SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6628 | snp | C/T | 0.33416 | 0.235408 | PAFAH1B1 | 17 | allele_origin=T(germline)/C(germline) | 17:2681819 | TGTGTCTCCTTCGGC[C/T]CCTCCTCCCTCTTTT | 5048 |
rs8797 | snp | A/C | 0 | 0 | utr-variant-3-prime | PAFAH1B1 | GRCh38.p7 | 17:2685528 | TTTGTTGCTCTCAGA[A/C]TGTGTAAAACAAAAT | 5048 |
rs758416 | snp | C/T | 0.46875 | 0.121031 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2645075 | aacctggtgaaaccc[C/T]gtctctacaaaaaat | 5048 |
rs768064 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2642510 | acgaggtatctcgga[G/T]atgagactcaaccaa | 5048 |
rs867092 | snp | C/T | 0.46885 | 0.12085 | intron-variant, upstream-variant-2KB | PAFAH1B1 | GRCh38.p7 | 17:2633788 | CTTCCTTGAAATACT[C/T]TCTTGGCTTTTGAGA | 5048 |
rs1029743 | snp | A/G | 0.453453 | 0.145282 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2659916 | GGAATGATCCCCTGT[A/G]TATCTCTGCCCTGGA | 5048 |
rs1029744 | snp | C/T | 0.450483 | 0.149354 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2659967 | TCTCCCAAGACTATA[C/T]AGTTTCATCTTGTTA | 5048 |
rs1049972 | snp | G/T | 0.0114282 | 0.0747228 | utr-variant-3-prime | PAFAH1B1 | GRCh38.p7 | 17:2683314 | CAACAGGTTTTTTTT[G/T]TTTCCAAGAGAGTTA | 5048 |
rs1050060 | snp | C/T | 0 | 0 | utr-variant-3-prime | PAFAH1B1 | GRCh38.p7 | 17:2682220 | GTTATTAGGGCTTTT[C/T]CTGAAATGTGTATCT | 5048 |
rs1050061 | snp | C/T | 0 | 0 | utr-variant-3-prime | PAFAH1B1 | GRCh38.p7 | 17:2682269 | GTGCTTAATAAATCT[C/T]CTGTAAGGATTTTAG | 5048 |
rs1063474 | snp | A/G | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | PAFAH1B1 | GRCh38.p7 | 17:2684507 | AGAATTGCATCCTCA[A/G]ATGATTATTGACTGT | 5048 |
rs1266470 | snp | A/G | 0.326976 | 0.237854 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2628758 | ttaattaccgtttca[A/G]tgtcactgcttgtta | 5048 |
rs1266471 | snp | C/T | 0.46865 | 0.121211 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2628852 | atttatccatctctt[C/T]taggttttctcattt | 5048 |
rs1266472 | snp | C/T | 0.207253 | 0.246318 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2628978 | tttggattttctctc[C/T]gctttccttggttaa | 5048 |
rs1266473 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2630365 | gctttccttcataca[C/T]gatgcttggtttcac | 5048 |
rs1266474 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2631416 | attcagatggttaca[A/G]aatttggctagagaa | 5048 |
rs1266475 | snp | C/T | 0.469937 | 0.118861 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2632026 | TTCATGTATCTCTCT[C/T]ATTCACTGTCATTAC | 5048 |
rs1803913 | snp | C/T | | | utr-variant-3-prime | PAFAH1B1 | GRCh38.p7 | 17:2685216 | CACGGCTGGACTGAA[C/T]GGGCCTTTTTATCTT | 5048 |
rs1803914 | snp | A/G | 0.029116 | 0.117091 | utr-variant-3-prime | PAFAH1B1 | GRCh38.p7 | 17:2683180 | CATTTTACACAACCC[A/G]GATATGTTGTATATT | 5048 |
rs1803915 | snp | C/T | 0.00212277 | 0.0325097 | synonymous-codon | PAFAH1B1 | GRCh38.p7 | 17:2680220 | TGGGGGGAAGTTTAT[C/T]TTGAGTTGTGCTGAT | 5048 |
rs2058165 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2661614 | tgatgcctccagctt[C/T]gttctttttgcttag | 5048 |
rs2228614 | snp | A/T | 0.00866737 | 0.0652576 | PAFAH1B1 | 17 | allele_origin=T(germline)/A(germline) | 17:2674081 | TGTGAAGACATTCAC[A/T]GGACACAGAGAATGG | 5048 |
rs2301165 | snp | A/C/G | 0 | 0 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2666326 | TGACTTTGAGGAATT[A/C/G]ATACTGAAAGAACTC | 5048 |
rs2317293 | snp | C/T | 0.469445 | 0.119766 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2621227 | CTCTCCCTCCTACCA[C/T]CCTTCACCCTCCGAA | 5048 |
rs2317295 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2624373 | gcgttctactgttac[C/T]agtttactgtattag | 5048 |
rs2317296 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2664466 | GCTAGAGTGCAGTGA[C/T]GCGGTCTTGGCTCAC | 5048 |
rs2317297 | snp | C/T | 0.287606 | 0.247155 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2673797 | ATATGGCTGGAAATA[C/T]TTTTAAGTGTGCATT | 5048 |
rs2439996 | snp | A/G | 0.478685 | 0.10101 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2626640 | TTGAACCAGGGAGTC[A/G]GAGGTTGCAGTGAGC | 5048 |
rs2439997 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | PAFAH1B1 | GRCh38.p7 | 17:2634677 | CATTAGATAAGATTT[C/T]AGGAAAAAAAAAAAT | 5048 |
rs2439998 | snp | A/G | 0.206336 | 0.246157 | intron-variant, upstream-variant-2KB | PAFAH1B1 | GRCh38.p7 | 17:2634257 | TCCAGCTACTTGAGA[A/G]GCTGAGGCAGGAGAA | 5048 |
rs2531855 | snp | A/G | 0.161267 | 0.233723 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2625966 | CAGAAAAACGTTAAT[A/G]AAAGCCAGGCGTGGT | 5048 |
rs2531856 | snp | A/T | 0.454664 | 0.143571 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2626104 | AAAAATACAAAAAAA[A/T]TTAGCTAGGCATAGT | 5048 |
rs2873425 | snp | A/G | 0 | 0 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2621787 | ccactatgtccagct[A/G]atttttgtatttttt | 5048 |
rs2873426 | snp | C/T | 0.469445 | 0.119766 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2643489 | ggctgcctctgggct[C/T]aggtgatgcttgcac | 5048 |
rs3029951 | snp | A/C/T | 0.0341408 | 0.126114 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2664694 | tctctctctctctct[A/C/T]tctctctcCATCTAT | 5048 |
rs3029954 | in-del | -/TA | | | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2664983 | CAGCCCTTGAGTGTA[-/TA]TAACAAGTGGTAAAG | 5048 |
rs3213695 | snp | A/C | 0.0001006 | 0.00709154 | utr-variant-5-prime | PAFAH1B1 | GRCh38.p7 | 17:2638240 | GCTTTTTGATTTCCC[A/C]AAGGAGGGACATACC | 5048 |
rs3213696 | snp | C/T | 0.155793 | 0.231571 | PAFAH1B1 | 17 | allele_origin=T(germline)/C(germline) | 17:2670358 | AGGATAGTGCTTTAA[C/T]AGTAATTTCTATCAT | 5048 |
rs3213697 | snp | C/T | 0.192088 | 0.2432 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2670564 | TTTGTATGAGTATTT[C/T]TTGGTAAGAAAAACT | 5048 |
rs3785957 | snp | C/T | 0.192401 | 0.243274 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2657875 | CATCCCTTCTTCCTC[C/T]TTCCTTTTTTCTTTA | 5048 |
rs3785958 | snp | C/T | 0.207864 | 0.246424 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2658003 | CAACCTGACTTTGCC[C/T]TATGAGTTTTTGAAA | 5048 |
rs4362427 | snp | C/G | 0.195526 | 0.243993 | upstream-variant-2KB | PAFAH1B1 | GRCh38.p7 | 17:2592426 | acgaggtcaagggat[C/G]gagaccatccgggcc | 5048 |
rs4556824 | snp | C/T | 0 | 0 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2631562 | ctctatccctgcatt[C/T]tgcgtggctctctaa | 5048 |
rs4609889 | snp | A/C | 0.380919 | 0.21298 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2640167 | acttaagtagttccc[A/C]aaaataaggatattc | 5048 |
rs4790087 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2673141 | CTGGTGTTGCAGTCA[C/T]TTCGACTTTAACCCG | 5048 |
rs4790088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2680662 | CCTCAACCTTTCCCA[C/T]TGGCAGGTGTATACT | 5048 |
rs4790089 | snp | C/G | 0.17461 | 0.238362 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2680817 | ATGGACCAAAGCCTG[C/G]GTAAGGTGGGCTAAT | 5048 |
rs4790090 | snp | A/T | 0.0103295 | 0.0711199 | utr-variant-3-prime | PAFAH1B1 | GRCh38.p7 | 17:2682488 | CTAATAGCAACTCAT[A/T]TATTTCATTTTGGTC | 5048 |
rs4790348 | snp | A/G | 0.206947 | 0.246265 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2650542 | TACAGGGATGTCGGC[A/G]CAGTCTTGGGACCTA | 5048 |
rs4790352 | snp | A/G | 0.339429 | 0.233457 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2675256 | GATCCGACCACCTCA[A/G]CTTCCCAAAGTTCTG | 5048 |
rs4790353 | snp | G/T | 0.338976 | 0.23363 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2675354 | TTTTTAAAACTACAT[G/T]TCAATAAACAAAGGA | 5048 |
rs4790354 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2676159 | TGGGCCGATCGATCA[C/T]CTGAGGTTAGGAGTT | 5048 |
rs4790355 | snp | G/T | 0.322483 | 0.239262 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2680682 | AGGTGTATACTATCA[G/T]ATACTAGAAACTCAG | 5048 |
rs4790356 | snp | A/G | 0.273318 | 0.24891 | utr-variant-3-prime | PAFAH1B1 | GRCh38.p7 | 17:2682935 | CCTATCTGTAAGTGG[A/G]TAAGTCTGTATGTGT | 5048 |
rs6502385 | snp | A/G | 0.363985 | 0.222503 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2594755 | TTTGATGCTGTTAAC[A/G]TTCAGCTTCGAGGCT | 5048 |
rs6502400 | snp | A/G | 0.081446 | 0.184634 | intron-variant, upstream-variant-2KB | PAFAH1B1 | GRCh38.p7 | 17:2612303 | ccgcctcgtgggttc[A/G]agtgattctcctgcc | 5048 |
rs6502438 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2643031 | atgagatagatatat[A/G]tcttcttatttctcc | 5048 |
rs6502440 | snp | A/G | 0.33875 | 0.233717 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2650770 | ACCATTTTTTTGTGT[A/G]TGTATAATGCCATTC | 5048 |
rs6502442 | snp | C/T | 0.457388 | 0.139608 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2651979 | cctaaaaatctcagc[C/T]tccccctattcatcc | 5048 |
rs6502449 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2667757 | TGGCTTTCCAGGAGT[A/G]TGGGAATATACAAGC | 5048 |
rs6502457 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2674723 | ATAGTATAAATGTTT[C/T]TTTAAATGAAGACTA | 5048 |
rs6502458 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2674741 | TAAATGAAGACTAAT[C/T]CATATGGCAGCCTCT | 5048 |
rs6502460 | snp | G/T | 0.273587 | 0.248885 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2676971 | ATCGAGCTAACTTGG[G/T]GAAATCCCGTCTCTA | 5048 |
rs7207159 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2646933 | GTGGGCACCACCTTC[A/G]TAGAAACACTGGGTG | 5048 |
rs7207614 | snp | C/T | 0.469049 | 0.120489 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2657304 | GCTGTAAGGCAGTGG[C/T]GCCATCTTGGCTCAC | 5048 |
rs7207987 | snp | A/T | 0.165527 | 0.235296 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2671569 | AGTTCTTTCTAATGC[A/T]TTTTTTTTTTTTACC | 5048 |
rs7209087 | snp | C/G | 0.356597 | 0.226135 | intron-variant, upstream-variant-2KB | PAFAH1B1 | GRCh38.p7 | 17:2634902 | GGTGTGGTGGCTCAA[C/G]CCTGTAATCCGAGCA | 5048 |
rs7209145 | snp | A/C | 0.264906 | 0.249555 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2675080 | gatctcggctcactg[A/C]aacctccgcctccca | 5048 |
rs7209407 | snp | A/G | 0.384785 | 0.210554 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2604955 | TTTGAGGTTGGAGAG[A/G]CACGTCTGAGCCAGA | 5048 |
rs7209580 | snp | C/G | 0.352287 | 0.228117 | intron-variant, upstream-variant-2KB | PAFAH1B1 | GRCh38.p7 | 17:2635124 | GCTGAGATTGTGCCA[C/G]TGCCCTCCTGGGCAA | 5048 |
rs7209748 | snp | C/G | 0.357024 | 0.225933 | intron-variant, upstream-variant-2KB | PAFAH1B1 | GRCh38.p7 | 17:2635219 | TATTTAAGACAATAC[C/G]TAGCACATAATATAA | 5048 |
rs7210936 | snp | A/G | 0.468148 | 0.122112 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2672049 | aaggcaggaaggatt[A/G]cttgaggacaggagt | 5048 |
rs7211181 | snp | A/C | 0.383632 | 0.211288 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2663081 | tcacgccattgcacc[A/C]cagcctgggcaataa | 5048 |
rs7211338 | snp | A/C | 0.357238 | 0.225832 | intron-variant, upstream-variant-2KB | PAFAH1B1 | GRCh38.p7 | 17:2635184 | aaaaaaGACCAAGTC[A/C]TTTTCCCCATTAAAC | 5048 |
rs7211841 | snp | A/G | 0.355954 | 0.226437 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2650994 | TTTGGGAAGACCTTC[A/G]CTAATCATGACTACA | 5048 |
rs7212391 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2657312 | GCAGTGGCGCCATCT[C/T]GGCTCACTGCAATAC | 5048 |
rs7212585 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2644377 | tgaaaccccatctct[A/T]ctaaaaatacaaaaa | 5048 |
rs7213173 | snp | G/T | 0.351853 | 0.228311 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2632573 | tttaacgtACAGTTG[G/T]CCCtctgtatctgtg | 5048 |
rs7213463 | snp | A/G | 0.130008 | 0.219321 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2650907 | GGTACTGAGTCACCC[A/G]TGGTCATGTGTTGCA | 5048 |
rs7213741 | snp | A/G | 0.355954 | 0.226437 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2651036 | TTTTACTTTCTTAAG[A/G]CCTTTTTGTTTTCAT | 5048 |
rs7214105 | snp | A/G | 0.350327 | 0.228986 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2601993 | ATCAAAGTTTATCAT[A/G]TATGAATGAACAGTG | 5048 |
rs7215780 | snp | A/T | 0.42666 | 0.176893 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2648762 | ccattcctgatggtt[A/T]aaaaaaaaaaaccct | 5048 |
rs7216462 | snp | A/C | | | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2635952 | caaaaatagaaaaat[A/C]caaaaaaaaaaaaaa | 5048 |
rs7216704 | snp | C/T | 0.324145 | 0.238752 | downstream-variant-500B | PAFAH1B1 | GRCh38.p7 | 17:2685728 | AAGAGTGACACGAAT[C/T]GGTGTCAGGGCAGTA | 5048 |
rs7216860 | snp | A/G | 0.358515 | 0.225221 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2597679 | ctctcaaagttctgg[A/G]attacagatgtgagc | 5048 |
rs7217392 | snp | C/T | 0.45198 | 0.147323 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2606803 | TTTTGTCATATTTGC[C/T]TCAGAGCtttttttt | 5048 |
rs7218235 | snp | A/G | 0.263809 | 0.249618 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2660973 | atagtatctcattgt[A/G]gttttgatttgcatt | 5048 |
rs7219015 | snp | C/T | 0.279461 | 0.248258 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2652298 | cgggtgcctgtagtc[C/T]cagctactcgggagg | 5048 |
rs7219416 | snp | A/G | 0.286825 | 0.247273 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2652177 | acactttgggaggcc[A/G]aggcgggcaaatcac | 5048 |
rs7219436 | snp | A/G | 0.224709 | 0.248717 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2652213 | caggagatcgagacc[A/G]tcctggctaacacgg | 5048 |
rs7221255 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2663985 | ggcgtgagccaccgc[G/T]cccagccTctggtct | 5048 |
rs7221826 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2656068 | actgagactacagac[A/G]tctgccaccacgccc | 5048 |
rs7223347 | snp | A/T | | | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2652004 | tcatccttccctgcc[A/T]ccctaaacccctcat | 5048 |
rs7223411 | snp | A/T | 0.149665 | 0.228982 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2673883 | ATTAGCTCCTTAATG[A/T]TATGTCTGTTAGCTT | 5048 |
rs7223817 | snp | C/T | 0.259951 | 0.249802 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2652287 | gggcgtggtggcggg[C/T]gcctgtagtcccagc | 5048 |
rs7224765 | snp | A/G | 0.258288 | 0.249863 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2678237 | aggaaccccatcgct[A/G]ctaaaaacacaaaat | 5048 |
rs7224954 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2619406 | gctaattaaaaaaaa[A/T]ttttttggtagagac | 5048 |
rs7225738 | snp | C/T | 0.469445 | 0.119766 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2643307 | cccttttgtggagaa[C/T]ggggtctcgctatat | 5048 |
rs7225921 | snp | G/T | 0.451856 | 0.147493 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2656101 | ctaattttttttgta[G/T]ttttagtagagacgg | 5048 |
rs8064409 | snp | C/G | 0.356597 | 0.226135 | intron-variant | PAFAH1B1 | GRCh38.p7 | 17:2643797 | agctcctgacctcaa[C/G]agatcacctgcttcg | 5048 |