| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs16855 | snp | C/T | 0.491936 | 0.0629843 | intron-variant, upstream-variant-2KB | RNF144A, RNF144A-AS1 | GRCh38.p7 | 2:6919242 | CCCTCCCCCTTCCTG[C/T]GCTGGAGCAGCTCTC | 9781 |
| rs28293 | snp | G/T | 0.434253 | 0.168969 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7055015 | CACCATGCCCTGCAG[G/T]TGCTTTACTCTTCCT | 9781 |
| rs89983 | snp | A/C | 0.327211 | 0.237778 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7055061 | GCATTGACAGGCTGG[A/C]ACCTCCTCTTTGAAA | 9781 |
| rs177922 | snp | C/T | 0.29432 | 0.24604 | intron-variant | RNF144A | GRCh38.p7 | 2:7003568 | acctaggctagctgg[C/T]acagcctattgctct | 9781 |
| rs309261 | snp | A/G | 0.408359 | 0.193449 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7070302 | aagcctgtagtcaca[A/G]ctactcgggaggctg | 9781 |
| rs309262 | snp | C/T | 0.406296 | 0.19512 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7069294 | AATCTGTTGGCCACA[C/T]AGATGAAACAGCCAG | 9781 |
| rs309263 | snp | C/T | 0.432357 | 0.171014 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7069084 | TTTGGAGGCTGACTG[C/T]GCTGATTGGCTTCCT | 9781 |
| rs309264 | snp | G/T | 0.430583 | 0.172886 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7067929 | gctgaaaacaggcca[G/T]gtgatcagacatcac | 9781 |
| rs309265 | snp | C/G | 0.406468 | 0.194981 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7067505 | gtttctgagcccaga[C/G]ggcagccaatcaaaa | 9781 |
| rs309266 | snp | C/T | 0.398894 | 0.200825 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7066887 | tttaaaactagaaag[C/T]gaagccaaggacttg | 9781 |
| rs309267 | snp | A/C | 0.448639 | 0.159445 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7066720 | caagtatgcaacaca[A/C]catggcgataatttt | 9781 |
| rs309268 | snp | C/G | 0.430583 | 0.172886 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7064487 | TGGGTTAGCCTCCCC[C/G]TGGAGTCACAATAGA | 9781 |
| rs309269 | snp | A/G | 0.459687 | 0.136129 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7063937 | gacttcccagccccc[A/G]gaaccataagctaaa | 9781 |
| rs309270 | snp | C/T | 0.460027 | 0.135605 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7063393 | TAAACCCATAATCAC[C/T]CCCATCTAACTCTTC | 9781 |
| rs309271 | snp | A/C | 0.402982 | 0.197728 | downstream-variant-500B, intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7062365 | TTTTAACTCTGTACC[A/C]GTCTTGAGATTTCCT | 9781 |
| rs309272 | snp | A/G | 0.399073 | 0.200692 | intron-variant | RNF144A | GRCh38.p7 | 2:7061970 | AGCAACTGGATTTTG[A/G]AATGATGAGTTACTT | 9781 |
| rs309273 | snp | A/G | 0.499087 | 0.0213463 | intron-variant | RNF144A | GRCh38.p7 | 2:7060733 | AGTGGGTCTCAGAAG[A/G]GGTTATAAATTCTTG | 9781 |
| rs309274 | snp | C/T | 0.399611 | 0.200291 | intron-variant | RNF144A | GRCh38.p7 | 2:7060717 | GGTTATAAATTCTTG[C/T]AGGTGAGAAGAGAGT | 9781 |
| rs309275 | snp | A/C | 0.397452 | 0.201886 | intron-variant | RNF144A | GRCh38.p7 | 2:7059864 | ATTAAATTTTAAGTA[A/C]TTCATATTAAGCAAG | 9781 |
| rs309276 | snp | C/T | 0.498503 | 0.0273153 | intron-variant | RNF144A | GRCh38.p7 | 2:7059826 | AGGATTTTCAGCTGG[C/T]TTAGTGATTCTCTCT | 9781 |
| rs309277 | snp | C/T | 0.407158 | 0.194426 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7057133 | AGAGCATGACAGCTT[C/T]AAACCTCTAATTTTC | 9781 |
| rs309278 | snp | C/T | 0.46974 | 0.119223 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7057068 | TCCCTTCTCACCTCC[C/T]GTTGATGTATGGGCA | 9781 |
| rs309279 | snp | C/T | 0.43088 | 0.172575 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7056826 | CATGAGATACACAAA[C/T]AAGGAAGCCACAAGG | 9781 |
| rs309280 | snp | C/G | 0.407158 | 0.194426 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7056501 | GGATGGTTGGTGTGT[C/G]GCTGAAGTACTCAAG | 9781 |
| rs309281 | snp | C/T | 0.39979 | 0.200158 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7056308 | GGGAAGCACAGAGGG[C/T]ACATCTTACCATGGG | 9781 |
| rs309282 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7056102 | AAATAAAGTCATTAA[C/T]TCTAATGCTAAAATC | 9781 |
| rs309283 | snp | C/T | 0.430136 | 0.173352 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7055300 | TCTCTGAGCTGCAGT[C/T]TCACACACTGAATGG | 9781 |
| rs309284 | snp | C/G | 0.436123 | 0.166908 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7053960 | tgcccagagagagaa[C/G]cagagcttgtccatc | 9781 |
| rs309285 | snp | A/G | 0.40263 | 0.198 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7053725 | ATTtgtaaggtacat[A/G]gatatgctttggtta | 9781 |
| rs309286 | snp | C/T | 0.321053 | 0.23969 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7053004 | AAATACTTCCATATG[C/T]GTTTAAACTTCTACA | 9781 |
| rs309287 | snp | A/G | 0.499977 | 0.00339449 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7051930 | CTTCCAAGAGTATCA[A/G]TGAATCCCCCAGTAT | 9781 |
| rs309288 | snp | G/T | 0.450726 | 0.155587 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7050495 | GACTAATGCAGGTCC[G/T]CTTCAGTCTCTCGTG | 9781 |
| rs309289 | snp | A/T | 0.451856 | 0.147493 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7050066 | CTTTGAAGGAAGAAC[A/T]GTTTGCCTTTCCCAG | 9781 |
| rs309290 | snp | A/C | 0.464285 | 0.132992 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7049569 | GATTTGAGTTTTCAA[A/C]GACACGAAAATGAGG | 9781 |
| rs309291 | snp | G/T | 0.462363 | 0.131916 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7049529 | CACAAAGGATGAAGA[G/T]GACAAAAATTCAACT | 9781 |
| rs309292 | snp | C/T | 0.462253 | 0.132093 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7049266 | TTTTCAGAAACACTG[C/T]ATAGTGGCTGAGCAC | 9781 |
| rs309293 | snp | C/T | 0.434543 | 0.168653 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7049223 | GAGGAGGGTAAGGGA[C/T]GAGAAACAGAGATAT | 9781 |
| rs309294 | snp | C/T | 0.45762 | 0.139261 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7048304 | GGAGATGGTGCCCAT[C/T]GCAGGACAAACACTG | 9781 |
| rs309295 | snp | A/G | 0.332106 | 0.236133 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7048107 | AACCCAGTCCTGTCT[A/G]TTTTCAAGCCAGCAA | 9781 |
| rs309296 | snp | C/T | 0.457388 | 0.139608 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7047948 | GGACCCAGTGTTCCT[C/T]CCACCACACATGGCT | 9781 |
| rs309297 | snp | C/T | 0.463234 | 0.130503 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7047685 | TACAAAAAAGCCTTA[C/T]GCTTGAACTGGAGGT | 9781 |
| rs309298 | snp | A/G | 0.317451 | 0.240729 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7046319 | AGTCACCCAGGATGT[A/G]CATTTTCGGATGAAG | 9781 |
| rs309299 | snp | C/T | 0.432944 | 0.170387 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7046115 | TATCTAGAAGGTATT[C/T]TAAACTTGACTTGTT | 9781 |
| rs309300 | snp | A/G | 0.497502 | 0.035255 | intron-variant | RNF144A | GRCh38.p7 | 2:7045050 | cggaaggtcagggaa[A/G]gctgtccagaggacg | 9781 |
| rs309301 | snp | C/G | 0.408188 | 0.193589 | intron-variant | LOC101929452, RNF144A | GRCh38.p7 | 2:7071418 | CACGCTCCTTCTTTG[C/G]ACAAGGTCTTagggc | 9781 |
| rs309302 | snp | A/G | 0.352721 | 0.227922 | utr-variant-3-prime, intron-variant | RNF144A | GRCh38.p7 | 2:7042046 | AGGGGCAGTCAAATT[A/G]GCACCTACTGGCTCT | 9781 |
| rs309303 | snp | A/G | 0.420892 | 0.182472 | utr-variant-3-prime, intron-variant | RNF144A | GRCh38.p7 | 2:7041429 | ATTTAGAAAATCCCT[A/G]TGTGTCAAAATTACA | 9781 |
| rs309304 | snp | A/G | 0.464841 | 0.127841 | utr-variant-3-prime, intron-variant | RNF144A | GRCh38.p7 | 2:7041355 | TTGAATTCGTTAGAA[A/G]AAACAGCGTCACCTC | 9781 |
| rs309305 | snp | A/G | 0.422315 | 0.181128 | intron-variant | RNF144A | GRCh38.p7 | 2:7039346 | tggatggatagaGAG[A/G]TGTATGATGGTTAAt | 9781 |
| rs309306 | snp | A/G | 0.49998 | 0.00319482 | intron-variant | RNF144A | GRCh38.p7 | 2:7020359 | TGTCCAGGTAATACA[A/G]CCAGCACCACCAGCC | 9781 |
| rs309307 | snp | C/G | 0.494976 | 0.0498674 | intron-variant | RNF144A | GRCh38.p7 | 2:7019639 | TGCCGAATTCTCGAT[C/G]AGTGGCCACCCCAGG | 9781 |
| rs309308 | snp | A/G | 0.356811 | 0.226034 | intron-variant | RNF144A | GRCh38.p7 | 2:7019481 | CTGAGTTTCAGAGAC[A/G]ACTTGAAAGGCGATG | 9781 |
| rs309309 | snp | A/G | 0.261884 | 0.249717 | intron-variant | RNF144A | GRCh38.p7 | 2:7019354 | ACATGCTGGCGCCGC[A/G]CGTGGACCGGGACTT | 9781 |
| rs309310 | snp | A/T | 0.465368 | 0.126951 | intron-variant | RNF144A | GRCh38.p7 | 2:7018101 | GTCTCGGTCTCTTCA[A/T]GCACGTGATTTGTCA | 9781 |
| rs309311 | snp | C/T | 0.463989 | 0.129263 | intron-variant | RNF144A | GRCh38.p7 | 2:7016816 | AAAATCATTGAACTG[C/T]CTCAGTTTTCTTCCA | 9781 |
| rs309312 | snp | A/G | 0.48995 | 0.0701706 | intron-variant | RNF144A | GRCh38.p7 | 2:7009114 | TATGGGTCTCCTGTC[A/G]CCCATGTGGAGGGTG | 9781 |
| rs309313 | snp | A/G | 0.293551 | 0.246177 | intron-variant | RNF144A | GRCh38.p7 | 2:7008464 | TATAAGAACCCACTC[A/G]GGGCAGGAAGGCCAG | 9781 |
| rs309314 | snp | C/T | 0.488302 | 0.0755777 | intron-variant | RNF144A | GRCh38.p7 | 2:7008456 | CGGTCACACTGGCCT[C/T]CCTGCCCCGAGTGGG | 9781 |
| rs309315 | snp | A/G | 0.294832 | 0.245947 | intron-variant | RNF144A | GRCh38.p7 | 2:7007824 | CCGTTTGTTCTATCT[A/G]TTCAATATGAAAACC | 9781 |
| rs309316 | snp | A/G | 0.267091 | 0.249415 | intron-variant | RNF144A | GRCh38.p7 | 2:7006467 | TGACATTGAGGAGGC[A/G]GGTGTCCCTTCCCAA | 9781 |
| rs309317 | snp | C/T | 0.486529 | 0.0809556 | intron-variant | RNF144A | GRCh38.p7 | 2:7006404 | CCCAGGAGCATTTTG[C/T]AGCACAGGCTGAGAT | 9781 |
| rs309318 | snp | A/G | 0.296619 | 0.245615 | intron-variant | RNF144A | GRCh38.p7 | 2:7006083 | TTAGACTGGGACAGA[A/G]CATAGCTGTCATGAT | 9781 |
| rs309319 | snp | C/T | 0.48666 | 0.0805725 | intron-variant | RNF144A | GRCh38.p7 | 2:7005304 | ACCCCAGGAGCCAGC[C/T]TGCAGAGCAGACATG | 9781 |
| rs309320 | snp | A/G | 0.294576 | 0.245994 | intron-variant | RNF144A | GRCh38.p7 | 2:7004746 | GAAGAGCTGAGAAAC[A/G]TCGAAGTCCTGTAGT | 9781 |
| rs309321 | snp | C/G | 0.488846 | 0.0738428 | intron-variant | RNF144A | GRCh38.p7 | 2:7004557 | TTCAAATCAAGAATG[C/G]AGTCGCAGGTTTGCC | 9781 |
| rs309322 | snp | A/G | 0.4862 | 0.0819127 | intron-variant | RNF144A | GRCh38.p7 | 2:7003096 | tatgtgtatatatac[A/G]tacaaatatatacat | 9781 |
| rs309323 | snp | A/C | 0.355525 | 0.226637 | intron-variant | RNF144A | GRCh38.p7 | 2:7015620 | GTTTCATTGTATGAC[A/C]CCGGAGTATTTCAGA | 9781 |
| rs309324 | snp | A/G | 0.2776 | 0.248472 | intron-variant | RNF144A | GRCh38.p7 | 2:7015154 | TATGCCTACCCTCAC[A/G]ACTTCCCTCCATGAC | 9781 |
| rs309325 | snp | A/G | 0.00102222 | 0.0225847 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RNF144A | GRCh38.p7 | 2:7014501 | TGGGCAGCTAATTGC[A/G]GTTTCTAATCCTTCT | 9781 |
| rs309326 | snp | A/G | 0.499653 | 0.0131743 | intron-variant | RNF144A | GRCh38.p7 | 2:7013950 | agtacccagagcctc[A/G]atgtgaacccaagcT | 9781 |
| rs309327 | snp | A/T | 0.499515 | 0.0155675 | intron-variant | RNF144A | GRCh38.p7 | 2:7013607 | CCAAGAGAAACTAGA[A/T]GTAGAGCTTATATAA | 9781 |
| rs364891 | snp | A/G | 0.289762 | 0.246818 | missense, intron-variant, nc-transcript-variant | RNF144A | GRCh38.p7 | 2:6996936 | TCTGCGATGACCACA[A/G]CAAGGTACCGGCCCA | 9781 |
| rs365483 | snp | C/T | 0.459118 | 0.137002 | intron-variant | RNF144A | GRCh38.p7 | 2:7027432 | CACAGAAATACTGTG[C/T]GTTAAGGGAAGCAGG | 9781 |
| rs365775 | snp | C/T | 0.346811 | 0.230494 | intron-variant | RNF144A | GRCh38.p7 | 2:7035315 | AATCTTACTTGACTG[C/T]AGCCCACAGGGAGAC | 9781 |
| rs367107 | snp | A/G | 0.496778 | 0.0400063 | intron-variant, nc-transcript-variant | RNF144A | GRCh38.p7 | 2:7031474 | ctctgtggactgcca[A/G]gccctaaaagggtct | 9781 |
| rs367495 | snp | C/G | 0.31503 | 0.241394 | intron-variant, nc-transcript-variant | RNF144A | GRCh38.p7 | 2:7031352 | CCTAAACAGAACGTA[C/G]TTCCGTAGAAGGACA | 9781 |
| rs367906 | snp | C/T | 0.294576 | 0.245994 | intron-variant | RNF144A | GRCh38.p7 | 2:7000041 | TTAGCAATTGCTAGG[C/T]CAGTCCCTTTCACAC | 9781 |
| rs368831 | snp | C/T | 0.342582 | 0.232225 | intron-variant | RNF144A | GRCh38.p7 | 2:7011459 | ACTAGGGCTCAAACC[C/T]ACATGTGGCTGATTC | 9781 |
| rs369808 | snp | G/T | 0.294576 | 0.245994 | intron-variant | RNF144A | GRCh38.p7 | 2:6999777 | TTATTCCTGCAGTTC[G/T]AAACCCAAACTTAGA | 9781 |
| rs372346 | snp | G/T | 0.496483 | 0.0417852 | intron-variant | RNF144A | GRCh38.p7 | 2:7033707 | CCAGAGTGGGGTGGG[G/T]CCACATGGGAGGGAG | 9781 |
| rs372417 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RNF144A | GRCh38.p7 | 2:7057859 | TGTCCACTAATAAAT[A/C]TCTGCTTAACATTTG | 9781 |
| rs376219 | snp | A/G | 0.451192 | 0.148398 | synonymous-codon, nc-transcript-variant | RNF144A | GRCh38.p7 | 2:7024447 | CATCGAGCGAGACGA[A/G]GGCTGCGCGCAGATG | 9781 |
| rs376348 | snp | G/T | 0.485392 | 0.0842056 | intron-variant | RNF144A | GRCh38.p7 | 2:6997820 | ATGTAGGTCAAAGGG[G/T]ATGAAGTTGCAGTTA | 9781 |
| rs377617 | snp | C/T | 0.382473 | 0.212016 | intron-variant | RNF144A | GRCh38.p7 | 2:7026376 | AGAAAATTCATCTTG[C/T]CATGCTGATTCATTA | 9781 |
| rs378548 | snp | A/G | 0.295088 | 0.245901 | intron-variant | RNF144A | GRCh38.p7 | 2:6997186 | GAGTCTTCTTGTTGA[A/G]GCCTTCACACAGTTC | 9781 |
| rs380605 | snp | A/G | 0.496842 | 0.0396107 | intron-variant, nc-transcript-variant | RNF144A | GRCh38.p7 | 2:7031299 | ATCTCCAGCTCCTAC[A/G]GCAGTACCCAGCACA | 9781 |
| rs381214 | snp | A/G | 0.49121 | 0.0657086 | intron-variant | RNF144A | GRCh38.p7 | 2:7010523 | GCCTAAAACTACAGC[A/G]AGTCTGATTTTTGTC | 9781 |
| rs388038 | snp | C/T | 0.263535 | 0.249633 | intron-variant | RNF144A | GRCh38.p7 | 2:6999081 | GCTTTTGGTCTCAAT[C/T]TGAGTGGCTTATTTG | 9781 |
| rs388773 | snp | C/T | 0.484214 | 0.0945481 | intron-variant | RNF144A | GRCh38.p7 | 2:7010627 | TTTGAAACCTGATGA[C/T]GAGACAGCACTGCTG | 9781 |
| rs389323 | snp | G/T | 0.497359 | 0.0362457 | intron-variant | RNF144A | GRCh38.p7 | 2:7029705 | TGTGACTCCACCAGA[G/T]TCCCTCTGCCCTGGC | 9781 |
| rs389351 | snp | A/G | 0.295599 | 0.245806 | intron-variant | RNF144A | GRCh38.p7 | 2:6998034 | ACGTATACAAAAAAT[A/G]AATATCAAAACTTCA | 9781 |
| rs389411 | snp | A/G | 0.335559 | 0.234904 | intron-variant | RNF144A | GRCh38.p7 | 2:7012454 | CTCAAGTCAGAGTTT[A/G]AGCAACAGCTCCCTT | 9781 |
| rs391109 | snp | C/T | 0.357451 | 0.225731 | intron-variant | RNF144A | GRCh38.p7 | 2:7029065 | GGTCATGGCCTTCTG[C/T]TCCTTTCAATCAACT | 9781 |
| rs392051 | snp | A/G | 0.497151 | 0.037632 | intron-variant | RNF144A | GRCh38.p7 | 2:7031069 | cagctgtaaatacag[A/G]tgaaggtttgctcgt | 9781 |
| rs392409 | snp | C/G | 0.357238 | 0.225832 | intron-variant | RNF144A | GRCh38.p7 | 2:7024681 | CCCCATGGCGCTCAT[C/G]AGTTAATGTTTTCAC | 9781 |
| rs392709 | snp | C/G | 0.387453 | 0.208822 | intron-variant | RNF144A | GRCh38.p7 | 2:7024615 | TGTTACACAGGAGTA[C/G]GCACCAAGCTCTTTA | 9781 |
| rs392740 | snp | G/T | | | intron-variant | RNF144A | GRCh38.p7 | 2:6996710 | agtgagctagattgc[G/T]ccactttactccaac | 9781 |
| rs392904 | snp | C/G | 0.49645 | 0.0419827 | intron-variant | RNF144A | GRCh38.p7 | 2:7035168 | AGAAGGAACAAAACA[C/G]GGCAAGAGAGAGACA | 9781 |
| rs397865 | snp | G/T | 0.264906 | 0.249555 | intron-variant | RNF144A | GRCh38.p7 | 2:6999735 | TGTGGTAGGCAGTCA[G/T]CAGGCCTAGTTCTTT | 9781 |
| rs399101 | snp | C/T | 0.496175 | 0.0435625 | intron-variant | RNF144A | GRCh38.p7 | 2:7037793 | AGTAAAAGATCTTTA[C/T]GGGCCATTATCAGCC | 9781 |