAGAACCC[C/G]TACCTTTGGCCGCCT | 494470 |
rs553398725 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46421981 | CATTGGACTGGGAAC[A/C/T]AATAGATAGAGAGGG | 494470 |
rs553405461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46446827 | TCCCTCCTGCAGTTA[C/T]TCTTGTCAACCTGCA | 494470 |
rs553445412 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46343459 | ATGCATAGGAAACAA[G/T]TCGAGAAGCCAGCCA | 494470 |
rs553470137 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46383119 | AAGGGCCTAGCCTAG[A/G]CCGGGGTAGGTGCTG | 494470 |
rs553472004 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346351 | AATTCAGTGGCATTA[C/T]GTACATTCACAGTAC | 494470 |
rs553507314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380218 | TGCTGCCTTTTGGCT[A/G]TGCCAGTCTCCTCTC | 494470 |
rs553509629 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375922 | CCCTGCCTTTGATGA[A/G]ACTGTACAATTTTGG | 494470 |
rs553524777 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374841 | ATGGAAAGTGCCTGC[A/G]TGCCTGGAGAGAGGG | 494470 |
rs553529490 | in-del | -/GTGA | 0.487305 | 0.0786545 | intron-variant | RNF165 | GRCh38.p7 | 18:46334714 | TGTGTGTGTGTGTGT[-/GTGA]GAGAGAGAGAGAGCG | 494470 |
rs553555965 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415540 | CAAAAAAAATAAAAA[A/C]AATAAAAAAATAAAT | 494470 |
rs553565825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390615 | TGATAGAAATAAGCC[A/G]TTTTCTCTTTTCTTT | 494470 |
rs553578533 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337230 | AAGAGAAAAAAGAAA[A/C]GAAAAGAAAAAAGAA | 494470 |
rs553581552 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46416072 | ACATGTCATGGGGGT[A/G]GAGAGGAAGAAAAAC | 494470 |
rs553598324 | snp | G/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332575 | GGGTGCCCCTCCAAG[G/T]CTCCCCGTTTGCCCA | 494470 |
rs553643429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405294 | CTCTGGGAGGTGCCC[A/G]TGGCCAGACAGGTTG | 494470 |
rs553643930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416544 | CTCAATAAACGACAA[C/T]GCCATTTGTATCAGT | 494470 |
rs553679752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375112 | GGCTTTATCTGCATC[G/T]GCCTGAGTCTCTTCT | 494470 |
rs553694538 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390026 | AGCCACCATGAAATG[C/G]TCATTTCTAACCAGT | 494470 |
rs553741540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351246 | AGATGACCTAGCCCT[A/G]CAGAGTCACCACCTC | 494470 |
rs553789327 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46453910 | TTGAGCCCAGGAGTT[C/T]GAGACCAGCCTGGCC | 494470 |
rs553826425 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356108 | TATTCTCTCCTTTAT[C/T]GACTACTGAAGTATT | 494470 |
rs553847212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396740 | GACTGCAGAGAAGGG[A/T]CACCAGCAGCCTTCA | 494470 |
rs553864036 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46344609 | CCTTGGCCTCCACAG[C/G]GGACCTCGGCATCCA | 494470 |
rs553869348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370275 | AGGGGAAACATCGTT[A/T]TTCCCATTTTACAGA | 494470 |
rs553881758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365035 | GGGGTCTCTGGGAGT[A/T]CCCTTTCTTCTAATG | 494470 |
rs553888142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385304 | GAGATGAAAGTGGTG[G/T]CTTGTGAGGACAAGT | 494470 |
rs553993575 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434662 | GGACTCCCAAGGATG[C/T]TCGGAGCACACTTTC | 494470 |
rs554006170 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428085 | GCTTGGAGGGGGTCT[A/G]TGGGAAACAAGGAGA | 494470 |
rs554010465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420031 | GATGGTTGGGAATCT[A/G]ATTTTACTGACCCTG | 494470 |
rs554034444 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46340429 | TGTTCATTGAATACT[G/T]ACTTGGGGCCAAACA | 494470 |
rs554054702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419284 | CCAGTTCAAGGAAAT[A/C]ATTGAGCCATCCTCC | 494470 |
rs554070539 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46414081 | CATCCCCCAGCAGTT[C/T]TCATCTGAATCCACG | 494470 |
rs554077185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426184 | ATTTCATCAAGCTTC[C/T]TGACTCCCTGGGCTC | 494470 |
rs554131396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46454573 | CTTGTGTGTTCCAGT[G/T]AGGTTACAGTATTCC | 494470 |
rs554159599 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46369464 | GACAGGCCAGCTTCC[A/G]GGGAATGTTGAAGTC | 494470 |
rs554167855 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405917 | CACTCCCTTCCTCCT[C/T]CCGGAGTGGGATTCT | 494470 |
rs554174216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408370 | CCCAGAGCCAGAGTT[G/T]GCCTTAGGCTGATGT | 494470 |
rs554177965 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46345930 | GGACCCAAGTTGTTC[A/C]GTGGCTGGAGAGTCA | 494470 |
rs554179691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341657 | AATGAACTTCAACAA[C/T]AAAAATTCCTCATAC | 494470 |
rs554203592 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46446131 | GTATTCTTCCACCAG[A/C]GAGCACTACTGTCTG | 494470 |
rs554214810 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46346561 | TCAGGCAGTCTTTAG[A/C]TTGACCACCTACCAG | 494470 |
rs554269410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425334 | TGCAACAGGGACCCT[A/G]GGCAGACCTGTGCTT | 494470 |
rs554270885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358738 | TCCTTCTTGTCCCTA[C/T]ACTGACCAGCTTCTC | 494470 |
rs554282881 | in-del | -/CAA | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46417323 | CCTCAGAGTCAAAGG[-/CAA]CAACATCCTGTAATG | 494470 |
rs554302773 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46375180 | GGCTCCTTCCAGGCC[A/G]CCCTGGCCGCATTCT | 494470 |
rs554315321 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46351893 | GGTGTGTGTTGGGAT[-/G]GGATACCAAGAATGT | 494470 |
rs554329172 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460966 | TTCCTCCTCCCTCGC[G/T]CCTCCCACAACCTCA | 494470 |
rs554330861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419312 | TCCGTAGCCAGCCCT[A/G]GGCCAGACCTCAGGG | 494470 |
rs554338314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439641 | TTTCTGAAGTTGGTG[C/T]CCATAGAGGTAAAAC | 494470 |
rs554352027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432902 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 494470 |
rs554366203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415700 | CCAAGTGATGCTGAG[A/C]AAGTCTTTCTAACCC | 494470 |
rs554375667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341006 | TGGCAAGAACAGAAA[A/G]TACGTAGCAGGAGGG | 494470 |
rs554383388 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46359315 | TCACAAAACGATGAA[C/T]GTGACAAAGGGAGTG | 494470 |
rs554417370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46426946 | TTCAGACATCACTGA[C/T]CGTTGATTTGTCATG | 494470 |
rs554444543 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46353061 | CCATCCTCCAAGTTG[G/T]TGTCAAACCACCGGC | 494470 |
rs554472063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46370846 | TGGAACTCAGGGGGC[A/G]TGAGGTCAGCATGAG | 494470 |
rs554480334 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388336 | ACAAAACAAAACAAA[A/G]CAAAAACCTTGTTTA | 494470 |
rs554481300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353605 | ATCCCTCTACAAATG[A/G]AAGTGTGTGGGAGGA | 494470 |
rs554490851 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396418 | TGCAGAGACATTCTA[C/T]CTGCCCAGACACAGA | 494470 |
rs554491059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386361 | CATCAAATATATAGT[C/T]ATTTCATTTGAGACA | 494470 |
rs554503251 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355861 | AAATATCCAGTATGG[-/C]CCTGCCATGTTGGGT | 494470 |
rs554528213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46358480 | TTTTGAAGCCTGAAG[C/T]GTACCCGAAAGGTAA | 494470 |
rs554547662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366058 | AGCACTTTGGGAGGC[A/C]AAGGAGGGCGGATCA | 494470 |
rs554580015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447229 | TGTCTTTCCATTACT[C/T]AGTGCCTCTGGCTTG | 494470 |
rs554592447 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373869 | GATCCCCCTCCCACC[C/T]CCGGTCCCAGACCCT | 494470 |
rs554605261 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414996 | TCTCAGCTCATGGAC[A/T]CTCCATCGGCTTCAG | 494470 |
rs554618690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46439750 | CAAACAATAAAAAAA[C/T]AAGAGAATAGTATAA | 494470 |
rs554641844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46391832 | CATATAACACATGTA[A/C]AGACCACATACCCTG | 494470 |
rs554690687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385394 | TGCATGTGTGTGTGA[A/G]TGTGCGTGTGCATAT | 494470 |
rs554701535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381442 | CCATCTATTGCTCAC[C/T]CAGTGCTCTCAGGGA | 494470 |
rs554715463 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46386552 | ACCCCCCATCAATCC[A/T]TCCATCCATCCATCC | 494470 |
rs554730397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419912 | TTCTTTCCTGTCTTC[C/T]TTTCTCATGTATTTC | 494470 |
rs554843550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407951 | AAGATCCAGAGAGGT[G/T]GTCAGGGAAGCCTTC | 494470 |
rs554878233 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369976 | ACATGCACACACACG[A/C]ACCCTAGACTTGGGA | 494470 |
rs554881249 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349615 | GCCAGGGGAAGCTGC[C/T]AGTGGTCACAGTTCT | 494470 |
rs554884229 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46359169 | TTCAATTCAGTCTGA[C/T]AATCTGAGTTTCCAC | 494470 |
rs554932961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46415296 | GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCAGG | 494470 |
rs554949430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382199 | CCCATCCCTCCTGGA[C/T]GGTCTGTCATCTTCC | 494470 |
rs554962431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440162 | ATCTTTGTTCTCTCG[C/T]TTCCCCGGTCCTGAT | 494470 |
rs554971255 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46334732 | AGAGAGAGAGAGAGC[A/G]CGCGCGCGAGAGCAT | 494470 |
rs554988987 | in-del | -/CCCTGCCCTAGCAGGGGATGCTAGGAGG | 0.0611083 | 0.163768 | intron-variant | RNF165 | GRCh38.p7 | 18:46437138 | CTCCGGGAGGCTGGT[-/CCCTGCCCTAGCAGGGGATGCTAGGAGG]CCCTGCCCTAGCAGG | 494470 |
rs555008887 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440862 | TATTGGTTTATAGGG[-/T]TTTTTTTTTCCTTGA | 494470 |
rs555010499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376408 | GCGTGGCCCTGGACT[A/G]CCTAGTTTTGAACTT | 494470 |
rs555015105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360185 | TCTCTCCTGGCAGTG[G/T]GGTTCATTCAAGGGC | 494470 |
rs555015960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46432564 | AGTAGGGTCAGTGGG[C/T]TTGCATAGGAGTCTA | 494470 |
rs555037242 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46397690 | TGTGTGTGTGTGGTT[A/T]TGCTGGGGTGTGAGG | 494470 |
rs555044179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394160 | TGATGAGACAGATGG[G/T]GTCCCCTGCCGAGGG | 494470 |
rs555055326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394618 | TGGGCAAATGGAATA[C/G]AGTTTCCCCTGGTTT | 494470 |
rs555064040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46450896 | CAGAGGGGTGCAGTC[C/T]AGATTCTAGAAACCT | 494470 |
rs555069969 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46368536 | CTGGGTTTTGTTCCC[A/G]GCTCCACTGGTCATT | 494470 |
rs555102826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46443100 | CTCTGTCTGTTAATT[A/G]GGGTGTCTAGACCAT | 494470 |
rs555104812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405745 | TCCAGGATGGGTTGA[A/G]TATGATGTCTATGTG | 494470 |
rs555133689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363045 | ACCAGAATGGAAGCT[C/T]TCAATGGCATGAGTT | 494470 |
rs555168439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400103 | TTACCCATCGCTTGG[C/T]TTCATTTCTCCTGGC | 494470 |
rs555191819 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46427018 | TAGGGACCAAACAGA[G/T]CAGCTGCTGCCTGGT | 494470 |
rs555202450 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446887 | TCTTCAGGACTGCTT[C/T]TGAGCCCTTTTGCTG | 494470 |
rs555207798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421361 | CCATGCTCACCTGTT[C/T]GTGATCATTCATTCA | 494470 |
rs555218741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389741 | ATTTCTTTCCTTTTT[G/T]TTTTTCAGACAAGGT | 494470 |
rs555234526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46348054 | AATACTGAACCTCGT[A/G]GGAAACAGACAGACG | 494470 |
rs555273307 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46348461 | TAAGGGCTGAGGGTA[C/T]AAGAAAGTGAGGTAG | 494470 |
rs555273438 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46342190 | AGCCTTTGCCACCCT[A/T]CCTGACTAGCTAGTA | 494470 |
rs555341522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46424045 | CATGGTACCTCCTCC[A/G]AAAACACTCACTTCG | 494470 |
rs555354861 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454377 | ACACAGCTGGACTCT[A/T]AAGCAGGCAGATCAT | 494470 |
rs555380739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412632 | TCTCTCCTCCCTACT[C/G]CAGTAGCTGGCTGTT | 494470 |
rs555384365 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46345093 | GCTTCGGGGCAGGGG[A/T]GCCTGGGATGCAGGG | 494470 |
rs555393214 | snp | A/C/G | 0.00358938 | 0.0422398 | intron-variant | RNF165 | GRCh38.p7 | 18:46413011 | CACAGCCCCCTCTCC[A/C/G]AGAAGCTGGAGGAGT | 494470 |
rs555412889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384189 | CTTCCAGCCCAACCT[C/T]ATCTACTGGGCCAAC | 494470 |
rs555427468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379437 | ACTTACCCTCACACC[C/T]ACCTTCCCTCCCCGA | 494470 |
rs555437600 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378619 | GCAGGCAGGGCCACT[C/G]TTTATCAAATAGGAG | 494470 |
rs555455913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418000 | CAGAGCAAGACTCTT[A/T]AAAAAAAAAAGTATA | 494470 |
rs555456794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407198 | GCCAGGGCTTCTGCT[A/C]CCCTTTCTGGGGCCT | 494470 |
rs555467870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356221 | CAATCCGTGACCAGC[C/T]GACCCTGTTCCAGGT | 494470 |
rs555506865 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449658 | AGTGAGCTCTCATAA[-/G]ATCTGATGGTTTTAC | 494470 |
rs555527678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46339676 | CAGTTCTTCTTTCTG[A/G]ACAAGAGAACTTCTC | 494470 |
rs555528721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436421 | TTTATGCTGTTCTTG[A/C]AACTTTTAGGTCAAA | 494470 |
rs555550713 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362594 | CAGCCAAGCCTCACT[C/T]GTTTTGACTAATGAG | 494470 |
rs555555565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438152 | GGCACAAGAAATCTC[C/T]AAAACACAGTTCTGG | 494470 |
rs555588948 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46452799 | TAGGGTGCATTGGTC[G/T]AGAGCACTCTTAGAG | 494470 |
rs555597379 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408601 | ATGGGAACTGTGGGG[C/T]ATCCTAAAGGGGGCA | 494470 |
rs555668041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46438807 | GCTGTTCCAGGGATT[C/T]GGGCTGATAATGGCT | 494470 |
rs555673033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379023 | GCCTGGAGTAGGGAA[A/G]GAGCGGGGCACCAGA | 494470 |
rs555688299 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46364305 | CTGCCCTCCCCACCT[C/T]CACCTATGCACTTTT | 494470 |
rs555698473 | snp | A/G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443332 | ATCTTATTTTATTTT[A/G/T]GGAATTCACTAGGTT | 494470 |
rs555708703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46401531 | AGTGATTTGCCCATG[A/T]TCACCCTGCTACTCA | 494470 |
rs555733959 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46363285 | TCTTAATTCTTCTAC[C/G]ACCTTTGGCTGCAGA | 494470 |
rs555738247 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450006 | GGAGAGTAATAGCAC[C/T]CACATTATAGATCAG | 494470 |
rs555748371 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46363772 | AGGAAACATACTTTT[C/T]AAGGTTGGGTCTCCT | 494470 |
rs555781894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406369 | TCTTACTGCCATTGC[C/T]CTGTGGGTGCTGGCC | 494470 |
rs555795856 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436811 | AATTAGGAAGATTTA[A/G]TTGCAATTTGGATTG | 494470 |
rs555812126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374069 | AGGCTGGGGCATTCT[A/T]GTCATCCCTGTCCCC | 494470 |
rs555845669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400771 | GCTTTCAGTAGCCCC[A/G]TCACTGTGCTCCTAA | 494470 |
rs555893450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46359529 | AATAGCAAGCTGACT[A/G]GTGGGGCTGGAGATA | 494470 |
rs555898267 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46437377 | GCCAGGAGATAGGCA[G/T]CCTGGTAATTGGATG | 494470 |
rs555911671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384212 | GGGCCAACCCCTCCC[G/T]CCATCTAGAATTCCA | 494470 |
rs555919325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363840 | TCATAGGGGCCACCG[C/T]TGAGGGTGTGACCTC | 494470 |
rs555922681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374435 | TCTCCTCCCGCCAGC[A/C]CCTGGCAGCCTTTAT | 494470 |
rs555926473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369210 | GTATCTAGAAGCAAC[G/T]TGTGGTTGTTTCCAG | 494470 |
rs555932890 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457958 | GGTTTGGGAGTGCCC[A/G]TGTTCCTGGTCTCTG | 494470 |
rs555947466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46453511 | GGTAAAAAGGAGAAT[A/T]AAAAGAATTAAGGGA | 494470 |
rs555955487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357218 | TCCTGTTCCTCCCAC[C/T]TCACCCTTGCTACCC | 494470 |
rs555972233 | in-del | -/GT | 0.156658 | 0.231921 | intron-variant | RNF165 | GRCh38.p7 | 18:46397561 | CTGGGGTGTGAGGGT[-/GT]GTGTGTGTGTGTGTG | 494470 |
rs555977958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395151 | GGAGGGATTAAAAGA[C/T]GGAAGTTGAACCAGT | 494470 |
rs555989807 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46369569 | TTAGGTTTGCAGGGC[A/G]GGATTCCCTATTCCC | 494470 |
rs556017998 | snp | A/G | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333101 | GCTTGTCCCCAGCTG[A/G]ACTGTCACAGGGCAC | 494470 |
rs556025639 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46396509 | CCTGAGTCCCAAGAC[C/G]TAGCAGGTGCCTGGC | 494470 |
rs556087153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380102 | AACTGCCCACCCAGT[G/T]GGGGTGGAGTGCAGG | 494470 |
rs556106564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390658 | AGTTAGTCCATCAGC[C/T]CCCATTCAGCAGCAT | 494470 |
rs556113870 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345282 | AGAGGTCATCTGGGG[C/T]GAGGGGGCAGCAGCC | 494470 |
rs556130696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356836 | TTATTCAGGCATGGT[G/T]CAAGAGACAGAGGCT | 494470 |
rs556147310 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360623 | GGCAGCCCCAGGCGA[A/T]AGACCCCTGCATTAG | 494470 |
rs556149797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418733 | AAATACAATTATGTG[C/G]AAAGATAGTTACAGA | 494470 |
rs556162499 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339076 | CACACATGGATGTTC[C/T]CAGTGGAGGCTCTGC | 494470 |
rs556179389 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46350785 | TAAAGTGTCCTAACA[A/C]GCTGGCGAGCCAGGC | 494470 |
rs556180927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407291 | ACCCAGTCTTTTGGG[G/T]TAAGATTCTTCTTCT | 494470 |
rs556223057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400655 | GTTCAGGAAGTTCCC[A/G]GGTGTGTCAGCGTGC | 494470 |
rs556244975 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46375380 | CAACATGGGCAAAAC[C/G]CTGTCTCTACTAAAA | 494470 |
rs556246154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46374553 | TTTCATTCAGGAGAA[C/T]GTCTTCAGGGTTCAC | 494470 |
rs556262444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46413165 | TGCAAGCTGGGAACC[A/C]TGCCAGGTCCTCTTC | 494470 |
rs556267602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46430264 | TCACCCTTCCCCCTC[A/G]ATACCTTGAAGGTAG | 494470 |
rs556294646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390421 | ACTTCATCAGCCATC[C/T]TTGGCCTGACAGCCA | 494470 |
rs556334745 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF165 | GRCh38.p7 | 18:46372981 | AGGGAGGGGGACCCT[C/T]CTGCTGGGAAACTGG | 494470 |
rs556370265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418181 | TAGTGAGACCCCTAT[C/T]TCTACAAAAAATAAA | 494470 |
rs556379318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424093 | AAATTCATACACAAA[C/T]AAAATGCCAAGTATA | 494470 |
rs556382509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412715 | TCCTGACTACCCCCA[C/T]CCCTCCCAACTCTTA | 494470 |
rs556414522 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46425410 | GTGGGTGGCAGGCCA[G/T]GTAGAGATGTCAGGT | 494470 |
rs556460116 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438736 | TGGATTTCTAAGTTT[G/T]CATCCAACTGGCTCC | 494470 |
rs556465121 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459275 | AACACTAGAAACTTC[C/T]CTTTGTCTCTCTGGG | 494470 |
rs556478069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46439001 | GACAAGGACCTGGGT[C/T]TTCTGACAGCTGCTG | 494470 |
rs556490118 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46431723 | CTGGAAAGAAAGTCA[C/T]TGCCTTGCATGAGAA | 494470 |
rs556505856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340263 | GAAAGGGGAGGGCTT[A/T]TCTTGGAACGACTCA | 494470 |
rs556510550 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46396571 | ATGTGAAATTATTTC[A/T]ATTTGTTTTCTTGAA | 494470 |
rs556549697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46352588 | GTTGCTCCACCCTCC[C/T]TAGGATATGGCCCTT | 494470 |
rs556574118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391327 | ACTGTGTCCCATGGG[C/T]TCTCTGTTGGCCAAA | 494470 |
rs556593675 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46410683 | GAAGGGGAGCCTCCC[C/T]GACAAACAAACAAGT | 494470 |
rs556622019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46453843 | ATCATAGTTAAAAGG[A/G]GGCTGGGCACACTGG | 494470 |
rs556683863 | snp | G/T | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461735 | AGAAGAATAGAGAGA[G/T]TGAGCTGAGAATTTG | 494470 |
rs556688147 | in-del | -/GT | 0.477236 | 0.104229 | intron-variant | RNF165 | GRCh38.p7 | 18:46335055 | GGCGCGTGTGTGTGT[-/GT]GTGTGTGTGTGTCTG | 494470 |
rs556690295 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46409761 | ATGGGCCCTTCAGGC[A/G]TCTTGCTTTCTTGGC | 494470 |
rs556708213 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46448533 | TATGGCCTCATTTAG[C/T]TTCCTGTGGTCAGTA | 494470 |
rs556709714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445968 | TGTAGTTTCCCCTTA[C/T]CTGGATTTTACTGGT | 494470 |
rs556751578 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390196 | AGGTGGGAACTGGGC[A/C/T]GATTCCTGCTGGGAC | 494470 |
rs556751641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46434682 | AGCACACTTTCAGAA[C/T]TGCTGGACTAGATCA | 494470 |
rs556789709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364953 | GGCCCTCTGGTCCCA[C/G]CTGGGTCTCTCCTAC | 494470 |
rs556796064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398512 | ACAATTGGCCAGCAA[A/T]TCTGGACAGTGTCCG | 494470 |
rs556804159 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46358611 | GGTGGCTGTGGAGAA[A/G]GGAGGGGTGACTGTC | 494470 |
rs556824015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391730 | TCCTCTGTTCACTCA[A/C]CCTTCCCAAGATCTG | 494470 |
rs556864168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428270 | AAAAATTAGCTGGGT[A/G]TGGTGGCAGGCGCCT | 494470 |
rs556872026 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46361129 | CCCAGTGTAAAAAAA[A/T]TTTTTTAACCCCTTG | 494470 |
rs556931454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349584 | CTCTCATTCCCAGTG[A/G]CATTTTTGCTGGCCA | 494470 |
rs556968377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350095 | GCATACCCCATGATA[C/G]ATACCCAGAGAAATA | 494470 |
rs556968488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343632 | CCGCGACTTCACTGC[C/T]TATCTGCCAAGGGAG | 494470 |
rs556984550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46393987 | GATGCAGTGGGGCTG[A/G]CCCCTGGCATCATGG | 494470 |
rs557005088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344023 | CCTTGAAACATGCCT[G/T]GGTGTGCCGCTGTGT | 494470 |
rs557022338 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457188 | CCTGACCGAACCAAC[A/G]ACAGCCCCAATCTTC | 494470 |
rs557027417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366031 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 494470 |
rs557126335 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366927 | CTGTGTCTTGCTGGA[A/T]GGAACAGATTTTCTA | 494470 |
rs557149653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399027 | AGTTACCACGACACC[A/C]GGGAGTCTGCAGTTC | 494470 |
rs557152290 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46368275 | GCTGAGATTGGCTTG[C/G]GACGTGGAGGCCTAA | 494470 |
rs557154167 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457322 | AGGCGGGAGGGGGGG[A/G]TTCTCGTTTTATTTT | 494470 |
rs557156310 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423893 | TTTCTTCCTCCTTTC[C/T]CTCGTTCCTCCTTCT | 494470 |
rs557188865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355435 | TCATTCTCTAGGCTC[C/T]GGTGAGGATCACAGG | 494470 |
rs557189581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367627 | TCTTAAAACCCACAT[A/T]GCCTAAAGCTTCTGA | 494470 |
rs557212593 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46453019 | AGTGCCTGGTATCTA[C/T]TAAGTGCCCAGGAAT | 494470 |
rs557302406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46388017 | CAAGCTGGCACTTGC[A/G]TTCCAAGCAGGCCTC | 494470 |
rs557319337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338798 | AATTCCTGGTTCTTT[A/C]AAAGGGTCATCATTT | 494470 |
rs557337495 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417054 | CTAGTTGCTTAGCAA[G/T]CAAGATATGGAGTCT | 494470 |
rs557365136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404595 | CCATCTCTACTAAAA[A/C]TACCAAAATTAGCAG | 494470 |
rs557365645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388549 | CTTGGCCATGATCAA[A/G]GGCGCAGGAAGCACA | 494470 |
rs557408074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364495 | CCCAGAGAACCCTTC[A/G]TGATGCCGACAGACA | 494470 |
rs557426898 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46399142 | GCTGCTGCCCACGAG[G/T]TTGGCCAAGCAGAGG | 494470 |
rs557436268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46338042 | TGAAGAGAAGGGGAT[A/G]TAACACTTAGGTTGA | 494470 |
rs557471464 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343917 | CCTTGACCCCGAGCT[C/G]AAGGCTGGCATAAGT | 494470 |
rs557477186 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46378690 | TGGCATGAACCCATA[A/C]ATACACATTCTACTT | 494470 |
rs557477450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383640 | GCTCACTGCAAGCTC[C/T]GCCTCCAGGGTTCAT | 494470 |
rs557487075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46373021 | GTGTCTGTGCATGTG[C/T]GAGTGTGTGTGTGTG | 494470 |
rs557502749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411194 | CGACAGCCCCTTGGG[A/G]AAGGCAGTGTGAGGC | 494470 |
rs557568908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411380 | AGATGAGCTGACACT[A/G]TGTGACTATCCTGAA | 494470 |
rs557600172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422572 | CTGAGGACCCAAGAC[G/T]TGCTCTCTCCTTACT | 494470 |
rs557628424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405364 | CACAGGGCTGGCACT[C/T]GGAAGGGGGCCTGGC | 494470 |
rs557637641 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341459 | GTGCTTTGGAGAGTA[A/G]AAGACCATGAAGACA | 494470 |
rs557648169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46443240 | TTTAAAATTTGTGTC[A/T]GTTTTTTGCCTTCTT | 494470 |
rs557650354 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46400142 | TGCTCCTCCAGCTCC[A/C]GCTCTAGGCCTTGTT | 494470 |
rs557664302 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383345 | AATGAGGGAACCAGC[A/G]GGATGATGCACCTGG | 494470 |
rs557712702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423208 | CTACAGAAGCACCCA[A/G]GGGCCTGGAAACATT | 494470 |
rs557717557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407605 | GAGGCTAATCCCTTC[C/T]AATGCAGAGGGTATT | 494470 |
rs557739911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429645 | ACAACTTTTTCTTTT[C/T]CTGGTCATAATAATT | 494470 |
rs557751334 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411823 | CATGCAGGAATCACA[A/G]CCTGGGGCTGAGCCG | 494470 |
rs557757737 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46367700 | TACCAAACTGGCCTC[G/T]GTGTCCCCACCAGTA | 494470 |
rs557779676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46449454 | ACCTTGGTGCTGACA[A/C]AAACCCAAGCCTTGA | 494470 |
rs557790417 | in-del | -/CTTT | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46431954 | TAATTCCTCCATCTG[-/CTTT]CTTTTTCTTCCAAAA | 494470 |
rs557792266 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46417897 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGTGGG | 494470 |
rs557794157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338874 | TGGGCTGACTGACTC[C/T]CCGGCTCACCCTGCT | 494470 |
rs557806255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427636 | CCTTCAACCAGCCTC[A/G]AACCCGCAGCCCCTT | 494470 |
rs557835104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46339513 | TTCCCTGTGACTGGA[C/T]GATTCAGGAACTACA | 494470 |
rs557837233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46451020 | TCTCATTAGTAAAGA[A/G]GGAGAGCTGGGTATC | 494470 |
rs557856748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350555 | AAGAACCCCTGCAGC[A/C]GTTACAGCAACATTT | 494470 |
rs557893510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344551 | CCCCCAGCGTGGAGA[C/T]ACTGGCCTTCCTTAA | 494470 |
rs557928132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435546 | CTCTGCTCCCAGCCA[C/T]CCTCTGGGCCAGATG | 494470 |
rs557946036 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449631 | TTCCCACATGCTTTT[C/T]TTATGATAGTGAGTG | 494470 |
rs557990362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412564 | GCCGATGTCCAGTCA[C/T]GTGCTGATGAGGCTG | 494470 |
rs557994148 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46356147 | CCTCACTCTGTGATA[G/T]GCAGAAGCTGAAAAA | 494470 |
rs558043432 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457021 | ACCACGTAGGAACCA[C/T]GTAGGGGTCTCTAGC | 494470 |
rs558056025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356749 | AGCCCTTCTGATGGC[A/G]TTGTCATCTGCTCCT | 494470 |
rs558111441 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46428630 | CTTGGAATGAGGCTA[C/G]GGCGAATTGACATGT | 494470 |
rs558125321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383664 | GGTTCATGCCATTCT[C/T]CTGCCTCAGCCTCCC | 494470 |
rs558139555 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383802 | GTGATCCGCCCACCT[C/G/T]GGCCTCCCAAAGTGC | 494470 |
rs558178836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419965 | TTCTCTCATGCACAC[C/T]TCCCCTCCCCAATAC | 494470 |
rs558191254 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420600 | CTGTAATCTCAGCAC[A/T]TTGGGAGGCTGAGGA | 494470 |
rs558200853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378984 | GGACCTCACTGTCCC[C/G]AGGGCTCACCTGCTC | 494470 |
rs558202672 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458590 | AATGGGTAAAAGTAA[C/G/T]AGGCGGGCAGATTTT | 494470 |
rs558208186 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46423524 | CATGTTATTTCCATT[C/T]GGCAAGCCACCAGGC | 494470 |
rs558234262 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333293 | TCTGGGCAGTGTGTC[C/T]CTGTGTAGACTGTTG | 494470 |
rs558236309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341963 | GGGAACGGGAGGGAG[C/G]CCGACCCAGTAGCGT | 494470 |
rs558255588 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405776 | AGCCATCCAGGCAAA[G/T]AATTTCTTAAGGTCT | 494470 |
rs558266601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365556 | TCGCCCAGCCTGGAG[A/T]GCAATGGTGCGATCT | 494470 |
rs558283854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46374453 | TGGCAGCCTTTATTC[C/T]ACTTTCTGTCTCTGT | 494470 |
rs558329825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46379369 | CTCACGAGACTAAGC[A/G]CTGGTTTCTTTTCAG | 494470 |
rs558358829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447794 | ATGGCCTGGCTCCCC[G/T]GTATCCTTGGCTCCC | 494470 |
rs558371439 | snp | A/C | 0.000144728 | 0.00850548 | intron-variant | RNF165 | GRCh38.p7 | 18:46334430 | GCCGGGGGCTCAGGG[A/C]ACACCCGCGAGGACG | 494470 |
rs558413656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375688 | TGCATCCTGGGAGTT[C/T]TCTTGTTCCCAGCAA | 494470 |
rs558414128 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46436212 | TGCAGAGTTCAGGGG[-/A]AAAAAATCTATCTAT | 494470 |
rs558428656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370856 | GGGGCGTGAGGTCAG[C/T]ATGAGCTTTGGAAGC | 494470 |
rs558444094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46448298 | CCTGGCCTTCTTGTG[C/T]CCTGGCTCCCTGGCA | 494470 |
rs558482748 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46387262 | AACCAGGCCCCACCT[C/T]CAGAGAGTCCCATTC | 494470 |
rs558486055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400714 | CAGCCTGTCGGGAAG[C/T]CTCTGTTGTCTCCCT | 494470 |
rs558496979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395226 | TCCAGGAAGAGTGCA[A/G]GGGTCCTTGAGCCCA | 494470 |
rs558508942 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46352980 | TGGCACTGTGGGTGG[A/G]ACTAGCATGCCCTCC | 494470 |
rs558523407 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46366768 | TGTGCATTCTTTTAT[C/T]CATTCACATGCTCAT | 494470 |
rs558527359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360315 | TGTTTGTGGCCAGCC[A/G]TGGAGGAACACAGAG | 494470 |
rs558536369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360795 | TGGAATCCTACCTAG[C/G]TAGCACCAGGCAGGG | 494470 |
rs558553242 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46347375 | TGGCCATCCTGCTGA[A/G]ATTCTCTGCCTCCTC | 494470 |
rs558613294 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46440288 | TGAGAGAGAGAGAGA[C/G]AGAGAGAGACCATAT | 494470 |
rs558641295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46415159 | CATGACCTCTGCCAG[A/G]GTTTGACTGACACTC | 494470 |
rs558648161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46392387 | TGTCCACTCTGTAAG[A/C]TCCCCCAGGCTAAGG | 494470 |
rs558669115 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355429 | TCTGCCTCATTCTCT[A/G]GGCTCTGGTGAGGAT | 494470 |
rs558676614 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46432943 | GAGCGAGACTCCGTC[A/T]CAAAAAATAAATAAA | 494470 |
rs558690580 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46353773 | GGGAAAGGAAACGGG[A/C]CCTCCAGAAGAGATA | 494470 |
rs558730271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382052 | CAGCTGGAGCAGGCT[A/C]TCTTCCCTCCTGCCT | 494470 |
rs558741184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371249 | TATTACAATTCAAGA[C/T]GAGATTTGCATGGGG | 494470 |
rs558749431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46409249 | GAAAAAAGGGGAACA[A/G]CAATATGAGATACCT | 494470 |
rs558808538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383070 | TCCATCTCATGCCTG[C/T]CTTCTTCTCAGCATG | 494470 |
rs558808554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46377166 | ATTGCAAATATATTC[A/T]TATGAAATATCTGAA | 494470 |
rs558828869 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46404943 | CAGCTGGTATGTATG[-/A]TACATGCAGAAGACA | 494470 |
rs558839380 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342342 | AATACCTGCTTTCCC[A/G]CCATAGCTGGTGGGA | 494470 |
rs558866552 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369742 | GGGGGTCCTTATTCC[A/T]CTCATCACGCACACC | 494470 |
rs558868307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46378097 | TTGGCCCTGAGATTT[A/G]CATTTGAGCTAACTG | 494470 |
rs558885858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403389 | GAGAGAGCCCTCCCT[C/G]CCCCCCGTCTCCCTC | 494470 |
rs558898244 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46403928 | TGCACTCTGGTATTC[A/T]TCATCTACCAACTTG | 494470 |
rs558905079 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385569 | TCTGCTGATAGGTAG[A/G]AGCAGGAACAAAACT | 494470 |
rs558908555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441095 | GGCTCAAGTGATCCT[C/G]CTGCCTCAGCCTCCC | 494470 |
rs559015730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46387364 | TTGGGGAACCACTCT[A/G]AAGTAAGGAAAGCAG | 494470 |
rs559023119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398346 | GGTAGGGAGGGGGAG[C/T]GACACCAGGCGAGCA | 494470 |
rs559062287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46439860 | TTTTTGAGACGGAGT[C/G]TCGCTCTGTCGCCAG | 494470 |
rs559062664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408042 | GGGGTGGCAGGGATT[A/G]GGGAAAAAGCCAAGG | 494470 |
rs559065641 | in-del | -/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388739 | GCAGCTTTTTCAGAA[-/G]GTGGGCTCAGGATAA | 494470 |
rs559068987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427710 | CAAGCAGGTATTTAC[C/T]GGGTGCCAGCACCAA | 494470 |
rs559076258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440419 | ATTGGTGTGAATATA[C/G]AGTATAGGAAGAAAC | 494470 |
rs559092768 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456234 | TTGCCCTGGGAAGGT[G/T]GGGTATGAAATGTTC | 494470 |
rs559104039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365142 | AGCATCCTGCCTTCT[C/T]GTTAGAGGTGGGAAA | 494470 |
rs559125798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46353499 | GGTGCCTGGCAGGTC[A/G]TAGGCACTCAATGAA | 494470 |
rs559129775 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459495 | GAGACAGTGGGCCCT[C/T]GTCCCCTCCCCCCTC | 494470 |
rs559163064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416033 | CCTTCCTGACTTTGC[C/T]GCTGGCATTTTCATG | 494470 |
rs559175826 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418013 | TTAAAAAAAAAAAGT[A/G]TAATGTAAGACACAT | 494470 |
rs559182213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428167 | TGTAATCCCAGCACG[C/T]TGGGAGGCCGAGGCT | 494470 |
rs559207120 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457290 | GAAAAAGGATTTTGT[A/T]TTTCACCCAATTTGG | 494470 |
rs559212622 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420527 | AACGTGGTCCAGGTA[A/G]CCACCCTAGCATGTC | 494470 |
rs559221587 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46410762 | ACTCATTCCTCTTGT[C/T]CTCATTGGTTTGGCT | 494470 |
rs559245953 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46353150 | CTTGCATTTTCCATC[A/T]TATCCAAAAGACTAT | 494470 |
rs559285324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360348 | TGCTCCCCTGCAACA[C/G]TGCAGGTGCTCCCCA | 494470 |
rs559286930 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46455027 | TGGCTTCTACATAAC[A/G]GTAAACTATTTTCAA | 494470 |
rs559298360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336950 | AACTTGGTGCACCAA[A/G]GTCCCTGGCTTAAGT | 494470 |
rs559300926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426487 | GTGTGCCAGGTGGGC[A/G]TCAGGCGAGCCCAGC | 494470 |
rs559319346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389318 | ATTTACTTATGTGCA[C/T]CTTTCCCAACAATGC | 494470 |
rs559339542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408595 | CACATCATGGGAACT[A/G]TGGGGCATCCTAAAG | 494470 |
rs559345283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347740 | GCCTGCTCCTAGGAG[A/G]CACTTTGAATTTTAT | 494470 |
rs559375894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46386068 | AAATAAAGTATTGGG[A/G]TTCACCCTCAGTTTT | 494470 |
rs559382629 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349901 | TCTATGGGCCCCATG[C/T]AATATGCATTTACAC | 494470 |
rs559398218 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46376700 | TTTTTGAGATGGAGT[C/G]TTGCTCTGATGCCAA | 494470 |
rs559413632 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359132 | CCATGAGAGGAAGAC[A/G]TTAGAAGCTAGAACA | 494470 |
rs559424547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365566 | TGGAGTGCAATGGTG[C/T]GATCTTGGCTCACTG | 494470 |
rs559448709 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347073 | GGATGGGGAGAGGTC[A/C]CTGAGGCCTGGAGAA | 494470 |
rs559494929 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380791 | GGGTTGCAAAGCTAG[A/T]GCTCCCCCAACCCCC | 494470 |
rs559542358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428278 | GCTGGGTGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 494470 |
rs559543554 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383601 | ACTCTGTCACCCAGA[C/T]TGGAGTACAGTGGTG | 494470 |
rs559550749 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46409479 | TGAAGAAATGACACT[A/G]AGAATCTGGATTTGA | 494470 |
rs559560842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342919 | GGAGTGGAGCTGTAA[A/G]CACAATATATGTATA | 494470 |
rs559644406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393318 | GTTCTGGGCCGGTGG[A/G]GAGCAGTCTCGAGGT | 494470 |
rs559649920 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364729 | TCTCTCTGCCCATCC[A/G]TGCTCACATACTGAT | 494470 |
rs559693834 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | RNF165 | GRCh38.p7 | 18:46394745 | TTCATGTCCACACCA[A/C]TGTTCAAGGACGACT | 494470 |
rs559697533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46348231 | TGGGCCAAGGGGCTG[G/T]GGGGGGTGAGGGGAG | 494470 |
rs559717397 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386507 | CCAGAACTAGAATCC[A/G]GGTCTTTTGCTAAGC | 494470 |
rs559732785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342364 | CTGGTGGGACCGATT[C/G]TGAATGCTAGGCTCT | 494470 |
rs559749921 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442036 | GGCATGGTGGCGCGC[A/G]CCTGTAGTCCCAGCT | 494470 |
rs559785923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415423 | CCCAGCTACTCGGGA[A/G]GCTGAGGCAGAAGAA | 494470 |
rs559796373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379190 | GAGTTGCTGGAAACG[C/T]TATCATTCTGGCAAG | 494470 |
rs559808113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399253 | GGGACTGGTACTCTG[C/G]ACGTCCAGGGCAGTG | 494470 |
rs559826491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367758 | TCAGAGCCCAGATCC[C/T]CTGAATGTTAGGTTA | 494470 |
rs559844366 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340652 | TAGCCCAGTCTTGAC[C/G]TGGAAGGGTGATCTT | 494470 |
rs559845012 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456761 | TGCAAGCACATTTTG[C/T]GGAAAGAGGAGTTGG | 494470 |
rs559859464 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335491 | TTGTATTCTGCCTCT[A/G]GACTCACATTTCTCG | 494470 |
rs559859544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46373767 | TATCTGAATCTTACA[C/T]GTGGGGAAGCTGAGT | 494470 |
rs559860258 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46334946 | TTTTCGTCTTTAACC[C/G/T]TTTTTGTGCATCGCC | 494470 |
rs559914600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367184 | GGGGTTTTCCAAGAG[A/C]CTTATGCAATATTTA | 494470 |
rs559937421 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374043 | TTTCTTCCTGCAGCA[C/T]GAGCAGGGCCAGGCT | 494470 |
rs559947215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398722 | AGACCAGTGCCCTTA[A/G]AGCTCCTGGCACCTG | 494470 |
rs559981115 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342428 | TGGCCTGCCAAGCTT[C/T]GAGGGGGTCTAGACC | 494470 |
rs560023176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46361437 | ACATTAATATTTAAC[G/T]GAGTATGGCAGGCAC | 494470 |
rs560040174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46401754 | AGCTTCCTGGAGTCA[C/T]GGGACTTTAAAGTTG | 494470 |
rs560099346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442171 | CCGTCTCAAAAAAAA[A/G]AAAAAGAAAAAGAAA | 494470 |
rs560109267 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392883 | ACCTCCTGGTCTTTG[C/G]GGAGTGACTCCTAAT | 494470 |
rs560129803 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46434175 | CTGTCAAGAGAAAGA[A/G]TTGGATAGTCAGTGG | 494470 |
rs560137124 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46406662 | CAGTGTGCCCTGGCT[A/G]ACAAGTTTGACCACA | 494470 |
rs560144258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46345197 | AAGGAAGTTTGCGCC[C/T]GCTGGAACCTGAAGA | 494470 |
rs560148132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46418444 | TCAGTATTTAATTAA[C/T]TTTAAAAGTTACTAA | 494470 |
rs560172041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384354 | GTGTACATGTATGTG[C/T]GTGGGGGGGATTCTT | 494470 |
rs560213025 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46364038 | CTGCAACCTCTGCTT[C/T]CTGGGTTCAAGCAGT | 494470 |
rs560247374 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394458 | CCTGATGCCTAAGGC[A/G]TCTCTGGGGATGTGC | 494470 |
rs560247461 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372788 | TGTGCATTTCGAGAG[C/T]GCCAAAATCCATACG | 494470 |
rs560251144 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353884 | CCTGGCTGGGCCCTA[G/T]GTCACTCTGCCTCCC | 494470 |
rs560261674 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46418272 | TGAGATGGGAGGATC[G/T]CTTGAGCCCAGGAGA | 494470 |
rs560303449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431314 | GGCTCTCTGTTCATG[A/C]CAAAGAGTAGGTCAC | 494470 |
rs560305835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419023 | GCAATGATTCCCTCC[C/T]GGAGAATTTTTGGCT | 494470 |
rs560318132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419540 | AGCAGGCACAATCTC[A/G]GCCTGAGGGGCCTTT | 494470 |
rs560367156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46453063 | TACCTTGATGCTTTT[C/G]CCTAACCCATGTGCT | 494470 |
rs560372849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390735 | GGAAGGCGGTGGCTC[A/G]GAATCCTATACTGGG | 494470 |
rs560411392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425035 | CCCTGCCCCTCCCTG[G/T]TGCCTTTGGAGAGGG | 494470 |
rs560424800 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332823 | ACTGTGATTTTTACC[A/G]TCTCCTATTTATCAG | 494470 |
rs560458417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444765 | GGCATGAGCCACTGT[A/G]CCTGGCTCATTTTGG | 494470 |
rs560467713 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46445556 | CCTTCTATGTAGCTG[A/C]CTCTTCTCTCCAAAT | 494470 |
rs560476037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46437841 | CCCACTCTGTCACAG[C/T]TGCAGCCCTGCCTAG | 494470 |
rs560476860 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429222 | CAGGCAGAAATTCTT[C/T]GGATTTTCATTTCTT | 494470 |
rs560487997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357722 | GGCAGGAATTGCCTC[C/T]GATGAGGGGTCTGTT | 494470 |
rs560491003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358185 | GGATGAGTCATGCAG[A/G]CCTCATGAGCTGGAC | 494470 |
rs560491400 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425609 | GTCTTCCCTGAAGAA[C/G]CCTTGCTGCCTTCCA | 494470 |
rs560513005 | snp | A/G | 0.000105452 | 0.0072605 | intron-variant | RNF165 | GRCh38.p7 | 18:46435440 | AGGGAGGAAGGGAGG[A/G]AGGAGGGAGGTCTTG | 494470 |
rs560519084 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46346051 | TTGTAAGTGGCACGA[C/G]CTATGGCAGCCATGG | 494470 |
rs560542816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46345330 | TCCCCGGGCAGGTGC[A/G]GTGGGAGTGTTGATT | 494470 |
rs560560595 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46340615 | AGATAAAAGAGCTTG[C/G]AGCAGTCCAGGGTTT | 494470 |
rs560579167 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413303 | TGGACCATGTGGTGA[C/T]GTCCCAGGGACCCTG | 494470 |
rs560636236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374298 | TTTTAACCATTAAGT[A/G]CCACAGTTTAGTGAT | 494470 |
rs560637047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391352 | GCCAAATGGGACGAC[A/G]TTACAGCTCTTTCAG | 494470 |
rs560645952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352656 | TTTCCAAGCATCAAG[A/G]TGGAGGAAGAAGGGA | 494470 |
rs560667395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46431761 | GAGCCCTGGGCAGAA[C/T]TGCTCCTTACACAGA | 494470 |
rs560670518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46454245 | AATCATGAATAATGA[A/T]GGCAAAAAAATAGTA | 494470 |
rs560694984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379820 | CCCGTTCAAGAGATG[C/G]CTAGAGGCTGTCCTG | 494470 |
rs560695583 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46369371 | GTAGAATCCTGGTGT[A/G]TGTGTGTGCTGGGGT | 494470 |
rs560697641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374751 | AGCACACAAAAGCAG[C/G]AAGGCTCTGGCTGAA | 494470 |
rs560702195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385460 | CACAAGGATGTCCAG[A/G]TTGAAACCCAGGAGC | 494470 |
rs560708129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369874 | TAGAGCCCGGGGCCC[A/G]TTGGGCCCATCTGCT | 494470 |
rs560743481 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442383 | AGGACTACAAACTTT[C/T]TAGTTAGCATTATGA | 494470 |
rs560748239 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377756 | TGTGATGGGGCATTG[C/T]GAGATGAATAGGAGT | 494470 |
rs560793993 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438052 | GGTCTGTACAGCAAC[A/C]AGACCACACCATGTT | 494470 |
rs560814074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46341056 | GGGGCGGAGGCACAT[A/G]TGCAGGCCTACAGGG | 494470 |
rs560821338 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46453325 | GAAGGAAATGAGTGG[C/T]GTATTCAAGTCCAGG | 494470 |
rs560869997 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390785 | GCACCACTTCTGAGC[C/T]GGGCACCCTTATTCT | 494470 |
rs560922923 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412824 | GATGGCACACCTGTG[A/G]GCCAGGGGCCACCAT | 494470 |
rs560934164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406812 | CTCCTTGGCGTTGGG[C/G]CTGGCAGGTGGCTGG | 494470 |
rs560935916 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363460 | CTGGAGACAGTGCCC[G/T]TTCCTGGCTTCTCTA | 494470 |
rs560939154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418863 | GTCATTCAGCACCTC[C/T]GTGGTTTTCCATTCT | 494470 |
rs560946264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364607 | TTTAGGATTGGCTTA[C/T]AGCTGGATTTTGTTT | 494470 |
rs560950153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371344 | ATGGCCCACTGCAAG[A/G]AGGGTCACGGGGTCT | 494470 |
rs560988255 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441964 | GGTCAGGGGATCGAG[A/G]CCATCCTGGCTGACA | 494470 |
rs561010250 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46340437 | GAATACTTACTTGGG[C/G]CCAAACACTGCGCTA | 494470 |
rs561043951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407484 | TCTAATCCTATCACC[C/T]GACAGGACAGTGTTA | 494470 |
rs561046808 | in-del | -/TAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375596 | TAATAATAATAATAA[-/TAA]CTTGTCCTGGCTTCC | 494470 |
rs561056542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385974 | GTGGTGGTTCTGATG[C/T]TCTGGCCCCAAGAAC | 494470 |
rs561060663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358266 | CTGGGGTGGACAGGG[C/T]AGTGGGCTCCAGGAA | 494470 |
rs561137323 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46414691 | ACGCTCACAGACACA[G/T]GCACATACACACAGC | 494470 |
rs561140575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425574 | GGGCTGGAGCATCAG[C/G]ACCTCCAGCTCGGGA | 494470 |
rs561149689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414909 | GGGGAGCGTGCACTT[C/T]CACCCAGGGCTGCAG | 494470 |
rs561159487 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344974 | CCTCAGGACGGAGGG[G/T]GACATCAGACCTGTC | 494470 |
rs561196671 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431939 | ATTTCTCAACTCTGC[C/T]AATTCCTCCATCTGC | 494470 |
rs561203503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431403 | GGCTTCATTATACAG[C/T]GGCCAGTTGGGGACC | 494470 |
rs561251738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46396761 | GCAGCCTTCATGGTG[C/T]TGGCCATGTGCACCA | 494470 |
rs561253317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46419638 | GAGCGGAGTGGGCAG[C/T]GCACAGCTGGACCAG | 494470 |
rs561265830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365048 | GTTCCCTTTCTTCTA[A/G]TGCCCTATAAGTCTC | 494470 |
rs561298390 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46375340 | GGTGGGTCACTTGAG[A/C]CCAGGAGTTCAACAC | 494470 |
rs561314137 | in-del | -/TATAA | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460533 | TTTTGCATTTTTAAT[-/TATAA]TTTATTTATTTAGAA | 494470 |
rs561318285 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RNF165 | GRCh38.p7 | 18:46341222 | AGAGTTTGGACTGGC[A/T]TCTTTGGCCTTTGGG | 494470 |
rs561337358 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444630 | CACCATACCCAACTA[A/G]TTTAAACATTTTTTT | 494470 |
rs561348591 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435153 | AGTGGTGAAGCTCAG[G/T]GCTTGCTAGACTGTG | 494470 |
rs561356015 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332950 | CTCTGGCCTTAGTGT[A/G]TGAACTGTGAGCCTG | 494470 |
rs561361801 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401248 | ATTTCCCAGGAGCTG[C/T]TACACTGGCCACACC | 494470 |
rs561383884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393641 | ACCCCACCCCCAGTT[C/T]TTCTCAAACCTTGAT | 494470 |
rs561395390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426300 | AGGCAAGGCAGTGAG[C/T]CTTTTAGAGACTCGG | 494470 |
rs561445572 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358371 | GGACAGCAGAGGCAG[G/T]AATGTACACAGCACA | 494470 |
rs561458291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388704 | TGGGTTTACTCACCA[A/G]TCCTAGACAACAGGA | 494470 |
rs561518994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362264 | GAGGCAGGGTTTTCC[G/T]TCAGGGGTTTTGCAA | 494470 |
rs561530278 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46455115 | TCATGATTGCTTTAC[G/T]ATAGTGCCTATCTTA | 494470 |
rs561550841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416905 | GGCCTAAGCCAGTCA[C/T]GTGGCCATGCCCAGA | 494470 |
rs561567219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455917 | GTGGGTGAAAACCAC[A/C]AGCCACCAGCTGAGT | 494470 |
rs561579906 | snp | A/C | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461838 | TGAGTTAGGTGGACA[A/C]GTATAGGACGTGCCC | 494470 |
rs561598601 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333648 | GTGACCCGTGCGCGG[G/T]GTGCAGGGACCTCAG | 494470 |
rs561613018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375882 | CCTGGGCTAAGGGCT[A/G]GGGAAATAGCAAAAC | 494470 |
rs561620329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435066 | CACAGCGGGCAGCCC[A/G]GAGACAGCCAGAGTT | 494470 |
rs561632949 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390888 | GGATAAATCACTTGA[-/G]GGAAGCACTCAGAAA | 494470 |
rs561696737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383701 | CTGGGACTACAGGCA[C/G]CCACCACCGCGCCCG | 494470 |
rs561725401 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46349772 | GCCTATCTAGTTGGG[C/T]ACCCCTTGCCCAGTA | 494470 |
rs561738714 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46428503 | CACTGCTCCACTCTA[C/T]CAGTTAGGAAACTTG | 494470 |
rs561749847 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46370919 | GGCACATTGTGGGAG[-/A]GGGGAGGTGTATTAG | 494470 |
rs561768904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46344170 | TAGGAAAGGAAGCGG[C/T]GGCTGCTGACTCAGC | 494470 |
rs561785251 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450478 | TTCCCTCCCCACCTC[C/T]GCTGGTGAGTAGGGT | 494470 |
rs561807765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338251 | CCCTCTTCTATGTGC[A/T]TATTTAAATTTTTAG | 494470 |
rs561811898 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46378787 | AAGCATCCAAGAGGA[A/T]GTTCTGGAGAGGAGC | 494470 |
rs561847053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422160 | AGATGGCCCACTTTC[A/G]TTTTCTTCATCTCTG | 494470 |
rs561893063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378443 | CCCCTGACCACCGTG[A/G]AGGGGCAGCGTGAGA | 494470 |
rs561897466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430000 | CTCCTCCCAGAGTCC[C/G]CGCCCTCCTGCTCCC | 494470 |
rs561924830 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458256 | CCCCAAAGGGAGCAG[A/G]GAGATAAGAGGACAG | 494470 |
rs561950783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337617 | CTAATACTAATATAC[A/G]ATCTCTCAATAAAGA | 494470 |
rs561960152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430528 | TAGGAAACAGGCTTT[A/G]TAGTTTTTGTTCCTA | 494470 |
rs561965391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350919 | GGAGGAGAAGAGGGC[C/T]GGGTTTAATTTGTGA | 494470 |
rs561971344 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420953 | GAATATCTGAACTCA[C/T]GACCTAAGACGAACT | 494470 |
rs561993791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400296 | CTTGGGCTTGGCCAG[C/T]GTCCTGCAGTGATGA | 494470 |
rs562002136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344911 | CCTCATCTTGGACAC[C/T]AGGGTGGTGGGCTGT | 494470 |
rs562010826 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458625 | TGAGGAAGAGCTTCT[A/G]GCACGACTGGTTCAT | 494470 |
rs562015091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373646 | CCACACTGGCTCCTC[A/G]GGCTCCAGGGACAGC | 494470 |
rs562071387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363513 | GAGACATCCACAAAT[C/T]AGGATGCACCCTGTG | 494470 |
rs562074968 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421115 | CACACTGACCACCTC[C/T]GTCCTGGGTCTCCTC | 494470 |
rs562080976 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46368691 | GCTGAGCATCAGGAG[C/T]GAGCAGCACACACTG | 494470 |
rs562090644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46405562 | TTGGAGAGAGAGGGC[A/G]AAGGAGACAGCGCAA | 494470 |
rs562131489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46362826 | AGCACAACATACGAG[A/G]GCCAAGAGGAATCTT | 494470 |
rs562134836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46356971 | GAGTTCAGGTGGGGG[A/G]CAAGTGGCTTTGTCC | 494470 |
rs562137604 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377035 | CCCCTACCTCAGGGA[C/G]TGGTCAGGCACCTAG | 494470 |
rs562141866 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420758 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 494470 |
rs562180947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46447437 | AAGGCTGGGAGATGT[A/G]AAGTTCCTTGCAGCT | 494470 |
rs562270083 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46424372 | TGGGAGGGGGATTTG[A/G]GCAGGGAATGGAATG | 494470 |
rs562280207 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374770 | GCTCTGGCTGAACTG[C/G]GGGGGCTAGAGACCC | 494470 |
rs562359398 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356823 | CTAGATGTTGGTCTT[A/T]TTCAGGCATGGTGCA | 494470 |
rs562395796 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400071 | TCCCTGGAGCACTGG[A/G]ACCCCCACGGTACCT | 494470 |
rs562403389 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383992 | GCTGTAACATGACTT[A/T]AAAAGGACACACAGT | 494470 |
rs562406701 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397071 | TTCTGTCAGGAGTCC[A/G]TGAGGTTGGCTTCCC | 494470 |
rs562415194 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444340 | TTTTTCCCTAAAATA[-/T]TTTTTCTGTCATCTA | 494470 |
rs562464129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406581 | GGTCCTGGCTTGCCC[A/G]GGGTCTCCCTGCCAG | 494470 |
rs562465686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429126 | ACCAAAGCCAGAATC[C/T]ATAAGGCAGAGAGGC | 494470 |
rs562479677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422693 | CAAAAGGAGGGTAGA[C/T]GTTGCAGGGAATTTG | 494470 |
rs562481534 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347501 | GGAGCTGGGGGCTTC[A/G]TGTCCTCCCTCTGAA | 494470 |
rs562528875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417612 | CCCCAACCTTTTCTT[C/T]TTCCTGCTTCATTTT | 494470 |
rs562541190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423566 | TCTCTGGGCATACCA[C/T]GTGGAGACGTGTATG | 494470 |
rs562578078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416960 | TGCCTTTAATGGGAG[A/G]AGCTTGTATGGGAGG | 494470 |
rs562610630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378818 | GCTGCTATGGATGGT[A/G]GGGAGCTGCACAACG | 494470 |
rs562613932 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458283 | ACAGAAGAATGGAGA[C/T]GGGAAAATCCACCAA | 494470 |
rs562665337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344627 | ACCTCGGCATCCACA[A/G]TGGGCTCATTCCCTG | 494470 |
rs562675987 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46373269 | AATGCCCAGCCAAAG[A/G]CCAGAGAGTGTAACA | 494470 |
rs562676164 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46430618 | GACGGGTTCCTTCAA[C/T]GTTTGCATCTTTTTT | 494470 |
rs562730160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46444715 | TGGACTAAAATGATC[C/T]TCCTGCCTTGGCCTC | 494470 |
rs562740234 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435065 | GCACAGCGGGCAGCC[A/C/T]GGAGACAGCCAGAGT | 494470 |
rs562741674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46431188 | TGAGAATGATGGTTT[A/C]CAGTTTCATCCATGT | 494470 |
rs562753995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424999 | CTCCAGCCCTGTGGC[C/T]GGCTGTCCTGTCTTC | 494470 |
rs562761710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46437735 | ATCCTGACCTTAAGC[C/T]GCAACCCAGGGCCTG | 494470 |
rs562831597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46363566 | CCTGCAAACCTCCCT[C/T]CTGTGTGCTGGTTGA | 494470 |
rs562871441 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376340 | GGAAAACTGAGGTTC[C/T]GTGTGGTTAAGGAGC | 494470 |
rs562872104 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398610 | AGTGGGAAGAGAAGG[G/T]CTGGAGTTGGGCTGA | 494470 |
rs562903930 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394924 | GAACATTTGACTAAC[A/C]TGAACTTTCACGTAT | 494470 |
rs562925310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409379 | GCTCAAGGGATCCTT[G/T]GAGGTTTGGCCCATC | 494470 |
rs562984691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403576 | TGCAATGTGTCAGAT[A/G]CCTCATGAAAATCAG | 494470 |
rs563005921 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393082 | GCAGGATGAGTCCTT[C/T]GCAATGTGAGGAGTC | 494470 |
rs563014844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418930 | ACTAGGAAACAATAG[C/T]GAGTTAATGTGTTGC | 494470 |
rs563079733 | snp | G/T | 5.8279e-05 | 0.00539779 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433247 | GCCGCCACTTCCACC[G/T]GGGCCCCCCGCAGCC | 494470 |
rs563080575 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459966 | GCCGCGGGTCCACCG[A/T]GGACGCCAATCAATC | 494470 |
rs563106162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351939 | TCCTCCTGCACCGTG[C/T]ATCTACGCAGTTTTT | 494470 |
rs563141726 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46433778 | TCAGAAGCCAGTGTG[G/T]GTCCCCATTGCATCA | 494470 |
rs563152299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427959 | GAAAAGCAGCCAGGG[A/C]GATGGGAGCACAAAC | 494470 |
rs563157966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46359912 | TTAAATCTGAATGGA[C/T]AGATTTTAGTCACAG | 494470 |
rs563170788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46385048 | AGAGTGGTGTGCAGG[A/G]CTCCCTTTCAGTTGG | 494470 |
rs563180030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46397420 | GTGTGTGTGCATGTG[C/G]TGTGTGTGTGTGGTC | 494470 |
rs563198927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46348811 | CAAATTAAAGTCCCT[A/G]GTAAGTCCTGCAACC | 494470 |
rs563198958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342433 | TGCCAAGCTTCGAGG[A/G]GGTCTAGACCCCCAA | 494470 |
rs563231720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365631 | GCCTCAGCCTCCCCA[A/G]TAGCTAGGATTACAG | 494470 |
rs563283941 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46447981 | CCTGACTCCCCTGTG[A/C]CCTGGCCCCCTTATA | 494470 |
rs563287514 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455890 | ACCTGACTCCCAGGG[A/G]AAGAGCAGGCTGTGG | 494470 |
rs563294549 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382991 | TACTCACTCCCCCCA[A/C]CCCCTGGGTCTGGAA | 494470 |
rs563298212 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418750 | AAGATAGTTACAGAC[C/T]CAGAAAAGAGCTATC | 494470 |
rs563318915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440579 | TAAATATTTCACTAT[A/G]TATCTCGAGAGATAA | 494470 |
rs563322001 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456820 | GTTGGGGAGGACCCA[C/T]CTCTCCAGAATGGCG | 494470 |
rs563334243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343039 | GGCTACATAATATTC[C/T]ACTTGAATAGTGGCT | 494470 |
rs563336056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366019 | AACTCTTGGCTGGGC[A/G]CGGTGGCTCACACCT | 494470 |
rs563344629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354811 | TTTGACATTCATTTT[A/G]TGTGTGCTCCATACA | 494470 |
rs563348738 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46421098 | GTTAGTTGATTGTGA[G/T]GCACACTGACCACCT | 494470 |
rs563349508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398035 | TGGTCATGTGGAGGT[A/G]TGAGGGTGTGTGTAC | 494470 |
rs563392920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46392512 | AGAGCCACTCCAGGA[A/G]TCTCTGAAGGCTCCC | 494470 |
rs563428981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360478 | TTGGAATTCCAAACA[A/C]CTCATTTACAAACAG | 494470 |
rs563429711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382546 | CTCACTGCTTATTTT[A/G]CTTACTACTGAGAGT | 494470 |
rs563430357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372256 | CATAGTATTCTGGAG[A/G]GAGCCCAGTTTGAGA | 494470 |
rs563443119 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46449737 | GTGAAGAGGTGCTTT[A/C]CACCATGGCTGTAGG | 494470 |
rs563472826 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405269 | GAGGGCTCCCCAGAA[A/G]TAGTAGAGTCTCTGG | 494470 |
rs563473291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379308 | CTTTGACAAACACAA[A/G]ACCCTCTCCTTAAAC | 494470 |
rs563490704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367268 | CCTGGCTTTCCAGGT[A/G]TAGGGTAGACCAGAT | 494470 |
rs563494243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354063 | ACTCTAAACCAGGAA[A/G]GCAGGAGCCACAACG | 494470 |
rs563498935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367841 | ACAATTCGGATTTCT[C/T]GGCTCTGCTTCTGGA | 494470 |
rs563508177 | snp | A/C/T | 0.00103921 | 0.0227714 | intron-variant | RNF165 | GRCh38.p7 | 18:46450421 | TTGCTCTGTCTGGTA[A/C/T]CAACTGGGTTGGTGG | 494470 |
rs563509654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386982 | GCACTGCTGCGTGCC[A/G]CTGCTGAACCAGGCA | 494470 |
rs563535581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416195 | TCTCAAGGAAACACA[C/T]GGATCTGCAGGAAAG | 494470 |
rs563542032 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409516 | AAGAGACGTCTGACT[C/G]TGAGCTGCTGAGTAT | 494470 |
rs563581565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382939 | CCATCCCCTTATTTT[A/G]TGAAGACAACGTCAT | 494470 |
rs563618456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378220 | AGGTCGTGGTGTCCA[A/C]AAGCAAGACAAGGAC | 494470 |
rs563629779 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339956 | TGGTTTTTAGGCTAC[A/G]GAAGCAACAGTTCTG | 494470 |
rs563669272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46377367 | TGGTCTAGACACACA[A/G]TGATGTGTGTCTTTC | 494470 |
rs563685368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415690 | CCAACCTGGGCCAAG[A/T]GATGCTGAGCAAGTC | 494470 |
rs563686622 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334630 | CAGCCCCTTCCCCTA[A/G]TACCTAGCCCTGTAT | 494470 |
rs563721005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381463 | CTCTCAGGGACATCC[G/T]TTGAGTCCCTGTTTG | 494470 |
rs563729679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404363 | AAGGATAGGAAGAAG[A/G]ATGACAGGAAGACAT | 494470 |
rs563730752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336289 | CCAATCTCTAAATAC[A/C]ATTGCAGGATGCTGA | 494470 |
rs563757500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442768 | TGTCTAGAACTCTAC[G/T]TATGAATTTGTTTTC | 494470 |
rs563773028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398657 | GTCTGAATTGCAGGG[A/G]TCCACGCTGCTGAAC | 494470 |
rs563846689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394212 | AACAAGGGCCTGAAG[A/G]GACAAGGTGCCTGCC | 494470 |
rs563851868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404870 | AGTTCCATTTTAGAG[C/T]TGGAGAAACAGAGGC | 494470 |
rs563862069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46361309 | AATCCCTGTAGCCTT[A/G]CTCTTCTGAAAAAGA | 494470 |
rs563868782 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384058 | TTTCTTAACAGCAGA[C/G]AGAGGCAGTCGGGGT | 494470 |
rs563883478 | snp | G/T | 6.95024e-05 | 0.0058946 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433474 | CAGCAGCTCCTGGAA[G/T]CCCAGCACCGCAGGC | 494470 |
rs563948976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415778 | GCCCATAATTCATTG[C/T]ACTGGATGGTTGTAG | 494470 |
rs563953213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343100 | CTCAAAATGCCATAG[G/T]TTCTAGGCCGCTTGG | 494470 |
rs563964931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46393789 | TCACCTTTTGGAGAG[C/T]CTGGCAGGTCATGAG | 494470 |
rs563998771 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363081 | TGATTTGTTCACTGC[C/T]ATATCCCCATTGTCT | 494470 |
rs564039518 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450235 | GGTGGAGAAGTTGCA[C/T]GCTGGGCTCATGGAG | 494470 |
rs564058658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46434926 | GGGTGCATAGAGCCT[A/G]TAGGAGGCGAGTCTG | 494470 |
rs564060111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360568 | GCCTTCCAGACTTTC[C/T]CTCTCTCTTCTCCTC | 494470 |
rs564076346 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413339 | ATGCTCCCATCCCCA[A/G]ATCTATCTGCATTAG | 494470 |
rs564094928 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46361354 | TATGTTTATAATGAT[A/T]TAGAAATCATTACAT | 494470 |
rs564120438 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46428395 | GCCTGGTGACAGAGC[C/G]AGACTCCATCTCAAA | 494470 |
rs564129378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337489 | GTGGTCGTGTAGCCC[A/G]GGCCATCTGCTCATT | 494470 |
rs564140769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349647 | GAGTGGGCTCTTGGC[C/T]ACTGGGGGTGCTTGC | 494470 |
rs564165752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46338118 | CTCGCCTAAAAACCC[A/G]TTTTGAGTTGTGTTT | 494470 |
rs564175847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343696 | GCACTGTGCTTTCCT[C/T]GTGATGAGAAGAGCT | 494470 |
rs564181957 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425095 | ATCAGGGCCCTGCCT[C/G]CAGTGTCCCCTCCCT | 494470 |
rs564199317 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46393287 | AAACTTTGTGGGGTG[A/T]CTGTTCCCAGCTCTT | 494470 |
rs564206863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354870 | ATTGACTCTTTAAAG[A/G]CAAACATCAGTGCCA | 494470 |
rs564241619 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46382988 | TAATACTCACTCCCC[A/C]CACCCCCTGGGTCTG | 494470 |
rs564270086 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454658 | GGAGACTTGGCATCC[A/G]GGCCTTGCCCCACGG | 494470 |
rs564327978 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46362801 | CTAGTCCTCTTCCTT[A/C]AATTCTAGAAGCACA | 494470 |
rs564334015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46443411 | TACCATTTTGTGTGT[A/T]ATGCAAAACTCTTAC | 494470 |
rs564340208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356479 | TGATATTTACCAGAG[C/T]CCTGAGCCTGAGGGC | 494470 |
rs564354058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383339 | GTTGCTAATGAGGGA[A/G]CCAGCAGGATGATGC | 494470 |
rs564387060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405420 | GACAGACAGTGGGAA[C/T]AGTGAGGTGCTACAG | 494470 |
rs564415847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378370 | GAGTCAGCACCAGGG[A/C]CAGAATCCAGGCTCC | 494470 |
rs564427940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378752 | GCAGAGGGTGCAAGA[A/G]GGTGGGGCTTGGCAT | 494470 |
rs564430032 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362713 | ATGCCCTGCGACAAC[C/G]ACATCAGGTTGAATG | 494470 |
rs564484179 | in-del | -/TTA | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46429545 | CTGTTCTAATATAGC[-/TTA]TTATTTGTTTTATTG | 494470 |
rs564491717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410946 | GGGCACCAGTGTGTG[C/T]CAGGTGCTGGCTGTG | 494470 |
rs564502744 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46400537 | CCATCCTGTGTTAAG[G/T]GTTTGGGGAACAGAG | 494470 |
rs564518656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46453382 | AGTGTTTACTCCTAC[C/T]GAGGATGCACGCCTC | 494470 |
rs564530784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340582 | GTCCACACGAATGGC[A/G]GAACGTCCTGACTGC | 494470 |
rs564542412 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420415 | CAGGGCCGGGCTTGT[G/T]TAAGCATACTGTGTG | 494470 |
rs564542608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436711 | CTCATTCTCAGGTAC[A/G]CTCTCCATTAAATTG | 494470 |
rs564592792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399901 | CAACCCACATGGCAG[G/T]TGGCTTTTCCAAAGC | 494470 |
rs564606568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46454104 | GGCAAGAGGGCAAGG[C/T]CGTCTCAAAAAAAAA | 494470 |
rs564634299 | in-del | -/CAG | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46368910 | ACATAGTGTTTAGAA[-/CAG]CAGTGCATGGCACAC | 494470 |
rs564643310 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46446396 | GAAGAGTTGGCTGGG[C/T]GTGGTGGCTCATGCC | 494470 |
rs564655720 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429888 | TCCCAAAGTGTTGGG[A/T]TTATGGATGTGAGCC | 494470 |
rs564657036 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46436096 | AGATTCTGGTTCTAG[C/G]TCATAAGAGAGCTGA | 494470 |
rs564657401 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440464 | ATTCCTTATTATTCA[C/T]AGTTTCAGGCAGCCA | 494470 |
rs564664604 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46377238 | AAATATCCTTTAAAG[-/A]AAAAAAGTTTCATAA | 494470 |
rs564686545 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46364711 | ACATTCCTGTCCTGA[A/G]GCTCTCTCTGCCCAT | 494470 |
rs564694506 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46425780 | GCACTGTCCTCCTCC[C/G]TGGGAGGCCCCCCGT | 494470 |
rs564705426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400185 | CTGGATATTCCCGAC[A/C]CTCATGCTGGTCACC | 494470 |
rs564720970 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397392 | GTGTGTGTGGTCATG[C/T]TGAGGTGTGAGGGTG | 494470 |
rs564761971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358948 | TGTCCCCACAGAGCC[C/T]CAGGTCCCCTACCCC | 494470 |
rs564763579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46365543 | AAGGCTTGCTCTGTC[A/G]CCCAGCCTGGAGTGC | 494470 |
rs564766885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394850 | AGGTATTTTATTACA[A/G]GCTAGTTCTTTGAAA | 494470 |
rs564790047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388881 | TAAAAACAGACCTAA[C/G]AACACAGAGATAAAG | 494470 |
rs564813409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369956 | ACACACACGCACACA[A/C]GCACACATGCACACA | 494470 |
rs564839357 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46385533 | GCTCTGGAGCTCCAA[A/G]TCCCCCAGATTCTGC | 494470 |
rs564846941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381027 | CTCATGTCCTCTGGC[A/C]ATGTGTGGGAGTGTG | 494470 |
rs564870128 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46359561 | AGAGCCAAGAGAATG[G/T]AAGAACTGAGGCCTG | 494470 |
rs564904740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385991 | CTGGCCCCAAGAACC[C/T]CTTGTCTCCGGAAGG | 494470 |
rs564928824 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349473 | ACCATCATCTTGGGG[C/G]TTAAGATTCAACATA | 494470 |
rs564951941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432076 | AGTGGGTATTGGGAG[A/G]AGCAGACATGTACTG | 494470 |
rs564961176 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332642 | CTATGGTGATTGCCC[A/G]TTGGCATCTCTGAGG | 494470 |
rs564968962 | snp | A/C/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460291 | TGGGGCTGTAGCAAC[A/C/G]TCTGTCAGGCCCCCT | 494470 |
rs564970827 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429137 | AATCTATAAGGCAGA[C/G]AGGCCTGACTTATGG | 494470 |
rs564975533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375259 | TTCCCTTTCATCAAA[A/G]ATACTTGTCCTGGCC | 494470 |
rs564994206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402451 | AATATTGCATGGAAC[A/C]TGCTTATACTAAAAA | 494470 |
rs565025423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391488 | TCAGTGTCCTCATCC[A/G]TCATGTGTGTTGAAC | 494470 |
rs565059836 | snp | A/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459730 | CTGTGCTTCTGCTCC[A/C]GGCACTGGTCAGGGA | 494470 |
rs565069737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46352796 | TTATATACTGAAGGC[C/T]ATGTGCCCAGCTGAA | 494470 |
rs565079731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382248 | TCCCATGGAGGCAGG[A/G]GTTGCTTAGATCTGC | 494470 |
rs565082686 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389927 | AGAGACAGGGTTTTG[C/T]CATGTTGCCCAGGCT | 494470 |
rs565108274 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412097 | GATCTCAGCTCAGCG[A/G]GAGACAACGGCTCAT | 494470 |
rs565110701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347052 | AGGGAGATATCTTAG[C/T]GCACGGGATGGGGAG | 494470 |
rs565186461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46348118 | TGTTCTCTTAGCCTG[C/T]GGCAGACATCCTGGG | 494470 |
rs565190101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46391908 | ATACTACACACACCA[A/G]CACACACTTATACAC | 494470 |
rs565207485 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458093 | TCCGGTCCTGCTACC[A/T]CACCTAGATGTTGTG | 494470 |
rs565208808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414959 | GGGGCTGAGCTAAGC[C/T]GCAGTCCTGCTGGGC | 494470 |
rs565209737 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370752 | CAAGACCCAATGGAC[A/G]GTTGGGTTGTGACAG | 494470 |
rs565212028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46425775 | TTTCTGCACTGTCCT[C/T]CTCCCTGGGAGGCCC | 494470 |
rs565212658 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46361981 | TTGAAGATAATAGCT[C/T]ATTTATATCCCTGAG | 494470 |
rs565218639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432655 | AGGATGCTTATGTAT[C/T]CATTAAAGATACACT | 494470 |
rs565242677 | snp | A/C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365216 | GTATGGATGGCAGGG[A/C/G]GTGGCCTAAGCTCAG | 494470 |
rs565259901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398086 | CATGCTGACGTGTGA[G/T]GGTGTGTGCGCATGT | 494470 |
rs565287458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46427149 | AAGAACCACTCTGGG[A/G]ATGGAGATGGTGGAG | 494470 |
rs565295380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46347633 | GTGGATGTAATGTAC[C/T]CACCGTGAGTGGCTC | 494470 |
rs565330737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341866 | TTTGTCTTTCTTGAA[A/G]AGACAGACCCCAAAG | 494470 |
rs565348666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46420913 | TTAATTTACTTGAGT[C/T]TTTGTTAAAAATATA | 494470 |
rs565352138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358444 | TGGGACTGGGAATCA[C/T]GTAAAATGAGGCCAC | 494470 |
rs565466042 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333689 | ACTAAGGGCGCTCGT[A/G]CCCGTCTCTCTGCAC | 494470 |
rs565467373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352398 | AGCTCCCAAATCTGA[G/T]AACACCTGCTATGGA | 494470 |
rs565529431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352830 | AGGGGTTGCATTACC[A/G]TAGAAGGAGAGAACA | 494470 |
rs565604094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46366478 | TACTGCACTCAGATA[C/T]TCATTTTATGATGAG | 494470 |
rs565610424 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379979 | TGGAACGTCAGAGAA[G/T]AGATGAGGCTCCAAA | 494470 |
rs565613726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428424 | AAACAAAAAGAAAAA[C/G]AAAAACAAAAACAAA | 494470 |
rs565617592 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46431548 | AGGGGAGGGGCACAC[A/G]CTTAGGTAACAGTGT | 494470 |
rs565622066 | snp | A/T | 0.116838 | 0.211584 | intron-variant | RNF165 | GRCh38.p7 | 18:46440714 | GTTATACTTTGTATC[A/T]ATCAAGATCCGAATA | 494470 |
rs565626487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364773 | TTCTGAGGATCGCAC[A/G]GCCACCGAGGTCATA | 494470 |
rs565647259 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46375596 | TAATAATAATAATAA[C/T]AACTTGTCCTGGCTT | 494470 |
rs565656632 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404181 | TATGATTCTTGATTT[C/G]TCGAAAACTGCTCAA | 494470 |
rs565662248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385355 | AGATTGTTTTGTCTG[A/G]AAGGAAGGACTTGCA | 494470 |
rs565701222 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RNF165 | GRCh38.p7 | 18:46375983 | TTTCTTGTCTACGAA[C/G]TGGATGATAATAGCT | 494470 |
rs565718183 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46396420 | CAGAGACATTCTACC[C/T]GCCCAGACACAGAGC | 494470 |
rs565726467 | snp | A/G | 8.24002e-05 | 0.0064182 | missense | RNF165 | GRCh38.p7 | 18:46456628 | ACACAACTGGGAGCC[A/G]ACAGCTGAGGGAGGA | 494470 |
rs565789195 | snp | G/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458766 | TGCCTACCGGTGCAG[G/T]CGCTGGGAGAGACAA | 494470 |
rs565805656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391595 | GGGTAGTTTGCACAG[A/C]CAGGCTTTCCCACCT | 494470 |
rs565873730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46364110 | GGACCACCATGTCCG[A/G]CTAATTTTTGTGTTT | 494470 |
rs565874116 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46454576 | GTGTGTTCCAGTGAG[G/T]TTACAGTATTCCCCA | 494470 |
rs565888164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347109 | GGAGGGCCTCCCGGA[A/G]GAGGCAGGACTGGAG | 494470 |
rs565903609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385663 | CAGCTGTCCCCCTTT[A/G]GAGCATGAACTGAGC | 494470 |
rs565913448 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | RNF165 | GRCh38.p7 | 18:46397643 | GAGGGTGTGTGTGTG[G/T]GTGGGGTCATGCTGG | 494470 |
rs565921808 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344968 | CATGTCCCTCAGGAC[A/G]GAGGGGGACATCAGA | 494470 |
rs565928643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408380 | GAGTTGGCCTTAGGC[A/T]GATGTGACTGGTGTC | 494470 |
rs565973170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46398278 | GTGTGCATGTGGTGT[A/G]TGTGTGAGTGTGTGT | 494470 |
rs565981294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46392189 | ACATGCACACATACT[C/G]TGGTCATCCTTGCCT | 494470 |
rs565993841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46392779 | CCCAGCCCGGACGGG[A/G]CCTGTGTGAGGAACA | 494470 |
rs566010320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414774 | CTCCTTTGCCCCAGT[G/T]CGGAGGGCAGGTTGC | 494470 |
rs566066423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409101 | ATGTGGAGCACCTAA[A/C]AGTGCCTGGCATACA | 494470 |
rs566066964 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46415078 | CAAGTCAGCCTGTGC[A/G]CTGCTGCAGTTTCAG | 494470 |
rs566072880 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404226 | CACCTGCGAGTTCTT[C/T]CCTGGTGCTACGTTA | 494470 |
rs566074845 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333135 | TGACACGGTGGCTGC[A/G]CCTCCACGTGTGAAT | 494470 |
rs566089933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448142 | CTGGCTTTCTTGTGT[A/G]TCAACCCCCATGCCC | 494470 |
rs566094050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366637 | GAGTCATGGCTGAGA[A/G]GAATAGTAGGGTTTC | 494470 |
rs566123222 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354522 | TTAGAGGCCGAACTT[A/G]AGAAACCTTTACAAG | 494470 |
rs566129777 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46403369 | GAAAGCTCTCCCTGC[C/T]CCCGGAGAGAGCCCT | 494470 |
rs566134127 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405691 | GCCCGGTAAATGGAC[C/T]TGATTTGGATGGTTT | 494470 |
rs566161647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360749 | GGCCCCCCTTGCCCT[C/T]TAATACGCCTGGGCA | 494470 |
rs566219651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46360112 | TGAGACGCATCACAA[A/G]TCCATGCAATGGCCC | 494470 |
rs566240236 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46440749 | TTACACATTGTGATT[G/T]GTTGATATGTCACAT | 494470 |
rs566339768 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416671 | CTCAGCTGGGAAGTC[C/G]TTTTGGTCTTCTTGG | 494470 |
rs566347844 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411837 | AGCCTGGGGCTGAGC[C/G/T]GTGTATGTGTGATCT | 494470 |
rs566352449 | snp | G/T | 0.00263434 | 0.0361971 | intron-variant | RNF165 | GRCh38.p7 | 18:46433548 | GACCCGGATGGGGTC[G/T]GGTGAGGGGGCAGGG | 494470 |
rs566367395 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449376 | CTTTAAAAAACATTG[C/T]ATTAAAATATCGTTA | 494470 |
rs566367726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394466 | CTAAGGCATCTCTGG[A/G]GATGTGCAGTTCTGT | 494470 |
rs566368515 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458358 | CCAGATTAGCTGGAA[G/T]TCTGCCACCTTCCTT | 494470 |
rs566385655 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46387233 | AGCTGAGGCATGCAT[A/G/T]AAAAAAGGCAGATAA | 494470 |
rs566403959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427538 | TCTGCCTGACCTGGC[C/T]CTCCCATGCCACAGC | 494470 |
rs566405342 | snp | A/C | 1.78586e-05 | 0.00298814 | intron-variant | RNF165 | GRCh38.p7 | 18:46450825 | CAGCAGGCCAGCCTG[A/C]ATAGTCAGGGAATGG | 494470 |
rs566407431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354420 | GGGGTCCTCATGCAC[A/G]AAGTGCAGGATTGGA | 494470 |
rs566409371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405740 | GGCCATCCAGGATGG[G/T]TTGAATATGATGTCT | 494470 |
rs566430800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372955 | TAATGCCACCATCAT[A/C]AGCCTCACTCAGGGA | 494470 |
rs566466931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416982 | TATGGGAGGGTAAGC[A/T]TACAAGGAGGGGAGA | 494470 |
rs566496098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46450164 | AAAAGGGACATAAGA[A/G]CAGGAAAGACAATAG | 494470 |
rs566521878 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371635 | AGACAGCAGCTGTTA[C/G]TATTGATGATAAGCC | 494470 |
rs566534940 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369675 | AGCCTATCTCATTTA[A/G]TTCTGCTTTGCTTTG | 494470 |
rs566607566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46451373 | AGAGCCCAGGAAACT[A/G]AGTTTAAAATTTTTT | 494470 |
rs566613384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368853 | TGCATGATGACAATG[C/T]CTACCTGATAGAGTG | 494470 |
rs566624877 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46363003 | CAGAAAAAGTGTAGA[A/G]TTAAAACCAGACCAA | 494470 |
rs566625384 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46414775 | TCCTTTGCCCCAGTG[C/T]GGAGGGCAGGTTGCA | 494470 |
rs566663511 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436894 | ACGGAGTACTCAGGG[A/C]CCTTGCATATGGCTG | 494470 |
rs566667033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389595 | ATTACGCTTTCCCCA[A/G]CCCATCCCTCATCGC | 494470 |
rs566672083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363655 | GCTGTCAAGTCACAG[C/G]CCTGCCCATGGGAGA | 494470 |
rs566695798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430107 | TTTGTTGTTCCTCTT[C/T]CTTGGTTTGTGTTAG | 494470 |
rs566698257 | in-del | -/GGGTCAGTGTGGC | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46433128 | CCCGGGTGGGCACAA[-/GGGTCAGTGTGGC]GGCCGCTCGTGCTGG | 494470 |
rs566708114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424033 | GGGCATTTACTGCAT[C/G]GTACCTCCTCCGAAA | 494470 |
rs566720087 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457593 | ACACTAAACCAGGGA[A/G]GGCTCGGCCCTCAGC | 494470 |
rs566727818 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440028 | AGAGACAGGGTTTCA[A/C]CATGTTGGCCAGGAT | 494470 |
rs566752427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46437093 | CTGCATTCCTGACCA[C/G]TACCTGCCCCAAGAA | 494470 |
rs566775521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345040 | GCTTGGGAGGCAGCT[C/T]CTGCCTCGCTCCTTC | 494470 |
rs566777870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46384177 | GCCCCGGCCGTGCTT[C/T]CAGCCCAACCTCATC | 494470 |
rs566856840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351110 | GTCTGCAGAGCCCGG[A/G]AGGGAGGCAGGGATG | 494470 |
rs566871436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445776 | TTGCTTGTTATATAA[C/T]GTCTGAAAACAGAGA | 494470 |
rs566874996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351541 | CCATTGTCCTCCCTC[A/G]GCAGCCCAGCCCCTT | 494470 |
rs566886978 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459526 | CCAATTCTCTGCCCC[A/C]GGCTAATATTAGGGA | 494470 |
rs566906883 | in-del | -/ACCAGAGTGGAAGTTGTGGTGCAG | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46409577 | TCCTGGCCACATCTA[-/ACCAGAGTGGAAGTTGTGGTGCAG]ACCAGAGTGGAAGTT | 494470 |
rs566918504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345583 | GGACTAGACGTGTGC[A/G]CAGCAGAGAGCAGAG | 494470 |
rs566944684 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46384502 | AATCCCTTGCCCTTT[C/T]CTTGAATATTTCTCA | 494470 |
rs566954759 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459109 | AGGGTGGTCTAGGAA[A/G]CTCACTCCTCTCTTA | 494470 |
rs566960539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379374 | GAGACTAAGCGCTGG[G/T]TTCTTTTCAGGGCTC | 494470 |
rs566999511 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420330 | AAAGGGGCATCAGAC[A/G]AAACAATTCTCCCAG | 494470 |
rs567004129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368933 | TGGCACACAGTAATT[G/T]CTTAGTGAATGTTTA | 494470 |
rs567033050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369545 | TCTGCTGGTCAGTGA[A/G]GTGTTGCTTTAGGTT | 494470 |
rs567052023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340156 | TTTGTAAAAATTCCC[A/G]GCTTAACATTGTATG | 494470 |
rs567104412 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360080 | TTGATGAGGAGCACT[C/T]TAGGTCCAGAATACC | 494470 |
rs567217728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400582 | CAGGGAACACCCGCA[C/T]CTGTTTAGGGTGGTT | 494470 |
rs567244590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384614 | CTACTCAGATTCCCT[A/G]GAGAAGCAGCAAAGC | 494470 |
rs567245590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405747 | CAGGATGGGTTGAAT[A/C]TGATGTCTATGTGAG | 494470 |
rs567261810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412350 | TTGGTTGCCTGGCAG[C/T]CCCAGAGGGTTACCA | 494470 |
rs567271511 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46387423 | GGAGTGAATCCAGTA[C/T]AAAAACAGCATTAGC | 494470 |
rs567273875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406196 | GCCTGCATCCAGAGT[C/T]GTCACAAACTTCCAC | 494470 |
rs567280502 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436523 | AAAGATTGATGTGCC[A/G]TTGTGTCATTTTTCA | 494470 |
rs567293280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363720 | GTTATAATGAGCTGG[C/T]CTTGTAGTCCCAGCT | 494470 |
rs567323024 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415418 | ATAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 494470 |
rs567356386 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46444854 | ACTGTTACTCTAACC[C/T]AGTGAATTTCCTATT | 494470 |
rs567413758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364104 | AGGCAGGGACCACCA[C/T]GTCCGGCTAATTTTT | 494470 |
rs567483418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424693 | AAAGAGATTTCAGCA[G/T]GTGTGTGGGATCAGC | 494470 |
rs567504186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46407627 | GAGGGTATTTCCAGA[C/T]CTGAGACTCCAGCCG | 494470 |
rs567510513 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429244 | TCATTTCTTTTTGCA[A/C]AGATTTATTTTTAAA | 494470 |
rs567524648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46408229 | TGGAGGCTACTGATT[C/T]AGGGGAAGGTCCGCA | 494470 |
rs567537932 | snp | C/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333142 | GTGGCTGCGCCTCCA[C/T]GTGTGAATTTGCAGG | 494470 |
rs567547319 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46427255 | CAGGTACCTGTGCCC[A/G]CCTTCCTCTGGCTGC | 494470 |
rs567552243 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368406 | CCACTGGGTGGGAAA[C/T]GAAGACTTCCAGAAT | 494470 |
rs567563905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385169 | GTCTGTTGGGTTAGA[G/T]AATATGTTTGGTTGG | 494470 |
rs567644016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345708 | TATTAAACTAAACAA[A/G]CAACTCTTCTACCTC | 494470 |
rs567661053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419089 | CTGATGTCCCCGAGT[A/T]CACCCCAGAAGTAGG | 494470 |
rs567719318 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF165 | GRCh38.p7 | 18:46433723 | TTCAGAGGCATCCAC[C/T]TCAGGCAGTGAGCAC | 494470 |
rs567743958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380563 | GCGTTTCCTCAGGTC[C/G]TAGTGCTTCATCCTT | 494470 |
rs567756115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374924 | TGGTCTTGAGGGCCT[C/T]CCCAGTCACTGCACT | 494470 |
rs567831024 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46396530 | GGTGCCTGGCACACA[C/G]TAGCTTTTCAGATAA | 494470 |
rs567835224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370135 | CAATCTGGGTCCCCA[C/T]TTCCTTCCCTGCTTT | 494470 |
rs567837510 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46454328 | CCTCCTTTTTCTAGC[A/T]GGGTCAGCTAAACGA | 494470 |
rs567840315 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332343 | GGCCTGAGAGATCCA[C/T]GGGCTTATGGGAGAG | 494470 |
rs567906738 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396460 | GTCACCTCTCAGGAT[A/G]GTGAACTCCATGACA | 494470 |
rs567914162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46446542 | CGGGCGTGGTGTGGC[A/C]TGCCTGTAGTCCCAG | 494470 |
rs567919694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46411068 | AAGGCAGGTAAGACA[C/T]GCCTGATGGATTCAG | 494470 |
rs567940868 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46370575 | TGTGTCTGGTCCCAG[A/G]TGGCAGTCATCGCTA | 494470 |
rs567968287 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399310 | AGCTTGGACGTGGGC[C/T]GCGCTTGCATGGGGA | 494470 |
rs567976570 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407510 | TGTTAGCCTGTTGAC[A/G]TTCTTCCTTGTAGAT | 494470 |
rs567978298 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46441814 | AATGGCGTGAACCGG[A/G]AGGCGGAGCTTGCAG | 494470 |
rs567997222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439421 | CCTCCTGCCATCTCG[C/T]TCCTGTAGGATCTGA | 494470 |
rs568019829 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46403475 | TACCTAGACTACATT[G/T]ATTATTTCTATCCAC | 494470 |
rs568045834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46348389 | TGGCCAGCGTTGCTG[A/G]TGGTTGATTGTCTTT | 494470 |
rs568060652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383020 | AACCTCATGCACCCC[C/G]TAGCCTGCTGGGCCA | 494470 |
rs568082923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46349185 | ATCTTAGCACATTTG[G/T]ACTGCAGTAACAAAA | 494470 |
rs568084463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382682 | GTCCACCACAGCCCC[A/G]TGAAGTTAGGCAGGT | 494470 |
rs568106777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46335463 | ATGCATTTAGATTCA[A/T]TTTTTTTCTTTTTTG | 494470 |
rs568136184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355954 | CCTCTGTAGTGGGCG[A/G]AGGCATGGCTGAGGG | 494470 |
rs568187954 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456965 | GCTGACAGACGGGCC[C/T]CTCAATCCTGTCCTC | 494470 |
rs568193441 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444743 | CTCCCAAAATGCTGG[A/G]ATTAGAGGCATGAGC | 494470 |
rs568221630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46449149 | TCCTGATTTTAAAGA[C/T]TGGAAAACTGAGGAA | 494470 |
rs568228353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46449917 | GGTTTGAAATCCTGG[C/T]TCTGTCCCTTGGTTG | 494470 |
rs568232222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405052 | AAGACCCCACCAATT[A/T]TTTTTTTGGTAAGGC | 494470 |
rs568232905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372406 | CTACCCCTCCCAGAG[A/G]CTGCATACAGACCCA | 494470 |
rs568258162 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46350025 | CACCCATGTTCCACA[A/T]GCCAATACATGCACA | 494470 |
rs568265027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442392 | AACTTTCTAGTTAGC[A/G]TTATGAATTCTTTTT | 494470 |
rs568297298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350496 | TGGGGGTCACACGAG[A/G]GGTGTCAAGAGGGGC | 494470 |
rs568309546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46367928 | TCCATGATTCTGATG[C/T]CCAGTTACGGTTGAG | 494470 |
rs568311398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398989 | GGCTCCTGGGTGTGG[C/T]CGCCAGAGATCCTGA | 494470 |
rs568318898 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF165 | GRCh38.p7 | 18:46335280 | CGCGGGCTTTGTTTT[C/T]AACTGTGATAAATGG | 494470 |
rs568329352 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46367553 | TGGGTCTATTGGACC[C/T]ATTGCCTTGTGCCCT | 494470 |
rs568365066 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458414 | CATTTGCACTGCTCT[A/G]TAAGCCTCCCCCTCA | 494470 |
rs568384704 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355243 | CAAGCATGAGCCACC[C/G]GGCCCGGCCTGTTTT | 494470 |
rs568395903 | in-del | -/CTCCCTGCCCCCGGAGAGAGCC | 0.00636936 | 0.0560724 | intron-variant | RNF165 | GRCh38.p7 | 18:46403361 | CTCCTAGAGAAAGCT[-/CTCCCTGCCCCCGGAGAGAGCC]CTCCCTGCCCCCCGT | 494470 |
rs568421860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373414 | AGTCACCCAGCAAGT[C/T]GTGGGCTCTCTCCAG | 494470 |
rs568505726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399255 | GACTGGTACTCTGGA[C/T]GTCCAGGGCAGTGCT | 494470 |
rs568513821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46423133 | CAGTTAAACCCTGTG[A/G]AATGCAAGCCCTAAA | 494470 |
rs568525178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388463 | TTTGTTCCTGAAACA[C/T]ATGTTGGGACCTGCA | 494470 |
rs568535588 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46384364 | ATGTGTGTGGGGGGG[-/A]TTCTTGATACTTCTT | 494470 |
rs568547025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383505 | AACCTTTGGTATTAT[A/G]TTCTCCATTGGACAA | 494470 |
rs568570868 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372246 | AGGTTGGCAGCATAG[C/T]ATTCTGGAGAGAGCC | 494470 |
rs568572107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356535 | CCAGGGGTTGATTCT[C/T]GCCTCTGTTGTCCTG | 494470 |
rs568576264 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46422439 | GCTGTATCCATGCAG[A/G]GGGGAGAGGAGGCTC | 494470 |
rs568597366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383762 | GGTTTCACCGTGTTG[A/G]CCAGGATGGTCTTGA | 494470 |
rs568619213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46338747 | GCCTTGCTAAATGAG[A/G]CATTTTAGACACTGA | 494470 |
rs568635379 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46373217 | ATGGGCCTCCAGGGC[A/T]TTAAGCTTGATCCCT | 494470 |
rs568660103 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46378924 | TTCCTCCCCAGTGTG[A/G]CTCTGATGAATAAGC | 494470 |
rs568660670 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46383775 | TGGCCAGGATGGTCT[C/T]GATCTGACCTCGTGA | 494470 |
rs568668279 | in-del | -/AA | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46446670 | GCGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 494470 |
rs568672870 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370960 | CACTGCTAATAAAGA[C/T]GTACGCGACACTGGG | 494470 |
rs568694634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405135 | TATTTTCAACATGTC[C/T]ATGGTGTACAGTGTG | 494470 |
rs568737555 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440339 | TATATTGTTATAATT[G/T]TTCTATTTTGTTATT | 494470 |
rs568755671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405574 | GGCGAAGGAGACAGC[A/G]CAAGAGGAAAAATGC | 494470 |
rs568759246 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398581 | GAGGAACCCATGGGT[A/G]GGAGATCAGGGAGAG | 494470 |
rs568762773 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46417798 | CACCTGAGGTCAGGA[A/G]TTTGAGACCAGCCTG | 494470 |
rs568770081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400001 | GCAAGCTGGGGCCAC[A/G]CCCCAGGTGTTCTGA | 494470 |
rs568798958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411918 | GAGGAAGGGCAGGGG[C/G]ACCATGGAGCCCAGC | 494470 |
rs568811951 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375274 | AATACTTGTCCTGGC[C/T]GGGCACAGTGGCTCA | 494470 |
rs568822757 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377845 | CCTGGTCTATTTAGC[A/G]TGTGATGCTCAGGTA | 494470 |
rs568828492 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46416025 | GTCCTCAGCCTTCCT[C/G]ACTTTGCTGCTGGCA | 494470 |
rs568869810 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372856 | AAGGACTGTGTAGTG[A/G/T]CCAGGAAGCCTCCCG | 494470 |
rs568887224 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457247 | AATCAAAGGTGGAAG[A/G]AAAAAAAAGCCAAAT | 494470 |
rs568900672 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351377 | AGTTCCAAGCAAAGG[C/T]GTCCCTTCCGTGGAT | 494470 |
rs568912875 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349277 | GAATCCAAGCTCAAG[G/T]TGCCAGCAGGTTTGT | 494470 |
rs568913280 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373023 | TCTGTGCATGTGCGA[-/GT]GTGTGTGTGTGTGTA | 494470 |
rs568930791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46423160 | TAAAGCCTTTCCTTT[A/G]GGGGATGTCCAAAGG | 494470 |
rs568932854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430043 | TGCAGAGATCCCTGC[A/G]CAGCTGTGTGCTTGG | 494470 |
rs569005782 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397721 | GTGTGTGTGCATGTG[-/GT]GTGTGTGTGTGATCA | 494470 |
rs569013478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442540 | AATTCTAATCCTTTT[A/G]TATTTATTGAGACTT | 494470 |
rs569024147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46442998 | ACGGGGTATATCTCT[C/T]TCCTCCTTTTACTTG | 494470 |
rs569027746 | in-del | -/TCGG | 0.117188 | 0.211804 | intron-variant | RNF165 | GRCh38.p7 | 18:46440710 | TCTGTTATACTTTGT[-/TCGG]ATCAATCAAGATCCG | 494470 |
rs569045009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367937 | CTGATGCCCAGTTAC[A/G]GTTGAGAATCATCTG | 494470 |
rs569049634 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46344544 | ACTCCCACCCCCAGC[A/G]TGGAGACACTGGCCT | 494470 |
rs569077253 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46394348 | CAGAGAGAGCTCCCT[C/T]CTTCTAGCTTGCCAG | 494470 |
rs569083959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46338823 | TCATTTTGGAGCTGC[C/T]CCTCTTTTGGCCGAT | 494470 |
rs569085830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46344992 | CATCAGACCTGTCTC[C/T]CTCCCTAAGGGCTGG | 494470 |
rs569103596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436354 | GAAGGAAATAGAAAT[G/T]CAGTAAAATGGTGAC | 494470 |
rs569117923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356610 | ACTACTCACTCTGAA[C/T]ACACAGAAGGGAGTA | 494470 |
rs569122364 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363839 | TTCATAGGGGCCACC[A/G]TTGAGGGTGTGACCT | 494470 |
rs569122435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46339430 | AAATCATGTTTTAGC[A/G]ATGTATGCAGTGTAT | 494470 |
rs569159907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362533 | GGTTTTCTGTCCCTG[C/T]AAACCCTGAAGAACA | 494470 |
rs569173749 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371954 | TGTTTATTAAATACT[C/G]ACTCCTAACGTACTA | 494470 |
rs569182195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356053 | AGGACGAACTTGGCT[A/C]CATGCAGGCCCCTGG | 494470 |
rs569254055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46444270 | TTAAAGTTTATCGAA[A/C]TTTTTGGATCTGTGA | 494470 |
rs569299447 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340797 | GTGCTAGACAGTTGC[C/G]CCTTCCCTTCACAAC | 494470 |
rs569304888 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389047 | TTGGCTCAAGGTCCA[A/C]AACAGATTGGGAACA | 494470 |
rs569326998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389567 | TTGTCAGGGGCAACC[A/G]TGGGGGTGGATTATT | 494470 |
rs569333935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432797 | AAAAATACAAAAAAT[C/T]AGCCGGGCGCGGTGG | 494470 |
rs569334382 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46425990 | GGAAGCAGCAAGCCG[C/G]CTCTTTGGGGCCTCT | 494470 |
rs569362965 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46423153 | CAAGCCCTAAAGCCT[A/G/T]TCCTTTGGGGGATGT | 494470 |
rs569365568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417337 | GGCAACATCCTGTAA[C/T]GACCAGTGAGGTCCT | 494470 |
rs569379146 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46384166 | CCAAGACCACTGCCC[C/T]GGCCGTGCTTCCAGC | 494470 |
rs569427949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373871 | TCCCCCTCCCACCCC[C/T]GGTCCCAGACCCTGT | 494470 |
rs569441420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46379311 | TGACAAACACAAAAC[C/T]CTCTCCTTAAACTTA | 494470 |
rs569454599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46347175 | CCTTGGGGAGTGATC[A/G]GGTCAGCCCTGCTCC | 494470 |
rs569492946 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46341566 | ACGCCAGAATGGCAG[A/T]TGGAAGGGGATTGTG | 494470 |
rs569493458 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459489 | CTGGGTGAGACAGTG[A/G]GCCCTCGTCCCCTCC | 494470 |
rs569508796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412860 | GTTATAGATAAGGAC[C/T]GAGGCCCAAAGGGGA | 494470 |
rs569567810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46455661 | GACCAACATGGTGAA[A/T]CCCTGTCTCTACAAA | 494470 |
rs569574483 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46374389 | CCTACCCCAATGAAA[A/C]CTCTGTCCCCATTAA | 494470 |
rs569634983 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365273 | CAGAAACCCACGCCC[C/T]CTGTCAGTGGTCCCC | 494470 |
rs569683705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353552 | TACCCCACTGTCACT[A/G]GTAAGGGATGTTACC | 494470 |
rs569689226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46371663 | GCCTCTCTGGGAAAT[A/G]AGAGCTGAAACAATG | 494470 |
rs569720066 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350818 | ACTCAGTCTTATTTA[C/T]GGCCAATATTATATC | 494470 |
rs569733502 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386551 | GACCCCCCATCAATC[C/T]ATCCATCCATCCATC | 494470 |
rs569801864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366725 | TCTGCCACGGAAGCT[G/T]TCTCTGACCTTCCTA | 494470 |
rs569832696 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46420515 | CCAGACAATGCTAAC[A/G]TGGTCCAGGTAGCCA | 494470 |
rs569844741 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380484 | GGGGCGCTTGCACAG[G/T]GCTTGTGGTGTGCCA | 494470 |
rs569878938 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403671 | TAATTTGAGGTCAGG[A/G]GTTCGAGACCAGTCT | 494470 |
rs569892828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447759 | CTGAGGCCTGCGGTC[C/T]CCTGTGCCCTGGCTG | 494470 |
rs569898068 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371053 | AATCATTACAGAAAG[A/C]AAAGGAGGAGCAAAG | 494470 |
rs569920137 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373938 | GAAGCAGATGGACAG[A/T]TGCTCCGACAAAGGG | 494470 |
rs569927959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376062 | GAACAGGGCCGGGCC[C/T]GGGGTCATCACAGCA | 494470 |
rs569941286 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46335173 | CGGGGCGTCCGGCCC[G/T]TGGGTGTTGTGCTGT | 494470 |
rs569945026 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46387319 | CTGCATTGAAACAAG[A/C]CCCCATCCTCCATGA | 494470 |
rs569978063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46448648 | CAAAAGAGATCCCAG[C/T]GGGAGCTCTTGGGCC | 494470 |
rs569982420 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | RNF165 | GRCh38.p7 | 18:46340213 | TGGTATGGTTTAGCT[A/C]CAGATAAACCAATAT | 494470 |
rs570034682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46383041 | TGCTGGGCCAGCTTG[A/G]CCAGATCATGGCATC | 494470 |
rs570047936 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46403378 | CCCTGCCCCCGGAGA[A/G]AGCCCTCCCTGCCCC | 494470 |
rs570050125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46409723 | TTAGGCTCCCCTTTT[C/G]TAAAAGGGAGGATTC | 494470 |
rs570089463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398331 | AGGAAGAAGGAAGCA[A/G]GTAGGGAGGGGGAGC | 494470 |
rs570096760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46441667 | GCTGAGGCAGGCAGA[G/T]CATGAGGTCAGGAGA | 494470 |
rs570108601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403909 | AAAACAAAATCAGAT[C/T]CATTGCACTCTGGTA | 494470 |
rs570115765 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402325 | ACCTCCTTCCCTCTA[A/C]ATCTGATTTTCTCAA | 494470 |
rs570133839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427412 | CCTGAAGGCCCCTTG[C/G]ACAGAGTGGGTACTC | 494470 |
rs570151883 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46392796 | CTGTGTGAGGAACAC[A/C/G]CATGCAGTGGCACCG | 494470 |
rs570191273 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46354460 | ATCAGGGCCCATAGG[C/T]GCCCAAACCCAGTAG | 494470 |
rs570208944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46433569 | GGGGGCAGGGCCAGG[A/G]CGTGGGCAGGGCCAG | 494470 |
rs570246035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421187 | AAAGAATTCCCAGTC[G/T]TTCTGTCTGTAATTC | 494470 |
rs570266155 | snp | A/G | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46348555 | GGGCTACTGCTGGGA[A/G]GGTGGGAAACTTCAG | 494470 |
rs570283885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428139 | GGGGAGGCCGGGCGC[A/G]GTGGCTCACGTCTGT | 494470 |
rs570311519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46334450 | CCGCGAGGACGCAGG[A/G]CGAGCGGTGGCTTCC | 494470 |
rs570330110 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445778 | GCTTGTTATATAACG[A/T]CTGAAAACAGAGATT | 494470 |
rs570378484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354216 | AGATGCCAGCACCAG[A/G]GACAGGGGACACCTC | 494470 |
rs570380327 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380149 | CTTCTTCTCCATCTT[C/T]GTGTCTCTGCCTTGG | 494470 |
rs570404006 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46349272 | GCTGGGAATCCAAGC[A/T]CAAGGTGCCAGCAGG | 494470 |
rs570452294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347972 | ATAACCATAAGGGCA[G/T]TAGCAGATGCTCACG | 494470 |
rs570453170 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461870 | TTCATAAGGCTTGGG[C/T]AGTCATTTGGCGAGT | 494470 |
rs570454210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386272 | TCCGACACCCTTCTA[C/G]TCTTTAATCATCAGC | 494470 |
rs570459913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46449061 | AGCACTTACTACATA[C/T]CAGGCACTGTTCTAA | 494470 |
rs570481876 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336257 | TGATTAAATCATTAC[C/T]ATCCTCATTAATACC | 494470 |
rs570550262 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401706 | GAACACAAATCCTCA[A/T]GTCAGCCCCGTGAGG | 494470 |
rs570589969 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421113 | TGCACACTGACCACC[C/T]CCGTCCTGGGTCTCC | 494470 |
rs570609909 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434656 | TTGCAGGGACTCCCA[A/G]GGATGCTCGGAGCAC | 494470 |
rs570626926 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449131 | TCCCACAAAAGAGTA[C/T]TATCCTGATTTTAAA | 494470 |
rs570626978 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46410512 | ACTGACAGCCTCAGC[C/T]GAAGGCTCACCCTTA | 494470 |
rs570646873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46456367 | AGGCTGATCTGAAAG[C/T]GCTTCCTGGCGGAGG | 494470 |
rs570732966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403934 | CTGGTATTCTTCATC[C/T]ACCAACTTGGGTGAC | 494470 |
rs570735277 | snp | G/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337258 | GAATCCCAGCAAAAT[G/T]GTTTTCCATTAAACA | 494470 |
rs570762147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46366813 | AACATGTACGTGTGG[A/G]CTACCTGCCATAAGT | 494470 |
rs570794987 | in-del | -/CGTGTG | 0.0197687 | 0.0974348 | intron-variant | RNF165 | GRCh38.p7 | 18:46334671 | AGAAAGATACATGAC[-/CGTGTG]TGTGTGTGTGTGTGT | 494470 |
rs570811424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378546 | GCCCAGAGGTGTCAG[A/G]TGATCCCTCCATTTG | 494470 |
rs570859332 | in-del | -/GCAGGGGTGCCTGGGAT | 0.105569 | 0.204058 | intron-variant | RNF165 | GRCh38.p7 | 18:46345085 | TGAGGCTGCTTCGGG[-/GCAGGGGTGCCTGGGAT]GCAGGGGTGCCTGGG | 494470 |
rs570861784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363780 | TACTTTTTAAGGTTG[A/G]GTCTCCTTGGACTTT | 494470 |
rs570903361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46434425 | TAGTGAGAAGAATGA[C/T]TTTTTAAAACATATT | 494470 |
rs570907876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398855 | CTCTCTCGTCTGGTC[A/G]TTATCTCAAATGAGA | 494470 |
rs570918384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399329 | CTTGCATGGGGATCA[C/T]GCGGGCATCAAAGGA | 494470 |
rs570960345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402415 | GATAAAATGAACATA[C/T]TTTTGATGTAAATAT | 494470 |
rs570965232 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445458 | TGCTCTTTGTTCAAC[C/T]TACTAAAATTTCACC | 494470 |
rs570996295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364124 | GGCTAATTTTTGTGT[C/T]TTTAATAGAACTGGG | 494470 |
rs571019327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343956 | GCTGCTCTTGTTGGG[A/C]CACTGAGCGGGACAT | 494470 |
rs571026190 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368868 | TCTACCTGATAGAGT[A/G]GTTGGGAGAATTTAG | 494470 |
rs571125627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383756 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGATGG | 494470 |
rs571159193 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457908 | GGCCCTGGCTCTGAG[G/T]TCACATCAGCTAGGT | 494470 |
rs571191710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422985 | GATTCTCCAACTGTT[C/T]CTAGTGTCAGATTAC | 494470 |
rs571195199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369422 | CAGGGCAGGGAGGAA[C/G]CTGATTGACTCGGGA | 494470 |
rs571214641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380713 | AGACTCTGGAGCCTC[A/G]AACCCAGCCTGTGTG | 494470 |
rs571214972 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46395648 | ACCATAATTCCTGCT[G/T]CAGGGGATAAGATCT | 494470 |
rs571273385 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46381221 | CACTGCCTTTGTCTT[C/T]TGTGGCCAAAGCCTG | 494470 |
rs571299978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46430796 | CAAGAGCTTCCTGTT[A/G]TTGCATGGATCCAAC | 494470 |
rs571309690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46400994 | CAGAGATGACCTCCC[A/G]CAAAGCTAAGCCTTG | 494470 |
rs571311684 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460929 | CCCACCACAACCCTG[C/T]CTCTCCATCATGAAC | 494470 |
rs571337738 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435731 | TCCCTGGGGGGAGAG[C/T]AGAAAGGAGAATTCC | 494470 |
rs571360176 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356418 | AGTGGGGGTGGGGAG[A/G]TGCTTATTTTATGCC | 494470 |
rs571362016 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF165 | GRCh38.p7 | 18:46359734 | GACCCAGGCTCCTTC[C/T]ACTTATTGCTCTGCC | 494470 |
rs571443621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352292 | ACTCTTTCCCCACCT[A/G]GAATCTACACTTTTG | 494470 |
rs571467198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345796 | TTCAGGCAGGTCAGT[C/T]CAGGCTGTGCCCCGA | 494470 |
rs571482844 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460247 | TCCCCTAAGCCCCCC[A/G]CCTGTAGGCGGGACA | 494470 |
rs571506875 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457311 | CCCAATTTGGGAGGC[A/G]GGAGGGGGGGGTTCT | 494470 |
rs571519592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375089 | TCCCCACAAACCTCA[C/T]CCAGGCAGGCTTTAT | 494470 |
rs571556186 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46403252 | CCAGACTCGAATCTA[C/T]TCTGACCTGATAAGC | 494470 |
rs571557293 | snp | C/T | 0 | 0 | intron-variant | RNF165 | GRCh38.p7 | 18:46346371 | ATTCACAGTACTGTG[C/T]GAACATCACTACTTT | 494470 |
rs571558059 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452876 | CTTTGGACAACTTCT[C/T]GGCTTTTCTGGCCCC | 494470 |
rs571601938 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46419205 | TTACTACAGACGGCA[A/C]TGGAGCTTGATGGGA | 494470 |
rs571616469 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423611 | CATGTGCTGGAAGGC[C/T]GTGACACTGATGTGG | 494470 |
rs571626192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414736 | AGGGCAAACACAGCA[C/T]GTGGAATCCTGGTCC | 494470 |
rs571636339 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460865 | TAATTTGCACTTGTC[A/G]GCAGACTGGGGTAAT | 494470 |
rs571663288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357954 | CCCTGGCTTGTAGCC[A/G]CATCACTCCAGTCTC | 494470 |
rs571681167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384736 | AAATGGCCCATCATG[A/G]CCAAGCACAGTGGCT | 494470 |
rs571684118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341370 | AGATGGCTCACATCA[C/G]GGAGTTTACTGTAAG | 494470 |
rs571716431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439566 | CACACTGCAAGAAAC[A/G]ACTGCTTGCAGCATA | 494470 |
rs571725296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351738 | CGCCTGGAAACAGAG[A/G]CCTAGGTTTAAGTCC | 494470 |
rs571726646 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46454526 | GGAGTATATAGGGCA[A/C]AGCGAGGCAGAGAGC | 494470 |
rs571734716 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365844 | GTGGCTAGATTTGCA[C/T]GGGGGTGAGGGTGTG | 494470 |
rs571814496 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46446893 | GGACTGCTTCTGAGC[C/T]CTTTTGCTGTCACCC | 494470 |
rs571815266 | in-del | -/ACACACACACAC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404787 | CACACACACACACAT[-/ACACACACACAC]ACACACACACACAAC | 494470 |
rs571822797 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46365323 | AGGGTTACGCAGGGT[C/T]GAGTCCAGGAGGTCT | 494470 |
rs571831245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380231 | CTGTGCCAGTCTCCT[C/T]TCCTATGGCATCTGG | 494470 |
rs571835582 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459745 | CGGCACTGGTCAGGG[A/G]GTCTGGGAAGAGTGG | 494470 |
rs571883393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46359203 | GCAATTTCTGCATGA[C/T]GCCAGGCCCAGGGGT | 494470 |
rs571883724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46366018 | TAACTCTTGGCTGGG[C/T]GCGGTGGCTCACACC | 494470 |
rs571911751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46424298 | CAGAGGCAGGCAAGG[C/T]CCCTGGGGGTCTGGG | 494470 |
rs571925055 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460256 | CCCCCCGCCTGTAGG[C/T]GGGACAAACACTCCC | 494470 |
rs571932251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390050 | AACCAGTGACCAGAG[G/T]CTCTGTTCCCCAATT | 494470 |
rs571945494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46374715 | CTTCAACAGAGTCTC[A/G]TACGGAGGTCTAGTA | 494470 |
rs571950031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432874 | GGCGTGAATCCGGGA[A/G]GCGGAGCTTGCAGTG | 494470 |
rs571954477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345207 | GCGCCCGCTGGAACC[C/T]GAAGAGTCCAGCCCT | 494470 |
rs571970434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46430840 | GAGGGTATGGATTAT[A/G]TTGTTTTGAAGTTAA | 494470 |
rs571993267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46424965 | CCAGCGCTGAACCCC[A/G]GCTCTTGAGGCTGAG | 494470 |
rs571995390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46387314 | GGGATCTGCATTGAA[A/G]CAAGCCCCCATCCTC | 494470 |
rs572066524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384814 | TTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGGC | 494470 |
rs572111933 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46396745 | CAGAGAAGGGACACC[A/C]GCAGCCTTCATGGTG | 494470 |
rs572113564 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46427449 | CAGGAGGGGCTGCTG[C/T]GAGGCAGGCAGCTGC | 494470 |
rs572118718 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390643 | TTTTCTCTGTAGGAC[A/T]GTTAGTCCATCAGCC | 494470 |
rs572154548 | snp | A/G | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333474 | TGTCTCTGAGAATGC[A/G]TTCTTGGCACGCGTC | 494470 |
rs572160356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46453160 | GTAAATGATTTCAAC[A/C]GCAGTTATTGAGTAC | 494470 |
rs572168645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46340908 | GGGTAGTGTGTATAC[A/G]GGAGGGAGGAGGAGG | 494470 |
rs572173369 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46396943 | TGGGCAGCCTGGGGG[G/T]TTCCCCTTTCCTTTG | 494470 |
rs572179371 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391373 | GCTCTTTCAGGTTGT[C/T]CTGGGAATCAGAGGC | 494470 |
rs572181211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380847 | GCAGGTCCCCATCAC[A/G]CTCGCCCCAGCCTTC | 494470 |
rs572190463 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46340434 | ATTGAATACTTACTT[A/G]GGGCCAAACACTGCG | 494470 |
rs572210414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418783 | CTGGCTATATCCATG[A/C]TCTGGGCTGTGAGGG | 494470 |
rs572226807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46413260 | GTTTTATAAAGCAGC[A/G]TCGCTCAAGCCCAGC | 494470 |
rs572255243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46453920 | GAGTTTGAGACCAGC[C/T]TGGCCATCATAGAGA | 494470 |
rs572265343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46375757 | AGGAGATATTTTGAG[A/G]TGGGAGCAGCACATA | 494470 |
rs572272339 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347881 | TGGATTTGTTCAGCT[A/C]ATCTAACACATACCC | 494470 |
rs572272842 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF165 | GRCh38.p7 | 18:46362822 | TAGAAGCACAACATA[C/T]GAGAGCCAAGAGGAA | 494470 |
rs572290310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391789 | ACTATACAATACATC[C/G]ACACACATAATACAC | 494470 |
rs572325312 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332519 | TAGAAGTCACTTTCC[C/T]GGAGTCAGCCTCAAC | 494470 |
rs572325978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447097 | TTTAGGAGTGGGTTG[C/T]GGTGGGCCAGGATAA | 494470 |
rs572334868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46407913 | ACAGAGATTGGTGGC[A/G]TCTTCAGGATTTCAC | 494470 |
rs572342923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46446157 | GTCTGGTTGTTGCTT[C/G]TTTTGTGATGTTAGC | 494470 |
rs572354050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402708 | GTTTTGCCATGTTGC[C/T]CAAACTGATCTCAAA | 494470 |
rs572395817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46402340 | AATCTGATTTTCTCA[A/G]TCCAGCTCCAATGGA | 494470 |
rs572445846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414895 | ACAGCCTTGTGAATG[A/G]GGAGCGTGCACTTCC | 494470 |
rs572446211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46439096 | GCTGGACCTGGGCTG[G/T]GCAAAGAGGAGGATG | 494470 |
rs572452018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381072 | CATGCCACACTACTG[C/T]GCCTCAGTTTTTCTA | 494470 |
rs572516491 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378812 | AGGAGCGCTGCTATG[C/G]ATGGTGGGGAGCTGC | 494470 |
rs572554274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358789 | TCAGGGAGAAACCCA[C/T]GGGCAGAGTGACACA | 494470 |
rs572565102 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46426238 | TTGGCTTTCAGGAAA[A/C]ACCTTGCTTCAAATT | 494470 |
rs572573762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46432481 | GTCCTGGCTGGCCAG[C/G]CTTCAGTGAAATTCT | 494470 |
rs572576645 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46393592 | CTGTTTAATCAGCAA[A/G]GTGTAAGGTCTTAGA | 494470 |
rs572612098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46386457 | GAGGGGTTAATATCA[A/T]TTTTTTTTTCCCTAA | 494470 |
rs572627736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46353074 | TGGTGTCAAACCACC[A/G]GCCTGTGGCGATTGG | 494470 |
rs572628584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426963 | GTTGATTTGTCATGG[A/G]CCCAGATATACTATC | 494470 |
rs572647877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385953 | TAGATGACCTCATGG[A/C]GGTGTGTGGTGGTTC | 494470 |
rs572649853 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | RNF165 | GRCh38.p7 | 18:46343219 | CTCTGCCCACCAGCA[G/T]CCCCTTCCATCGAGA | 494470 |
rs572657584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420275 | AGAATGGATGGCTTC[A/G]GGAGCCAGGCTTGGG | 494470 |
rs572676774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420032 | ATGGTTGGGAATCTA[A/G]TTTTACTGACCCTGG | 494470 |
rs572689317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46420714 | GCCAGGTGTGGTGGT[A/G]TGTGCCTGTAATCCC | 494470 |
rs572777444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46422594 | CTCCTTACTGCCATG[C/T]TTCTTCCCCCCGACC | 494470 |
rs572819910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347987 | GTAGCAGATGCTCAC[A/G]TAGCACTTACTCTGT | 494470 |
rs572853835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46435630 | ATATGCCCATCGTAG[A/G]ACACAGTGTTCATGG | 494470 |
rs572854633 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372334 | TCCTGAGGCAAGTCA[A/C]TTCGCTCTTCCTGCC | 494470 |
rs572884208 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46435056 | GAGACCTCTGCACAG[C/G]GGGCAGCCCGGAGAC | 494470 |
rs572899457 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | RNF165 | GRCh38.p7 | 18:46441986 | TGGCTGACACGGTGA[A/T]ACCCCGTCTCTACTA | 494470 |
rs572916692 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46428893 | GACAGTGCTGGGTGA[C/G]AGTCTTGACAATACC | 494470 |
rs572963919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46349741 | CTTGTCCAGATTCCT[C/T]GAAGTGGAGTTTCTT | 494470 |
rs572980682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388124 | ACTGAAGGTTACATG[G/T]TTATTTGGGATTACA | 494470 |
rs573004092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388669 | CCTCAAGACATGAAG[A/G]AGGGGCTTGGGGCTG | 494470 |
rs573014389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46383679 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 494470 |
rs573016762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362595 | AGCCAAGCCTCACTC[A/G]TTTTGACTAATGAGA | 494470 |
rs573016869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355580 | CCCATCTGTGCCTAT[C/G]TGAGGACCGCCTATT | 494470 |
rs573017515 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46433759 | GATCTGACAGGGGCT[-/C]CCCTCAGAAGCCAGT | 494470 |
rs573025705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412578 | ATGTGCTGATGAGGC[C/T]GCCTGGTTGGTCAGT | 494470 |
rs573029221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46356211 | CTGCAAATGTCAATC[C/T]GTGACCAGCCGACCC | 494470 |
rs573054803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389183 | ACAAGGAAACAGGGA[A/G]ACATCCACTGTATTT | 494470 |
rs573125348 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46444460 | TTCTGATGGTGTGCT[A/T]CATTTTGGATTATTA | 494470 |
rs573128536 | in-del | -/C | 0.0225045 | 0.103662 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389746 | TTCCTTTTTTTTTTT[-/C]CAGACAAGGTCTCAC | 494470 |
rs573138122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46350568 | GCAGTTACAGCAACA[C/T]TTGGGTAGAGGTGGA | 494470 |
rs573154492 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357680 | AAGATGCCTCCAGAT[A/G]CCTGGGAGTCACCCT | 494470 |
rs573168787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46413190 | CTCTTCTCTCTCGAG[G/T]GGAATTAGAATAAGG | 494470 |
rs573169420 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | RNF165 | GRCh38.p7 | 18:46340432 | CATTGAATACTTACT[-/G]TGGGGCCAAACACTG | 494470 |
rs573174374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412003 | GCAGAGTAATTGGAT[C/G]TGACTTGCAGCAGGC | 494470 |
rs573197603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46378754 | AGAGGGTGCAAGAGG[A/G]TGGGGCTTGGCATCA | 494470 |
rs573217056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436410 | TACAGGAATTCTTTA[C/T]GCTGTTCTTGCAACT | 494470 |
rs573239773 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431052 | TCCTCTTGCCCCCCA[C/T]CCCTGGACAGGCCCC | 494470 |
rs573245330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46357262 | AGTGGTAACAGTGGT[C/G]AGTACCCAGCATTTA | 494470 |
rs573245666 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382665 | TGTCCATCTCCTCTG[A/T]TGTCCACCACAGCCC | 494470 |
rs573282343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405795 | TTCTTAAGGTCTGGG[A/G]ATGGTGAGAGGTTCT | 494470 |
rs573308263 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46373096 | CTAGAAACTCCAAAG[G/T]TAACTAGTAAATAGA | 494470 |
rs573310173 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF165 | GRCh38.p7 | 18:46379009 | CTGCTCCTAATTAGG[C/T]CTGGAGTAGGGAAGG | 494470 |
rs573323869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46451785 | ATTCTAGCCTGGACA[A/G]CAGAGCAAGACCCTG | 494470 |
rs573337553 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366529 | AGGCATGGAGAATTG[C/T]TCACTGGTTTTCTTC | 494470 |
rs573370349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46394666 | AACTAATGACCCTGG[C/T]GAGGTTACTTCTAAA | 494470 |
rs573373234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46406289 | CGGGACTGGATGCCC[C/T]GGGCAGGCGTGGGAG | 494470 |
rs573424870 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342430 | CCTGCCAAGCTTCGA[-/G]GGGGGTCTAGACCCC | 494470 |
rs573461245 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46363828 | GGTCACATGAATTCA[C/T]AGGGGCCACCGTTGA | 494470 |
rs573476922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46400750 | TGAATAGCCTAAATT[G/T]TGTCGGCTTTCAGTA | 494470 |
rs573517494 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418751 | AGATAGTTACAGACC[C/T]AGAAAAGAGCTATCA | 494470 |
rs573541588 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368964 | CTGTCATCATTTCTA[C/T]GTGCCAGGCACTATG | 494470 |
rs573559916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46443104 | GTCTGTTAATTGGGG[A/T]GTCTAGACCATTTGC | 494470 |
rs573596518 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454211 | AATATTAAGCTAAAA[A/T]TTTTAACTATTAAAG | 494470 |
rs573651626 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370023 | CTCTGGGGGCCATAA[A/C]AGCTTCTTGCTGCCT | 494470 |
rs573654241 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344817 | GTGTGTGTGTCCCCA[A/G]CCTCTGTGCTGAGGA | 494470 |
rs573664260 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389560 | TTTGCTGTTGTCAGG[A/G]GCAACCGTGGGGGTG | 494470 |
rs573708501 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352664 | CATCAAGATGGAGGA[A/C]GAAGGGAAAGGTTAG | 494470 |
rs573725335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46356832 | GGTCTTATTCAGGCA[C/T]GGTGCAAGAGACAGA | 494470 |
rs573741657 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359592 | AGAGCCATGGACTCC[A/T]CCTGAAAGCCCATGT | 494470 |
rs573765246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436482 | AGTGTAAAATAATCT[A/G]TCAATGGAAAAGAAT | 494470 |
rs573767245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46407230 | TGCAGTTTTCACCCC[A/G]CAGAGTGGGAGACCA | 494470 |
rs573778703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46417499 | AAAGCACTTTGCCTG[G/T]ATATCTGCCAGTTCA | 494470 |
rs573827136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46429777 | AATACTCTTTTTTTT[C/T]CCTTTCTTTTATTGA | 494470 |
rs573839496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46384200 | ACCTCATCTACTGGG[C/T]CAACCCCTCCCTCCA | 494470 |
rs573847339 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46350645 | GTTCCTCCTGCCACG[C/G]TCGGTGGTGGCACTG | 494470 |
rs573883096 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46430552 | GTTCCTAATTTTCTC[C/T]CTATCATTTCCTCCA | 494470 |
rs573884126 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46344612 | TGGCCTCCACAGGGG[A/T]CCTCGGCATCCACAG | 494470 |
rs573913922 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46418054 | TTTTTTTCTAGCAGC[C/T]ACATTAAAAAAGTGA | 494470 |
rs573924839 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404709 | AGTGAGCCGAGACCG[C/T]GCCGCCACACTCCAG | 494470 |
rs573949080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410076 | TGGGCCCTGCTGTTT[C/T]ACTTATGTGGTGAGG | 494470 |
rs573968232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46451991 | TCAGTGGTTGCCAGT[G/T]GGGAGGGAGGGAGGA | 494470 |
rs573973249 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458667 | TGCTCTGGCCACCTG[C/T]AGGCAGAAAGTGGGG | 494470 |
rs573989019 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46366067 | GGAGGCCAAGGAGGG[C/T]GGATCACCTGAGGTC | 494470 |
rs574014562 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459232 | GTGTCCCAGGTTCCA[C/G]TCTGGGCTCTTCACT | 494470 |
rs574029239 | snp | C/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457528 | ATCTAGGCGGGGCTC[C/G]CCAGGCCCAGGGCTC | 494470 |
rs574049094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46415252 | AAGGCGAGGCACAGT[G/T]GTTCACACCTGTAAT | 494470 |
rs574062110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363870 | CCAGGGTCACCTTTC[A/C]GTGGGTCTGAGGCCC | 494470 |
rs574077922 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333589 | TCCCTTGTGCCCGCA[G/T]TCAGGCTCTACACGT | 494470 |
rs574081552 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341991 | CGTATTGGGAGAGGA[A/G]AGGGCAGGGAGTAGG | 494470 |
rs574093830 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340444 | TACTTGGGGCCAAAC[A/G]CTGCGCTAAGGGGGA | 494470 |
rs574124291 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46357384 | AGGTAACTGAGAGTA[A/C]GCAAATGATCCACAA | 494470 |
rs574137879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46452856 | TACCCCTTATAACTC[C/T]GTTACTTTGGACAAC | 494470 |
rs574205513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440535 | TAGTATATTTGGAAA[C/G]AAATCCAGGCATCAT | 494470 |
rs574219508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395894 | ATTCTATGGGAAAGC[C/T]CAGTAGTTCTTCCGA | 494470 |
rs574223529 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46364578 | CCTTCACACCTACTG[C/T]CTGATGCCTGGATTT | 494470 |
rs574259928 | in-del | -/A | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457247 | AATCAAAGGTGGAAG[-/A]AAAAAAAAGCCAAAT | 494470 |
rs574267213 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46441213 | GCCTAGGCTGATCCT[C/G]TACTTCTGTGCTCAA | 494470 |
rs574273669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389516 | CACAGCTGATGAGAG[C/T]AGAGACAGTCTCCCA | 494470 |
rs574333001 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46342064 | TGTCTGCAAAGAGGG[G/T]TTTTTTCGCAATTCA | 494470 |
rs574334350 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378244 | CAAGGACCCTGCACA[C/T]GCCCTTGCGTGCCCT | 494470 |
rs574340045 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390659 | GTTAGTCCATCAGCC[C/G]CCATTCAGCAGCATT | 494470 |
rs574357564 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355870 | GTATGGCCCTGCCAT[A/G]TTGGGTATGTGACTG | 494470 |
rs574371455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46334606 | GGCGGACGTGGTTCC[C/T]CCAAATCACAGCCCC | 494470 |
rs574402844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46456425 | CCTCCCTCCATAGCC[A/G]GGCAGTTCCCCAGGA | 494470 |
rs574425864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447871 | CCCATGCCCTGACTC[A/C]CTTGTGCCCTGGCCT | 494470 |
rs574437404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354680 | CACATCTTGGAAACT[A/G]GGATGCGCCTTATAA | 494470 |
rs574441804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46434664 | ACTCCCAAGGATGCT[C/T]GGAGCACACTTTCAG | 494470 |
rs574458365 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443476 | GCTACTTCTTTTGTA[A/G]GTTTTATCTCTATGT | 494470 |
rs574459924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46348788 | TGGAGAGTCGGTGTG[C/T]GTATTAGCAAATTAA | 494470 |
rs574481568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46366249 | GTGAGCCAAGATCAC[A/G]CCAGTGCACTCCAGC | 494470 |
rs574486140 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448449 | AGTGGAAAGGGGCAG[A/C]GTGGCAGGGTGTGGT | 494470 |
rs574505949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46403535 | GACTCTTTCATTTCA[A/G]TGACTACTTATTGAA | 494470 |
rs574551286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46398482 | TGGTGGGCACAGGAA[A/G]CTGACACAGGTGAGA | 494470 |
rs574557132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46373944 | GATGGACAGTTGCTC[C/G]GACAAAGGGGCTGTG | 494470 |
rs574560138 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415834 | ACAGGTAAAGTGATA[C/T]GCTGATATGACTGGG | 494470 |
rs574567431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46397994 | TGCGGAGGTGTGAGG[A/G]TGTGTGTGCATGTGG | 494470 |
rs574593686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46371863 | TACTGCAGCATCCTC[A/G]CTGTTCAGATAGACT | 494470 |
rs574616663 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46375697 | GGAGTTCTCTTGTTC[A/C]CAGCAATTTTATGTT | 494470 |
rs574623328 | snp | C/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457387 | ATGTTTACAGTGCAC[C/G]GAGTGTGGAAGGGGG | 494470 |
rs574702477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46428252 | CGTCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 494470 |
rs574729170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372649 | AGGGGTTGGGGGTCT[C/T]CTGTTAGAATTGGGG | 494470 |
rs574775564 | in-del | -/T | 0.130008 | 0.219321 | intron-variant | RNF165 | GRCh38.p7 | 18:46363946 | TTCTTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 494470 |
rs574781902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46342928 | CTGTAAACACAATAT[A/G]TGTATACTTTTTACA | 494470 |
rs574785238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372984 | GAGGGGGACCCTCCT[G/T]CTGGGAAACTGGAAG | 494470 |
rs574791079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367770 | TCCCCTGAATGTTAG[G/T]TTAGAGGTATGGCTC | 494470 |
rs574792919 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46350993 | TGCAGCCATAAATCA[-/T]GGCAGACGCCAGCAG | 494470 |
rs574799312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368157 | TCCTTGGACCTCCAT[A/G]AGACTTTGTGCTTGA | 494470 |
rs574819555 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438017 | GGCACTCGTAGGGCC[A/G]GATTCTGGGAAGAAC | 494470 |
rs574843090 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46441026 | TAGATACAGGGTCTT[G/T]CTCTGTCACCCAGGC | 494470 |
rs574904878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46404056 | AACCACTTCAAAATC[C/T]ATTACAGATTTGTCA | 494470 |
rs574932518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387910 | GACTGGGGCAGTCAC[A/G]CCTAATCAACCGTGG | 494470 |
rs574964823 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46404516 | CCCAGCACTTTGGGT[G/T]GCCGAGGCAGGTGGA | 494470 |
rs574984798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347019 | AGTGGTCATGCTGGC[C/T]AGAAAGTGTGGCCTA | 494470 |
rs574997222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337953 | ACCCCTACCTTTGGC[C/T]GCCTGTGTACTCAGT | 494470 |
rs575059601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46405339 | GGGAGCCAGGGAAGC[C/T]CTGCAGGTCCACAGG | 494470 |
rs575102307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411309 | AAGATAATTATGGTG[A/G]CATTGGCTGGAGAAA | 494470 |
rs575191975 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46428859 | AATTCCCTGTGTGGC[C/G]CACATTATAATTCTG | 494470 |
rs575198826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343642 | ACTGCCTATCTGCCA[A/G]GGGAGAGAATTGACT | 494470 |
rs575271152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46398527 | ATCTGGACAGTGTCC[A/G]GTGAGATATCAGAGA | 494470 |
rs575278389 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46428695 | ACATAGTAAGAAAAG[A/G]AAAGAGTTTTAAAAA | 494470 |
rs575289695 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46441955 | GGATCACGAGGTCAG[A/G]GGATCGAGACCATCC | 494470 |
rs575296776 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425297 | GGAGCAGGCAGAGCT[A/G]GCTCTGGTCAGCTGG | 494470 |
rs575314637 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46434777 | GTAGGAGGTCAGAAG[C/G]AGAAGAGGTCACCAT | 494470 |
rs575321795 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350453 | AGGTCCATGTCAGTA[A/G]AGCATGAGAGAAGGG | 494470 |
rs575328364 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458099 | CCTGCTACCTCACCT[A/G]GATGTTGTGAGGATT | 494470 |
rs575330595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399048 | TCTGCAGTTCAACAT[C/G]GTCCCAGGAGATCAG | 494470 |
rs575347725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46354832 | GCTCCATACACAAAG[A/C]TTTGGGGCCTATAAG | 494470 |
rs575374214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46338085 | TGTTCTTAACTAGCA[A/G]TCTTGTAGCATTTCA | 494470 |
rs575388007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46367004 | AACAAGAGGAAATTC[A/T]TCGTATACTTAGTTT | 494470 |
rs575396728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46368279 | AGATTGGCTTGGGAC[A/G]TGGAGGCCTAAATAA | 494470 |
rs575411054 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46344539 | TGCCCACTCCCACCC[C/G]CAGCGTGGAGACACT | 494470 |
rs575411091 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46369795 | AAGTAAGACTTTGCA[G/T]GCGCATTTCAAGAGA | 494470 |
rs575436155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46355441 | TCTAGGCTCTGGTGA[A/G]GATCACAGGAGATCC | 494470 |
rs575469383 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372589 | GAGGACACGTGACCA[C/T]GGTCACAGGCAGGTG | 494470 |
rs575484097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46362043 | AATGGAGCTTGAATT[A/G]GGCTGGAGTTAGCCT | 494470 |
rs575495524 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346693 | TCTCACTCATATAAA[C/G]TACGAGACACCCGAA | 494470 |
rs575510987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46368612 | TTTCAGGACAGCTCT[A/G]TGGAGTCGAGTCTTA | 494470 |
rs575534770 | in-del | -/AGCCCAGCCCCTTCCTGCTA | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46351544 | TTGTCCTCCCTCAGC[-/AGCCCAGCCCCTTCCTGCTA]AGCCCAGCCCCTTCC | 494470 |
rs575554658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416196 | CTCAAGGAAACACAC[A/G]GATCTGCAGGAAAGC | 494470 |
rs575558580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46350199 | CCCCTACCCCACCAT[C/T]GCTGAATTCAAACAA | 494470 |
rs575570046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46416706 | ACTCACATTGCTGCA[A/G]TCAGCTGGGACAGAT | 494470 |
rs575570495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46363294 | TTCTACCACCTTTGG[C/T]TGCAGAGGAAGCAAA | 494470 |
rs575597182 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46345954 | AGAGTCAGAGCTGGC[C/T]CTTGGAGCTCTAGTC | 494470 |
rs575626072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46378253 | TGCACATGCCCTTGC[A/G]TGCCCTAGCTCTAGT | 494470 |
rs575634415 | snp | C/T | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461727 | AGAAGAAGAGAAGAA[C/T]AGAGAGAGTGAGCTG | 494470 |
rs575651488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46373039 | GTGTGTGTGTGTGTA[C/T]GTGTGCATGTGCACA | 494470 |
rs575689903 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459462 | TTTCAGACTGGGCTG[G/T]GGGCACACGTGCTGG | 494470 |
rs575697488 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424276 | CAGAGAATGGCTGTC[A/G]AGGGCCCAGAGGCAG | 494470 |
rs575724634 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460289 | CGTGGGGCTGTAGCA[A/C]CGTCTGTCAGGCCCC | 494470 |
rs575750345 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436876 | TAATTCAATTCAGCA[C/T]ACACGGAGTACTCAG | 494470 |
rs575758882 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46373563 | GTGGTAACGAGAGAC[A/T]GCACAGTGCCTGGAC | 494470 |
rs575794144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46411950 | CCCTGGAGTGGGGTC[A/G]ATGATGCCAGGCTCC | 494470 |
rs575805799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46443321 | CACTTTATTTTATCT[G/T]ATTTTATTTTGGGAA | 494470 |
rs575853041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46436641 | TGAATGCTATGGGAG[C/T]TTCTAGGTGCAGGAA | 494470 |
rs575866910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46370344 | CAAGATAAGACTAAT[A/G]AGGTGCTAAGCCAAA | 494470 |
rs575903753 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46418867 | TTCAGCACCTCCGTG[A/G]TTTTCCATTCTCTCT | 494470 |
rs575905373 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46405378 | TCGGAAGGGGGCCTG[C/G]CTGAAATGTGCAGGC | 494470 |
rs575918151 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388415 | TCCTGGGACCCTTCA[A/G]TGACCTAGCAGCTGC | 494470 |
rs575922353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46399815 | CCTCACCAGGCCCTG[C/T]TCTTATTCTTCTCCT | 494470 |
rs575929176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46365066 | CCCTATAAGTCTCTG[A/G]TTCTCCTGATATTCC | 494470 |
rs576012814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46419444 | ATGCTTGTTTTGCAG[A/G]TTGGAAAGCTGAAGT | 494470 |
rs576045855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46380975 | GAAGCACATTTGTCA[C/T]AGAGAGCACCTTTGA | 494470 |
rs576081540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385983 | CTGATGCTCTGGCCC[C/T]AAGAACCCCTTGTCT | 494470 |
rs576088707 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453793 | AAAAACTAGAAAGAG[A/C]TATGAAAGCAACATA | 494470 |
rs576089166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391229 | TCACATGAGTGATCT[C/T]GCTTAGTCTTGAGGT | 494470 |
rs576091234 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373606 | ATAGATCCCCAGTGA[C/T]GTTGAGGCTGAGAGC | 494470 |
rs576109053 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF165 | GRCh38.p7 | 18:46375189 | CAGGCCGCCCTGGCC[A/G]CATTCTTTTGTGCTG | 494470 |
rs576123233 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450677 | TATACATGCTGAGCA[C/T]ACATGTGCACATTTT | 494470 |
rs576129393 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46341009 | CAAGAACAGAAAGTA[A/C]GTAGCAGGAGGGAAG | 494470 |
rs576140286 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RNF165 | GRCh38.p7 | 18:46415364 | CTCTACTAAAAATAC[-/A]AAAAAATTTTTTATA | 494470 |
rs576152346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385399 | GTGTGTGTGAGTGTG[A/C]GTGTGCATATGTGTG | 494470 |
rs576152754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46414834 | GCCGTGTTAGATTCA[C/T]TGGGAGCCATTTCAC | 494470 |
rs576165843 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332597 | GTTTGCCCAGCTTCC[C/T]GTGCTGCCCATTTCT | 494470 |
rs576175677 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333284 | CCTGGGTTTTCTGGG[C/T]AGTGTGTCTCTGTGT | 494470 |
rs576192459 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341614 | AGACTTCTAGTCCTT[A/T]ACATACAGATTCCTG | 494470 |
rs576256604 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438870 | TTCACCTGCATTTTC[G/T]CATTTGATGCTCCAA | 494470 |
rs576258215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF165 | GRCh38.p7 | 18:46382200 | CCATCCCTCCTGGAC[A/G]GTCTGTCATCTTCCC | 494470 |
rs576311366 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375537 | CCAGCCTGGGTGACA[A/G]AGTGAGACTCTGTCT | 494470 |
rs576327980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46440218 | GTTTCGCTTTCCAGG[A/G]TTTCAGTTACCCATG | 494470 |
rs576343221 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435238 | GAGCTCTTGAGAACT[A/G]GTGGCCTGGGTAGCC | 494470 |
rs576369437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46397020 | CAGTGCTGGCTGTGC[A/G]AGCGTGGCCCAGATT | 494470 |
rs576371430 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46376723 | GATGCCAAGGCTGGA[A/G]TGCAGTGGTGCAATC | 494470 |
rs576403057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46397802 | CTGAGGTGTGAGGGT[G/T]TGTGTGCATGTGGTG | 494470 |
rs576414707 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46341045 | GTGTTGATGGCGGGG[A/C/T]GGAGGCACATGTGCA | 494470 |
rs576455332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46341617 | CTTCTAGTCCTTTAC[A/G]TACAGATTCCTGGTT | 494470 |
rs576489732 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333323 | GGCAAAGACCTCAGT[A/G]AATGAGTGAATTTCA | 494470 |
rs576514876 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449660 | TGAGCTCTCATAAGA[A/T]CTGATGGTTTTACAA | 494470 |
rs576552996 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447098 | TTAGGAGTGGGTTGC[A/G]GTGGGCCAGGATAAG | 494470 |
rs576565407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46447304 | TTGTCTTGGGAGGGA[A/G]CTTTGGTCCCCTAGT | 494470 |
rs576580597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46421466 | TGAGACAGACCTAGG[A/C]TCTGCCTTCATGGAG | 494470 |
rs576595874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426313 | AGCCTTTTAGAGACT[C/T]GGGGACCTTGTCACT | 494470 |
rs576606650 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378242 | GACAAGGACCCTGCA[C/T]ATGCCCTTGCGTGCC | 494470 |
rs576635930 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46347584 | ATTCTTACCTGCCAG[C/G]TGAGTTTAATCCTCA | 494470 |
rs576652799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427056 | CAGACCCTACATGAT[A/T]TAGGGCTGAGGAGAG | 494470 |
rs576668933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46376182 | AACAGCCTTGGCAGC[A/T]AAACGGTCACCTGCC | 494470 |
rs576693468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46359075 | TCAGTTGTCCTCCCC[A/G]TAAAAGGAGAGGCAG | 494470 |
rs576711358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46334735 | GAGAGAGAGAGCGCG[C/T]GCGCGAGAGCATGCT | 494470 |
rs576748885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46347391 | ATTCTCTGCCTCCTC[C/T]CCTGCCCCTCTGCCC | 494470 |
rs576785126 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461155 | AGCCGGGAGGCTCAG[C/G]TTTTCAAATCTGCTC | 494470 |
rs576790609 | snp | A/G | 0.00121114 | 0.0245785 | intron-variant | RNF165 | GRCh38.p7 | 18:46375275 | ATACTTGTCCTGGCC[A/G]GGCACAGTGGCTCAC | 494470 |
rs576858392 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420591 | GGCTCACGCCTGTAA[C/T]CTCAGCACTTTGGGA | 494470 |
rs576878139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382290 | AAATCAGGCAGTGCA[A/G]GAGCCCGTGCCTGGC | 494470 |
rs576938974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46381533 | GGAGGGAAAAACATC[C/T]TTCAAGACTCTCAGG | 494470 |
rs576939789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46382793 | AAGCCTAGGTTCTTA[A/G]ATTAGAGACTATGCA | 494470 |
rs577009878 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF165 | GRCh38.p7 | 18:46410452 | GTGAAGGACTGAACC[C/T]GTTAGGCTGTGAGAC | 494470 |
rs577050467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46377189 | TATCTGAAAAAGGTA[C/T]ATAATGTACCCCTTT | 494470 |
rs577069699 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46432965 | ATAAATAAATAAATA[A/C]ATAAAAAATAAAGAT | 494470 |
rs577099988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403025 | CTTGTTGCTCTCAGA[A/G]CACGAGACTCACTTC | 494470 |
rs577111807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46397129 | GTGTTGTCTGGGAGG[G/T]CCCTGCCGGAGGCGT | 494470 |
rs577113627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46403448 | GCCAACTCACCTAAG[C/T]GTAGTATCCATTACC | 494470 |
rs577131065 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46433645 | AGGCTCCTAGACTCC[C/T]GGCTTCTCTCCCTGG | 494470 |
rs577137171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46427158 | TCTGGGGATGGAGAT[G/T]GTGGAGGGAAGAAGC | 494470 |
rs577171923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46397941 | ATGATGCTGGGGTGC[A/G]AGGGTGTGTGTGCAT | 494470 |
rs577218593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46387367 | GGGAACCACTCTGAA[A/G]TAAGGAAAGCAGCTT | 494470 |
rs577225007 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390786 | CACCACTTCTGAGCC[A/G]GGCACCCTTATTCTT | 494470 |
rs577332548 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46384233 | TAGAATTCCACTCTG[G/T]TTATTAAGACCACCT | 494470 |
rs577353056 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46342853 | CCCTCTGTGATCATG[G/T]GAGTGAAATGCAGTC | 494470 |
rs577381007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46410201 | TTTCTTAAGGCCCCA[A/G]ATGCTTAGCCAAGCT | 494470 |
rs577391083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46343390 | TCAGTTTTCCCATCA[C/G]TCAAATGGGCACATC | 494470 |
rs577392694 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF165 | GRCh38.p7 | 18:46420947 | GTAGGAGAATATCTG[A/C]ACTCATGACCTAAGA | 494470 |
rs577473189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46372582 | ACCATGTGAGGACAC[A/G]TGACCATGGTCACAG | 494470 |
rs577517945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF165 | GRCh38.p7 | 18:46356860 | AGAGGCTTTACATTC[A/G]GGGAAAACGGAAACT | 494470 |
rs577542504 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF165 | GRCh38.p7 | 18:46406637 | TGACTCTACCTGGCC[C/T]GGGTGCCCTCAGTGT | 494470 |
rs577546293 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381898 | CACCGGCGAGCAGGT[A/G]TCTTTGGAGAGATGT | 494470 |
rs577568893 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411835 | ACAGCCTGGGGCTGA[A/G]CCGTGTATGTGTGAT | 494470 |
rs577606089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389365 | ACTGTAAGTTCTAAA[C/T]ACACTGGATAAAGTC | 494470 |
rs577611235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46448693 | AGTTCTGCCTTTTTC[A/G]GAGGGCAGGCCTTCT | 494470 |
rs577612056 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF165 | GRCh38.p7 | 18:46407306 | GTAAGATTCTTCTTC[A/T]CCTCCTAACCAGTCT | 494470 |
rs577614827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46395159 | TAAAAGATGGAAGTT[A/G]AACCAGTTATTTCCA | 494470 |
rs577648255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46449521 | AGTGATATGGTTTGG[A/C]TCTGTATCCCCACCC | 494470 |
rs577677228 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384060 | TCTTAACAGCAGACA[C/G]AGGCAGTCGGGGTGA | 494470 |
rs577678493 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409806 | GAGATTACTGTCATT[-/C]TTTCTCATAACTGCA | 494470 |
rs577690095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46402311 | TGTATTTAGTTAAAA[C/T]CTCCTTCCCTCTAAA | 494470 |
rs577718461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418224 | TAGCTTTGTGTGGTC[A/G]CACATGCCCATAGTC | 494470 |
rs577761307 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430009 | GAGTCCCCGCCCTCC[A/T]GCTCCCCTGTGGAAT | 494470 |
rs577772887 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459345 | GATGCTTGCTAATTT[C/T]CTTCTGACACTCACA | 494470 |
rs577776919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46412733 | CTCCCAACTCTTAGA[A/G]AATGACAAGGCCGCC | 494470 |
rs577853744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46424174 | GAAGGTCTTGGAGGG[C/T]TCCCAAGGGAGTTAA | 494470 |
rs577863507 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459679 | TCCCACTTCTTTAGC[C/T]GGGCAGCTGTTTGGG | 494470 |
rs577864526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369250 | AGCCAATTGAAGGGT[A/G]GTTCAAGGTGGCAGC | 494470 |
rs577875390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46374561 | AGGAGAACGTCTTCA[C/G]GGTTCACCTGTGCTG | 494470 |
rs577898632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46345162 | GGAACCAGAGGGATA[A/G]GGCAGCAAGGGACAA | 494470 |
rs577932298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46369725 | AGGTAACTCATAAAC[C/T]GGGGGGTCCTTATTC | 494470 |
rs577933330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46418749 | AAAGATAGTTACAGA[C/T]CCAGAAAAGAGCTAT | 494470 |
rs577959676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46426096 | AATCCATCACCTTGG[C/T]GGTTAGGATTTGAAC | 494470 |
rs577960030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46419506 | CCCCTGAGAGCCTGC[C/T]GGGACTCTCCTCTAG | 494470 |
rs577997936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46452069 | GTATCATACTCTAAC[A/G]GTGGATACATGACAT | 494470 |
rs578001596 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383018 | GGAACCTCATGCACC[C/T]CCTAGCCTGCTGGGC | 494470 |
rs578006965 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339113 | TTGTGCAAGAGGAGA[C/G]ATACAGGTTTACAAG | 494470 |
rs578014687 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF165 | GRCh38.p7 | 18:46395963 | GGCTTGCTGCTCTTG[A/G]CTGGGCTCTGTCACA | 494470 |
rs578074827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46351984 | TATATTTCCTGGGAG[C/G]CTCTGGAGTGAATAG | 494470 |
rs578091601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390712 | TAAGGAGATACAAAG[C/G]AAATGTGGGAAGGCG | 494470 |
rs578113886 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46445997 | GTTGCATTCTTGTGT[A/T]GTCACTTAAGATGTT | 494470 |
rs578134814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46352616 | CTTTTCTGCATGGTC[C/T]AGGATGGTTCACACC | 494470 |
rs578158387 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400654 | TGTTCAGGAAGTTCC[C/T]GGGTGTGTCAGCGTG | 494470 |
rs578171488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46364960 | TGGTCCCAGCTGGGT[C/G]TCTCCTACACTCTCA | 494470 |
rs578171870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46358098 | CTGTTTCCAAATAAG[G/T]TCACACTCACAGGTA | 494470 |
rs578176728 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404336 | CCCAAGTAATTTTGA[C/T]GGATGTGGGTCAAGG | 494470 |
rs578215108 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441121 | CTCCCAAGTAGCTGG[G/T]ACTACAGGTGTGCAC | 494470 |
rs578237464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF165 | GRCh38.p7 | 18:46385434 | GAGGGATTCTGAAGA[C/G]GAAGGTGTTGCACAA | 494470 |
rs745310271 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390707 | CAGGCTAAGGAGATA[C/T]AAAGGAAATGTGGGA | 494470 |
rs745373360 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422351 | AGTTGCATGAAATCC[A/G]AATTTCTCCCAGGCT | 494470 |
rs745401337 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400091 | CCACGGTACCTCTTA[C/G]CCATCGCTTGGCTTC | 494470 |
rs745423513 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392822 | CACCGCTCCTGCACC[C/G]AGGAGGACAACACGC | 494470 |
rs745435382 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367698 | TCTACCAAACTGGCC[G/T]CGGTGTCCCCACCAG | 494470 |
rs745461215 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434230 | CTCTTTTCCACTCTT[A/G]CAAATTAATGAAGAC | 494470 |
rs745470319 | snp | C/G | 1.65111e-05 | 0.0028732 | intron-variant | RNF165 | GRCh38.p7 | 18:46447528 | CCTGGCTAAATCACA[C/G]CACCCTATGGTTCAC | 494470 |
rs745492938 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398970 | GAGCTCTTGTTAAAG[A/G]GCAGGCTCCTGGGTG | 494470 |
rs745510919 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408855 | GCCTTCATCCCAGTG[A/G]TACTGTTATCTGTTT | 494470 |
rs745515938 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376285 | TCTCTGTGTCAAGAA[C/T]CTCTATGAGGTAAAT | 494470 |
rs745522492 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339446 | ATGTATGCAGTGTAT[C/T]TAATGTTTGACCCAG | 494470 |
rs745539152 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365286 | CCCCTGTCAGTGGTC[C/T]CCACCCTACACTCCC | 494470 |
rs745541694 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435780 | GAAGGCTTTCTGGAG[C/T]AGGTGCATCTCAAGG | 494470 |
rs745543592 | snp | A/C | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447633 | CCTCAGCACTATCAG[A/C]ATTACCTAGCCACTC | 494470 |
rs745553808 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448140 | ACCTGGCTTTCTTGT[A/G]TATCAACCCCCATGC | 494470 |
rs745580971 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408118 | AAGTAGCTCAGATAG[C/G]TCGGGGCAGTGGATT | 494470 |
rs745607795 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429109 | CTGCAGCCCCCGGAC[C/T]CACCAAAGCCAGAAT | 494470 |
rs745608048 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375075 | GGATTTGGGGTTTCT[C/G]CCCACAAACCTCACC | 494470 |
rs745618327 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447351 | GAGCCTGGATTGCTC[A/T]AGCTCCTTCAGACCT | 494470 |
rs745661274 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416771 | CTGTCATTCTCCAGC[A/C]GGTTAGCCTGGGCTT | 494470 |
rs745701028 | in-del | -/AAAAAAAAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441863 | CGAGACTCCATCTCA[-/AAAAAAAAA]AAAAAAAAAGAGGCC | 494470 |
rs745707247 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361763 | GAGCCAGGAGCTGCT[A/G]CAGGTCACCACCCAT | 494470 |
rs745754817 | snp | G/T | 2.16579e-05 | 0.00329067 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433198 | CTTCCAGGTGCCCCC[G/T]TTCAAAGGTCTCAGC | 494470 |
rs745810179 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376394 | TGGTAGAGGCCACAG[C/T]GTGGCCCTGGACTGC | 494470 |
rs745870605 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425592 | CTCCAGCTCGGGAGT[C/T]AGTCTTCCCTGAAGA | 494470 |
rs745887287 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387911 | ACTGGGGCAGTCACG[C/T]CTAATCAACCGTGGC | 494470 |
rs745904547 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342592 | GATGCCGTCTCAGAG[C/T]AGGCCTGGCTGGCTT | 494470 |
rs745956021 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348082 | ACGCAGGAACAGCAT[C/G]GCCCTAAGGTATGTG | 494470 |
rs745976399 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420462 | AGGAAGGGGCCCCAT[C/T]GAAGTGGCTTTCTGA | 494470 |
rs745977022 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46387228 | CGTCCAGCTGAGGCA[G/T]GCATAAAAAAAGGCA | 494470 |
rs745993621 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371459 | TTCTCAGTCATCTCA[A/G]AGAGACTCAGTGAGA | 494470 |
rs745995027 | snp | C/G | 1.64871e-05 | 0.00287111 | intron-variant | RNF165 | GRCh38.p7 | 18:46447730 | CCTTGCGCCTATTGA[C/G]TGCCAGTGGTGGTCT | 494470 |
rs746014957 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446906 | GCCCTTTTGCTGTCA[A/C]CCTAATAGTGTTTTG | 494470 |
rs746043388 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443672 | ACCTCAGTGGACACT[G/T]GAGTAGCTGTGACAG | 494470 |
rs746050985 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430667 | TCTGTCTTCTCATTC[C/T]GGTTTCTGAGAGTCC | 494470 |
rs746097222 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364338 | CCAACCAAAGTTTGC[G/T]TGGGTCAAAAATTCA | 494470 |
rs746143530 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429498 | TTCTGATATTGCTTA[C/T]GTTATTCATATTGTG | 494470 |
rs746170021 | snp | A/C | | | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433304 | TGGCCCACCCCGTGC[A/C]GTCGCAGCCAGGCCT | 494470 |
rs746195496 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372694 | AGGAGGGAGCTGAGC[C/T]TTCTCGGGCTCTGGC | 494470 |
rs746202402 | snp | A/G | 3.7386e-05 | 0.00432338 | missense | RNF165 | GRCh38.p7 | 18:46455996 | CCCAGGATGGCAAGG[A/G]CAAGAAGGATGAGGG | 494470 |
rs746211122 | snp | G/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332812 | CAGCTCCACATACTG[G/T]GATTTTTACCATCTC | 494470 |
rs746248771 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404734 | CTCCAGCCTGGGGCA[C/T]AGAGCGAGACTCCAT | 494470 |
rs746268263 | in-del | -/AC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383406 | ATATAAAATATGTAT[-/AC]ACACACACACATGTT | 494470 |
rs746269485 | in-del | -/AT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403966 | CCATCATAGAAGCTC[-/AT]TCTTTAGGGGATTCT | 494470 |
rs746274757 | snp | C/T | 3.89658e-05 | 0.00441377 | intron-variant | RNF165 | GRCh38.p7 | 18:46433517 | CCAGGTTGGTGCTGC[C/T]TGGGGCGGAGGTGGG | 494470 |
rs746275702 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372082 | TAGAAGAAAGGGACT[A/G]GCATCCACACAGATG | 494470 |
rs746283491 | snp | C/T | 3.3095e-05 | 0.00406773 | intron-variant | RNF165 | GRCh38.p7 | 18:46456110 | TTTTGATTCCCTCTC[C/T]CCTCTCTTATAGGTA | 494470 |
rs746317683 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442699 | GTTCAGGTCTTTTAT[A/G]TTCTTACTGATTTTT | 494470 |
rs746324317 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456849 | CGACTGTCCCCATCC[A/G]CCTGGCTGAGCAGGA | 494470 |
rs746366726 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391460 | TACGGTTGTGGTTGC[C/T]GCTATTCCACCCTCA | 494470 |
rs746374337 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358212 | GGACCCCCTGTGAGG[G/T]CTGCAAGCGTTCAGA | 494470 |
rs746391012 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345842 | TACACTCCTCTGGCA[C/T]TTGGGTCCATCCAGG | 494470 |
rs746414837 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413265 | ATAAAGCAGCGTCGC[A/T]CAAGCCCAGCCCTAT | 494470 |
rs746455408 | in-del | -/TCGTA | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458459 | CCAGTCTCAATGCCC[-/TCGTA]TCAATAAGACCGGGG | 494470 |
rs746498667 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339039 | GATGGGAAAGCTGAG[C/T]TGATTTACTGTGACA | 494470 |
rs746513593 | in-del | -/TAC | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337803 | CTTTTCTTTTTACTT[-/TAC]TTTTTTTTTTTTGTG | 494470 |
rs746518719 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432205 | GGATTTTTGCTTAGA[A/G]AGAATTTGTAAGGTT | 494470 |
rs746522189 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407973 | GAAGCCTTCCTGGGG[C/G]AGGTGGCATAGCAGC | 494470 |
rs746559892 | snp | A/T | 1.65124e-05 | 0.00287331 | intron-variant | RNF165 | GRCh38.p7 | 18:46447519 | CTTCTCTAACCTGGC[A/T]AAATCACACCACCCT | 494470 |
rs746605062 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46456591 | GAGCAAGAAATGCCC[C/T]ATCTGCCGAGTGGAC | 494470 |
rs746674363 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349825 | CTGCACACGATCCAC[C/T]CAGCACCTGATGCTC | 494470 |
rs746699743 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415897 | AGGGACCTGGAGTGC[C/T]AGGTGGGAGGAGAGG | 494470 |
rs746704347 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459342 | TTGGATGCTTGCTAA[C/T]TTCCTTCTGACACTC | 494470 |
rs746718474 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426566 | GGACCCACCTCACTC[A/G]GGCCCCCACCCCCTG | 494470 |
rs746721746 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410712 | GTGGAAATCTGTCAC[A/T]AAGGAAGCAAACACA | 494470 |
rs746752278 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458255 | ACCCCAAAGGGAGCA[A/G]AGAGATAAGAGGACA | 494470 |
rs746799714 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383388 | TGTAAGGAAAAATAC[-/GT]ATATATAAAATATGT | 494470 |
rs746827610 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392350 | TTCAGCTCAGGGTTC[C/T]CTGCTATGCAGATTG | 494470 |
rs746829085 | in-del | -/GTGT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334672 | GAAAGATACATGACC[-/GTGT]GTGTGTGTGTGTGTG | 494470 |
rs746832284 | snp | A/C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369644 | AGCTCCTTGCTGGAG[A/C/G]TGGGGGCACTTTTCT | 494470 |
rs746846310 | snp | C/G | 2.50423e-05 | 0.00353843 | intron-variant | RNF165 | GRCh38.p7 | 18:46433182 | ATGTCTCTGTCCTTG[C/G]CTTCCAGGTGCCCCC | 494470 |
rs746863888 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409115 | ACAGTGCCTGGCATA[C/G]AGGGGGTGCAATAGA | 494470 |
rs746903034 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360288 | TGCTGGGCACAGAGG[C/T]GGGGTATCATGTGTT | 494470 |
rs746927597 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402259 | GCTACTTACTGAGCA[G/T]GTATTATATACTATG | 494470 |
rs746966788 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380877 | CCTTCCCACGTCTCA[C/G]CACTGCAGTGGAGAA | 494470 |
rs746979059 | snp | C/G | 2.70091e-05 | 0.00367476 | intron-variant | RNF165 | GRCh38.p7 | 18:46334388 | GGATCGCCGCAGGCA[C/G]CGGGGCGGGGGCGGG | 494470 |
rs746987203 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343259 | AAGTGGAGTGGAGGC[A/G]GATAAGAGAAGGCTG | 494470 |
rs746988859 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436923 | TGAGTGATTGGAACA[C/T]ACACAAGGGCCTACA | 494470 |
rs747016260 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351873 | CAGCAAACGGTAAAT[A/C]TATTGGTGTGTGTTG | 494470 |
rs747018544 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385868 | AGGTATCTGGGGCTG[A/G]AAGAGTTGCTTTTAC | 494470 |
rs747051153 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354089 | CAACGTTCACCAGGC[C/T]CCCCAATTCTCTCCT | 494470 |
rs747075008 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364195 | TCAAGTGATCTGCAA[A/G]CCTCAGCCTCCCAAA | 494470 |
rs747080382 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418283 | GATCGCTTGAGCCCA[G/T]GAGACAGAAGCTGCA | 494470 |
rs747106528 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395079 | TCGCTGGAACTCAAG[C/T]TTATGCCTGAAGTCA | 494470 |
rs747111994 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363001 | CACAGAAAAAGTGTA[C/G]AGTTAAAACCAGACC | 494470 |
rs747130457 | snp | A/G | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332598 | TTTGCCCAGCTTCCC[A/G]TGCTGCCCATTTCTG | 494470 |
rs747161701 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443464 | TTTGCATCCTTTGCT[A/G]CTTCTTTTGTAGGTT | 494470 |
rs747173285 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420572 | GGTTTGGGCCAGATG[C/T]GGTGGCTCACGCCTG | 494470 |
rs747182142 | snp | A/T | 5.2415e-05 | 0.00511906 | intron-variant | RNF165 | GRCh38.p7 | 18:46455949 | TGCCCCAGGTAATGA[A/T]TACTACTCTCTCTGC | 494470 |
rs747202178 | snp | C/G | 1.79322e-05 | 0.00299429 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433494 | GCACCGCAGGCTGGT[C/G]TCGCACCCCAGGTTG | 494470 |
rs747211714 | in-del | -/C | 3.93988e-05 | 0.00443822 | intron-variant, frameshift-variant | RNF165 | GRCh38.p7 | 18:46433250 | CCACTTCCACCTGGG[-/C]CCCCCCGCAGCCGCA | 494470 |
rs747308680 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415003 | TCATGGACACTCCAT[C/T]GGCTTCAGATAACAT | 494470 |
rs747421511 | snp | G/T | 1.74631e-05 | 0.00295487 | intron-variant | RNF165 | GRCh38.p7 | 18:46450808 | TAAGAAGGTGGGTCT[G/T]CCAGCAGGCCAGCCT | 494470 |
rs747430609 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390671 | GCCCCCATTCAGCAG[A/C]ATTTATGGGGTGTGG | 494470 |
rs747431703 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436310 | AAGTATATACATTGT[-/G]GGGGGAGAGAGAAAG | 494470 |
rs747462342 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454855 | GGCTGATTTCGCTCA[C/T]GACTAGATTTCTTCT | 494470 |
rs747475340 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422215 | GTTAGCTTATGTAGT[A/G]TACCCCAGACTCTCA | 494470 |
rs747525527 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367629 | TTAAAACCCACATTG[C/T]CTAAAGCTTCTGACA | 494470 |
rs747529245 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398700 | GTCTAGCCCCACAGG[C/T]TCTGTAAGACCAGTG | 494470 |
rs747565394 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433862 | ACTCCTGCATGGTGC[A/G]GGAGGAAATTTGACT | 494470 |
rs747565533 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421623 | ATTGTCCCATTATGC[A/G]CAGAGGTTTTCTTCT | 494470 |
rs747589792 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429594 | GTTTACTGTTGAGCC[A/G]AGTATAACATCATAC | 494470 |
rs747622582 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349798 | CAGTAACCCACAGCT[A/G]CATTTGACACGCTGC | 494470 |
rs747644970 | snp | G/T | 1.66156e-05 | 0.00288228 | intron-variant | RNF165 | GRCh38.p7 | 18:46456473 | CTGCTCCGCTCAGTG[G/T]CCCTCAGCTCTTGCC | 494470 |
rs747653589 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445478 | AAAATTTCACCCCAT[G/T]TATGCAGATCTTAGT | 494470 |
rs747682413 | in-del | -/TGTGAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334713 | GTGTGTGTGTGTGTG[-/TGTGAG]AGAGAGAGAGAGCGC | 494470 |
rs747697683 | snp | A/C | 1.64735e-05 | 0.00286993 | missense | RNF165 | GRCh38.p7 | 18:46456579 | GTGGCTCGCCATGAG[A/C]AAGAAATGCCCCATC | 494470 |
rs747711953 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46427886 | GGCAACCCTGGGGCT[A/G]GTGGGCAGGGTGGTA | 494470 |
rs747717666 | in-del | -/CAGTTCT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351707 | GAAAGATAACTTAGA[-/CAGTTCT]CAGTTACATCGCCTG | 494470 |
rs747718065 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348349 | CTTTGTTGGCCCTCC[A/T]GGTCAACATGGCAGC | 494470 |
rs747744913 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458146 | CGTGTTCTATGCTCT[C/T]TTCTGAGAACCTTGT | 494470 |
rs747807984 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359262 | GCCTGTGGGGTTATG[G/T]TCTGTCTGCTGGGAG | 494470 |
rs747811667 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392215 | TGCCTCCAACTCATC[A/C]CCATCCTGTTCCCCT | 494470 |
rs747842042 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424711 | GTGTGGGATCAGCAG[C/G]ATCACTGCAGGTCAC | 494470 |
rs747845289 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368825 | TTGAACCTCAATATC[A/C]TCATGTTTCAAATGC | 494470 |
rs747917153 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384589 | CATAATGCCTCCCAT[A/G]TACCCAAACCTACTC | 494470 |
rs747931588 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378280 | TAGTTTACACACACC[A/G]TAGTTTCTCCCTTTG | 494470 |
rs747959303 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372002 | CTTCCGAGAGCTGAC[C/T]GTAGGGTCCTGGATG | 494470 |
rs747970688 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450932 | CTGGTTAGATGCTCT[A/G]AAGCTGTAATAACTT | 494470 |
rs748012692 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368354 | CTCCCTTTCTGCCTC[C/T]ACCCCCTGCTCATAT | 494470 |
rs748020220 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342489 | GGGACTTTGAGAGAC[A/T]GGGAGGGTGCATGGT | 494470 |
rs748024464 | snp | G/T | 3.01555e-05 | 0.00388289 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334269 | GCCGCCGCGCGAGGA[G/T]CCAGGATGGTCCTGG | 494470 |
rs748100241 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377593 | GGAGGTTGAGCTAGG[A/G]AGCCAGGGAGAGGTT | 494470 |
rs748103597 | in-del | -/C | 1.7134e-05 | 0.00292689 | intron-variant | RNF165 | GRCh38.p7 | 18:46334394 | CCGCAGGCACCGGGG[-/C]GGGGGCGGGCGCCGC | 494470 |
rs748125223 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352900 | GTTGGTGCTTAGAAC[A/C]CACACGTCAGGTCTT | 494470 |
rs748139468 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449773 | TGAGGCTCTCCAACT[A/G]TGTGGAACTGTGAGT | 494470 |
rs748146992 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390623 | ATAAGCCGTTTTCTC[-/TT]TTCTTTTCTCTGTAG | 494470 |
rs748159582 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419393 | TGGGGGAACTTCATA[A/G]CATTCCCCCTGCTAG | 494470 |
rs748188019 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362004 | TCCCTGAGGATTTCA[A/T]AGGCATTTACAGATG | 494470 |
rs748206689 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371503 | GGAGAAGTTAAAGGA[A/G]ATTGGACATTTTAAA | 494470 |
rs748215981 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370710 | TACCATCTCTGTCCT[C/T]GTTCTCTTGAGCCAC | 494470 |
rs748236747 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383720 | CACCGCGCCCGGCTA[-/C]ATTTTTTGTATTTTT | 494470 |
rs748246525 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345520 | GTATTCCCTAAGTCA[C/G]GCCCCATCCCTGCAC | 494470 |
rs748246830 | snp | G/T | 1.86093e-05 | 0.0030503 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433308 | CCACCCCGTGCAGTC[G/T]CAGCCAGGCCTCAGC | 494470 |
rs748249514 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385402 | TGTGTGAGTGTGCGT[G/T]TGCATATGTGTGCAG | 494470 |
rs748332550 | snp | C/T | 3.34437e-05 | 0.0040891 | missense, intron-variant | RNF165 | GRCh38.p7 | 18:46450779 | ATTGAGAGGTTCACC[C/T]TCCCCCACAAGTATA | 494470 |
rs748344837 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454672 | CGGGCCTTGCCCCAC[A/G]GTCATTCTCTAGGTA | 494470 |
rs748355234 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403245 | ATCTCTCCCAGACTC[A/G]AATCTATTCTGACCT | 494470 |
rs748355629 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412822 | CAGATGGCACACCTG[C/T]GGGCCAGGGGCCACC | 494470 |
rs748362352 | snp | G/T | 1.65721e-05 | 0.0028785 | intron-variant | RNF165 | GRCh38.p7 | 18:46450449 | TGGAGATGCCATTAT[G/T]GTTATCATCCCTTTT | 494470 |
rs748383793 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422021 | GACCCATGGCAGCCC[C/T]GGGGGCTAAGCCAAG | 494470 |
rs748417530 | snp | A/C | 2.03772e-05 | 0.00319189 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433221 | GTCTCAGCATCCTCA[A/C]GCTACCTCCTGCCGC | 494470 |
rs748474775 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379717 | GCCACCCTGGGGAGC[G/T]AATGTACTTTCTGAA | 494470 |
rs748486809 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417671 | GACATATTTTCTTAT[A/G]TATCTACTTATTGGA | 494470 |
rs748509248 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355545 | ATGTTCCTTCCCTCC[C/T]CAAACCAGCGGTCCC | 494470 |
rs748517258 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452904 | CCCTCCCTGTCCACC[A/T]CCCCCTTTTAAAATG | 494470 |
rs748528447 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416131 | GCACATCTGGGAAAA[G/T]GCTGGGTGTGGGAGG | 494470 |
rs748546595 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398662 | AATTGCAGGGGTCCA[C/T]GCTGCTGAACTGAGA | 494470 |
rs748570669 | in-del | -/ACACACACACACACAT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404772 | CACACACACACAAAC[-/ACACACACACACACAT]ACACACACACACAAC | 494470 |
rs748609783 | snp | C/T | 1.64931e-05 | 0.00287163 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46435346 | TCCCAGCTTCGACTT[C/T]GGCCAACTGCAGACA | 494470 |
rs748648046 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431940 | TTTCTCAACTCTGCT[A/G]ATTCCTCCATCTGCT | 494470 |
rs748649523 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430954 | AACGTGCGGGTTTGT[C/T]ACATAGGTATACACG | 494470 |
rs748673691 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406703 | ATGTGGGCTCACAGT[A/G]TACAGGTTGGGCACA | 494470 |
rs748705818 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447140 | GTAGGTCTAGGTGTA[C/G]AGTTCTCTCTCTTTG | 494470 |
rs748708776 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359149 | TAGAAGCTAGAACAA[C/T]GCAATTCAATTCAGT | 494470 |
rs748714770 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334605 | CGGCGGACGTGGTTC[C/T]CCCAAATCACAGCCC | 494470 |
rs748752028 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382874 | CACCCATCCCTCCTG[A/G]ACCGTCAGAGCCTCG | 494470 |
rs748757781 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424455 | GGATTTCGAAGGTCA[C/G]CGCTGGTCCTTGTTT | 494470 |
rs748841985 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391674 | TTGCACACCACTTAC[C/T]TGGTGTAAAGGGCTT | 494470 |
rs748877321 | snp | A/G | 1.8332e-05 | 0.00302748 | missense | RNF165 | GRCh38.p7 | 18:46456013 | AAGAAGGATGAGGGG[A/G]AGGAGTCAGACACAG | 494470 |
rs748903366 | snp | C/T | 8.2426e-05 | 0.0064192 | intron-variant | RNF165 | GRCh38.p7 | 18:46447720 | AGACGGACTCCCTTG[C/T]GCCTATTGAGTGCCA | 494470 |
rs748911538 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436652 | GGAGCTTCTAGGTGC[A/G]GGAAGTCGTGGCTTT | 494470 |
rs748929683 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390747 | CTCGGAATCCTATAC[G/T]GGGCTGGGCTCAGGT | 494470 |
rs748936398 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400871 | AAAGCCTCAGGATCA[A/G]GTCTCGTGCAGACAT | 494470 |
rs748947848 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400229 | CTGCTCCTATACCCT[C/T]CTCTGAGCCTTTCAC | 494470 |
rs748948633 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430255 | GATTGGAAATCACCC[C/T]TCCCCCTCAATACCT | 494470 |
rs748956167 | snp | C/T | 4.75003e-05 | 0.00487318 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334249 | CGCGCGCAGCCGCCG[C/T]CGCCGCCGCCGCGCG | 494470 |
rs748956352 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361119 | TTTCCTGATGCCCAG[C/T]GTAAAAAAATTTTTT | 494470 |
rs748974660 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342294 | TGCATACGGCAAGGA[A/G]CCTCATCAAGACCAA | 494470 |
rs749001260 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435509 | GGCGCAGGAGGCCTA[A/G]TTCTCAGGCCCCAGC | 494470 |
rs749035462 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376099 | AGCTGCTCTGAGTGT[C/T]ACCCTCACCTGTGGC | 494470 |
rs749066319 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385721 | TGCCCCTCCCCAGCC[C/T]CTTGCTCCAAGCCTG | 494470 |
rs749080958 | in-del | -/TTTTAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443908 | TTAGTTTGAAGAACT[-/TTTTAA]AACACTTCTTGTAGT | 494470 |
rs749094556 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449626 | GCAGTTTCCCACATG[C/T]TTTTCTTATGATAGT | 494470 |
rs749097199 | in-del | -/CC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437041 | GCTTTCTTTATAGAG[-/CC]AAACCTCCTTGTCTT | 494470 |
rs749111550 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376417 | TGGACTGCCTAGTTT[C/T]GAACTTTGTTCCTGG | 494470 |
rs749124305 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461261 | GAGAACTGGGAGATC[C/T]TTAGGGTCCCTTAGA | 494470 |
rs749137397 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | RNF165 | GRCh38.p7 | 18:46447663 | CCTCGAATGCACCAC[C/T]TTCCCAGAAACTCCT | 494470 |
rs749155158 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394980 | TAATGTCCATGCAAA[A/G]CCTCATGTAGCCTGT | 494470 |
rs749155747 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351723 | AGTTCTCAGTTACAT[C/T]GCCTGGAAACAGAGG | 494470 |
rs749173305 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418117 | ATCTTAGCACTTGAA[A/G]GCAGGAGGGTCACCT | 494470 |
rs749223307 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384897 | AAAATAGAATAAGAA[A/T]ATGTCCTGCCTTTTC | 494470 |
rs749259150 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416902 | ATTGGCCTAAGCCAG[A/T]CACGTGGCCATGCCC | 494470 |
rs749262979 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428352 | AGGTGGAGATTGCAG[C/T]GAGCTGAGATCGTGC | 494470 |
rs749303055 | in-del | -/TGGG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340433 | CATTGAATACTTACT[-/TGGG]GCCAAACACTGCGCT | 494470 |
rs749305089 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384277 | CCAGGGGGCTGGGAT[A/G]CCCAAGGCCTCACCT | 494470 |
rs749332098 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402435 | GATGTAAATATATCT[A/C]AATATTGCATGGAAC | 494470 |
rs749336552 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344536 | ATGTGCCCACTCCCA[C/T]CCCCAGCGTGGAGAC | 494470 |
rs749342505 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380249 | CTATGGCATCTGGCA[C/T]AGCTGGTGCAGAACC | 494470 |
rs749353553 | in-del | -/CACG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392097 | AACATACACACACAC[-/CACG]CATACACACACTGTG | 494470 |
rs749370010 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379545 | CCTGGCCAACAGCAC[C/T]GCCCTCATTTGTTTC | 494470 |
rs749382725 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411981 | CTGGGCTAAAAGCCT[C/T]TTGTCAGCAGAGTAA | 494470 |
rs749409475 | snp | A/G | 3.30202e-05 | 0.00406313 | intron-variant | RNF165 | GRCh38.p7 | 18:46450424 | CTCTGTCTGGTACCA[A/G]CTGGGTTGGTGGAGA | 494470 |
rs749428072 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441176 | TTTTTAAATTTTTGT[A/G]GAGACAGAGTCTTGC | 494470 |
rs749429920 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343649 | ATCTGCCAAGGGAGA[G/T]AATTGACTGGATTGC | 494470 |
rs749506865 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385598 | CTTACTTTGAAATGC[-/A]CAGACAGAAAATCTT | 494470 |
rs749517828 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353848 | TGGGAGATGGAGTAG[C/T]GGGGCCTTGTGGTGG | 494470 |
rs749651454 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337017 | TACAATGTCAAGAGC[A/G]TCTTTGGACATCCGC | 494470 |
rs749652124 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401681 | GCATGCTTCAGGCTG[C/T]TCGTTAAGTGAACAC | 494470 |
rs749678147 | in-del | -/AT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354628 | CCTGCCAGCCACAGC[-/AT]CAGCACCATGCTAAG | 494470 |
rs749679715 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406466 | TTCCAGAAAACCCAA[C/G]AGCAGGATGTCCTTG | 494470 |
rs749681689 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395920 | TCCGATCTCATTTAG[A/G]CTCATTGGGGCTCAC | 494470 |
rs749717067 | snp | A/G | 9.67258e-05 | 0.00695367 | intron-variant | RNF165 | GRCh38.p7 | 18:46456125 | CCCTCTCTTATAGGT[A/G]TTGGTGACCAATCAC | 494470 |
rs749717359 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347717 | GTTGCCATGCACAGA[G/T]TCCCCCTGCCTGCTC | 494470 |
rs749749597 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429717 | TACAAATTCTTACCA[A/G]ACTCTCTATCACATT | 494470 |
rs749769398 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405661 | GCTTGAGGGGTAGGG[C/T]TGGGGAGGAGCAGGG | 494470 |
rs749778449 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444425 | ATTTTTACTGAGACT[C/T]TGTTAATTTTTTAGT | 494470 |
rs749885183 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378014 | GGGTTTAAGAGGCAT[G/T]TGGGAAGAGGGTGAG | 494470 |
rs749887065 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410614 | TGGTTATGACCTGGA[A/G]CCATGCCCAGAAACA | 494470 |
rs749894346 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400778 | GTAGCCCCGTCACTG[A/T]GCTCCTAATGGCAAA | 494470 |
rs749932692 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409507 | TGACAGTAGAAGAGA[C/T]GTCTGACTCTGAGCT | 494470 |
rs749933150 | in-del | -/AAG | 1.64762e-05 | 0.00287016 | intron-variant | RNF165 | GRCh38.p7 | 18:46447701 | ACAGATGGTAAGTGA[-/AAG]AAGACGGACTCCCTT | 494470 |
rs749965573 | snp | A/T | 1.64808e-05 | 0.00287057 | intron-variant | RNF165 | GRCh38.p7 | 18:46447711 | AGTGAAAGAAGACGG[A/T]CTCCCTTGCGCCTAT | 494470 |
rs749973905 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449366 | ATTTATTTGACTTTA[A/G]AAAACATTGCATTAA | 494470 |
rs749985724 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377346 | AACTCGCTATATGCC[A/G]GGAATTGGTCTAGAC | 494470 |
rs750018617 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419168 | TGCTGGGTGCCCTTG[C/T]TACTCTCCCCTGCCT | 494470 |
rs750050927 | snp | A/C/T | 2.36644e-05 | 0.00343972 | intron-variant | RNF165 | GRCh38.p7 | 18:46433547 | GGACCCGGATGGGGT[A/C/T]GGGTGAGGGGGCAGG | 494470 |
rs750070792 | in-del | -/CGCAGC | 0.000296223 | 0.0121665 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334237 | CACAAAGGGCCCGCG[-/CGCAGC]CGCAGCCGCCGCCGC | 494470 |
rs750074163 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385495 | CTAGCGTGGCTCTAC[C/T]GACTCTAGTGGACAG | 494470 |
rs750111325 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363715 | TCACCGTTATAATGA[G/T]CTGGCCTTGTAGTCC | 494470 |
rs750116194 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405149 | CTATGGTGTACAGTG[A/T]GGCATACTGGTGGGG | 494470 |
rs750118787 | snp | G/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333185 | TGATGTTACATATCC[G/T]CCTGCTGGCTGTGGA | 494470 |
rs750139613 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429076 | GAAGGGAAGGGGGTC[C/T]GGTGCCGCTTGCTCA | 494470 |
rs750179025 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394873 | CTTTGAAAATAGATG[C/T]CCTGGTAGAGGATGC | 494470 |
rs750229042 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428165 | TCTGTAATCCCAGCA[A/C]GTTGGGAGGCCGAGG | 494470 |
rs750232813 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399149 | CCCACGAGGTTGGCC[-/A]AGCAGAGGTAGCTGT | 494470 |
rs750240804 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458132 | TATTCTCTGTCCAGC[A/G]TGTTCTATGCTCTCT | 494470 |
rs750291047 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371410 | GCTCTGACAATGCAA[C/T]CTCATCCCAGGGATG | 494470 |
rs750309140 | snp | C/T | 3.30743e-05 | 0.00406645 | missense, intron-variant | RNF165 | GRCh38.p7 | 18:46450743 | TTGGGTAATGTGACT[C/T]GGGGAGCTGTACAGA | 494470 |
rs750342501 | in-del | -/GTGAGAGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334714 | TGTGTGTGTGTGTGT[-/GTGAGAGA]GAGAGAGAGCGCGCG | 494470 |
rs750352225 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414053 | GTAGGGTGCTCTACA[A/G]TTTTCAAGGCACCAT | 494470 |
rs750366288 | snp | A/C/G | 0.000139735 | 0.00835773 | intron-variant | RNF165 | GRCh38.p7 | 18:46455927 | ACCACCAGCCACCAG[A/C/G]TGAGTCTGCCCCAGG | 494470 |
rs750386579 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357442 | AGGATCAGAAATAAA[G/T]AACAGGGTGTCAGGC | 494470 |
rs750400575 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398250 | GTGGGGTCATGCGGA[G/T]GTGTGAGGGTGTGTG | 494470 |
rs750440197 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412782 | GCTGCTAACAGCCAA[C/T]GCGGAGTGACCACGT | 494470 |
rs750458818 | in-del | -/TTAA | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460499 | ATCGTGGGTTCTTAT[-/TTAA]TTATTTTTATAGTTG | 494470 |
rs750516529 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413776 | ACATTACATATGCAC[A/G]TGGTAAGAATTCCTA | 494470 |
rs750522044 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338249 | TACCCTCTTCTATGT[A/G]CATATTTAAATTTTT | 494470 |
rs750548715 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431458 | AACCAGAAGTATCTG[A/C]AGAGCTCTTCCTAGG | 494470 |
rs750561620 | snp | A/G | 1.64743e-05 | 0.00287 | missense | RNF165 | GRCh38.p7 | 18:46456556 | TTTCACCAACTGTGC[A/G]TGGACCAGTGGCTCG | 494470 |
rs750576640 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374490 | GACTACTTGAGGCCC[C/T]TCATGTCAGTGGAAT | 494470 |
rs750579464 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391658 | TGACATATTAAAATG[C/T]TTGCACACCACTTAC | 494470 |
rs750585667 | snp | C/T | 1.68704e-05 | 0.00290429 | intron-variant | RNF165 | GRCh38.p7 | 18:46435412 | GTGAGTCTTCAGGGC[C/T]CCTGGGGGAGGAAGG | 494470 |
rs750609943 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350347 | CCCCACTATGATGGA[C/G]AAAACAATCATCACA | 494470 |
rs750612945 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416407 | CAAGCACCCAGATTG[C/T]ATCCAGCCCTGTCCT | 494470 |
rs750661939 | snp | A/G | 1.64895e-05 | 0.00287132 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456647 | GCTGAGGGAGGAATT[A/G]GCCAGTGGACACCCC | 494470 |
rs750675247 | snp | C/T | 1.64895e-05 | 0.00287132 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46435316 | GCGTGTATCTGTCCA[C/T]CCCCACCGCCTCCAT | 494470 |
rs750697501 | snp | A/G | 0.000192215 | 0.00980157 | intron-variant | RNF165 | GRCh38.p7 | 18:46334437 | GCTCAGGGCACACCC[A/G]CGAGGACGCAGGGCG | 494470 |
rs750698005 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348947 | GTGTGTGTGTGTGTG[A/T]GATTTCTAGAAGCAT | 494470 |
rs750731058 | in-del | -/TGTGTGTGTGTGAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334705 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGAG]AGAGAGAGAGAGCGC | 494470 |
rs750744626 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457987 | TGGCTGCTTCTCTGA[C/T]TCTTTGATAACCTTG | 494470 |
rs750756417 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425050 | GTGCCTTTGGAGAGG[C/G]AGTCTCGGGCCTTCC | 494470 |
rs750773286 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392775 | GGTACCCAGCCCGGA[C/T]GGGGCCTGTGTGAGG | 494470 |
rs750811656 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369230 | GTTGTTTCCAGATAC[A/C]CAGGAGCCAATTGAA | 494470 |
rs750850453 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437508 | GACCACAGACTTCTG[A/C]CCTAGGTCATTCCAG | 494470 |
rs750876392 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424308 | CAAGGCCCCTGGGGG[C/T]CTGGGAGAGATGAGG | 494470 |
rs750905210 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353781 | AAACGGGCCCTCCAG[A/G]AGAGATAACCAGATA | 494470 |
rs750921883 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | RNF165 | GRCh38.p7 | 18:46450286 | ATCCAAGGCGTTTTC[C/T]ACCCAACAGGTCGTC | 494470 |
rs750931291 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378573 | TTTGATGTATGGTCC[A/T]ATTGTTCCAGTTTCA | 494470 |
rs750959087 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401687 | TTCAGGCTGCTCGTT[A/G]AGTGAACACAAATCC | 494470 |
rs750974798 | snp | A/C | 3.90793e-05 | 0.00442019 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334326 | GTGTTTGGCTCTGTG[A/C]GAAACAGAGGTATCG | 494470 |
rs750974858 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453223 | ATAGAGGAAATGGCA[A/G]CATTTCAGTAATTAA | 494470 |
rs750984302 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436487 | AAAATAATCTATCAA[A/T]GGAAAAGAATGAATT | 494470 |
rs750986814 | in-del | -/TC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440486 | AGGCAGCCACTGGTG[-/TC]CTGGAACATATCCCT | 494470 |
rs751009676 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451891 | ATTCTTAAGTAAAAG[A/C]AGTTAGCCCAAAATG | 494470 |
rs751032645 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385412 | TGCGTGTGCATATGT[A/G]TGCAGGGAGGGATTC | 494470 |
rs751081515 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428842 | ACTACTAGGAAATGT[A/G]AAATTCCCTGTGTGG | 494470 |
rs751121692 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417573 | GTGAAGGTTCTCTTG[A/G]CAGTCATATTTAAAA | 494470 |
rs751127322 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428136 | CAAGGGGAGGCCGGG[C/T]GCAGTGGCTCACGTC | 494470 |
rs751198229 | snp | C/G | 1.8667e-05 | 0.00305502 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433273 | CAGCCGCAGCAGCTC[C/G]CTCCCGACTTCCCGC | 494470 |
rs751198907 | snp | C/G/T | 3.43225e-05 | 0.0041425 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433464 | CCTCCTGCAGCAGCA[C/G/T]CTCCTGGAAGCCCAG | 494470 |
rs751201500 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393855 | AGACCTGGGTTCAAA[C/T]CTTGCCTCTGCCACT | 494470 |
rs751297669 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403655 | GGCCGAGGCGGGTGG[A/T]TAATTTGAGGTCAGG | 494470 |
rs751306725 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432710 | CGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 494470 |
rs751340502 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455237 | TATCAGTGAATAAAT[A/G]AGTCAACAGTGGTTG | 494470 |
rs751378678 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344348 | AGGCGCTCTCCATGT[C/T]TTCCCCCTTCTCCCC | 494470 |
rs751424343 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356388 | TAGCGCAGGGTCAAA[G/T]GGTGGTGATGCTGGA | 494470 |
rs751428473 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453891 | GCGGTGGCAGGAGGA[C/T]AGATTGAGCCCAGGA | 494470 |
rs751452764 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380117 | GGGGGTGGAGTGCAG[A/G]GGCCTCGAACCTCTG | 494470 |
rs751471453 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460132 | AATGTTCCCAGCCTC[C/T]GTGCAAGTATTCTTA | 494470 |
rs751490269 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421963 | TAGGCCCTTGGCATA[A/C]TCCATTGGACTGGGA | 494470 |
rs751510621 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367230 | GGTTCAATTCTGCTC[C/T]GCCTCCCATCCTGGC | 494470 |
rs751520377 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355248 | ATGAGCCACCGGGCC[C/T]GGCCTGTTTTAATAT | 494470 |
rs751521556 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421064 | CTTCTGTTTTGGGTC[G/T]GAAATTGCTTCTTCT | 494470 |
rs751537757 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406237 | TCTTGTTGCATTGAA[C/T]CCCCCTCTCAACCTC | 494470 |
rs751566459 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378187 | CATTTATCAATTTAT[A/G]TTGGGGAAGCAAGTT | 494470 |
rs751576420 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389816 | TCACTGCAGCCTCGA[A/C]TGCCCAGTCTCAGCT | 494470 |
rs751610513 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433006 | CCTCCATCAGGTACA[C/T]GCACACAGCCTTCAC | 494470 |
rs751622988 | snp | G/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457438 | AAAAGGAGCTGATGG[G/T]GTCTTATCCTGGCCT | 494470 |
rs751642179 | snp | G/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333818 | CGCCCTCTCCGGCCC[G/T]CGGGCGGCCAGGGAC | 494470 |
rs751674027 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445001 | TATAATAGCTATTTT[A/G]GCATCCTTGTTATTT | 494470 |
rs751675723 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348801 | TGCGTATTAGCAAAT[G/T]AAAGTCCCTGGTAAG | 494470 |
rs751693487 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405374 | GCACTCGGAAGGGGG[A/C]CTGGCTGAAATGTGC | 494470 |
rs751726037 | snp | C/T | 1.67217e-05 | 0.00289147 | intron-variant | RNF165 | GRCh38.p7 | 18:46435253 | AGTGGCCTGGGTAGC[C/T]CCTGACACGAGGGCT | 494470 |
rs751738104 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347617 | TGGATTAAACGAGAC[A/G]GTGGATGTAATGTAC | 494470 |
rs751749477 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454241 | GGAAAATCATGAATA[A/G]TGATGGCAAAAAAAT | 494470 |
rs751751692 | snp | C/T | 3.29712e-05 | 0.00406011 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46456523 | CTCTCTTCCAGACGC[C/T]TACCCTGTATGCATC | 494470 |
rs751752608 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375696 | GGGAGTTCTCTTGTT[C/T]CCAGCAATTTTATGT | 494470 |
rs751776759 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382475 | GAATCCCTCCCCTTA[C/T]ATGCAATGAATGTTT | 494470 |
rs751787323 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414945 | TGTGTGAGGGAGTAG[C/G]GGCTGAGCTAAGCCG | 494470 |
rs751795532 | in-del | -/AC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414469 | TGCAGACATACATGT[-/AC]ACACACACACACATC | 494470 |
rs751803630 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46391924 | CACACACTTATACAC[A/G]TACACCATGCACACA | 494470 |
rs751841730 | snp | A/G | 8.71017e-05 | 0.00659873 | intron-variant | RNF165 | GRCh38.p7 | 18:46456094 | AGGTAGGAGACCGCC[A/G]TTTTGATTCCCTCTC | 494470 |
rs751848269 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424191 | CCCAAGGGAGTTAAC[A/G]TCTGCCCAGGGTAGT | 494470 |
rs751851896 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358890 | TTTTGACTTAAAGAC[A/C]ACAGTGAGAGGAGAG | 494470 |
rs751851903 | snp | A/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456731 | TTCTGAGCCATTTGA[A/C]GTAGAGGAAAAGCCT | 494470 |
rs751883235 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401300 | AATTCCAGCTGATGG[C/T]AGAGGGGATGTGGTG | 494470 |
rs751927442 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377868 | CTCAGGTAACCATGT[C/G]TAGAGCAAAGGGTAC | 494470 |
rs751938107 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422800 | TCCTCTTCTGAGCAG[A/T]TAGTGGGCCTCTGCA | 494470 |
rs751939236 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358019 | ATGGCCTATCATGAC[A/G]TTGTATTAGGGCCAC | 494470 |
rs751977043 | snp | A/G | 1.76855e-05 | 0.00297362 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334229 | GAGCCGCGCCACAAA[A/G]GGCCCGCGCGCAGCC | 494470 |
rs752024290 | snp | C/T | | | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435323 | TCTGTCCACCCCCAC[C/T]GCCTCCATCCCAGCT | 494470 |
rs752029170 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368083 | GGGCTTGAGACTCCA[C/T]GTGGGTAATTGTGAT | 494470 |
rs752037755 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405546 | AAAAGTGGGTGAAAG[A/G]TTGGAGAGAGAGGGC | 494470 |
rs752080188 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409405 | CCATCTGCAGGTAAA[C/T]GGTGGTGGTGATGCA | 494470 |
rs752130268 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352338 | TTTGCACTGGCTATA[C/T]TGGGTACACATCATC | 494470 |
rs752138435 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426260 | CTTCAAATTTCTACT[G/T]TGTTACTTATCAGAT | 494470 |
rs752138733 | in-del | -/CGCTTC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456366 | AGGCTGATCTGAAAG[-/CGCTTC]CGCTTCCTGGCGGAG | 494470 |
rs752156694 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449167 | GAAAACTGAGGAATA[C/G]AGAGGCTAAGTAACT | 494470 |
rs752171893 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408820 | GTCAAAAGACTTTGA[A/G]CTTAGATAGTCTGTG | 494470 |
rs752175569 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361421 | TATGCAGCATATATG[C/T]ACATTAATATTTAAC | 494470 |
rs752209397 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370272 | GGGAGGGGAAACATC[A/G]TTATTCCCATTTTAC | 494470 |
rs752226829 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403579 | AATGTGTCAGATGCC[G/T]CATGAAAATCAGATC | 494470 |
rs752297471 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379984 | CGTCAGAGAAGAGAT[A/G]AGGCTCCAAAGGCAG | 494470 |
rs752316959 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402809 | CCTGGCCCCATTCTC[C/T]TTTTATTTGTGAACT | 494470 |
rs752340141 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453422 | CACTTCAACAGGCAC[A/G]AGGAAATTGTGAAGA | 494470 |
rs752375372 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46450391 | CTCCGCCGTACGGGA[A/G]AGCTATGAGGTATGT | 494470 |
rs752402498 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347518 | GTCCTCCCTCTGAAG[C/T]GGGCAACCCTCTTGG | 494470 |
rs752404716 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411634 | GCTGTGACGAGAGCC[C/T]ATCCCAGGGAGGGGC | 494470 |
rs752409762 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339240 | TAAAACTACCCTGAA[C/T]TGAGTGATCACTCTC | 494470 |
rs752446188 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437766 | AGTTCTTTTCACTCT[C/T]CTTCTTGGACTCAGT | 494470 |
rs752490015 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379148 | CCCCCAGGCCCCCCA[A/G]CCCTCTGATTTTATC | 494470 |
rs752491132 | snp | C/G | | | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388996 | GCTTATTGACTCTCG[C/G]TTCACGAGGAATTCT | 494470 |
rs752497821 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353648 | GAGAGTGGGAGTGAC[A/G]GGGCCCTGGAGACGC | 494470 |
rs752512498 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355205 | TTATCCACCCACTTC[A/G]GCATCCCAAAGTGCT | 494470 |
rs752516588 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366279 | CCTGGGCAACAAGAG[C/G]AGAACTCTGGCTCAA | 494470 |
rs752530963 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452354 | GCACGATCTTGACTC[A/T]CTGCAACCTCCACCT | 494470 |
rs752545053 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420949 | AGGAGAATATCTGAA[C/T]TCATGACCTAAGACG | 494470 |
rs752606267 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365923 | GTCACTCAGAAGGAA[A/G]TTCAAATCCTGAGAA | 494470 |
rs752633252 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431326 | ATGCCAAAGAGTAGG[A/T]CACTAAAGCTGTCTA | 494470 |
rs752646371 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403851 | CCATTGCACTCCAGC[C/T]TGGCAACAGAGTGAG | 494470 |
rs752658783 | snp | A/G | 3.29794e-05 | 0.00406061 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435305 | CGGAGTCAGGAGCGT[A/G]TATCTGTCCACCCCC | 494470 |
rs752694014 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358792 | GGGAGAAACCCATGG[A/G]CAGAGTGACACACGC | 494470 |
rs752708071 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456419 | CCACAGCCTCCCTCC[A/G]TAGCCGGGCAGTTCC | 494470 |
rs752723452 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382226 | TTCCCCTCCTGCTGA[A/G]GACAGGTCCCATGGA | 494470 |
rs752796703 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346674 | GGTGAGGATGAAAGA[C/G]AGTTCTCACTCATAT | 494470 |
rs752812060 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428277 | AGCTGGGTGTGGTGG[C/T]AGGCGCCTGTAGTCC | 494470 |
rs752813227 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391309 | GGGGTAAGCACCTGA[A/G]CCACTGTGTCCCATG | 494470 |
rs752813621 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381667 | AGACCCTGTTTCTAC[C/T]AAAAATAAAAAAAAT | 494470 |
rs752832204 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414229 | GGACCTGAACACAAC[C/T]TGCCTGACTCTCTGG | 494470 |
rs752876765 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380338 | TTCCTCTGGCGACTT[G/T]GGGAGTGTGCGCAGG | 494470 |
rs752892999 | snp | C/T | 6.58989e-05 | 0.00573978 | missense | RNF165 | GRCh38.p7 | 18:46447691 | CCTCCTCCACACAGA[C/T]GGTAAGTGAAAGAAG | 494470 |
rs752901343 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390454 | GACAGTGTTTGAAGA[C/T]GGGTCACTGCTTCTA | 494470 |
rs752917140 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422650 | AGATGGTGACTGTCC[A/G]GTTTGGCAACTTTAA | 494470 |
rs752924672 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335331 | TTTCCCCACATCCCC[-/T]CTCCCTCACATTCTG | 494470 |
rs752930167 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398713 | GGCTCTGTAAGACCA[C/G]TGCCCTTAAAGCTCC | 494470 |
rs752940984 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411688 | TGAAAAAGTCTTCAT[-/G]TTCCAAAGGGGTGAG | 494470 |
rs752960292 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400481 | TCCAGTGGGGACCCT[C/T]AGTCTGTAACGGGCA | 494470 |
rs752985517 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368022 | GCTTGTTAAACATGC[A/G]GATTCCTGGGCCTGG | 494470 |
rs752990255 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340364 | GTACTTCATGTGTTT[A/C]GTTGTTCATTCATTC | 494470 |
rs753016760 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433691 | CCAAGTGGGTCTCTG[C/T]AGGAAGTAGCTATTG | 494470 |
rs753067526 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367536 | GGTTATTGAATAATA[A/G]GTGGGTCTATTGGAC | 494470 |
rs753120078 | snp | A/C/G | 3.29458e-05 | 0.00405857 | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447610 | CTCAGTTCCAGGTGC[A/C/G]GCCCATCCCTCAGCA | 494470 |
rs753151762 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46387418 | CTTTGGGAGTGAATC[C/T]AGTACAAAAACAGCA | 494470 |
rs753158719 | snp | C/T | 1.65422e-05 | 0.0028759 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456686 | CACCAGGTCCCCCCA[C/T]GGCCATAGCCCTTGC | 494470 |
rs753163026 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447884 | TCCCTTGTGCCCTGG[A/C]CTTCTTGTGTCCTGG | 494470 |
rs753178604 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339004 | CTGGCCCTCTTTGTT[C/T]TCGTGCTCTTCCCAG | 494470 |
rs753222388 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350523 | GGGCAAGCATGGTCA[A/G]GAGCGCCCCCAACCC | 494470 |
rs753229819 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407856 | CATTACATCATCACA[A/G]ATGTCACAAAGCTGC | 494470 |
rs753324500 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428022 | CTAATGAGTCTCCAG[A/T]GAAAGCTGAAGGCTC | 494470 |
rs753332208 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435659 | GGTCCTGCAGTGGGG[A/G]AGGGGGACAGGGATA | 494470 |
rs753337614 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378878 | CCTATGAAGCACCCC[A/G]CTATGGTCCTGTCTA | 494470 |
rs753381897 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344200 | CACCAGCCTGCAGGT[A/G]GAGAGGGGGTGGAGG | 494470 |
rs753413256 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410748 | TGACCAGGAGGGCCA[C/T]TCATTCCTCTTGTTC | 494470 |
rs753422154 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411501 | CCCCTTTGCTATCGA[C/T]TGATTCATTTCAACA | 494470 |
rs753459441 | snp | A/G | 5.96427e-05 | 0.00546057 | intron-variant | RNF165 | GRCh38.p7 | 18:46334341 | CGAAACAGAGGTATC[A/G]CTTTTTCCTTTCGGG | 494470 |
rs753471662 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343139 | TAACCCACCTCCCTT[A/G]GACTGCTGTCCAGCC | 494470 |
rs753541674 | in-del | -/GAAG | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458527 | GAAATTCCATACAGT[-/GAAG]GAAATTTGAGTCTGT | 494470 |
rs753549998 | in-del | -/CTCCC | 1.65323e-05 | 0.00287505 | intron-variant | RNF165 | GRCh38.p7 | 18:46456106 | CCATTTTGATTCCCT[-/CTCCC]CTCCCCTCTCTTATA | 494470 |
rs753556282 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420135 | CATGGCGCCTCCACT[C/T]ACCGGCTGCTGTCTG | 494470 |
rs753622760 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396384 | AGAGAGAAGTGAAGC[A/G]TTAGTGGGTTCAGGC | 494470 |
rs753629130 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454884 | CTTTGCCAAAATATT[C/T]ACCAAGTACTAATAC | 494470 |
rs753632259 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419326 | TAGGCCAGACCTCAG[G/T]GAGGGTGAAAAGCCT | 494470 |
rs753658803 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352774 | CTGTAAAGGAAGCTG[G/T]GAAGTCTTATATACT | 494470 |
rs753683720 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450210 | CTCAGGGTGTACTGA[-/GT]GGGTTACAGGTGGAG | 494470 |
rs753691945 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395533 | TATTGTCATCTTTGC[C/T]TTAAGGATGAGTTTG | 494470 |
rs753695892 | in-del | -/GTGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398282 | GCATGTGGTGTGTGT[-/GTGA]GTGTGTGTGTTCACA | 494470 |
rs753716904 | snp | A/G | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333361 | AAATAATTATTGTGA[A/G]CTTTGTGCTCTCCAA | 494470 |
rs753746188 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347580 | ACTCATTCTTACCTG[A/C]CAGGTGAGTTTAATC | 494470 |
rs753752172 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433555 | ATGGGGTCGGGTGAG[A/G]GGGCAGGGCCAGGGC | 494470 |
rs753752250 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438597 | TGTGAGGCAGTGCAA[C/T]GGATTGAGCCCAGGC | 494470 |
rs753764316 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397258 | GTGAGGACTGGGGGT[-/G]GGAGGGGAAGTGAGA | 494470 |
rs753778617 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414901 | TTGTGAATGGGGAGC[A/G]TGCACTTCCACCCAG | 494470 |
rs753793036 | snp | A/G | 1.76253e-05 | 0.00296856 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433484 | TGGAAGCCCAGCACC[A/G]CAGGCTGGTCTCGCA | 494470 |
rs753797832 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390253 | TTCCCATCACTGTCT[A/G]AATCACCCCATCTTT | 494470 |
rs753828224 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367951 | CGGTTGAGAATCATC[C/T]GAGGCCAGTGAGTCT | 494470 |
rs753886454 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356566 | GGCAGGCACGGAATG[C/T]GTACTTCTTGCCTCC | 494470 |
rs753888204 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404586 | TGGTGAAACCCATCT[C/G]TACTAAAAATACCAA | 494470 |
rs753939787 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399563 | GGATGAGTGGACTTT[C/G]ATGGGAAAACGGTGA | 494470 |
rs753970433 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421988 | CTGGGAACCAATAGA[C/T]AGAGAGGGAGGAAAG | 494470 |
rs753989511 | snp | G/T | 1.71155e-05 | 0.00292531 | intron-variant | RNF165 | GRCh38.p7 | 18:46435420 | TCAGGGCCCCTGGGG[G/T]AGGAAGGGAGGAAGG | 494470 |
rs754004622 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367400 | GTGGGAGGTAGGAAA[A/C]AATTTGTCCATAGTA | 494470 |
rs754023776 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410425 | TGGAGGAGGAGGCAG[A/C]CAGCCAGCTGTGTGA | 494470 |
rs754041647 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338749 | CTTGCTAAATGAGGC[A/G]TTTTAGACACTGAGG | 494470 |
rs754044059 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431721 | CTCTGGAAAGAAAGT[C/G]ACTGCCTTGCATGAG | 494470 |
rs754090588 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375748 | GCAAGTTGGAGGAGA[C/T]ATTTTGAGGTGGGAG | 494470 |
rs754125165 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429083 | AGGGGGTCCGGTGCC[A/G]CTTGCTCATGCTGCA | 494470 |
rs754125258 | snp | C/G | 1.64735e-05 | 0.00286993 | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447594 | GCTGGCTTGAGTCCT[C/G]CTCAGTTCCAGGTGC | 494470 |
rs754131265 | snp | C/G/T | 3.29898e-05 | 0.00406128 | intron-variant | RNF165 | GRCh38.p7 | 18:46447733 | TGCGCCTATTGAGTG[C/G/T]CAGTGGTGGTCTGAG | 494470 |
rs754192315 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459698 | CAGCTGTTTGGGGGA[C/T]AAGAGAGGGCCAGGG | 494470 |
rs754203631 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384350 | TGGTGTGTACATGTA[A/T]GTGTGTGGGGGGGAT | 494470 |
rs754263728 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361220 | CTAAGCTGGGCTTCA[A/C]CCCAGCTCCAGATGG | 494470 |
rs754273567 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430317 | CTGGATTAATTCTTG[-/A]AAAATCTCAAGCTGT | 494470 |
rs754277127 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426297 | CCCAGGCAAGGCAGT[A/G]AGCCTTTTAGAGACT | 494470 |
rs754280021 | snp | A/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458909 | CAGTAGCTCCAGTGT[A/T]TGAAAATGTCTCCAG | 494470 |
rs754321306 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372992 | CCCTCCTGCTGGGAA[A/C]CTGGAAGCTCTGTGT | 494470 |
rs754353632 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370226 | ATCTAAGGGGTTCAC[A/G]TGATATCCTTACGAT | 494470 |
rs754372032 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446488 | CCAGCCTGGACAACA[C/T]GGTGAAACCCCATCT | 494470 |
rs754414122 | in-del | -/AAAAAAAAAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441862 | GCGAGACTCCATCTC[-/AAAAAAAAAA]AAAAAAAAAGAGGCC | 494470 |
rs754414852 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360359 | AACAGTGCAGGTGCT[C/T]CCCACAATGGTGCTC | 494470 |
rs754415729 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425276 | CTCCCAGGATCCCAC[A/G]TCCCTGGAGCAGGCA | 494470 |
rs754436371 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402767 | TGGCCTCCCAAAGTA[C/G]TGGGATTGCAGGCAT | 494470 |
rs754483214 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347298 | TCTGGAGCATCGGGC[C/G]CTCTCATTTCATTGT | 494470 |
rs754503207 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392148 | ACACAACAAACACAC[A/T]TGCACACCACACACG | 494470 |
rs754532852 | snp | C/T | 2.0332e-05 | 0.00318835 | intron-variant | RNF165 | GRCh38.p7 | 18:46334349 | AGGTATCGCTTTTTC[C/T]TTTCGGGGTCTGCTT | 494470 |
rs754534844 | snp | C/T | 3.29554e-05 | 0.00405914 | missense | RNF165 | GRCh38.p7 | 18:46450386 | CACACCTCCGCCGTA[C/T]GGGAGAGCTATGAGG | 494470 |
rs754586197 | snp | A/G | 0.00100214 | 0.0223622 | intron-variant | RNF165 | GRCh38.p7 | 18:46433141 | AAGGGTCAGTGTGGC[A/G]GCCGCTCGTGCTGGT | 494470 |
rs754627326 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378905 | TCTAACCCACCTTCC[A/T]CTCTTCCTCCCCAGT | 494470 |
rs754640793 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378239 | CAAGACAAGGACCCT[C/G]CACATGCCCTTGCGT | 494470 |
rs754650579 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410760 | CCACTCATTCCTCTT[A/G]TTCTCATTGGTTTGG | 494470 |
rs754652370 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370402 | AGCTTGTGTCTTCAA[C/T]CAATTCTTTACACAG | 494470 |
rs754684141 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436753 | AAAAGATAGATTGCA[C/T]TACAGCCAACTTCTG | 494470 |
rs754713852 | snp | A/C | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333484 | AATGCGTTCTTGGCA[A/C]GCGTCCTGCGTTAAC | 494470 |
rs754760872 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409792 | TTCAAGGCATCCTGG[A/T]GATTACTGTCATTCT | 494470 |
rs754763631 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365083 | TCTCCTGATATTCCT[A/G]CTTTATCACCATTCC | 494470 |
rs754772011 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450914 | ATTCTAGAAACCTTT[A/G]CTCTGGTTAGATGCT | 494470 |
rs754850721 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419365 | TGTAAGACACTTTCA[A/G]TGGGGGAGGAGGTGG | 494470 |
rs754878939 | snp | G/T | 3.35374e-05 | 0.00409482 | intron-variant | RNF165 | GRCh38.p7 | 18:46435247 | AGAACTAGTGGCCTG[G/T]GTAGCCCCTGACACG | 494470 |
rs754893708 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429501 | TGATATTGCTTATGT[C/T]ATTCATATTGTGGAA | 494470 |
rs754910066 | snp | C/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333776 | CGTGTTCACGCCGCC[C/T]ATGTCTGTGCAGGGG | 494470 |
rs754919143 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382611 | CAGTTAGCCTTGCAT[A/G]ACTTAAGTTTCCCAT | 494470 |
rs754962054 | in-del | -/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460213 | CACCAGACTTTTTTT[-/C]CTTTTTTTCCTAAAG | 494470 |
rs754974034 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429234 | CTTTGGATTTTCATT[G/T]CTTTTTGCAAAGATT | 494470 |
rs754997026 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345334 | CGGGCAGGTGCGGTG[A/G]GAGTGTTGATTGAGG | 494470 |
rs755002268 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395011 | GGAGACAGCTTCTTT[C/T]GGACCAAGAATCTGC | 494470 |
rs755016217 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405283 | AATAGTAGAGTCTCT[A/G]GGAGGTGCCCGTGGC | 494470 |
rs755041288 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455475 | GACAGCAAAAATGAT[A/G]TCCACTTGACCTCTT | 494470 |
rs755052138 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390332 | GTGACTCTTCCTGCC[C/T]GCTGGGTGTTGGTGC | 494470 |
rs755056021 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335046 | AAGATGCTTGGGCGC[-/GT]GTGTGTGTGTGTGTG | 494470 |
rs755088302 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424668 | GAAGCTATTTGAGGC[C/G]CCTGCCAGCAAAGAG | 494470 |
rs755103568 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389334 | CTTTCCCAACAATGC[C/T]GATAAATAAAACATC | 494470 |
rs755107888 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411505 | TTTGCTATCGATTGA[-/T]TCATTTCAACATACA | 494470 |
rs755130485 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367519 | TGAGGCAGGGTAGAA[C/T]TGGTTATTGAATAAT | 494470 |
rs755208796 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355451 | GGTGAGGATCACAGG[A/C]GATCCTTGCTGTCTG | 494470 |
rs755277475 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447779 | TGCCCTGGCTGCTAC[A/G]TGGCCTGGCTCCCCT | 494470 |
rs755278175 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421428 | TATTAGGATCTGTGC[C/T]AGGCAGTAGGGGTAA | 494470 |
rs755292837 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366200 | GGGAGGCTGAGGCAG[A/G]AGACTCGCTTGAACC | 494470 |
rs755302464 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450636 | CTTCCAGCTCCCAAT[A/C]CATATCCTGTGTGCA | 494470 |
rs755305587 | snp | C/G | 3.30584e-05 | 0.00406548 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456679 | TTTCCTTCACCAGGT[C/G]CCCCCACGGCCATAG | 494470 |
rs755314787 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375792 | AGAAGCCCTTTTGAG[G/T]GTCCCTCCAATCCCA | 494470 |
rs755319184 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338893 | GCTCACCCTGCTCCT[C/T]GCTGGCGGGTGCACC | 494470 |
rs755340958 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337063 | TGCCCCTTTAACAGC[C/T]GGCTCCCTTCTGCTG | 494470 |
rs755345808 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431896 | CCATTCCTTCTTGAC[C/T]ACTCCTTTGGTAGGT | 494470 |
rs755391255 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386996 | CGCTGCTGAACCAGG[A/C]ACTTGGCCAACATTC | 494470 |
rs755397000 | snp | A/G | 1.71129e-05 | 0.00292509 | intron-variant | RNF165 | GRCh38.p7 | 18:46435422 | AGGGCCCCTGGGGGA[A/G]GAAGGGAGGAAGGGA | 494470 |
rs755406820 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374758 | AAAAGCAGCAAGGCT[C/T]TGGCTGAACTGGGGG | 494470 |
rs755430864 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349357 | GCATGGCAGATGGTG[A/C]GAGGGACTCCTCTGG | 494470 |
rs755456531 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416508 | GAACATTGAGAGCAC[A/T]ACTCAAAATTGAGTC | 494470 |
rs755469051 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361250 | GGAAAACAAAAGACA[A/G]AGATGAACTCTCAAC | 494470 |
rs755493485 | snp | A/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458946 | AGGCTGGAGATCTCA[A/C]CAGTGGGGAAAGTAC | 494470 |
rs755538296 | snp | A/C/G | 1.64806e-05 | 0.00287054 | missense | RNF165 | GRCh38.p7 | 18:46456571 | GTGGACCAGTGGCTC[A/C/G]CCATGAGCAAGAAAT | 494470 |
rs755562331 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410620 | TGACCTGGAGCCATG[A/C]CCAGAAACACTCAAA | 494470 |
rs755573558 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426390 | TTTCCCTCCCCTATG[A/G]GTTCTTCTGTCCTCC | 494470 |
rs755587827 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383617 | TGGAGTACAGTGGTG[C/T]GATCTCAGCTCACTG | 494470 |
rs755652053 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant | RNF165 | GRCh38.p7 | 18:46447714 | GAAAGAAGACGGACT[C/T]CCTTGCGCCTATTGA | 494470 |
rs755663052 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368201 | TTCCAGGCTAAGCTT[A/G]TTGGAAGTTCACTAA | 494470 |
rs755669275 | snp | C/T | 0.000100873 | 0.00710113 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334236 | GCCACAAAGGGCCCG[C/T]GCGCAGCCGCCGCCG | 494470 |
rs755670323 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400809 | ATCCTGCCATTCCAC[C/T]ATTTGAATCTTCCCC | 494470 |
rs755694074 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341977 | GCCCGACCCAGTAGC[A/G]TATTGGGAGAGGAGA | 494470 |
rs755711203 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant | RNF165 | GRCh38.p7 | 18:46450289 | CAAGGCGTTTTCTAC[C/T]CAACAGGTCGTCCAT | 494470 |
rs755722422 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409508 | GACAGTAGAAGAGAC[A/G]TCTGACTCTGAGCTG | 494470 |
rs755734364 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377369 | GTCTAGACACACAAT[A/G]ATGTGTGTCTTTCAG | 494470 |
rs755747651 | in-del | -/GCC/GCCGCC/GCCGCCGCC | 0.167887 | 0.23777 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334241 | AAGGGCCCGCGCGCA[-/GCC/GCCGCC/GCCGCCGCC]GCCGCCGCCGCCGCC | 494470 |
rs755812529 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419244 | ACTTGGGAGGTGCAG[A/G]TGCTCTCAGAGTTTG | 494470 |
rs755817822 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352546 | AGAGTGGTGCTCAAT[A/T]TCAAGGACTCAGGTG | 494470 |
rs755869922 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429197 | AATTCTTTTCTGGCT[C/G]ACTTGCAGTCAGGCA | 494470 |
rs755880383 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372449 | CCAGGGCAGCCTGAA[A/G]ATAGTGACATAAAGG | 494470 |
rs755903797 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363768 | GGGCAGGAAACATAC[G/T]TTTTAAGGTTGGGTC | 494470 |
rs755918653 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414347 | CCTTCCAAACCAGGG[C/T]TCTGTGTAGGTGCTG | 494470 |
rs755930624 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461192 | AGACGTCCCAATGAC[C/G]TTGAGCAAGTCCCTT | 494470 |
rs755960875 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404519 | AGCACTTTGGGTGGC[C/T]GAGGCAGGTGGATTA | 494470 |
rs755974462 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339600 | ACCTTGACTTCAGGA[-/T]TTTGGAAACCCCATC | 494470 |
rs755981557 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396871 | GGCATGACGTGGGTT[-/G]GGTGGATTTTCCGCT | 494470 |
rs755990444 | snp | C/G | 1.86607e-05 | 0.00305451 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433299 | CCCGCTGGCCCACCC[C/G]GTGCAGTCGCAGCCA | 494470 |
rs755993903 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362698 | AGTGAACAAAGAATA[A/G]TGCCCTGCGACAACC | 494470 |
rs756041403 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435519 | GCCTAGTTCTCAGGC[C/T]CCAGCGTTTGCCTCT | 494470 |
rs756043619 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346497 | GGACTTCTTGGGGGC[C/T]GAGGGGATGGGAAAC | 494470 |
rs756130487 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381489 | GTTTGGTCCTTCTCA[A/C]GGTCCTTCTATTTCC | 494470 |
rs756145977 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364772 | TTTCTGAGGATCGCA[C/T]GGCCACCGAGGTCAT | 494470 |
rs756146988 | snp | C/G | 1.68821e-05 | 0.0029053 | intron-variant | RNF165 | GRCh38.p7 | 18:46435413 | TGAGTCTTCAGGGCC[C/G]CTGGGGGAGGAAGGG | 494470 |
rs756228024 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421138 | GTCTCCTCAGTTCAT[G/T]CTGGACCTGCAACTG | 494470 |
rs756228555 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398271 | AGGGTGTGTGTGCAT[A/G]TGGTGTGTGTGTGAG | 494470 |
rs756239086 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343825 | TGCAGTAGGTGGGAA[-/G]GGAGCAGTAATTGCC | 494470 |
rs756298145 | snp | G/T | 1.64882e-05 | 0.00287121 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435324 | CTGTCCACCCCCACC[G/T]CCTCCATCCCAGCTT | 494470 |
rs756298531 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446277 | TTCATTTATTAGCTG[A/G]AAAACTTTTACAAAG | 494470 |
rs756358093 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383113 | CAGGCCAAGGGCCTA[C/G]CCTAGGCCGGGGTAG | 494470 |
rs756386910 | in-del | -/AC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383408 | ATAAAATATGTATAC[-/AC]ACACACACATGTTAA | 494470 |
rs756388166 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458758 | TTATTGAGTGCCTAC[C/T]GGTGCAGGCGCTGGG | 494470 |
rs756403457 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426936 | ATGTCTGTTTTTCAG[A/G]CATCACTGATCGTTG | 494470 |
rs756405563 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336437 | TAAAGTTTACTTTCA[C/T]GGCAAACATGCCCAC | 494470 |
rs756410971 | snp | C/G | 8.5492e-05 | 0.00653748 | intron-variant | RNF165 | GRCh38.p7 | 18:46456116 | TTCCCTCTCCCCTCT[C/G]TTATAGGTATTGGTG | 494470 |
rs756413883 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430668 | CTGTCTTCTCATTCC[A/G]GTTTCTGAGAGTCCC | 494470 |
rs756447348 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445264 | GTCTTCTTCCAGCAG[G/T]ACTAGAATATCCCTA | 494470 |
rs756491360 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349070 | TACTGTGGAGGTAGG[A/G]AGACTGAGAAAAAGG | 494470 |
rs756493487 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334718 | TGTGTGTGTGTGTGA[A/G]AGAGAGAGAGAGCGC | 494470 |
rs756515258 | snp | A/G | 1.96992e-05 | 0.00313834 | utr-variant-5-prime, missense, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334335 | TCTGTGCGAAACAGA[A/G]GTATCGCTTTTTCCT | 494470 |
rs756516786 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383497 | AAAACCATAACCTTT[A/G]GTATTATATTCTCCA | 494470 |
rs756530950 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46456564 | ACTGTGCGTGGACCA[A/G]TGGCTCGCCATGAGC | 494470 |
rs756530974 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360038 | ATCTCAAGGTCTCTA[C/T]CATAGTCATCATGTC | 494470 |
rs756539065 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458010 | TAACCTTGGGCAAGT[C/T]CCTTTCTTTCTCTGT | 494470 |
rs756557793 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389918 | ATTTTTTGTAGAGAC[A/G]GGGTTTTGCCATGTT | 494470 |
rs756557947 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359085 | TCCCCGTAAAAGGAG[A/T]GGCAGTAACATCCAC | 494470 |
rs756574477 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442684 | TTAGTCGACAGTATT[G/T]TTCAGGTCTTTTATA | 494470 |
rs756579251 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348010 | TACTCTGTGCCAGGC[A/G]CCCTCCTAAGCACTT | 494470 |
rs756583943 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425098 | AGGGCCCTGCCTCCA[C/G]TGTCCCCTCCCTGTT | 494470 |
rs756605296 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424424 | AGTTAACGTGGCAGC[A/C]ATTTATTTGGAAGAG | 494470 |
rs756736803 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391571 | TATGGGGCAGGCCCT[C/G]CTCGAGCAGGGTAGT | 494470 |
rs756744711 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438897 | CCAACATTACCATGA[G/T]GAGCTACTGTTATCA | 494470 |
rs756757719 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461143 | CCTGGACTGGGGAGC[C/T]GGGAGGCTCAGGTTT | 494470 |
rs756769500 | in-del | -/TATCCCCC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340437 | AATACTTACTTGGGG[-/TATCCCCC]CCAAACACTGCGCTA | 494470 |
rs756774086 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384649 | CAACAGAGAGGGGAC[C/T]CATTCCCTATCTCCC | 494470 |
rs756822409 | snp | C/T | 3.29451e-05 | 0.00405851 | utr-variant-5-prime, synonymous-codon | RNF165 | GRCh38.p7 | 18:46447617 | CCAGGTGCGGCCCAT[C/T]CCTCAGCACTATCAG | 494470 |
rs756823994 | in-del | -/CT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380127 | GCAGGGGCCTCGAAC[-/CT]CTCTGCCTTCTTCTC | 494470 |
rs756830597 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351485 | GAGCCAAATGGTAAG[G/T]TTTGCTAAGGCTGTC | 494470 |
rs756845941 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350735 | CTGGGGGAATGAAAG[A/C]GATCATATGATACTA | 494470 |
rs756864511 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384733 | AGAAAATGGCCCATC[A/G]TGGCCAAGCACAGTG | 494470 |
rs756879392 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417613 | CCCAACCTTTTCTTC[C/T]TCCTGCTTCATTTTT | 494470 |
rs756935888 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361570 | ATGCTTTCAAAGATG[A/G]TCTTGCTTATTCCAT | 494470 |
rs756954409 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393904 | TTAATCCTTCTGAAT[A/G]TTAGTTGATGTGAGG | 494470 |
rs756969330 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428148 | GGGCGCAGTGGCTCA[A/C]GTCTGTAATCCCAGC | 494470 |
rs757007119 | in-del | -/TGA | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332633 | GAACAAGCTCTATGG[-/TGA]TTGCCCGTTGGCATC | 494470 |
rs757013910 | snp | A/C | 1.65263e-05 | 0.00287452 | missense, intron-variant | RNF165 | GRCh38.p7 | 18:46450735 | AGGACAGGTTGGGTA[A/C]TGTGACTCGGGGAGC | 494470 |
rs757021316 | snp | C/T | 1.87138e-05 | 0.00305885 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433275 | GCCGCAGCAGCTCGC[C/T]CCCGACTTCCCGCTG | 494470 |
rs757107684 | snp | G/T | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439669 | AACTTGGAGATAGTG[G/T]ATGTTACCTTGGCAC | 494470 |
rs757159135 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394093 | CTGCCACACACCAGA[C/G]TCTAATTTCCTCCCT | 494470 |
rs757242856 | snp | C/T | 1.65061e-05 | 0.00287277 | intron-variant | RNF165 | GRCh38.p7 | 18:46450422 | TGCTCTGTCTGGTAC[C/T]AACTGGGTTGGTGGA | 494470 |
rs757278787 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389190 | AACAGGGAAACATCC[A/G]CTGTATTTATTCACC | 494470 |
rs757296747 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371257 | TTCAAGACGAGATTT[G/T]CATGGGGACACAGCC | 494470 |
rs757313406 | snp | C/G | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336261 | TAAATCATTACCATC[C/G]TCATTAATACCACCA | 494470 |
rs757355884 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405424 | GACAGTGGGAACAGT[G/T]AGGTGCTACAGCAGT | 494470 |
rs757379954 | snp | C/T | 1.67075e-05 | 0.00289023 | intron-variant | RNF165 | GRCh38.p7 | 18:46435255 | TGGCCTGGGTAGCCC[C/T]TGACACGAGGGCTCT | 494470 |
rs757422747 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411711 | GGGGTGAGGCCCTAC[C/T]GAAGGAATCTCAGAT | 494470 |
rs757434390 | in-del | -/GTGTGTGT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334674 | AAGATACATGACCGT[-/GTGTGTGT]GTGTGTGTGTGTGTG | 494470 |
rs757434804 | snp | A/T | 1.64887e-05 | 0.00287125 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46435310 | TCAGGAGCGTGTATC[A/T]GTCCACCCCCACCGC | 494470 |
rs757445737 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414963 | CTGAGCTAAGCCGCA[A/G]TCCTGCTGGGCCTTT | 494470 |
rs757477744 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445043 | TTGTTTCCATGGATC[A/G]ATTTTTCACCTGATT | 494470 |
rs757525258 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410650 | ATCTATCACCAATAA[C/T]TGTCCATGGGCCTGG | 494470 |
rs757564388 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443696 | GTGACAGAGACTGTA[C/T]GGCTTTTGAAGCCCC | 494470 |
rs757566261 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457746 | TTAACCAGATGATGC[A/G]GATAAGACAGCATAG | 494470 |
rs757610726 | snp | G/T | 0.000106729 | 0.00730433 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334231 | GCCGCGCCACAAAGG[G/T]CCCGCGCGCAGCCGC | 494470 |
rs757630176 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350507 | CGAGGGGTGTCAAGA[C/G]GGGCAAGCATGGTCA | 494470 |
rs757656762 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390683 | CAGCATTTATGGGGT[A/G]TGGAATATCAGGCTA | 494470 |
rs757680315 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422852 | AACTTTGGGAGACAA[A/G]ATAAATTCTGAGAAA | 494470 |
rs757685138 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368120 | AAATGGTGGGAAACT[A/G]CTGCTCTAGACCTTA | 494470 |
rs757697296 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | RNF165 | GRCh38.p7 | 18:46455980 | TTCTCATAGCGAAGA[C/G]CCCAGGATGGCAAGG | 494470 |
rs757758083 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341819 | TACCAATCAGTATCC[C/T]GAAATCTGAGTTGGA | 494470 |
rs757771262 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377197 | AAAGGTATATAATGT[A/G]CCCCTTTTAAATTCA | 494470 |
rs757791483 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345426 | AGTCTCAGTTTCCCC[C/T]AGCAGAGAGGTGGTG | 494470 |
rs757843582 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350629 | GAAGCTCTCTGCTGG[C/T]GTTCCTCCTGCCACG | 494470 |
rs757855863 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447167 | TTTGTTTTCTCAAAG[C/T]GGTAAAAATATAGCC | 494470 |
rs757866689 | in-del | -/TT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415620 | TTTATTGAGAACGTG[-/TT]TTGGTGGTGCTGAGA | 494470 |
rs757920923 | snp | A/C | 5.5881e-05 | 0.00528558 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433265 | GCCCCCCGCAGCCGC[A/C]GCAGCTCGCTCCCGA | 494470 |
rs757928130 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417040 | GCCACACCAATCTTC[C/T]AGTTGCTTAGCAAGC | 494470 |
rs757928549 | snp | A/G | 4.02406e-05 | 0.00448539 | intron-variant | RNF165 | GRCh38.p7 | 18:46433154 | GCGGCCGCTCGTGCT[A/G]GTCGTCATGGAGATG | 494470 |
rs757959760 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361492 | AGACAGTGCCACAGT[A/G]CAAAGCAAGGCTTCC | 494470 |
rs757967987 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459294 | TGTCTCTCTGGGCCT[C/T]AGTTTCCTCAGTTAC | 494470 |
rs757975111 | in-del | -/TG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397668 | GCTGGGGCAGAATTG[-/TG]TGTGTGTGTGTGTGT | 494470 |
rs758007224 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403591 | GCCTCATGAAAATCA[G/T]ATCCGGCTGGGTGCA | 494470 |
rs758019125 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393148 | TTTCTGATCAGATTT[A/G]CTGACATCGTGGGTC | 494470 |
rs758045408 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367372 | AAATTGGAGGATTGC[A/G]TTTATGTTCAGTGTG | 494470 |
rs758072343 | snp | A/G | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439528 | TGTGTCCTAATTACC[A/G]GGGACCACTTCAATG | 494470 |
rs758079664 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437794 | AGTCCTGGCTTCTCA[G/T]TTCTAACTCTGCTCC | 494470 |
rs758095333 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402872 | ATAGAATCAGGTCTC[A/G]GTACCTCTAGTATTC | 494470 |
rs758096218 | in-del | -/CA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382596 | GAATCTCAGCAGGCT[-/CA]GTTAGCCTTGCATGA | 494470 |
rs758105943 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439855 | TTGTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 494470 |
rs758155601 | snp | A/G | 1.64852e-05 | 0.00287094 | intron-variant | RNF165 | GRCh38.p7 | 18:46450403 | GGAGAGCTATGAGGT[A/G]TGTTGCTCTGTCTGG | 494470 |
rs758165779 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355242 | ACAAGCATGAGCCAC[C/T]GGGCCCGGCCTGTTT | 494470 |
rs758185239 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411819 | TGGACATGCAGGAAT[A/C]ACAGCCTGGGGCTGA | 494470 |
rs758191830 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380012 | CAGAGGCCACCCCAC[A/C]CCCAAATCCCTCCCA | 494470 |
rs758320120 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365988 | ATCAGTGCAAAGTGG[A/G]GTCTAATTAAGAGAT | 494470 |
rs758371603 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387898 | TCCAGCTCTTAGGAC[C/T]GGGGCAGTCACGCCT | 494470 |
rs758380764 | snp | C/T | 5.30912e-05 | 0.00515197 | intron-variant | RNF165 | GRCh38.p7 | 18:46455946 | GTCTGCCCCAGGTAA[C/T]GAATACTACTCTCTC | 494470 |
rs758395720 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420352 | TTCTCCCAGGAGAAA[C/T]GGGAGGCAGAGGAAT | 494470 |
rs758399908 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396469 | CAGGATGGTGAACTC[C/T]ATGACAGTATGGGCC | 494470 |
rs758417523 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371666 | TCTCTGGGAAATGAG[A/T]GCTGAAACAATGGTT | 494470 |
rs758430073 | snp | C/T | 1.76496e-05 | 0.0029706 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433485 | GGAAGCCCAGCACCG[C/T]AGGCTGGTCTCGCAC | 494470 |
rs758458032 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46387117 | GATTTTTGGTGGTCT[A/C]ACAGCAGTGACACTC | 494470 |
rs758481226 | in-del | -/TGAG | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333728 | GCACCTCCACATGTC[-/TGAG]TGCACGTCCCTCTCC | 494470 |
rs758483514 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443344 | TTTGGGAATTCACTA[C/G]GTTTACAATATTCCT | 494470 |
rs758495215 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414267 | TGTCTTCTTCCTTAA[C/G]GGAAACTGCTTTAAT | 494470 |
rs758532211 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357971 | ATCACTCCAGTCTCC[A/G]CCTCTGTTGTCACAG | 494470 |
rs758540378 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447031 | ATTGGTTCATCCTCA[C/G]TGCAATTCATCAATT | 494470 |
rs758578900 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381692 | AAAAATTAGCTAGGC[G/T]TAATAGCAAGTGCTT | 494470 |
rs758579053 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391348 | GTTGGCCAAATGGGA[C/T]GACATTACAGCTCTT | 494470 |
rs758620365 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456465 | GTGTGTCCCTGCTCC[A/G]CTCAGTGTCCCTCAG | 494470 |
rs758666850 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390635 | CTCTTTTCTTTTCTC[G/T]GTAGGACAGTTAGTC | 494470 |
rs758701178 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383835 | GGATCACAGGCGTGA[A/G]CCACCGCGCCCGGCC | 494470 |
rs758708147 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455610 | GGGAGGCTGAGGCAA[A/G]CAGATCACCTGAGCT | 494470 |
rs758718916 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356797 | TCTCCCCGCAGCTTC[A/C]TGCCTCAATTCTAGA | 494470 |
rs758721993 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385012 | GACAGTATCTCTGTT[C/T]CCTCCCCCTCAAAGA | 494470 |
rs758828124 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448773 | TGGGCTCCTGACATT[G/T]CAAGCTGCATGGAAT | 494470 |
rs758829209 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433742 | GGCAGTGAGCACTGT[C/T]CTGATCTGACAGGGG | 494470 |
rs758859763 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367565 | ACCCATTGCCTTGTG[A/C]CCTCATAATCAGGCT | 494470 |
rs758872735 | in-del | -/GA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453273 | AATGATCATTCTCTG[-/GA]GAGAGAGAGAGTTTT | 494470 |
rs758899800 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403969 | TCATAGAAGCTCATT[A/C]TTTAGGGGATTCTAC | 494470 |
rs758918430 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447893 | CCCTGGCCTTCTTGT[A/G]TCCTGGCTCCCTGGC | 494470 |
rs758927096 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368953 | TGAATGTTTACTGTC[-/A]ATCATTTCTATGTGC | 494470 |
rs758946200 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376009 | TAGCTCAGAGGGTGG[A/C]CTGAGGGTGAGATGA | 494470 |
rs758977425 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370227 | TCTAAGGGGTTCACA[C/T]GATATCCTTACGATC | 494470 |
rs759019628 | snp | A/G | 1.68829e-05 | 0.00290537 | intron-variant | RNF165 | GRCh38.p7 | 18:46450686 | TGAGCACACATGTGC[A/G]CATTTTTCTCTTTCC | 494470 |
rs759021042 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380851 | GTCCCCATCACACTC[A/G]CCCCAGCCTTCCTTC | 494470 |
rs759027810 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453313 | GAGAAGAACATAGAA[A/G]GAAATGAGTGGTGTA | 494470 |
rs759033021 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412508 | TAGGAGATGAGCCTC[A/T]TACTGAGTGCAGCCC | 494470 |
rs759061979 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455007 | CTACATAATGATTCT[A/G]CATATGGCTTCTACA | 494470 |
rs759077024 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345008 | CTCCCTAAGGGCTGG[A/G]TCAGGAGGGAAGCTG | 494470 |
rs759108903 | snp | A/C | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389690 | TACTAGATTTTATTC[A/C]AGCCATAGCAGCTCT | 494470 |
rs759125026 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421719 | CAACTGGAGCTAAAT[A/G]CTGGCCCTTTGCTGC | 494470 |
rs759161314 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344254 | TGAGAATTCAGTGGA[C/G]ACCTGTCTCAAGGAA | 494470 |
rs759164998 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356145 | GCCCTCACTCTGTGA[C/T]ATGCAGAAGCTGAAA | 494470 |
rs759212631 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391132 | CAAAATGGCACCAAT[C/T]GCCTCCATAAACAGG | 494470 |
rs759246188 | snp | C/T | 6.60589e-05 | 0.00574675 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435290 | CCCTTCTGGTGCAGG[C/T]GGAGTCAGGAGCGTG | 494470 |
rs759254223 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355091 | AGTAGCTAGGACTAC[A/G]GGAACATGCCACCAT | 494470 |
rs759274632 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335377 | GATTTTCCCCTCTTC[C/T]CCCCACCTCCACTCC | 494470 |
rs759304074 | snp | A/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336003 | GAGGAAGGCATTGCT[A/T]TTTAAGCGGCAGTAT | 494470 |
rs759319985 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365661 | GGCACATGCCACCAA[A/G]TCCAGCTAATTTTTA | 494470 |
rs759342539 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337875 | TTTTCACAATAGATG[C/T]CTGGAGCGATAGGAG | 494470 |
rs759357080 | in-del | -/TGTG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348903 | CTCTCTCTCTTTCTG[-/TGTG]TGTGTGTGTGTGTGT | 494470 |
rs759373467 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373303 | CACATTTCCTCAGAG[C/T]TTGCCCAGTGCTTTC | 494470 |
rs759410060 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373945 | ATGGACAGTTGCTCC[G/T]ACAAAGGGGCTGTGT | 494470 |
rs759419543 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396390 | AAGTGAAGCGTTAGT[A/G]GGTTCAGGCTCTTGC | 494470 |
rs759424174 | snp | C/T | 1.65091e-05 | 0.00287303 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435360 | TCGGCCAACTGCAGA[C/T]ACCTCAGCCCAGGTA | 494470 |
rs759432561 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350099 | ACCCCATGATACATA[A/C]CCAGAGAAATACAGG | 494470 |
rs759447744 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383754 | ACAGACGGGGTTTCA[C/G]CGTGTTGGCCAGGAT | 494470 |
rs759486898 | snp | C/T | 1.65364e-05 | 0.0028754 | intron-variant | RNF165 | GRCh38.p7 | 18:46456503 | CGGGCCTCTGACTCT[C/T]CCTCCTCTCTTCCAG | 494470 |
rs759502607 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435746 | CAGAAAGGAGAATTC[C/T]GAGGAACTGGGTTGT | 494470 |
rs759512956 | in-del | -/TGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355908 | TGATGACGACAATGG[-/TGA]TGATGATGATGATGA | 494470 |
rs759537625 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392599 | TGGGGAGCCCTTGTC[C/T]GGGGTGATGGGTCAG | 494470 |
rs759537764 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383214 | CACCCAGGGGAGGCA[A/G]TGGGTGTTGGGGGCT | 494470 |
rs759584283 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346590 | AGCTGCGGGACTTTG[A/G]CCCTCTCTGAGCCTC | 494470 |
rs759606400 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357458 | AACAGGGTGTCAGGC[A/C]AGAAAACAGCAGTGT | 494470 |
rs759627813 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400438 | TGGGAGAGTGCCATT[A/G]TGGCCCCTGTCACCT | 494470 |
rs759678390 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340277 | TATCTTGGAACGACT[C/T]AGATTTTCAGGATGA | 494470 |
rs759688087 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367996 | CTAGGCAGCACCCCC[A/T]GCTGGGAGGGGCTTG | 494470 |
rs759701862 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457597 | TAAACCAGGGAGGGC[C/T]CGGCCCTCAGCTACT | 494470 |
rs759714693 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341530 | TGAGTTTAGTGTACA[A/G]ATAAGCACATAGAAC | 494470 |
rs759723252 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377630 | TAAAGGGAGAGGCAC[A/G]TATGAAGGCTCTATG | 494470 |
rs759753172 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411297 | TGAGTTTGCTGAAAG[A/G]TAATTATGGTGGCAT | 494470 |
rs759765763 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351276 | CTGTGAGTGGAGCTC[A/G]GGACTTCCCTCCAGT | 494470 |
rs759805883 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352024 | TGCAATGGAGTCTTC[C/T]TGCCCTGGTGGCCTG | 494470 |
rs759807029 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376822 | ACTACAGGCACGCAC[C/T]ACCATGCCTGGCTAA | 494470 |
rs759848167 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363226 | CAGCCAAGAACATCC[C/T]TCCTTCTCTGGGCTT | 494470 |
rs759873010 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460700 | AACTTTATTTCGTCC[A/G]AACTATCAGGGTGTG | 494470 |
rs759902563 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385208 | ATGTCATGGGCCAGG[A/G]GAATCTTGTCCTGCC | 494470 |
rs759911386 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404183 | TGATTCTTGATTTCT[C/T]GAAAACTGCTCAATG | 494470 |
rs759938099 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362251 | ATGGATTCTTGGGGA[A/G]GCAGGGTTTTCCTTC | 494470 |
rs759963982 | snp | C/T | 1.73288e-05 | 0.00294348 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433373 | CCCTGCACCAGTCGC[C/T]GACCCCGCTGCCCAC | 494470 |
rs759965811 | in-del | -/CGGA | 4.01421e-05 | 0.00447989 | intron-variant | RNF165 | GRCh38.p7 | 18:46433522 | TGGTGCTGCCTGGGG[-/CGGA]CGGAGGTGGGGACCC | 494470 |
rs759976089 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428613 | CCAGTGGCTCCTGGG[A/C]ACTTGGAATGAGGCT | 494470 |
rs759990738 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359157 | AGAACAATGCAATTC[A/T]ATTCAGTCTGACAAT | 494470 |
rs760018649 | snp | C/G | 0.000106544 | 0.00729797 | intron-variant | RNF165 | GRCh38.p7 | 18:46450821 | CTGCCAGCAGGCCAG[C/G]CTGCATAGTCAGGGA | 494470 |
rs760026123 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371098 | GTGGCAGGCAAGAGG[A/G]TGTGTGCAGAGGAAC | 494470 |
rs760033347 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374629 | TTATGCCTTCTCTTT[-/G]GTGCTCTAATTCTTT | 494470 |
rs760047002 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393628 | AAGGTCTAAGGTCAC[C/T]CCACCCCCAGTTCTT | 494470 |
rs760062176 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46427641 | AACCAGCCTCAAACC[C/T]GCAGCCCCTTCGAGC | 494470 |
rs760082150 | snp | A/C | 1.90761e-05 | 0.00308832 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433252 | CACTTCCACCTGGGC[A/C]CCCCGCAGCCGCAGC | 494470 |
rs760130002 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446480 | GTTCAAGACCAGCCT[G/T]GACAACATGGTGAAA | 494470 |
rs760150051 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440980 | GTTGTGTAGGATTGG[C/T]ATTATTATTTTTAAT | 494470 |
rs760169745 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404733 | ACTCCAGCCTGGGGC[A/G]CAGAGCGAGACTCCA | 494470 |
rs760176983 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420110 | TCAGGGGCGTGTGGA[A/G]GTCAACTCCCATGGC | 494470 |
rs760203317 | in-del | -/TG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406019 | TCGCATACATACCCC[-/TG]TGTGTGTGTACACCC | 494470 |
rs760217521 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354561 | GAGCTGGTTAGAATA[G/T]CTCCAGGGTCTCTGC | 494470 |
rs760228233 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373872 | CCCCCTCCCACCCCC[A/G]GTCCCAGACCCTGTG | 494470 |
rs760305326 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353561 | GTCACTGGTAAGGGA[A/T]GTTACCTAAAAACCC | 494470 |
rs760308803 | in-del | -/G | 1.90547e-05 | 0.00308658 | intron-variant | RNF165 | GRCh38.p7 | 18:46450844 | TCAGGGAATGGGGCA[-/G]GGGGGGTTGTCTAAT | 494470 |
rs760332878 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335694 | TTTAGTGCGCCCCAG[A/G]GGCCCGATTGGGCAA | 494470 |
rs760383408 | snp | A/G | 2.641e-05 | 0.00363377 | intron-variant | RNF165 | GRCh38.p7 | 18:46456087 | AGATGTGAGGTAGGA[A/G]ACCGCCATTTTGATT | 494470 |
rs760387162 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364958 | TCTGGTCCCAGCTGG[A/G]TCTCTCCTACACTCT | 494470 |
rs760421083 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395441 | CTAGTAGCATCCCTG[A/G]CTTGGTTGTTGAGAA | 494470 |
rs760520063 | in-del | -/GTG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397668 | TGCTGGGGCAGAATT[-/GTG]TGTGTGTGTGTGTGT | 494470 |
rs760522134 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358755 | CTGACCAGCTTCTCA[C/T]CCCTTCCTTCTCACA | 494470 |
rs760534133 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415334 | GACCACCCTGGCTAA[C/T]ACGGTGAAACCCCAT | 494470 |
rs760536175 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405185 | CTCTGGGACACAGGG[A/G]GGTCAAGTGACTTGG | 494470 |
rs760538573 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456396 | GGCTTCATGGTTTCC[C/T]ATCTCAGCCACAGCC | 494470 |
rs760539909 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382950 | TTTTATGAAGACAAC[A/G]TCATACTCTTCTTGG | 494470 |
rs760553028 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423800 | TCATTTAGCTAGGAT[A/G]TTGGAGGATTCCATG | 494470 |
rs760614121 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361568 | GGATGCTTTCAAAGA[C/T]GGTCTTGCTTATTCC | 494470 |
rs760624262 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414887 | GTGTCATCACAGCCT[G/T]GTGAATGGGGAGCGT | 494470 |
rs760643108 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448474 | TGTGGTCTGTGGGTA[A/G]AGGGCTCAGGGCTAA | 494470 |
rs760661626 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391230 | CACATGAGTGATCTC[A/G]CTTAGTCTTGAGGTG | 494470 |
rs760674259 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400984 | ATGCTGGAGGCAGAG[A/G]TGACCTCCCGCAAAG | 494470 |
rs760680092 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367231 | GTTCAATTCTGCTCC[A/G]CCTCCCATCCTGGCT | 494470 |
rs760689839 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383578 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 494470 |
rs760752395 | snp | A/G | 4.94752e-05 | 0.00497344 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456652 | GGGAGGAATTAGCCA[A/G]TGGACACCCCATTTC | 494470 |
rs760755694 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408341 | TGTCATCTCTTGGTC[C/T]CACCTCCCTTCTACC | 494470 |
rs760776993 | in-del | -/AAAAAA | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461648 | ACAAAACTCAGTCCA[-/AAAAAA]AAAAAAAAAAAAAAG | 494470 |
rs760799992 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340076 | GTTCCCTCAATCCTA[C/T]TCCACAACTGTCACA | 494470 |
rs760838801 | in-del | -/TTTA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449304 | GAGTCAGACTCTGTC[-/TTTA]TTTAAAATATTGATA | 494470 |
rs760843544 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407715 | AAGAGCAGGGCAGTA[C/T]ATGCTGGGAGCTGGT | 494470 |
rs760861503 | snp | C/T | 1.64746e-05 | 0.00287002 | utr-variant-5-prime, synonymous-codon | RNF165 | GRCh38.p7 | 18:46447578 | GGATCTCAGTGTGGA[C/T]GCTGGCTTGAGTCCT | 494470 |
rs760861743 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351118 | AGCCCGGGAGGGAGG[C/T]AGGGATGCACAATCT | 494470 |
rs760887401 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361182 | GTAATACCTTTTGAA[A/G]CTCCTTAGAGCCTTT | 494470 |
rs760889903 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338518 | TCTCAGCCATTGTCT[A/G]AGTGTGTGTGTTGAG | 494470 |
rs760928363 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438894 | GCTCCAACATTACCA[-/T]GAGGAGCTACTGTTA | 494470 |
rs760942302 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426232 | CCACATTTGGCTTTC[A/G]GGAAACACCTTGCTT | 494470 |
rs760964978 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403357 | TGTGCTCCTAGAGAA[A/G]GCTCTCCCTGCCCCC | 494470 |
rs760968724 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371029 | TCCACATGGCTAGGG[A/G]GGCCTCACAATCATT | 494470 |
rs760986738 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449281 | GTGAGGCAGGCCATG[A/C]CAGAACAGAGTCAGA | 494470 |
rs761005919 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46427404 | CAGAGAAACCTGAAG[G/T]CCCCTTGGACAGAGT | 494470 |
rs761031058 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438915 | GCTACTGTTATCATC[A/G]TCTTAGAGATGAGGC | 494470 |
rs761049350 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412391 | AGGCAAACATGTCCC[C/T]GCCAGTCTGCTGCTG | 494470 |
rs761056154 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370051 | CCTGTGGCCCCCTCA[A/G]TGTGAAGGAGCTGAG | 494470 |
rs761091595 | snp | A/G | 0.000115587 | 0.00760132 | intron-variant | RNF165 | GRCh38.p7 | 18:46334449 | CCCGCGAGGACGCAG[A/G]GCGAGCGGTGGCTTC | 494470 |
rs761112841 | snp | G/T | 1.73845e-05 | 0.00294821 | intron-variant | RNF165 | GRCh38.p7 | 18:46450657 | CCTGTGTGCATGTGG[G/T]CATTTATACATGCTG | 494470 |
rs761129889 | in-del | -/ATGAACCAAAGCTTAGGCACAATTG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396694 | CTGGCTGTCGGGACC[-/ATGAACCAAAGCTTAGGCACAATTG]ATAGGGGACTGCAGA | 494470 |
rs761148182 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369261 | GGGTGGTTCAAGGTG[A/G]CAGCATCCATCATCA | 494470 |
rs761148224 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379784 | GGAAGAGGAGTTTGA[C/T]ACAAGGGATCTGTTT | 494470 |
rs761152840 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46335888 | TTCTTCATTGTGTAG[C/T]TCAGTGAATGGTCAA | 494470 |
rs761169998 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352362 | CATCATCCTGTCCCA[A/G]GCTTATTTCATGTGG | 494470 |
rs761245857 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411516 | TTGATTCATTTCAAC[A/G]TACATTTGGTAAGTT | 494470 |
rs761251829 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360199 | GTGGTTCATTCAAGG[-/G]CTTCCTCCTCTCCCG | 494470 |
rs761277811 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437555 | CCATGTCCAGCCCAA[C/G]GTCGTCCACCCCCTG | 494470 |
rs761288430 | snp | G/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333143 | TGGCTGCGCCTCCAC[G/T]TGTGAATTTGCAGGA | 494470 |
rs761296963 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453156 | ATTCGTAAATGATTT[C/G]AACCGCAGTTATTGA | 494470 |
rs761303433 | snp | C/T | 2.26621e-05 | 0.00336609 | intron-variant | RNF165 | GRCh38.p7 | 18:46433541 | AGGTGGGGACCCGGA[C/T]GGGGTCGGGTGAGGG | 494470 |
rs761310305 | snp | C/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388657 | GAGGTTTAGGTTCCT[C/G]AAGACATGAAGAAGG | 494470 |
rs761328549 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364811 | CAGAAGAGTCAGGTC[C/T]ACTGGATATCTCTGG | 494470 |
rs761330055 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395401 | TGGGTGTTTGGCAGC[A/T]TTCCTGGCACCTCCC | 494470 |
rs761399292 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444544 | ATCACAGCTCATTGT[A/G]GCCTCAACTTCCTGG | 494470 |
rs761419681 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425394 | CCTGGGGTAGCCCCG[A/G]GTGGGTGGCAGGCCA | 494470 |
rs761440413 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372827 | ATTCTAACCACACTG[C/T]GGTGCTATTATGTAA | 494470 |
rs761464445 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347388 | GAAATTCTCTGCCTC[C/T]TCTCCTGCCCCTCTG | 494470 |
rs761489527 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442990 | TAGCACTTACGGGGT[A/G]TATCTCTTTCCTCCT | 494470 |
rs761550903 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358395 | CAGCACACCCAGCCA[C/T]AGGACAGGATCTGCG | 494470 |
rs761575722 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456337 | GCGTCTAAGACAAAG[C/T]TGTGGCTTTGTTTCA | 494470 |
rs761616494 | snp | C/T | 1.97932e-05 | 0.00314582 | intron-variant | RNF165 | GRCh38.p7 | 18:46450851 | AATGGGGCAGGGGGG[C/T]TGTCTAATTGACTCT | 494470 |
rs761619571 | snp | A/C | 1.64732e-05 | 0.0028699 | missense | RNF165 | GRCh38.p7 | 18:46447676 | ACTTTCCCAGAAACT[A/C]CTCCTCCACACAGAT | 494470 |
rs761622198 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382085 | GCCTGGGCATCTGTA[A/G]AGCCAGGTTGGCTTT | 494470 |
rs761629897 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442158 | ACAGAGCGAAACTCC[A/G]TCTCAAAAAAAAAAA | 494470 |
rs761659549 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455254 | GTCAACAGTGGTTGA[C/T]TGAAAGAATAAATGA | 494470 |
rs761685405 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423680 | AGGCCTGGATGCCAG[C/T]CCCAACTTGGCCATG | 494470 |
rs761719530 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399474 | GACCTCCTGTGAGGA[A/G]CCGGTTTTATGGGAT | 494470 |
rs761740642 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345173 | GATAGGGCAGCAAGG[A/G]ACAACTGGAAGGAAG | 494470 |
rs761773072 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422479 | CATGTTGAGTAGAAC[A/G]TGAAGTCTGTCTTTG | 494470 |
rs761782053 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409126 | CATACAGGGGGTGCA[A/G]TAGAAATGTCAGCCA | 494470 |
rs761834386 | in-del | -/GTGTGTGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334710 | TGTGTGTGTGTGTGT[-/GTGTGTGA]GAGAGAGAGAGAGCG | 494470 |
rs761861418 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434548 | TTCTGGAAAACCTCT[C/T]TGTTCATTTGTGACA | 494470 |
rs761863942 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365774 | TCCCAAAGTGGGACA[C/T]CTCACTTTGCTGCTG | 494470 |
rs761870004 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336984 | AGCCATGGCCATAGC[A/G]TCTTAATTGTTTAAT | 494470 |
rs761940714 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413275 | GTCGCTCAAGCCCAG[A/C]CCTATCCAGAAGTGG | 494470 |
rs761949232 | snp | C/G | 1.64757e-05 | 0.00287012 | missense | RNF165 | GRCh38.p7 | 18:46456547 | ATGCATCTCTTTCAC[C/G]AACTGTGCGTGGACC | 494470 |
rs761951884 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426141 | TGACACCAACATTCA[G/T]ACCACAGCACTCTCT | 494470 |
rs761959347 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446055 | TGGCACCAAGATTAA[C/G]GCTTGAGTAGATTCA | 494470 |
rs762015984 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369144 | TATGATCTAAAAGGC[C/G]ATGTTTTTGTTTTCC | 494470 |
rs762022792 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361098 | TAACTGGGCTGTGAG[C/T]ACATTTTTCCTGATG | 494470 |
rs762023051 | in-del | -/TGTT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440715 | TATACTTTGTATCAA[-/TGTT]TCAAGATCCGAATAA | 494470 |
rs762056958 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437276 | TTAGCTCTGCTCCAG[C/T]GGGGGCCAGCCTAGT | 494470 |
rs762074461 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452017 | GAGGAATGAATGGGT[A/G]GAGCATAGGGGAGTC | 494470 |
rs762086251 | in-del | -/CAAAAAA | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461646 | GAACAAAACTCAGTC[-/CAAAAAA]AAAAAAAAAAAAAAA | 494470 |
rs762086411 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432235 | TTTCTTGTCATCAAG[C/G]TCAATTTTATTTAGA | 494470 |
rs762112784 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359778 | CTTTTCAAAGTCATA[C/T]ATGGCCCAAGATGGC | 494470 |
rs762113179 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383616 | TTGGAGTACAGTGGT[A/G]CGATCTCAGCTCACT | 494470 |
rs762118223 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378515 | AACTGGAAAGGCTTC[A/G]GGGAGCTTGGAGAAA | 494470 |
rs762121308 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438835 | GCTTTTTGCATCTGT[A/G]TAGTGCTCTACAAAG | 494470 |
rs762129850 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422760 | TACTCCAGGTCACAC[C/G]CCCGCCCTTTGCTGG | 494470 |
rs762136474 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354077 | AGGCAGGAGCCACAA[C/T]GTTCACCAGGCTCCC | 494470 |
rs762185699 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420700 | AAATACAAAAATTAG[C/T]CAGGTGTGGTGGTGT | 494470 |
rs762209819 | snp | G/T | 1.97389e-05 | 0.0031415 | utr-variant-5-prime, missense, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334316 | CGTGCTTCCAGTGTT[G/T]GGCTCTGTGCGAAAC | 494470 |
rs762213989 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343030 | GCTTTTAATGGCTAC[A/G]TAATATTCCACTTGA | 494470 |
rs762229759 | snp | C/T | 1.654e-05 | 0.00287571 | intron-variant | RNF165 | GRCh38.p7 | 18:46450256 | GCTCATGGAGAAACC[C/T]TGAATCCTTGCTCTA | 494470 |
rs762289368 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46387581 | CACCTGGGTGTAGCT[A/C]TGGAGGGCATGAAGC | 494470 |
rs762316026 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341909 | AGGAGCTTTGCCTCC[A/G]CTACTTTGCAAAAGG | 494470 |
rs762331156 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394756 | ACCACTGTTCAAGGA[C/T]GACTGTGGATCCTGA | 494470 |
rs762360518 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377940 | TTCTGGGGCAGGAAG[A/G]CTGCTATGGATGGTG | 494470 |
rs762360978 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396180 | ATTGGCCAAAGCAAG[A/T]CACAAAGCCAGCCCA | 494470 |
rs762365482 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | RNF165 | GRCh38.p7 | 18:46450837 | CTGCATAGTCAGGGA[A/G]TGGGGCAGGGGGGTT | 494470 |
rs762375507 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386282 | TTCTACTCTTTAATC[A/G]TCAGCATTGTCATCG | 494470 |
rs762384771 | snp | C/T | | | synonymous-codon | RNF165 | GRCh38.p7 | 18:46450304 | CCAACAGGTCGTCCA[C/T]GAAATCCGAAACTAC | 494470 |
rs762416448 | snp | C/T | 1.69815e-05 | 0.00291384 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433449 | CCTGCACCAGCAATA[C/T]CTCCTGCAGCAGCAG | 494470 |
rs762420874 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346112 | GCTTGAGGACAGCTT[A/G]GGTTTAACTGGGCAG | 494470 |
rs762468863 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372199 | CAGAGGCACTGAAGG[G/T]TCCTCCCTGGGGCCC | 494470 |
rs762491250 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442860 | GATTGTCATTTTTCA[A/G]GATGAATTGACCCCT | 494470 |
rs762512959 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455106 | AACAGTGTTTCATGA[C/T]TGCTTTACGATAGTG | 494470 |
rs762530856 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457957 | TGGTTTGGGAGTGCC[C/T]GTGTTCCTGGTCTCT | 494470 |
rs762586428 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381964 | AAGCACCCGCAGGGC[A/C]TCCCTTCTCTTAGGT | 494470 |
rs762605573 | snp | C/T | 1.66416e-05 | 0.00288453 | intron-variant | RNF165 | GRCh38.p7 | 18:46450701 | ACATTTTTCTCTTTC[C/T]AGGAGCTGCTGCAGC | 494470 |
rs762645873 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412572 | CCAGTCATGTGCTGA[C/T]GAGGCTGCCTGGTTG | 494470 |
rs762676335 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381074 | TGCCACACTACTGCG[C/T]CTCAGTTTTTCTATC | 494470 |
rs762676977 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367764 | CCCAGATCCCCTGAA[C/T]GTTAGGTTAGAGGTA | 494470 |
rs762742491 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402733 | CTCAAACTCCTGGGC[C/T]CAAATGATCCTCTGG | 494470 |
rs762764082 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46389838 | GTCTCAGCTGATCCT[C/T]CCACCTCAGCCTCCC | 494470 |
rs762777097 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367006 | CAAGAGGAAATTCAT[A/C]GTATACTTAGTTTCC | 494470 |
rs762804201 | snp | A/G | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46338106 | TAGCATTTCAGACTC[A/G]CCTAAAAACCCATTT | 494470 |
rs762810373 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399363 | TGGGGTGCTGGCCCC[A/T]TCCCTCCATCATGTG | 494470 |
rs762824638 | snp | C/T | 8.24151e-05 | 0.00641878 | intron-variant | RNF165 | GRCh38.p7 | 18:46447555 | TCACTGAGGCTGTTT[C/T]CCTGCAGGGATCTCA | 494470 |
rs762831813 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431341 | TCACTAAAGCTGTCT[A/G]GAATGTCTGTGTGCC | 494470 |
rs762832740 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434303 | TACCATATTAAAAAT[A/G]AAAACTAAAAAGTTT | 494470 |
rs762838408 | in-del | -/GGAACCC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422105 | ACCTGGAGTACATAA[-/GGAACCC]GGAAAGAATGGCCTT | 494470 |
rs762863923 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339718 | GCATCAGAAAGACCC[A/G]CTAAGTTAATGAGTT | 494470 |
rs762865445 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375213 | TGTGCTGTCACTGGC[C/T]GCATCTATATATTGA | 494470 |
rs762913859 | snp | A/C/G | 5.02023e-05 | 0.0050099 | intron-variant | RNF165 | GRCh38.p7 | 18:46435403 | CACTGACTGGTGAGT[A/C/G]TTCAGGGCCCCTGGG | 494470 |
rs762984133 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347083 | AGGTCACTGAGGCCT[A/G]GAGAAAATCAGGAGG | 494470 |
rs762999531 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415286 | AACACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 494470 |
rs763006210 | snp | A/C/G | 3.99339e-05 | 0.00446829 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334310 | CTATCTCGTGCTTCC[A/C/G]GTGTTTGGCTCTGTG | 494470 |
rs763027450 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348917 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 494470 |
rs763042540 | in-del | -/CCAC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355743 | CTCCCCTCTATCTCT[-/CCAC]CCACCCATCATGTGC | 494470 |
rs763057572 | snp | A/G | 4.38914e-05 | 0.00468442 | intron-variant | RNF165 | GRCh38.p7 | 18:46334402 | ACCGGGGCGGGGGCG[A/G]GCGCCGCGGGCGGCC | 494470 |
rs763076622 | snp | C/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457570 | CCCAGCTATATCCCC[C/G]CAGTTCCACACTAAA | 494470 |
rs763100826 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437125 | CAGAAAGAAGGAGGC[C/T]CCGGGAGGCTGGTCC | 494470 |
rs763129672 | in-del | -/GCAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437543 | GGGCTGCAAGCCCAT[-/GCAA]GTCCAGCCCAAGGTC | 494470 |
rs763168391 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342874 | AAATGCAGTCATATT[G/T]TTGTTCATCTATTTG | 494470 |
rs763178230 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423965 | TTTTATCCAGTATCT[C/T]ATTATCCTCCTGTCT | 494470 |
rs763186023 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401052 | CCCTCCCCATAAGTG[A/T]GCAAGGGGCACACTG | 494470 |
rs763190628 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451598 | CCAGGAATTCAAGAC[A/C]AACCTGAGCAAAATA | 494470 |
rs763191063 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435976 | GCTGAGTCTTTGCAG[A/G]TAATGGGCCCCTGAG | 494470 |
rs763215851 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409364 | AGAGGGAAGGAATGA[A/G]CTCAAGGGATCCTTT | 494470 |
rs763234078 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459273 | GCAACACTAGAAACT[C/T]CCCTTTGTCTCTCTG | 494470 |
rs763263235 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341653 | AGGAAATGAACTTCA[A/G]CAATAAAAATTCCTC | 494470 |
rs763281600 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450141 | CAAGGCTTGGTTCTT[G/T]ATGAAAGAAAAGGGA | 494470 |
rs763356849 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352260 | AATGGGAAGGCAGCC[A/G]GTATGGACTCCATCA | 494470 |
rs763421558 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395259 | TCTCCAGGGGACTGT[A/G]TGACCATCTCCATGG | 494470 |
rs763473711 | snp | A/G | 2.07166e-05 | 0.00321836 | intron-variant | RNF165 | GRCh38.p7 | 18:46433528 | CTGCCTGGGGCGGAG[A/G]TGGGGACCCGGATGG | 494470 |
rs763489890 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418598 | CTAGATTGCAGTTCC[A/G]CAATGGCAAGGATTT | 494470 |
rs763509796 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394571 | CTCTGCTCACATAGC[A/C]ACAGAGGGGAAGTCT | 494470 |
rs763516057 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404907 | AGTTCAGAGAAGTTA[C/T]GTGAGGTGCTCAAGG | 494470 |
rs763526911 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460885 | ACTGGGGTAATCCTT[G/T]CACTTGCTACACTTG | 494470 |
rs763558259 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442901 | GAAACATCCTTCCTT[A/G]TCCTTGGTAATATCC | 494470 |
rs763571593 | snp | C/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332947 | ATTCTCTGGCCTTAG[C/T]GTGTGAACTGTGAGC | 494470 |
rs763573459 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378115 | TTTGAGCTAACTGCT[C/T]TTCCAGATTGAATGC | 494470 |
rs763581036 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428727 | CTCAATAATTTTTTA[C/T]ATAGAATACATATTG | 494470 |
rs763650153 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404376 | AGGATGACAGGAAGA[C/T]ATGAGCAGGTATTAA | 494470 |
rs763693942 | snp | C/G | 1.86475e-05 | 0.00305342 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433272 | GCAGCCGCAGCAGCT[C/G]GCTCCCGACTTCCCG | 494470 |
rs763740144 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403648 | TTTGGGAGGCCGAGG[C/T]GGGTGGATAATTTGA | 494470 |
rs763772124 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346131 | TTAACTGGGCAGAGA[C/G]AGAAGGGATGGCATT | 494470 |
rs763775017 | snp | A/G | 1.93793e-05 | 0.00311276 | intron-variant | RNF165 | GRCh38.p7 | 18:46450848 | GGGAATGGGGCAGGG[A/G]GGTTGTCTAATTGAC | 494470 |
rs763791164 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452391 | TTCAAGCAATTCTCC[C/T]ACGTCAGCCTCCCAA | 494470 |
rs763794861 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441323 | TGCCTAGGCCCAAAT[C/G]ATTCTCCTGCCTTAG | 494470 |
rs763802311 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356383 | CAAAATAGCGCAGGG[C/T]CAAAGGGTGGTGATG | 494470 |
rs763813967 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455148 | TGAACTTTCTGGATA[A/G]AAAGATAAATCCAAC | 494470 |
rs763831725 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421906 | GCATCACAAAGCTGC[G/T]CTTGGCTGTAAAGGA | 494470 |
rs763963281 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342986 | TCACAGACATTTTCA[C/T]ATTCTGCTATGCTGT | 494470 |
rs763969251 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367092 | GGAAGACACTGGAGT[C/T]GGGTGGATGAAAGGC | 494470 |
rs763997034 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435569 | GCCAGATGGTCCCAC[A/G]TGAGCCTGGTTCTAG | 494470 |
rs764093451 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347612 | TCATCTGGATTAAAC[C/G]AGACGGTGGATGTAA | 494470 |
rs764147448 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383230 | TGGGTGTTGGGGGCT[A/G]AAGACAGAGAGGGTC | 494470 |
rs764176845 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444875 | ATTTCCTATTTCAGA[A/C]ATTGCATTTTTCATC | 494470 |
rs764185183 | snp | A/C | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333060 | TGGCAACAAAGCTTG[A/C]GGTGAAGGCTCTTTG | 494470 |
rs764189051 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415443 | AGGCAGAAGAATGGC[A/G]TGGACCTGGGAGGTA | 494470 |
rs764194821 | snp | A/T | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46338126 | AAAACCCATTTTGAG[A/T]TGTGTTTTAACTTTT | 494470 |
rs764202738 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424954 | TCAAAAAGGAGCCAG[C/T]GCTGAACCCCGGCTC | 494470 |
rs764211373 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458549 | ATTTGAGTCTGTATT[A/G]CTGCTACAAGGGTAA | 494470 |
rs764253381 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401203 | CCTCCCAGGCCTGTC[C/T]GTGAGTGAGGATTTG | 494470 |
rs764259549 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400677 | TCAGCGTGCCTCTCA[A/G]TGCAGTGGGCTCAGA | 494470 |
rs764348272 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429039 | CCTTCCCTTTGTCCT[A/G]TGTGATGGTAGACCA | 494470 |
rs764368131 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342922 | GTGGAGCTGTAAACA[A/C]AATATATGTATACTT | 494470 |
rs764374042 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436054 | CTGAGATGCAGGGTC[A/G]CTTGGTTTTGGATCC | 494470 |
rs764374547 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369105 | AACTAATAAATGGTA[A/G]GCCAGGATTTGAATC | 494470 |
rs764398046 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391388 | CCTGGGAATCAGAGG[C/T]GAGGCCTAGTACGGG | 494470 |
rs764453718 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377075 | GCAATGCATCTTACA[G/T]GTACTAGGAGAGGTT | 494470 |
rs764460818 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368550 | CAGCTCCACTGGTCA[C/T]TTAGGGAAAGCCAGT | 494470 |
rs764462430 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341671 | ATAAAAATTCCTCAT[A/G]CTCACATGACTTGTC | 494470 |
rs764466297 | snp | C/T | | | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46435319 | TGTATCTGTCCACCC[C/T]CACCGCCTCCATCCC | 494470 |
rs764478206 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336088 | AAGAAAGAGGGGGGC[C/T]GGATGCGATCTCCTT | 494470 |
rs764530177 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410228 | AGCTTGGCTTCTTGC[A/G]CCTCAGCTCTGCTGC | 494470 |
rs764538612 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450149 | GGTTCTTGATGAAAG[A/G]AAAGGGACATAAGAG | 494470 |
rs764541228 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385305 | AGATGAAAGTGGTGG[C/T]TTGTGAGGACAAGTG | 494470 |
rs764552104 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448927 | TCAGCTCCTCAGTCT[A/C]CTTATTTGTATAATA | 494470 |
rs764567837 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363459 | CCTGGAGACAGTGCC[C/T]GTTCCTGGCTTCTCT | 494470 |
rs764571293 | in-del | -/AAAAAAAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366293 | GCAGAACTCTGGCTC[-/AAAAAAAA]AAAAAAAAAAAAAAA | 494470 |
rs764633279 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403557 | CTTATTGAATGCTTC[C/T]GTATGCAATGTGTCA | 494470 |
rs764675650 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455043 | GTAAACTATTTTCAA[A/C]TAATCAGCATAAAAT | 494470 |
rs764684130 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386264 | GTAGACTGTCCGACA[A/C]CCTTCTACTCTTTAA | 494470 |
rs764762497 | snp | C/T | 1.68664e-05 | 0.00290395 | intron-variant | RNF165 | GRCh38.p7 | 18:46450687 | GAGCACACATGTGCA[C/T]ATTTTTCTCTTTCCA | 494470 |
rs764793618 | snp | C/T | 4.43882e-05 | 0.00471085 | intron-variant | RNF165 | GRCh38.p7 | 18:46433144 | GGTCAGTGTGGCGGC[C/T]GCTCGTGCTGGTCGT | 494470 |
rs764827093 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379089 | GGTGTTGGGGGCAAT[A/G]AAGGAAAGGGAAGGC | 494470 |
rs764851148 | snp | C/G | 0.000276789 | 0.0117609 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433257 | CCACCTGGGCCCCCC[C/G]CAGCCGCAGCAGCTC | 494470 |
rs764861440 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439309 | CAGGCCATGTGGGAT[C/T]CAGGCTCAGTAGCAG | 494470 |
rs764870432 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402771 | CTCCCAAAGTACTGG[G/T]ATTGCAGGCATGAGC | 494470 |
rs764884676 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384909 | GAAAATGTCCTGCCT[C/T]TTCCCTGGTAGATAC | 494470 |
rs764887279 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411629 | CCCCAGCTGTGACGA[C/G]AGCCCATCCCAGGGA | 494470 |
rs764911337 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453409 | CCTCACCTGCTGTCA[C/T]TTCAACAGGCACGAG | 494470 |
rs764934164 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425470 | CTTCCCCTCTTTCAG[C/T]CCCCTTTTCCTTGGA | 494470 |
rs764949482 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365856 | GCATGGGGGTGAGGG[C/T]GTGGGCAAGGAATGA | 494470 |
rs764999027 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407429 | TTGTCGTCATCATCA[C/T]TATTATTATGTGGCT | 494470 |
rs765014392 | snp | C/T | | | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388965 | CTCTGTGGCTGTTTA[C/T]TGGATTTCTTTAATA | 494470 |
rs765114143 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398881 | TGAGACACGTCGACA[A/T]CATCTAGTCATCGTC | 494470 |
rs765141141 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346947 | CTGTAGCCTAACTGG[C/G]GAGACCCCCGAACAC | 494470 |
rs765196037 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336165 | GCATTTCCTCTTAAA[A/G]CGGGTGTGGAACATT | 494470 |
rs765201268 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373415 | GTCACCCAGCAAGTC[A/G]TGGGCTCTCTCCAGG | 494470 |
rs765216182 | in-del | -/C | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332707 | AGATCGGGATCACCT[-/C]CCTATGCCCTTGCTC | 494470 |
rs765218292 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430591 | CTCTTTCCAGTGAAA[A/T]GTGCAATTTCTGACG | 494470 |
rs765226739 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406229 | CCAATAGCTCTTGTT[G/T]CATTGAACCCCCCTC | 494470 |
rs765232753 | in-del | -/TGGAC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402008 | GCTCTCACAAGTGGT[-/TGGAC]TGAACTTTCCCTTGG | 494470 |
rs765257508 | snp | A/G | 8.24586e-05 | 0.00642047 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435303 | GGCGGAGTCAGGAGC[A/G]TGTATCTGTCCACCC | 494470 |
rs765258112 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341931 | TGCAAAAGGCCATCC[C/T]TACACATGGGAGCAG | 494470 |
rs765276939 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391284 | CACCTTCACCTGTAG[C/T]GGGTGACCTGGGGTA | 494470 |
rs765283350 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422612 | CTTCCCCCCGACCGA[A/G]GTCCAGCTCTCTGTG | 494470 |
rs765304244 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456400 | TCATGGTTTCCCATC[A/T]CAGCCACAGCCTCCC | 494470 |
rs765307752 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411995 | TCTTGTCAGCAGAGT[A/C]ATTGGATCTGACTTG | 494470 |
rs765319176 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442423 | GACCCTGGGTAATTT[A/G]GAAGTTTATTATTTA | 494470 |
rs765324274 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368002 | AGCACCCCCAGCTGG[C/G]AGGGGCTTGTTAAAC | 494470 |
rs765360662 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400478 | AGATCCAGTGGGGAC[A/C]CTCAGTCTGTAACGG | 494470 |
rs765370277 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414206 | ATAGTGAGTGACTGA[C/T]TAAGACGGGACCTGA | 494470 |
rs765387294 | in-del | -/TGTCACTTCTCTGCTCAGATACCCTCCTCAGAGTCAAAGG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417284 | CAGAGAGTCAAGACC[lengthTooLong]CAACATCCTGTAATG | 494470 |
rs765429021 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391491 | GTGTCCTCATCCGTC[-/AT]GTGTGTTGAACACAC | 494470 |
rs765474346 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418485 | TATTTTGTTTGCACT[A/G]AGTCTCTGATGTCTT | 494470 |
rs765489759 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362134 | GCTCTGGGCTTAGGG[G/T]CAGGCCCAAGGTGAC | 494470 |
rs765508355 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352054 | GGCAGACCCTGTCAC[C/T]CCCAGGATGGCAGCC | 494470 |
rs765512328 | snp | A/C | 1.64743e-05 | 0.00287 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46447686 | AAACTCCTCCTCCAC[A/C]CAGATGGTAAGTGAA | 494470 |
rs765520339 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448667 | AGCTCTTGGGCCTAG[A/C]CTGCCTATCCAGTTC | 494470 |
rs765557983 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340313 | GAACCAAAAGCAAAC[C/G]CTTATAACCCCATAG | 494470 |
rs765590609 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356624 | ACACACAGAAGGGAG[C/T]ATTCAGATTCCATCA | 494470 |
rs765600137 | snp | C/T | 1.64727e-05 | 0.00286986 | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447609 | GCTCAGTTCCAGGTG[C/T]GGCCCATCCCTCAGC | 494470 |
rs765612440 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447833 | CGGCTTCCACATGAC[C/T]CAGCTCACCTGTGTA | 494470 |
rs765614464 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460768 | GGATACATTCCATAC[A/G]AAATGCAAACCTTTG | 494470 |
rs765619822 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46385236 | GCCTCACCAATTACA[A/G]GGTTGCTTCCTGGGC | 494470 |
rs765650695 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416524 | ACTCAAAATTGAGTC[C/T]CCACCTCAATAAACG | 494470 |
rs765674529 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454205 | CAAGGTAATATTAAG[-/C]TAAAATTTTTAACTA | 494470 |
rs765680462 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375917 | TCAGTCCCTGCCTTT[A/G]ATGAGACTGTACAAT | 494470 |
rs765696215 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362345 | GCCTGCTAGGTGAGT[A/G]TTTCAGGACACCCCT | 494470 |
rs765702592 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459778 | AAGAGGCAGGGTCAG[A/G]CCTCAGCATCTCACA | 494470 |
rs765707700 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394409 | CACTCTCGGAGATGA[C/T]ACAGCTCTCCCTCTC | 494470 |
rs765718015 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371176 | GAGAACAGTACAGGG[A/G]AAACAGCTCCCATGA | 494470 |
rs765760925 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411458 | GAGCAAGGATTTGCA[C/T]GGAGCCATTTGCATT | 494470 |
rs765762269 | in-del | -/G | 2.60393e-05 | 0.00360818 | intron-variant | RNF165 | GRCh38.p7 | 18:46433553 | GATGGGGTCGGGTGA[-/G]GGGGGCAGGGCCAGG | 494470 |
rs765770140 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383467 | ACAAGACTAGTTAAT[A/G]TCTAGCAGGACAGTA | 494470 |
rs765825306 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375179 | AGGCTCCTTCCAGGC[C/T]GCCCTGGCCGCATTC | 494470 |
rs765911045 | snp | G/T | 3.39905e-05 | 0.00412239 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433391 | CCCCGCTGCCCACCC[G/T]GCAGTTCCAGGACGT | 494470 |
rs765915439 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420786 | GGAGGTGGAGGTTGC[A/G]GTGAGCCTAGATCGC | 494470 |
rs765921115 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453246 | GTAATTAAGGGTGTC[A/T]TCTACAGGGGAAAAT | 494470 |
rs765923015 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437683 | TTGGGGGATACATCC[C/T]AAACCCCTCTCTTTC | 494470 |
rs765928876 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343099 | ACTCAAAATGCCATA[A/G]GTTCTAGGCCGCTTG | 494470 |
rs765951516 | snp | C/T | 1.64781e-05 | 0.00287033 | intron-variant | RNF165 | GRCh38.p7 | 18:46450293 | GCGTTTTCTACCCAA[C/T]AGGTCGTCCATGAAA | 494470 |
rs765962170 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417126 | ACAAATCTTGTCACC[C/T]GTACCCTTGAAATGA | 494470 |
rs765965170 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386675 | AGTAGTGAACAAAAC[A/C]GGATCTTTTCCCTGT | 494470 |
rs765977961 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410726 | CAAAGGAAGCAAACA[C/T]ACCCCATGACCAGGA | 494470 |
rs765986134 | snp | A/G | | | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387648 | TGGGCATACAGACCC[A/G]TGGAGGGTGCAAGGG | 494470 |
rs766003347 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431252 | TTAAAAATTTGGTAG[C/G]TTCTCTTTCTCTTTT | 494470 |
rs766010987 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451917 | AAATGGCTGTGTACT[C/G]TATGTTTCCAAATAT | 494470 |
rs766032102 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420120 | GTGGAGGTCAACTCC[C/T]ATGGCGCCTCCACTC | 494470 |
rs766038006 | in-del | -/GAGAAATGCACAATTTGTCTGTCTATGCTGGAAGATG | 1.85955e-05 | 0.00304916 | frameshift-variant | RNF165 | GRCh38.p7 | 18:46456031 | GAGTCAGACACAGAT[lengthTooLong]GAGAAGATGTGAGGT | 494470 |
rs766056385 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386778 | GGGGAGCTGGACATG[A/C]GGCTCTCAGAGGAAC | 494470 |
rs766090519 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396353 | AGTTCCTGGAAGCTC[A/G]TGGCCCATCAGTGAG | 494470 |
rs766093639 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353566 | TGGTAAGGGATGTTA[C/T]CTAAAAACCCTTAAT | 494470 |
rs766093688 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365645 | AGTAGCTAGGATTAC[A/C]GGCACATGCCACCAA | 494470 |
rs766095435 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335758 | CAGCTGTCCCCAGCC[C/T]CGCGCCTCTCCCCAG | 494470 |
rs766121767 | snp | A/G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430423 | TTTGGACACTTCACA[A/G/T]GGAGATGTCTTTCGG | 494470 |
rs766137110 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444777 | TGTGCCTGGCTCATT[C/T]TGGATTATTTTTATT | 494470 |
rs766174118 | in-del | -/TG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334999 | CCCGCCCCCCGCAAC[-/TG]TCTTTGTATGACAGT | 494470 |
rs766183506 | snp | C/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333280 | TGGCCCTGGGTTTTC[C/T]GGGCAGTGTGTCTCT | 494470 |
rs766277308 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372501 | ACCCCATGTGGGGCC[A/G]CCTTAGTAAGCCCCC | 494470 |
rs766306072 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347525 | CTCTGAAGCGGGCAA[A/C]CCTCTTGGGGCACTG | 494470 |
rs766325052 | snp | A/C | 3.29473e-05 | 0.00405864 | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447591 | GATGCTGGCTTGAGT[A/C]CTGCTCAGTTCCAGG | 494470 |
rs766334807 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391766 | CAAACACACACACGC[A/G]CACACACACTATACA | 494470 |
rs766338395 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443322 | ACTTTATTTTATCTT[A/C]TTTTATTTTGGGAAT | 494470 |
rs766346177 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405259 | CATCAGCTCTGAGGG[A/C]TCCCCAGAAATAGTA | 494470 |
rs766359278 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346595 | CGGGACTTTGGCCCT[C/T]TCTGAGCCTCAGTCT | 494470 |
rs766393820 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358756 | TGACCAGCTTCTCAC[C/T]CCTTCCTTCTCACAT | 494470 |
rs766434105 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414897 | AGCCTTGTGAATGGG[A/G]AGCGTGCACTTCCAC | 494470 |
rs766440722 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434620 | GAAAATGGTTTTGAC[C/T]TCTTGAACCACCTGA | 494470 |
rs766472566 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376757 | GCCACTGCAACATCC[A/G]CCTCCCAGGTTCAAG | 494470 |
rs766476892 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342177 | CAAGAGTGGTGAAAG[A/C]CTTTGCCACCCTTCC | 494470 |
rs766513629 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417124 | GAACAAATCTTGTCA[C/T]CTGTACCCTTGAAAT | 494470 |
rs766530822 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448524 | TGCACTTCATATGGC[C/T]TCATTTAGTTTCCTG | 494470 |
rs766575045 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413926 | CATGTTTACTTTTCT[A/G]CACATACACTGTAAT | 494470 |
rs766590679 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340133 | GTTTCTCTATGGATC[C/T]AAACAGCTTTGTAAA | 494470 |
rs766590868 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407733 | GCTGGGAGCTGGTGC[C/T]GGGCTCAATGCCTTG | 494470 |
rs766612529 | snp | C/T | 1.64939e-05 | 0.0028717 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456653 | GGAGGAATTAGCCAG[C/T]GGACACCCCATTTCC | 494470 |
rs766680504 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46338575 | GAGTAAAGTCAGGAC[C/T]TAACCCCAAATTGAG | 494470 |
rs766735446 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384310 | TGCTCCCCGTAGTGT[A/C]CAGTCTTCCCGAGGA | 494470 |
rs766752245 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408216 | AAAGAGGCTGTGATG[A/G]AGGCTACTGATTCAG | 494470 |
rs766767819 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361191 | TTTGAAACTCCTTAG[A/G]GCCTTTGGGTGCTCT | 494470 |
rs766781618 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425153 | AGGCTGGCTCAGTAG[C/T]TGAGCACAGCGGGAA | 494470 |
rs766804686 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426245 | TCAGGAAACACCTTG[C/T]TTCAAATTTCTACTT | 494470 |
rs766824752 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393518 | AGCTTCATACCCTGT[A/C]TGGACGCCCCCCGCC | 494470 |
rs766828629 | snp | A/G | 1.92739e-05 | 0.00310429 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433248 | CCGCCACTTCCACCT[A/G]GGCCCCCCGCAGCCG | 494470 |
rs766860057 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344130 | CACTGTATCCCTTAG[A/G]TCTAAGTGCTGGCCT | 494470 |
rs766864219 | snp | A/C | 7.80975e-05 | 0.00624841 | intron-variant | RNF165 | GRCh38.p7 | 18:46334469 | GCGGTGGCTTCCCCC[A/C]ACCCCATTTTAGGGG | 494470 |
rs766864232 | in-del | -/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457314 | ATTTGGGAGGCGGGA[-/G]GGGGGGGGTTCTCGT | 494470 |
rs766914293 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392842 | GGACAACACGCCTGG[A/G]TGGAGTTGGACCCTT | 494470 |
rs766964226 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424060 | GAAAACACTCACTTC[A/G]CAACTTTATTGGAGA | 494470 |
rs766973088 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352611 | TGGCCCTTTTCTGCA[C/T]GGTCCAGGATGGTTC | 494470 |
rs766981743 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439042 | TGTGGTGTGCATGGA[A/G]TCTGTGAGAGTGACT | 494470 |
rs767003965 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386302 | CATTGTCATCGTTGC[C/T]TTCATCTCTGACATT | 494470 |
rs767005145 | in-del | -/GGGAGGAA | 1.69661e-05 | 0.00291252 | intron-variant | RNF165 | GRCh38.p7 | 18:46435418 | CTTCAGGGCCCCTGG[-/GGGAGGAA]GGGAGGAAGGGAGGG | 494470 |
rs767060304 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352450 | TGGAGTAGGTTTATT[A/G]GGTCAGATGTAAGTT | 494470 |
rs767090867 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419070 | TACTGGACCATGAGT[C/T]TTTCTGATGTCCCCG | 494470 |
rs767129772 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419495 | CCCAAGTCACTCCCC[C/T]GAGAGCCTGCCGGGA | 494470 |
rs767135575 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395409 | TGGCAGCATTCCTGG[C/T]ACCTCCCCACTAGAT | 494470 |
rs767182665 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428910 | GTCTTGACAATACCC[A/G]TTTTCACCCCATTCT | 494470 |
rs767208436 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370605 | ATTTGCCACCCTTCT[C/T]ACGTCTGATCTTAAA | 494470 |
rs767226711 | snp | A/G | 2.26544e-05 | 0.00336552 | intron-variant | RNF165 | GRCh38.p7 | 18:46433542 | GGTGGGGACCCGGAT[A/G]GGGTCGGGTGAGGGG | 494470 |
rs767226759 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347410 | GCCCCTCTGCCCAGC[C/T]GAGCTGCCTGAGTGC | 494470 |
rs767235119 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443057 | GAATGGACAGCATAT[A/T]CTTGGCAATTGTTTT | 494470 |
rs767261521 | snp | A/G | 2.78563e-05 | 0.00373194 | intron-variant | RNF165 | GRCh38.p7 | 18:46455925 | AAACCACCAGCCACC[A/G]GCTGAGTCTGCCCCA | 494470 |
rs767277595 | snp | C/G | | | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435302 | AGGCGGAGTCAGGAG[C/G]GTGTATCTGTCCACC | 494470 |
rs767279163 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413982 | TCATGCAGCATGCTC[A/G]GGTTCCTCTCTTAGA | 494470 |
rs767289176 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339097 | GAGGCTCTGCTGTAG[-/T]TTGTGCAAGAGGAGA | 494470 |
rs767302927 | in-del | -/GTGG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396864 | GGTTCTTGGCATGAC[-/GTGG]GTTGGGTGGATTTTC | 494470 |
rs767316559 | snp | C/T | 1.71917e-05 | 0.00293182 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433467 | CCTGCAGCAGCAGCT[C/T]CTGGAAGCCCAGCAC | 494470 |
rs767316842 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346383 | GTGCGAACATCACTA[C/T]TTTCTATTTCCAAAA | 494470 |
rs767318963 | snp | A/G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372352 | CGCTCTTCCTGCCTC[A/G/T]GTCCCACCATTGCTC | 494470 |
rs767324966 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456369 | GCTGATCTGAAAGCG[C/G]TTCCTGGCGGAGGCT | 494470 |
rs767326865 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441382 | GTGCCACTGCATCTG[A/G]TAATTTTGGTAGTTT | 494470 |
rs767406317 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357416 | TCAATATGAAATTGT[A/G]AAAAGTGCTGAGGAT | 494470 |
rs767429386 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384405 | GCAGAGATGCTCTTC[C/T]TCAGAGATCTGCCCC | 494470 |
rs767453292 | snp | G/T | 4.94597e-05 | 0.00497266 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456642 | CGACAGCTGAGGGAG[G/T]AATTAGCCAGTGGAC | 494470 |
rs767494422 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356552 | CCTCTGTTGTCCTGG[A/G]CAGGCACGGAATGCG | 494470 |
rs767510460 | snp | C/G | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336374 | CTACCTTCTCCCTCA[C/G]CCCCCCCAACAAAAA | 494470 |
rs767545177 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342916 | GGGGGAGTGGAGCTG[-/T]AAACACAATATATGT | 494470 |
rs767552105 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383721 | ACCGCGCCCGGCTAA[-/T]TTTTTTGTATTTTTA | 494470 |
rs767557487 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406275 | AGTGGCCACTGTCAC[A/G]GGACTGGATGCCCCG | 494470 |
rs767572227 | in-del | -/CAAAAA | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461646 | GAACAAAACTCAGTC[-/CAAAAA]AAAAAAAAAAAAAAA | 494470 |
rs767574834 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422517 | GCCTCCTCTGGACTA[C/T]ATCTCCCTCCACCTG | 494470 |
rs767579826 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383763 | GTTTCACCGTGTTGG[C/T]CAGGATGGTCTTGAT | 494470 |
rs767634173 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447455 | GTTCCTTGCAGCTCT[A/G]GCAGGGTGTCACTCC | 494470 |
rs767640781 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380237 | CAGTCTCCTCTCCTA[C/T]GGCATCTGGCACAGC | 494470 |
rs767642072 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431353 | TCTAGAATGTCTGTG[G/T]GCCTTGAGGGTGAGA | 494470 |
rs767660780 | snp | C/G | 3.29783e-05 | 0.00406055 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435311 | CAGGAGCGTGTATCT[C/G]TCCACCCCCACCGCC | 494470 |
rs767662059 | in-del | -/TAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375563 | TGTCTCTAATAATAA[-/TAA]TAATAATAATAATAA | 494470 |
rs767667739 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392702 | GGTCCTGTGCCTTGT[C/T]AGTCTCTCCCCTCTG | 494470 |
rs767689494 | in-del | -/CT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437971 | AGCTCCCAAAGCTCC[-/CT]GAGCCTGGAGTCACC | 494470 |
rs767737682 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426177 | CTACCATATTTCATC[A/G]AGCTTCCTGACTCCC | 494470 |
rs767809806 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348834 | CTGCAACCAAGAGAG[C/T]CCTTTGGTTTTGCTT | 494470 |
rs767816180 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383453 | CTGCTAAATTAGACA[C/G]AAGACTAGTTAATAT | 494470 |
rs767828306 | snp | C/G | 3.29484e-05 | 0.00405871 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46456552 | TCTCTTTCACCAACT[C/G]TGCGTGGACCAGTGG | 494470 |
rs767876200 | snp | A/T | 1.64749e-05 | 0.00287005 | missense | RNF165 | GRCh38.p7 | 18:46450372 | TAAATCCCAGCAGAC[A/T]CACCTCCGCCGTACG | 494470 |
rs767880736 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361540 | CACACGGTTCCCCTC[C/T]ACAGTTTCTTTTGGA | 494470 |
rs767883064 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343041 | CTACATAATATTCCA[C/T]TTGAATAGTGGCTCA | 494470 |
rs767931438 | snp | C/T | 0.000178142 | 0.00943606 | intron-variant | RNF165 | GRCh38.p7 | 18:46334435 | GGGCTCAGGGCACAC[C/T]CGCGAGGACGCAGGG | 494470 |
rs767952080 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377966 | TGGTGGTGGACTGCA[A/C]AACAGAGGTGGTGCA | 494470 |
rs767959620 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46402521 | TACATGTGTGTGTTT[G/T]TTTTTCTTTTCGAGA | 494470 |
rs767988983 | snp | C/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333083 | GCTCTTTGATTGGGT[C/T]TTGCTTGTCCCCAGC | 494470 |
rs768038891 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46387606 | TGAAGCAAGAAAAAC[A/C]TTCCCCACTTGGAAG | 494470 |
rs768052715 | snp | A/C | 4.44356e-05 | 0.00471336 | intron-variant | RNF165 | GRCh38.p7 | 18:46433537 | GCGGAGGTGGGGACC[A/C]GGATGGGGTCGGGTG | 494470 |
rs768066501 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451802 | AGAGCAAGACCCTGT[A/G]TCAAACAAAGAAAGA | 494470 |
rs768066675 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356223 | ATCCGTGACCAGCCG[A/G]CCCTGTTCCAGGTGT | 494470 |
rs768074906 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347261 | TGTGGCTGTCACCCT[C/T]GTCTGAATTTTCTTT | 494470 |
rs768104226 | snp | A/G/T | 6.26669e-05 | 0.00559734 | missense | RNF165 | GRCh38.p7 | 18:46456057 | AATTTGTCTGTCTAT[A/G/T]CTGGAAGATGGAGAA | 494470 |
rs768123927 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397454 | CTGAGGTGTGAGGGG[-/GT]GTGTGTGTGTGTGTG | 494470 |
rs768132142 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391701 | GCTTGGGACATGTCA[A/G]TCTCCAGTCAGCATC | 494470 |
rs768149937 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348281 | GGAGAGTCATGCAGA[C/G]GGGTCACTGGGACAG | 494470 |
rs768176427 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444518 | CACCTAGGCAGAAGT[C/G]CAGTGGTGGCATCAC | 494470 |
rs768179718 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359152 | AAGCTAGAACAATGC[A/G]ATTCAATTCAGTCTG | 494470 |
rs768180775 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415174 | AGTTTGACTGACACT[C/T]ATCGAAATGTGAATA | 494470 |
rs768195493 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423656 | CACACTGCAGCACTG[A/G]GACTCAGGAGGCCTG | 494470 |
rs768206389 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457030 | GAACCATGTAGGGGT[C/T]TCTAGCTATTTCTGT | 494470 |
rs768206647 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428229 | TTCTGGCCAACATGG[C/T]GAAACCCCGTCTCTA | 494470 |
rs768247841 | in-del | -/TGTGTG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348901 | CTCTCTCTCTCTTTC[-/TGTGTG]TGTGTGTGTGTGTGT | 494470 |
rs768267808 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358340 | AGGGCCTAGTGTGAG[A/G]AAGTGAACGAGTGAA | 494470 |
rs768268720 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424569 | TAGGACCCTGGCGGC[A/G]GTACAACACTGAACA | 494470 |
rs768351014 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445616 | CCTCCTGGAAATAAG[A/G]TCTCTGAATCCTCAA | 494470 |
rs768368346 | snp | A/C | 4.5042e-05 | 0.00474542 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334253 | CGCAGCCGCCGCCGC[A/C]GCCGCCGCGCGAGGA | 494470 |
rs768378242 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381965 | AGCACCCGCAGGGCC[C/T]CCCTTCTCTTAGGTC | 494470 |
rs768419256 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396688 | CTCGGCCTGGCTGTC[A/G]GGACCATGAACCAAA | 494470 |
rs768443606 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367807 | CTTCTTGAGTGTCAG[A/T]ATCACTTCAGTGCTT | 494470 |
rs768446499 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422460 | GAGGAGGCTCCCTGG[A/G]GGCCATGTTGAGTAG | 494470 |
rs768468233 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390750 | GGAATCCTATACTGG[G/T]CTGGGCTCAGGTTCC | 494470 |
rs768501782 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377492 | AGGAGGGGCAGCAAG[A/T]GGCTGGAGGGGATTT | 494470 |
rs768505481 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408278 | CTTTAAGAAACTGTG[A/G]AGGGGCTACTGAGAA | 494470 |
rs768514176 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384922 | CTTTTCCCTGGTAGA[C/T]ACAGCCCAGAGCCAG | 494470 |
rs768577505 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409110 | ACCTAACAGTGCCTG[A/G]CATACAGGGGGTGCA | 494470 |
rs768615306 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449690 | AGGGACCTCCCCATT[C/T]GCTTGGCACTCATTC | 494470 |
rs768696810 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351810 | AGTGTCCCACCGTGG[C/T]GGCAGGGCCTGGCTA | 494470 |
rs768696816 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339892 | CTGCCCCACCCTGTC[A/C]TTCCCATCTTTAAAT | 494470 |
rs768697507 | snp | A/C | 5.38924e-05 | 0.00519069 | intron-variant | RNF165 | GRCh38.p7 | 18:46334407 | GGCGGGGGCGGGCGC[A/C]GCGGGCGGCCGGGGG | 494470 |
rs768705176 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448335 | CAGCTCCCCTCTCTT[C/T]GCAGCTCCTATTCAC | 494470 |
rs768726510 | in-del | -/AA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440714 | GTTATACTTTGTATC[-/AA]TCAAGATCCGAATAA | 494470 |
rs768752326 | snp | C/T | 2.06154e-05 | 0.00321049 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433213 | TTTCAAAGGTCTCAG[C/T]ATCCTCACGCTACCT | 494470 |
rs768757193 | snp | G/T | 1.65179e-05 | 0.00287379 | intron-variant | RNF165 | GRCh38.p7 | 18:46450427 | TGTCTGGTACCAACT[G/T]GGTTGGTGGAGATGC | 494470 |
rs768827036 | snp | A/G | 0.000131787 | 0.00811641 | missense | RNF165 | GRCh38.p7 | 18:46450365 | CAGGGACTAAATCCC[A/G]GCAGACACACCTCCG | 494470 |
rs768829145 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353929 | AGCTCTAAGGGTTTT[A/G]TTGGAAGCCTGGAAA | 494470 |
rs768831473 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451649 | AAATTTTGAAAAGTT[A/G]AAAAGTTAAAAAGTT | 494470 |
rs768848735 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437140 | TCCGGGAGGCTGGTC[C/T]CTGCCCTAGCAGGGG | 494470 |
rs768872449 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369794 | AAAGTAAGACTTTGC[A/G]TGCGCATTTCAAGAG | 494470 |
rs768885924 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379603 | CCACAGGGCAAAGTC[A/G]CTCTTTGAAGCCACC | 494470 |
rs768905194 | in-del | -/CA | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461221 | TTGGCCCCTGAGTCT[-/CA]GTTTTCTGGGTGGGG | 494470 |
rs769022529 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353384 | GAAAGCACCAGGTGC[A/T]ATGTCTGGGCCGTGA | 494470 |
rs769049598 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438668 | GTCCATGAATAAGGC[-/A]CTGTCCTTCTGCAGG | 494470 |
rs769059982 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445361 | GTCTCTATTGTATGA[C/T]CAAGGACTCTCTGCT | 494470 |
rs769073072 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429777 | AATACTCTTTTTTTT[-/T]CCTTTCTTTTATTGA | 494470 |
rs769081619 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396087 | GCAGGAATCTTAGAG[A/G]CACAGAGACCAAGAG | 494470 |
rs769125082 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341242 | TGGCCTTTGGGAGCT[C/T]TGAGGGGAGAGGGCT | 494470 |
rs769166070 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364680 | TCTCCTTTGGTGATT[C/G]ACATGGCTTCTTGGG | 494470 |
rs769169518 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405698 | AAATGGACTTGATTT[G/T]GATGGTTTGAGTCTG | 494470 |
rs769171241 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415043 | AAGCCCAGGAAATGG[G/T]CAGGGGAGGGAGCAG | 494470 |
rs769209270 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357035 | AGCTTGCAAAATCCA[C/T]ATTCCCAGGCCCTAC | 494470 |
rs769224422 | in-del | -/TTGT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413133 | ACTCGGTTTTGAAAA[-/TTGT]TTGGTTAAAACATTG | 494470 |
rs769244849 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373721 | AGGACAGGGCTGTCT[C/T]CAGGATCTCTGCAGG | 494470 |
rs769253823 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372799 | AGAGCGCCAAAATCC[A/C]TACGTTTCCTTTATT | 494470 |
rs769255742 | in-del | -/TGTGTGAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334711 | GTGTGTGTGTGTGTG[-/TGTGTGAG]AGAGAGAGAGAGCGC | 494470 |
rs769266279 | snp | A/C/T | 4.98131e-05 | 0.00499044 | intron-variant | RNF165 | GRCh38.p7 | 18:46435267 | CCCCTGACACGAGGG[A/C/T]TCTCCATCCCTTCTG | 494470 |
rs769273657 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413425 | GTCAGTTCTGAGTGG[C/G]ATAGGTGAGCGCTCC | 494470 |
rs769348452 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434278 | TATGTGGGTTTTGAC[C/T]ATTGATGTTTACCAT | 494470 |
rs769426377 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390726 | GGAAATGTGGGAAGG[C/T]GGTGGCTCGGAATCC | 494470 |
rs769468049 | in-del | -/GAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434884 | AAAAAGGGTTGAGGA[-/GAG]GAGAAGAGCATGATG | 494470 |
rs769487299 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372156 | GCCTTAGGAGCTGGA[C/T]GGGGCTATACCTCAA | 494470 |
rs769494711 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376343 | AAACTGAGGTTCCGT[G/T]TGGTTAAGGAGCATG | 494470 |
rs769514663 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389709 | CATAGCAGCTCTCTC[C/T]AGGAAGTGAAATGGT | 494470 |
rs769550205 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366962 | TGGCTTAGGGCCCAG[A/T]CATCCCGTTGGACTT | 494470 |
rs769566553 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339457 | GTATTTAATGTTTGA[C/T]CCAGATTGTCTGAAC | 494470 |
rs769583513 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384765 | CTCATGCCTGTAATC[C/T]CAGTGCTTTGGGAGA | 494470 |
rs769595032 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432600 | AAAGGCCAAGCTTTA[C/G]GAACCTTAAAACTTT | 494470 |
rs769596041 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350165 | TTTTCTCTGACATGT[C/T]ACCTGTGCCCCTATG | 494470 |
rs769610551 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390648 | TCTGTAGGACAGTTA[A/G]TCCATCAGCCCCCAT | 494470 |
rs769631841 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant | RNF165 | GRCh38.p7 | 18:46447532 | GCTAAATCACACCAC[C/T]CTATGGTTCACTGAG | 494470 |
rs769639085 | snp | C/T | | | utr-variant-5-prime, missense, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334315 | TCGTGCTTCCAGTGT[C/T]TGGCTCTGTGCGAAA | 494470 |
rs769668186 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448188 | CTGGCCCCCTTATAT[A/C]CTGGCTCCCCTGTGC | 494470 |
rs769673412 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383945 | TCTTGCCATGGAAGG[C/T]CAGTGACTCTTAGGG | 494470 |
rs769676334 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348419 | TTGTCAAGAATAAAG[A/T]GCACAGAACCTCTGT | 494470 |
rs769685079 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416791 | AGCCTGGGCTTGTTC[C/T]TATGGTAGAGGCAGG | 494470 |
rs769719598 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436929 | ATTGGAACACACACA[A/G]GGGCCTACAGGGAAG | 494470 |
rs769723750 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426970 | TGTCATGGACCCAGA[A/T]ATACTATCCTGGGAG | 494470 |
rs769784703 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437249 | TAGGATGCTGATTCT[C/T]CTCCCTTGTAATTAG | 494470 |
rs769800181 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444957 | CTCTTCTCTGTTTTC[A/G]TGTTTTCTTTTGTAT | 494470 |
rs769834288 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400995 | AGAGATGACCTCCCG[C/T]AAAGCTAAGCCTTGA | 494470 |
rs769908461 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370652 | GAGGCCTCCCCAGAA[C/T]GCCCCATGCCAGGTG | 494470 |
rs769910053 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451443 | ATGTCCTTCAATAGA[C/T]GAAAGATAGATAAAC | 494470 |
rs769918739 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360909 | GGCCCAGAGGCCAGG[C/T]GTCAGCCCCACAGCA | 494470 |
rs769979165 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353237 | GTGGTGGACAGTAGA[C/T]ACTGAATGAAAGCTG | 494470 |
rs769997352 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46450064 | GTGCTTAGAACAGTG[C/T]CTGCCATGAAGGTTA | 494470 |
rs770000150 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378421 | ATGTCCTCCAGCACA[C/T]TCATTCCCCCTGACC | 494470 |
rs770011144 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46387326 | GAAACAAGCCCCCAT[C/T]CTCCATGATTCCAGT | 494470 |
rs770042717 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395139 | GAGCTATGGGGTGGA[A/G]GGATTAAAAGATGGA | 494470 |
rs770048495 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383851 | CCACCGCGCCCGGCC[A/G]CCATGTTGGTTTTCT | 494470 |
rs770083690 | snp | A/T | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461846 | GTGGACACGTATAGG[A/T]CGTGCCCTTTCATAA | 494470 |
rs770095408 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377754 | TATGTGATGGGGCAT[G/T]GTGAGATGAATAGGA | 494470 |
rs770102873 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404273 | GAAGATGTAGGTGGT[A/G]TGAGTATGCTGGATG | 494470 |
rs770208180 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346170 | GTGGCAGATCCTCAA[A/G]TGTGCCAGGCCTAGG | 494470 |
rs770230470 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379453 | ACCTTCCCTCCCCGA[C/G]TCCATTTTACAGATG | 494470 |
rs770260871 | snp | A/G | 1.65756e-05 | 0.00287881 | intron-variant | RNF165 | GRCh38.p7 | 18:46433520 | GGTTGGTGCTGCCTG[A/G]GGCGGAGGTGGGGAC | 494470 |
rs770309932 | snp | A/G | 1.66468e-05 | 0.00288498 | intron-variant | RNF165 | GRCh38.p7 | 18:46435262 | GGTAGCCCCTGACAC[A/G]AGGGCTCTCCATCCC | 494470 |
rs770314768 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414645 | TTCATGATCATGCCA[C/T]GTACCACACAATACA | 494470 |
rs770319666 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416157 | GGAGGTCAAAATCAA[A/G]GCTAAAAATCAGTGC | 494470 |
rs770323430 | snp | A/G | 1.6517e-05 | 0.00287372 | intron-variant | RNF165 | GRCh38.p7 | 18:46447520 | TTCTCTAACCTGGCT[A/G]AATCACACCACCCTA | 494470 |
rs770326194 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428654 | GACATGTGTGGCAAG[C/T]ACAAAATAGCCACCA | 494470 |
rs770364006 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366836 | CCATAAGTCAGACGC[C/T]GTGCTAGGTACTAGG | 494470 |
rs770379895 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421647 | TTCTTCTGTAATTGT[A/G]TCCTGTCTCTAACCA | 494470 |
rs770381837 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421530 | AAATGCCTTGTTAGG[-/A]TTGTGGCAGGAATGT | 494470 |
rs770381894 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433870 | ATGGTGCGGGAGGAA[A/G]TTTGACTAGGGAACT | 494470 |
rs770382345 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392670 | ACACTGGGCCAGCCT[C/T]GGGCTGAGGGTGACA | 494470 |
rs770382919 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381890 | TCAGGCACCACCGGC[A/G]AGCAGGTGTCTTTGG | 494470 |
rs770395387 | snp | A/G | 1.8338e-05 | 0.00302798 | missense | RNF165 | GRCh38.p7 | 18:46456011 | GCAAGAAGGATGAGG[A/G]GGAGGAGTCAGACAC | 494470 |
rs770399387 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358221 | GTGAGGGCTGCAAGC[A/G]TTCAGAGAAAAGGGC | 494470 |
rs770433876 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397094 | GGCTTCCCCTGGGCC[C/T]GGCCTGGAACCCAGG | 494470 |
rs770467729 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339223 | TCCAACCTCAACAAT[A/G]ATAAAACTACCCTGA | 494470 |
rs770469880 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432215 | TTAGAGAGAATTTGT[A/T]AGGTTTTCTTGTCAT | 494470 |
rs770476632 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447297 | ATGGACTTTGTCTTG[A/G]GAGGGAGCTTTGGTC | 494470 |
rs770556084 | snp | A/T | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337711 | TCCTGCTGTTTAGAT[A/T]TTCCCCCCTTGCTTT | 494470 |
rs770564436 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459366 | GACACTCACACTCCC[C/T]AACATCAACACATCT | 494470 |
rs770615726 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335047 | GATGCTTGGGCGCGT[-/GT]GTGTGTGTGTGTGTG | 494470 |
rs770650482 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348572 | GTGGGAAACTTCAGA[C/G]AAAAGAGCAGAGTGG | 494470 |
rs770651576 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407980 | TCCTGGGGGAGGTGG[A/C]ATAGCAGCTGAGCTT | 494470 |
rs770652998 | in-del | -/GA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440275 | ATTTTGAGAGACTGA[-/GA]GAGAGAGAGAGAGAG | 494470 |
rs770669181 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373875 | CCTCCCACCCCCGGT[A/C]CCAGACCCTGTGCCC | 494470 |
rs770686313 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362912 | GGGAAGAAAAATCAC[C/T]GGGAGGGATAGTGGC | 494470 |
rs770739271 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407290 | TACCCAGTCTTTTGG[A/G]GTAAGATTCTTCTTC | 494470 |
rs770740276 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359332 | TGACAAAGGGAGTGT[G/T]CAGGCAGCTGTGGGG | 494470 |
rs770757191 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383744 | TATTTTTAATACAGA[C/T]GGGGTTTCACCGTGT | 494470 |
rs770767415 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | RNF165 | GRCh38.p7 | 18:46456613 | CGAGTGGACATTGAG[A/G]CACAACTGGGAGCCG | 494470 |
rs770779833 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458410 | CCCTCATTTGCACTG[C/T]TCTGTAAGCCTCCCC | 494470 |
rs770783895 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360782 | CGAGGCGGGTATGTG[A/G]AATCCTACCTAGGTA | 494470 |
rs770787580 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424790 | TGACTGTGAGGGGAA[C/G]TGCCCTGGCCTTTGG | 494470 |
rs770790819 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437312 | CGAGGGGTTTTGTGA[-/T]TGATTGTGCTAACTG | 494470 |
rs770830154 | snp | A/G | 6.48109e-05 | 0.00569221 | intron-variant | RNF165 | GRCh38.p7 | 18:46334395 | CGCAGGCACCGGGGC[A/G]GGGGCGGGCGCCGCG | 494470 |
rs770831330 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415962 | TGAAAATGGAAACCA[A/G]TTTGGACACCCAGTG | 494470 |
rs770846783 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352958 | TTGTCTACCCTTCTT[A/G]CATTAGTGGCACTGT | 494470 |
rs771047478 | snp | G/T | 1.64738e-05 | 0.00286995 | missense | RNF165 | GRCh38.p7 | 18:46447678 | TTTCCCAGAAACTCC[G/T]CCTCCACACAGATGG | 494470 |
rs771050715 | snp | G/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461383 | GGCATGGTGGCTCAC[G/T]CCTGTAATCCCAGCA | 494470 |
rs771059181 | in-del | -/CCGCAG | 1.89396e-05 | 0.00307724 | intron-variant, cds-indel | RNF165 | GRCh38.p7 | 18:46433254 | TTCCACCTGGGCCCC[-/CCGCAG]CCGCAGCCGCAGCAG | 494470 |
rs771061609 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351945 | TGCACCGTGCATCTA[C/T]GCAGTTTTTCTCCTA | 494470 |
rs771070831 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383452 | GCTGCTAAATTAGAC[A/G]CAAGACTAGTTAATA | 494470 |
rs771094002 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386444 | GGAAGCAGAGGCAGA[-/G]GGGTTAATATCAATT | 494470 |
rs771161273 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383066 | GGCATCCATCTCATG[C/T]CTGCCTTCTTCTCAG | 494470 |
rs771169815 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404123 | TCATCTTTTTTCTTT[A/G]TGCAAAAATTTAAAT | 494470 |
rs771176324 | snp | G/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332624 | TTCTGCATGGAACAA[G/T]CTCTATGGTGATTGC | 494470 |
rs771209000 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404710 | GTGAGCCGAGACCGC[A/G]CCGCCACACTCCAGC | 494470 |
rs771219476 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395104 | AAGTCAACGCTGACT[A/G]GCTGGACTCCCATTT | 494470 |
rs771245295 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359589 | CTGAGAGCCATGGAC[C/T]CCACCTGAAAGCCCA | 494470 |
rs771287447 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371072 | GGAGGAGCAAAGGCA[C/T]GTCTTACATGGTGGC | 494470 |
rs771336042 | snp | A/C/T | 1.81952e-05 | 0.00301617 | intron-variant, missense, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433500 | CAGGCTGGTCTCGCA[A/C/T]CCCAGGTTGGTGCTG | 494470 |
rs771377413 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380672 | AGGGAGCAGGGACTT[C/T]TGAGGTCTCCAACCC | 494470 |
rs771403461 | snp | C/G | 1.75038e-05 | 0.00295831 | intron-variant | RNF165 | GRCh38.p7 | 18:46450813 | AGGTGGGTCTGCCAG[C/G]AGGCCAGCCTGCATA | 494470 |
rs771411341 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459327 | CCTAAGGAGGTTGGA[C/T]TGGATGCTTGCTAAT | 494470 |
rs771450485 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345775 | ACAGAATTTGGTGAC[A/G]TTTCATTCAGGCAGG | 494470 |
rs771454801 | snp | A/C | 1.8238e-05 | 0.00301972 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433334 | TCAGCGCCCACATGG[A/C]CCCGGCCCACCAGCA | 494470 |
rs771470879 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455791 | AGTGAGCCAAGATCA[C/T]GCTATTGCACTCCAG | 494470 |
rs771476754 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412447 | GCTGCCTGTCAGGCT[C/G]TGAAAACAGAGCAGA | 494470 |
rs771490989 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347875 | TGATCATGGATTTGT[G/T]CAGCTCATCTAACAC | 494470 |
rs771511070 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335397 | ACCTCCACTCCACAT[C/T]TCTTTCATTTTCTTT | 494470 |
rs771540373 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356931 | CGGCTGGAAAGGCGT[A/G]ATCTGTGCCCTGCAT | 494470 |
rs771550049 | snp | G/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337292 | GTAGCGTGTTCTGCT[G/T]TGCTGAATTACTTCC | 494470 |
rs771551433 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | RNF165 | GRCh38.p7 | 18:46456584 | TCGCCATGAGCAAGA[A/G]ATGCCCCATCTGCCG | 494470 |
rs771552798 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454947 | TAAAGAAGGGTAAGT[A/C]ATGAGTCCATGCCAT | 494470 |
rs771583285 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386458 | AGGGGTTAATATCAA[-/T]TTTTTTTTCCCTAAG | 494470 |
rs771602258 | snp | A/G | 0.000115442 | 0.00759656 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435347 | CCCAGCTTCGACTTC[A/G]GCCAACTGCAGACAC | 494470 |
rs771611020 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458169 | AACCTTGTGGGGTGT[C/T]GGGATGGGGGTGCTG | 494470 |
rs771612599 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445548 | GGAGCCCTCCTTCTA[C/T]GTAGCTGCCTCTTCT | 494470 |
rs771626101 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394306 | CTAGTTGCGTCCCAG[C/T]TCACTGGTCATATCC | 494470 |
rs771630281 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355940 | ATGATGCAGATGGGC[C/T]TCTGTAGTGGGCGGA | 494470 |
rs771642193 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451688 | TATGAACTTGTAGTC[C/G]TAGTTACTAGGGAGG | 494470 |
rs771674682 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412713 | GGTCCTGACTACCCC[A/C]ACCCCTCCCAACTCT | 494470 |
rs771702518 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444547 | ACAGCTCATTGTAGC[C/T]TCAACTTCCTGGGCT | 494470 |
rs771710070 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373842 | GGCAGAGCTGGGGCT[C/T]GCTAGCCCTCAGATC | 494470 |
rs771733671 | snp | C/G | 2.32631e-05 | 0.00341043 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334286 | CAGGATGGTCCTGGT[C/G]CACGTCGGCTATCTC | 494470 |
rs771753224 | in-del | -/AG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404880 | TAGAGTTGGAGAAAC[-/AG]AGGCATAGGAAGTTC | 494470 |
rs771774131 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359308 | AAGCAGTTCACAAAA[C/T]GATGAACGTGACAAA | 494470 |
rs771792464 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457296 | GGATTTTGTTTTTCA[C/T]CCAATTTGGGAGGCG | 494470 |
rs771857432 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415219 | AAGGCAGTGACCTTA[C/T]CAGTAAGTTGCTGAA | 494470 |
rs771871965 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358692 | CGGCCCTTACTGACA[G/T]GTTCCAGACCCCCAG | 494470 |
rs771924415 | snp | A/C | 2.35114e-05 | 0.00342858 | intron-variant | RNF165 | GRCh38.p7 | 18:46334377 | CTTCGGAGCGTGGAT[A/C]GCCGCAGGCACCGGG | 494470 |
rs771945257 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424746 | CCAGGAAACTAGGGC[C/T]TGGAGAAGTCCATGG | 494470 |
rs771948550 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377605 | AGGGAGCCAGGGAGA[C/G]GTTATCAGGTAAAGG | 494470 |
rs771969378 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436898 | AGTACTCAGGGCCCT[G/T]GCATATGGCTGAGTG | 494470 |
rs771974511 | in-del | -/ACCC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355746 | CCCCTCTATCTCTCC[-/ACCC]ATCATGTGCACACAT | 494470 |
rs772003907 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378399 | CCTGGTCTTTTCAGC[C/G]TGGGGCATGTCCTCC | 494470 |
rs772021760 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428373 | GAGATCGTGCCACTG[A/C]ACTTCAGCCTGGTGA | 494470 |
rs772059580 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423690 | GCCAGCCCCAACTTG[A/G]CCATGACTACTCTAG | 494470 |
rs772118878 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342507 | GAGGGTGCATGGTGG[A/T]CCAGAAACTCTCCAG | 494470 |
rs772123117 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404554 | AGGTCGGGAGGTCGA[G/T]ACCAGCCTGACTAAC | 494470 |
rs772147906 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420240 | CTCTTCTTCTAAACT[A/C]TTCCCCATCATCACA | 494470 |
rs772163294 | in-del | -/CGGC | 7.06939e-05 | 0.00594491 | intron-variant | RNF165 | GRCh38.p7 | 18:46334412 | GGCGGGCGCCGCGGG[-/CGGC]CGGCCGGGGGCTCAG | 494470 |
rs772212755 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459578 | GGGAGAGGGAAGCTG[C/T]TTACTTTGGGGGTAG | 494470 |
rs772232328 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369990 | GCACCCTAGACTTGG[A/G]AATGATTCTGGTGTG | 494470 |
rs772234768 | in-del | -/AC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404755 | AGACTCCATCTCAAA[-/AC]ACACACACACACAAA | 494470 |
rs772244848 | snp | A/C | 1.9832e-05 | 0.00314891 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433234 | CACGCTACCTCCTGC[A/C]GCCACTTCCACCTGG | 494470 |
rs772287706 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438848 | GTGTAGTGCTCTACA[A/C]AGAGTTTTCACCTGC | 494470 |
rs772289927 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412230 | AATCCTGCCATGATC[A/T]TATGTCCCAGTTTGG | 494470 |
rs772294221 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370718 | CTGTCCTCGTTCTCT[C/T]GAGCCACTCTCTGGG | 494470 |
rs772306693 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346816 | CTGGGACAGTTTTAG[A/G]GGTCTTAGGGGAGTG | 494470 |
rs772329853 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380471 | GGAATAGTTATGAGG[G/T]GCGCTTGCACAGTGC | 494470 |
rs772337604 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348144 | CTGGGGAGGGCAATG[A/C]CTGGGGGAGCTGATG | 494470 |
rs772350754 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355554 | CCCTCCCCAAACCAG[C/T]GGTCCCAGCTCCCAT | 494470 |
rs772366437 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393432 | GGCAGACGCCAGAAG[C/G]GTGCGCTGTTTCCTC | 494470 |
rs772374949 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453145 | GCACTGGATTTATTC[A/G]TAAATGATTTCAACC | 494470 |
rs772396400 | snp | C/T | 1.67891e-05 | 0.00289729 | synonymous-codon, intron-variant | RNF165 | GRCh38.p7 | 18:46450784 | GAGGTTCACCTTCCC[C/T]CACAAGTATAAGAAG | 494470 |
rs772442823 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403262 | ATCTATTCTGACCTG[A/C]TAAGCATGACTTTTA | 494470 |
rs772443354 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454729 | TTTCTCTTTGCAAAA[C/T]GATCTTGAAGTCAGC | 494470 |
rs772500024 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363366 | GATGTTAAAAAATAT[C/T]GAAAGGAACACACCA | 494470 |
rs772507102 | snp | A/T | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388465 | TGTTCCTGAAACACA[A/T]GTTGGGACCTGCACG | 494470 |
rs772526234 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335741 | CCCTATTTTATCCAG[C/G]CCAGCTGTCCCCAGC | 494470 |
rs772562343 | snp | A/G | | | intron-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388942 | TGCCATGAAGCTCAT[A/G]TACTTAACTCTGTGG | 494470 |
rs772562681 | in-del | -/GTGTGTGTGT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334672 | GAAAGATACATGACC[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 494470 |
rs772604250 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354137 | TTATGAATTGTTTCA[C/T]TTCTTCCCACACTGC | 494470 |
rs772618486 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411401 | CTATCCTGAATAGGA[C/T]GTATGCTCTGAGTCA | 494470 |
rs772627004 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383419 | TATACACACACACAT[G/T]TTAATGAGAAAACTA | 494470 |
rs772637176 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420722 | TGGTGGTGTGTGCCT[A/G]TAATCCCAGTTACTC | 494470 |
rs772650570 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407053 | GAACTCGACTTTTGC[C/T]TCGGCCTCTACCACC | 494470 |
rs772709315 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337320 | TCCTGTTCTTATTTT[A/G]TGGGTAATTTTTTCT | 494470 |
rs772713590 | snp | G/T | 1.65941e-05 | 0.00288041 | intron-variant | RNF165 | GRCh38.p7 | 18:46456486 | TGTCCCTCAGCTCTT[G/T]CCGGGCCTCTGACTC | 494470 |
rs772739785 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431029 | GGTATTTCTCCTAAT[G/T]CTCTCCCTCCTCTTG | 494470 |
rs772761320 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365498 | ATTTTGTGATCTTGA[A/G]TTTTTTTTTGTTGTT | 494470 |
rs772798368 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446454 | GGTGGGTGGATCACT[G/T]GAAGTCAGGAGTTCA | 494470 |
rs772801242 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335413 | TCTTTCATTTTCTTT[C/T]AATAAAAAATTCCCA | 494470 |
rs772827548 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430395 | CTTCAGAACCACCTC[A/T]TTGCTCTCATTGTTT | 494470 |
rs772831345 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396269 | CACAAGGGAGCAGAA[A/G]TGAAGAGGAGGGAAT | 494470 |
rs772842597 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382945 | CCTTATTTTATGAAG[A/G]CAACGTCATACTCTT | 494470 |
rs772897519 | snp | C/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457317 | TTGGGAGGCGGGAGG[C/G]GGGGGTTCTCGTTTT | 494470 |
rs772916766 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444577 | TCAAGTGATCCTTCA[A/G]CCTCAGCCTCCTGAG | 494470 |
rs772921467 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364924 | ACAGCCCTGACCCAG[A/G]TCTCAGGAGAGCTGG | 494470 |
rs772960511 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368963 | ACTGTCATCATTTCT[A/G]TGTGCCAGGCACTAT | 494470 |
rs772981896 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347461 | CCCCTGGAAAGAGAG[A/T]CACGTGGAGGGGTCG | 494470 |
rs773001124 | in-del | -/TGAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334715 | GTGTGTGTGTGTGTG[-/TGAG]AGAGAGAGAGAGCGC | 494470 |
rs773051312 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400682 | GTGCCTCTCAGTGCA[G/T]TGGGCTCAGACTCAG | 494470 |
rs773078953 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370342 | TCCAAGATAAGACTA[A/G]TAAGGTGCTAAGCCA | 494470 |
rs773106150 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419093 | TGTCCCCGAGTTCAC[C/T]CCAGAAGTAGGCTGT | 494470 |
rs773124237 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375417 | AAATTAGCTGGGTAT[A/G]GTGGTACACACCTGT | 494470 |
rs773139122 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358693 | GGCCCTTACTGACAG[A/G]TTCCAGACCCCCAGG | 494470 |
rs773168440 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348521 | CTGGGACAGTTACCT[C/T]CACAGGAAGAGGTAC | 494470 |
rs773172740 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424759 | GCCTGGAGAAGTCCA[C/T]GGGGCTGTCCAGGTC | 494470 |
rs773183076 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448073 | ATACCCTGACTTTTC[A/G]GTGCCCTGGCCCCCT | 494470 |
rs773185335 | in-del | -/T | 0.000602773 | 0.01735 | intron-variant | RNF165 | GRCh38.p7 | 18:46335866 | TGCATTTATCAAATC[-/T]TTTTTTTTCTTCATT | 494470 |
rs773207003 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418277 | TGGGAGGATCGCTTG[A/G]GCCCAGGAGACAGAA | 494470 |
rs773220605 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368488 | TTCCCTGTGGGTCTG[C/T]GTGTGCCCAGGTCAC | 494470 |
rs773238497 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362069 | AGCCTGCCAAAGGCC[A/C]CCCTGCCACCCCAAG | 494470 |
rs773242132 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46363945 | TTCTTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 494470 |
rs773251421 | snp | G/T | 2.16603e-05 | 0.00329084 | utr-variant-5-prime, missense, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334294 | TCCTGGTCCACGTCG[G/T]CTATCTCGTGCTTCC | 494470 |
rs773259648 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435709 | AGTGAGGGATATGAA[C/T]CAGTGGTCCCTGGGG | 494470 |
rs773335260 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434759 | AGATAGAAGGTGAGC[A/G]CTGTAGGAGGTCAGA | 494470 |
rs773355653 | snp | C/T | 1.83337e-05 | 0.00302762 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433326 | GCCAGGCCTCAGCGC[C/T]CACATGGCCCCGGCC | 494470 |
rs773364115 | in-del | -/TGTGTGTG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46348901 | CTCTCTCTCTCTTTC[-/TGTGTGTG]TGTGTGTGTGTGTGT | 494470 |
rs773365883 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440168 | GTTCTCTCGCTTCCC[C/T]GGTCCTGATATTACA | 494470 |
rs773414483 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351050 | CCCTAGCGGGCAGAC[C/T]CCAGAGCTCACGTGT | 494470 |
rs773443078 | snp | C/T | | | utr-variant-5-prime, synonymous-codon | RNF165 | GRCh38.p7 | 18:46447585 | AGTGTGGATGCTGGC[C/T]TGAGTCCTGCTCAGT | 494470 |
rs773471669 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394279 | AAAGCGAGAGCCCTG[A/G]CCTGGGAATCTCTAG | 494470 |
rs773482802 | snp | C/T | 1.95452e-05 | 0.00312605 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433242 | CTCCTGCCGCCACTT[C/T]CACCTGGGCCCCCCG | 494470 |
rs773503360 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361153 | CCCCTTGACACCATA[C/T]TGAGTCTTTTCTAGT | 494470 |
rs773534422 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380506 | GGTGTGCCAGGCATC[A/G]TTCTCAGGGCTCTAC | 494470 |
rs773538085 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426214 | CTGTTCCCTTCTGCC[C/T]GTCCACATTTGGCTT | 494470 |
rs773568779 | in-del | -/AAAAAAA | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461647 | AACAAAACTCAGTCC[-/AAAAAAA]AAAAAAAAAAAAAAG | 494470 |
rs773595042 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370008 | TGATTCTGGTGTGGA[C/T]TCTGGGGGCCATAAC | 494470 |
rs773619605 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344842 | TGAGGAGAGAGACAG[C/T]GGAGGTAGCTGGGCC | 494470 |
rs773620308 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379757 | ACATGTGACTTCAGG[A/T]CCACAGACAGGGGAA | 494470 |
rs773633899 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438874 | CCTGCATTTTCTCAT[C/T]TGATGCTCCAACATT | 494470 |
rs773649290 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403346 | GAAGCCTGTGCTGTG[C/T]TCCTAGAGAAAGCTC | 494470 |
rs773650541 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412238 | CATGATCATATGTCC[C/T]AGTTTGGGGAAGGAT | 494470 |
rs773653701 | snp | A/G | 1.74178e-05 | 0.00295103 | intron-variant | RNF165 | GRCh38.p7 | 18:46450656 | TCCTGTGTGCATGTG[A/G]GCATTTATACATGCT | 494470 |
rs773729862 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448605 | GAAGATGCCTGCCTC[A/G]CCCATCTCACAGGGC | 494470 |
rs773742085 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444538 | GGTGGCATCACAGCT[C/T]ATTGTAGCCTCAACT | 494470 |
rs773758873 | in-del | -/GTGTGTGTGAGAGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334708 | TGTGTGTGTGTGTGT[-/GTGTGTGTGAGAGA]GAGAGAGAGCGCGCG | 494470 |
rs773794109 | snp | A/G | 1.66263e-05 | 0.00288321 | intron-variant | RNF165 | GRCh38.p7 | 18:46456469 | GTCCCTGCTCCGCTC[A/G]GTGTCCCTCAGCTCT | 494470 |
rs773804423 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395377 | TGCAGGGGCTGTTCC[A/G]TGCTTTGTTGGGTGT | 494470 |
rs773810778 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453149 | TGGATTTATTCGTAA[A/G]TGATTTCAACCGCAG | 494470 |
rs773810946 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377974 | GACTGCACAACAGAG[A/G]TGGTGCAGGATAGAG | 494470 |
rs773850789 | snp | C/G | 2.22393e-05 | 0.00333454 | intron-variant | RNF165 | GRCh38.p7 | 18:46433538 | CGGAGGTGGGGACCC[C/G]GATGGGGTCGGGTGA | 494470 |
rs773947286 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457057 | CTGTGGATGGCAGCC[A/G]GAGCATGTTAGCTTA | 494470 |
rs773955576 | in-del | -/CCTTATT | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390792 | TTCTGAGCCGGGCAC[-/CCTTATT]CTTGGTGCTTCATTC | 494470 |
rs773958750 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413802 | TCCTATGGTGCAAAA[G/T]GATGTACATACAGAG | 494470 |
rs773958870 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404970 | GACATATTCAGCTCC[A/G]TTTGGCTCCAAAGTC | 494470 |
rs774001074 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347379 | CATCCTGCTGAAATT[A/C]TCTGCCTCCTCTCCT | 494470 |
rs774050528 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400319 | AGTGATGACAGGAAC[C/G]TGATTGTTCATTTCT | 494470 |
rs774059734 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382909 | TGCCAAACACCACCA[C/T]GAGCTCATGTAGTCC | 494470 |
rs774133427 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335320 | GCACGGTCCCCTTTC[C/T]CCACATCCCCTCTCC | 494470 |
rs774153739 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440522 | GAAAAGGAGAAACTA[C/G]TATATTTGGAAACAA | 494470 |
rs774188523 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362972 | TGTGGAGTCCACAGA[A/G]ATCTTTCCACGCCCA | 494470 |
rs774195436 | in-del | -/AGG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46456293 | GAGGATGAAAAGTGT[-/AGG]AGAACAGTGTGGTGT | 494470 |
rs774196363 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367833 | TGCTTGAGACAATTC[A/G]GATTTCTCGGCTCTG | 494470 |
rs774220018 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349228 | GGTGGCTTATAAATA[A/G]CAGAAGTTTGTTTCC | 494470 |
rs774229723 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423663 | CAGCACTGGGACTCA[G/T]GAGGCCTGGATGCCA | 494470 |
rs774249096 | in-del | -/TGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355910 | TGACGACAATGGTGA[-/TGA]TGATGATGATGATGA | 494470 |
rs774255561 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409121 | CCTGGCATACAGGGG[A/G]TGCAATAGAAATGTC | 494470 |
rs774315618 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422474 | GGGGCCATGTTGAGT[A/G]GAACGTGAAGTCTGT | 494470 |
rs774321724 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435589 | CCTGGTTCTAGCAAT[A/T]AGCTCAGATATTACT | 494470 |
rs774329531 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399451 | ATTTGTACTGGGCCT[C/T]GGCACGTGACCTCCT | 494470 |
rs774351479 | snp | A/T | 2.05219e-05 | 0.0032032 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433215 | TCAAAGGTCTCAGCA[A/T]CCTCACGCTACCTCC | 494470 |
rs774358266 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376579 | GGATGTTGCAAGATT[A/T]TGCCCCTGTGACTTG | 494470 |
rs774358329 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451487 | TCCAGATAATGGAAT[A/T]TTATTCTGCAATAAA | 494470 |
rs774377523 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344788 | CAAAGAACTGGTCCT[C/T]GCATGGCCCAGAGGT | 494470 |
rs774383086 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422443 | TATCCATGCAGAGGG[A/G]AGAGGAGGCTCCCTG | 494470 |
rs774385080 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341168 | ATGTGGGAGAAAAGG[A/C]TTGAAGAGGTTTTGA | 494470 |
rs774386447 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418324 | ATTATGCCATTGCAC[A/T]CCAGCCTGAGTGACA | 494470 |
rs774401799 | snp | A/G | 1.64776e-05 | 0.00287028 | utr-variant-5-prime, missense | RNF165 | GRCh38.p7 | 18:46447565 | TGTTTCCCTGCAGGG[A/G]TCTCAGTGTGGATGC | 494470 |
rs774447195 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379715 | CAGCCACCCTGGGGA[A/G]CTAATGTACTTTCTG | 494470 |
rs774456603 | snp | A/T | 1.6473e-05 | 0.00286988 | missense | RNF165 | GRCh38.p7 | 18:46447673 | ACCACTTTCCCAGAA[A/T]CTCCTCCTCCACACA | 494470 |
rs774473356 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351826 | GGCAGGGCCTGGCTA[C/T]GTCAATCCACTGCGC | 494470 |
rs774519389 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346560 | ATCAGGCAGTCTTTA[A/G]CTTGACCACCTACCA | 494470 |
rs774538980 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438469 | AGGATTGGGATGACT[C/G]TGTTCCAAGTTCCTT | 494470 |
rs774546923 | in-del | -/GTGAGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334714 | TGTGTGTGTGTGTGT[-/GTGAGA]GAGAGAGAGAGCGCG | 494470 |
rs774550637 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360922 | GGCGTCAGCCCCACA[A/G]CAAGTGACTTTCCAT | 494470 |
rs774574061 | snp | A/G | 2.24268e-05 | 0.00334857 | intron-variant | RNF165 | GRCh38.p7 | 18:46334421 | CCGCGGGCGGCCGGG[A/G]GCTCAGGGCACACCC | 494470 |
rs774576815 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409760 | GATGGGCCCTTCAGG[C/T]GTCTTGCTTTCTTGG | 494470 |
rs774618831 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437191 | GAGGCCCGCCTGGTC[C/T]ACCCTTGGGCTCTTT | 494470 |
rs774627855 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428175 | CAGCACGTTGGGAGG[C/G]CGAGGCTGGCGGACC | 494470 |
rs774632245 | snp | A/G | 3.30978e-05 | 0.0040679 | intron-variant | RNF165 | GRCh38.p7 | 18:46450249 | ATGCTGGGCTCATGG[A/G]GAAACCTTGAATCCT | 494470 |
rs774648767 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359742 | CTCCTTCTACTTATT[G/T]CTCTGCCATTCACAA | 494470 |
rs774657994 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369129 | TTGAATCTAGACCTC[C/T]ATGATCTAAAAGGCC | 494470 |
rs774686070 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343013 | CTGTTTTCACAAGCA[C/T]TGCTTTTAATGGCTA | 494470 |
rs774750026 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378479 | TGGGCTTTTGCACCG[C/T]TTTCTGTAAGTCACC | 494470 |
rs774766491 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353981 | CACCCCCTCATTTTA[C/T]GGGGACTTGGCCAAG | 494470 |
rs774775066 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429996 | AGATCTCCTCCCAGA[A/G]TCCCCGCCCTCCTGC | 494470 |
rs774783187 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400501 | TGTAACGGGCAGTTC[A/G]TAAGACTGTGTGACC | 494470 |
rs774789878 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411370 | TGGCCTTTGCAGATG[A/G]GCTGACACTATGTGA | 494470 |
rs774849565 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396144 | GGCTTGGAGCTAGAA[C/G]AGTCACTTCCACCTT | 494470 |
rs774859195 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422565 | TTGCTCCCTGAGGAC[A/C]CAAGACTTGCTCTCT | 494470 |
rs774871419 | snp | C/T | 0.000132482 | 0.00813779 | intron-variant | RNF165 | GRCh38.p7 | 18:46456117 | TCCCTCTCCCCTCTC[C/T]TATAGGTATTGGTGA | 494470 |
rs774877881 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410424 | GTGGAGGAGGAGGCA[A/G]CCAGCCAGCTGTGTG | 494470 |
rs774880051 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361403 | GTGTCGATCTGCTGT[A/G]CATATGCAGCATATA | 494470 |
rs775001127 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413506 | GCCTTGTCTTATTAG[A/C]CCTGCGACCTGGACT | 494470 |
rs775005957 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429387 | TCAACCGCAGTGCGC[C/T]TTTAACTCTTCTTCA | 494470 |
rs775021113 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459389 | ACACATCTTCAAGGC[A/G]GCAGAGCTGTGCGCC | 494470 |
rs775036631 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356300 | GAAGCTTGCATTCTA[C/G]TGGGGAAGGCAGACA | 494470 |
rs775038296 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371189 | GGGAAACAGCTCCCA[C/T]GAATCAATTATCTCC | 494470 |
rs775052906 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346011 | TGAGGGCTGGTGGAC[A/G]TTTTGTGTTTTGACT | 494470 |
rs775088401 | in-del | -/GTGTGTGAGAGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334710 | TGTGTGTGTGTGTGT[-/GTGTGTGAGAGA]GAGAGAGAGCGCGCG | 494470 |
rs775120005 | snp | C/G | 1.81539e-05 | 0.00301275 | intron-variant | RNF165 | GRCh38.p7 | 18:46450834 | AGCCTGCATAGTCAG[C/G]GAATGGGGCAGGGGG | 494470 |
rs775126542 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366969 | GGGCCCAGTCATCCC[A/G]TTGGACTTCTGAGAT | 494470 |
rs775156274 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367714 | CGGTGTCCCCACCAG[C/T]AGCCTGTGACTTTGT | 494470 |
rs775167162 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455050 | ATTTTCAAATAATCA[A/G]CATAAAATGAAAAAC | 494470 |
rs775198185 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408218 | AGAGGCTGTGATGGA[A/G]GCTACTGATTCAGGG | 494470 |
rs775200935 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390734 | GGGAAGGCGGTGGCT[C/G]GGAATCCTATACTGG | 494470 |
rs775244524 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376353 | TCCGTGTGGTTAAGG[A/G]GCATGGCCAGACAAC | 494470 |
rs775275721 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434284 | GGTTTTGACTATTGA[C/T]GTTTACCATATTAAA | 494470 |
rs775287332 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389710 | ATAGCAGCTCTCTCC[A/G]GGAAGTGAAATGGTC | 494470 |
rs775363001 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant | RNF165 | GRCh38.p7 | 18:46447550 | ATGGTTCACTGAGGC[C/T]GTTTCCCTGCAGGGA | 494470 |
rs775370678 | in-del | -/AC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356609 | AACTACTCACTCTGA[-/AC]ACACAGAAGGGAGTA | 494470 |
rs775412605 | in-del | -/AAAAAAAA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441864 | GAGACTCCATCTCAA[-/AAAAAAAA]AAAAAAAAAGAGGCC | 494470 |
rs775473426 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397244 | TCCTAGGGTCAGGAG[A/T]GAGGACTGGGGGTGG | 494470 |
rs775473569 | in-del | -/CCA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355748 | CCTCTATCTCTCCAC[-/CCA]TCATGTGCACACATG | 494470 |
rs775490181 | snp | C/G | 4.94205e-05 | 0.0049707 | missense | RNF165 | GRCh38.p7 | 18:46450345 | AGCTTCACTTCCTTG[C/G]TCTCCAGGGACTAAA | 494470 |
rs775492402 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407448 | TATTATGTGGCTTTA[C/T]TTCTCTCCCCAAATA | 494470 |
rs775512105 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350963 | TCCCTCTGCCCCTGG[C/T]GTGTGTGCAGGAGGT | 494470 |
rs775513125 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425137 | ACACTGGGGAAGAGT[A/G]AGGCTGGCTCAGTAG | 494470 |
rs775516384 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447434 | GGAAAGGCTGGGAGA[C/T]GTAAAGTTCCTTGCA | 494470 |
rs775526902 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381916 | TTTGGAGAGATGTGC[G/T]ACTCCCTTGCTCTCT | 494470 |
rs775545275 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343620 | AGCCTGAGTACTCCG[A/C]GACTTCACTGCCTAT | 494470 |
rs775560258 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46376591 | ATTATGCCCCTGTGA[-/C]TTGGAAAGAAATTTC | 494470 |
rs775578549 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445958 | CTGTTTTTCCTGTAG[-/T]TTCCCCTTACCTGGA | 494470 |
rs775600070 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350228 | AATATTTCAACAGGA[A/G]ATGCAGGCCTTATCT | 494470 |
rs775605907 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459533 | TCTGCCCCAGGCTAA[C/T]ATTAGGGACTGGGGA | 494470 |
rs775639367 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435927 | TCAGGACTGAGGAGG[C/G]GAGCTGGGGAGAGAG | 494470 |
rs775639458 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451587 | ATCACTTTGGGCCAG[G/T]AATTCAAGACCAACC | 494470 |
rs775653354 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400667 | CCCGGGTGTGTCAGC[A/G]TGCCTCTCAGTGCAG | 494470 |
rs775690055 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369030 | GTAGTTTAAGTGTTA[C/T]TCTACAGAGATTAAG | 494470 |
rs775770813 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359120 | TTCATAGGGCTCCCA[C/T]GAGAGGAAGACGTTA | 494470 |
rs775779725 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378439 | ATTCCCCCTGACCAC[C/T]GTGGAGGGGCAGCGT | 494470 |
rs775781835 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368500 | CTGCGTGTGCCCAGG[A/T]CACCTTGATCAAAGC | 494470 |
rs775817079 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352077 | TGGCAGCCCTGTCCT[A/C]TACCTCCCAGGCCTT | 494470 |
rs775821551 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341626 | CTTTACATACAGATT[C/T]CTGGTTGGGGTAGGA | 494470 |
rs775830163 | snp | G/T | 1.83407e-05 | 0.0030282 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46456012 | CAAGAAGGATGAGGG[G/T]GAGGAGTCAGACACA | 494470 |
rs775856932 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394496 | TGGGTCACGAGTCTC[C/G]ATCCTCCACCTTCCC | 494470 |
rs775871859 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377764 | GGCATTGTGAGATGA[A/G]TAGGAGTTTGATAAA | 494470 |
rs775884897 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46386119 | GCCAAGGCCCATCTG[C/T]CCAGGGGCCATGTTC | 494470 |
rs775885361 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372198 | TCAGAGGCACTGAAG[A/G]GTCCTCCCTGGGGCC | 494470 |
rs775962389 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404845 | ACAACTCAATGAAGT[A/C]GGGATTATTAGTTCC | 494470 |
rs775968050 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412724 | CCCCCACCCCTCCCA[A/G]CTCTTAGAAAATGAC | 494470 |
rs775973088 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395239 | CAGGGGTCCTTGAGC[C/T]CACGTCTCCAGGGGA | 494470 |
rs776029160 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381174 | AGGAGGCATTGCTGT[C/T]TTTGTCAGCCAGGCA | 494470 |
rs776030565 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358486 | AGCCTGAAGCGTACC[C/T]GAAAGGTAACCCACT | 494470 |
rs776033062 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429569 | GTTTTATTGTTAATA[C/T]AGAAATGATGTTTAC | 494470 |
rs776077693 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379314 | CAAACACAAAACCCT[C/G]TCCTTAAACTTAACT | 494470 |
rs776094595 | snp | C/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332924 | GCCCGTGGGTGGGCC[C/T]CTGAAGCATTCTCTG | 494470 |
rs776107075 | in-del | -/GGGCAGGGCCAGGGCGT | 2.60444e-05 | 0.00360853 | intron-variant | RNF165 | GRCh38.p7 | 18:46433556 | TGGGGTCGGGTGAGG[-/GGGCAGGGCCAGGGCGT]GGGCAGGGCCAGGAC | 494470 |
rs776111318 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46427845 | GGAGTGGGAGAGAAG[A/G]GAGTTCTCAGAGCTC | 494470 |
rs776132211 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361559 | GTTTCTTTTGGATGC[G/T]TTCAAAGATGGTCTT | 494470 |
rs776150375 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421687 | GGCTTCTTTCCCTTA[C/T]TCCTGGTCCATGATG | 494470 |
rs776165171 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379911 | TGGCCTCCTTGGCCC[A/T]CTGGGACGTTGCTGC | 494470 |
rs776173953 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365646 | GTAGCTAGGATTACA[A/G]GCACATGCCACCAAG | 494470 |
rs776213163 | in-del | -/GTGTGAGAGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334712 | TGTGTGTGTGTGTGT[-/GTGTGAGAGA]GAGAGAGAGCGCGCG | 494470 |
rs776229595 | in-del | -/CA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406073 | TCCCACATACACACT[-/CA]CACACACTGACCTTG | 494470 |
rs776245421 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420787 | GAGGTGGAGGTTGCA[A/G]TGAGCCTAGATCGCA | 494470 |
rs776274146 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422740 | GCCAAAAAGGGCCCT[C/G]GAAGTACTCCAGGTC | 494470 |
rs776281736 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356431 | AGGTGCTTATTTTAT[A/G]CCTGGCACTCAGAAA | 494470 |
rs776297290 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453262 | TCTACAGGGGAAAAT[A/G]ATCATTCTCTGGAGA | 494470 |
rs776312976 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46337734 | CTTGCTTTTCTATCC[C/T]CACCCTCACCCACCC | 494470 |
rs776317162 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416018 | GGGGTTTGTCCTCAG[C/T]CTTCCTGACTTTGCT | 494470 |
rs776321880 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398847 | CTTCTGCCCTCTCTC[A/G]TCTGGTCATTATCTC | 494470 |
rs776326589 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432411 | CCTTAAAAGTGTATG[C/G]AAAACAACTTCTGGT | 494470 |
rs776333346 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431283 | CACTTTGTAATCAAA[C/T]GACCGATCACTCTTA | 494470 |
rs776344786 | snp | C/G | 1.6477e-05 | 0.00287024 | missense | RNF165 | GRCh38.p7 | 18:46456616 | GTGGACATTGAGACA[C/G]AACTGGGAGCCGACA | 494470 |
rs776351776 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354926 | TTCTTTTTCACCATA[G/T]ACACACTCCTTCATT | 494470 |
rs776367123 | snp | C/T | 4.95552e-05 | 0.00497747 | intron-variant | RNF165 | GRCh38.p7 | 18:46447526 | AACCTGGCTAAATCA[C/T]ACCACCCTATGGTTC | 494470 |
rs776371284 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375064 | GCTTTGCCGGAGGAT[C/T]TGGGGTTTCTCCCCA | 494470 |
rs776401796 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46335865 | CTGCATTTATCAAAT[A/C]TTTTTTTTTCTTCAT | 494470 |
rs776409478 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46447316 | GGAGCTTTGGTCCCC[C/T]AGTTTAAAGAAATTT | 494470 |
rs776410906 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397095 | GCTTCCCCTGGGCCC[A/G]GCCTGGAACCCAGGC | 494470 |
rs776470974 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383749 | TTAATACAGACGGGG[C/T]TTCACCGTGTTGGCC | 494470 |
rs776516168 | snp | A/G/T | 3.2948e-05 | 0.00405871 | missense | RNF165 | GRCh38.p7 | 18:46447684 | AGAAACTCCTCCTCC[A/G/T]CACAGATGGTAAGTG | 494470 |
rs776543734 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369974 | ACACATGCACACACA[C/T]GCACCCTAGACTTGG | 494470 |
rs776544301 | snp | C/T | 4.40306e-05 | 0.00469184 | intron-variant | RNF165 | GRCh38.p7 | 18:46334400 | GCACCGGGGCGGGGG[C/T]GGGCGCCGCGGGCGG | 494470 |
rs776565244 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341525 | AGAATTGAGTTTAGT[G/T]TACAGATAAGCACAT | 494470 |
rs776590828 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406006 | TCCCCTCAGACACTC[A/G]CATACATACCCCTGT | 494470 |
rs776628256 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400389 | CAGTGCATAGATATG[A/G]CTTTAAGAGCTCTGA | 494470 |
rs776659763 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359400 | CAAAGGCCTCCTGAG[C/T]AGGTGGCACATGGAG | 494470 |
rs776663968 | snp | A/G | 1.65855e-05 | 0.00287967 | intron-variant | RNF165 | GRCh38.p7 | 18:46456489 | CCCTCAGCTCTTGCC[A/G]GGCCTCTGACTCTCC | 494470 |
rs776671251 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448549 | TTCCTGTGGTCAGTA[C/T]CTCCCTAGGCTTTGG | 494470 |
rs776672074 | snp | G/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457521 | AGAGTTCATCTAGGC[G/T]GGGCTCCCCAGGCCC | 494470 |
rs776687664 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418362 | ACACTGTCTCCAAAA[A/G]AAAGGTGAAAATGGG | 494470 |
rs776722490 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395119 | AGCTGGACTCCCATT[A/T]TATGGAGCTATGGGG | 494470 |
rs776753456 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351311 | AGTTTGAGGGCTGGG[A/G]GCAGGGATGGGCTGT | 494470 |
rs776754506 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433933 | ATTCTAACACCCAAG[C/T]ACCCTAAAGAATACC | 494470 |
rs776769303 | in-del | -/TTTTG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407557 | TCTTGTTTAGTGTTT[-/TTTTG]TTTTGTTTTGTTTTG | 494470 |
rs776777835 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428456 | AAACAAAACCAGGCC[A/G]AGGGGTTTGGATTTC | 494470 |
rs776778722 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449838 | TTGGGTATTTCTTCA[C/T]AGCAGAGTGAGAATG | 494470 |
rs776819070 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377623 | TATCAGGTAAAGGGA[A/G]AGGCACATATGAAGG | 494470 |
rs776938961 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351186 | AAGGAGCTTCCCACT[A/G]GAGTCGACACTAAAT | 494470 |
rs776949892 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341463 | TTTGGAGAGTAGAAG[A/T]CCATGAAGACAAACG | 494470 |
rs776961545 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372018 | GTAGGGTCCTGGATG[A/G]GCCATATCAGGAGAT | 494470 |
rs776962645 | in-del | -/ACATTCATCAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378917 | CCACTCTTCCTCCCC[-/ACATTCATCAG]AGTGTGGCTCTGATG | 494470 |
rs776971638 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46417132 | CTTGTCACCTGTACC[C/G]TTGAAATGAAATATA | 494470 |
rs777003105 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403396 | CCCTCCCTGCCCCCC[A/G]TCTCCCTCTAGGTTG | 494470 |
rs777019560 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380712 | GAGACTCTGGAGCCT[C/T]GAACCCAGCCTGTGT | 494470 |
rs777050455 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449969 | ATCTATTGTACCTCA[-/G]TTTACCCCATCAGTA | 494470 |
rs777077140 | snp | A/G | 1.73933e-05 | 0.00294895 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433371 | CGCCCTGCACCAGTC[A/G]CTGACCCCGCTGCCC | 494470 |
rs777077458 | in-del | -/C | 1.77002e-05 | 0.00297486 | intron-variant, frameshift-variant | RNF165 | GRCh38.p7 | 18:46433358 | ACCAGCACAGCGGCG[-/C]CCTGCACCAGTCGCT | 494470 |
rs777104037 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394388 | AAATGTAATTGTGAC[A/G]GGGTTCACTCTCGGA | 494470 |
rs777104345 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404148 | TTAAATATGATTTAC[A/G]GTCTAAAACCCCTCA | 494470 |
rs777119091 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46413263 | TTATAAAGCAGCGTC[A/G]CTCAAGCCCAGCCCT | 494470 |
rs777138749 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442679 | TCAAGTTAGTCGACA[G/T]TATTGTTCAGGTCTT | 494470 |
rs777207018 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432166 | CTTGGCCTCATTAAA[A/G]GCCTCCCTTTGGCAC | 494470 |
rs777228356 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393114 | CTTCCTGCTGTCTGA[A/G]CTTCACAAATCCAGA | 494470 |
rs777228419 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345817 | TGTGCCCCGACTCCC[A/G]GGGTGGCTATACACT | 494470 |
rs777228558 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440917 | CAGTGCACTGCTTGC[C/T]TCATTGAATGGTTTG | 494470 |
rs777244329 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361529 | CTGTGCCCGGCCACA[C/T]GGTTCCCCTCCACAG | 494470 |
rs777250722 | snp | A/G | 6.79198e-05 | 0.00582712 | intron-variant | RNF165 | GRCh38.p7 | 18:46450682 | ATGCTGAGCACACAT[A/G]TGCACATTTTTCTCT | 494470 |
rs777270990 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459340 | GATTGGATGCTTGCT[A/G]ATTTCCTTCTGACAC | 494470 |
rs777302024 | snp | C/T | 1.93676e-05 | 0.00311182 | intron-variant, synonymous-codon | RNF165 | GRCh38.p7 | 18:46433251 | CCACTTCCACCTGGG[C/T]CCCCCGCAGCCGCAG | 494470 |
rs777302163 | snp | A/C | 1.76424e-05 | 0.00297 | intron-variant | RNF165 | GRCh38.p7 | 18:46450818 | GGTCTGCCAGCAGGC[A/C]AGCCTGCATAGTCAG | 494470 |
rs777314394 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344989 | GGACATCAGACCTGT[C/G]TCCCTCCCTAAGGGC | 494470 |
rs777316294 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46356944 | GTGATCTGTGCCCTG[A/C]ATTGCAATGCTGAGT | 494470 |
rs777316988 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384530 | TCATGGATACACACC[C/G]CATGATACACACACC | 494470 |
rs777334305 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370368 | AGCCAAAATTAGAAG[A/C]AGGGAAATCAGTGTG | 494470 |
rs777354009 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349808 | CAGCTACATTTGACA[C/T]GCTGCACACGATCCA | 494470 |
rs777364735 | snp | C/T | 2.44263e-05 | 0.00349465 | intron-variant | RNF165 | GRCh38.p7 | 18:46334380 | CGGAGCGTGGATCGC[C/T]GCAGGCACCGGGGCG | 494470 |
rs777371217 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46439635 | TTGGTATTTCTGAAG[C/T]TGGTGCCCATAGAGG | 494470 |
rs777416072 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393279 | TTTGCGGAAAACTTT[A/G]TGGGGTGACTGTTCC | 494470 |
rs777469031 | snp | C/G | 7.95071e-05 | 0.00630454 | intron-variant | RNF165 | GRCh38.p7 | 18:46433178 | GGAGATGTCTCTGTC[C/G]TTGCCTTCCAGGTGC | 494470 |
rs777507989 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46456588 | CATGAGCAAGAAATG[C/T]CCCATCTGCCGAGTG | 494470 |
rs777524438 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46360757 | TTGCCCTCTAATACG[A/C]CTGGGCACACGAGGC | 494470 |
rs777558794 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410883 | CCTTTGTAATGTTTA[C/T]GGGAGGCCCTGCCTC | 494470 |
rs777563860 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415896 | GAGGGACCTGGAGTG[C/T]CAGGTGGGAGGAGAG | 494470 |
rs777591536 | snp | G/T | 1.64738e-05 | 0.00286995 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46450334 | CCCTTACCCTCAGCT[G/T]CACTTCCTTGCTCTC | 494470 |
rs777636715 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344344 | GTGGAGGCGCTCTCC[A/T]TGTCTTCCCCCTTCT | 494470 |
rs777637520 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381319 | AAGAGCAGGTTTAGC[C/T]GCAAGAAACAGTGAC | 494470 |
rs777653265 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437900 | TGGGCAGAGGGTGGG[C/T]GGAGGGTGAGCACCT | 494470 |
rs777655555 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425452 | CCTTTCAGGCTGCCT[A/G]TTCTTCCCCTCTTTC | 494470 |
rs777680319 | in-del | -/CAAGCCCA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46437544 | GGCTGCAAGCCCATG[-/CAAGCCCA]TCCAGCCCAAGGTCG | 494470 |
rs777740698 | in-del | -/T | | | intron-variant, downstream-variant-500B | RNF165, LOC105372095 | GRCh38.p7 | 18:46387668 | GGGTGCAAGGGCCCC[-/T]GAATGGGAACAGACC | 494470 |
rs777743295 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452400 | TTCTCCCACGTCAGC[C/T]TCCCAAGCAGCTGGG | 494470 |
rs777744829 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443367 | ATATTCCTATTTAGC[A/G]TATCACACTCTACCC | 494470 |
rs777786714 | snp | C/G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379279 | TTTAAGCTTATTGAC[C/G/T]GTACTTGTCTCCACT | 494470 |
rs777795896 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46379711 | CATTCAGCCACCCTG[G/T]GGAGCTAATGTACTT | 494470 |
rs777819848 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372579 | GACACCATGTGAGGA[C/T]ACGTGACCATGGTCA | 494470 |
rs777825780 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46441048 | CACCCAGGCTGGAGT[A/G]CACCTTGGCTCACTG | 494470 |
rs777871846 | snp | A/G | 1.78557e-05 | 0.0029879 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433492 | CAGCACCGCAGGCTG[A/G]TCTCGCACCCCAGGT | 494470 |
rs777878386 | snp | C/G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46378414 | CTGGGGCATGTCCTC[C/G/T]AGCACATTCATTCCC | 494470 |
rs777891354 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46362908 | AAAGGGGAAGAAAAA[A/T]CACCGGGAGGGATAG | 494470 |
rs777906227 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382372 | CTACATAGCTCAGAG[C/T]CCTGGGTTGGTCCTG | 494470 |
rs777922048 | snp | A/C | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46332546 | CAACTCCTCCCCTTG[A/C]CACCCACTGGGCTGG | 494470 |
rs777930331 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428391 | TTCAGCCTGGTGACA[C/G]AGCGAGACTCCATCT | 494470 |
rs777980014 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419815 | AGCCTATAGCTCTGC[C/T]TTTCCCAGGCATCTC | 494470 |
rs777983026 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371925 | CATTTACTCTTATCC[A/G]TTCAACTAACAGCTG | 494470 |
rs777991974 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381732 | GCTACACTGGAGGTT[G/T]AGGTGGGAGGATCGC | 494470 |
rs778042992 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404629 | ATGGTGGCGGGAGCC[C/T]GTAATGCCAACTACT | 494470 |
rs778046746 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414356 | CCAGGGCTCTGTGTA[A/G]GTGCTGCTTACAGGC | 494470 |
rs778066612 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46399880 | TTCCCTGAGGGTGGC[C/G]CCTCACAACCCACAT | 494470 |
rs778105748 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46357381 | TGGAGGTAACTGAGA[C/G]TAAGCAAATGATCCA | 494470 |
rs778113243 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46347638 | TGTAATGTACCCACC[A/G]TGAGTGGCTCCTGGC | 494470 |
rs778134305 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422692 | CCAAAAGGAGGGTAG[A/G]TGTTGCAGGGAATTT | 494470 |
rs778141123 | snp | C/T | 1.68074e-05 | 0.00289887 | missense, intron-variant | RNF165 | GRCh38.p7 | 18:46450785 | AGGTTCACCTTCCCC[C/T]ACAAGTATAAGAAGG | 494470 |
rs778167990 | snp | C/G | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389539 | GTCTCCCACCCCGGT[C/G]TAGAGTTTGCTGTTG | 494470 |
rs778192386 | snp | A/G | 2.64897e-05 | 0.00363925 | intron-variant | RNF165 | GRCh38.p7 | 18:46455947 | TCTGCCCCAGGTAAT[A/G]AATACTACTCTCTCT | 494470 |
rs778200531 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455653 | ACCAGCCTGACCAAC[A/C]TGGTGAAACCCTGTC | 494470 |
rs778221183 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340646 | GAGTCCTAGCCCAGT[C/G]TTGACCTGGAAGGGT | 494470 |
rs778223262 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433821 | GTCGGGGACGGGTAA[C/T]TGGTGGTCCACGATC | 494470 |
rs778237839 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346417 | TTAAATCACCCGAAA[C/T]AGAAACTAAGAGCTC | 494470 |
rs778300853 | snp | A/G | 4.94189e-05 | 0.00497062 | utr-variant-5-prime, synonymous-codon | RNF165 | GRCh38.p7 | 18:46447611 | TCAGTTCCAGGTGCG[A/G]CCCATCCCTCAGCAC | 494470 |
rs778332621 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371023 | CACAGTTCCACATGG[C/G]TAGGGAGGCCTCACA | 494470 |
rs778403172 | snp | A/C | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458096 | GGTCCTGCTACCTCA[A/C]CTAGATGTTGTGAGG | 494470 |
rs778415043 | in-del | -/CT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414237 | ACACAACCTGCCTGA[-/CT]CTCTGGGCAGATGTG | 494470 |
rs778439607 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408787 | TATCTTGGAACAGAT[A/G]GTTGTGAATGAGCTG | 494470 |
rs778445000 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415789 | ATTGCACTGGATGGT[G/T]GTAGGGCTGAATTTG | 494470 |
rs778446548 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401874 | CGGAGGCTTCACACT[A/G]GGAGGGACCATCAGC | 494470 |
rs778451844 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366501 | ATGATGAGGCCCAGA[C/T]AATTTGGTGAGGAGG | 494470 |
rs778453412 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392980 | CCTGGAAGGGAAATC[A/G]GCAACCATAAGGCAG | 494470 |
rs778476821 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369509 | AAGGGAGTCAGGGAA[A/C]GAGAAATGCCTCAGA | 494470 |
rs778482978 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46359223 | GGCCCAGGGGTTCAG[C/G]GTGGGCCAGGTGGGC | 494470 |
rs778516474 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366935 | GCTGGAAGGAACAGA[-/T]TTTTCTAACACTGGC | 494470 |
rs778564942 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368805 | GGGGAAATCATTGAA[C/T]ATCTTTGAACCTCAA | 494470 |
rs778613535 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46425280 | CAGGATCCCACATCC[C/T]TGGAGCAGGCAGAGC | 494470 |
rs778614980 | snp | C/G | 1.64754e-05 | 0.00287009 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46450301 | TACCCAACAGGTCGT[C/G]CATGAAATCCGAAAC | 494470 |
rs778636580 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377501 | AGCAAGTGGCTGGAG[C/G]GGATTTTCCTGGAGG | 494470 |
rs778675551 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454981 | AATTTGAGACTTTAC[A/G]TAATGGTAAACTACA | 494470 |
rs778695142 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365178 | GTTGCTCTTTGGAAC[C/T]TAACCTGGCTGAAGG | 494470 |
rs778696962 | snp | A/G | 3.4411e-05 | 0.00414781 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334264 | CCGCCGCCGCCGCGC[A/G]AGGAGCCAGGATGGT | 494470 |
rs778698119 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445568 | CTGCCTCTTCTCTCC[-/A]AATCATGGTACCACA | 494470 |
rs778700409 | snp | A/G | 0.000184281 | 0.00959721 | intron-variant | RNF165 | GRCh38.p7 | 18:46435248 | GAACTAGTGGCCTGG[A/G]TAGCCCCTGACACGA | 494470 |
rs778717011 | in-del | -/TCC | | | | | GRCh38.p7 | 18:46459828 | GAGACCACTGGTAAG[-/TCC]TCCTCCTGCTCAACT | 494470 |
rs778743562 | snp | C/T | | | | | GRCh38.p7 | 18:46378279 | CTAGTTTACACACAC[C/T]GTAGTTTCTCCCTTT | 494470 |
rs778750289 | snp | C/G/T | 0.000108622 | 0.0073689 | | | GRCh38.p7 | 18:46334366 | TTCGGGGTCTGCTTC[C/G/T]GAGCGTGGATCGCCG | 494470 |
rs778762604 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343168 | CCATGTGGGGAGGAG[A/G]TAGTGAGTGGATCAG | 494470 |
rs778770380 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46353647 | AGAGAGTGGGAGTGA[C/T]GGGGCCCTGGAGACG | 494470 |
rs778793402 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436826 | ATTGCAATTTGGATT[G/T]AATTCTGTCCCTCAG | 494470 |
rs778810034 | in-del | -/GGGGCG | 2.78734e-05 | 0.00373308 | intron-variant | RNF165 | GRCh38.p7 | 18:46334389 | ATCGCCGCAGGCACC[-/GGGGCG]GGGGCGGGGGCGGGC | 494470 |
rs778814800 | in-del | -/GG/GGGG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397487 | CATGCTGAGGTGTGA[-/GG/GGGG]GGGTGTGTGTGTGTG | 494470 |
rs778818413 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46419377 | TCAATGGGGGAGGAG[A/G]TGGGGGAACTTCATA | 494470 |
rs778832927 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46381541 | AAACATCCTTCAAGA[C/T]TCTCAGGTGGCCTGG | 494470 |
rs778835340 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46387008 | AGGCACTTGGCCAAC[A/G]TTCTCTTCTAATTCA | 494470 |
rs778894370 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46455561 | GAACTTTATGGCCGG[G/T]CAAGGTGGCTCACAT | 494470 |
rs778998241 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440036 | GGTTTCACCATGTTG[G/T]CCAGGATGGTCTCGA | 494470 |
rs779027403 | snp | A/G | 1.6517e-05 | 0.00287372 | intron-variant | RNF165 | GRCh38.p7 | 18:46450429 | TCTGGTACCAACTGG[A/G]TTGGTGGAGATGCCA | 494470 |
rs779027870 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370687 | GGGGATCAAGGAATA[G/T]AATAAGATACCATCT | 494470 |
rs779028612 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390333 | TGACTCTTCCTGCCC[A/G]CTGGGTGTTGGTGCA | 494470 |
rs779047577 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355462 | CAGGAGATCCTTGCT[C/G]TCTGAAAGCCTTGGA | 494470 |
rs779063296 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344618 | CCACAGGGGACCTCG[G/T]CATCCACAGTGGGCT | 494470 |
rs779080278 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46421532 | ATGCCTTGTTAGGAT[C/T]GTGGCAGGAATGTGT | 494470 |
rs779083311 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403818 | GGAAGGTGGAGGTTG[C/T]AGTGAGCTGAGATCA | 494470 |
rs779106269 | snp | C/T | | | upstream-variant-2KB | RNF165 | GRCh38.p7 | 18:46333180 | GAGCCTGATGTTACA[C/T]ATCCGCCTGCTGGCT | 494470 |
rs779113441 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46380302 | TCTTGGAAGATGGTG[C/T]CCACGGGGGCTGTTG | 494470 |
rs779116664 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389341 | AACAATGCTGATAAA[C/T]AAAACATCACTGTAA | 494470 |
rs779166503 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431914 | TCCTTTGGTAGGTGC[C/T]TGGTGTTCAATTTCT | 494470 |
rs779176029 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46454439 | AATTATACGGGACTA[C/T]GGATGTAATTCTGAT | 494470 |
rs779187358 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407823 | CCACCCATGTGAAAA[G/T]TTGGGTGACACCACA | 494470 |
rs779203055 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46398457 | AGCCCCTTACCCCCA[A/C]GGTGCCTGCTGGTGG | 494470 |
rs779209171 | snp | A/G | 6.85096e-05 | 0.00585236 | intron-variant | RNF165 | GRCh38.p7 | 18:46435428 | CCTGGGGGAGGAAGG[A/G]AGGAAGGGAGGGAGG | 494470 |
rs779231293 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367531 | GAATTGGTTATTGAA[C/T]AATAGGTGGGTCTAT | 494470 |
rs779269862 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46433682 | CGGCAGTCACCAAGT[G/T]GGTCTCTGTAGGAAG | 494470 |
rs779294835 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396815 | GCATCCAAGGACGGG[C/T]GTGGTGGGGCCCTGT | 494470 |
rs779362637 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446860 | TTGTCCTAACTCTGG[A/C]CAGTGGGAGCCTCTT | 494470 |
rs779395526 | snp | C/G | 4.95921e-05 | 0.00497932 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334246 | GCCCGCGCGCAGCCG[C/G]CGCCGCCGCCGCCGC | 494470 |
rs779416809 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358229 | TGCAAGCGTTCAGAG[A/G]AAAGGGCATGTTTTG | 494470 |
rs779422536 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383892 | CTAACTTTACAGAGT[-/C]CCAGGGTCTGCTCAG | 494470 |
rs779438431 | snp | A/G | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46337266 | GCAAAATGGTTTTCC[A/G]TTAAACAGGGGTAGC | 494470 |
rs779449704 | snp | C/T | 1.6522e-05 | 0.00287414 | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456682 | CCTTCACCAGGTCCC[C/T]CCACGGCCATAGCCC | 494470 |
rs779454055 | snp | A/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46459063 | GAAAACCAAGAATTC[A/T]TCGGAAGATGGCTTT | 494470 |
rs779485406 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406652 | CGGGTGCCCTCAGTG[G/T]GCCCTGGCTGACAAG | 494470 |
rs779526539 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349429 | CACTCTTGGAATCGA[A/G]TCACTTCTCGAAGAC | 494470 |
rs779537057 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342110 | TTATCTTATTTCCTC[C/T]TTGGCACAGCCCATG | 494470 |
rs779545444 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435450 | GGAGGGAGGAGGGAG[G/T]TCTTGCCAGATCTGT | 494470 |
rs779546924 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46424434 | GCAGCCATTTATTTG[A/G]AAGAGGGATTTCGAA | 494470 |
rs779563574 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343899 | AAGCACAGACACAGG[A/G]CTCCTTGACCCCGAG | 494470 |
rs779582267 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46409750 | ATTCAGGATAGATGG[C/G]CCCTTCAGGCGTCTT | 494470 |
rs779592010 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396508 | CCCTGAGTCCCAAGA[C/G]CTAGCAGGTGCCTGG | 494470 |
rs779610716 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367385 | GCATTTATGTTCAGT[A/G]TGGGAGGTAGGAAAC | 494470 |
rs779615264 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46368219 | GGAAGTTCACTAAAT[G/T]CATTCATCCTGGAAG | 494470 |
rs779624631 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345528 | TAAGTCAGGCCCCAT[C/T]CCTGCACAGGTGCAC | 494470 |
rs779632651 | snp | C/T | 1.98438e-05 | 0.00314984 | intron-variant | RNF165 | GRCh38.p7 | 18:46334340 | GCGAAACAGAGGTAT[C/T]GCTTTTTCCTTTCGG | 494470 |
rs779683863 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391647 | GCTTGGTTTGGTGAC[A/G]TATTAAAATGTTTGC | 494470 |
rs779782954 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384896 | TAAAATAGAATAAGA[A/C]AATGTCCTGCCTTTT | 494470 |
rs779787787 | in-del | -/GCC | 0.162533 | 0.2342 | cds-indel, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334242 | AAGGGCCCGCGCGCA[-/GCC]GCCGCCGCCGCCGCC | 494470 |
rs779809234 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46340869 | TGAGCTTGCTGCAGA[A/G]GCGGGTTTGCAATGT | 494470 |
rs779825130 | snp | C/T | 1.65888e-05 | 0.00287996 | synonymous-codon, intron-variant | RNF165 | GRCh38.p7 | 18:46450707 | TTCTCTTTCCAGGAG[C/T]TGCTGCAGCTCGAGG | 494470 |
rs779873055 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46394169 | AGATGGGGTCCCCTG[A/C]CGAGGGACAGAATTT | 494470 |
rs779873238 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46418086 | AACAGGCTAAGTGTG[A/G]TTGCTTATGCCTATA | 494470 |
rs779887105 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46371501 | AGGGAGAAGTTAAAG[C/G]AGATTGGACATTTTA | 494470 |
rs779904541 | snp | C/T | 1.64833e-05 | 0.00287078 | intron-variant | RNF165 | GRCh38.p7 | 18:46447718 | GAAGACGGACTCCCT[C/T]GCGCCTATTGAGTGC | 494470 |
rs779913029 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449524 | GATATGGTTTGGCTC[C/T]GTATCCCCACCCAAA | 494470 |
rs779919995 | in-del | -/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460384 | AAATGAAAAAAAAAA[-/T]CACAAAAAACAAAAA | 494470 |
rs779955407 | snp | C/G | 3.73343e-05 | 0.00432039 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46433300 | CCGCTGGCCCACCCC[C/G]TGCAGTCGCAGCCAG | 494470 |
rs779956776 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46411839 | CCTGGGGCTGAGCCG[C/T]GTATGTGTGATCTTT | 494470 |
rs779979331 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46389234 | AGAAAGTTAAGTGCA[C/T]GAGCATTTAGGAAAG | 494470 |
rs779994418 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351625 | GGGGCACATCAGGGG[C/T]TTTATAGGCATCATC | 494470 |
rs780000907 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461242 | TCTGGGTGGGGTGAG[A/T]GAGGAGAACTGGGAG | 494470 |
rs780102711 | snp | C/G | | | synonymous-codon | RNF165 | GRCh38.p7 | 18:46450349 | TCACTTCCTTGCTCT[C/G]CAGGGACTAAATCCC | 494470 |
rs780103916 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355335 | AGCAGTGGTCCCGAG[A/G]TCCCTCTGAAGAGGA | 494470 |
rs780107962 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46452756 | TCATTGTCAAGCCAA[A/G]GACCGTCTTCACTCC | 494470 |
rs780123284 | snp | A/G/T | 3.29751e-05 | 0.00406038 | intron-variant, missense | RNF165 | GRCh38.p7 | 18:46435330 | ACCCCCACCGCCTCC[A/G/T]TCCCAGCTTCGACTT | 494470 |
rs780156738 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46404573 | AGCCTGACTAACATG[A/G]TGAAACCCATCTCTA | 494470 |
rs780170262 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365288 | CCTGTCAGTGGTCCC[C/T]ACCCTACACTCCCCA | 494470 |
rs780231111 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395907 | GCCCAGTAGTTCTTC[C/T]GATCTCATTTAGGCT | 494470 |
rs780249569 | snp | G/T | | | intron-variant, nc-transcript-variant | RNF165, LOC105372095 | GRCh38.p7 | 18:46388163 | GTGAAGGGAGATAGC[G/T]ACATAGTAAGATGGC | 494470 |
rs780257372 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373638 | GAGTGCTGCCACACT[A/G]GCTCCTCGGGCTCCA | 494470 |
rs780270004 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420463 | GGAAGGGGCCCCATC[A/G]AAGTGGCTTTCTGAA | 494470 |
rs780289833 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46349168 | TGCCATCTTTTCCCA[C/T]TATCTTAGCACATTT | 494470 |
rs780344056 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46406384 | CCTGTGGGTGCTGGC[C/T]GGGGCTGGCCAGCTG | 494470 |
rs780353640 | snp | A/G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374554 | TTCATTCAGGAGAAC[A/G/T]TCTTCAGGGTTCACC | 494470 |
rs780400310 | snp | G/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458083 | CAGCCCCATTTCCGG[G/T]CCTGCTACCTCACCT | 494470 |
rs780416053 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46431514 | TCCCCCAGTTTCACC[C/G]TGGGGCTGTGGAGGG | 494470 |
rs780436042 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405613 | TTCCTGGGATGCTGA[C/T]CTGGGCCCCTGGGGC | 494470 |
rs780468307 | in-del | -/AAAT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432947 | AGACTCCGTCTCAAA[-/AAAT]AAATAAATAAATAAA | 494470 |
rs780481677 | snp | C/T | | | intron-variant, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46336480 | GGCTGAGGGGTGAGT[C/T]GGTCTGTGGGTAAAA | 494470 |
rs780535790 | in-del | -/TGTGTGTGAG | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334709 | GTGTGTGTGTGTGTG[-/TGTGTGTGAG]AGAGAGAGAGAGCGC | 494470 |
rs780538919 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46436208 | TGCCTGCAGAGTTCA[C/G]GGGAAAAAAATCTAT | 494470 |
rs780555546 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46367664 | ACAAGTTGTATTCAT[A/G]TGACTTTTGGCAAGT | 494470 |
rs780584683 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46444392 | GTCTTTACTTACCCA[A/T]GTGGCTGACTGCTTG | 494470 |
rs780593307 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46403971 | ATAGAAGCTCATTCT[G/T]TAGGGGATTCTACTG | 494470 |
rs780660043 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46351528 | CAGAGCCGCCCTGCC[A/G]TTGTCCTCCCTCAGC | 494470 |
rs780674708 | snp | C/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46456874 | GCAGGAGAGAGGGAG[C/G]TGGCGGTGCCCAGCG | 494470 |
rs780682596 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46448036 | TCCATATGACCTAGC[C/T]CCCCTGTGTTCTCAA | 494470 |
rs780732718 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46382732 | GGGAAAGAAAGACAG[G/T]CTCATGGAGTGTCCC | 494470 |
rs780741914 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46377342 | TGGGAACTCGCTATA[C/T]GCCAGGAATTGGTCT | 494470 |
rs780780425 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46428149 | GGCGCAGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 494470 |
rs780781368 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46339406 | TATAGCAAGCTGTGG[A/G]TTAATGGGAAATCAT | 494470 |
rs780867396 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345926 | TTGGGGACCCAAGTT[G/T]TTCAGTGGCTGGAGA | 494470 |
rs780924850 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46400006 | CTGGGGCCACACCCC[A/C]GGTGTTCTGATCTTC | 494470 |
rs780948077 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410827 | TCAATTGTCCAGGCT[C/T]ATGAAAGTGGTCAGC | 494470 |
rs780968237 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46461184 | TCCATGACAGACGTC[C/G]CAATGACCTTGAGCA | 494470 |
rs780976943 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46416753 | ATTTGTATATCACAT[A/G]GTCTGTCATTCTCCA | 494470 |
rs780980281 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407992 | TGGCATAGCAGCTGA[G/T]CTTTGAAGTCTGAGT | 494470 |
rs781024685 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46393333 | AGAGCAGTCTCGAGG[A/T]GTGGGGTGCATCTGG | 494470 |
rs781036594 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46361608 | TCTTGATCCTTGTTA[A/C]TGTTCTTCTCAGTAC | 494470 |
rs781053832 | snp | C/T | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460109 | AGGACTCAAGCTCCT[C/T]TTCTGCAAATGTTCC | 494470 |
rs781066996 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46426803 | CTGATGTCATTTTAG[C/G]CTGGGGAAATATGAC | 494470 |
rs781071934 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439794 | ATATGTTATCCAGCT[A/G]TGACATCAACTCATG | 494470 |
rs781102431 | snp | A/G | 1.65078e-05 | 0.00287291 | intron-variant | RNF165 | GRCh38.p7 | 18:46450423 | GCTCTGTCTGGTACC[A/G]ACTGGGTTGGTGGAG | 494470 |
rs781109444 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396473 | ATGGTGAACTCCATG[A/G]CAGTATGGGCCTTAT | 494470 |
rs781118711 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429538 | TCCTTTTCTGTTCTA[A/C]TATAGCTTATTATTT | 494470 |
rs781155445 | snp | G/T | 1.65312e-05 | 0.00287495 | missense, intron-variant | RNF165 | GRCh38.p7 | 18:46450737 | GACAGGTTGGGTAAT[G/T]TGACTCGGGGAGCTG | 494470 |
rs781157523 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344522 | GAGCTAATGGGAGAA[C/T]GTGCCCACTCCCACC | 494470 |
rs781162054 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46453999 | GCACCTGTAGTCCCA[A/G]CCACTTAGGAAGCTG | 494470 |
rs781202625 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46412760 | CGCCTCGGGCAGGTA[C/T]GGAGATGCTGCTAAC | 494470 |
rs781219812 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46370388 | AAATCAGTGTGCAGA[A/G]CTTGTGTCTTCAACC | 494470 |
rs781245982 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365203 | TGAAGGGGAGGGGGT[A/G]TGGATGGCAGGGAGT | 494470 |
rs781281202 | in-del | -/AC | | | intron-variant | RNF165 | GRCh38.p7 | 18:46383407 | ATATAAAATATGTAT[-/AC]ACACACACATGTTAA | 494470 |
rs781309515 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46369690 | GTTCTGCTTTGCTTT[A/G]AGTGGGCTAGAAACC | 494470 |
rs781324392 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46352998 | TAGCATGCCCTCCAT[A/G]GCTTCACCCAAATAG | 494470 |
rs781334654 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373578 | AGCACAGTGCCTGGA[C/T]GCTGAGGGCTTTATA | 494470 |
rs781399733 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46395842 | GATGGGAGGAAGGAG[C/T]TGAGTAGAGAACCAC | 494470 |
rs781406375 | in-del | -/GTGTGTGTGTGTGAGAGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46334704 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGAGAGA]GAGAGAGAGCGCGCG | 494470 |
rs781427059 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46372647 | TAAGGGGTTGGGGGT[C/G]TCCTGTTAGAATTGG | 494470 |
rs781446534 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46430632 | ACGTTTGCATCTTTT[C/T]TCCTCCCATTCCCCA | 494470 |
rs781460853 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46354939 | TAGACACACTCCTTC[A/G]TTTTGCTTTTAATAT | 494470 |
rs781478267 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391452 | AAGGACACTACGGTT[C/G]TGGTTGCCGCTATTC | 494470 |
rs781487801 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422302 | CTTTCCCAAGCACCC[G/T]GCCTCTGAATGACTC | 494470 |
rs781489581 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405516 | GGGAGTGGCTGTTGG[A/C]GATGTGGAAACAGCA | 494470 |
rs781498502 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46415051 | GAAATGGGCAGGGGA[A/G]GGAGCAGAAGCCAAG | 494470 |
rs781530192 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445160 | CTGTTAAGTAGTTAC[A/G]TTTGTTTTATTCATT | 494470 |
rs781536101 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46429385 | CCTCAACCGCAGTGC[A/G]CTTTTAACTCTTCTT | 494470 |
rs781586500 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46414476 | CATACATGTACACAC[A/G]CACACATCACAGGTG | 494470 |
rs781621080 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46443794 | TAAAGACAATTTTTC[A/G]TAGGAAAAATAATTT | 494470 |
rs781639530 | snp | A/G | 1.87587e-05 | 0.00306252 | synonymous-codon | RNF165 | GRCh38.p7 | 18:46455994 | ACCCCAGGATGGCAA[A/G]GGCAAGAAGGATGAG | 494470 |
rs781663586 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46422991 | CCAACTGTTCCTAGT[A/G]TCAGATTACTCAAGT | 494470 |
rs781687391 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440292 | AGAGAGAGAGAGAGA[C/G]AGAGACCATATTCAC | 494470 |
rs781691736 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46346906 | GCAGTTACTGAGAAC[A/C]TGCTTTGGCACAGAC | 494470 |
rs781709020 | in-del | -/GGTG/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397490 | GCTGAGGTGTGAGGG[-/GGTG/GT]TGTGTGTGTGTGTGT | 494470 |
rs781713279 | snp | G/T | 1.64806e-05 | 0.00287054 | intron-variant | RNF165 | GRCh38.p7 | 18:46447710 | AAGTGAAAGAAGACG[G/T]ACTCCCTTGCGCCTA | 494470 |
rs781741265 | snp | C/G/T | 0.000103611 | 0.00719685 | utr-variant-5-prime, nc-transcript-variant | RNF165 | GRCh38.p7 | 18:46334234 | GCGCCACAAAGGGCC[C/G/T]GCGCGCAGCCGCCGC | 494470 |
rs781745576 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46358207 | GAGCTGGACCCCCTG[G/T]GAGGGCTGCAAGCGT | 494470 |
rs781757684 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46408440 | CTGGAGGCAGCAGAA[C/T]GTCCATAGAGGTTAA | 494470 |
rs796106651 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46391069 | TTGAACTCTGCTTTT[G/T]TTGGCTGGGTGGCTG | 494470 |
rs796112315 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46365355 | TTTTGGGATGACCTA[C/T]GTCTGTCTCTAGAAG | 494470 |
rs796128060 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46343431 | TGCCTTACTGGACTC[A/G]TCACATGAAGTAATG | 494470 |
rs796217600 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46449371 | TTTGACTTTAAAAAA[C/T]ATTGCATTAAAATAT | 494470 |
rs796225851 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46355376 | TCTCTCTCAGGGCCT[C/T]GGGCTCCTCACTGGT | 494470 |
rs796242477 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374356 | TTATCTTCACCATCC[A/C]TCTCCAGAACTTTCT | 494470 |
rs796261448 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46342071 | AAAGAGGGGTTTTTT[C/T]GCAATTCAAAGCTCT | 494470 |
rs796277632 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46392183 | CCACACACATGCACA[C/T]ATACTGTGGTCATCC | 494470 |
rs796315104 | multinucleotide-polymorphism | CAC/TAT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46420580 | CAGATGCGGTGGCTC[CAC/TAT]CCTGTAATCTCAGCA | 494470 |
rs796315510 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46438145 | ACACATTGGCACAAG[A/G]AATCTCCAAAACACA | 494470 |
rs796336376 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445914 | ATCCTTTTTTTTTTT[-/T]CTCCAATGTATTTGT | 494470 |
rs796352343 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46350296 | AGGCCAGCCGCAGAG[C/T]CTGGGCCTTTGATAC | 494470 |
rs796362584 | in-del | -/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345128 | TGCGATGCAGGGCTG[-/C]CTGGCTGCCACCTGC | 494470 |
rs796378129 | in-del | -/AA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46364406 | TGGTCTAAGAAACTT[-/AA]AAAAAAAAAAAGCTC | 494470 |
rs796393122 | snp | A/C | | | intron-variant | RNF165 | GRCh38.p7 | 18:46451080 | ATATTACATACATAT[A/C]CATGTATAGGTGTCA | 494470 |
rs796459876 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46344693 | CCTGCCCCCTCTGCC[G/T]GTGACGTTTGGGACT | 494470 |
rs796495377 | in-del | -/GGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46410411 | TCCCACAGTTAAGGT[-/GGA]GGAGGAGGCAGCCAG | 494470 |
rs796501611 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373653 | GGCTCCTCGGGCTCC[A/G]GGGACAGCCCACCAG | 494470 |
rs796522717 | snp | A/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46457198 | CCAACGACAGCCCCA[A/G]TCTTCCCGTCTTTAT | 494470 |
rs796528364 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46401024 | GAACTGGAAACGCTG[A/G]GGAGGCCAGACCCCC | 494470 |
rs796533366 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46366028 | CTGGGCGCGGTGGCT[C/G]ACACCTGTAATCCCA | 494470 |
rs796535623 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46460986 | CCACAACCTCAGCCC[A/C]CCCAGCCGGTATCCT | 494470 |
rs796559401 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442112 | AGCTTGCAGTGAGTC[C/G]AGATCGCGCCACTGC | 494470 |
rs796592193 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396825 | ACGGGCGTGGTGGGG[C/G]CCTGTCTCTGGAAAC | 494470 |
rs796608986 | snp | G/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46373725 | CAGGGCTGTCTCCAG[G/T]ATCTCTGCAGGTGTG | 494470 |
rs796628587 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46435031 | AATCTACCACAGACA[C/T]ACCAAGGGAGAGACC | 494470 |
rs796653835 | in-del | -/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46405049 | GCAAGACCCCACCAA[-/T]TTTTTTTTTTGGTAA | 494470 |
rs796667545 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF165, LOC105372095 | GRCh38.p7 | 18:46390516 | AGACGGGCATATATA[G/T]TCTATCTATTTTCAG | 494470 |
rs796675910 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46341325 | AGGTCAGGGAGGGGG[-/G]TGGGACAGGCGTGGG | 494470 |
rs796719999 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46423944 | CCTTCCCTCTTTCTT[C/T]TCCTCTTTTATCCAG | 494470 |
rs796730129 | snp | A/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432970 | TAAATAAATAAATAA[A/T]AAATAAAGATAACAC | 494470 |
rs796731400 | in-del | -/AAAAAA | | | downstream-variant-500B | RNF165 | GRCh38.p7 | 18:46461662 | AAAAAAAAAAAAAAA[-/AAAAAA]GAGGGAAAGAGGGAG | 494470 |
rs796762570 | in-del | -/GAGA | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440274 | GCATTTTGAGAGACT[-/GAGA]GAGAGAGAGAGAGAG | 494470 |
rs796779914 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46375150 | TCCCAACTCCCCCCG[C/T]CCTCAGAGGCCCCAG | 494470 |
rs796787249 | in-del | ATCAA/TCGGATCTGTT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46440711 | CTGTTATACTTTGTA[ATCAA/TCGGATCTGTT]CAAGATCCGAATAAG | 494470 |
rs796789770 | in-del | -/TT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46445903 | TACTTCTCCATATCC[-/TT]TTTTTTTTTTCTCCA | 494470 |
rs796792563 | snp | C/G | | | utr-variant-3-prime | RNF165 | GRCh38.p7 | 18:46458313 | AATTCCAACCCAAAC[C/G]CAACTTTCTTTCTCC | 494470 |
rs796825581 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46432696 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 494470 |
rs796829125 | snp | C/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46434639 | TGAACCACCTGAAAG[C/G]GTTGCAGGGACTCCC | 494470 |
rs796871554 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46446619 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 494470 |
rs796891670 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46396218 | AGATGGGGAAATAGA[C/T]TCTACCTCTTGACTG | 494470 |
rs796944777 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345319 | CAGCTTGGTCTTCCC[C/T]GGGCAGGTGCGGTGG | 494470 |
rs796953007 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46384983 | ACTTCTTGATGGTCA[C/T]CTTTGTGCCCGTAGA | 494470 |
rs796962974 | in-del | -/A | | | intron-variant | RNF165 | GRCh38.p7 | 18:46439712 | TTTTTATTAAAAAAA[-/A]CCCTTTTTATTATAG | 494470 |
rs796983736 | in-del | -/GT | | | intron-variant | RNF165 | GRCh38.p7 | 18:46397490 | TGCTGAGGTGTGAGG[-/GT]GTGTGTGTGTGTGTG | 494470 |
rs796987783 | in-del | -/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46374768 | GGCTCTGGCTGAACT[-/G]GGGGGGGCTAGAGAC | 494470 |
rs797002918 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46442833 | GACTTATATATATTA[A/G]GATATTAAAAGGATT | 494470 |
rs797009475 | snp | C/T | | | intron-variant | RNF165 | GRCh38.p7 | 18:46407102 | ACTATAAATTGCATC[C/T]TACCACACAAAGTTG | 494470 |
rs797015499 | snp | A/G | | | intron-variant | RNF165 | GRCh38.p7 | 18:46345757 | AAACCTTTGAATGCA[A/G]ATACAGAATTTGGTG | 494470 |