SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs141718010 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21054942 | ACCATAGTGAGGCAC[A/T]AGTCTAGGGATACCA | 26524 |
rs141767697 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038370 | ATAATTCCATCTTTT[-/T]TTTTTTAATTTAAAA | 26524 |
rs141778268 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21020321 | GAACAATTCTATTAT[C/T]ATCCTATTATTTGCC | 26524 |
rs141785776 | snp | A/C/G | 0.00279242 | 0.0372774 | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972825 | TTGTTCCCATTTTAC[A/C/G]CAAGTTGGTCACAGA | 26524 |
rs141897751 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040377 | GACAGACCTTGTCTC[-/A]AAAAAAAAAAAAAAA | 26524 |
rs141913189 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:21050748 | GCCTTGCTTACCATC[A/G]CCGTGCCAAATACGC | 26524 |
rs141913267 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:20987707 | AAAGGCGAAAGGGAG[A/G]TCACACCATTTGCAA | 26524 |
rs141959381 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20986849 | ACATATCCTATGCAT[A/G/T]TAACAAAATATCACA | 26524 |
rs141971390 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | LATS2 | GRCh38.p7 | 13:21012739 | TGAACAGCGCTAGCA[A/C]AGGGCGGGAGCTGTG | 26524 |
rs141992182 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | LATS2 | GRCh38.p7 | 13:21049872 | ATGCCTATAATCCCA[A/G]CTCTTTCGGATGCCG | 26524 |
rs141993097 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:20985836 | GGATCATCTGAGGTC[A/G]GAAGTTTGAGACCAG | 26524 |
rs141995731 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | LATS2 | GRCh38.p7 | 13:20984184 | GGTGATCTGCCCACC[C/T]TGGCCTCCCAAAGTG | 26524 |
rs142033815 | snp | A/G | 0.000577201 | 0.0169784 | missense | LATS2 | GRCh38.p7 | 13:20988128 | TTGTCGCCGCCCTCG[A/G]GCTCGTTGGGGCCCG | 26524 |
rs142061899 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:20992242 | CCCATGGCAGCAGCA[A/C]GCAAGGGTAGGTGGA | 26524 |
rs142095268 | in-del | -/AGATATAT/AT | 0.305934 | 0.243663 | intron-variant | LATS2 | GRCh38.p7 | 13:21007531 | AGTCGTAGGGGATGG[-/AGATATAT/AT]ATATATATATATAGT | 26524 |
rs142105650 | snp | A/G | 6.64099e-05 | 0.00576199 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981491 | GAGCACCTCGGGTGC[A/G]ATGTAGTTTGGAGTC | 26524 |
rs142152183 | snp | C/G | 0.000153988 | 0.00877328 | missense | LATS2 | GRCh38.p7 | 13:20983447 | GATCAGCAGGCTCAT[C/G]ATGTCCCCACCAGGG | 26524 |
rs142193763 | in-del | -/CTCACGGATGACAT | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024580 | CTTCCTGCATAGCGC[-/CTCACGGATGACAT]CTCACTTTGACGGTC | 26524 |
rs142208157 | in-del | -/AAAAATAAAAAT | 0.326976 | 0.237854 | intron-variant | LATS2 | GRCh38.p7 | 13:20987213 | ATAAATTAAAAAATA[-/AAAAATAAAAAT]AAAAAAAACACAAAT | 26524 |
rs142292013 | in-del | -/G | 0.0248432 | 0.108648 | intron-variant | LATS2 | GRCh38.p7 | 13:21060048 | CATTTCTCATCCAAA[-/G]GCCTCAGAACAGCCG | 26524 |
rs142294481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009410 | ACTGGTTCCAATTTG[C/T]TGCTGGATCATTGGT | 26524 |
rs142301699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21036713 | GGGACACGGAGGTTA[C/T]AGTGAGCCAAGATGG | 26524 |
rs142338418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035621 | AATAATCTCAGCAGT[A/G]AACGTTTGGTGTGAC | 26524 |
rs142359259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030960 | GTCTTTACGACACTT[C/T]CATTTCAGAAAGACA | 26524 |
rs142389190 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:21034582 | GAAGGTGCCTATTCC[C/T]GATGACACTGTGGAC | 26524 |
rs142394061 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | LATS2 | GRCh38.p7 | 13:21034004 | CTGGTAGGACAACGA[C/T]CTTATTATTAAGTAA | 26524 |
rs142447314 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | LATS2 | GRCh38.p7 | 13:21022345 | AAGTGCATGTACTGA[C/G]TCAGGACTGAGAACC | 26524 |
rs142485410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996888 | ATTCATAAATATTAA[A/G]TGAAAAATTATTTTG | 26524 |
rs142593118 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21003427 | CAACTAATTTTTGTC[C/T]GTCTTTCTTTTTTTT | 26524 |
rs142619969 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | LATS2 | GRCh38.p7 | 13:21013791 | GGCAACACAGCAAGA[C/T]CCCGTCTCTACAAAA | 26524 |
rs142694965 | snp | A/G | | | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989195 | GCCGTCAGCGCCGAA[A/G]CTTGGGCCCTCGTAG | 26524 |
rs142801103 | snp | C/G | 0.0792508 | 0.182605 | intron-variant | LATS2 | GRCh38.p7 | 13:21042909 | GAATTGCTTGAACCT[C/G]GGAGGCAGAAGTTGC | 26524 |
rs142804110 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21016838 | ACACAACACCTGAAC[G/T]AACTCTCTTTATCAC | 26524 |
rs142843444 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:20979624 | GCAAATGCTGACCAA[A/G]GATTCATGGGTACAT | 26524 |
rs142866652 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | LATS2 | GRCh38.p7 | 13:20985622 | CGCACACCTGTAGTC[C/T]CAGCTCTCAGGAGGC | 26524 |
rs142900440 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | LATS2 | GRCh38.p7 | 13:21002128 | CCATGTTAGCTAAGA[C/T]GGTCTCGATCTCCTG | 26524 |
rs142910797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028989 | AGTTCTGGTAACTTT[G/T]AAAAATAGATTCCTT | 26524 |
rs142945405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038002 | CCCACGTTTGTAGTC[A/C]CAGCTACCTGGGTGG | 26524 |
rs142969829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21052894 | TATGTCAAAGGCACC[A/G]ATGCTTCCTGTCCTC | 26524 |
rs143007708 | snp | C/T | 0.021333 | 0.101051 | intron-variant | LATS2 | GRCh38.p7 | 13:20977310 | TGAGGCATGAGAACC[C/T]GGAAGGCAGAGGTTG | 26524 |
rs143027949 | snp | C/G/T | 0.0135063 | 0.0812451 | intron-variant | LATS2 | GRCh38.p7 | 13:21010824 | ATAAGGTCTGACTTA[C/G/T]GTTGACCAATCAGAG | 26524 |
rs143161995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21007352 | GGAATGTCAGGACAT[A/G]CATCCTCCATACTGA | 26524 |
rs143202552 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | LATS2 | GRCh38.p7 | 13:21036330 | AGCCACTGTGCCTGG[A/C]CAAAAGCCCATTTTA | 26524 |
rs143263468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21045436 | ACATTACAATTTCAG[A/G]AGACCTCAGCAACTT | 26524 |
rs143287640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050397 | ACCAAGGGGAACCAC[C/T]TTCATGTCATCTAAC | 26524 |
rs143305057 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061985 | CAGAAAAGGACAGAC[A/G]GCTATTGGGACAGTG | 26524 |
rs143330178 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21012590 | AGTCAAATTTTCTAC[A/C]TAGTAGTGTTCCTAT | 26524 |
rs143340763 | in-del | -/C | | | frameshift-variant | LATS2 | GRCh38.p7 | 13:20989297 | GGGGTTGGCATGAGC[-/C]CCCTTTCCTGCAGTG | 26524 |
rs143343911 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016075 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 26524 |
rs143377449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047290 | GCTATGTAATAGAGA[C/T]GGATGCTTAGGACAG | 26524 |
rs143402079 | snp | C/T | 1.65116e-05 | 0.00287324 | missense | LATS2 | GRCh38.p7 | 13:20991374 | CGATGCTCCTGCTGC[C/T]AGTCTGCTTGAGAGC | 26524 |
rs143449172 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:21044320 | AATAACAAATAACAC[C/T]GTTAGCCTTTTCCTA | 26524 |
rs143531605 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:21003397 | TAGCTGGGACTACAG[A/G]TGCGCCACCACACAC | 26524 |
rs143535162 | snp | A/C/G/T | 0.0013027 | 0.0254932 | missense | LATS2 | GRCh38.p7 | 13:20989211 | CTTGGGCCCTCGTAG[A/C/G/T]GGGTACCGCTCAGCT | 26524 |
rs143588109 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20992695 | CTGAAAATGTAGAAC[A/G]GGGAGCTCCGGAAAG | 26524 |
rs143590005 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21032199 | GTTTTATAGGTAAGA[C/G]CTATGTGCTGCAATT | 26524 |
rs143631255 | snp | A/G | 4.96742e-05 | 0.00498344 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975256 | CATCGGCCCCATTCC[A/G]CCCCAGGCGGTGGTC | 26524 |
rs143698126 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:20994393 | GAGCTATGTTTTAAA[C/T]ACTGAAGGAAATGGG | 26524 |
rs143741195 | snp | A/G | 8.24232e-05 | 0.0064191 | missense | LATS2 | GRCh38.p7 | 13:20988108 | CCTTGGCGCTTTTGC[A/G]GCTCTTGTCGCCGCC | 26524 |
rs143755377 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:20995505 | GTGTTCTGGTGTCTA[C/G]CGTGTAGAAAGAGAT | 26524 |
rs143768575 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:21056409 | CTCTATTAGACAGCT[C/T]TGTACATTATATTTT | 26524 |
rs143772707 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21049154 | TCTTCCTGGAGACAT[A/T]GGAGGTCAAAGGACT | 26524 |
rs143804776 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20990645 | AGGCTTGAGCCACTG[C/T]GCCTGGCCATGAATC | 26524 |
rs143882901 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21060353 | CGCAGGTGAGCTTAC[A/C]TCAGAAGAGAAAGCC | 26524 |
rs143886370 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | LATS2 | GRCh38.p7 | 13:20998365 | GTCTCAAACAAACAA[A/T]CAAAAATTAATTAAT | 26524 |
rs143948304 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | LATS2 | GRCh38.p7 | 13:21029501 | ATTGCATTTATAAAA[C/G]ATATTGGAATGTCGG | 26524 |
rs143951018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20978540 | TGCGAACAATGATAT[A/C]ATATCCAAATAAAGA | 26524 |
rs144004880 | in-del | -/GGT | 0.0248432 | 0.108648 | intron-variant | LATS2 | GRCh38.p7 | 13:21008377 | AGGGGCAGCCCGCTG[-/GGT]GGTGTTGTTAGAATG | 26524 |
rs144074278 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LATS2 | GRCh38.p7 | 13:21044908 | GCTTTTTATTTTTTG[C/T]AGAGATGGGGAGTCT | 26524 |
rs144081478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980133 | CCAATTAAAATAACA[G/T]AACTGAAAAACATAA | 26524 |
rs144082538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21043167 | ACATAGTGAAACCCC[A/G]TCTCTGCTAAAAATA | 26524 |
rs144119196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981810 | AGCTGCTCCATAGGG[A/G]CAGCCTGCTGTTCCT | 26524 |
rs144140968 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047024 | ATCATGTGGGTAAGA[A/G]TTATTACTACAGAAC | 26524 |
rs144245359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046262 | ATGGGAGAGAAATGT[C/T]CATTTGTCATTTTCA | 26524 |
rs144289902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21055520 | GGCCTGTGTAAACAA[C/T]GTGAGAGCAAAATTT | 26524 |
rs144300061 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008923 | GGGAAAACTGGAAAC[C/T]ATCTAAATGTCCATC | 26524 |
rs144361960 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21027544 | TGTAGTAAGTCCCAT[A/G]TAAGTGTGGGTCTAT | 26524 |
rs144404651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004462 | AAAAGCTTCTGTAAT[A/G]CAAGGGAGAATCAAA | 26524 |
rs144411531 | snp | A/G | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060926 | CCCCCGGAGACAGCG[A/G]AAGCAGAGGCGCGCC | 26524 |
rs144453954 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21021450 | TGCACTCCAGAGCCC[A/G]GGCAGCAGAGTGAGA | 26524 |
rs144464647 | snp | G/T | 0.000153988 | 0.00877328 | missense | LATS2 | GRCh38.p7 | 13:20981642 | CTGTCCTGTCTGACA[G/T]GGCTCCCTTCACCCA | 26524 |
rs144489503 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:20996117 | ACAGATCTCAATGCT[A/G]GAGTTGAAGCCATCA | 26524 |
rs144509764 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21032912 | AAAACCTCATAGCCT[G/T]GTGGCAGGGGAGGTG | 26524 |
rs144577478 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LATS2 | GRCh38.p7 | 13:21054671 | CAGGGCAGTCGAGAC[C/T]GGACATTTCTATGTC | 26524 |
rs144582350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038293 | TGATCTGATGGGCTA[C/T]AGGACCTCAATTCTG | 26524 |
rs144663667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043405 | GATGCATACAACTCT[A/G]AAGGTACGGTTATCT | 26524 |
rs144696152 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LATS2 | GRCh38.p7 | 13:21002194 | CTGGGATTACACGTG[C/T]GAGCCACTGCGCCCG | 26524 |
rs144787936 | snp | A/G | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21006291 | TTAGTGAGCAGAGAA[A/G]GAAGACCAGGCCCAA | 26524 |
rs144792361 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20985302 | AGCTTCTGCAGAGCA[A/C]AGGAAACAACAGAGT | 26524 |
rs144810264 | in-del | -/GT | 0.0209421 | 0.100162 | intron-variant | LATS2 | GRCh38.p7 | 13:21004546 | CACTGACCAGCACAC[-/GT]GTGTGTCAGCATGAA | 26524 |
rs144849048 | in-del | -/GT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20983013 | AAAAAAAAAAAAAAA[-/GT]AAACCTGAAATCCAC | 26524 |
rs144855804 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LATS2 | GRCh38.p7 | 13:21037879 | TGCAGCTACAGGTGG[A/G]TCCTGTCCGCCAACT | 26524 |
rs144863654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004901 | TACACAAAATCCACA[A/G]GGGGAGTCATCATGT | 26524 |
rs144886469 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21048273 | ATCCTAGAAGTGACT[C/T]GGTATGTCTGGGAAG | 26524 |
rs144901841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022111 | TGAAAAATACCAATG[A/C]CCAGAATCCACCCTG | 26524 |
rs144970358 | in-del | -/T | 0.136166 | 0.22258 | intron-variant | LATS2 | GRCh38.p7 | 13:21054987 | TCTTAAGTGAATATG[-/T]AAAAAATAGTACCTA | 26524 |
rs144978189 | in-del | -/T/TT | 0.0236746 | 0.106192 | intron-variant | LATS2 | GRCh38.p7 | 13:21005805 | GAGACCCCTACTCTA[-/T/TT]TAAAAAAAAAAAAAA | 26524 |
rs145000849 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21021668 | GCAGCTTAATTTTTG[A/G]AGAATTGAGGACACC | 26524 |
rs145008601 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | LATS2 | GRCh38.p7 | 13:21017915 | ACAGGCGTGAACCAG[C/G]ATGTCCAGCCTGATT | 26524 |
rs145052665 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20987584 | TAAGCGAGGACATAC[A/C]CTAAAACTTAATTTG | 26524 |
rs145113867 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:20991880 | GAGTCATATATTACA[C/T]GCCTACTGTTTACAA | 26524 |
rs145117380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21026138 | AGAAGAGAAGGAAAC[A/G]AATTATTTGCATCCA | 26524 |
rs145120725 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | LATS2 | GRCh38.p7 | 13:20983707 | TGATCTTGACAAACA[C/T]AGACTTGTCCATCTT | 26524 |
rs145164340 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983285 | GAGGCCGAAATCTGT[A/G]AGTTTAATGTGACCA | 26524 |
rs145227490 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | LATS2 | GRCh38.p7 | 13:20998705 | GCGGCGCTCCCGGCG[A/C]TCTTGGGCAGGTGGG | 26524 |
rs145230507 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061527 | GGGCGCTCACGCCGC[A/G]GTTCCAAAGCGCAGA | 26524 |
rs145269828 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20989584 | CACATCCCGAGGTGC[A/G]TCCCTGCCCCCTGGG | 26524 |
rs145325971 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973465 | TCAAATATAAATCAC[C/T]TTAAATAGGAATCAT | 26524 |
rs145334455 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21005121 | TGGTGTCATGACTAG[A/G]TAGAGGCCCATGTTT | 26524 |
rs145384605 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:21056276 | ATTCCTGGACTCAAG[C/T]GATCCCCCCGCCTCG | 26524 |
rs145432416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008700 | CAACAGCAAGTGTTG[A/G]CAAAGTTAGAGAGAT | 26524 |
rs145468370 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | LATS2 | GRCh38.p7 | 13:20990502 | TAAATACAGACGAGG[A/T]CTCCCTCTGTTGCCC | 26524 |
rs145592764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21002723 | TTAGAGACAGGGTCT[C/T]GCTCTGTCACCCAGG | 26524 |
rs145596116 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:21006712 | CCACTTACTCGACAA[A/T]GGCACATAGGCGTGC | 26524 |
rs145604868 | snp | A/G | 0.00168015 | 0.0289353 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975215 | GGAGAAGTCAATGGC[A/G]CTGAAGAAGGGGTGG | 26524 |
rs145691003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057154 | AATCCAGCTTACATT[A/C]TTAAGATCCTTACCA | 26524 |
rs145719220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053518 | GCAACATCTGTTGAA[A/C]GACACAGGTAGTCAC | 26524 |
rs145737186 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | LATS2 | GRCh38.p7 | 13:21030371 | GACACGGGTGGATCA[C/T]GAGGTCAGGAGATCG | 26524 |
rs145797074 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21022994 | ATTTTCTCTGATTAG[C/G]CAGGAAAGGGGGTGT | 26524 |
rs145840066 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21026428 | CCCATTGATGCTGTT[G/T]TATAAGTGGTCCCTC | 26524 |
rs145865279 | in-del | -/A | 0.0170251 | 0.090679 | intron-variant | LATS2 | GRCh38.p7 | 13:21045361 | ACCCGAATAAACACC[-/A]AAAAAAGGGGCTAAG | 26524 |
rs145945763 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:20997816 | GCAGAAGTATTTCAC[A/G]TGCATTGCCATGTGA | 26524 |
rs145980105 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000795 | ATAAGCAAAAACAAA[A/G]CAGGCAACTTTCAAT | 26524 |
rs146066011 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | LATS2 | GRCh38.p7 | 13:21020151 | TCAGTTCACATAAAA[C/T]ATACCTGAAAACACA | 26524 |
rs146074368 | in-del | -/GGG | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024515 | GTGGGGTTCAGTGGC[-/GGG]GGTTCTCGCCAGGGC | 26524 |
rs146140963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21034350 | GCATTGGGGTGGCCA[C/T]GTGCCCAGGTGAAGT | 26524 |
rs146145347 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063158 | GAGTGCAGTGGCACA[A/C]TCATAACTTACTGCA | 26524 |
rs146259834 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21016966 | TCTCAGACATAAGAG[C/G]GATTACAGCATCAAA | 26524 |
rs146320345 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | LATS2 | GRCh38.p7 | 13:20998992 | CTTGTCCACGCAGGA[C/G]AGGGATCCCCGCGAC | 26524 |
rs146343904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21016476 | GTAGAGACAGGGTTT[C/T]ACTATGTTGGCCAAG | 26524 |
rs146387162 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21035777 | CCCAGCTCCCAAAGG[A/G]CTGCAGGGACCAACA | 26524 |
rs146479948 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LATS2 | GRCh38.p7 | 13:21043198 | CAAAAATTAGCCAGG[C/T]GTGGTGTTGCGTGCC | 26524 |
rs146529403 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047027 | ATGTGGGTAAGAGTT[A/G]TTACTACAGAACTAC | 26524 |
rs146578805 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | LATS2 | GRCh38.p7 | 13:21057359 | ACTTAAAACACTTGT[C/G]ACAATTAACTTGACA | 26524 |
rs146602298 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:21028199 | GTTTTTTGTCCTTGC[A/G]ATAGTTTCCTGAGAA | 26524 |
rs146731231 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | LATS2 | GRCh38.p7 | 13:21009926 | ACAGAAGGGCCAGGC[A/G]TGGTGGCTCATGCCT | 26524 |
rs146765369 | snp | A/G | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:20976452 | AAAATAAATTGGACT[A/G]CATAAAAATTTAAAA | 26524 |
rs146819002 | snp | A/G | 5.00396e-05 | 0.00500173 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989219 | CTCGTAGGGGGTACC[A/G]CTCAGCTGGTGGTAG | 26524 |
rs146839607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21056556 | TTTCCTAATAGCAAG[A/C]GACCCAACAGGATGG | 26524 |
rs146852814 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:20994167 | GAAAAATCAGCAAGG[A/G]GACCACAAGTGAAGA | 26524 |
rs146872572 | in-del | -/TTC | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062803 | TCATCCTCCTCCCCT[-/TTC]CCCTCTCTTTCAATC | 26524 |
rs146899010 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:20984253 | TTGTTTTTTTATATC[C/T]ATATATAGACATGAA | 26524 |
rs146901823 | snp | C/G | 0.292523 | 0.246357 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060613 | ACTGGCCCGTGAGCC[C/G]GCGGCGCGGCCGCGG | 26524 |
rs146904043 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21048671 | AAACCCTGTCTCTAC[A/T]AACTAAACATAAAAA | 26524 |
rs146914300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21045048 | GCTGTGTATTAATGT[A/G]TAACTGGTGCCACCT | 26524 |
rs146923938 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:20984059 | TCTCAGCCTCCCGAG[C/T]AGCTGGGACTACATG | 26524 |
rs146933483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21018947 | CACTGTGCCTGGACC[C/T]GAGTCCCTCTTTACG | 26524 |
rs146933786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20981401 | AAAGCTAGAGCCAGC[A/G]AGACTCAGCTCACGT | 26524 |
rs146957910 | in-del | -/GGGCTCC | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023147 | ATAGCGCTGCATCGA[-/GGGCTCC]GGGCTCCGAGGGCTC | 26524 |
rs147009773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21031238 | TTAGATCTGTACATG[A/G]ATGCTTTTCACCACA | 26524 |
rs147038091 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LATS2 | GRCh38.p7 | 13:21002506 | CAGCCTCCAGAGTAG[C/T]TGGGACTACAGGTGC | 26524 |
rs147129744 | snp | C/T | 0.000214272 | 0.0103484 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045754 | AGCTGCAGAGGTGCC[C/T]GATTCATTAGCAAAA | 26524 |
rs147156074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051279 | TTGGTCCTGAGGATG[C/T]AGAAAGACTGATTTG | 26524 |
rs147172274 | snp | A/G/T | 0.000831861 | 0.0203781 | missense | LATS2 | GRCh38.p7 | 13:20988207 | GCTCCGACTTGCTGC[A/G/T]CAGCAGCAGGTGCTT | 26524 |
rs147198702 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | LATS2 | GRCh38.p7 | 13:21055063 | GTTCCTTCAGTTTCA[C/T]AGAGAATGAAAGCAT | 26524 |
rs147227478 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:20995576 | AGTTAGACTGTGACA[C/T]AGGATAGATGAAAGG | 26524 |
rs147261893 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038169 | AGGCCGGAGAAAGAC[A/G]CAGAAGGGGCAACCA | 26524 |
rs147289953 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | LATS2 | GRCh38.p7 | 13:20982059 | GGATTTAAACAACAT[G/T]AACAAAGGTTACTTC | 26524 |
rs147300161 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:20978628 | ACTAGCATTTTCTTC[C/T]ACCTTTGCCATCCCT | 26524 |
rs147302467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042620 | TGAGCCTGGAAGGTC[A/G]AGGCTGCAGTGAGCA | 26524 |
rs147389119 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21055853 | GGCAGACGGGCCAGG[C/G]CTCCAGCCAGATGCT | 26524 |
rs147410952 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024442 | CTCTGAATGATAATA[A/C]TAATAAATGATAATA | 26524 |
rs147440484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028995 | GGTAACTTTTAAAAA[C/T]AGATTCCTTAAGGTG | 26524 |
rs147515729 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008270 | GCTGGGGTTCTCAAG[A/G]GGCACCCCCTGCTCT | 26524 |
rs147545133 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21012696 | GCAGATTTTTTAAGG[G/T]AACGAGCAGAAAGAG | 26524 |
rs147587032 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20989727 | CGGTTCCCAAAGCGC[A/T]GCTCCCTCACAGAAA | 26524 |
rs147596822 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20986296 | AGGAAAGGAAATCAG[G/T]ATATCAAAGGGATAC | 26524 |
rs147628171 | snp | C/T | 9.88386e-05 | 0.00702919 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975120 | CAAGGGCTTTCTTCA[C/T]CTACGGGGTCGAAAT | 26524 |
rs147633185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21036124 | TGGTCTCGAACACCC[A/G]ACCTCGGATGATCCA | 26524 |
rs147706247 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | LATS2 | GRCh38.p7 | 13:21035447 | TTTAAATGAAGCCCC[C/T]ACACAGAATTGCATG | 26524 |
rs147758795 | in-del | -/AAC | 0.498982 | 0.0225409 | intron-variant | LATS2 | GRCh38.p7 | 13:21036775 | AAAACTCCGTCTCAA[-/AAC]AACAACAACAACAAC | 26524 |
rs147765759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051920 | CAAGGTCACACTACT[A/G]CACTCCAGCCTGGGA | 26524 |
rs147767071 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LATS2 | GRCh38.p7 | 13:21015010 | AGTGCGCTCACCGCC[A/G]TATCCCTGGGGTCCA | 26524 |
rs147787318 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21021529 | AAGGCATTTCTGATA[C/T]GCACGTTTAAGTTTC | 26524 |
rs147810046 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21018615 | CCTGAGAGTGACATG[C/G]TGTTTCATACCAAGA | 26524 |
rs147871895 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | LATS2 | GRCh38.p7 | 13:21038336 | TGTGTGTGTGGTATA[C/T]GTATTATATAGTTTA | 26524 |
rs147892150 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21004947 | TGACTCCAAGGGACA[A/G]AGACCAGCCCCGGCG | 26524 |
rs147978028 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | LATS2 | GRCh38.p7 | 13:21006723 | ACAATGGCACATAGG[C/T]GTGCCTCACTGCACA | 26524 |
rs148029816 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | LATS2 | GRCh38.p7 | 13:21003401 | TGGGACTACAGGTGC[A/G]CCACCACACACAACT | 26524 |
rs148084153 | snp | C/T | 1.74934e-05 | 0.00295743 | synonymous-codon, missense | LATS2 | GRCh38.p7 | 13:20975332 | CAGCTTCACCTGGGC[C/T]GGAATGTGGAGCGTG | 26524 |
rs148105702 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:20985474 | CCAGATATGGTGGCT[C/T]ACGCCTGTAATCCCA | 26524 |
rs148106190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049221 | GGAGGTATCCAGAGG[C/G]TCAATTCCCAGCCAT | 26524 |
rs148126167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20994461 | GGGCACAAAGTACAT[A/G]CAGAGTCACAGAGTG | 26524 |
rs148138215 | snp | A/C/T | 0.000659516 | 0.0181475 | missense | LATS2 | GRCh38.p7 | 13:20988120 | TGCGGCTCTTGTCGC[A/C/T]GCCCTCGGGCTCGTT | 26524 |
rs148156960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21044477 | TTCCGCTTCATGCAA[C/T]TGTAATTTTTAAGAT | 26524 |
rs148189470 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | LATS2 | GRCh38.p7 | 13:20978018 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 26524 |
rs148240343 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21036341 | CTGGCCAAAAGCCCA[C/T]TTTAACAGGAAAGTG | 26524 |
rs148317971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21016283 | TGAGACAGCGTACCC[A/G]GCCTATTTTTATTTT | 26524 |
rs148335438 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | LATS2 | GRCh38.p7 | 13:21028684 | CAAGCAATTCTCCTG[C/T]CTCAACCTCCCAATT | 26524 |
rs148431484 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21059502 | CTCGGGAGACTGAGG[C/T]AGGAGATCGCTTGAA | 26524 |
rs148431566 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996746 | ACTCCATATCAAATT[A/C/T]AGCAAAACCTGACAT | 26524 |
rs148449356 | snp | A/G | 3.72308e-05 | 0.00431439 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988706 | GCCCAATTCATACAG[A/G]TCCACGTTGAGGCTG | 26524 |
rs148472236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21020269 | ACATCAGCCAAGTGA[A/G]TATCTGAAAGTACAC | 26524 |
rs148502905 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:20979208 | GACGCTATGTTACTG[A/G]TAAGGCTTCCAGTCA | 26524 |
rs148597245 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010225 | AAACAAACAAACAAA[A/C]AACCCACAAAGGAAT | 26524 |
rs148603382 | in-del | -/AAAC/AAACAAAC/AAACAAACAAAC/AACAAAC | 0.191461 | 0.24305 | intron-variant | LATS2 | GRCh38.p7 | 13:21010201 | TAGACTCTGTCAAAA[lengthTooLong]AAACAAACAAACAAA | 26524 |
rs148638117 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | LATS2 | GRCh38.p7 | 13:21029541 | CTCATGCCTGTAATC[C/T]CAGGACTTTGGGAGG | 26524 |
rs148673026 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21018211 | TACTTAGAATTCACT[C/G/T]AGAAAGTAAACACTT | 26524 |
rs148683497 | snp | G/T | 1.64762e-05 | 0.00287016 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20987938 | CTGCTGGTAGGTTTT[G/T]ATGACATTCTCCACG | 26524 |
rs148716564 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21009146 | GGAACCGCTCAGTCA[C/T]GTGTGGTGAGTGATG | 26524 |
rs148724601 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046330 | TCGTGGAAATATACC[A/G]CTTGGAAAGAAAAGA | 26524 |
rs148810933 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LATS2 | GRCh38.p7 | 13:21043839 | AGCTGAAACACAACC[A/G]CAAAGAACACAGGGG | 26524 |
rs148821048 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:20980981 | CATTTTACACAACTG[A/G]CACCTGCCACTTTTG | 26524 |
rs148832667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20990617 | AAAACCAGGCCACAC[A/G]GTGTTGGGTTACAGG | 26524 |
rs148865677 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21039137 | AATTTAATTTGAAAG[C/G]CACTAAGAAAAAAAA | 26524 |
rs148891423 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036777 | AACTCCGTCTCAAAA[A/C]AACAACAACAACAAC | 26524 |
rs148908674 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21002996 | GCATGAGTCACTGCA[A/C]CTGGCCTATTTTATC | 26524 |
rs148935054 | snp | C/T | 3.3112e-05 | 0.00406877 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975255 | TCATCGGCCCCATTC[C/T]GCCCCAGGCGGTGGT | 26524 |
rs148990286 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:20994235 | ACCGTACTCATGAGC[C/T]GGCTTGTTTATAAAT | 26524 |
rs149021951 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21010727 | TCACACATGTACTTT[G/T]AATTCCTGGAAAACC | 26524 |
rs149026722 | in-del | -/TA | 0.089084 | 0.191327 | intron-variant | LATS2 | GRCh38.p7 | 13:21022237 | GCATGCATGTGTGCC[-/TA]TGTGTGTGGACGTAT | 26524 |
rs149042415 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | LATS2 | GRCh38.p7 | 13:21022263 | ACGTATGCATATGTG[C/T]GTGTGCATGTATTTG | 26524 |
rs149063121 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023553 | GAGCCCAGACAGTGT[C/T]TGAGATTGATGGTCA | 26524 |
rs149084733 | snp | C/T | 0.00138331 | 0.0262629 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983726 | CTTGTCCATCTTGGC[C/T]CTCTTTAACCTGTTG | 26524 |
rs149115314 | snp | A/G | 0.030665 | 0.119967 | intron-variant | LATS2 | GRCh38.p7 | 13:21036156 | CCCCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 26524 |
rs149166120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20998939 | TCCCGGTGACCTTGC[A/G]CACACGGCGCAAGGG | 26524 |
rs149202388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050393 | ACAGACCAAGGGGAA[A/C]CACCTTCATGTCATC | 26524 |
rs149266675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032839 | TCGAAGGGTGGACCA[C/T]GGCTGGCTGGGGAAT | 26524 |
rs149309276 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20995876 | ACCAATTACTAATTA[C/T]TTACAGAGTAATGTG | 26524 |
rs149360336 | in-del | -/T | 0.0225045 | 0.103662 | intron-variant | LATS2 | GRCh38.p7 | 13:21014520 | ATATGCTAGATAATA[-/T]ATTTTTTTAGAAAAC | 26524 |
rs149362900 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023881 | AGGAGGCTGAGGCAG[C/G]AGAATCGCTTGAACC | 26524 |
rs149401941 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:20984912 | CAAAATATGTTACAA[C/G]CCTAGAGTAACTGAA | 26524 |
rs149412419 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | LATS2 | GRCh38.p7 | 13:21019887 | GCTGAGGAAGGAGAA[C/T]TGCTTGAACCCAGGA | 26524 |
rs149434310 | snp | C/T | 0.00333839 | 0.0407192 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975100 | TACCTTCGCTGGCAT[C/T]GTTCCAAGGGCTTTC | 26524 |
rs149473829 | in-del | -/A | 0.077417 | 0.180873 | intron-variant | LATS2 | GRCh38.p7 | 13:20989863 | TATATACACAATAAT[-/A]AAAACCACACAAAAC | 26524 |
rs149487732 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | LATS2 | GRCh38.p7 | 13:21000384 | AGACTCTGTCATAAT[A/C]ATAATAATAATAATA | 26524 |
rs149489019 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:20977207 | TTGAAACCAGCCTGA[A/C]CAACATGATGAAGCC | 26524 |
rs149530843 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LATS2 | GRCh38.p7 | 13:21058188 | TCAAGACAGAGTCAA[C/T]GCATTTGAATTTACC | 26524 |
rs149553710 | snp | C/T | 8.25185e-05 | 0.0064228 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046000 | ATTTCCAGAATAAGT[C/T]GTGGCAGGAAAAGTC | 26524 |
rs149570091 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | LATS2 | GRCh38.p7 | 13:20992379 | CAGGCTGGGGGCGGC[C/T]GTGGGTGCAGAGCTG | 26524 |
rs149575397 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21054408 | GCAAGTCTCCACCTC[A/C]AAAAGAAAAAAAATT | 26524 |
rs149602943 | in-del | -/CT | 0.0387552 | 0.1337 | intron-variant | LATS2 | GRCh38.p7 | 13:21050113 | CGACAGAGGGAGACT[-/CT]GTCTCATAGACAGAT | 26524 |
rs149645238 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21004394 | AGCTGAGATTGCGCC[A/T]TTGCACTCTAGCCTG | 26524 |
rs149677867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026394 | TGTTCAGCATCTTTC[A/G]TGCAGCATGATTTTG | 26524 |
rs149709453 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | LATS2 | GRCh38.p7 | 13:21050094 | CACTGCACTCCAGCC[C/T]AGGCGACAGAGGGAG | 26524 |
rs149875994 | in-del | -/CTC | 0.00478085 | 0.0486577 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063192 | CACATCAGCCTTGAA[-/CTC]CTGAGCTCAAGCCAT | 26524 |
rs149889017 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:20993771 | ACCACCGCCTACTTC[A/G]GGAGCTATGCGATGA | 26524 |
rs149932312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051232 | CTTGAGCAGTGCACA[A/G]CCTGAACACCCACAC | 26524 |
rs150004293 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | LATS2 | GRCh38.p7 | 13:21035001 | TTTGGTAGGCCAGGG[C/T]GGGAGGATCACTTGA | 26524 |
rs150046964 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | LATS2 | GRCh38.p7 | 13:20998690 | GCCCCTCCCCTGAGC[A/G]CGGCGCTCCCGGCGA | 26524 |
rs150108495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980621 | CAAGCAATGGTTTCT[G/T]GAGAATGCTGCACGT | 26524 |
rs150150190 | in-del | -/AACTA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987430 | AAATCATTAGTTACT[-/AACTA]AACACTTAAAAGAAT | 26524 |
rs150163527 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:20976366 | AAGAAAACATAGGGT[A/G]AAATCTTCATGAACC | 26524 |
rs150196333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20994724 | ACACAGTGAGACCCC[A/G]TCTCTACACAAAAAT | 26524 |
rs150288953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048027 | GACTGTGCAGACATT[G/T]AGCTATTAGATCCAG | 26524 |
rs150322094 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | LATS2 | GRCh38.p7 | 13:21010027 | CAACATGATGAAACC[C/T]TGTCTCTACTAAAAA | 26524 |
rs150350694 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | LATS2 | GRCh38.p7 | 13:21000123 | GTGGTGGCTCACGCC[C/T]GTAATCCCAACACTT | 26524 |
rs150370668 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | LATS2 | GRCh38.p7 | 13:21005880 | GTACTTTGGGAGGCC[A/G]AGGTTGGTGGATCAC | 26524 |
rs150375162 | snp | A/G | 0.000115309 | 0.00759218 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983624 | TAGGGTCTTCATGGC[A/G]TACAGGGCGTGAGTG | 26524 |
rs150394036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992255 | CACGCAAGGGTAGGT[A/G]GAGATGGGGGGATGG | 26524 |
rs150403621 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028724 | TACAGGCATGCACCA[C/T]CACGCCCTGCTAATT | 26524 |
rs150428840 | snp | C/T | 0.00224392 | 0.0334204 | missense | LATS2 | GRCh38.p7 | 13:20989274 | TCGAAGCTGGGCCTC[C/T]GCGTCACTGGGGTTG | 26524 |
rs150446393 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | LATS2 | GRCh38.p7 | 13:20987195 | GCAAGACTCCGTCTA[A/C]AAATAAATTAAAAAA | 26524 |
rs150490560 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21050211 | AGGAGGAACAGTAAG[A/G]CTTTTGGGGGTGGAG | 26524 |
rs150515011 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | LATS2 | GRCh38.p7 | 13:21059720 | CCTGTAATCCCAGCA[C/G]TCTGGGAGACGGAGG | 26524 |
rs150544057 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21026188 | GTATGAAAGATGTAT[A/G]CACCAGTAAAATCAC | 26524 |
rs150586388 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | LATS2 | GRCh38.p7 | 13:20985839 | TCATCTGAGGTCGGA[A/C]GTTTGAGACCAGCCT | 26524 |
rs150596037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020894 | CCACGCCAGACTGGA[C/T]CAAGGACACACTCTT | 26524 |
rs150687923 | snp | A/G | 3.30022e-05 | 0.00406202 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988133 | GCCGCCCTCGGGCTC[A/G]TTGGGGCCCGCACGG | 26524 |
rs150689681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21007204 | AATTTTTAAGTTATA[C/T]TTCCAAAGGCTCAGA | 26524 |
rs150722345 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:21029716 | GAATCACTTGAACCC[A/G]GGAGGCAGAGGTTGC | 26524 |
rs150809660 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | LATS2 | GRCh38.p7 | 13:21050944 | CCACAGCCACGTGAG[A/G]GGGGGCAGGAAAAGG | 26524 |
rs150850950 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | LATS2 | GRCh38.p7 | 13:20982489 | CTAATTTTGTTATTT[C/T]TAGTAGAGACGGGGT | 26524 |
rs150903403 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | LATS2 | GRCh38.p7 | 13:21040587 | CCCAAAGTAAGCAAG[C/T]GGGAAGAGCTGTCTG | 26524 |
rs150909869 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981494 | CACCTCGGGTGCGAT[A/G]TAGTTTGGAGTCCCC | 26524 |
rs150944797 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | LATS2 | GRCh38.p7 | 13:21013963 | GCAACAGAGCAAGAC[C/G]CCCAACTTGAAAACA | 26524 |
rs150999745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009586 | TTCCAGGTATATGTG[C/G]TGCATTAGCCACACC | 26524 |
rs151040671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21005274 | GGTGAACAGAAAAGA[C/T]TGCACACAGAGAAAT | 26524 |
rs151158219 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047504 | TGCCCCTTCCCTCAC[C/T]CACTCCCCCTTACTC | 26524 |
rs151158447 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LATS2 | GRCh38.p7 | 13:20984016 | GCTCACTGCAGCCTC[C/T]GCCTCCTGGGTTCCA | 26524 |
rs151223161 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | LATS2 | GRCh38.p7 | 13:20983472 | CCAGGGATGTAGTCC[A/G]TCACAAAGTACAGGC | 26524 |
rs151235724 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010228 | CAAACAAACAAAAAA[A/C]CCACAAAGGAATAAC | 26524 |
rs151316034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20987023 | CATGGCGAAACCCCC[A/G]TCTCTACTAAAAACA | 26524 |
rs180788093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014507 | TCTGAGTGAAATGTA[C/T]ATGCTAGATAATATT | 26524 |
rs180795147 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21040954 | CAATCACATTCTACT[G/T]CCCCCTTGAGGCATG | 26524 |
rs180809202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21031720 | AAAAAGTGAGCTGAG[C/T]GTGGCGAAGTGTGCC | 26524 |
rs180809643 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21049191 | TAGTGGGGGTGTCTC[A/G]TGGGATGAAACCATG | 26524 |
rs180816064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20996931 | TAGAATAGAAGCTAG[C/T]AGGGCTAAATACTAT | 26524 |
rs180849304 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21060324 | CATCTCCAGAGTCCG[G/T]CTGGGGAGCTAAGCG | 26524 |
rs181012995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20989745 | TCCCTCACAGAAAGG[A/G]CAGAACTGTATCCAC | 26524 |
rs181023104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20978642 | CCACCTTTGCCATCC[C/T]TGAGACAGCAAGGCC | 26524 |
rs181047243 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999945 | TGAGGCAGAAGAATG[A/G]CTTGAACCTGGGAGG | 26524 |
rs181055962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21018086 | TCAGCTTCAGTAACA[C/T]GTAGGATCACTGGCT | 26524 |
rs181056923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000332 | GTTGCAATGAGCCGA[A/G]ATTGCACCACTGTAC | 26524 |
rs181062581 | snp | C/T | | | missense, intron-variant | LATS2 | GRCh38.p7 | 13:20979714 | GGGTTTCTGTGGGAG[C/T]AGGTGCCAAAAAGGG | 26524 |
rs181065247 | snp | C/T | 0.00390959 | 0.0440399 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046041 | TTGTTAGTCCAGTTT[C/T]CTTTTACCATAAATA | 26524 |
rs181074147 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21027695 | TAAGGTAGTTTAAGG[A/T]CTCTACCTGTGTTCT | 26524 |
rs181075017 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21009084 | CCCCTTGTCCTGCCA[C/G]CGATTTGGGCCAGAA | 26524 |
rs181081556 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21036085 | TGTATTTTTAATAGA[C/T]GGGTTTCACCATGTT | 26524 |
rs181081714 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054805 | GCTTATGAAAAATGT[A/C]AAACATACAAAAAGG | 26524 |
rs181121166 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:20992250 | AGCAGCACGCAAGGG[C/T]AGGTGGAGATGGGGG | 26524 |
rs181140471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028094 | CTTCCCCCACCCCAC[A/T]ACAGTCCCCAGAGTG | 26524 |
rs181151282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009505 | GGGTAAGCTAAAACA[A/G]TTAACAGACTGTTAA | 26524 |
rs181181398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046278 | CATTTGTCATTTTCA[C/T]GCAACGTTAATGCTA | 26524 |
rs181349235 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974757 | TCAAGTGAAGTAATC[A/G]ACGGACTAATTTAAA | 26524 |
rs181479659 | snp | A/C | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21055444 | AACTCACAAAACAAA[A/C]ACACCTCATTCTCTA | 26524 |
rs181486501 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | LATS2 | GRCh38.p7 | 13:21036527 | CGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 26524 |
rs181624868 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21044149 | GACATAACAATCCTC[A/T]CTATATACAAGTTAA | 26524 |
rs181627273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21018573 | AGGAAGACTGTGGTC[A/G]CTTCCCTGATGTCCT | 26524 |
rs181656601 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:20980273 | GACAATTCACTGTAA[A/G]CCAAACACTCCTTGT | 26524 |
rs181660661 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975308 | GATGAGGTCCCTGGC[C/T]TCAGGGCTCAGCTTC | 26524 |
rs181687639 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21058666 | GATTCTAGTAATTCA[C/T]CTTGGTAATTTTGCA | 26524 |
rs181692095 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21031881 | TTCTGTCTGTGCATC[A/C]CTAACCCTGTATTTT | 26524 |
rs181692481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014827 | GAAACTCCTTTCTCA[A/G]AACTCACAAATACCA | 26524 |
rs181711234 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20997346 | TGGACCTAACCACTA[C/T]GAAGCCTGGAAAATG | 26524 |
rs181716673 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21040268 | GATGTGCGCCTGTGG[A/T]CTCAGTTACTTTGGA | 26524 |
rs181721697 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21000916 | GCTTGATTAGAACAT[A/G]AAAAAAATTAAAGTA | 26524 |
rs181736028 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063398 | TGTAAAAATAATTTT[C/T]AAAACACTTGTGGAA | 26524 |
rs181756742 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026734 | ACAGAGGCAAGAGGA[C/G/T]TGTTTGAGCCCAGGA | 26524 |
rs181763883 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:20995845 | GCTCTTTGAATGTGT[A/G]TATCATGCACTATTT | 26524 |
rs181793265 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:21031046 | TCAATATATGCAGCA[G/T]TTATACTGTCTAATG | 26524 |
rs181795349 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21048829 | GCAACAAGAGCGAAA[C/T]TCCGTCTCAAAAAAT | 26524 |
rs181801919 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:20985266 | CCCAAAGTAGACAAA[C/T]GGGACTATATTAAGC | 26524 |
rs181809156 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:21013853 | ACACATGCCTGTGGT[C/T]CCAGCTACTCAAGAG | 26524 |
rs181878924 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21005282 | GAAAAGATTGCACAC[A/C]GAGAAATCAGAGAAA | 26524 |
rs181962345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21059241 | TTGAATTTTTTACCG[A/G]CCAAATGTATACTCT | 26524 |
rs181962933 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21049877 | TATAATCCCAGCTCT[C/T]TCGGATGCCGAGGCA | 26524 |
rs181976722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21022354 | TACTGAGTCAGGACT[A/G]AGAACCATTGCTCAA | 26524 |
rs182137888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022108 | CTCTGAAAAATACCA[A/G]TGCCCAGAATCCACC | 26524 |
rs182146691 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20984880 | TAGGCAAAAAGAACA[A/G]AATTGTTACCTGACT | 26524 |
rs182188572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986230 | AAAAAAAGAAACTAA[A/G]AATAGAACTACCATA | 26524 |
rs182203607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21008478 | TGTAGGTATTTATGT[C/T]TCACCAAACCAGGAG | 26524 |
rs182205821 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974237 | TCTCCACACACCAGA[C/T]GTCGGAAATCACAGC | 26524 |
rs182213055 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21011617 | CTTTGCCTTGGCCTA[C/G]GAATTTAAAAAATCT | 26524 |
rs182236686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029071 | TCCAATCTGTGTACT[C/T]TTATTTCTTTTTTCT | 26524 |
rs182238187 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047403 | TGATGAATGTTTATA[C/T]AACCAGCTGCTCTAA | 26524 |
rs182241924 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21022997 | TTCTCTGATTAGCCA[A/G]GAAAGGGGGTGTGGG | 26524 |
rs182242777 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040416 | AGAAAAAGAAAGAAA[G/T]GTCTTTGCTGTGGAA | 26524 |
rs182243391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21006301 | GAGAAAGAAGACCAG[A/G]CCCAAGACACACATG | 26524 |
rs182508715 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21015819 | ATTCTCTCGTCTCAG[C/T]CTCCCGAGTAGCTGG | 26524 |
rs182517500 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20976330 | GTTGTTTTCATAGAG[C/T]TAAAACTGTAGAGCT | 26524 |
rs182527713 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051405 | TTGCCCAAAGAATTA[C/T]GGGGATCTGAAATAG | 26524 |
rs182543903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002182 | CCTCCTAAAGTGCTG[C/G]GATTACACGTGTGAG | 26524 |
rs182550323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20981878 | CAAGGTAGAAATGAC[A/G]GTGAAGAATCACAGG | 26524 |
rs182564515 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21038425 | CCAGGCTGGCCTTGA[A/T]CTTATAAGCTCAAGC | 26524 |
rs182569714 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21056774 | TTCCATGGAGGAGCA[C/T]AATTCTTCAGGAAGG | 26524 |
rs182574274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21019815 | CCCATCTCTACTAAA[A/G]ATACAAAAATTAGCT | 26524 |
rs182594955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037247 | CCATCTCTACAAAAA[C/T]ACAAAAATTAGCCAG | 26524 |
rs182757600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001295 | TGGCATGGTTTCAGG[A/G]GTCCTGGATCCTATA | 26524 |
rs182768038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997975 | AGTTTTAACATTCCA[A/C]CTATGAGGTTTGGCT | 26524 |
rs182823720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033587 | ATGGAGAAGGTGACA[A/G]ACACACACGGTATCG | 26524 |
rs182829649 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21010092 | GAAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAC | 26524 |
rs182831384 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21028759 | TATTTTAGTAGAGAC[A/G]GGATTTCACCATGTT | 26524 |
rs182844423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20993431 | GCAGCACAAAAAACA[C/T]AGGCTGTAAACTGTG | 26524 |
rs182861547 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21056549 | TTGCAGCTTTCCTAA[C/T]AGCAAGCGACCCAAC | 26524 |
rs182863034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20994342 | ACTTCCTATCTGTAC[A/C]TTAAATCTCAGAAGA | 26524 |
rs182873743 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21019090 | GCTGCTTTCTCCCTA[A/C/T]GTGGTCTAAGGGAGT | 26524 |
rs183061810 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21034326 | CTTCCTTACTGACAG[C/T]GCCCAGTTGCATTGG | 26524 |
rs183063631 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051948 | GGAGTCAGAGCAAGA[C/T]CCTGTTTAAAAAGCA | 26524 |
rs183075474 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061601 | CACGTGACCCCGCCT[C/T]CCGCGTCACTCTCGG | 26524 |
rs183075546 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:21016493 | CTATGTTGGCCAAGC[C/T]GGTCTCAAACTGCTG | 26524 |
rs183104104 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015582 | AACTTTTAAAAGTTT[C/T]CTAGGTAGTTGTTTT | 26524 |
rs183148503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21032880 | GGGCGACAGCATGAG[C/T]GAACCCAGTGTGGGA | 26524 |
rs183148670 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007624 | ATATATATATATAGT[A/G]TATATATATATATAT | 26524 |
rs183151686 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:20987443 | CTAACTAAACACTTA[A/G]AAGAATAAATGGAAT | 26524 |
rs183151910 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050369 | AACCCCAGAAGCCTC[C/T]AGGCCCCCACAGACC | 26524 |
rs183353117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20982673 | CCCCACAAAGGCCCC[A/G]TGACACCTTGTAGCC | 26524 |
rs183399548 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047014 | ACATCAAATGATCAT[A/G]TGGGTAAGAGTTATT | 26524 |
rs183403479 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21019929 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACCCCA | 26524 |
rs183437445 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21041165 | TTTTAGTACAGACAG[C/G]GTTTCACCATGTTAG | 26524 |
rs183588306 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20979376 | GGTGTGGGTGGGGGA[C/G]ACAGTGGATCAGCAG | 26524 |
rs183589633 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024868 | ACACCTCAATTGAGA[A/T]GAGCCCCATCTCAAG | 26524 |
rs183589922 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007684 | TATATATATATATAG[A/T]ATATATATATATATA | 26524 |
rs183602853 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062174 | TTAGCCAGGCGTGGT[A/G]GCTCATGCCTGTAAT | 26524 |
rs183622656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042652 | TGACCTCACCACCAC[A/G]CTCCAGACTGTACAA | 26524 |
rs183625707 | snp | A/C/T | 5.17347e-05 | 0.00508578 | intron-variant | LATS2 | GRCh38.p7 | 13:20983812 | AGAGTCCAGCCTGTG[A/C/T]AGAAGGAAAAGGAAG | 26524 |
rs183626753 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | LATS2 | GRCh38.p7 | 13:21038924 | GGCGGAGGTTGTAAT[C/G]AGCTGAGATCACCCC | 26524 |
rs183635387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21004042 | GTCAAATCTCCCTGT[A/G]AGAAAAACATACGCC | 26524 |
rs183648875 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21004422 | CTGGGCAACAAGAGC[A/G]AAACACTGTCTCAAA | 26524 |
rs183706883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997720 | CAGGGCTTACGAGGA[C/T]GGGTGGGAACTGGAA | 26524 |
rs183835770 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20986673 | ATTGGTGCAAACATA[C/T]AGCTGGATAGAAGGA | 26524 |
rs183842644 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21031349 | GGACAACCTCATATC[A/G]TCCCACAAGTCACTG | 26524 |
rs183849552 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21048859 | TAAAAAATAAAAATA[A/T]AAATAAAAATAAAAA | 26524 |
rs183930270 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | LATS2 | GRCh38.p7 | 13:20975769 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 26524 |
rs184016089 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061794 | ACTGGCTGCTATCTG[C/T]CCCCAAACTTGAGTA | 26524 |
rs184085147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21021973 | TTTCCACACTTTCTT[C/T]GTTAGAGGAGCTGAT | 26524 |
rs184089998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004881 | TCACCAGGAAAATAA[A/G]TAATTACACAAAATC | 26524 |
rs184104237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20984266 | TCCATATATAGACAT[A/G]AATATGGAATGAAAA | 26524 |
rs184106965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058426 | TCAATCCCCACCCTA[C/T]CCCACCCCTTGGTGG | 26524 |
rs184113766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040034 | GCCGAGATAGCTCCA[C/T]TGTATTCCAGCCTGG | 26524 |
rs184130300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21054486 | GGACTGGGTAGGATA[C/T]AGCAGGGCAAAGTCT | 26524 |
rs184167431 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041567 | GACCAGGAAAATGTA[C/T]CAATGCTGAGCCACA | 26524 |
rs184333872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017770 | AGCTAGAATTACAGG[C/T]GCCCACCACCACACC | 26524 |
rs184385215 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974466 | AGATTTCTCATCAAT[A/G]TTCTTCAGTTTTTAT | 26524 |
rs184411149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013891 | TGGGAGGATCGCTTG[A/C]GCCCAGGAGATTGAG | 26524 |
rs184415578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21039872 | TGAGGTCAGGAGTTC[A/G]AGACCAACCTGACCA | 26524 |
rs184457118 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:21035727 | ATCTGTACTGCACAC[G/T]GGGATAGAAGAGCAG | 26524 |
rs184473854 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:20999986 | AGTGAGTCAAGATCA[C/T]GCAGCAGAGCAAGTC | 26524 |
rs184495289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20995540 | AGATATCTGTTCAAT[C/G]AATGATTGAGTGAGT | 26524 |
rs184497457 | snp | C/G/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973886 | GACTACAGAAACGGA[C/G/T]ATGTGTCCGTGATTA | 26524 |
rs184506438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996492 | AAACAATTCTCCTGC[C/T]TCAGCTTCCCGAATA | 26524 |
rs184510622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020449 | CAATTTACCCAGGAA[A/G]GTTAGGCCAGGAAGT | 26524 |
rs184519159 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048704 | TAGCCAGGCATGGTG[A/G]CGGGTGCCTATAATC | 26524 |
rs184529778 | snp | A/G/T | 0.00239401 | 0.0345304 | intron-variant | LATS2 | GRCh38.p7 | 13:21030312 | GGAACTCTGCTGGCC[A/G/T]GGCGTGGTGGCTCAC | 26524 |
rs184532318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21012675 | CAAGTATGGTATAAG[C/T]GCTTTGCAGATTTTT | 26524 |
rs184534140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999342 | TACAGGTACAAACCA[C/T]ACGTCTTTTTGAAAC | 26524 |
rs184548366 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058114 | TCAGTCACTTCAATC[A/T]AGCCTTACCCTTCTT | 26524 |
rs184550702 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:20977848 | TTCAATTAGGGCGCA[C/G]ATAATGCCAGATTCC | 26524 |
rs184631685 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994832 | AGTAGGGCAGGCTGG[A/G]CAACAAAGTAAGAAT | 26524 |
rs184767678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21012482 | ATCTCATGGGACCAT[C/G]ATCATACATGTGGCC | 26524 |
rs184788550 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973217 | ATACTGACAGTCACG[A/G]CGACAGGCACAGCAG | 26524 |
rs184889128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029940 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC | 26524 |
rs184907461 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007944 | TTTGTATTTTTAGTA[A/G]AGACAGGGTTTGCCA | 26524 |
rs184983946 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058864 | TTAATTACAGTTAAA[C/T]AGACGTCATAAACAG | 26524 |
rs184988977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21047988 | ACACAATATAATATA[A/G]TAAAGTCACTGAAAT | 26524 |
rs185011478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21034877 | AATTATAGAAGATTA[C/G]AAATTGTAAAAATTT | 26524 |
rs185015936 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008556 | AGTTCATAAAGGCAG[C/T]GGTAAAGTCTGAATT | 26524 |
rs185056070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053018 | GAGGCAGGCAGATCA[C/T]GAGGTCAGGAGATCG | 26524 |
rs185118347 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21001999 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 26524 |
rs185120389 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21027826 | GAGATTGTATTTGGA[G/T]TCTGCTGGATCCACA | 26524 |
rs185122509 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046157 | CTTTTGAAAATGTTC[C/T]TTCCTTCCATTTTTG | 26524 |
rs185129198 | snp | C/T | 1.67142e-05 | 0.00289081 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981482 | TTTGCGGAGGAGCAC[C/T]TCGGGTGCGATGTAG | 26524 |
rs185135613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009136 | CTGGCAAATAGGAAC[C/T]GCTCAGTCACGTGTG | 26524 |
rs185196564 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007687 | ATATATATATAGTAT[A/G]TATATATATATAGTA | 26524 |
rs185238924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21043686 | CATGATCCTTACTTT[C/T]AGTGTATTTGTGTTT | 26524 |
rs185326327 | snp | C/T | 1.66857e-05 | 0.00288835 | missense | LATS2 | GRCh38.p7 | 13:20989218 | CCTCGTAGGGGGTAC[C/T]GCTCAGCTGGTGGTA | 26524 |
rs185345631 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063173 | ATCATAACTTACTGC[A/G]GCCCACATCAGCCTT | 26524 |
rs185349536 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21026393 | GTGTTCAGCATCTTT[C/T]GTGCAGCATGATTTT | 26524 |
rs185367439 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | LATS2 | GRCh38.p7 | 13:21005819 | TATAAAAAAAAAAAA[A/C]AAAAAAACGGAGGCC | 26524 |
rs185371443 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20985608 | GCTGAGCATGGTGTC[A/G]CACACCTGTAGTCCC | 26524 |
rs185410852 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21022615 | CAAAGTCAGAGGAAA[G/T]CTTTTTGTTTATTGT | 26524 |
rs185569296 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:20978303 | CACATGACCACCAGG[C/G]CATGTGAAAATTCCA | 26524 |
rs185673345 | snp | A/T | 0.0539704 | 0.155153 | intron-variant | LATS2 | GRCh38.p7 | 13:20999634 | TAATTTTTTAAAAAA[A/T]TTTTTTGTAGAGATG | 26524 |
rs185679828 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21015129 | AGTGTTCCAGGGAAA[C/G]TGTATAACTCTCTTG | 26524 |
rs185683518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997418 | AAAGAGGCACTTTAA[C/G]AAAACGGCGAGGTGG | 26524 |
rs185712819 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032660 | TTCTAATGTGGCCCA[C/G]GGAAAAGATTGGACA | 26524 |
rs185716714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049947 | CCAACACAGTGAAAC[A/G]CTGTCTCTACTAAAA | 26524 |
rs185791088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21056677 | GCTCCAGCTAGGGAG[C/T]TAGAACACCCCTCCC | 26524 |
rs185802651 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017298 | CACAATTTCATAAAA[A/T]CACTTCCCTTACATA | 26524 |
rs185813697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044856 | TGCCTCAGCATCCCA[C/T]GTAGTTGGGACTACA | 26524 |
rs185845417 | snp | C/T | 0.00110659 | 0.0234962 | missense, synonymous-codon | LATS2 | GRCh38.p7 | 13:20975348 | GGAATGTGGAGCGTG[C/T]TCTCCCAGTTGATCA | 26524 |
rs185858479 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:21040978 | AGGCATGTGTTCACC[G/T]TTTTTTTTTTCTGAG | 26524 |
rs185862846 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | LATS2 | GRCh38.p7 | 13:21023135 | CTCCCGGCATCCATA[C/G]CGCTGCATCGAGGGC | 26524 |
rs185867410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21007224 | AAAGGCTCAGAATCT[C/T]TGTAACAAGTTTCCA | 26524 |
rs185883672 | snp | A/G | 0.179425 | 0.239831 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061004 | GCCCCTGCCCCGCCG[A/G]GATCCCGGCCGCCCC | 26524 |
rs185915620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037339 | AACCCCAGAGGGGGA[G/T]GTTGCAGTAAGCCAG | 26524 |
rs185917076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21018421 | AAAATTCTGCCCTGG[A/G]GCAGATGAAAAGTAC | 26524 |
rs185931130 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20990598 | AAACAAAACAAAGCA[A/C]AACAAAACCAGGCCA | 26524 |
rs185933526 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000497 | TTATTAAGTTTTTTT[A/T]ATCCCGATTTAATGA | 26524 |
rs185937862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20979863 | AGGTGAATTTCATTA[A/C]GATGCTGAACATACA | 26524 |
rs185954629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21036452 | TATTACCACTTTCTA[G/T]TATCACACACATCCA | 26524 |
rs185958586 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LATS2 | GRCh38.p7 | 13:21054860 | CCTAAACCTACCACC[C/T]GGTTTTGTTTGGTAC | 26524 |
rs186033784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040632 | GTGGCTGAGACACTG[C/T]AGAGAGCTCCTCTGT | 26524 |
rs186168094 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21059679 | CTTGTTCAAAATTCT[G/T]GTCAGGTGGGGCGCG | 26524 |
rs186271135 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046407 | GGTTAGAGCACATGA[C/T]ATCTACGGCTGTCCC | 26524 |
rs186417570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21055664 | AAACCCACACTGGCT[A/G]CCAAACACACATCAA | 26524 |
rs186494250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21031725 | GTGAGCTGAGCGTGG[C/T]GAAGTGTGCCTGTAG | 26524 |
rs186503267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997168 | GCAAGACAAACTGAG[G/T]TTTCACTGGTTTACT | 26524 |
rs186525057 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:20989408 | CCCTCGGGGCTGAGG[G/T]TCTTGAACCCTGGGC | 26524 |
rs186546082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029493 | GGATTTATATTGCAT[C/T]TATAAAAGATATTGG | 26524 |
rs186549375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047670 | TTATAACTGTAAACC[A/G]CGACCCTGCTTCACA | 26524 |
rs186551491 | snp | C/T | 0.000799201 | 0.019974 | intron-variant | LATS2 | GRCh38.p7 | 13:21022203 | ACATGTGTGCAACTA[C/T]GTAAGTGTGTGAATA | 26524 |
rs186705548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986254 | TACCATACAATCTAC[C/T]AAACCCATTATTGGG | 26524 |
rs186709546 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21014611 | ACGACGCTGACCATC[A/C]ATGCAGCAACTGAAA | 26524 |
rs186726434 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:21049636 | GCTTTTCACTCAGCT[A/G]TGAAAGGACAAGAGC | 26524 |
rs186745617 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LATS2 | GRCh38.p7 | 13:20985001 | CAGAAATAAGTCCAC[A/G]TATTTACAGCCACCT | 26524 |
rs186786672 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21040293 | TTTGGAGGTTGAGGC[A/G]GAGAATTGCTTGAGC | 26524 |
rs186858641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009508 | TAAGCTAAAACAATT[A/T]ACAGACTGTTAAGTA | 26524 |
rs186956411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21005359 | CTGGGACCCAGAGCC[A/G]GCCTCTGGCACTCCT | 26524 |
rs187019259 | snp | A/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062640 | GCAAGTGATGCTGAG[A/G]GTCAATATAGTGTTT | 26524 |
rs187031862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21025249 | ATACAAAAATTAGAC[A/G]GGTATGGTGGCAAGC | 26524 |
rs187036182 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:21042923 | TGGGAGGCAGAAGTT[C/G]CAGTGAGCCGAGATT | 26524 |
rs187040615 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21028176 | TGAGTGAGAACATGC[A/G]GTGTTTGGTTTTTTG | 26524 |
rs187063723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992803 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAA | 26524 |
rs187073479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038515 | ACCTATTTTATCTCT[C/T]TCTTTCTTTTCAGTC | 26524 |
rs187086342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21019832 | TACAAAAATTAGCTG[A/G]GGGTGGTGGTGCACT | 26524 |
rs187086548 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973557 | GCACATACATCTATA[C/T]TTCTAAGAAAATACG | 26524 |
rs187109753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21057545 | TAACAGGCCGGGCGC[A/G]GTGGCTCATGCCTGT | 26524 |
rs187282453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21033092 | TCCAGGTATAGTAGA[A/G]CAGGGTGTTAGCAGC | 26524 |
rs187318337 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LATS2 | GRCh38.p7 | 13:20998140 | AGGCCAAGGTAGGAT[C/T]GCTTGAGGCCAGGAG | 26524 |
rs187324521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20976514 | AAAAAGGCAACAAAA[C/T]GGGAGAACAGATTTC | 26524 |
rs187351657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000980 | CGATTTGTTAAAGAG[A/G]GCATGACAATAACAT | 26524 |
rs187378669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999445 | ATCGTTCCAATTTTC[A/G]TATCTGCTGCAGAAG | 26524 |
rs187382172 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:20978106 | ATTTTCAGTAGAGAC[A/G/T]GGGTTTCACTACGTT | 26524 |
rs187395365 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21037016 | AAGTCAGTAATATCC[A/C]TAAGAAGGTGTGTAG | 26524 |
rs187396415 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21034338 | CAGTGCCCAGTTGCA[C/T]TGGGGTGGCCACGTG | 26524 |
rs187400583 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21052134 | TAACACCCGCTACTG[G/T]CTACCTGACAGGCTT | 26524 |
rs187408966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21016665 | CAGCCAACCCCCAGG[A/G]AACAGCAGCTCTCTG | 26524 |
rs187466231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20994455 | GCCTCTGGGCACAAA[G/T]TACATGCAGAGTCAC | 26524 |
rs187585747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002263 | GGATGGTCTAAGATG[G/T]TTGGTTACACAACAG | 26524 |
rs187587806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981953 | GAGAGGCTGGAAGAA[C/T]TGCGGGGACAGCACT | 26524 |
rs187607679 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21018706 | TCGCCCTGTCTGGAG[G/T]GCAGTGGCTCGATCA | 26524 |
rs187616034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980308 | GGCCCCTACGGAGCC[A/G]GGCCTTCCTCACGGG | 26524 |
rs187662246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015741 | GTCTCACTCTGTCAC[C/G]CAGGCTGGAGTGCAA | 26524 |
rs187675772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20975978 | TGCAAACCATCATGA[C/T]GCTCATTCAAATACT | 26524 |
rs187679748 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024585 | TGCATAGCGCCTCAC[A/G]GATGACATCTCACTT | 26524 |
rs187684651 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007626 | ATATATATATAGTGT[A/G]TATATATATATATAT | 26524 |
rs187690915 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987492 | TCTTCCAAAATCCCA[C/T]AATCTCAATTTACAA | 26524 |
rs187702478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21011686 | AAATACCAGCTGGCT[A/G]TTGTAGACTTAACAG | 26524 |
rs187704490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21041914 | CCTACCCACACCATG[C/T]AGATGTTCCCCCTAT | 26524 |
rs187727532 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972922 | CCTGAGACAGCCCTG[C/T]CTGTGCTGTGCAACC | 26524 |
rs187887692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21012584 | TTTTCTAGTCAAATT[C/T]TCTACCTAGTAGTGT | 26524 |
rs187905755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048166 | TTTGTGCTCTAAGCA[A/T]CTGTTTTGAAATACC | 26524 |
rs187913534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028936 | TGCATACTGACCTTG[C/T]ATCCTGTGACCATGC | 26524 |
rs187913718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21010247 | CAAAGGAATAACACA[A/G]AGAGTTAAGTGAGCA | 26524 |
rs187925695 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20993689 | GGAAGAGTTGCAGAG[A/G]GAAGGCAGCGGTGGT | 26524 |
rs187950921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997803 | CAATGTCTAAGCAGC[A/G]GAAGTATTTCACGTG | 26524 |
rs187951960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047078 | CTCGTTACATGGAAC[A/G]CGATGTCACAAAGGC | 26524 |
rs188015205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020508 | AATTTACAAGACCTT[A/C]CATCTACTTACTAAG | 26524 |
rs188019219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004629 | GTGGGCTTCCTGGCC[A/C]CCTGCCTCCAACCTG | 26524 |
rs188023259 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:20983986 | CCTAGGCTGGAGTGC[A/G]GTGGCACAATCTCAG | 26524 |
rs188171678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20994934 | GTCCTTATCTAGAAT[C/T]GTAGGTGGCTATTCC | 26524 |
rs188172625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21033595 | GGTGACAGACACACA[C/T]GGTATCGCTGAAGGC | 26524 |
rs188181339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986853 | ATCCTATGCATGTAA[C/T]AAAATATCACATGTT | 26524 |
rs188202694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024367 | TTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 26524 |
rs188211677 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21029956 | TGGTGAAACCCTGTC[C/T]CTACTAAAAATACAA | 26524 |
rs188250926 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061618 | CGCGTCACTCTCGGC[C/T]GCATACCAGTCCGGG | 26524 |
rs188397322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049099 | ATGCAAAGAAGCCTT[C/T]AGGCTCCACCCACCA | 26524 |
rs188449848 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LATS2 | GRCh38.p7 | 13:21051535 | AGATGAGCCCAAGTT[C/T]CTGGTTTGAAAAATG | 26524 |
rs188458791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21016076 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 26524 |
rs188475956 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21022067 | AGAAAAGACTATTTT[C/T]GTGGGTTCTCAAACT | 26524 |
rs188477996 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21005098 | GGGAACCATTAGTCA[A/G]GAGGGCTTGGTGTCA | 26524 |
rs188495153 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041310 | ATGGCCCCTGATTCA[A/C]TGAGCAGCTGGTGTG | 26524 |
rs188501244 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | LATS2 | GRCh38.p7 | 13:21007547 | ATATATATATATAGT[A/G]TATATATATATATAT | 26524 |
rs188502406 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:21058596 | AATTTACACTTAAAC[C/T]ATTTCAAACTCGATG | 26524 |
rs188520682 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21040182 | GCTTCAGACTAGGAG[C/T]TCAAGACCACCGTGG | 26524 |
rs188555704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017859 | TTGAACTCCTGACCT[C/G]AGGTGATCCGCCTGC | 26524 |
rs188561042 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21000078 | TGTTAGCACCAAAAT[A/G]AAATAAAAAATTATA | 26524 |
rs188718735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20979639 | AGATTCATGGGTACA[G/T]GAGCAAATCAGATGT | 26524 |
rs188818570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21018445 | AAAGTACTGCATGAG[A/G]CAGCTAGAGTTCAGA | 26524 |
rs188833050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000589 | TAATGATGTCTGTCA[A/G]ATTTAGGTATAATAT | 26524 |
rs188957404 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21039257 | TTTCTTCCTTCTCCT[C/G]TTATTAATATTTCAG | 26524 |
rs188970483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004064 | ACATACGCCAATTTT[A/C]AAAAGCAGCACACAA | 26524 |
rs188983587 | snp | A/C | 0.00597247 | 0.0543191 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061942 | GCCACCAAGTTACCA[A/C]CTAGTGGCTGGACAC | 26524 |
rs189028613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996679 | AGCCACCGTGCCTGG[A/G]CTGATAGAAGATTCT | 26524 |
rs189048695 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21031576 | CCTGTCTGGGGCTGG[G/T]TGTGGTGGCTCATGC | 26524 |
rs189050169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21036522 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 26524 |
rs189067198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058225 | ATTTCTTCACACCAA[C/T]TGTTTTTAAAAAGTC | 26524 |
rs189070256 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | LATS2 | GRCh38.p7 | 13:21057669 | GCTGGGCATGGTGGC[A/G]GGCGCCTGTAGTCCC | 26524 |
rs189208187 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20983011 | AAAAAAAAAAAAAAA[A/C]AGTAAACCTGAAATC | 26524 |
rs189240419 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21020085 | TTTACGAAAGTGGTT[G/T]AAGGAGAGTGGATGT | 26524 |
rs189313724 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974733 | GTTTTCTTGGTGAAG[A/G]GCAGAATTTCAAGTG | 26524 |
rs189346417 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21014366 | CATGAGCCAAAGACA[A/G]CCCTGACAACCAGGG | 26524 |
rs189348508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040006 | TGAATCCGGAAGGCA[C/G]AGGTTGCAGTAAGCC | 26524 |
rs189402556 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:20989453 | TTCTGCCCAGCACAG[A/G]GTCAGTGGACTCCCC | 26524 |
rs189426979 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21045312 | CCAAAACAAGAAAAG[G/T]GAAGCCAGTCTCTTT | 26524 |
rs189435124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008930 | CTGGAAACTATCTAA[A/C]TGTCCATCACCAGGA | 26524 |
rs189437099 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027324 | CTATGCTTTTTTCCC[C/G]AAAGTTTTTAGCTGT | 26524 |
rs189472812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030423 | TGAAACCCCGTCTCT[A/G]CTAAAAATGCACAAA | 26524 |
rs189478343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048800 | CGAGATCGCACCATC[A/G]CACTCCAGCCTGGGC | 26524 |
rs189488905 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | LATS2 | GRCh38.p7 | 13:21013466 | ATTTTCTGTAGAGAA[C/G]ATCCAAACGGCCAGG | 26524 |
rs189518662 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984603 | TATAAAAAAAATCTA[A/G]GAGTAAATTTAACCA | 26524 |
rs189560765 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LATS2 | GRCh38.p7 | 13:21049709 | GTTCCATGTTAAAGC[C/T]AGGATGCAGGGATGT | 26524 |
rs189579427 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21035915 | CCTTCCCCTTTTTTC[A/C/G]GGGAACAGAGTCTTG | 26524 |
rs189628114 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20995546 | CTGTTCAATGAATGA[C/G/T]TGAGTGAGTGACTGA | 26524 |
rs189640223 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973956 | ATAAGTTCAGTATAT[G/T]ACAAATGTTTCAGTT | 26524 |
rs189731244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21006199 | TGCCTCAGCTTATCA[C/T]GTGTGAGGAAAAAAA | 26524 |
rs189731425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986129 | AGGTGCATGGAAAGA[C/T]GCTCATTAACCATCA | 26524 |
rs189778668 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007685 | ATATATATATATAGT[A/G]TATATATATATATAG | 26524 |
rs189877754 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21026654 | GACATACGGTAGGTA[A/T]GTTTGACTTAAATTG | 26524 |
rs189894659 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21054491 | GGGTAGGATATAGCA[A/C/G]GGCAAAGTCTCCACG | 26524 |
rs189950600 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21040659 | CTGTAGAGGGGAGCA[C/T]GTGGGGAGGATAAGA | 26524 |
rs189962638 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:21022664 | CCCGCGTTTACTGCC[C/T]GAGCCACAGAAATGT | 26524 |
rs190060567 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061244 | CCTTCCCGGAGCCTC[C/G]GCACCACAGTAGGTG | 26524 |
rs190079259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997177 | ACTGAGGTTTCACTG[C/G]TTTACTGCTGCTACT | 26524 |
rs190125134 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LATS2 | GRCh38.p7 | 13:21043707 | ATTTGTGTTTCTGTA[C/T]TGGAAACAGCACTGG | 26524 |
rs190227451 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023323 | CTCCTGCCTCAGTCT[C/G]CTGACACACTGGGAC | 26524 |
rs190231526 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:21041097 | CCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGACTA | 26524 |
rs190278246 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046178 | TCCATTTTTGTAGTT[C/T]CTATAGAGAACCTAA | 26524 |
rs190279947 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:20981840 | TAGTTTGGAGACACA[A/C]GTGGTGAGGTTGGCG | 26524 |
rs190295434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20978457 | TATTAAATGACTGAC[A/G]ATTATTTAACTACTT | 26524 |
rs190298376 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | LATS2 | GRCh38.p7 | 13:21037520 | TTTGAGAGCTTGCAC[A/G]GTTCTGGGTCTTAGA | 26524 |
rs190318148 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019328 | ATTATTATTATTATT[A/C]TTATTATTATTATTT | 26524 |
rs190328728 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21017426 | GCGATCCACCAGCCT[A/C/T]GGCCTCTCAAGGTAC | 26524 |
rs190349761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053549 | TCAGCACCGAATCTG[A/C]GTCCTCAGTTCCACA | 26524 |
rs190386086 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005533 | TTTTCTGACAGGAAG[A/G]GTAATAAGATATGGG | 26524 |
rs190431973 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:21040388 | TCTCAAAAAAAAAAA[A/G]AAAGAAAGAAAAAGA | 26524 |
rs190573870 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035107 | CAAAACAAAACAAAA[A/G]AGCAAGAAAAGAAAT | 26524 |
rs190580172 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999911 | CACACACCTATATAG[C/T]CCCAGCTACTAGGGA | 26524 |
rs190615811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20993107 | ACAGTGGGGGAGGCC[A/G]TGCAGGGCTGCTCTG | 26524 |
rs190654609 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985086 | ACTAGATATCCATAT[A/G]CAGAAGAATGAAACT | 26524 |
rs190672516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21059166 | AATACGGGCAAACTT[G/T]CCTTTAAAAATGTAC | 26524 |
rs190682706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21022299 | GCATGTGTGTGTGAG[C/T]GTGCATGTGTGTGAA | 26524 |
rs190721649 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047126 | TCTACCTACCCCAGG[A/C]CTCGTTCACGGCCTA | 26524 |
rs190873265 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028945 | ACCTTGTATCCTGTG[A/T]CCATGCTAAATTATT | 26524 |
rs190877321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21010730 | CACATGTACTTTGAA[G/T]TCCTGGAAAACCCAT | 26524 |
rs190885311 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20997967 | TATCCTAAAGTTTTA[A/G]CATTCCAACTATGAG | 26524 |
rs190919796 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21060252 | GGAAAGCTCCCCAGA[A/G]GTTCTGGAGTTGGGC | 26524 |
rs190926859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015139 | GGAAACTGTATAACT[C/T]TCTTGGTCCAGTAAT | 26524 |
rs190929167 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033349 | CCAAGGAAATCCTGA[A/C]AGGAGGAGTCAGCTG | 26524 |
rs190932282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20997519 | ACCACACCCCAGCTC[C/T]AAACCTCCCCATGGG | 26524 |
rs190936168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20975421 | TCTTGGGCAGTTCTG[A/G]GACAGCGTGTGATGA | 26524 |
rs190960225 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21032731 | TTCCCTGGATGGTAC[C/T]GACACAAATGGGAAT | 26524 |
rs191132759 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20986659 | GAGATGAGAAGTTAA[C/T]TGGTGCAAACATACA | 26524 |
rs191132834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015777 | CGACCTCTGCTAACT[A/G]CAACCTCCGCCTCCC | 26524 |
rs191138469 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21014769 | TACCTTTTTAAAAAA[C/G]AATGTTTGTTGAGTG | 26524 |
rs191148368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20976042 | GAAAAACAAACAGGA[A/G]AAACTTCATAGGGAA | 26524 |
rs191151978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051074 | TAGAAGATGTGTGAC[A/G]CATACGCCGTGTCAG | 26524 |
rs191195613 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21040017 | GGCAGAGGTTGCAGT[A/G]AGCCGAGATAGCTCC | 26524 |
rs191203472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058238 | AACTGTTTTTAAAAA[A/G]TCAGTAAGAAATACT | 26524 |
rs191222544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009209 | AAGAAGCAGATGTGC[A/G]AAGGTACAGCTCTTT | 26524 |
rs191380583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21031826 | CACCCACTGCACTCC[A/G]GCCTGGGTGACAGAG | 26524 |
rs191412587 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007668 | ATATATATATAGTGT[A/G]TATATATATATATAG | 26524 |
rs191414607 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024724 | CTGATGTTAAAAGAT[A/G]TATATTTCAACCCAA | 26524 |
rs191419306 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21007281 | CCATTTTGTTTAAAA[C/T]TTGGCTGTTACCCTA | 26524 |
rs191427459 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:20992230 | GGGAAAGATGGGCCC[A/G]TGGCAGCAGCACGCA | 26524 |
rs191428361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20987669 | TGCACAGCTATCTCT[A/G]ATTCTTCAGAAGAGT | 26524 |
rs191434229 | snp | C/T | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062035 | GACGTTTGCCAGAAG[C/T]GGTGGCTCACGCCTG | 26524 |
rs191442463 | snp | A/G | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21042285 | AAATTTCCATTTTAA[A/G]GTATTTTAATTAAAA | 26524 |
rs191448863 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027905 | TGAACATACTCTCTC[C/T]ATTTATTTATTTATT | 26524 |
rs191477948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21056678 | CTCCAGCTAGGGAGT[C/T]AGAACACCCCTCCCA | 26524 |
rs191513369 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062763 | TGCACTATTTTGACA[A/G]TCTCACCCAGCCTTC | 26524 |
rs191632074 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21016145 | TAGGCACTCGCCATC[A/G]TGCCCAGCTAATTTT | 26524 |
rs191700506 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21028663 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGCAATTC | 26524 |
rs191727894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20979902 | GTTAAGTGGGAAAGC[A/G]CGTTGAAGCATCGCA | 26524 |
rs191758756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21021021 | CCTGATATGCTGTCT[A/G]GGATTTATTTTAAGA | 26524 |
rs191760776 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:20998211 | GTGAGAAAATTAGCT[A/G]GGCATGGTGGTGGGT | 26524 |
rs191771861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20976689 | AGGACATGAAAATAA[A/G]CTCAATATAATTAAA | 26524 |
rs191776276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004668 | ACATCTGCTTTGGCA[A/G]GAAGCGCTTTGCTCT | 26524 |
rs191778698 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:20984154 | GGCCAGGCTGGTCTT[C/G]AACTCCTGACCTCAG | 26524 |
rs191939999 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:20980468 | TAATCCTTGCTAAGT[A/G]TAAACTGGGATGTTA | 26524 |
rs191947180 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21056258 | CACCCAAGCTCGTCT[A/C]GAATTCCTGGACTCA | 26524 |
rs191960793 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LATS2 | GRCh38.p7 | 13:21018888 | CGACCTCAAATAATC[C/T]GCCTGCCTTGGCCTC | 26524 |
rs192000494 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21010075 | CATGGTGGTGTGTGC[C/T]TGAAATCCCAGCTAC | 26524 |
rs192020775 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046981 | GGCAACTTCTCAGAG[C/T]GCACCATGGCCACAT | 26524 |
rs192039034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041445 | TTTGTTTACATTTCT[A/T]CCCTAACCTCATTCC | 26524 |
rs192076191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21052918 | TGTCCTCCCCAACCT[A/G]CAAAACCTTTCTCTC | 26524 |
rs192251285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001272 | AGTTCCCTATTAGTA[A/C]ACACACATGGCATGG | 26524 |
rs192291773 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | LATS2 | GRCh38.p7 | 13:21037163 | TAATCTCAGCACTCC[A/G]GGAGGCCAAGGCATG | 26524 |
rs192293712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:20995177 | GGTTAGCTGTTACAG[G/T]TCACAAAGGTATCTT | 26524 |
rs192293758 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:21038742 | GTCTTACCAGGTGGC[C/T]GAGGCGGGCGGATCA | 26524 |
rs192299144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21019873 | CAGCTACTCGGGAGG[C/G]TGAGGAAGGAGAATT | 26524 |
rs192321129 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LATS2 | GRCh38.p7 | 13:21057564 | GCTCATGCCTGTAGG[C/T]GGGTGGATCACGAGG | 26524 |
rs192323123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21012668 | TGGTAAACAAGTATG[A/G]TATAAGCGCTTTGCA | 26524 |
rs192347336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024578 | CTCTTCCTGCATAGC[A/G]CCTCACGGATGACAT | 26524 |
rs192392312 | snp | C/T | 0.0142736 | 0.0832652 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061630 | GGCCGCATACCAGTC[C/T]GGGCGGGGCGCCTGC | 26524 |
rs192483377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035530 | GCCAGGCAAAATTGG[A/G]GTTCCAGGCAACAAA | 26524 |
rs192535806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051560 | AAAATGGGGCCAGTG[G/T]TGGTGCCATTCTCTG | 26524 |
rs192560018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999495 | TTTTTTTTTGACAGG[G/T]TCTTGCTCTGTCACC | 26524 |
rs192564687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025338 | CAGAGGTTGCAATGA[A/G]CCAAGATCATGCCAC | 26524 |
rs192578835 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034413 | CCAAGTAACTGGGTC[C/T]TGACCGGGGAGGTGT | 26524 |
rs192588363 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017156 | CCTGGCACTTGAATG[A/G]CAGCCAGCACAGTGA | 26524 |
rs192732862 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21011791 | TCATTAGGTGATTTC[A/G]TTGTTGTGTGAACAT | 26524 |
rs192739453 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973216 | AATACTGACAGTCAC[A/G]ACGACAGGCACAGCA | 26524 |
rs192744424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047671 | TATAACTGTAAACCG[C/T]GACCCTGCTTCACAG | 26524 |
rs192793665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017468 | GCATGAGCCACCACA[C/T]CTGGATGATTCTTTA | 26524 |
rs192810150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21054357 | GGGCTGCTGTGAGCC[A/G]AGGTCATTCCACTGC | 26524 |
rs192820340 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007686 | TATATATATATAGTA[G/T]ATATATATATATAGT | 26524 |
rs192824312 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:21033629 | TGTAAGCGTCTCCAA[G/T]GTTGACAGACGGCAC | 26524 |
rs192837891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043208 | CCAGGCGTGGTGTTG[C/T]GTGCCTGTAATCGCA | 26524 |
rs192945639 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20994512 | GGAATGGCAAGAGGT[C/T]GGAGCCAGGATGCGG | 26524 |
rs192975792 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21002579 | GATGGGGTTTCGCCA[C/T]GTTGCCCAGGATGGT | 26524 |
rs192988243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029990 | TTAGCAGGGCATGGT[A/G]GCATGCACCTGTAAT | 26524 |
rs193006365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21020093 | AGTGGTTGAAGGAGA[A/G]TGGATGTACATCCTT | 26524 |
rs193025732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057957 | TAATAAAGCCCATTA[C/G]AGAGAGCAGCAGTGA | 26524 |
rs193091713 | snp | C/T | 0.00268695 | 0.0365548 | intron-variant | LATS2 | GRCh38.p7 | 13:20983187 | GGTTAGTGACATCTA[C/T]ACATAGAAAGTGCAT | 26524 |
rs193114497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20978132 | ACGTTGGCCAGGCTA[A/G]TCTCGATCTCCTGAC | 26524 |
rs193181597 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20982286 | GGCTATAAGAGAGGG[C/G]TCCTTGGGAGGCTGT | 26524 |
rs193192464 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048212 | GTAACTTCACATTCC[A/G]ACAAAAACGGAGAGG | 26524 |
rs193205965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21039641 | TGCTCTGCAACATGG[A/G]AGGCCTTGTGGGCAC | 26524 |
rs193207660 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004329 | ATCCCAGCTACTCGG[A/G]AGGCTGAGGCAAGAG | 26524 |
rs193260521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20987014 | TCTGACCAACATGGC[A/G]AAACCCCCGTCTCTA | 26524 |
rs199516698 | in-del | -/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974424 | TCTTTTTTTTTTTTT[-/T]ACATTATTGCACAGA | 26524 |
rs199533183 | in-del | -/CC | 0.0275645 | 0.114116 | intron-variant | LATS2 | GRCh38.p7 | 13:21041276 | CGCGCCTGGCCCACT[-/CC]CTTTTCTTATTAAGC | 26524 |
rs199542359 | in-del | -/GA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007530 | TAGTCGTAGGGGATG[-/GA]GATATATATATATAG | 26524 |
rs199543001 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975060 | TTGTTATTGGGCGAG[A/G]TGAGTGTGTCCCAGG | 26524 |
rs199547214 | snp | A/G | 4.98351e-05 | 0.0049915 | missense | LATS2 | GRCh38.p7 | 13:20988173 | TCCATGCCTGCGCAC[A/G]GGCTGTCCAGGTCGT | 26524 |
rs199667500 | in-del | -/AAA | 0.0554779 | 0.157039 | intron-variant | LATS2 | GRCh38.p7 | 13:21013978 | CCCCAACTTGAAAAC[-/AAA]AGAAGAAGAAAGAAG | 26524 |
rs199685272 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032292 | ATTTTTTGAGACAGA[C/G]TCTCGCTCTGTCACC | 26524 |
rs199706697 | snp | A/T | 4.94205e-05 | 0.0049707 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045784 | AGGCAACAAGGAATA[A/T]CTGATTTCCCTCAAG | 26524 |
rs199726268 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998381 | CAAAAATTAATTAAT[A/T]AATTAAATTAAGAAA | 26524 |
rs199747073 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020525 | ATCTACTTACTAAGG[C/T]AATGTTAAGGGAAAA | 26524 |
rs199759999 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056150 | GTCTTTTTTTTTGGT[-/G]GGGGGGGCAGGGTCT | 26524 |
rs199808327 | in-del | -/TTATTATTA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019299 | TCTCACTTGGATTTG[-/TTATTATTA]TTATTATTATTATTA | 26524 |
rs199809075 | in-del | -/CCAGGGTGGTCAGGA | 0.0463947 | 0.145069 | intron-variant | LATS2 | GRCh38.p7 | 13:21037804 | GCAGAGTGGGCAGGG[-/CCAGGGTGGTCAGGA]CCAGGGCGGGTAGGG | 26524 |
rs199845909 | in-del | -/TG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007703 | TATATATATATAGTA[-/TG]TATATATATATATAT | 26524 |
rs199850920 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019337 | ATTATTATTATTATT[-/A]TTATTTGAGACAGAG | 26524 |
rs199885099 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059337 | GTGCGGTGGCTTACG[-/C]CTGTAATCCCAGCAG | 26524 |
rs199906951 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057805 | ACTCCATCTCAAAAA[A/T]AAAAAAAAAATGAAA | 26524 |
rs199932609 | in-del | -/CCT | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062800 | GGTTCATCCTCCTCC[-/CCT]CCTCCCTCTCTTTCA | 26524 |
rs199989605 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998383 | AAAATTAATTAATTA[A/T]TTAAATTAAGAAAAA | 26524 |
rs200000616 | snp | A/G | 0.000702099 | 0.0187232 | missense | LATS2 | GRCh38.p7 | 13:20988653 | AGGGAGTCCCGGCGG[A/G]CCAGGGTGGCAGCCG | 26524 |
rs200017724 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994854 | AGTAAGAATGTGTCT[A/C]AAAAAAAAAAAAATA | 26524 |
rs200043464 | snp | C/G | 0.00199792 | 0.0315431 | missense | LATS2 | GRCh38.p7 | 13:20981562 | GCGCCCTCTGCTCTA[C/G]GGTCTTCAGCCTGTC | 26524 |
rs200061443 | snp | C/G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012227 | AAATGCATATCTATA[C/G/T]AGGACACTTAACATG | 26524 |
rs200079087 | in-del | -/G | 0.0142736 | 0.0832652 | intron-variant | LATS2 | GRCh38.p7 | 13:20989688 | TCATGCCCAAATTGT[-/G]GGGGGGCTGAGTTTA | 26524 |
rs200121518 | in-del | -/TCA/TCATA | 0.0752113 | 0.178743 | intron-variant | LATS2 | GRCh38.p7 | 13:21000376 | CAGAGCAAGACTCTG[-/TCA/TCATA]TCATAATAATAATAA | 26524 |
rs200203792 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982999 | TCTGTCTCAAAAAAA[-/C]AAAAAAAAAAAAAGT | 26524 |
rs200214946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21026731 | AAGACAGAGGCAAGA[A/G]GATTGTTTGAGCCCA | 26524 |
rs200221089 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019990 | AAAAAAAAAAAAAAA[C/T]GCCCTAAACTCATTT | 26524 |
rs200228153 | snp | C/T | 1.65932e-05 | 0.00288034 | intron-variant | LATS2 | GRCh38.p7 | 13:20991436 | GGAGAGGTAAGTGCA[C/T]GTCATCCTAAAACAA | 26524 |
rs200249485 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036796 | AACAACAACAACAAA[A/C]AACAACAACAAAAAA | 26524 |
rs200295556 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017638 | TTCTTTTTTTTTTTT[G/T]GTTTTTGAGATGGAG | 26524 |
rs200317656 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005820 | TAAAAAAAAAAAAAA[-/C]AAAAAACGGAGGCCA | 26524 |
rs200348220 | snp | A/G | 0.000197021 | 0.00992328 | missense | LATS2 | GRCh38.p7 | 13:20988629 | GGCGCCTCCAGGCCC[A/G]GCTTCTGCAGGGAGT | 26524 |
rs200359250 | snp | A/G | 0.00697544 | 0.0586435 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988271 | GCCTCCGTACTCCAC[A/G]TCCAGCGGGAAGGCG | 26524 |
rs200369113 | snp | A/C/T | 0.000414741 | 0.0143947 | missense | LATS2 | GRCh38.p7 | 13:20988170 | TGCTCCATGCCTGCG[A/C/T]ACAGGCTGTCCAGGT | 26524 |
rs200462227 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058939 | TTACAACGGTTGTTA[A/C]AGAAAAAAAAAAAAC | 26524 |
rs200506247 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988283 | CACGTCCAGCGGGAA[A/G]GCGCCTGCGCCGCCC | 26524 |
rs200511475 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21031697 | GACCCTGTCTCTATA[A/G]AAAAGTTAAAAAGTG | 26524 |
rs200559897 | in-del | -/AATA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009190 | ACAAATGAATGAATG[-/AATA]AAGAAGCAGATGTGC | 26524 |
rs200567208 | in-del | -/CT | 0.00914312 | 0.0669923 | intron-variant | LATS2 | GRCh38.p7 | 13:20981405 | CTAGAGCCAGCGAGA[-/CT]CAGCTCACGTCTGAA | 26524 |
rs200590477 | snp | C/T | 0.00199797 | 0.0315435 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974818 | TGTGAGGGCACCGGC[C/T]CCGGGACCCTGACCT | 26524 |
rs200597884 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026327 | TTGTCACTATGAGTT[A/T]ACCATTCTCTAAACT | 26524 |
rs200608951 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030391 | TCAGGAGATCGAGAC[C/T]ATCCTGGCCAACACG | 26524 |
rs200620820 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20977622 | TAAAATAATTATTAA[A/T]TAAATGGTAATTAAA | 26524 |
rs200664265 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045913 | ACTGTTTGGTCCTGC[A/G]GGTAGCCCCTGAACC | 26524 |
rs200704585 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045982 | TTGCAGTCGCTGCCG[A/G]CTATTTCCAGAATAA | 26524 |
rs200722927 | snp | C/T | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062325 | AAAAAAAAAAAAAAA[C/T]AACGTCTGATGCACA | 26524 |
rs200736030 | in-del | -/G | 0.0111196 | 0.0737302 | intron-variant | LATS2 | GRCh38.p7 | 13:21022226 | TGTGAATATGTGCAT[-/G]CATGTGTGCCTATGT | 26524 |
rs200751057 | snp | A/G | 0.000235444 | 0.0108474 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989192 | GGGGCCGTCAGCGCC[A/G]AAGCTTGGGCCCTCG | 26524 |
rs200838920 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054803 | TTGCTTATGAAAAAT[-/G]TCAAACATACAAAAA | 26524 |
rs200852337 | snp | C/T | 6.68583e-05 | 0.00578141 | missense | LATS2 | GRCh38.p7 | 13:20981613 | CATCATCCCAGAGGT[C/T]GCTGGGCTCCATGCT | 26524 |
rs201011483 | snp | A/C | 0.00672662 | 0.0576026 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988940 | ACCCCCGGTCTCCGG[A/C]GGCGTCTTGCTCTGG | 26524 |
rs201033230 | snp | C/T | 0.000247062 | 0.0111117 | missense | LATS2 | GRCh38.p7 | 13:20988000 | GCGAGTAGCTCTTGA[C/T]GCGTGACTCTCTCTT | 26524 |
rs201051843 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037968 | CCCTTTTCAGAATGA[G/T]GGGGGCTAGACACGG | 26524 |
rs201095232 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987223 | AAATAAAAAATAAAA[A/T]TAAAAAAAACACAAA | 26524 |
rs201100789 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21000489 | ATCAAAAGTTATTAA[-/G]TTTTTTTTATCCCGA | 26524 |
rs201109040 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:20989818 | TAAAAGACTTTCTAG[-/T]TTTTTTTTGTCTATA | 26524 |
rs201216594 | snp | C/T | 0.000115784 | 0.00760779 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981557 | CTTCCGCGCCCTCTG[C/T]TCTAGGGTCTTCAGC | 26524 |
rs201224061 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057634 | CGTCTCTACTAAAAG[-/T]TAAAAAAAAAAAAAA | 26524 |
rs201239635 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007921 | CGAATCATCACAACC[A/G]ACTAATTTTTGTATT | 26524 |
rs201272637 | snp | A/T | 0.00199792 | 0.0315431 | missense | LATS2 | GRCh38.p7 | 13:20983328 | AAAATGTTATCAGGC[A/T]TGATGTCTCGGTGGA | 26524 |
rs201277800 | in-del | -/ATAAAAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020144 | AGTCAGTCAGTTCAC[-/ATAAAAT]ATAAAATATACCTGA | 26524 |
rs201288154 | snp | A/G | 0.000247372 | 0.0111187 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988118 | TTTGCGGCTCTTGTC[A/G]CCGCCCTCGGGCTCG | 26524 |
rs201349070 | snp | C/T | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023157 | ATCGAGGGCTCCGGG[C/T]TCCGAGGGCTCCGAA | 26524 |
rs201357445 | in-del | -/AAT/AATAAT | 0.354665 | 0.227036 | intron-variant | LATS2 | GRCh38.p7 | 13:20977620 | TTAAAATAATTATTA[-/AAT/AATAAT]AATAAATGGTAATTA | 26524 |
rs201397018 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21050200 | TGCTGAAAGCCAGGA[-/G]GAACAGTAAGGCTTT | 26524 |
rs201430841 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009582 | GGATTTCCAGGTATA[C/T]GTGGTGCATTAGCCA | 26524 |
rs201433877 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058942 | CAACGGTTGTTACAG[-/A]AAAAAAAAAAACATA | 26524 |
rs201475650 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000490 | TCAAAAGTTATTAAG[-/T]TTTTTTTATCCCGAT | 26524 |
rs201481097 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032291 | TATTTTTTGAGACAG[A/T]GTCTCGCTCTGTCAC | 26524 |
rs201531181 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045817 | TTTCTGATAAGGTCC[A/G]AACTTTGGGGTGGCT | 26524 |
rs201541943 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055317 | GGACTTTAAAAAAAA[-/T]GGGGATATCAAGCAA | 26524 |
rs201550910 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017639 | TCTTTTTTTTTTTTT[G/T]TTTTTGAGATGGAGT | 26524 |
rs201571099 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026328 | TGTCACTATGAGTTA[A/C]CCATTCTCTAAACTA | 26524 |
rs201580031 | snp | A/G | 0.000348493 | 0.0131956 | intron-variant | LATS2 | GRCh38.p7 | 13:20981443 | GAGACCTCCTGCGGG[A/G]TGGCTGGCCATGGCG | 26524 |
rs201596095 | in-del | -/GAGG | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998762 | AGGCGGGGCGGGGCC[-/GAGG]CGACAACCTTGGGCT | 26524 |
rs201597110 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023683 | AAAAAAAAAAAAAAA[-/AC]AAACCTCGGCCGGGC | 26524 |
rs201638691 | in-del | -/A | 0.00624044 | 0.0555092 | intron-variant | LATS2 | GRCh38.p7 | 13:20981420 | CTCAGCTCACGTCTG[-/A]AGGGAAGGAGACCTC | 26524 |
rs201647689 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018387 | AAGATGAGGAGACAA[-/G]GGGTTGACATGGAAA | 26524 |
rs201653116 | in-del | -/CTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976135 | CGTTCAGTAAATGCA[-/CTT]GTTGTAGAGATGTGT | 26524 |
rs201681793 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21021900 | GGGTGAAAGCTCCTC[-/A]AGACTTCTCAAGCTG | 26524 |
rs201689644 | snp | A/G | 1.68712e-05 | 0.00290436 | intron-variant | LATS2 | GRCh38.p7 | 13:20989323 | CAGTGGAAAAAACAG[A/G]AAGACAGCATCAGAG | 26524 |
rs201705042 | in-del | -/TTATTA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019299 | TCTCACTTGGATTTG[-/TTATTA]TTATTATTATTATTA | 26524 |
rs201728408 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003648 | GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTTGA | 26524 |
rs201734683 | snp | A/C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038753 | TGGCCGAGGCGGGCG[A/C/G]ATCACCTGAGGTCAG | 26524 |
rs201836681 | snp | C/T | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062806 | ATCCTCCTCCCCTCC[C/T]TCTCTTTCAATCTCT | 26524 |
rs201894248 | snp | C/T | 9.88354e-05 | 0.00702908 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983591 | CACCTGATTCCGGTT[C/T]AGGACATCCTTTTTC | 26524 |
rs201896922 | snp | C/T | | | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988832 | GGCCTGCTTGTGGTG[C/T]GGGTGCGGCACGTAG | 26524 |
rs201910561 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024116 | CTGTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 26524 |
rs201912534 | snp | A/C | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973982 | CAGTTCCCCCCCCCC[A/C]AAGAATCCAATCACA | 26524 |
rs201914308 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020523 | ACATCTACTTACTAA[-/G]GAAATGTTAAGGGAA | 26524 |
rs201940969 | in-del | -/CA | 0.0193772 | 0.0965046 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974025 | ACACAAATCACTTCT[-/CA]GTTACACATCTGCAT | 26524 |
rs202010116 | snp | C/T | 0.00153287 | 0.0276421 | missense | LATS2 | GRCh38.p7 | 13:20988627 | GCGGCGCCTCCAGGC[C/T]CGGCTTCTGCAGGGA | 26524 |
rs202027345 | snp | A/G | 0.000214177 | 0.0103461 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975174 | ATGGTGGGAACGTAG[A/G]GGGCTGGCTGCTTCC | 26524 |
rs202040927 | snp | A/C/G | 3.49921e-05 | 0.00418271 | missense | LATS2 | GRCh38.p7 | 13:20988224 | AGCAGCAGGTGCTTC[A/C/G]GGTAGGGCGGAGGCG | 26524 |
rs202048651 | in-del | -/TC | 0.0236746 | 0.106192 | intron-variant | LATS2 | GRCh38.p7 | 13:20987339 | TTTGTGTGATTTAAA[-/TC]TGTTACATTTTAATT | 26524 |
rs202198238 | snp | C/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973514 | ATATTGTGTTTATCT[C/G]TGTGTGTGTGTGTGT | 26524 |
rs202224882 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988022 | CTCTCTCTTCTCTTC[A/G]TCTCTGCTGTTTTTG | 26524 |
rs202227113 | in-del | -/AAAAG | 0.0437281 | 0.141251 | intron-variant | LATS2 | GRCh38.p7 | 13:21043344 | ACCGTCTAAAAAAAA[-/AAAAG]AACTCTATTATACTG | 26524 |
rs267603775 | snp | A/G | | | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983567 | GTCCCTCTCGGCCTT[A/G]ACGTGGGCCACCTGA | 26524 |
rs367560172 | in-del | -/AAC/AC/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21025413 | AAAAAAAAAAAAAAA[-/AAC/AC/C]ATTATGGTCATGAGT | 26524 |
rs367586777 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983582 | GACGTGGGCCACCTG[A/G]TTCCGGTTCAGGACA | 26524 |
rs367587292 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20987751 | TTGGCCCCAGAACCA[G/T]ACTGTCGCCCATTAG | 26524 |
rs367606968 | snp | G/T | 0.00185154 | 0.0303707 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988853 | CGGCACGTAGAGCCC[G/T]GCGGCAGGGGGTGGG | 26524 |
rs367611609 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21018316 | CAGGACATTTGTGAC[A/G]TGGGTGTTGGGCGAG | 26524 |
rs367693247 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054714 | TACCTGAGCAAAGAA[A/G]TACTAAGTGGCCGTG | 26524 |
rs367791420 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007555 | TATAGTATATATATA[-/C]TATATATATATATAT | 26524 |
rs367799502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21039899 | ACCAACATAGTGAAA[A/T]CCCATCTCTACTAAA | 26524 |
rs367835552 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21036899 | GGAAGTATAAATTCA[A/G]TTGAATGATTTTTAA | 26524 |
rs367839042 | snp | A/G | 6.67416e-05 | 0.00577636 | intron-variant | LATS2 | GRCh38.p7 | 13:20979672 | ACAGCAAGCAGATGC[A/G]TGGTTCCTCTCACAT | 26524 |
rs367900258 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21010574 | ACATGACTGTGTTTT[C/T]ATAAAATTACATCAG | 26524 |
rs367902164 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057558 | GCGGTGGCTCATGCC[C/T]GTAGGCGGGTGGATC | 26524 |
rs367947803 | in-del | -/AA/AAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994854 | GTAAGAATGTGTCTC[-/AA/AAA]AAAAAAAAAAAAATA | 26524 |
rs367950299 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040332 | AGGCTACAGTGAGCC[A/G]AGATTGCGCCACTGC | 26524 |
rs367963331 | snp | C/T | 0.000153988 | 0.00877328 | missense | LATS2 | GRCh38.p7 | 13:20989154 | TAGTCCACGTACGGC[C/T]GCGGCATCTCCTCCA | 26524 |
rs367984462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981342 | TTAGTAGCTTTCAGG[C/T]TTCTATGAGGACAAA | 26524 |
rs367994284 | in-del | -/TGT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976140 | AGTAAATGCACTTGT[-/TGT]AGAGATGTGTCTACT | 26524 |
rs368016185 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976093 | ATGTGACCTTACATG[C/G]TCAACTGCACAAACC | 26524 |
rs368025904 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017061 | AAATTCATCTTCATT[A/T]GTGCTTCTTACCCAG | 26524 |
rs368085296 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005537 | CTGACAGGAAGAGTA[A/G]TAAGATATGGGTAAG | 26524 |
rs368085590 | snp | C/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061738 | CCCACGGCCTCCCTG[C/G]TGGCCTGCGGTAGCT | 26524 |
rs368174602 | snp | A/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024690 | TCTTATACCCACATT[A/T]AAAAAAAAAAAAAAA | 26524 |
rs368206215 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992485 | GGCTCTGATGAAGGC[A/G]CCCCCTTCACCTTTC | 26524 |
rs368239343 | in-del | -/A | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047044 | TACTACAGAACTACA[-/A]CTGCAGCATGGAAAT | 26524 |
rs368357711 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21009787 | TGAGGATGAGGTATG[C/G]GTGGAAAAAGAGGCC | 26524 |
rs368361503 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027861 | ACTGTGAGAACTGCC[A/G]TCTTAACAGTATTGA | 26524 |
rs368367737 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044641 | TTGGATTGTATTCAG[A/G]TATACGAATTGCTAA | 26524 |
rs368369677 | snp | C/G | 1.66407e-05 | 0.00288446 | missense | LATS2 | GRCh38.p7 | 13:20989271 | CCTTCGAAGCTGGGC[C/G]TCCGCGTCACTGGGG | 26524 |
rs368370954 | snp | A/C | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062341 | AACGTCTGATGCACA[A/C]CCAAATTTAACCTGA | 26524 |
rs368467707 | snp | C/G/T | 3.36832e-05 | 0.00410374 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988196 | CAGGTCGTACTGCTC[C/G/T]GACTTGCTGCGCAGC | 26524 |
rs368473445 | snp | C/T | 1.71628e-05 | 0.00292935 | missense, intron-variant | LATS2 | GRCh38.p7 | 13:20979780 | CAACACTCCACCAGT[C/T]ACAGAGTTGAGTGTA | 26524 |
rs368487061 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992704 | TAGAACGGGGAGCTC[C/T]GGAAAGGAGTCCACA | 26524 |
rs368510782 | snp | A/G | 2.43034e-05 | 0.00348584 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989114 | CTGGTGGCCGGGCCC[A/G]TGGGGGCCGACTCCG | 26524 |
rs368544702 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998608 | CCAACCCCACCCCCA[C/T]GGAAAGGCCCCTGGA | 26524 |
rs368577911 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20984532 | TCTAGTTTCATTCTT[C/G]TGCATATGGATATCT | 26524 |
rs368636896 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039082 | AGTAATTTAAATTCC[C/T]ACATTAAAAAGGTAT | 26524 |
rs368641859 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056162 | GGTGGGGGGGGCAGG[A/G]TCTCACTCTGGTTGC | 26524 |
rs368644979 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21025645 | TCGTCATTAGGTCTG[C/T]ACTCATTGACCCAGA | 26524 |
rs368651471 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998088 | AGGTAACTTCCACTT[A/G]AGTTGTAGCTGACGC | 26524 |
rs368659820 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036516 | GCGGTGGCTCACGCC[C/T]GTAATCCCAGCACTT | 26524 |
rs368665309 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21001580 | AGTTAACTGTGTTGC[A/G]GTTCTAACCCATGAG | 26524 |
rs368671052 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | LATS2 | GRCh38.p7 | 13:21032669 | GGCCCAGGGAAAAGA[C/T]TGGACACCCCTAAAT | 26524 |
rs368692697 | snp | C/G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986491 | AATGGAACTGGAGGT[C/G/T]ATTATGTTAAGTGAA | 26524 |
rs368713145 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975029 | GGTGAATTCGTAAAA[C/T]GCGTGCTCAGGATGC | 26524 |
rs368736874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21012825 | GTTCATCTTTGAAAT[A/G]TGGTTAGGAACCCTT | 26524 |
rs368752326 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020640 | GTAGTCAGAATTCCT[A/G]CCATCCATCAAACAG | 26524 |
rs368849287 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21011728 | TGATAGAATGTATTA[A/C]TACAGTCATGCATTC | 26524 |
rs368927673 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21008145 | GGAGCTGACAGGCCA[C/G]TAGGATGGCACAGAG | 26524 |
rs368946130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20977946 | TTTGAAACAGAGTCT[C/T]GCTCTGTCATCCAGG | 26524 |
rs369060203 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981272 | GTGCATGTCTTCCAA[C/T]CCCCTGAAGCAAGAG | 26524 |
rs369090182 | snp | A/G | 4.9652e-05 | 0.00498232 | intron-variant | LATS2 | GRCh38.p7 | 13:20991409 | CCAGCCATCTCCTGG[A/G]AGGGAAGTAAAGGAG | 26524 |
rs369166799 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975127 | TTTCTTCATCTACGG[A/G]GTCGAAATTCGAGGT | 26524 |
rs369167901 | snp | C/T | 0.00155952 | 0.0278806 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988646 | CTTCTGCAGGGAGTC[C/T]CGGCGGGCCAGGGTG | 26524 |
rs369318746 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034393 | GGCTGCTTAAACCCC[C/T]ATGACCAAGTAACTG | 26524 |
rs369330158 | snp | C/G | 1.64743e-05 | 0.00287 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045955 | TGGCTGTTTTAACCC[C/G]TCACGAATCTCTTGC | 26524 |
rs369339596 | in-del | -/AT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040560 | AACCAACGAAATCAT[-/AT]GTCAGAGAGACCCAA | 26524 |
rs369414029 | in-del | -/TAG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007710 | TATAGTATGTATATA[-/TAG]TATATATATATAGTA | 26524 |
rs369416563 | snp | A/G | 0.000765506 | 0.0195491 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988286 | GTCCAGCGGGAAGGC[A/G]CCTGCGCCGCCCAGC | 26524 |
rs369432620 | snp | A/C | 1.64732e-05 | 0.0028699 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983651 | AGTGTCCACCTTACA[A/C]GCAAGGCACACTTCT | 26524 |
rs369472122 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21030532 | AAGCGGAGCTTGCAG[C/T]GAGCTGAGATCACAC | 26524 |
rs369490836 | snp | C/G/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973980 | TTCAGTTCCCCCCCC[C/G/T]CAAAGAATCCAATCA | 26524 |
rs369559801 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | LATS2 | GRCh38.p7 | 13:21034732 | CCTGGGGCCGCTGCC[C/G]AGCCTACACAGCTAG | 26524 |
rs369590717 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997548 | GGATGGTCCAGGCCT[C/T]TGTTGCAGGTACATC | 26524 |
rs369608584 | in-del | -/AG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030607 | AAAAAAAAAAAAAAA[-/AG]AAAAGAAAAAAAAAA | 26524 |
rs369626520 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030027 | TACTCAGGAGGCTGA[C/T]TCAGGAGAATTGCTT | 26524 |
rs369635157 | in-del | -/GTGTGTGT | 0.279461 | 0.248258 | intron-variant | LATS2 | GRCh38.p7 | 13:21044690 | CTATGAGGTGTAGGG[-/GTGTGTGT]GTGTGTGTGTGTGTG | 26524 |
rs369697670 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20985521 | AGGCAGGCGGATTAC[C/T]TGAGGTCAGGAGTTT | 26524 |
rs369736688 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991009 | ACACCTTCCCCTAGG[C/T]AGGAAGTACTAAGGT | 26524 |
rs369747828 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21052897 | GTCAAAGGCACCGAT[A/G]CTTCCTGTCCTCCCC | 26524 |
rs369778035 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013431 | TGTTTGCTGATTCCA[A/G]AGTCTGTGGAAAAAG | 26524 |
rs369800545 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985828 | AGACAGGTGGATCAT[A/C]TGAGGTCGGAAGTTT | 26524 |
rs369935029 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21008456 | TCCTTCTCATAATAA[C/T]GCTAAATGTAGGTAT | 26524 |
rs370004533 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20987986 | CTTAAAGGCGTATGG[C/T]GAGTAGCTCTTGATG | 26524 |
rs370015346 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:20992775 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 26524 |
rs370131826 | in-del | -/CGGA | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21030583 | ACAAGAGTGAGAGAC[-/CGGA]TCCGTCTCAAAAAAA | 26524 |
rs370189931 | in-del | -/GT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045110 | GAAAAGTGAGACTGT[-/GT]TGCCACAATTTTGAC | 26524 |
rs370235404 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007760 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 26524 |
rs370240707 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20982263 | GATACACTACATAGA[-/T]GCAGGTTGGCTATAA | 26524 |
rs370241513 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21031551 | AGTTTCCATTTCTCT[G/T]TAAAGATTTCCTGTC | 26524 |
rs370255628 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979237 | CAACAGGCTATTAGT[A/C]AAGTTTTTGGGGAGT | 26524 |
rs370265384 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | LATS2 | GRCh38.p7 | 13:20979834 | ATCCCTACACAGGCA[C/T]GAATTCTCCTCCGAG | 26524 |
rs370269023 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061368 | GGCGCGGTCTACACC[C/G]TCGGGGGCGTCCTGG | 26524 |
rs370271192 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991939 | ACTGGCCCTTAGAGA[G/T]CTGACTCGTAGAAGA | 26524 |
rs370297723 | snp | C/T | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:20995187 | TACAGTTCACAAAGG[C/T]ATCTTATGTGTTTCT | 26524 |
rs370308177 | in-del | -/CCC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048391 | AAAATAGAGAAAACA[-/CCC]CAGCCATACTATCTT | 26524 |
rs370325396 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005246 | ACTCAAAAGGAGGCT[C/T]GAAAAACTGTCTGGT | 26524 |
rs370331787 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023964 | GGCAACAAGAGTGAA[A/G]CTCCCTCTCAAGAAA | 26524 |
rs370335321 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982859 | AGCCAGAGGTGGTGG[C/T]GCGTGACTGTAATCC | 26524 |
rs370337187 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055975 | GGGTCTTTGAGGAAG[A/G]CAGTGATTGCATTCC | 26524 |
rs370354132 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990713 | GGGCCCATGTGCTCC[A/T]TCTTGGGAAAGTAAC | 26524 |
rs370366341 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013844 | GGTGTGACCACACAT[A/G]CCTGTGGTCCCAGCT | 26524 |
rs370385231 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046897 | GCATTTTGACCTAAA[C/T]AGTAAAATTAAAATA | 26524 |
rs370394984 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997732 | GGACGGGTGGGAACT[A/G]GAAGACACTCCTTCA | 26524 |
rs370448263 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043104 | CTTGGGAGGCCGAAC[A/G]AAGCAGGCAGATCAC | 26524 |
rs370483004 | snp | A/G | 6.67278e-05 | 0.00577577 | missense | LATS2 | GRCh38.p7 | 13:20981610 | ACACATCATCCCAGA[A/G]GTCGCTGGGCTCCAT | 26524 |
rs370486084 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20991689 | GAGACTTAAATTCTG[C/T]TTCTCCTCAGAAAAC | 26524 |
rs370596856 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21032981 | GTACAAGAAATAAGT[A/G/T]GAGATCAGATTGGAA | 26524 |
rs370604792 | snp | A/C/T | 6.60452e-05 | 0.0057462 | missense | LATS2 | GRCh38.p7 | 13:20988140 | TCGGGCTCGTTGGGG[A/C/T]CCGCACGGAGGCTCT | 26524 |
rs370614058 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:20998023 | GCACTCTGGCCCTAT[C/T]GTGTCTGCGTGGGCC | 26524 |
rs370681584 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060844 | ATCCGTGGGACCGCT[A/G]CGCCGCCGGACCGGG | 26524 |
rs370692017 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042764 | GAGGCCTAAGAGGGC[A/G]GATCACAAGGTCAGG | 26524 |
rs370695534 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015024 | CGTATCCCTGGGGTC[C/T]AACACATGGCCTGGC | 26524 |
rs370715357 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005883 | CTTTGGGAGGCCGAG[A/G]TTGGTGGATCACCTG | 26524 |
rs370724860 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024584 | CTGCATAGCGCCTCA[C/T]GGATGACATCTCACT | 26524 |
rs370816273 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21021458 | AGAGCCCGGGCAGCA[A/G]AGTGAGACTCTGTCT | 26524 |
rs370885678 | snp | C/T | 1.77666e-05 | 0.00298043 | intron-variant | LATS2 | GRCh38.p7 | 13:20983191 | AGTGACATCTACACA[C/T]AGAAAGTGCATGTGG | 26524 |
rs370944795 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21009822 | TGGAGGTCTATATGA[A/G]ATCACCTGGGTCCTT | 26524 |
rs370958624 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:20986910 | TAAATAAAAAATAAA[C/T]GGCTGGGTGTGGTGG | 26524 |
rs370973977 | snp | A/C/T | 0.000261513 | 0.0114321 | missense | LATS2 | GRCh38.p7 | 13:20988851 | TGCGGCACGTAGAGC[A/C/T]CGGCGGCAGGGGGTG | 26524 |
rs370996218 | snp | A/G | 1.85761e-05 | 0.00304758 | intron-variant | LATS2 | GRCh38.p7 | 13:20975414 | CCTCACATCTTGGGC[A/G]GTTCTGGGACAGCGT | 26524 |
rs371007153 | snp | C/T | 6.87651e-05 | 0.00586326 | intron-variant | LATS2 | GRCh38.p7 | 13:20981457 | GGTGGCTGGCCATGG[C/T]GCATGTACCTTTGCG | 26524 |
rs371095072 | snp | A/G | 1.72534e-05 | 0.00293708 | synonymous-codon, missense | LATS2 | GRCh38.p7 | 13:20975319 | TGGCCTCAGGGCTCA[A/G]CTTCACCTGGGCTGG | 26524 |
rs371115757 | in-del | -/AAAA | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974364 | AACATGGGAAAAAAT[-/AAAA]AACAAAAACCATTGT | 26524 |
rs371123024 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997470 | AGTATCAGGCCCTGC[C/T]AGTATCTTGAGGCTG | 26524 |
rs371131272 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21016692 | TCTGCTGCAAATACC[A/G]AGGCGCCAAGAGCAG | 26524 |
rs371136597 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978688 | TCAGCCCACTCCACA[G/T]GAAGATGACAAAGAT | 26524 |
rs371149587 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027860 | AACTGTGAGAACTGC[C/T]GTCTTAACAGTATTG | 26524 |
rs371157941 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21009644 | CATCATAGCTGTTAC[A/G]TAACAATCACAGCAT | 26524 |
rs371228267 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051206 | AGACAAGCCCTCTTA[C/T]ATGTAGGGCCCTTGA | 26524 |
rs371256486 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012068 | ATAACAAAATGATCT[G/T]AAATGAAGCATGTTA | 26524 |
rs371266176 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975201 | TTCCGGATGTCACTG[A/G]AGAAGTCAATGGCGC | 26524 |
rs371331193 | snp | A/G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040167 | TGAGGCAGGCGTATC[A/G/T]CTTCAGACTAGGAGT | 26524 |
rs371343498 | in-del | -/CAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036792 | CAACAACAACAACAA[-/CAA]AAAACAACAACAAAA | 26524 |
rs371346898 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054341 | TGAACCTGGGAGGCG[A/G]GGGCTGCTGTGAGCC | 26524 |
rs371362441 | snp | C/T | 5.34431e-05 | 0.00516901 | missense | LATS2 | GRCh38.p7 | 13:20988873 | CAGGGGGTGGGAAAG[C/T]GAGGCCGGCGCCTGG | 26524 |
rs371394634 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984586 | ATGCCATTTACAACA[A/G]CTATAAAAAAAATCT | 26524 |
rs371430796 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029133 | GAAGATGAAAGAGGA[C/T]ATCACACTGTATTAC | 26524 |
rs371513911 | snp | C/T | 0.00030216 | 0.0122878 | missense | LATS2 | GRCh38.p7 | 13:20989197 | CGTCAGCGCCGAAGC[C/T]TGGGCCCTCGTAGGG | 26524 |
rs371569585 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045815 | GCTTTCTGATAAGGT[C/T]CGAACTTTGGGGTGG | 26524 |
rs371577718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051554 | GTTTGAAAAATGGGG[A/C]CAGTGGTGGTGCCAT | 26524 |
rs371583865 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003131 | TGACAATAATTAACA[C/T]AAAGATTTAACAAAA | 26524 |
rs371627985 | in-del | -/CC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030153 | AAAAGAAATCCACCC[-/CC]ATGGTCTAATCATCT | 26524 |
rs371635207 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023447 | CACCGTGTGGGTAGA[A/G]TAGAACCCAACTGCA | 26524 |
rs371652277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037364 | AGCCAGATCATGCCA[C/T]TGCATTCCAGCCTGG | 26524 |
rs371733790 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007565 | ATATATATATATATA[-/C]TATATATATATATAT | 26524 |
rs371745650 | snp | A/G | 4.94189e-05 | 0.00497062 | missense | LATS2 | GRCh38.p7 | 13:20983587 | GGGCCACCTGATTCC[A/G]GTTCAGGACATCCTT | 26524 |
rs371767931 | in-del | -/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974588 | TAGTAAGAAAAAATG[-/G]ATATAAACAAAATAA | 26524 |
rs371770242 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21014896 | TCTAAGATCTTGTCT[A/G]CTTTATGACACGTTA | 26524 |
rs371772552 | snp | A/G | 1.67033e-05 | 0.00288987 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989213 | TGGGCCCTCGTAGGG[A/G]GTACCGCTCAGCTGG | 26524 |
rs371775408 | snp | A/G | 0.000107939 | 0.0073456 | missense | LATS2 | GRCh38.p7 | 13:20989028 | GGCCGCCCGTAGTGC[A/G]CGCCCTGCAGCGGGA | 26524 |
rs371793780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21043199 | AAAAATTAGCCAGGC[A/G]TGGTGTTGCGTGCCT | 26524 |
rs371803284 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015760 | GCTGGAGTGCAATGG[C/T]GCGACCTCTGCTAAC | 26524 |
rs371824520 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21054727 | AAATACTAAGTGGCC[A/G]TGTCCCTAGCCAGAT | 26524 |
rs371851186 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017140 | AGCCATGAACAAAGC[A/G]CCTGGCACTTGAATG | 26524 |
rs371859722 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976628 | TTGATTTAAAAAGGG[G/T]AATGGACTTGAGGAG | 26524 |
rs371872148 | snp | A/C/G | 0.000161987 | 0.00899818 | missense | LATS2 | GRCh38.p7 | 13:20988309 | CGCCCAGCGCCAGGG[A/C/G]ATGCTCCTCCTTGGC | 26524 |
rs371910588 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21010359 | TCTGGTAAAACCGAA[A/G]GGCCCCAGGGACAAA | 26524 |
rs371927873 | snp | C/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047389 | TATTCTTCACCCCGT[C/G]ATGAATGTTTATATA | 26524 |
rs371970700 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972964 | GTCACAGGGGAAGCA[C/T]GGGGGAGTTACAACA | 26524 |
rs371989086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21034490 | CTTCCCTGGCTCAGA[C/T]CTGGAACACCACTGC | 26524 |
rs371994166 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034025 | TATTAAGTAAAGCAC[A/G]TCACAGCACCAGGAA | 26524 |
rs372044956 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032500 | TGGAACTCCTGGCCT[C/T]AAGCAATCGCCCACC | 26524 |
rs372110765 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998745 | CCTTGTCAATGCGGG[C/G]CGAGGCGGGGCGGGG | 26524 |
rs372140528 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21006950 | GTTATTTTTTAAATG[A/C]TGTCAAGTAGGTTGG | 26524 |
rs372162495 | snp | A/C | 4.46967e-05 | 0.00472719 | missense | LATS2 | GRCh38.p7 | 13:20989121 | CCGGGCCCGTGGGGG[A/C]CGACTCCGGGGAAAA | 26524 |
rs372186448 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:20983044 | TACCTTAAAAAAAAA[-/A]TGCATATCACACTAT | 26524 |
rs372228474 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995766 | GTTTTACTCCATTAT[-/A]CTAGTTTGCACACGT | 26524 |
rs372262014 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998739 | CCAAGGCCTTGTCAA[C/T]GCGGGGCGAGGCGGG | 26524 |
rs372319546 | snp | C/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047247 | TGACCCTGGACCAGT[C/G]CCTTCGCCTCCCTCA | 26524 |
rs372320989 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045187 | TGTTAATAGTTACAC[C/T]CCCTGTAACAGCATA | 26524 |
rs372390097 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20992709 | CGGGGAGCTCCGGAA[A/G]GGAGTCCACAGTTAC | 26524 |
rs372397921 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040396 | AAAAAAAAAAAGAAA[A/G]AAAAAGAAAAAGAAA | 26524 |
rs372456985 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002522 | TGGGACTACAGGTGC[A/G]TTACCACCACACCCA | 26524 |
rs372482520 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010741 | TGAATTCCTGGAAAA[C/T]CCATACCTCTGCTTA | 26524 |
rs372492229 | snp | C/G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978577 | TTTCTTTAGATACAG[C/G/T]TGACCCTTGAACAAC | 26524 |
rs372530318 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041354 | GGAAGGCTGCCTCTC[A/G]GTGCACATCCTGACC | 26524 |
rs372660233 | in-del | -/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024116 | AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAAACAG | 26524 |
rs372824007 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042468 | TTGGAGGTTAAGGCC[A/G]CTTGAGTCTGGAAGT | 26524 |
rs372864277 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059083 | AATTTTAAGCAAAAC[A/G]CTTGTGCAAGATCAC | 26524 |
rs372913919 | snp | A/C/G | 7.00493e-05 | 0.00591781 | missense, intron-variant | LATS2 | GRCh38.p7 | 13:20979791 | CAGTCACAGAGTTGA[A/C/G]TGTACCCTGCAAGAC | 26524 |
rs372930048 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032709 | GACCCTGAGAGGCCT[A/G]CCATGGTTCCCTGGA | 26524 |
rs372962495 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029636 | TTGCTACTAAAAATA[C/G]AAAAATTAGCCGGGT | 26524 |
rs372979732 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986140 | AAGATGCTCATTAAC[C/G]ATCAGGGAAATGCAA | 26524 |
rs372997332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023811 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAATTA | 26524 |
rs373012826 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20988002 | GAGTAGCTCTTGATG[C/T]GTGACTCTCTCTTCT | 26524 |
rs373045868 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049512 | AGCTACCAGGTGAGT[A/G]GATGGCTGAGGCCCT | 26524 |
rs373064421 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009034 | AGGCCCAGGTTGTTC[A/G]TCCCACTGCCCATGC | 26524 |
rs373069985 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21035668 | GAACAATATTTATGA[C/T]CTCCAATATTTTTCA | 26524 |
rs373075270 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21016288 | CAGCGTACCCGGCCT[A/G]TTTTTATTTTTTTTG | 26524 |
rs373077961 | in-del | -/A | 0.473174 | 0.112665 | intron-variant | LATS2 | GRCh38.p7 | 13:21030613 | AAAAAAAAAAAAAAG[-/A]AAAAAAAAAAGAAAA | 26524 |
rs373080553 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | LATS2 | GRCh38.p7 | 13:20975404 | GTTAGTTTCTCCTCA[C/T]ATCTTGGGCAGTTCT | 26524 |
rs373089416 | in-del | -/TAAG | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994841 | GGCTGGGCAACAAAG[-/TAAG]AATGTGTCTCAAAAA | 26524 |
rs373091661 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044236 | CACAAACATCTCCTC[C/T]GAGAAATGTAAATTC | 26524 |
rs373118597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20982400 | CACCGCAACCTCTGC[C/T]TCCCGGGTTCAAGCG | 26524 |
rs373133372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20996598 | GTTGGCCAGGCTGGT[C/T]TCGAACTCCTGACCT | 26524 |
rs373148609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21040968 | TTCCCCCTTGAGGCA[C/T]GTGTTCACCTTTTTT | 26524 |
rs373167364 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974179 | TGCTGTGAATGGCAA[A/G]ATATGGTAATTTTAT | 26524 |
rs373245196 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038747 | ACCAGGTGGCCGAGG[A/C]GGGCGGATCACCTGA | 26524 |
rs373276729 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007683 | GTATATATATATATA[-/G]TATATATATATATAT | 26524 |
rs373324657 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993605 | GACAGATTGGAAAAT[C/G]GTAATAAGAACAGAC | 26524 |
rs373339307 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035046 | GACCAGCCCGAGAAA[A/C]ATAGCAAGACTCCAT | 26524 |
rs373374500 | snp | A/G | 8.23676e-05 | 0.00641693 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975131 | TTCATCTACGGGGTC[A/G]AAATTCGAGGTGTCC | 26524 |
rs373475512 | snp | A/G | 3.42624e-05 | 0.00413884 | intron-variant | LATS2 | GRCh38.p7 | 13:20981458 | GTGGCTGGCCATGGC[A/G]CATGTACCTTTGCGG | 26524 |
rs373499293 | in-del | -/TA | 0.141596 | 0.225274 | intron-variant | LATS2 | GRCh38.p7 | 13:21007723 | TATATATATATATAG[-/TA]TATATATATATAGTA | 26524 |
rs373546130 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20989404 | GCTGCCCTCGGGGCT[A/G]AGGGTCTTGAACCCT | 26524 |
rs373557414 | in-del | -/GTGT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044690 | CTATGAGGTGTAGGG[-/GTGT]GTGTGTGTGTGTGTG | 26524 |
rs373563720 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055004 | AAAAATAGTACCTAC[A/G]GATAAACTGTGTTCT | 26524 |
rs373607209 | snp | C/T | 8.85716e-05 | 0.00665417 | intron-variant | LATS2 | GRCh38.p7 | 13:20983198 | TCTACACATAGAAAG[C/T]GCATGTGGCACACTT | 26524 |
rs373640437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20991584 | GTGTGCCCTGCAGGT[A/G]CCTGATGGCAAAAGC | 26524 |
rs373643179 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052293 | CAGGAGATAAGACCA[C/G]GGAAAAATTACCAAA | 26524 |
rs373724424 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991509 | TGGGACACTTCGCCT[C/G]TGTACTGCTGAGAAC | 26524 |
rs373725855 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21033224 | TAGGAACCTTTGTTA[C/G]ACCAGACCTGGTTGA | 26524 |
rs373729998 | snp | C/T | 8.815e-05 | 0.00663832 | missense | LATS2 | GRCh38.p7 | 13:20975337 | TCACCTGGGCTGGAA[C/T]GTGGAGCGTGTTCTC | 26524 |
rs373818643 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008601 | TCACAAGAAGTCCAA[C/T]GTCACCAGCAATCAT | 26524 |
rs373820700 | snp | C/T | 0.000542692 | 0.0164636 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988889 | GAGGCCGGCGCCTGG[C/T]GGTCCTCCCTGGCCC | 26524 |
rs373945996 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21021567 | AACAAAACCCTTTGC[C/G]AAGTTCTTACTCCAG | 26524 |
rs374081136 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004961 | AGAGACCAGCCCCGG[A/C]GTTCTAAATGCCTGG | 26524 |
rs374085888 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | LATS2 | GRCh38.p7 | 13:20999606 | CCTGTAGTCAGGAGC[A/C]AGTATGCTTGGCTAA | 26524 |
rs374103407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986931 | GGTGTGGTGGCTCAC[A/G]CGTGTAATTCCAGCA | 26524 |
rs374153836 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011607 | CTGGTGGAGACTTTG[C/T]CTTGGCCTAGGAATT | 26524 |
rs374190894 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039024 | GCTTAAGGGGAGAGG[A/G]GATTATGACACAGAG | 26524 |
rs374211521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20986489 | TGAATGGAACTGGAG[A/G]TCATTATGTTAAGTG | 26524 |
rs374290112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20998031 | GCCCTATCGTGTCTG[C/T]GTGGGCCTCTGTCTG | 26524 |
rs374295752 | in-del | -/A | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062228 | CAAGAGAATCACTGG[-/A]ACCCGGGAGGCGGAG | 26524 |
rs374368520 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21032297 | TTGAGACAGAGTCTC[C/G]CTCTGTCACCCAGGC | 26524 |
rs374488676 | in-del | -/TAAAAATAAAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048863 | AAATAAAAATAAAAA[-/TAAAAATAAAAA]AAACCTACTGAATCT | 26524 |
rs374496670 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995542 | ATATCTGTTCAATGA[A/C]TGATTGAGTGAGTGA | 26524 |
rs374509341 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039494 | ATATTGTTAGAATTA[A/G]GCCAAATAAATATCC | 26524 |
rs374514931 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056368 | ACATAAGCTTACAGT[C/G]TCGGGGAAAAAGACA | 26524 |
rs374522537 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21025519 | GTTTCTTGAAAGGAA[A/C]AGTACCAGCTTATTC | 26524 |
rs374578315 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21001835 | GGTGAGCCGAGACAG[C/T]GCCCCTGCACTCCAG | 26524 |
rs374586338 | snp | C/G/T | 4.29528e-05 | 0.0046341 | intron-variant | LATS2 | GRCh38.p7 | 13:20979842 | ACAGGCATGAATTCT[C/G/T]CTCCGAGGTGAATTT | 26524 |
rs374588173 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | LATS2 | GRCh38.p7 | 13:20998513 | CAGCAGGGTGGTCTT[C/T]AAAAGAATCTCTGAC | 26524 |
rs374594463 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015864 | AGCATCATGCCCAGC[C/T]AATTTTTGTATTTTT | 26524 |
rs374595657 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21005320 | ACTTGACCTTGACAG[A/G]GTGTAGCGTAAGCCA | 26524 |
rs374596801 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036943 | AATACAAATAAGAAT[C/G]GTAAAAATGCTCTCA | 26524 |
rs374601847 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990564 | TGGCCTCAGCCTCCC[A/C]AAGAGTTGGGATTAC | 26524 |
rs374613235 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20984401 | CTAGAACTCCAAGAG[A/C]CATCTAATCTTTCAG | 26524 |
rs374620767 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21034891 | ACAAATTGTAAAAAT[A/T]TAACTATGAAAAAAA | 26524 |
rs374622852 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006529 | ATCATCAGAGCTGAA[A/G]CATGAACAGATTAAA | 26524 |
rs374629084 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21022004 | TTTTTTTTTGTGACT[A/G]AACTGAAAGTATAGT | 26524 |
rs374636710 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013696 | AAGGGCCAGGTGCAG[C/T]GGCTCGAGCCTGCAA | 26524 |
rs374642050 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037874 | GATCCTGCAGCTACA[A/G]GTGGGTCCTGTCCGC | 26524 |
rs374653974 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21014495 | AAAGGAAGTATTTCT[A/G]AGTGAAATGTATATG | 26524 |
rs374660528 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016918 | CCAAAGATAAGTAAA[A/C]CCAACTTGCCCGATC | 26524 |
rs374700037 | in-del | -/TGAG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028165 | ATTCCCATCTATGAG[-/TGAG]AACATGCGGTGTTTG | 26524 |
rs374711207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21009641 | TTTCATCATAGCTGT[C/T]ACATAACAATCACAG | 26524 |
rs374720953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024981 | CAGACCAGGCTTCCC[C/T]CATAACTTTTTGCCT | 26524 |
rs374805655 | in-del | -/AT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022238 | CATGCATGTGTGCCT[-/AT]GTGTGTGGACGTATG | 26524 |
rs374877162 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21009341 | CAGCCATCTCTCCCC[A/G/T]ACACCTGCTCCTCTC | 26524 |
rs374884189 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030591 | GAGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 26524 |
rs374973316 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032825 | CGTGGAAGTGGGACT[C/T]GAAGGGTGGACCACG | 26524 |
rs374990574 | snp | A/G | 8.79113e-05 | 0.00662932 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988226 | CAGCAGGTGCTTCGG[A/G]TAGGGCGGAGGCGGG | 26524 |
rs375002952 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21010866 | TCAACCAATCAGAAC[A/T]AAGCAAGTTTGACTC | 26524 |
rs375024406 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983609 | GACATCCTTTTTCCT[G/T]AGGGTCTTCATGGCG | 26524 |
rs375064398 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996670 | ATAGGTGTGAGCCAC[C/T]GTGCCTGGGCTGATA | 26524 |
rs375149933 | snp | C/G/T | 1.66574e-05 | 0.0028859 | missense | LATS2 | GRCh38.p7 | 13:20989224 | AGGGGGTACCGCTCA[C/G/T]CTGGTGGTAGGACGC | 26524 |
rs375179623 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007689 | TATATATAGTATATA[-/G]TATATATATAGTATG | 26524 |
rs375181961 | snp | C/G | | | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045866 | CTGGTGGCATCTTTG[C/G]TCCCCAGGACTTTGG | 26524 |
rs375183194 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:20983962 | ATACTACAGAGTCTC[A/G]CTCTGTCGCCTAGGC | 26524 |
rs375203969 | snp | A/C/G | 0.0178429 | 0.0930183 | intron-variant | LATS2 | GRCh38.p7 | 13:20998752 | AATGCGGGGCGAGGC[A/C/G]GGGCGGGGCCCGACA | 26524 |
rs375208071 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030435 | TCTACTAAAAATGCA[A/C]AAAATTAGCCAGCCG | 26524 |
rs375208842 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015352 | CACACTGCAGACACA[C/G/T]GAAGGACCAGGACCC | 26524 |
rs375212059 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992348 | TTTCAAACTGGGACA[A/T]ACGGCATCAGCAGGT | 26524 |
rs375213619 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038021 | CTACCTGGGTGGACC[A/G]CTTGAGCCCAGGAGG | 26524 |
rs375233026 | snp | A/G | 0.00637571 | 0.0560999 | intron-variant | LATS2 | GRCh38.p7 | 13:21030998 | AGATATAAAATTCTC[A/G]GTGTATTTTTTTCTT | 26524 |
rs375267518 | snp | A/G | 0.000313017 | 0.0125064 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045972 | CACGAATCTCTTGCA[A/G]TCGCTGCCGGCTATT | 26524 |
rs375282390 | snp | A/G | 1.6522e-05 | 0.00287414 | missense | LATS2 | GRCh38.p7 | 13:20988150 | TGGGGCCCGCACGGA[A/G]GCTCTGCTCCATGCC | 26524 |
rs375310896 | in-del | -/T | 0.380919 | 0.21298 | intron-variant | LATS2 | GRCh38.p7 | 13:21003445 | CTTTCTTTTTTTTCC[-/T]TTTTTTTTTTTTAAA | 26524 |
rs375328835 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057538 | AATCACGTAACAGGC[C/T]GGGCGCGGTGGCTCA | 26524 |
rs375342028 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010017 | CCAGCCTGGCCAACA[G/T]GATGAAACCCTGTCT | 26524 |
rs375364724 | in-del | -/TAC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007577 | ATATATATATATATA[-/TAC]TATATATATAGTATA | 26524 |
rs375367921 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996512 | CTTCCCGAATAGCTG[G/T]GATTACATGCATGAA | 26524 |
rs375374336 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995946 | TAGCCACGTGCAACA[A/G]GAAAATCCCTCACAC | 26524 |
rs375375919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982130 | GTTTTGAGTTAGAGA[A/G]AAAAGACTAAGTGAT | 26524 |
rs375414588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981067 | AGCACCCAGCTGCAC[A/G]CGGCACAACTCAGCC | 26524 |
rs375419483 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981040 | AAAAGGATCTTCCAA[C/T]GCTGTCACATAAGCA | 26524 |
rs375424015 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21010194 | CATGGAGCTAGACTC[C/T]GTCAAAAAAACAAAC | 26524 |
rs375424765 | in-del | -/AAGT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022206 | TGTGTGCAACTACGT[-/AAGT]GTGTGAATATGTGCA | 26524 |
rs375438520 | in-del | -/AGAGGGGAGCA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040648 | AGAGAGCTCCTCTGT[-/AGAGGGGAGCA]TGTGGGGAGGATAAG | 26524 |
rs375447416 | snp | C/T | 2.97119e-05 | 0.00385423 | missense | LATS2 | GRCh38.p7 | 13:20988852 | GCGGCACGTAGAGCC[C/T]GGCGGCAGGGGGTGG | 26524 |
rs375527776 | snp | C/T | 0.000155988 | 0.00883004 | missense | LATS2 | GRCh38.p7 | 13:20989050 | GCAGCGGGAAGTGTG[C/T]CCCTGCTGCCTCTAC | 26524 |
rs375559948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20984878 | CCTAGGCAAAAAGAA[A/C]AAAATTGTTACCTGA | 26524 |
rs375566927 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:20998468 | GCTGCACTGTCTCTG[A/G]CGGGATCCTGTGCTT | 26524 |
rs375645901 | snp | C/G | 0.000155988 | 0.00883004 | missense | LATS2 | GRCh38.p7 | 13:20988753 | GCAGGCTCTGCGGGG[C/G]GCTGTCGCTGGCGAA | 26524 |
rs375661998 | snp | A/T | 1.85372e-05 | 0.00304438 | intron-variant | LATS2 | GRCh38.p7 | 13:20975403 | GGTTAGTTTCTCCTC[A/T]CATCTTGGGCAGTTC | 26524 |
rs375787806 | snp | A/G | 3.34409e-05 | 0.00408893 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988187 | CAGGCTGTCCAGGTC[A/G]TACTGCTCCGACTTG | 26524 |
rs375829672 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027474 | ACAAACAAAAACCCT[C/T]AACCTCCGCCCTTTT | 26524 |
rs375849818 | in-del | -/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024122 | AAAAAAAAAGAAAAA[-/G]AAAAAACAGCTTGAA | 26524 |
rs375919132 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:20993578 | GCCCATGTGGGACAT[A/G]GGACATGAAGTGACA | 26524 |
rs375928401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008454 | CCTCCTTCTCATAAT[A/C]ACGCTAAATGTAGGT | 26524 |
rs375937159 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022582 | TCAAAATGTTTGAAA[-/A]GATCAAATGAACTGT | 26524 |
rs376003859 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004804 | TCCTTCTAAAACCTA[C/T]ACCAACCAAGACATT | 26524 |
rs376078182 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20985518 | CTGAGGCAGGCGGAT[C/T]ACTTGAGGTCAGGAG | 26524 |
rs376201762 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040198 | TCAAGACCACCGTGG[A/G]CAACATGGTGAAACC | 26524 |
rs376213206 | snp | C/G | 0.000153988 | 0.00877328 | missense | LATS2 | GRCh38.p7 | 13:20983338 | CAGGCTTGATGTCTC[C/G]GTGGATGAAGCCCAT | 26524 |
rs376233949 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982600 | ACAGGCGTGAGCCAC[C/T]ATGCCCAGCCAAATC | 26524 |
rs376259400 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005805 | TGAGACCCCTACTCT[A/T]TAAAAAAAAAAAAAA | 26524 |
rs376264549 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012853 | AACAAACTGAGGCTA[A/C]AATAGATTAGCTTTT | 26524 |
rs376277723 | in-del | -/CA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995880 | ATTACTAATTATTTA[-/CA]GAGTAATGTGGTAGG | 26524 |
rs376318141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991158 | CTGAATGAGGCAATG[G/T]GCCAGGAGACTGGCT | 26524 |
rs376321247 | snp | A/T | 1.85544e-05 | 0.0030458 | intron-variant | LATS2 | GRCh38.p7 | 13:20975406 | TAGTTTCTCCTCACA[A/T]CTTGGGCAGTTCTGG | 26524 |
rs376327437 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024515 | AGTGGGGTTCAGTGG[C/T]GGTTCTCGCCAGGGC | 26524 |
rs376333080 | snp | C/T | 4.94287e-05 | 0.00497111 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988091 | CTTTCCGCCTTTGTC[C/T]CCCTTGGCGCTTTTG | 26524 |
rs376401196 | snp | A/T | 0.000135207 | 0.00822102 | intron-variant | LATS2 | GRCh38.p7 | 13:20979829 | ACTCAATCCCTACAC[A/T]GGCATGAATTCTCCT | 26524 |
rs376445846 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017342 | CTTTTTCTTTTTTTT[-/T]GTTTTTAATTTTTGT | 26524 |
rs376467864 | snp | A/C/T | 0.00010539 | 0.00725843 | intron-variant | LATS2 | GRCh38.p7 | 13:20987841 | TTGCCAGTAGAGGGA[A/C/T]GAGCCGGGAACAAAT | 26524 |
rs376469173 | in-del | -/ACATACATACATAC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050173 | CATACATACATACAT[-/ACATACATACATAC]AGATGGAAAGCTGCT | 26524 |
rs376477507 | in-del | -/AGT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043010 | CAAAAAACAAAAAAC[-/AGT]AGGAGTGAAAGGGGT | 26524 |
rs376521798 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013368 | TGGACTATGACTAAT[A/G]TGCATGAGGGAATAT | 26524 |
rs376529851 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026423 | TGAAGCCCATTGATG[C/G]TGTTGTATAAGTGGT | 26524 |
rs376634897 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005047 | ATGGGAAGGACCATG[C/T]TGGTCCCACAGAAGA | 26524 |
rs376637350 | snp | G/T | 1.64789e-05 | 0.0028704 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975200 | CTTCCGGATGTCACT[G/T]GAGAAGTCAATGGCG | 26524 |
rs376637368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20981974 | GGACAGCACTCCTAG[C/T]GCTTAGGCCATAATC | 26524 |
rs376649294 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991606 | GGCAAAAGCCTAGCA[A/C]AAGCCACACCATAGA | 26524 |
rs376683920 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:21051042 | AGTCACAGAGAAGGG[C/T]GATCATGTCTGCCCT | 26524 |
rs376685837 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023747 | GGGAGGCTGAGCCGC[A/G]TGGATCACCTGAGGT | 26524 |
rs376701545 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975057 | TGCTTGTTATTGGGC[A/G]AGGTGAGTGTGTCCC | 26524 |
rs376704213 | in-del | -/CT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987340 | TTGTGTGATTTAAAT[-/CT]GTTACATTTTAATTT | 26524 |
rs376786994 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974862 | TGGTGGGGGTGCCTG[A/G]CCCCCATCTACACGT | 26524 |
rs376788053 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986844 | TCATTACATATCCTA[C/T]GCATGTAACAAAATA | 26524 |
rs376795301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20977311 | GAGGCATGAGAACCC[A/G]GAAGGCAGAGGTTGC | 26524 |
rs376833482 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992573 | CCGTTGAGGCTGGCT[A/G]TGGGACAAGGGCAAA | 26524 |
rs376896730 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21009534 | AAGTAAAAACACAAC[A/T]ACAAAAATGTAGGTA | 26524 |
rs376909649 | snp | A/G | | | missense | LATS2 | GRCh38.p7 | 13:20988189 | GGCTGTCCAGGTCGT[A/G]CTGCTCCGACTTGCT | 26524 |
rs376920019 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974751 | AGAATTTCAAGTGAA[A/G]TAATCGACGGACTAA | 26524 |
rs376966173 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022928 | TATACAAATAAGCAA[A/T]AGACTCCCCTTCTTC | 26524 |
rs376970905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040422 | AGAAAGAAATGTCTT[C/T]GCTGTGGAAGTTTGA | 26524 |
rs376976811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21058451 | TGGTGGAGTTTAGGA[A/G]CCCAAGGCTGGCTAT | 26524 |
rs377015028 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035048 | CCAGCCCGAGAAACA[C/T]AGCAAGACTCCATCT | 26524 |
rs377140113 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020434 | CCTCTAGGCACAGGG[C/T]AATTTACCCAGGAAA | 26524 |
rs377171544 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21017324 | ACATAGAGGTGATGC[A/G]ATCCTTTTTCTTTTT | 26524 |
rs377266289 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974759 | AAGTGAAGTAATCGA[C/T]GGACTAATTTAAAAC | 26524 |
rs377274695 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000061 | GAGCATTTTACAACT[A/G]TTGTTAGCACCAAAA | 26524 |
rs377277206 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21005852 | GCGCAGTGGCTTACG[C/T]CTATTAATCCCAGTA | 26524 |
rs377277425 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035182 | GTGGCTTTAATTCAA[A/G]AGCTATGAATTTCTG | 26524 |
rs377330170 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016344 | GGCTCAGTACAGTGG[C/T]GTGATCTCGGCTCAC | 26524 |
rs377391449 | in-del | -/TGGTCAGGACCAGGG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037810 | TGGGCAGGGCCAGGG[-/TGGTCAGGACCAGGG]CGGGTAGGGCCAGGG | 26524 |
rs377401953 | snp | A/G | 1.8517e-05 | 0.00304272 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988778 | GGCGAACACCTGGCT[A/G]CGGGAGCCCAGCACA | 26524 |
rs377469118 | snp | G/T | 0.000215031 | 0.0103667 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975246 | GCCTTCAGGTCATCG[G/T]CCCCATTCCGCCCCA | 26524 |
rs377473637 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038748 | CCAGGTGGCCGAGGC[A/G]GGCGGATCACCTGAG | 26524 |
rs377473754 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027128 | AGTCCATTGTCAGAT[-/A]TATGTATCAGTAATA | 26524 |
rs377473908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995372 | TCCAGCTTACCTCAG[A/G]CTGCTGTGTAAACAT | 26524 |
rs377502327 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042752 | CCAGCACTTTGGGAG[G/T]CCTAAGAGGGCGGAT | 26524 |
rs377579860 | snp | C/T | 1.95616e-05 | 0.00312737 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988667 | GGCCAGGGTGGCAGC[C/T]GGCCACTGCTGGACG | 26524 |
rs377626485 | snp | C/T | 1.66618e-05 | 0.00288628 | missense | LATS2 | GRCh38.p7 | 13:20989287 | TCCGCGTCACTGGGG[C/T]TGGCATGAGCCCCTT | 26524 |
rs377710938 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052959 | ACCGAACGCTGGGCC[A/G]GGCACGGTGGCTCAC | 26524 |
rs377715225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997726 | TTACGAGGACGGGTG[A/G]GAACTGGAAGACACT | 26524 |
rs377716734 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013732 | GCACTTAAGGAGCCT[C/G]AGGCAGGAGGATCAC | 26524 |
rs377723947 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034982 | ATGCCTGTAATCCCA[A/G]CACTTTGGTAGGCCA | 26524 |
rs377724358 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20997347 | GGACCTAACCACTAC[A/G]AAGCCTGGAAAATGT | 26524 |
rs377731878 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014780 | AAAAGAATGTTTGTT[A/G]AGTGGTTTAAGTTTA | 26524 |
rs386768685 | multinucleotide-polymorphism | GC/TA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013223 | TATGGTGACCATGAA[GC/TA]AGGCTGCCTCCCAGG | 26524 |
rs386768686 | in-del | -/CTCCGGGC/T | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023150 | GCGCTGCATCGAGGG[-/CTCCGGGC/T]TCCGAGGGCTCCGAA | 26524 |
rs386768687 | in-del | CCCGA/TCC | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023151 | CGCTGCATCGAGGGC[CCCGA/TCC]GGGCTCCGAGGGCTC | 26524 |
rs386768688 | multinucleotide-polymorphism | AC/GT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030316 | CTCTGCTGGCCGGGC[AC/GT]GGTGGCTCACACCTG | 26524 |
rs386768690 | in-del | CTGTCTCATAGACAG/GTCTC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050113 | CGACAGAGGGAGACT[CTGTCTCATAGACAG/GTCTC]ATAGATAGATAGATA | 26524 |
rs386768692 | in-del | CGT/TG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054986 | TGTCTTAAGTGAATA[CGT/TG]AAAAAATAGTACCTA | 26524 |
rs397751657 | in-del | -/GTAT/GTGT/GTGTGT | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973535 | TGTGTGTGTGTGTGT[-/GTAT/GTGT/GTGTGT]ATACACGCACATACA | 26524 |
rs397759027 | in-del | -/A | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21044872 | GTAGTTGGGACTACA[-/A]GGTGCACACCACCAC | 26524 |
rs397784855 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004450 | AAAAAAAAAAAAAAA[-/A]GCTTCTGTAATGCAA | 26524 |
rs397788847 | in-del | -/A | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:20987232 | TAAAAATAAAAAAAA[-/A]CACAAATGAAAAGTA | 26524 |
rs397817690 | in-del | -/AG | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21032291 | TATTTTTTGAGACAG[-/AG]TCTCGCTCTGTCACC | 26524 |
rs397937838 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995765 | AGTTTTACTCCATTA[-/A]TCTAGTTTGCACACG | 26524 |
rs397946193 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993061 | AAAAAAAAAAAAAAA[-/A]TGGGGGGGTGGAGAT | 26524 |
rs397957126 | in-del | -/AAAATATA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020154 | TTCACATAAAATATA[-/AAAATATA]CCTGAAAACACACCA | 26524 |
rs398021822 | in-del | -/A | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21021504 | AAAAAAAAAAAAAAA[-/A]GCTTTGTAAAAGGCA | 26524 |
rs398021823 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024705 | AAAAAAAAAAAAAAA[-/A]GTACTGATGTTAAAA | 26524 |
rs398021824 | in-del | -/A | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21025234 | AAAAAAAAAAAAAAA[-/A]TACAAAAATTAGACG | 26524 |
rs398021825 | in-del | -/A | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21026328 | TGTCACTATGAGTTA[-/A]CCATTCTCTAAACTA | 26524 |
rs398098662 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055316 | TGGACTTTAAAAAAA[-/A]TGGGGATATCAAGCA | 26524 |
rs398098663 | in-del | -/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061898 | CAGTCTTGGTGAAAG[-/G]AAAAAAAAAAGTTAG | 26524 |
rs527270776 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21013350 | AATAATAATCTCATT[G/T]CTTGGACTATGACTA | 26524 |
rs527312087 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043984 | CCTACTTTCAAAACT[C/G]CTGGGTTCTGTACGT | 26524 |
rs527346510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013885 | CTAAGATGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 26524 |
rs527384936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21052468 | TGATTCTCGTGCCTC[A/C]GCCACCCGAGTAACT | 26524 |
rs527390685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000046 | CACTGATAAAATAAA[G/T]AGCATTTTACAACTA | 26524 |
rs527421271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046672 | ACTAACCTCTCCCCC[A/C]TCACATGAGATGTGG | 26524 |
rs527479332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000728 | GAAATAATACTTTCT[A/G]TAAGTAAAACTCTAA | 26524 |
rs527516469 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051679 | AAAGCACAGGGCAGG[C/T]TGGGTCCAGTGGCTC | 26524 |
rs527570698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040612 | TGTCTGGGAGGCCAT[A/G]CTGTGTGGCTGAGAC | 26524 |
rs527631937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21027983 | TGTGCACAATGTGCC[A/G]GTTAGTTACATATGT | 26524 |
rs527650007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050943 | ACCACAGCCACGTGA[G/T]GGGGGGCAGGAAAAG | 26524 |
rs527664602 | snp | C/T | | | synonymous-codon | LATS2 | GRCh38.p7 | 13:20991306 | GACCCGCACAATCTG[C/T]TCATTCCTCGGGTCC | 26524 |
rs527686386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038118 | CTCAAAAACCGAAAC[A/G]AAACAAATCAGACTG | 26524 |
rs527686813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21045189 | TTAATAGTTACACCC[C/G]CTGTAACAGCATATA | 26524 |
rs527694109 | in-del | -/CAGA | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21026893 | ACTACTTAGTATTAT[-/CAGA]CAGACCTTTATACTT | 26524 |
rs527716154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20999345 | AGGTACAAACCATAC[A/G]TCTTTTTGAAACGAA | 26524 |
rs527774568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038592 | TGTTATGGTGGGGTA[C/T]TGGAAAGTTTCCAAT | 26524 |
rs527843182 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20987139 | GGCAGAGGTTGCAGC[C/G]AGCCAAGATCGCGCC | 26524 |
rs527896647 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21026338 | AGTTAACCATTCTCT[A/C]AACTACTAAATAAAT | 26524 |
rs527937541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981230 | GGTCTAGGTAGAGCC[C/T]GAGGGCCAGCAGACA | 26524 |
rs528021565 | in-del | -/GTCG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014170 | AACAGGGTAATATGA[-/GTCG]GGGGCAGGGGGAAAG | 26524 |
rs528021642 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21020193 | TGTGACATAGGGAAG[C/G]CTGGCAAGATTCTTC | 26524 |
rs528026146 | snp | C/T | | | missense | LATS2 | GRCh38.p7 | 13:20989248 | AGGACGCAAACGAAT[C/T]GCCGGTTCCTTCGAA | 26524 |
rs528037090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991919 | GCTGGCTATAGCAGC[A/G]GAGGACTGGCCCTTA | 26524 |
rs528050343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20985155 | AACAGATTAAAGACC[C/T]AGAAATAAGACCAGA | 26524 |
rs528122972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20985835 | TGGATCATCTGAGGT[C/T]GGAAGTTTGAGACCA | 26524 |
rs528232476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017896 | CTCCTAAAGTGCTGG[G/T]ATTACAGGCGTGAAC | 26524 |
rs528269517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21011233 | CTGCTTTTCCTCACT[C/T]GTCCTGAATCAAAAA | 26524 |
rs528273516 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973871 | ATGAAAGAGCATACG[A/G]ACTACAGAAACGGAC | 26524 |
rs528311814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21056654 | GCACCCCTCCAAGTT[C/T]TGGATACGCTCCAGC | 26524 |
rs528340100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21011872 | GGCTAGATGGTATAG[C/G]ATATTGTTCCTGGCT | 26524 |
rs528370526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050484 | CTACTCTGTAGTTTA[C/G]CACATTTCTTTCAAC | 26524 |
rs528398745 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994130 | ATGTGTATGTTTATT[A/G]TGCATCAAATCTAGG | 26524 |
rs528423373 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034792 | AGAAGAATTTCCTGC[C/T]GTTTCCCACAGTACA | 26524 |
rs528462274 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061634 | GCATACCAGTCCGGG[C/G]GGGGCGCCTGCGGCC | 26524 |
rs528470026 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20997710 | CTACTAAGCACAGGG[C/T]TTACGAGGACGGGTG | 26524 |
rs528502189 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21029094 | TTTTTTCTTTCCTTA[C/T]TGCACTAGCTAGGAC | 26524 |
rs528511429 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062043 | CCAGAAGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 26524 |
rs528540776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048816 | CACTCCAGCCTGGGC[A/G]ACAAGAGCGAAACTC | 26524 |
rs528543951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21017054 | CGGAAACAAATTCAT[C/T]TTCATTAGTGCTTCT | 26524 |
rs528547206 | in-del | -/ATC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21031346 | ACTGGACAACCTCAT[-/ATC]ATCCCACAAGTCACT | 26524 |
rs528626490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049368 | AGGAGCAGCAGCCCC[A/G]GGGAGCAAGGGGAAG | 26524 |
rs528686392 | in-del | -/A | 0.351418 | 0.228505 | intron-variant | LATS2 | GRCh38.p7 | 13:21019974 | AGTGAGACTCCATCT[-/A]AAAAAAAAAAAAAAA | 26524 |
rs528687390 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:21042932 | GAAGTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 26524 |
rs528732819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997675 | TGACACACCCTCTGC[G/T]CTCTTGGCTTGGTCC | 26524 |
rs528770161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043385 | AATCATCTTTTTAAC[A/T]AACTGATGCATACAA | 26524 |
rs528818757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20998013 | TAGAAACGGAGCACT[C/T]TGGCCCTATCGTGTC | 26524 |
rs528820593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030535 | CGGAGCTTGCAGCGA[A/G]CTGAGATCACACCAC | 26524 |
rs528841775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986312 | ATATCAAAGGGATAC[C/G]TGCACCCCATGTTTA | 26524 |
rs528865413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025418 | AAAAAAAAAAAATTA[C/T]GGTCATGAGTGAGGA | 26524 |
rs528914516 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058136 | ACCCTTCTTTCTGAT[C/G]ATCAGAATATTTCGG | 26524 |
rs528927341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20980498 | AAGAGGTCAGTCTGC[A/G]GGTGCCTGCAGCTGC | 26524 |
rs529006281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21019118 | AGTTCCCTAATTACT[C/G]TGTATTTCCATTTCC | 26524 |
rs529033793 | snp | C/T | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21057423 | GGTGAACGGCAAACA[C/T]TAAACAATGCCAAAT | 26524 |
rs529035253 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043071 | AGACGTGGTGACGCA[C/T]GCCTGTAATCCCAGC | 26524 |
rs529041307 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038922 | GAGGCGGAGGTTGTA[A/G]TGAGCTGAGATCACC | 26524 |
rs529055712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050504 | TTTCTTTCAACACTA[A/T]ATTTGCAGATTCATA | 26524 |
rs529108867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21005888 | GGAGGCCGAGGTTGG[A/T]GGATCACCTGAGGTC | 26524 |
rs529198767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21045324 | AAGGGAAGCCAGTCT[A/C]TTTCCACGATAGCTC | 26524 |
rs529226428 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20990114 | GCCCTGACAGCCTGG[-/C]CACTGAACAAAGGTC | 26524 |
rs529235648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038650 | TCATTGGCTATGACA[C/T]TGCCACTGTGCAAAG | 26524 |
rs529283068 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21010414 | CTACAGCAAAGCCCC[A/C]ACTCTACAGGCCCCA | 26524 |
rs529286441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21055976 | GGTCTTTGAGGAAGG[C/T]AGTGATTGCATTCCT | 26524 |
rs529297646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21049464 | ATGGGACATTTGCCC[A/G]GCCAGAGGCCTGCCT | 26524 |
rs529336735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21011066 | CTTTTGTTCACACAT[A/G]TATCAACATGGTAAT | 26524 |
rs529343119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042978 | CACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 26524 |
rs529406390 | in-del | -/ACAA | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:20980105 | ATGTTCTTAAAGATC[-/ACAA]ACAGAGGCACCAATT | 26524 |
rs529411212 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21012234 | TATCTATATAGGACA[A/C]TTAACATGAATGGAG | 26524 |
rs529469332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21037488 | ATGCTTGTCTCTGTG[C/T]TTCTCTGTTAGGTGT | 26524 |
rs529503929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20998048 | TGGGCCTCTGTCTGT[A/G]TCTGCCTGTCTCTCA | 26524 |
rs529525070 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21040325 | CAGGTCAAGGCTACA[A/G]TGAGCCGAGATTGCG | 26524 |
rs529553339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21031077 | AGAAGTCAGCTTTTA[A/G]TCTTATCTTTCTTCT | 26524 |
rs529608364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21031785 | GGATTGCTTGAGCCC[A/G]GGAAGGCTGCAGTGA | 26524 |
rs529611621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20985851 | GGAAGTTTGAGACCA[A/G]CCTGAACAACATGGT | 26524 |
rs529625145 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981975 | GACAGCACTCCTAGC[A/G]CTTAGGCCATAATCA | 26524 |
rs529633400 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20992546 | GGGAGGGTGAGCAGA[C/G]AGAAAAGAACACCGT | 26524 |
rs529636395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996184 | TTCAACACTTCCTTC[A/G]TCAGTGACCACTCCA | 26524 |
rs529636954 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024721 | GTACTGATGTTAAAA[A/G]ATGTATATTTCAACC | 26524 |
rs529640947 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21004537 | ATTACTGGGCACTGA[-/C]CAGCACACGTGTGTG | 26524 |
rs529733681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20997426 | ACTTTAACAAAACGG[C/T]GAGGTGGCTGAGGGG | 26524 |
rs529738889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042211 | TAATAAACATATCAT[C/T]TGACATACACATTAT | 26524 |
rs529746003 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026645 | AATGACTGAGACATA[C/G/T]GGTAGGTATGTTTGA | 26524 |
rs529755639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21036115 | TGGCCAGAGTGGTCT[C/T]GAACACCCGACCTCG | 26524 |
rs529759065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20989768 | GTATCCACTGTGCAG[C/T]AGCTGCTCCACTTCT | 26524 |
rs529854067 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20984303 | ATAAAAAAGAAAGTT[C/G]TTTCTCTAGGATACT | 26524 |
rs529935472 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | LATS2 | GRCh38.p7 | 13:21007744 | TATATAGTATATATA[-/G]TATATATATATATAT | 26524 |
rs529946320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017167 | AATGGCAGCCAGCAC[A/G]GTGAAATAAAACGGA | 26524 |
rs529999586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20982472 | TGCATCACCACGCCC[A/G]GCTAATTTTGTTATT | 26524 |
rs530008522 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062405 | TTTTCTTTCTGAGAA[G/T]TATTTTATGGTGTAG | 26524 |
rs530064931 | snp | A/C/G | 0.000170948 | 0.00924391 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988532 | CTTGCCAGGCGGACC[A/C/G]GGCCGCGGCTGGTGG | 26524 |
rs530097199 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21043892 | CAAGTGATTTACAGG[-/AGA]AGATTTTAAGCTCTG | 26524 |
rs530158779 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:20983019 | AAAAAAAAAGTAAAC[C/T]TGAAATCCACTACCT | 26524 |
rs530172073 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21021853 | GCACCTTTCACAGTG[C/T]CACAGAGACCAGTTC | 26524 |
rs530206319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053417 | CTGGTGTGCTTCCTC[C/T]TGAAGAATCTGATAG | 26524 |
rs530212615 | in-del | -/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047308 | TGCTTAGGACAGTGG[-/T]TGAGCACCGGGTCAG | 26524 |
rs530213928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008488 | TATGTTTCACCAAAC[C/T]AGGAGACTGGTTTGG | 26524 |
rs530303704 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974796 | GCCCTCGGCTTCCCT[A/G]TTGGCCTGTGAGGGC | 26524 |
rs530327797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053883 | GCAAATTCATAGAGA[C/T]AGAAAGAAGAGAGAT | 26524 |
rs530335085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21001937 | ATTTTTTTTTGAGGC[A/G]GAGTCTCGCTCTGTC | 26524 |
rs530381063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997578 | CACCATTTAATGATC[G/T]TCTCTGCTGTCCCTC | 26524 |
rs530386465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009147 | GAACCGCTCAGTCAC[A/G]TGTGGTGAGTGATGA | 26524 |
rs530414924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048137 | CATATTGCAGCCACA[C/G]TCATTTCAGTGACTT | 26524 |
rs530420148 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975101 | ACCTTCGCTGGCATC[A/G]TTCCAAGGGCTTTCT | 26524 |
rs530454151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21048739 | CTACTTGGGAGGCTG[A/G]GGCAGGAGAATCACT | 26524 |
rs530454937 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:20994798 | GAGGTTGAGGCAGGA[A/G]GATTGCTTGAGTCCA | 26524 |
rs530483526 | in-del | -/TTATTATTATTATTA | 0.448452 | 0.152042 | intron-variant | LATS2 | GRCh38.p7 | 13:21019299 | TCTCACTTGGATTTG[-/TTATTATTATTATTA]TTATTATTATTATTA | 26524 |
rs530501410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20985000 | CCAGAAATAAGTCCA[C/T]GTATTTACAGCCACC | 26524 |
rs530541435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21036758 | AGCCTGGGCGACAGA[A/G]CAAAACTCCGTCTCA | 26524 |
rs530623192 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:20979978 | GGGGTGGTGGGGGGC[A/G]GTGGCCATGGCCGCT | 26524 |
rs530668430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030938 | AGATTTTTGTTCCCC[C/T]GGAAATGTCTTTACG | 26524 |
rs530678287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024031 | ACAAGCAGGCATCCT[C/T]GGGAAGGGCCCCCCA | 26524 |
rs530685148 | in-del | -/AG | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:20982334 | TATTTTATTTGAGAC[-/AG]AGTTTCGCTCTTGTT | 26524 |
rs530690467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21010549 | AACAAAAAATCAAAT[A/T]GTGCAAATAACATGA | 26524 |
rs530695283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20979333 | GTGAACTATAGTTCC[C/T]GGAGTTCCGTGTGTT | 26524 |
rs530696354 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062559 | TAGAAATAATAGACT[A/G]GAAGCCAAATCCTCA | 26524 |
rs530705023 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004484 | AGAATCAAATTTTAA[C/T]AGTATACATCCTGTT | 26524 |
rs530723707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21011139 | AAATGCATGCCAATT[A/C]ACCATCAAATCATCT | 26524 |
rs530759264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21055400 | TTTTAAGTAACAAAC[C/T]ACAAACACTGGAATT | 26524 |
rs530759425 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063185 | TGCAGCCCACATCAG[C/T]CTTGAACTCCTGAGC | 26524 |
rs530776254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20977073 | ATAAACTAGACACAA[A/G]AAGACAGATACTGCA | 26524 |
rs530794099 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006138 | GCAAAACTGCATCTC[-/A]AAAAAAAAGAAAGAA | 26524 |
rs530826184 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049648 | GCTATGAAAGGACAA[C/G]AGCCACAAGAGACAC | 26524 |
rs530833220 | snp | A/G | | | intron-variant, missense | LATS2 | GRCh38.p7 | 13:21023100 | TGTCGCTCGAGCCGG[A/G]GACTCCTTTCCAAAG | 26524 |
rs530845018 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060806 | CCCGTGGGACGATGG[A/C]GCGGCCGGGAGGATG | 26524 |
rs530901808 | snp | A/G | 1.74154e-05 | 0.00295083 | intron-variant | LATS2 | GRCh38.p7 | 13:20983814 | AGTCCAGCCTGTGTA[A/G]AAGGAAAAGGAAGGA | 26524 |
rs530907015 | in-del | -/TAAC | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:21002355 | CATCTTTTAAAAAAT[-/TAAC]TAACTAATTAATTAA | 26524 |
rs531001985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001982 | GCAGTGGCACTATCT[C/T]GGCTCACTGCAAGCT | 26524 |
rs531123819 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979007 | CCTCAGGTAATCTGC[C/T]CACCTTGGCCTTCCA | 26524 |
rs531125144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009732 | CCTCCACATAACAGA[C/T]GACAATACACCAAGT | 26524 |
rs531125890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21003258 | TTAAATTTATTATTA[C/T]TATTTTTGAGAGGGG | 26524 |
rs531162123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002313 | TCTACTTTGCTGTCT[A/G]CTATGTATAATCTGG | 26524 |
rs531188279 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023534 | GACTCTCCACGCTGC[C/T]GGAGAGCCCAGACAG | 26524 |
rs531231864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042339 | ATGGGTGGGTTTAAT[A/C]TGCAAAAATTCACTA | 26524 |
rs531252408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996994 | CAGCCTCGTCTCTTC[C/T]GGAGAGCGGTGACAT | 26524 |
rs531275274 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999265 | TCCGACCGCTGGTGG[C/T]GCCGCAGGCCCCCGA | 26524 |
rs531311531 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20977313 | GGCATGAGAACCCGG[A/G]AGGCAGAGGTTGCAA | 26524 |
rs531344834 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21053184 | AGGATGCAGTGAGCC[A/G]AGAACATGCCACTGC | 26524 |
rs531422811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21035002 | TTGGTAGGCCAGGGC[A/G]GGAGGATCACTTGAG | 26524 |
rs531440857 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000979 | TCGATTTGTTAAAGA[C/G]AGCATGACAATAACA | 26524 |
rs531453079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001286 | ACACACACATGGCAT[G/T]GTTTCAGGGGTCCTG | 26524 |
rs531460724 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21035500 | GAGCCCCTCTCCCAG[A/G]GCCCCATCCATCAAG | 26524 |
rs531615493 | snp | G/T | 0.000131259 | 0.00810015 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989057 | GAAGTGTGCCCCTGC[G/T]GCCTCTACGCTGGCA | 26524 |
rs531637140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20987250 | CAAATGAAAAGTATA[G/T]CTGTAAAAAAATCAG | 26524 |
rs531637232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20993999 | GTGAATCACCAGCCT[A/G]TGCTCATTAACCCAG | 26524 |
rs531669701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033273 | GAGGATGGGAGAGAA[C/T]AGGGGGTAGAGGGGC | 26524 |
rs531672891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20987688 | CTTCAGAAGAGTCAA[A/G]GGGAAAGGCGAAAGG | 26524 |
rs531749775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032801 | CCGTAGAAGGCCACA[A/G]GGATGGGTCGTGGAA | 26524 |
rs531759229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21039154 | ACTAAGAAAAAAAAA[A/G]GGGAAAAGGCAAGGA | 26524 |
rs531761898 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21026805 | AATTTTTAATTTAAA[A/C]AACATTAGTAAATAA | 26524 |
rs531854592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013442 | TCCAGAGTCTGTGGA[A/G]AAAGTCCAATTTTCT | 26524 |
rs531869155 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017611 | CTTCCCTTCAAAAGA[C/T]GACTCATTTCTTTCT | 26524 |
rs531933508 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LATS2 | GRCh38.p7 | 13:21055901 | ACCACTATGTGGATG[C/T]ACCACACCAGCACTG | 26524 |
rs531959153 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21001175 | CAGGATTTTGAGGAA[A/T]GTTTGCTAAAATAAG | 26524 |
rs531962577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21040647 | CAGAGAGCTCCTCTG[C/T]AGAGGGGAGCATGTG | 26524 |
rs531978582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982380 | GCAATGGCGCGATCT[C/T]AGCTCACCGCAACCT | 26524 |
rs531979780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001316 | GGATCCTATATTTCT[A/G]TTCATGTGTAACAGT | 26524 |
rs531979820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009094 | TGCCAGCGATTTGGG[C/T]CAGAACTGAGTGCAT | 26524 |
rs531999310 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991953 | ATCTGACTCGTAGAA[A/G]AAAGAAAGGAGACAA | 26524 |
rs532012414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040746 | CCAGCTGCCAGGGAC[A/G]TGGGGGGCAGCCATG | 26524 |
rs532079424 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981423 | AGCTCACGTCTGAAG[A/G]GAAGGAGACCTCCTG | 26524 |
rs532149210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048021 | CTGTAAGACTGTGCA[C/G]ACATTGAGCTATTAG | 26524 |
rs532182709 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | LATS2 | GRCh38.p7 | 13:21007712 | TAGTATGTATATATA[-/G]TATATATATAGTATA | 26524 |
rs532188911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029319 | TGCTTACTCTATCTA[C/T]TGAGATGATGAAATG | 26524 |
rs532223360 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | LATS2 | GRCh38.p7 | 13:21054373 | AGGTCATTCCACTGC[A/C]CTCCAGCCTAGGCAA | 26524 |
rs532224333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21036044 | GCTGGGACTACAAGC[A/G]TGTGACACCACACCT | 26524 |
rs532224966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029766 | ACTGCACTGTGGCCT[A/G]GGCAACAGAGCGACA | 26524 |
rs532227217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041262 | CAGGTGTGAGCCACC[A/G]CGCCTGGCCCACTCC | 26524 |
rs532247708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20996120 | GATCTCAATGCTGGA[A/G]TTGAAGCCATCATAT | 26524 |
rs532258861 | snp | A/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023826 | TAAAAATACAAAATT[A/T]GCTGGGCATGGTGGC | 26524 |
rs532285334 | snp | C/G | 3.38301e-05 | 0.00411265 | missense | LATS2 | GRCh38.p7 | 13:20989182 | CCAGCGCCGTGGGGC[C/G]GTCAGCGCCGAAGCT | 26524 |
rs532303699 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:21003435 | TTTTGTCTGTCTTTC[-/T]TTTTTTTCCTTTTTT | 26524 |
rs532309911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023186 | AAGGCCGGGGAGTGG[A/G]ACCAGCTCCCACACA | 26524 |
rs532311875 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999536 | TACAGTGGCTCGATC[A/T]GGGCTCATTGCAGCC | 26524 |
rs532331013 | in-del | -/ACA | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21058980 | GCTTACCAAAAATAT[-/ACA]ACAAGATTTAGCACA | 26524 |
rs532353813 | snp | A/G | 0.000224871 | 0.0106012 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989024 | GTGCGGCCGCCCGTA[A/G]TGCGCGCCCTGCAGC | 26524 |
rs532386067 | in-del | -/AAAAAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048846 | CCGTCTCAAAAAATA[-/AAAAAT]AAAAATAAAAATAAA | 26524 |
rs532387548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20983917 | CTAGCTCATTTTACA[A/G]AAAGGAGAACAGAGA | 26524 |
rs532409148 | snp | C/T | 1.6582e-05 | 0.00287936 | missense | LATS2 | GRCh38.p7 | 13:20988168 | TCTGCTCCATGCCTG[C/T]GCACAGGCTGTCCAG | 26524 |
rs532469301 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21056214 | AGATCTGAGGGGGAG[G/T]TTCGCCATGAGATGG | 26524 |
rs532480589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21027744 | TGCTATTCTAGGTAC[C/T]TTGCAGTGCCATATG | 26524 |
rs532531463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982883 | GTAATCCCGGCTACT[C/T]GGGAGGCTGGAGGCA | 26524 |
rs532564861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20976037 | GTTTTGAAAAACAAA[C/T]AGGAAAAACTTCATA | 26524 |
rs532602850 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21027797 | TTCAATTAAAAAAAA[A/T]AAATAAACCTGCTGA | 26524 |
rs532631206 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032093 | AGGGTTTCACTTTCC[A/G]TTTTCTTACCATGTG | 26524 |
rs532695491 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974076 | GAGATACAATCATAG[C/T]GAAGAGGTCACCCGC | 26524 |
rs532716131 | in-del | -/CT | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21041005 | TGAGGCAGAGTCTCG[-/CT]CTGTCGCCCAGGCTG | 26524 |
rs532725276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058979 | AGCTTACCAAAAATA[C/T]ACAACAAGATTTAGC | 26524 |
rs532729045 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993597 | CATGAAGTGACAGAT[C/T]GGAAAATGGTAATAA | 26524 |
rs532770110 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21010649 | ATCCCTCAAGATGAA[C/T]CCTGAGCAGCCAACT | 26524 |
rs532777535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21019249 | CAGCTGAAAGGTTTT[A/T]AAAAATGAACTGTAC | 26524 |
rs532785845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21039478 | GCTTTTTTGGTGATG[C/T]ATATTGTTAGAATTA | 26524 |
rs532791356 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974640 | AAATTTTCAAAAATA[C/T]TGTTTTAATGCAGTG | 26524 |
rs532803491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014745 | GGGTCAAGGAAAGAA[G/T]AAATATGATACCTTT | 26524 |
rs532817178 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995493 | CAGTTCAGGTATGTG[C/T]TCTGGTGTCTAGCGT | 26524 |
rs532833212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053263 | AAAAAAAAAGCCCAA[C/T]TCAACCCCACCTGCC | 26524 |
rs532839920 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041074 | GCCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 26524 |
rs532860872 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21058112 | AGTCAGTCACTTCAA[A/T]CAAGCCTTACCCTTC | 26524 |
rs532924598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981084 | GGCACAACTCAGCCA[A/G]GAGCCTGAGACAGAA | 26524 |
rs532955043 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039106 | AAGGTATGTGGTGTG[C/T]CTTCTGGAAGAGCCA | 26524 |
rs533006253 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20999930 | AGCTACTAGGGAGGC[C/T]GAGGCAGAAGAATGA | 26524 |
rs533070440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21039277 | TAATATTTCAGCACG[C/T]GTGTTCAGTAACACC | 26524 |
rs533072981 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21006045 | GGGAGGCTGAGGCAG[A/G]AGAATCGCTGGAACC | 26524 |
rs533089128 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20994071 | TAGGTCAATGTGGAT[A/G]TTCTCAAATTCCCTC | 26524 |
rs533102000 | in-del | -/TAAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987224 | AATAAAAAATAAAAA[-/TAAAA]AAAACACAAATGAAA | 26524 |
rs533153103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21011824 | TAGAGTGTACTTACA[A/C]AAACCTAGATGCTAC | 26524 |
rs533153455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004327 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAAG | 26524 |
rs533160459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21006508 | AATAGCCAAAAAATA[A/G]GCCAGATCATCAGAG | 26524 |
rs533178681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050381 | CTCCAGGCCCCCACA[C/G]ACCAAGGGGAACCAC | 26524 |
rs533225750 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20997962 | AACCATATCCTAAAG[-/T]TTTAACATTCCAACT | 26524 |
rs533236710 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974033 | CACTTCTCAGTTACA[C/T]ATCTGCATTTCTTTA | 26524 |
rs533242888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037644 | TGGGGGAGAAAATTA[C/T]GGTGTCACGGGAGAG | 26524 |
rs533247709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046512 | GTATTAACAACTGAC[A/G]GCTCATTTAAAATAC | 26524 |
rs533272037 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991208 | TTGGACCCCTCTGCA[C/T]GTGGTTTTGTTGTCC | 26524 |
rs533283553 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061490 | CGGCGGTGGCGTGGA[C/T]GGCGACTGCTCCATC | 26524 |
rs533285739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040060 | CCTGGGCAATAAGAG[C/T]GAAACTCCATCTCAA | 26524 |
rs533322097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21056577 | AACAGGATGGGCCAT[C/T]TTATATTCAATTTCA | 26524 |
rs533365406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038464 | TGCCTCAGCCGACCA[A/G]ACTGTTGAGATTACA | 26524 |
rs533390772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20998170 | GTTCAAGACCAGCCT[A/G]GGCAAGACCCGCATG | 26524 |
rs533401112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032636 | ATGTGTGGTCCAAGA[A/C]AATTCTTCTTCTAAT | 26524 |
rs533424848 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023918 | GCAGAGGTAGCAGGG[-/A]GACGAGATCGCACCA | 26524 |
rs533433834 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004172 | GGGTGCAGTGGCTCA[C/T]GCCTCACCAACCCAG | 26524 |
rs533482476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992107 | AGCCTCCTTCCACCC[A/G]AAAGATGAGGTGGTG | 26524 |
rs533484206 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036016 | TGATTCTCGTGCCTC[A/C]GCCTCCTGAGTAGCT | 26524 |
rs533553782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21045514 | GAGAAGGTAGAGAAC[C/T]TTCAATTGTGAGTTC | 26524 |
rs533606003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986422 | GTCTGTGTACACCAT[A/G]GGATACTATTCAGCC | 26524 |
rs533613846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20993158 | GTCACAGAGCCACTC[C/T]GCAGAGAGAGATGCA | 26524 |
rs533628038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025632 | AAACTCTGTCTCATC[A/G]TCATTAGGTCTGCAC | 26524 |
rs533643699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20980629 | GGTTTCTTGAGAATG[C/T]TGCACGTGGTAGAGG | 26524 |
rs533685886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032964 | ACAGGAAGGCTGGGC[C/T]GGTACAAGAAATAAG | 26524 |
rs533699792 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018378 | TCCATCTGGCAAGAT[G/T]AGGAGACAAGGGTTG | 26524 |
rs533751950 | snp | C/T | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:20999059 | CCACAACCTTGTCCA[C/T]GCGAGGCAGGGGCCC | 26524 |
rs533762400 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21006077 | GGAAGGCAGAGGTTG[C/T]GGTGGGCCAATATCA | 26524 |
rs533829273 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993916 | GACTCTAACCACAAG[C/T]CTTTCCATCAGCACT | 26524 |
rs533875262 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015647 | GATTTTTTACAACCA[A/G]CAGTTTGCAAAAAGC | 26524 |
rs533890953 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21048163 | GACTTTGTGCTCTAA[A/G]CATCTGTTTTGAAAT | 26524 |
rs533923229 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21039530 | AGATCTGCATTTCTG[C/G]TTAGCATCTTTTCCA | 26524 |
rs533930640 | in-del | -/GTAGGCCAGGCACGGTGGCTCACACCT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982707 | TGTCTTAAAAATATA[-/GTAGGCCAGGCACGGTGGCTCACACCT]GTAATCCCAGCACTT | 26524 |
rs533972839 | snp | A/G | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:20994223 | TCCTAAAAGTGAACC[A/G]TACTCATGAGCCGGC | 26524 |
rs534019608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024975 | GCCCTGCAGACCAGG[C/T]TTCCCCCATAACTTT | 26524 |
rs534056591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025684 | GATCTTGCCTGACAC[A/T]GCTCACAACATTATT | 26524 |
rs534087578 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21013941 | GCACCACTGTACTCC[A/G]GCCTGGGCAACAGAG | 26524 |
rs534114301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981986 | TAGCGCTTAGGCCAT[A/C]ATCAAAAGGTAACAA | 26524 |
rs534126535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020702 | ACACTGTCCAGGGGC[C/T]AAAAGGTTGAAAATG | 26524 |
rs534141440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21018720 | GTGCAGTGGCTCGAT[C/G]ACGGCTGACTGCAGC | 26524 |
rs534156763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057038 | GAGTAAGAATGGAGT[G/T]AACTAGTAATGAACC | 26524 |
rs534185077 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987135 | AGGAGGCAGAGGTTG[C/T]AGCGAGCCAAGATCG | 26524 |
rs534209816 | snp | A/C | 0.00597247 | 0.0543191 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063496 | TGCAGTTACAATGAT[A/C]ATTTCAGCATTGTTT | 26524 |
rs534277971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20978602 | AACAACACAGTTTGA[A/G]GGTCACTTACACTAG | 26524 |
rs534300651 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047046 | CTACAGAACTACAAC[C/T]GCAGCATGGAAATGG | 26524 |
rs534312946 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:20980251 | AGGAGGTGGGCAAAA[C/G]CCACCGGACAATTCA | 26524 |
rs534347895 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062754 | CATTATCTGTGCACT[A/G]TTTTGACAGTCTCAC | 26524 |
rs534351654 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20980663 | GTAGACCTTCACTGG[G/T]CACCAAGGTTATTCA | 26524 |
rs534362683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20979455 | CAGATGGCCAAGGGT[C/T]TAATAGAATTTCAGA | 26524 |
rs534377018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017400 | GGCTGGTCTCAAACT[A/C]CTGGCCTCAAGCGAT | 26524 |
rs534408220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21055561 | TTTAATTTGGTCCTA[C/T]CAAACCCAATTCCAA | 26524 |
rs534437729 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974055 | ATTTCTTTAACAAAA[C/G]AGTAAGAGATACAAT | 26524 |
rs534455060 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034793 | GAAGAATTTCCTGCC[A/G]TTTCCCACAGTACAG | 26524 |
rs534460458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21010616 | CTGTCAAAGACACTG[C/T]GAACTCTGGAAGAGC | 26524 |
rs534477961 | in-del | -/ACAGCCAAGGTG | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21034251 | TATGCCCTGGTTGAC[-/ACAGCCAAGGTG]ACAGCCAAGGTGACA | 26524 |
rs534488245 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21003737 | GAGAGCCACCATACC[A/G]GGCCTAATTTTTGTC | 26524 |
rs534497052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057587 | TCACGAGGTCAGGAG[A/T]TCGAGACCATCCTGG | 26524 |
rs534613073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20998208 | AAAGTGAGAAAATTA[G/T]CTGGGCATGGTGGTG | 26524 |
rs534618970 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024111 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAGAAAA | 26524 |
rs534631583 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21016824 | ACTAATAAAACTCCA[A/C]ACAACACCTGAACTA | 26524 |
rs534646060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037753 | AAGTGGGCCTGGTCC[C/T]GCAGCAGGGCCAGCA | 26524 |
rs534650981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053961 | TTTGTTTGGGATGAT[G/T]AAAAAGTCTTATGTA | 26524 |
rs534668312 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21009979 | GCGAGGTGGACAGAC[C/T]GCCTGAGGTCAGGTG | 26524 |
rs534735884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048352 | TGTTTCCAATCTTAA[C/G]TTTTCTTCCCTTTCT | 26524 |
rs534822868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049993 | AGGTGTGACAGCACA[A/C]CCCTGTAGTCCAGCT | 26524 |
rs534869290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042443 | GCTTGAACTTATAAT[C/T]CCAGCACTTTTGGAG | 26524 |
rs534903212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997135 | TAAAACTAAGAGATT[A/G]GGGAGGGACTGAGAA | 26524 |
rs534914896 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048221 | CATTCCGACAAAAAC[A/G]GAGAGGTTCTCAAGG | 26524 |
rs534915836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037176 | CCGGGAGGCCAAGGC[A/G]TGTGGATCACCTGAG | 26524 |
rs534926444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991528 | ACTGCTGAGAACCTG[C/T]GATATGCTGCAGGAG | 26524 |
rs534950769 | snp | A/G | 3.29451e-05 | 0.00405851 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983630 | CTTCATGGCGTACAG[A/G]GCGTGAGTGTCCACC | 26524 |
rs535000342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001516 | CCTCAAGAAGGCTGG[A/C]TACTTCCATTTTCAG | 26524 |
rs535005158 | snp | C/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024226 | ATCACTTGAGGTCAG[C/G]AGTTCAAGACCAGCC | 26524 |
rs535010178 | snp | A/G | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:20984482 | AAAAATCAGTAGCAT[A/G]CATTAGATAGACTTG | 26524 |
rs535041898 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002208 | GTGAGCCACTGCGCC[A/C/T]GGCCAAAAAGCCATT | 26524 |
rs535082318 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20980942 | GAAGCATCCATCCAG[C/G]AGGCAAATGTTATGA | 26524 |
rs535095940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21041744 | CTAGAGGGGACACCA[C/T]GTGATAAAGTGCTTT | 26524 |
rs535135790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21056218 | CTGAGGGGGAGTTTC[A/G]CCATGAGATGGGGTT | 26524 |
rs535172813 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982591 | GCTAGGATTACAGGC[A/G]TGAGCCACCATGCCC | 26524 |
rs535184956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21035828 | GTGATTCCTAGAGCC[C/T]ACCTAGGACCTGCGC | 26524 |
rs535220198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20989388 | TGGTCCCCACTCTAG[C/T]GCTGCCCTCGGGGCT | 26524 |
rs535238179 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013271 | ACCAGTTACAGCCTT[C/G]CATGTTCTGCCCAAT | 26524 |
rs535262305 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:20998309 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 26524 |
rs535325454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030014 | CTGTAATCCCAGCTA[C/T]TCAGGAGGCTGACTC | 26524 |
rs535362853 | in-del | -/AT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026941 | ATATAGTAGTATCTC[-/AT]TGTGGTTTTAATTTG | 26524 |
rs535379664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992778 | GTGGTGGCTCACGCC[C/T]GTAATCCCAGCACTT | 26524 |
rs535414815 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21010711 | ATTTGCTGACTAGTC[A/G]TCACACATGTACTTT | 26524 |
rs535416264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032108 | GTTTTCTTACCATGT[A/G]CAGTAATGATGGATA | 26524 |
rs535424680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017967 | TGAGACTATCCCTTC[A/T]ATTAGGTGCCATGGT | 26524 |
rs535465548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21042505 | CCAGCCTGGGTAACA[C/T]AGTGAGATGCCATCT | 26524 |
rs535475110 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21002766 | GGTGCAATCAAAGCT[A/C]ACTCCAGCCTCTAAC | 26524 |
rs535499344 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036893 | AGGGTTGGAAGTATA[A/C]ATTCAATTGAATGAT | 26524 |
rs535505040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21003839 | TCAGCCTCCCAAAGT[C/G]CTGGGAGTACAGGCA | 26524 |
rs535515052 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21011427 | CTCCTGTTTTTAAAC[G/T]GGTCACTGTACCCAC | 26524 |
rs535538499 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20984720 | GTTCACCGACAGAAA[C/G]ATTTAATATTGTTAA | 26524 |
rs535614731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043824 | GTTTCTTTTTCTCAC[A/C]GCTGAAACACAACCG | 26524 |
rs535655724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044644 | GATTGTATTCAGGTA[C/T]ACGAATTGCTAAGAG | 26524 |
rs535655792 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | LATS2 | GRCh38.p7 | 13:21037829 | CAGGACCAGGGCGGG[C/T]AGGGCCAGGGTGGGC | 26524 |
rs535670603 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050948 | GCCACGTGAGGGGGG[-/T]GCAGGAAAAGGCTGA | 26524 |
rs535671297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20998836 | CGCAGCGACATTGTG[C/T]ACGCCGGGTGGGGGC | 26524 |
rs535682022 | snp | A/C | | | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988466 | CGGGTGCAAGATGTG[A/C]GCGGCCGTGACAGCC | 26524 |
rs535694662 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21030645 | GAACTCTACAATAAT[A/G]TATTTCCATTTAACT | 26524 |
rs535704548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20985254 | AGGCAAAAAAACCCC[A/G]AAGTAGACAAATGGG | 26524 |
rs535728474 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002660 | TGGGATTACAGGTGT[A/G]AGCCATGGTGCCTGG | 26524 |
rs535735056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21031616 | CAGCACTTTGGGAAG[C/T]TGGGGAGGGGGAGCA | 26524 |
rs535740363 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054686 | TGGACATTTCTATGT[C/T]GATGTCTGTTTATAC | 26524 |
rs535743022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038174 | GGAGAAAGACGCAGA[A/G]GGGGCAACCAGGAGC | 26524 |
rs535752054 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062847 | GCTCTTCCAGGGAAT[C/G]TTCTCAGATCTCTGT | 26524 |
rs535759135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986077 | AGCTAATGACCTGAA[C/T]AGACACTTGTCAAAA | 26524 |
rs535793722 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21013185 | CATGTGCTTGCCTGC[-/T]TAGGTGAGTTAGGCC | 26524 |
rs535925831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029398 | TGTTTAACCTTGTAT[A/T]TCTGGGATATATCCC | 26524 |
rs535970010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21060243 | ATCCCCGAGGGAAAG[C/T]TCCCCAGAAGTTCTG | 26524 |
rs535970434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20990239 | TGGGCCTGGCCTTCC[C/T]TTTGAGCTGTGCTCT | 26524 |
rs535975834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21030048 | AGAATTGCTTGAACC[C/T]GGGAGGGGGAGGTTG | 26524 |
rs535986104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20983969 | AGAGTCTCGCTCTGT[C/T]GCCTAGGCTGGAGTG | 26524 |
rs535989208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015123 | ATGCACAGTGTTCCA[A/G]GGAAACTGTATAACT | 26524 |
rs536020893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015951 | TGATTTGCCCACCTC[A/G]GCCTCCCAAAGTGTT | 26524 |
rs536062985 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20975828 | AGCTGGGATTACAGG[C/T]GCCTGCCACCACACC | 26524 |
rs536080395 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023761 | CGTGGATCACCTGAG[G/T]TCGGGAATTCAAGAC | 26524 |
rs536113070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024330 | AATCCCAACTACTGA[C/G]GAGACTGAGGCAGGA | 26524 |
rs536125640 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21048512 | AGCCCATCCACCCTC[C/T]ACCTACCATACAAAC | 26524 |
rs536163610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21009881 | CAAATCAGACTACAA[C/T]ACAGTGAGAGCAGAC | 26524 |
rs536186250 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005532 | TTTTTCTGACAGGAA[A/G]AGTAATAAGATATGG | 26524 |
rs536208009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20975715 | TTGAGATGGAGTCTC[A/G]CTGTGTTGCCCAGGT | 26524 |
rs536219127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058458 | GTTTAGGAGCCCAAG[A/G]CTGGCTATTTACAAC | 26524 |
rs536233801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013699 | GGCCAGGTGCAGCGG[C/T]TCGAGCCTGCAATCC | 26524 |
rs536234138 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21049169 | GGAGGTCAAAGGACT[-/C]CGGGGGTAGTGGGGG | 26524 |
rs536277703 | snp | C/T | 4.94205e-05 | 0.0049707 | missense | LATS2 | GRCh38.p7 | 13:20983400 | TCTGCGATGTAGAAC[C/T]GGGCCAGGTGCTCAG | 26524 |
rs536296306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051867 | GAGGCTGAGGTGGGA[A/G]AATCACTTAAACCCA | 26524 |
rs536317178 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21006904 | GAAAGGGACATTTGG[A/C]TGCAGACTGAACAGA | 26524 |
rs536342899 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022264 | CGTATGCATATGTGC[A/G]TGTGCATGTATTTGT | 26524 |
rs536381194 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997754 | ACTCCTTCAATCTAC[C/T]GCTCAGCTCTTAGCA | 26524 |
rs536429840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000956 | TTTATGTTGAAAGAA[C/G]AGTAATTTCGATTTG | 26524 |
rs536467749 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20999710 | CCATCCTCCTGCCTC[A/C]GCCTCCTAAAATGCT | 26524 |
rs536476041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21054045 | TGTATACTTAAGAAT[A/G]GTTAAAAGGATAAAT | 26524 |
rs536518557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995280 | TAATGTTTTACTGTG[C/T]ATTCTTCTTACAATA | 26524 |
rs536552531 | snp | C/T | 5.82191e-05 | 0.00539501 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988313 | CAGCGCCAGGGCATG[C/T]TCCTCCTTGGCGTCC | 26524 |
rs536554674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995777 | ATTATCTAGTTTGCA[A/C]ACGTGCCATTCTTCA | 26524 |
rs536599805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20983994 | GGAGTGCAGTGGCAC[A/G]ATCTCAGCTCACTGC | 26524 |
rs536608399 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984394 | AGCATTCCTAGAACT[C/T]CAAGAGCCATCTAAT | 26524 |
rs536700042 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21016039 | CTGTCACTCAGGCTG[G/T]AGTGCAGTGGTATGA | 26524 |
rs536732144 | in-del | -/A | 0.335559 | 0.234904 | intron-variant | LATS2 | GRCh38.p7 | 13:21006207 | TTATCATGTGTGAGG[-/A]AAAAAAAAAAAAAAT | 26524 |
rs536775730 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029536 | GGTGGCTCATGCCTG[C/T]AATCCCAGGACTTTG | 26524 |
rs536795947 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21007561 | TATATATATATATAT[A/G]TATATATATATATAT | 26524 |
rs536814604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047072 | AATGGCCTCGTTACA[C/T]GGAACGCGATGTCAC | 26524 |
rs536849713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040389 | CTCAAAAAAAAAAAA[A/G]AAGAAAGAAAAAGAA | 26524 |
rs536944577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21040919 | ATTATTAGGCCCAGA[A/G]AGACATTAAACTGAG | 26524 |
rs536988923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035118 | AAAAAAGCAAGAAAA[G/T]AAATCTAAAACGAGT | 26524 |
rs537000133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21052950 | GCTAGAAAAACCGAA[C/T]GCTGGGCCGGGCACG | 26524 |
rs537017932 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21059941 | CTCCCCTCCAGCCTG[C/G]GAGACAGAGCGAGAT | 26524 |
rs537064203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022738 | CACAAGGCCAATTTA[A/G]ATATGAGAGTGGGGA | 26524 |
rs537091174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047135 | CCCAGGCCTCGTTCA[C/T]GGCCTACTCTGCTGT | 26524 |
rs537091979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061007 | CCTGCCCCGCCGGGA[C/T]CCCGGCCGCCCCGGT | 26524 |
rs537101336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20999983 | TGCAGTGAGTCAAGA[C/T]CACGCAGCAGAGCAA | 26524 |
rs537138181 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051459 | AGTGGGTGCACTCAA[C/T]AGCACTAAGAGGTAG | 26524 |
rs537152971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21054150 | TGAACAATGGCTCCC[G/T]TTTTAAACATAGCTA | 26524 |
rs537153073 | in-del | -/A/AAAAAAAAAAAAAAGA | 0.235564 | 0.249583 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062924 | CCAGCAGAAGTGTGC[-/A/AAAAAAAAAAAAAAGA]AAAAAAAAAAAAAAG | 26524 |
rs537273600 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:20996322 | TGAGATTTCATTCAC[A/G]TCTCACATCCAGTCC | 26524 |
rs537314084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002833 | AGCTAGGATTACAGG[G/T]GCAGGCAATCACACC | 26524 |
rs537330910 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21042678 | TACAACAGAGCAAAA[A/C]CCTCTTAAACAGACA | 26524 |
rs537429266 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | LATS2 | GRCh38.p7 | 13:21007575 | TATATATATATATAT[A/G]TATATATATATAGTA | 26524 |
rs537533223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21047776 | TTCAAAGAATTAATT[C/T]ACATAGATCTATTGC | 26524 |
rs537553766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001386 | TGTATGTACGGGCTG[C/G]AGCCCCCAGTGTGAA | 26524 |
rs537578956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21027211 | TAAAGACTTTTCATT[C/T]TGTAAACATCCAATC | 26524 |
rs537606819 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044134 | TTATCAAAGCAGCTC[A/G]ACATAACAATCCTCA | 26524 |
rs537645699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041447 | TGTTTACATTTCTTC[C/G]CTAACCTCATTCCAT | 26524 |
rs537666676 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016339 | ACCCAGGCTCAGTAC[A/G]GTGGCGTGATCTCGG | 26524 |
rs537668794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020820 | CTCCCAAAGGCACCT[C/G]CATCCCTGCTGTCAT | 26524 |
rs537683150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20975772 | CACTGCAACCTCCGC[C/T]TCCTGGGTTCAAGCG | 26524 |
rs537731797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035753 | AGCAGGTTGCTCGCA[G/T]TGGAGGGACCCAGCT | 26524 |
rs537776394 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21029475 | ATTTTGGTAAGGATG[C/T]TTGGATTTATATTGC | 26524 |
rs537829150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20993826 | GCTTGGAGGAAGACA[C/T]GATATAAGACCACAT | 26524 |
rs537894056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980845 | TGTCTCTGGATTAAT[A/T]ACACCCCATTGTCAC | 26524 |
rs537898083 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:21006378 | CTGTGTACATCCCTT[A/T]AAAAAGTGAGCAGAC | 26524 |
rs537911668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21018764 | GTTCAAGTGATTCTC[C/T]TGCTTCAGCCTCCTG | 26524 |
rs537977783 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039895 | CCTGACCAACATAGT[A/G]AAATCCCATCTCTAC | 26524 |
rs537996639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21012410 | TAAGTAAGAGTTGGA[C/T]TATGAAGTTACAGCT | 26524 |
rs537998645 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21019700 | AAAAGGCGGCTGGGC[A/G]TGGTGGCTCATGCCT | 26524 |
rs538085713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982641 | TAAGGCTTGCTTTAA[C/T]GAGGCAGGTGATGGT | 26524 |
rs538103820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21021384 | AGTCTCAGGCAGGAG[A/T]GCTGCTTGAACCTGG | 26524 |
rs538129396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21006087 | GGTTGCGGTGGGCCA[A/G]TATCATGCCATTGCA | 26524 |
rs538137547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21045628 | CCAAACCATTCTGAC[G/T]GCCCCAGCTGTCCCA | 26524 |
rs538315557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981351 | TTCAGGCTTCTATGA[A/G]GACAAAAATATGACT | 26524 |
rs538334862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035015 | GCGGGAGGATCACTT[C/G]AGGCCAGGAGTTTCA | 26524 |
rs538339082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028178 | AGTGAGAACATGCGG[C/T]GTTTGGTTTTTTGTC | 26524 |
rs538377731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21028858 | CAGGTGTGAGCCACC[A/G]TACCCGGCCAAATTT | 26524 |
rs538400780 | snp | G/T | 3.29451e-05 | 0.00405851 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974993 | AAAGGGGTAGCCATT[G/T]TCATCAAAGAACCTT | 26524 |
rs538410141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057655 | AAAAAAAAAAATTAG[C/T]TGGGCATGGTGGCGG | 26524 |
rs538490070 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21036176 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCT | 26524 |
rs538512684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051675 | TGAAAAAGCACAGGG[C/T]AGGCTGGGTCCAGTG | 26524 |
rs538539855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21006677 | CTGGAAAATTCTGCC[A/G]CTGTCTCCATCAAAA | 26524 |
rs538562976 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047043 | TTACTACAGAACTAC[-/A]ACTGCAGCATGGAAA | 26524 |
rs538568719 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060861 | GCCGCCGGACCGGGG[A/G]TCCCGAGGCTGTCAG | 26524 |
rs538593305 | in-del | -/ATTATTATTATT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019331 | ATTATTATTATTATT[-/ATTATTATTATT]TGAGACAGAGTTTCA | 26524 |
rs538595173 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:21015866 | CATCATGCCCAGCTA[A/G]TTTTTGTATTTTTGT | 26524 |
rs538603231 | snp | A/G | | | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975273 | CCCAGGCGGTGGTCT[A/G]CGGAGCAGCACAGCT | 26524 |
rs538663790 | snp | C/T | 0.00019996 | 0.009997 | missense | LATS2 | GRCh38.p7 | 13:20988270 | GGCCTCCGTACTCCA[C/T]GTCCAGCGGGAAGGC | 26524 |
rs538686571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981917 | CACCGTGCTGAGCTG[A/G]CAGGAAGGCACTGCA | 26524 |
rs538755890 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042534 | CTCTAGAAAAAATTT[G/T]GAAAACTGGCCAGAC | 26524 |
rs538778858 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017887 | TGCCTTGGCCTCCTA[A/C]AGTGCTGGGATTACA | 26524 |
rs538787349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21006208 | TTATCATGTGTGAGG[A/G]AAAAAAAAAAAAATC | 26524 |
rs538824643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21006749 | GCACACACCTGTCTC[C/T]GACTGTGGGGCTTTA | 26524 |
rs538910692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21007520 | GAAGGAGTAGTTAGT[C/T]GTAGGGGATGGATAT | 26524 |
rs538926429 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | LATS2 | GRCh38.p7 | 13:20984489 | AGTAGCATACATTAG[A/G]TAGACTTGTATATGG | 26524 |
rs538941141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21039968 | ATCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 26524 |
rs538958324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000875 | TAGTAACTATGTACA[C/T]AAATCAGTTATGCCT | 26524 |
rs539047878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026970 | TTGCATTTCTCTGAT[A/G]ATGAATGATGTTGCT | 26524 |
rs539086505 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LATS2 | GRCh38.p7 | 13:21050531 | CATACACGTAGTATA[C/T]ATATAGCAGAAGCCT | 26524 |
rs539101901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20975524 | TCAGCAGCCACAAAA[A/G]GTCAGTGTCATTTCA | 26524 |
rs539136793 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21044766 | ATAGGGTCTCGCTCA[A/G]CTAACCAGGATTGGA | 26524 |
rs539147726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21058351 | ATACAAAAAAGAACA[C/T]CTCTCCCCTAACCCC | 26524 |
rs539148030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21051269 | ACCCTGTTACTTGGT[C/T]CTGAGGATGCAGAAA | 26524 |
rs539159835 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044848 | ATCCCTCCTGCCTCA[A/G]CATCCCATGTAGTTG | 26524 |
rs539171366 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20998908 | CCCTGGCGACGTTGT[A/C]CACGCAGGGTAGGAG | 26524 |
rs539222369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21038225 | AGGTGGAGCCTGTAC[C/T]GGGGGCAGGAGAGGC | 26524 |
rs539255638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992912 | TGGTGGTGTGTGCCT[A/G]TAGTTCCAGCTACTC | 26524 |
rs539275203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21052776 | CCTCTCTGAAACGTG[C/T]CTGCAGCCAGGTGCC | 26524 |
rs539341224 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:21001379 | CCATCCCTGTATGTA[C/T]GGGCTGCAGCCCCCA | 26524 |
rs539362504 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20987376 | AGTTTCATCAATAAT[A/T]ACCTTCTTCAGCACT | 26524 |
rs539370623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980896 | TGAAGGATTCCTCCT[A/G]TACTGAACCAGATGT | 26524 |
rs539378164 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037464 | TGGAATGAAAATGTT[C/T]ATGACGTAATGCTTG | 26524 |
rs539416723 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21012144 | GCAACTGTAACAGAA[C/T]AGTGTTTATCTAAAC | 26524 |
rs539417169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043010 | CAAAAAACAAAAAAC[A/G]GTAGGAGTGAAAGGG | 26524 |
rs539425559 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986733 | GTAAAAATGTATTCA[A/G]TATTTCAAAATAGCT | 26524 |
rs539454289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037061 | CCAGCTCTTTACAAT[A/G]AATTATGGGACATCT | 26524 |
rs539502641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21005308 | AGAAAGAAAATCACT[C/T]GACCTTGACAGGGTG | 26524 |
rs539539184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030807 | TTATACTTATTGATA[A/T]CTACTGTTTCTAGTG | 26524 |
rs539563222 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21033983 | AGGGGACCAGTCGCA[-/C]CCAGGCTGGTAGGAC | 26524 |
rs539575390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21031311 | TTTCCTTTCTATTCT[C/T]GGATTTCAATTTCAC | 26524 |
rs539586293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21045422 | AGATCAGAAAATACA[C/T]ATTACAATTTCAGGA | 26524 |
rs539625151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038752 | GTGGCCGAGGCGGGC[A/G]GATCACCTGAGGTCA | 26524 |
rs539633220 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062979 | TTCAATTTAATTTTT[C/T]GATAGTATCCTGTAT | 26524 |
rs539645866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20993581 | CATGTGGGACATGGG[A/C]CATGAAGTGACAGAT | 26524 |
rs539659110 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005782 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACCC | 26524 |
rs539659512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024798 | ATACTGACATTTTAT[A/G]TTCTCTTTTTTGCAC | 26524 |
rs539660720 | in-del | -/TC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032578 | GCCTTTTTTTTTCGT[-/TC]TTTTTTAAGCCCATC | 26524 |
rs539684280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980173 | ACCTGTGAATAGTCA[C/G]GTGAGGGTCAAGGGA | 26524 |
rs539698505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21018150 | GTAAACTGACAGTTC[A/G]AGGAGGTCTCTAAAA | 26524 |
rs539712726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025862 | CATACGGCCCTGTAC[A/G]TCTGGGTTGATTTTT | 26524 |
rs539718804 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035261 | ATAATGGATGTGGCA[-/T]TTTTTTTTTTAATTT | 26524 |
rs539827588 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21053561 | CTGCGTCCTCAGTTC[C/T]ACACTGAGGACAAAG | 26524 |
rs539832568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20990513 | GAGGTCTCCCTCTGT[C/T]GCCCAGGCTGGTCTC | 26524 |
rs539859253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21031773 | GCTGAGATGGGAGGA[C/T]TGCTTGAGCCCGGGA | 26524 |
rs539866882 | snp | A/G | 3.31658e-05 | 0.00407208 | intron-variant | LATS2 | GRCh38.p7 | 13:20991429 | AAGTAAAGGAGAGGT[A/G]AGTGCATGTCATCCT | 26524 |
rs539989522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20985936 | GTAATCCCAGCTGCT[C/T]GGTAGGCTGAGGCAG | 26524 |
rs540036228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017590 | GGTGTCATCAGCAAC[C/T]AGTGCCTTCCCTTCA | 26524 |
rs540066175 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972547 | GTAGAGACAGGGTTT[C/T]GCCATGTTGGCTAGG | 26524 |
rs540072640 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974400 | GGATAAAATGGTCTC[C/T]GTGACATTGAGCAGA | 26524 |
rs540097666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057365 | AACACTTGTCACAAT[C/T]AACTTGACATGATCT | 26524 |
rs540113351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21012622 | TTATGATTCTTTTCT[A/C]CTAGAAAATGCTATT | 26524 |
rs540174308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21011613 | GAGACTTTGCCTTGG[A/C]CTAGGAATTTAAAAA | 26524 |
rs540252813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024427 | GGCGACAGAGTGAGA[C/G]TCTGAATGATAATAA | 26524 |
rs540274183 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055178 | TTCATGAGAATACTC[A/G]TCAGTCAAGACTGCA | 26524 |
rs540293358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992999 | CGAGATCACGCCACT[A/G]CACTCCAGCCTGGCG | 26524 |
rs540312316 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057609 | CCATCCTGGCTACTA[C/T]GGTGAAACCCCGTCT | 26524 |
rs540322249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032328 | TGGAGTGCAATGGCG[C/T]GATCTTGGCTCACTG | 26524 |
rs540323864 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21025410 | AAAAAAAAAAAAAAA[A/C]AAAATTATGGTCATG | 26524 |
rs540327214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017653 | TGTTTTTGAGATGGA[A/G]TCTCACTCTGTCACC | 26524 |
rs540363313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026001 | GACTCTCCACCCAAG[A/G]CCTAGCCTGACCATC | 26524 |
rs540374760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21055916 | TACCACACCAGCACT[A/G]TCAAGCCAGGAAGCC | 26524 |
rs540386530 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21049847 | GGAAGCTGGCCGGGC[A/C]CTGTGGCTCATGCCT | 26524 |
rs540393587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008880 | GAGGAGACATAAAAA[A/G]GAATACTCACTGTAC | 26524 |
rs540415754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21010979 | TACCTTCAGTTTACA[C/T]TGAAGGCTGCAGCTC | 26524 |
rs540524663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21057916 | AGGGCTGCCCTCACA[C/T]TGGGGCCATCACAGG | 26524 |
rs540529425 | snp | A/G | | | synonymous-codon | LATS2 | GRCh38.p7 | 13:20987980 | GAAGAACTTAAAGGC[A/G]TATGGCGAGTAGCTC | 26524 |
rs540559024 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015175 | GATTCCTATTGAAAT[A/G]AGCTATCCTGTACTT | 26524 |
rs540565259 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21013167 | CTTGTATATGAAGGT[A/T]CTCATGTGCTTGCCT | 26524 |
rs540667621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20979861 | CGAGGTGAATTTCAT[C/T]AAGATGCTGAACATA | 26524 |
rs540683980 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010405 | CTGGTCACCCTACAG[C/T]AAAGCCCCCACTCTA | 26524 |
rs540703583 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21034383 | ACATTTCCAAGGCTG[C/T]TTAAACCCCCATGAC | 26524 |
rs540713023 | in-del | -/A | 0.0232847 | 0.105357 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973691 | GTACACTAAAAGAAC[-/A]AAAAAAAAAGTGAGA | 26524 |
rs540723594 | snp | A/T | | | missense | LATS2 | GRCh38.p7 | 13:20981621 | CAGAGGTCGCTGGGC[A/T]CCATGCTGTCCTGTC | 26524 |
rs540754792 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972805 | TAATCCTAATGAGGC[A/G]TATTTTGTTCCCATT | 26524 |
rs540758627 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20983983 | TCGCCTAGGCTGGAG[C/T]GCAGTGGCACAATCT | 26524 |
rs540770958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996863 | GCTACCCTCTGGGCT[A/G]TTCTTGCAGATTCAT | 26524 |
rs540772796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002983 | GTTGGGATTATAGGC[A/G]TGAGTCACTGCACCT | 26524 |
rs540811608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997423 | GGCACTTTAACAAAA[C/T]GGCGAGGTGGCTGAG | 26524 |
rs540843742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042776 | GGCGGATCACAAGGT[C/G]AGGAGATTGAGTCCA | 26524 |
rs540913488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21049171 | GAGGTCAAAGGACTC[A/G]GGGGTAGTGGGGGTG | 26524 |
rs540992808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028161 | TTCAATTCCCATCTA[C/T]GAGTGAGAACATGCG | 26524 |
rs541112633 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992305 | GCTCTCCAGGGTTTT[A/G]CTCCTGTCTGCAGGC | 26524 |
rs541134558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20982884 | TAATCCCGGCTACTC[A/G]GGAGGCTGGAGGCAG | 26524 |
rs541138472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995917 | AAGACTTTGATGACT[G/T]TGTGTCAGTCACCTA | 26524 |
rs541144164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035361 | ATTTCCTTGTTGGTT[C/T]TTCCCCTATTTACAT | 26524 |
rs541177303 | snp | A/G/T | 0.000211126 | 0.0102722 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988931 | GCTGGCGTAACCCCC[A/G/T]GTCTCCGGCGGCGTC | 26524 |
rs541200167 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21021745 | AGAGAACAGCGAGGC[C/T]AAGAGCATGCCCTTG | 26524 |
rs541204962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20989740 | GCTGCTCCCTCACAG[A/G]AAGGGCAGAACTGTA | 26524 |
rs541225574 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20983637 | GCGTACAGGGCGTGA[A/G]TGTCCACCTTACAAG | 26524 |
rs541259179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20977734 | TAAATTTTAATTTAC[C/T]ATTAAAATAATTAGA | 26524 |
rs541302147 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050171 | ATACATACATACATA[C/G]ATAGATGGAAAGCTG | 26524 |
rs541315683 | snp | C/T | | | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989258 | CGAATCGCCGGTTCC[C/T]TCGAAGCTGGGCCTC | 26524 |
rs541364366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061230 | GCCCCGCCGGGCGCC[C/T]TTCCCGGAGCCTCGG | 26524 |
rs541391234 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21016136 | CTGAGATTATAGGCA[C/T]TCGCCATCATGCCCA | 26524 |
rs541398903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995424 | AGATGTGGAAAGGGT[A/G]AGCAGCCCTGCCCCA | 26524 |
rs541417510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049301 | AGCTAAGGAGTGACA[C/T]GGCCTGAGTGGAAGG | 26524 |
rs541438379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21003112 | AATTTTCAAATAGGT[A/C]AGATGACAATAATTA | 26524 |
rs541484742 | snp | A/G | 0.000710552 | 0.0188354 | missense | LATS2 | GRCh38.p7 | 13:20988501 | CGGTGTTGGGGGCGG[A/G]CAGGGAGGGCTCGGC | 26524 |
rs541490057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997469 | CAGTATCAGGCCCTG[C/T]CAGTATCTTGAGGCT | 26524 |
rs541525254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20990892 | AGAATTGAGGAAAGA[A/C]GCCACCCTTGTCAAA | 26524 |
rs541534685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028623 | GTCACCAGGCTGGAG[C/T]GCAGTAGCGCGATCT | 26524 |
rs541623788 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022599 | ATCAAATGAACTGTA[C/T]CAAAGTCAGAGGAAA | 26524 |
rs541648656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022321 | GTGTGTGAATATCTG[C/T]ATATGCCTAAGTGCA | 26524 |
rs541650411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060597 | GGCCTCTGAGGGGCT[C/G]ACTGGCCCGTGAGCC | 26524 |
rs541702620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015322 | ACTGTCAGGATCCTG[C/G]CCTGGAAGAAGGCTC | 26524 |
rs541723435 | in-del | -/ATTTGTT | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20999762 | GGTGCCTGGCCTTAA[-/ATTTGTT]ATAAAATAAAATGAA | 26524 |
rs541768311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053836 | AAAAGGAAATATTGT[A/T]TGATTCCAGTTATGT | 26524 |
rs541865109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21035927 | TTCGGGGAACAGAGT[C/T]TTGCTCTGTCGCCCA | 26524 |
rs541889009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042844 | AAAAAATTAGCCGGG[C/T]GTGGTGGTGGGTGCC | 26524 |
rs541898683 | in-del | -/AAAAAAAAAAAAAAAAC | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023668 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAC]AAACCTCGGCCGGGC | 26524 |
rs541956882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21029568 | GAGGCCAAGGCAGGC[A/G]TATCACGAGGTCAGG | 26524 |
rs541979789 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976638 | AAGGGTAATGGACTT[C/G]AGGAGATATTTCCAA | 26524 |
rs542009974 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20978162 | CCTCGTAATCTGCCC[A/G]CCTCCGCCTCCCAAA | 26524 |
rs542015834 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:21037268 | AATTAGCCAGGCATG[A/G]CGGTGGGTGCCTGTA | 26524 |
rs542048565 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052864 | GCAGGTCTGGGTTGA[C/G]TCTGTGATCCTGTGT | 26524 |
rs542141994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21025035 | TTTTTATATATTTAA[C/T]AGGTTACTATCAATT | 26524 |
rs542173109 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21033451 | TGGAAACAAACACAC[C/G]GAGTTCAATACAGAA | 26524 |
rs542217688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21029155 | CTGTATTACTAATCT[C/T]AGAGGCAAGTTATTT | 26524 |
rs542237961 | snp | C/T | 0.000399281 | 0.0141238 | missense | LATS2 | GRCh38.p7 | 13:20988968 | TGGAAGGAGGGGCTG[C/T]GCTGCACTCCGTAGC | 26524 |
rs542239657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058687 | TAATTTTGCAAGACA[A/G]GCTAGCCTCTGCTCA | 26524 |
rs542253872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20982767 | GAGGCGGAGGCAGGC[A/G]GATCACCTGAGGTTG | 26524 |
rs542257276 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21007611 | TATATAGTGTGTATA[-/G]TATATATATAGTGTA | 26524 |
rs542307864 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048419 | CTTCACAAGAACAAT[A/C]AATGCAAGGGAGGGC | 26524 |
rs542322839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20977818 | ATGTGGGCAATTTAG[C/T]GAGTAGCTCAGCCAT | 26524 |
rs542371356 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047303 | GACGGATGCTTAGGA[A/C]AGTGGTGAGCACCGG | 26524 |
rs542464743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21016252 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCA | 26524 |
rs542469947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21009682 | AAATTCAATACCTTT[C/T]AAAATACAGAAACCA | 26524 |
rs542497919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21041129 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 26524 |
rs542501805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21016853 | TAACTCTCTTTATCA[C/T]GGCAGAGTCCTTAAC | 26524 |
rs542527140 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21048768 | CTTGAACCAGGGAGG[C/T]GGGGGTTGCAGTGAG | 26524 |
rs542585957 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981333 | TTGCAGAAATTAGTA[A/G]CTTTCAGGCTTCTAT | 26524 |
rs542680200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999809 | CCTTGGCCTTGCCAA[A/T]GATCACGAGACCAGC | 26524 |
rs542754470 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21008214 | GTAGGACAGACACTC[A/G]GGCACCGCATCCAGG | 26524 |
rs542785377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001269 | CAAAGTTCCCTATTA[C/G]TACACACACATGGCA | 26524 |
rs542805291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20994525 | GTCGGAGCCAGGATG[C/T]GGGAGGAGTGTGTCA | 26524 |
rs542882430 | snp | C/G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993471 | ATGCAGGCGTGGGCA[C/G/T]GGCAAGATGGCAGGG | 26524 |
rs542950360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020956 | ATCTTTAAGCCACAC[A/G]TCCGTGGTTGGGAAG | 26524 |
rs542980089 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21017334 | ATGCAATCCTTTTTC[-/T]TTTTTTTTGTTTTTA | 26524 |
rs542982152 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | LATS2 | GRCh38.p7 | 13:21028391 | GCCGCAATAAACATA[C/T]GTGTGCATGTGTCTT | 26524 |
rs542989723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21006346 | GGCCACTCTCTGGCC[C/T]TGGTCCCCAGCGCCC | 26524 |
rs543006393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20977441 | CAGAGACAGGAAGCA[A/G]AAGAGAGGCGAGCAG | 26524 |
rs543027922 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21008332 | ACTACAGCCTTGGGC[A/G]TGGGGTGGGGTGGGG | 26524 |
rs543064602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009044 | TGTTCGTCCCACTGC[C/T]CATGCTCTTTCTTCA | 26524 |
rs543111711 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21001112 | CAATAAAATGGCAAG[A/G]TAAGAATATACAAGC | 26524 |
rs543126939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046326 | GTGATCGTGGAAATA[C/T]ACCGCTTGGAAAGAA | 26524 |
rs543139906 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003173 | AATAATTCTTCAAAA[A/G]ATGAGACTGTTCCAT | 26524 |
rs543204870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048602 | TTTGGGAGGTCAAGG[C/T]GGGCGGATCATCTGA | 26524 |
rs543213326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033888 | CTAATGTCATAACCA[A/C]CCAAATATATATCAA | 26524 |
rs543290781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042011 | AAATGCAAACTTAAA[A/T]GATCACTTATGCCAA | 26524 |
rs543293198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21036008 | GGTTCAAGTGATTCT[C/T]GTGCCTCAGCCTCCT | 26524 |
rs543322078 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:20982365 | TGCCCAGGCTGGGGC[A/G]CAATGGCGCGATCTC | 26524 |
rs543325523 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20996723 | GCAGAACTGATACTA[C/T]TATTCACACTCCATA | 26524 |
rs543380179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048773 | ACCAGGGAGGCGGGG[A/G]TTGCAGTGAGCCGAG | 26524 |
rs543513326 | snp | A/G | 1.65146e-05 | 0.0028735 | missense | LATS2 | GRCh38.p7 | 13:20988143 | GGCTCGTTGGGGCCC[A/G]CACGGAGGCTCTGCT | 26524 |
rs543553219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001857 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 26524 |
rs543553530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995333 | GTTCTTTTCCCCAAG[C/G]CTCAATAGACACCTC | 26524 |
rs543555119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041210 | ACCTCCTGACCTCAT[G/T]ATCTGCCCGCCTTGG | 26524 |
rs543599839 | snp | A/T | 0.00676609 | 0.0577691 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988373 | GGCGGGGGCCGGGGC[A/T]GGCGCGGGCACCCAG | 26524 |
rs543644951 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:20982388 | GCGATCTCAGCTCAC[C/T]GCAACCTCTGCTTCC | 26524 |
rs543714031 | snp | A/G | 0.000171856 | 0.00926814 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989132 | GGGGCCGACTCCGGG[A/G]AAAAGGTAGTCCACG | 26524 |
rs543732833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014600 | CATGAGAAGGAACGA[C/T]GCTGACCATCCATGC | 26524 |
rs543749580 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022611 | GTACCAAAGTCAGAG[A/G]AAAGCTTTTTGTTTA | 26524 |
rs543754131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046423 | ATCTACGGCTGTCCC[A/G]AAATGCTTCCTGTAA | 26524 |
rs543809523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033053 | AGGAAAAGTCCACCC[A/G]GGGAATTACTGGGTC | 26524 |
rs543829505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032574 | CCCAGCCTTTTTTTT[C/T]CGTTCTTTTTTAAGC | 26524 |
rs543850372 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20976025 | CGGCCAACTGGGGTT[C/T]TGAAAAACAAACAGG | 26524 |
rs543914502 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21025003 | TTTTTGCCTGGTTTT[A/G]TTTTTTGATTCATTG | 26524 |
rs543915896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040482 | CCAGGAAGAGCCTGT[A/G]TAAAAAGGAATCTGA | 26524 |
rs543988842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058028 | TTTGAAGGCCGATTC[A/C]TTCTAGAGGAATTAC | 26524 |
rs544018233 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | LATS2 | GRCh38.p7 | 13:21037912 | CAGGCACCATCCTGA[-/G]GCCAGAGAAAAGGTT | 26524 |
rs544031881 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043044 | AAGCTGCAACAATAA[A/G]AACTCTCGGCCAGAC | 26524 |
rs544057635 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052281 | GTTTAATGAGGCCAG[A/G]AGATAAGACCACGGA | 26524 |
rs544106383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051390 | TGTCACAATGAAAGT[C/T]TGCCCAAAGAATTAT | 26524 |
rs544112387 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20976556 | TTGAAAAGGGGTTAG[A/T]ACCCAGAGAAAATAC | 26524 |
rs544115053 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020171 | CTGAAAACACACCAA[A/T]TCCCACTGTGACATA | 26524 |
rs544149774 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | LATS2 | GRCh38.p7 | 13:21059616 | CAACAACAACAACAA[A/C/T]AAAAAACACTCATAT | 26524 |
rs544164532 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057729 | GGTGTGAACCCAGGA[A/G]GAGGAGCTTGCAGTG | 26524 |
rs544195996 | snp | A/G | 4.94694e-05 | 0.00497316 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045993 | GCCGGCTATTTCCAG[A/G]ATAAGTCGTGGCAGG | 26524 |
rs544203168 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035763 | TCGCAGTGGAGGGAC[C/T]CAGCTCCCAAAGGGC | 26524 |
rs544214514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20986990 | CTGAGGTCAAGAGTT[C/T]GAGACCAGTCTGACC | 26524 |
rs544217694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999894 | ATAGCCAGGCGTGGT[A/G]GCACACACCTATATA | 26524 |
rs544221209 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:21018397 | AGACAAGGGTTGACA[C/T]GGAAAAACAAAATTC | 26524 |
rs544224936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21011081 | ATATCAACATGGTAA[C/T]GGTAGCTACCTCATA | 26524 |
rs544252093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20987467 | ATGGAATCACTACTA[A/G]ATACATTTTTCTTCC | 26524 |
rs544289099 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21038024 | CCTGGGTGGACCGCT[G/T]GAGCCCAGGAGGTCG | 26524 |
rs544313299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21019151 | CCGTGTACCTAATTT[G/T]TAATACATCTTAAGC | 26524 |
rs544347468 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982531 | GGTCAGGCTGGTCTC[G/T]AACTCCTGACCCCAG | 26524 |
rs544351170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21019950 | CTGCACCCCAGCCTG[C/T]GTAACAGGAGTGAGA | 26524 |
rs544395911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050322 | CACACTCTTGTAAAT[A/G]GCATCCAAATCAAGA | 26524 |
rs544446856 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21044981 | GATCTTCTTGACTGG[C/T]CTCCCAAAGTGCTGG | 26524 |
rs544481755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038381 | CTTTTTTTTTTAATT[A/T]AAAAAAATAGACAGG | 26524 |
rs544511310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051974 | AAGCACAGGGAGGGG[A/G]AGCTCACTGAAAACT | 26524 |
rs544550158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980275 | CAATTCACTGTAAGC[C/G]AAACACTCCTTGTGT | 26524 |
rs544567121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21007058 | ACTGACAAGGTAATT[C/T]GGTAAAGTATACAAA | 26524 |
rs544655177 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973625 | TCTTTGCTTTTTTAC[A/G]AAGGTTAGGAATATG | 26524 |
rs544681002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21012517 | GTTGCCCGAAACATC[A/G]TTATGCGGCACTTGA | 26524 |
rs544709514 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20989496 | GCAGGACCAGTTGCC[C/G]TAATGTGTTAGCAGA | 26524 |
rs544854297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999232 | GCAGCAGAAGCTCCA[A/G]CCCCAGCCGTGGCCG | 26524 |
rs544889734 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047191 | GTCCAAGTCAACACC[A/G]CCCTCAGCAGCCAGC | 26524 |
rs544891686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014302 | GGAGGACAATTAGCA[C/T]TGCAGCCGGCCACTC | 26524 |
rs544919764 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21048196 | CTAACTTTGTAAAAC[C/T]GTAACTTCACATTCC | 26524 |
rs544923877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046528 | GCTCATTTAAAATAC[C/T]TCATTATAATAAAAT | 26524 |
rs544944084 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994160 | GAACTCAGAAAAATC[A/C]GCAAGGAGACCACAA | 26524 |
rs544960364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040078 | AACTCCATCTCAAAA[A/T]AAAAAAAAAGAAAGA | 26524 |
rs545012841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014127 | GAATGTAGGAAAAAC[A/G]GATAAAAGTATTTTT | 26524 |
rs545021276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20994787 | CAGCTACTGAAGAGG[C/T]TGAGGCAGGAGGATT | 26524 |
rs545039722 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993634 | ACCTGTTTGTTAAAG[C/T]GGCGCCTGGACTACC | 26524 |
rs545045516 | snp | A/C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038357 | ATATAGTTTAATATA[A/C/T]AATTCCATCTTTTTT | 26524 |
rs545058056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982275 | AGATGCAGGTTGGCT[A/G]TAAGAGAGGGCTCCT | 26524 |
rs545080266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020861 | TGAGCACACCTACTA[C/T]GTCACAATGCAGTGT | 26524 |
rs545088319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21058618 | AACTCGATGGAGAAG[C/T]CAGAAGAATCCCTTC | 26524 |
rs545099351 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017036 | AGGAAAATATGGCAG[A/G]ACCGGAAACAAATTC | 26524 |
rs545109248 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20975846 | CTGCCACCACACCCG[G/T]CTGATTTTTGTATTT | 26524 |
rs545117236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013796 | CACAGCAAGACCCCG[C/T]CTCTACAAAACAATT | 26524 |
rs545134345 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993089 | GATACAGAAAGACCC[C/T]GGACAGTGGGGGAGG | 26524 |
rs545170563 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021793 | CAGTGCTGCTCCTGG[A/G]GTCCACACTGCAGTT | 26524 |
rs545186140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21045126 | TTGCCACAATTTTGA[C/T]GATTTCTCAAGCTTT | 26524 |
rs545219146 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20999321 | GGAAGACACCTGCTC[C/G]GCACATACAGGTACA | 26524 |
rs545257874 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20993159 | TCACAGAGCCACTCC[A/G]CAGAGAGAGATGCAG | 26524 |
rs545273282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033101 | AGTAGAGCAGGGTGT[C/T]AGCAGCAAAGACACT | 26524 |
rs545277702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008096 | CACTCTGGCTCCACC[A/G]TGGGGAGCCAGGTAT | 26524 |
rs545362575 | in-del | -/AAC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059599 | GACAACGTCTCAAAA[-/AAC]AACAACAACAACAAC | 26524 |
rs545368242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001182 | TTGAGGAATGTTTGC[G/T]AAAATAAGACTTTTG | 26524 |
rs545408408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21057215 | AACTACACTACAAGA[C/T]TCTAACAATCAGTGT | 26524 |
rs545435251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043342 | ACACCGTCTAAAAAA[A/C]AAAAAGAACTCTATT | 26524 |
rs545443998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050923 | ACGCATAGACATGCC[A/G]TGATACCACAGCCAC | 26524 |
rs545468109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997980 | TAACATTCCAACTAT[A/G]AGGTTTGGCTGAAAA | 26524 |
rs545504132 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987583 | TTAAGCGAGGACATA[C/T]CCTAAAACTTAATTT | 26524 |
rs545592423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986208 | GAACGACTATTATCA[A/G]AAAGGAAAAAAAAGA | 26524 |
rs545653533 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21054903 | AGGACCCCACAAGCT[C/G]TTCTGATTTTTTCTC | 26524 |
rs545656743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20993892 | TAAAAAAATGTGCCA[A/G]TTGGGGCTGACTCTA | 26524 |
rs545754267 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21029715 | AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG | 26524 |
rs545774867 | in-del | -/GTAA | 0.00199561 | 0.0315249 | intron-variant | LATS2 | GRCh38.p7 | 13:21022204 | CATGTGTGCAACTAC[-/GTAA]GTGTGTGAATATGTG | 26524 |
rs545800603 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973759 | AGAAAACAGGACTAA[C/G]AACATTCACTGAAGC | 26524 |
rs545854661 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061619 | GCGTCACTCTCGGCC[A/G]CATACCAGTCCGGGC | 26524 |
rs545889222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037888 | AGGTGGGTCCTGTCC[A/G]CCAACTCCCAGGCAC | 26524 |
rs545891015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21030958 | ATGTCTTTACGACAC[C/T]TTCATTTCAGAAAGA | 26524 |
rs545962056 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21007693 | TATAGTATATATATA[-/C]TATATAGTATGTATA | 26524 |
rs545983225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21031721 | AAAAGTGAGCTGAGC[A/G]TGGCGAAGTGTGCCT | 26524 |
rs545998652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20978964 | GACGGGTTTCGCCAT[A/G]TTGCCCAGGCTGGTC | 26524 |
rs546114110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20985871 | AACAACATGGTGAAA[C/T]CCTGTCTCTACAAAA | 26524 |
rs546119695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21056626 | CAATCGTTAAGAAAG[C/T]CTTGCCTCCTCTGCA | 26524 |
rs546151229 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053552 | GCACCGAATCTGCGT[C/T]CTCAGTTCCACACTG | 26524 |
rs546155551 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011794 | TTAGGTGATTTCGTT[A/G]TTGTGTGAACATCAT | 26524 |
rs546160521 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981134 | AATGTGTGGTCTGGG[A/C]AGACTGAGCAGAGGT | 26524 |
rs546178680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20979530 | AAATTTAAAAATAGA[C/T]AATTTAAAAAATAAT | 26524 |
rs546205927 | in-del | -/GTGTGTGT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044692 | ATGAGGTGTAGGGGT[-/GTGTGTGT]GTGTGTGTGTGTGTG | 26524 |
rs546247747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20984703 | ATGAAAAGAGATCCC[A/C]TGTTCACCGACAGAA | 26524 |
rs546261440 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030554 | AGATCACACCACTGC[A/C]CTCCAGCCTGGGCGA | 26524 |
rs546267348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21016404 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAACTGGG | 26524 |
rs546300135 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973169 | GTCAGAGCGCTGTGA[A/G]TAACAACATGGCACG | 26524 |
rs546386324 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973880 | CATACGGACTACAGA[A/C]ACGGACATGTGTCCG | 26524 |
rs546393697 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981410 | GCCAGCGAGACTCAG[C/T]TCACGTCTGAAGGGA | 26524 |
rs546411694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21011251 | CCTGAATCAAAAACT[G/T]AAACTAGCTACTAAA | 26524 |
rs546435647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21010149 | AGGTCGCAGTGAGCC[A/G]AGATCGCACCACTGC | 26524 |
rs546477956 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20983168 | ATTTAGTTGCTTGCA[A/G]TGGGGTTAGTGACAT | 26524 |
rs546480579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21003297 | TATCGCTCAGAGTTC[A/G]GGCTGGAGTGCAGTG | 26524 |
rs546522691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997597 | CTGCTGTCCCTCGGG[G/T]AAGCTGGCCTCACCC | 26524 |
rs546594979 | snp | A/G | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024119 | AAAAAAAAAAAAGAA[A/G]AAGAAAAAACAGCTT | 26524 |
rs546630082 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024682 | TTCCATTGTCTTATA[C/T]CCACATTAAAAAAAA | 26524 |
rs546697481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058113 | GTCAGTCACTTCAAT[A/C]AAGCCTTACCCTTCT | 26524 |
rs546771270 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006707 | AAGATCCACTTACTC[A/G]ACAATGGCACATAGG | 26524 |
rs546793556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21011879 | TGGTATAGCATATTG[C/T]TCCTGGCTACAAACC | 26524 |
rs546802700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20998207 | AAAAGTGAGAAAATT[A/G]GCTGGGCATGGTGGT | 26524 |
rs546811319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050012 | TGTAGTCCAGCTACT[C/T]GGAAGGCTGAGGCAG | 26524 |
rs546832278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21005114 | GAGGGCTTGGTGTCA[C/T]GACTAGGTAGAGGCC | 26524 |
rs546848190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050485 | TACTCTGTAGTTTAG[C/T]ACATTTCTTTCAACA | 26524 |
rs546857042 | in-del | -/AAGTT | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20984280 | TGAATATGGAATGAA[-/AAGTT]AAGATAAAAAAGAAA | 26524 |
rs546869992 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050725 | GCAGCGTGGGTGCTC[A/G]GCTCAAGGCCTTGCT | 26524 |
rs546922540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21036906 | TAAATTCAATTGAAT[A/G]ATTTTTAAAAACCCA | 26524 |
rs546935863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044570 | GTTACATTTCACTAA[A/T]TACATTTTTACCTGG | 26524 |
rs546940798 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029135 | AGATGAAAGAGGACA[C/T]CACACTGTATTACTA | 26524 |
rs546945015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991186 | GCTCTGGCCAGGCCA[C/G]GCCAGGTTGGACCCC | 26524 |
rs546959668 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21030544 | CAGCGAGCTGAGATC[A/G]CACCACTGCACTCCA | 26524 |
rs546980972 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20977442 | AGAGACAGGAAGCAG[-/AA]GAGAGGCGAGCAGGT | 26524 |
rs546996957 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20980002 | GGCCGCTTAGGTTTT[C/T]GTATTTTTAATCATT | 26524 |
rs547008923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001874 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAAATAGT | 26524 |
rs547070864 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:21002606 | TGGTCTGGAACTCCT[A/G]AGCTCAAGCAATCTG | 26524 |
rs547092955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042467 | TTTGGAGGTTAAGGC[C/T]GCTTGAGTCTGGAAG | 26524 |
rs547093503 | in-del | -/CA | 0.00398564 | 0.0444627 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973981 | CAGTTCCCCCCCCCC[-/CA]AAAGAATCCAATCAC | 26524 |
rs547126963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041311 | TGGCCCCTGATTCAC[C/T]GAGCAGCTGGTGTGG | 26524 |
rs547129446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21036223 | TTTTAGTAGAGACAG[A/G]GTTTCATCATGTTGG | 26524 |
rs547135177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996168 | CAAGATACCTGCAGT[A/G]TTCAACACTTCCTTC | 26524 |
rs547221704 | snp | C/T | 0.000402077 | 0.0141731 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989204 | GCCGAAGCTTGGGCC[C/T]TCGTAGGGGGTACCG | 26524 |
rs547254055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21037411 | CCATCTCAAAAATCA[C/T]AATAATTTTAAAAAT | 26524 |
rs547327091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040864 | TATGAGGATGGAAAT[A/G]AGAAAAGAATTCTTA | 26524 |
rs547393007 | snp | G/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061663 | CCCCTGCTCCTCCGC[G/T]GCCGCTCCGCCCAGC | 26524 |
rs547405135 | in-del | -/AAC | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:21059598 | GACAACGTCTCAAAA[-/AAC]AACAACAACAACAAC | 26524 |
rs547418555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21035030 | GAGGCCAGGAGTTTC[A/G]GACCAGCCCGAGAAA | 26524 |
rs547456141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982414 | CTTCCCGGGTTCAAG[C/T]GATTCTCATGCCTCA | 26524 |
rs547460221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20975543 | AGTGTCATTTCAGTC[A/G]ATGGCTCACAGCCTG | 26524 |
rs547625999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060885 | CTGTCAGGGGCGCCC[G/T]GCCGGGCGTCTAGTG | 26524 |
rs547641110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000886 | TACACAAATCAGTTA[C/T]GCCTATGAACAAGGG | 26524 |
rs547666301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015930 | TCTTGAACTCCTGAC[C/T]TCAGGTGATTTGCCC | 26524 |
rs547687289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20977965 | CTGTCATCCAGGTTG[C/G]AGTGCAGTGGCGTGA | 26524 |
rs547758811 | snp | G/T | 1.66824e-05 | 0.00288806 | missense | LATS2 | GRCh38.p7 | 13:20989293 | TCACTGGGGTTGGCA[G/T]GAGCCCCTTTCCTGC | 26524 |
rs547760697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996939 | AAGCTAGTAGGGCTA[A/C]ATACTATGGCACAAA | 26524 |
rs547781928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21027049 | TCTACTCAAATCTTT[C/T]GCCCATTTTTAAAGG | 26524 |
rs547785880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21034324 | TTCTTCCTTACTGAC[A/T]GTGCCCAGTTGCATT | 26524 |
rs547844574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20989893 | CCCCTCTACAAATAT[A/C]CAGATTGATTTCATC | 26524 |
rs547866094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21021272 | GAGGTCAGGAGTTCA[A/C]GACCAGCCTGGCTAA | 26524 |
rs547886581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21059013 | AATTTCCTAATAATC[A/G]GCCATGAGTTACTTT | 26524 |
rs548018255 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995919 | GACTTTGATGACTTT[A/G]TGTCAGTCACCTAGC | 26524 |
rs548044414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21053336 | CACAGAAGGACCTTC[C/T]TGACCTCCCCAATCT | 26524 |
rs548045004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023438 | CTTGTAAGACACCGT[C/G]TGGGTAGAATAGAAC | 26524 |
rs548063380 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974379 | AAAAAACAAAAACCA[C/T]TGTGTGGATAAAATG | 26524 |
rs548068453 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20980174 | CCTGTGAATAGTCAG[A/G]TGAGGGTCAAGGGAG | 26524 |
rs548077202 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017180 | ACAGTGAAATAAAAC[G/T]GACGATAGCCATTAA | 26524 |
rs548115758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21010440 | CCCCACCCTATAGTC[C/T]TTCCAATCAGCTTTT | 26524 |
rs548160027 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21015574 | TAATGCCCAACTTTT[-/AA]AAGTTTCCTAGGTAG | 26524 |
rs548164753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21042247 | TACACAGAAAATACC[C/T]TTGAGTCTTTTACTT | 26524 |
rs548165911 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20976196 | TCTTTATTGTTTACA[C/T]TTAGAATCAGGAGGA | 26524 |
rs548176686 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004263 | AACATGGTGAAACCC[C/T]GTCTCTGTTAAACAT | 26524 |
rs548195869 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004880 | GTCACCAGGAAAATA[A/C]GTAATTACACAAAAT | 26524 |
rs548202983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20976831 | AACTGAACACTCAGT[C/T]ACTGTTGGTGGGAAT | 26524 |
rs548208260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21029438 | TGATGTATCATCTTC[C/T]TACCAAATGCCATTT | 26524 |
rs548209751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21055291 | TTTATAAATATGACC[C/T]TCATGGATGTGGACT | 26524 |
rs548232750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20983970 | GAGTCTCGCTCTGTC[A/G]CCTAGGCTGGAGTGC | 26524 |
rs548249742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21036116 | GGCCAGAGTGGTCTC[A/G]AACACCCGACCTCGG | 26524 |
rs548283118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20983084 | AAGGGAAGGATGTCA[A/C]ACCAATTTATAAAAT | 26524 |
rs548297317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060679 | CGGCGCAGCCACCGG[A/G]GGCTGAGGGGCGGCG | 26524 |
rs548371859 | snp | C/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023906 | TGAACCCAGGAGGCA[C/G]AGGTAGCAGGGAGAC | 26524 |
rs548403424 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061825 | TTTGCCCTCTCGACT[A/G]CATTTGTATTAAAAG | 26524 |
rs548453129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21009902 | GAGAGCAGACAGCAA[A/G]GAAATAACACAGAAG | 26524 |
rs548489872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053914 | TACCAGAAGAAAGGG[A/G]AACAGGGAATTTTTA | 26524 |
rs548511816 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20996207 | CCACTCCATGCCACC[C/T]GCTGCAAGAGTAAGA | 26524 |
rs548598458 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046095 | ATTTAAAAAAAAAAA[A/C]TGTCAATAGTATCAG | 26524 |
rs548607717 | in-del | -/A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057635 | GTCTCTACTAAAAGT[-/A/T]AAAAAAAAAAAAAAA | 26524 |
rs548611782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21021967 | TATCTGTTTCCACAC[C/T]TTCTTCGTTAGAGGA | 26524 |
rs548621397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21059794 | CAACACGGCGAAACC[C/T]GTCTCTACTAAAAAA | 26524 |
rs548668532 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21018559 | TGCGCAGCAGGTCCA[A/G]GAAGACTGTGGTCGC | 26524 |
rs548698642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008497 | CCAAACCAGGAGACT[A/G]GTTTGGTCTCCTGAA | 26524 |
rs548701438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014849 | CAAATACCATGCAAC[C/T]TTCTTTTTCCAGCTG | 26524 |
rs548734138 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21052504 | TACAGGCGTGCACCA[A/C]CACACTCGGTTAATT | 26524 |
rs548735101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015606 | TTGTTTTAAATAGGA[C/T]TTGGGGAACTGTGAA | 26524 |
rs548817588 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20977247 | CTAAAAATACAAAAA[C/T]TAGCTGGTGTTGTGG | 26524 |
rs548862591 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056217 | TCTGAGGGGGAGTTT[C/T]GCCATGAGATGGGGT | 26524 |
rs548915168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041378 | CCTGACCACTGGCTG[A/T]CTTCTTTATGCCCTT | 26524 |
rs548944508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999355 | CATACGTCTTTTTGA[A/C]ACGAATGAAGAAGAA | 26524 |
rs548967311 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021106 | TGGGTCACTGTCAAA[A/G]CTGGTCAGTGAGTAT | 26524 |
rs548985636 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21006622 | TAAGTAGGCTGAATA[C/T]GTGTGAAGACTCTGC | 26524 |
rs549012624 | snp | C/G | 3.51549e-05 | 0.0041924 | missense | LATS2 | GRCh38.p7 | 13:20988568 | GAAGGAGTTGGTCCT[C/G]CTGGGCACTGGGCAG | 26524 |
rs549067266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038136 | ACAAATCAGACTGAG[G/T]AGGGTACTGTGCAGG | 26524 |
rs549129737 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974797 | CCCTCGGCTTCCCTA[C/T]TGGCCTGTGAGGGCA | 26524 |
rs549140140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000753 | CTCTAACAAATCTAC[C/T]ACTGTTCTAGATGGT | 26524 |
rs549140337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026353 | AAACTACTAAATAAA[C/T]AAAACTGTGCAGTAT | 26524 |
rs549155227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032059 | TTCCTCCTGGTGCTA[C/T]TGACTGCCTTAGTTC | 26524 |
rs549177245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026774 | CAGCCTAGGTAACAT[A/G]GCAAAACCTCATGTC | 26524 |
rs549177701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986619 | TAGTTACCAGAGGTG[A/G]GAAAGGGTGTGTGTG | 26524 |
rs549206866 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21034347 | GTTGCATTGGGGTGG[C/T]CACGTGCCCAGGTGA | 26524 |
rs549243886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028036 | CTGCACCCATTAACT[C/T]GTCATTTAGCATTAG | 26524 |
rs549258974 | in-del | -/A | 0.000722732 | 0.0189959 | intron-variant | LATS2 | GRCh38.p7 | 13:20989313 | CCTTTCCTGCAGTGG[-/A]AAAAAACAGGAAGAC | 26524 |
rs549265263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020252 | AAGTCTAGCTCTCCA[C/T]TACATCAGCCAAGTG | 26524 |
rs549295820 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991861 | AGAGGGTGCAGCTGC[C/T]GAAGAGTCATATATT | 26524 |
rs549317024 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013197 | TGCTTAGGTGAGTTA[C/G]GCCCATCCGCTATGG | 26524 |
rs549341189 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20981702 | AAATATAAAGTGAAT[C/T]TTCACTCTTCAATAA | 26524 |
rs549354573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21045197 | TACACCCCCTGTAAC[A/G]GCATATACACTAATT | 26524 |
rs549369727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057610 | CATCCTGGCTACTAC[A/G]GTGAAACCCCGTCTC | 26524 |
rs549393527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040345 | CCGAGATTGCGCCAC[C/T]GCACTACAGCCTCGG | 26524 |
rs549408939 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21012795 | ATCACACCCCCCCCC[C/G]ACCTCCTAGGAAATA | 26524 |
rs549460400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20987190 | ACAGAGCAAGACTCC[A/G]TCTAAAAATAAATTA | 26524 |
rs549516190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035007 | AGGCCAGGGCGGGAG[G/T]ATCACTTGAGGCCAG | 26524 |
rs549526130 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042476 | TAAGGCCGCTTGAGT[C/G]TGGAAGTTCCAGTCC | 26524 |
rs549614078 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044336 | GTTAGCCTTTTCCTA[G/T]GACTGCAACACCAGG | 26524 |
rs549625457 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974764 | AAGTAATCGACGGAC[C/T]AATTTAAAACAAAAC | 26524 |
rs549670690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058221 | CTGTATTTCTTCACA[A/C]CAACTGTTTTTAAAA | 26524 |
rs549677784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21060130 | TCGGGTGGGTTTTAC[C/T]TTCTTCAGGGTCCAT | 26524 |
rs549738360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046984 | AACTTCTCAGAGTGC[A/C]CCATGGCCACATGAA | 26524 |
rs549740977 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:20994006 | ACCAGCCTGTGCTCA[C/T]TAACCCAGTACCTGT | 26524 |
rs549807926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:20995174 | AAGGGTTAGCTGTTA[C/G]AGTTCACAAAGGTAT | 26524 |
rs549827407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20987699 | TCAAGGGGAAAGGCG[A/C]AAGGGAGGTCACACC | 26524 |
rs549844838 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20977549 | TGGTTGCACAATATT[A/G]TGAATGTACTTAATG | 26524 |
rs549979033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981381 | TGGAAGCATTAGGTC[C/T]TTGGAAAGCTAGAGC | 26524 |
rs549992152 | in-del | -/T | 0.461148 | 0.133852 | intron-variant | LATS2 | GRCh38.p7 | 13:21002375 | AACTAATTAATTAAC[-/T]TTTTTTTTTTTTTTT | 26524 |
rs550029793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022012 | TGTGACTGAACTGAA[A/C]GTATAGTGGGCCCTG | 26524 |
rs550041617 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019851 | TGGTGGTGCACTCCT[A/G]TAATCCCAGCTACTC | 26524 |
rs550058133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20977091 | GACAGATACTGCATG[A/G]CTCCACTTACAAGAA | 26524 |
rs550073541 | snp | A/G | 0.000566412 | 0.0168192 | intron-variant | LATS2 | GRCh38.p7 | 13:20983199 | CTACACATAGAAAGT[A/G]CATGTGGCACACTTC | 26524 |
rs550108062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20983891 | GGGGATGCCCTGGAA[C/T]TGAGAGGAACCTAGC | 26524 |
rs550108139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21021070 | TGGGAGGGTTATAGA[C/T]GAAACAAGACAGGCC | 26524 |
rs550136944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20976013 | GCGGTCAAAAAACGG[C/G]CAACTGGGGTTTTGA | 26524 |
rs550151935 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973242 | CAGCAGACTTGAGTA[C/T]GCCACTCACACAAAT | 26524 |
rs550154660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21039167 | AAGGGGAAAAGGCAA[C/G]GAACTGCTACACCCA | 26524 |
rs550171465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051691 | AGGCTGGGTCCAGTG[C/G]CTCACACATGTAATC | 26524 |
rs550223790 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21026848 | TTCTATGTGAATTTT[A/G]AGAAAATTCCAATTG | 26524 |
rs550269632 | in-del | -/CCCCTCCCACCAAAAGAAAG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058515 | TATTGTAAAATCATT[-/CCCCTCCCACCAAAAGAAAG]CCCCTCCCACCAACC | 26524 |
rs550282765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057424 | GTGAACGGCAAACAT[C/T]AAACAATGCCAAATT | 26524 |
rs550312916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020363 | TGACAAAAACCTCAA[C/T]TGCTTTTGCACCAAC | 26524 |
rs550397489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058246 | TTAAAAAGTCAGTAA[A/G]AAATACTGTTCAGAA | 26524 |
rs550439232 | in-del | -/ACATGGGCAGGCCATGTTGCCTGCCCATGTGGG | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:20993541 | TGGGGAGGTGCCGCC[lengthTooLong]ACATGGGACATGAAG | 26524 |
rs550449876 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21052758 | AGAAAAGCTTAAGTC[C/T]TTCCTCTCTGAAACG | 26524 |
rs550492088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044662 | GAATTGCTAAGAGAT[A/C]ATAAATGTATGGCTA | 26524 |
rs550515519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025558 | TACCTTTTGGTGTCA[C/T]GCAGGATGGATCACT | 26524 |
rs550524286 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034471 | GAGCCAGAGCCGGCA[C/T]GTCCTTCCCTGGCTC | 26524 |
rs550526586 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20998839 | AGCGACATTGTGCAC[G/T]CCGGGTGGGGGCCCT | 26524 |
rs550530106 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994957 | GCTATTCCAAAAGAT[A/G]GCAGGATGGCGCAGT | 26524 |
rs550580964 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973894 | AAACGGACATGTGTC[C/T]GTGATTAAACTTTTT | 26524 |
rs550642106 | in-del | -/GGGGCG | 0.0160261 | 0.0881779 | cds-indel | LATS2 | GRCh38.p7 | 13:20988343 | AAGCCCTCCGCAGCC[-/GGGGCG]GGGGCGGGGGCGGGG | 26524 |
rs550644426 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036966 | TGCTCTCAACATTTA[C/T]GCTAGTAATTCCATT | 26524 |
rs550675776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21043465 | GACTTTCCTACCTGA[A/G]TTTTCTGAACGCAAA | 26524 |
rs550678697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037042 | TGTAGAAGAATGTTC[A/G]TGACCAGCTCTTTAC | 26524 |
rs550681199 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013275 | GTTACAGCCTTGCAT[A/G]TTCTGCCCAATTGGA | 26524 |
rs550690041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21049550 | CACTCACATTCCTTA[C/T]AGGAGCAGCCACCTG | 26524 |
rs550723952 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21003494 | TGCCCAGGCTGGAGT[A/G]CAGTGACACAATCTT | 26524 |
rs550765751 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21005977 | AATTAGCCGGGAGTG[C/G]TGGCGCATGTCTGTA | 26524 |
rs550785420 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986593 | TCTCATAGAGGTAGA[C/G]AGTAGAATGATAGTT | 26524 |
rs550954522 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984839 | ATACTAAAATTCACA[A/G]GGAGCCCAAATACTC | 26524 |
rs551015635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004105 | AATGAATATAACATA[A/C]AAAAGAATATAACAT | 26524 |
rs551170831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992059 | GGCCACCACGGGAGA[A/G]GGCAGGTAAAATGGA | 26524 |
rs551249457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038839 | AAAAAATTAGCCGGG[C/T]GTGGTGGTGCATGCC | 26524 |
rs551296117 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986339 | TTTATTGCAGCACTA[A/C/T]TCACAACAGTAAAAA | 26524 |
rs551332040 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987078 | TAGGCACCTGTAACC[C/T]CAACTACTCGGGAAG | 26524 |
rs551359225 | in-del | -/AAAAAAA | 0.4021 | 0.198407 | intron-variant | LATS2 | GRCh38.p7 | 13:20993036 | TGTGACTCCATCTCC[-/AAAAAAA]AAAAAAAAAAAAAAA | 26524 |
rs551406734 | snp | C/T | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061602 | ACGTGACCCCGCCTC[C/T]CGCGTCACTCTCGGC | 26524 |
rs551442958 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015351 | TCACACTGCAGACAC[A/G]CGAAGGACCAGGACC | 26524 |
rs551449464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043595 | GAATTATTTCAAGGG[C/T]ATTAAATATGGTAAA | 26524 |
rs551479376 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20985968 | AGAATCACTTGAACC[A/C/T]GGGAGGCGGAGGTTG | 26524 |
rs551483365 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018260 | GAAAATAAGTGAAGG[C/T]AAGTTTCCTTCAGAC | 26524 |
rs551495458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21006050 | GCTGAGGCAGGAGAA[C/T]CGCTGGAACCCGGAA | 26524 |
rs551504920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20998181 | GCCTGGGCAAGACCC[A/G]CATGTTTGTAAAAAG | 26524 |
rs551513634 | snp | A/G | 1.74269e-05 | 0.00295181 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046056 | CCTTTTACCATAAAT[A/G]CAATCTTCTTAAAGT | 26524 |
rs551531128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21031950 | ATATTTGTAATAGCT[C/T]TTTAAAAATTGTTTA | 26524 |
rs551532523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999531 | TGGAGTACAGTGGCT[C/T]GATCAGGGCTCATTG | 26524 |
rs551641202 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009738 | CATAACAGACGACAA[A/T]ACACCAAGTACATGC | 26524 |
rs551687441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033302 | GCGAGAGAACACACG[A/C]TCCTGGTGTAGAGGA | 26524 |
rs551801241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044459 | CAAAAATACTTAGCT[C/T]ATTTCCGCTTCATGC | 26524 |
rs551897602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992705 | AGAACGGGGAGCTCC[A/G]GAAAGGAGTCCACAG | 26524 |
rs551959499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21010551 | CAAAAAATCAAATAG[C/T]GCAAATAACATGACT | 26524 |
rs551964950 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024089 | GTTAAAGTGTCTCGC[C/T]GTGCAAAAAAAAAAA | 26524 |
rs551986742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986427 | TGTACACCATGGGAT[A/G]CTATTCAGCCATAAA | 26524 |
rs552001556 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062569 | AGACTGGAAGCCAAA[A/T]CCTCAGTCTACTTCT | 26524 |
rs552043630 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:21011181 | CATGGCCGTTTCTAC[C/T]TCCTCTCATCTCTTT | 26524 |
rs552045516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21003693 | GTGATCCAGCCACCT[C/T]GGCCTCCCAAAGTGC | 26524 |
rs552052608 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21017327 | TAGAGGTGATGCAAT[A/C]CTTTTTCTTTTTTTT | 26524 |
rs552105102 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012190 | AAAGATAATGTAAAA[A/T]TATCATATAAAAGAT | 26524 |
rs552115382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981115 | GTTAAAGCTAGAGCC[C/G]GGAAATGTGTGGTCT | 26524 |
rs552128755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060813 | GACGATGGCGCGGCC[C/G]GGAGGATGGCCCCGG | 26524 |
rs552137582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991076 | GTGTCCCACGGTCTA[C/T]CACTTGGGGCTGCTC | 26524 |
rs552156184 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LATS2 | GRCh38.p7 | 13:21036767 | GACAGAGCAAAACTC[C/T]GTCTCAAAACAACAA | 26524 |
rs552219249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20978566 | AAAGAAACTGCTTTC[C/T]TTAGATACAGTTGAC | 26524 |
rs552242148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030515 | AATGGCGTGAACCTG[A/G]GAAGCGGAGCTTGCA | 26524 |
rs552354828 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21017868 | TGACCTCAGGTGATC[C/T]GCCTGCCTTGGCCTC | 26524 |
rs552484245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048786 | GGGTTGCAGTGAGCC[A/G]AGATCGCACCATCGC | 26524 |
rs552501186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20990003 | CATTTCTTCAGGCCA[A/G]CTGCTCCACTTGGCT | 26524 |
rs552504876 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055108 | ACAGTGTATTTTAAG[C/T]TTTAGTTTGAAGACA | 26524 |
rs552571264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015007 | CCTAGTGCGCTCACC[A/G]CCGTATCCCTGGGGT | 26524 |
rs552648949 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976179 | ACAAAACCTAGGGGA[C/G]TTCTTTATTGTTTAC | 26524 |
rs552663038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048227 | GACAAAAACGGAGAG[C/G]TTCTCAAGGTGATGC | 26524 |
rs552677788 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:20997424 | GCACTTTAACAAAAC[A/G]GCGAGGTGGCTGAGG | 26524 |
rs552688504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21054963 | AGGGATACCACAAGG[A/G]CTGTCCCTGTCTTAA | 26524 |
rs552699585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041468 | CTCATTCCATTAAAG[A/T]TTTAAATCACTTAAA | 26524 |
rs552717871 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032696 | AAATAATCCCTAAGA[A/C]CCTGAGAGGCCTACC | 26524 |
rs552731941 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21009761 | GTACATGCTGTGAGC[A/C]CACAGGGCAGTGAGG | 26524 |
rs552759237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20996407 | TTTTTGAGACAGAGG[C/T]TCGTTCTGTCCCCCA | 26524 |
rs552764888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997917 | CACTCAGCCCTTCCT[C/G]GTAAGGAAGCATTTT | 26524 |
rs552826015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002397 | TTTTTTTTTTGAGAC[A/T]GGGTCTCACTCTTGT | 26524 |
rs552839901 | in-del | -/CTCA | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21016806 | TTCATCAGAAAACCT[-/CTCA]CTAATAAAACTCCAC | 26524 |
rs552918007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21036130 | CGAACACCCGACCTC[A/G]GATGATCCACCCCCC | 26524 |
rs552943347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048371 | TCTTCCCTTTCTTTG[A/C]AAACTAAAATAGAGA | 26524 |
rs552943884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991529 | CTGCTGAGAACCTGC[A/G]ATATGCTGCAGGAGA | 26524 |
rs552958488 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054492 | GGTAGGATATAGCAG[A/G]GCAAAGTCTCCACGT | 26524 |
rs552989811 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21055637 | TTATTCTAATTTATC[C/T]TAGTGCTTCACAAAC | 26524 |
rs553125922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041854 | GGCACCATCCTGAGT[A/G]CTATAATTAAGAACA | 26524 |
rs553149814 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978732 | ATGATCCACTTTCAA[C/T]TATTAAAATAGTAAA | 26524 |
rs553211776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035872 | AAGTCATTCAGGGAG[C/G]AGAGAAAAGGCATTT | 26524 |
rs553222608 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019132 | TCTGTATTTCCATTT[A/C]CTCCCGTGTACCTAA | 26524 |
rs553253473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21037754 | AGTGGGCCTGGTCCC[A/G]CAGCAGGGCCAGCAC | 26524 |
rs553313431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21027617 | AATGCCACACTGTCT[G/T]GCTTAGCTTTAGAGA | 26524 |
rs553327304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041117 | AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC | 26524 |
rs553332344 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21050022 | CTACTCGGAAGGCTG[A/C]GGCAGGAGAATCCCT | 26524 |
rs553366032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035368 | TGTTGGTTTTTCCCC[C/T]ATTTACATCCTTGTT | 26524 |
rs553407852 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981050 | TCCAACGCTGTCACA[C/T]AAGCACCCAGCTGCA | 26524 |
rs553420114 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21002103 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 26524 |
rs553422477 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061967 | GGACACTAAAAATAG[A/G]GGCAGAAAAGGACAG | 26524 |
rs553437782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21021515 | AAAAAGCTTTGTAAA[A/C]GGCATTTCTGATATG | 26524 |
rs553445318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21034533 | TGGTGCACGCCAAGA[C/T]GGAGTCACTTGCTAA | 26524 |
rs553495557 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982594 | AGGATTACAGGCGTG[A/G]GCCACCATGCCCAGC | 26524 |
rs553519964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022104 | GGAGCTCTGAAAAAT[A/C]CCAATGCCCAGAATC | 26524 |
rs553572412 | in-del | -/AGG | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024342 | TGAGGAGACTGAGGC[-/AGG]AGAATTGTTTGAACC | 26524 |
rs553597183 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997536 | ACCTCCCCATGGGAT[-/G]GGTCCAGGCCTCTGT | 26524 |
rs553650202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022958 | CACTCTCCAGCTGGA[C/G]GCTTGGGCAAGGGTG | 26524 |
rs553678999 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21060221 | GGTTTGCTCCAGGCC[A/G]CACTCCATCCCCGAG | 26524 |
rs553693379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015055 | ACTGCTGGCACTCAC[A/G]TGTGGGCTGAGGCAA | 26524 |
rs553713313 | in-del | -/G | 0.00319297 | 0.0398282 | intron-variant | LATS2 | GRCh38.p7 | 13:21007571 | ATATATATATATATA[-/G]TATATATATATATAT | 26524 |
rs553736731 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975062 | GTTATTGGGCGAGGT[A/G]AGTGTGTCCCAGGCC | 26524 |
rs553868746 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20982695 | CTTGTAGCCTACTGT[C/T]TTAAAAATATAGTAG | 26524 |
rs553881824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21006804 | ACTTTTTAAGAGAGT[A/G]GCTGTGCATGTTTGG | 26524 |
rs553993614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20977172 | AGGCTGAGGTGGGTG[A/G]ATAACTTGAGGTCAG | 26524 |
rs554023070 | in-del | -/AAC | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047578 | TTTTAATAAACGAAG[-/AAC]AACTGATCCAAAAAG | 26524 |
rs554032036 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:20998542 | ACCCAAAGGCCTAGA[-/T]TTTTTTATGAGAACA | 26524 |
rs554053954 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018400 | CAAGGGTTGACATGG[A/T]AAAACAAAATTCTGC | 26524 |
rs554129253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057791 | GGTGACAGAGCGAGA[A/C]TCCATCTCAAAAATA | 26524 |
rs554137824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21001542 | TTCAGTCCTCAGATC[A/G]CACCATGGTTGGAGA | 26524 |
rs554178460 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | LATS2 | GRCh38.p7 | 13:20998518 | GGTGGTCTTCAAAAG[-/A]AATCTCTGACCCAAA | 26524 |
rs554182417 | in-del | -/GGC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042760 | TGGGAGGCCTAAGAG[-/GGC]GGCGGATCACAAGGT | 26524 |
rs554221066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022710 | GAGAGATGAGGACTA[G/T]GAAGCAAACACACAC | 26524 |
rs554244935 | snp | A/G | 0.000131785 | 0.00811635 | missense | LATS2 | GRCh38.p7 | 13:20983401 | CTGCGATGTAGAACC[A/G]GGCCAGGTGCTCAGG | 26524 |
rs554256304 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041495 | TAAACATGATAAAGT[G/T]GGGGGAAAGAACTGG | 26524 |
rs554306645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015955 | TTGCCCACCTCGGCC[A/T]CCCAAAGTGTTGGGA | 26524 |
rs554338611 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047129 | ACCTACCCCAGGCCT[C/T]GTTCACGGCCTACTC | 26524 |
rs554343737 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20978193 | GTGCTGGGATGACAG[C/G]CATGATCCACCACGC | 26524 |
rs554376526 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:21039990 | AGGCAGGAGAATCAC[C/T]TGAATCCGGAAGGCA | 26524 |
rs554430832 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999749 | AGACATGAGCTAGGG[C/T]GCCTGGCCTTAAATT | 26524 |
rs554443783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041937 | CCCCCTATAACCCAC[G/T]GCAACCAGAGAGAAA | 26524 |
rs554464191 | in-del | -/TCCACGACCTTG | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20998969 | GCCCTGGTGACCTTT[-/TCCACGACCTTG]TCCACGCAGGACAGG | 26524 |
rs554489329 | snp | A/G | 6.59272e-05 | 0.00574101 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988100 | TTTGTCCCCCTTGGC[A/G]CTTTTGCGGCTCTTG | 26524 |
rs554522440 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063561 | CCAGTCAAGGGGTAG[A/G]AAAATGAAAGGTAGA | 26524 |
rs554533135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21048553 | TACCTACTCAAGGCT[A/G]GACGTGGTGGCTCAC | 26524 |
rs554654666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20978060 | AGCTGAGACTACAGG[C/T]GCCCGCCCCCATGCC | 26524 |
rs554756335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995293 | TGTATTCTTCTTACA[A/G]TAATTATACAAAGAA | 26524 |
rs554765648 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21007568 | ATATATATATATATA[G/T]ATATATATATATATA | 26524 |
rs554774789 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053167 | TTGAACCCGGGAGGC[A/G]GAGGATGCAGTGAGC | 26524 |
rs554793199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995840 | TTAATGCTCTTTGAA[G/T]GTGTGTATCATGCAC | 26524 |
rs554795068 | snp | C/G | 0.000399281 | 0.0141238 | missense | LATS2 | GRCh38.p7 | 13:20988318 | CCAGGGCATGCTCCT[C/G]CTTGGCGTCCAAGCC | 26524 |
rs554883193 | snp | A/G | 3.73804e-05 | 0.00432305 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988736 | GTTCCGCGAGGGAGT[A/G]AGCAGGCTCTGCGGG | 26524 |
rs554885637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21002805 | TCAAACTTCCTGCCT[C/T]GGCCTCCCAAGTAGC | 26524 |
rs554936240 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:21045520 | GTAGAGAACCTTCAA[C/T]TGTGAGTTCAATTAT | 26524 |
rs554940742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996612 | TCTCGAACTCCTGAC[C/T]TCAGGTGATCCACCT | 26524 |
rs554954951 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045078 | TCCACTAATGTATCC[C/T]TTAATCCTAAACAAC | 26524 |
rs554974342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21038911 | CTTGAACCCGCGAGG[C/T]GGAGGTTGTAATGAG | 26524 |
rs554986663 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022301 | ATGTGTGTGTGAGTG[C/T]GCATGTGTGTGAATA | 26524 |
rs554993272 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21007115 | AAAACTGAAATTCCC[A/T]GGCTATGCAGTTTTT | 26524 |
rs555002794 | in-del | -/A | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024691 | CTTATACCCACATTA[-/A]AAAAAAAAAAAAAAG | 26524 |
rs555005646 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21038269 | GCTTCCGAGGAGAAC[C/T]GACTGGGGTGATCTG | 26524 |
rs555014005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21014193 | CAGGGGGAAAGGCGC[A/G]CAGGTCACTCCCAGG | 26524 |
rs555181985 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039290 | CGCGTGTTCAGTAAC[A/G]CCAAACGGTGGTTCC | 26524 |
rs555248008 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LATS2 | GRCh38.p7 | 13:20987826 | TGTGCGTGCTTCCTA[C/T]TGCCAGTAGAGGGAT | 26524 |
rs555256727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028442 | TCCTTTGGGTATATA[C/T]CCAGTAATTTATTTT | 26524 |
rs555283356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20982784 | ATCACCTGAGGTTGG[A/G]AGTTTGAGACCAGCC | 26524 |
rs555305837 | in-del | -/AG | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992530 | GAGCTGTAGGCAAAC[-/AG]GGAGGGTGAGCAGAG | 26524 |
rs555313062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21027111 | TATATATTCCAAATG[A/T]GAGTCCATTGTCAGA | 26524 |
rs555349755 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990246 | GGCCTTCCCTTTGAG[C/G]TGTGCTCTAAGGCCT | 26524 |
rs555427580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21018333 | GGGTGTTGGGCGAGG[C/T]ATGTGGCAATACTGA | 26524 |
rs555455265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20993781 | ACTTCGGGAGCTATG[C/T]GATGAGATCACGTCT | 26524 |
rs555456321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032965 | CAGGAAGGCTGGGCC[A/G]GTACAAGAAATAAGT | 26524 |
rs555476802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20987411 | TGTCAACTAAGGTAT[A/G]TTTAAATCATTAGTT | 26524 |
rs555491016 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21026553 | TTGCTATTACAAATA[A/G]AACTACTATAAATAT | 26524 |
rs555584783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980682 | CAAGGTTATTCACAA[C/T]CTCTCAAGGTCGTTA | 26524 |
rs555613521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21056430 | ATTATATTTTTATGA[C/T]ATACATTATGCAAAT | 26524 |
rs555643554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044940 | GCTATGTTGTCCAGG[C/G]TGGTCTCAAACTCCT | 26524 |
rs555649985 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979484 | GATATTAAAATGGGT[C/T]CAATTCCATGGCTTT | 26524 |
rs555669004 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21058543 | AAGAAAGCCCCTCCC[A/G]CCAACCCTGTGATTT | 26524 |
rs555677766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020766 | AGCTGACAACTACCC[G/T]ACATGGAACAGGCAA | 26524 |
rs555694526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004691 | TTTGCTCTAATAGCA[C/T]CATGGGGCTGTTCAA | 26524 |
rs555729930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033055 | GAAAAGTCCACCCGG[A/G]GAATTACTGGGTCAG | 26524 |
rs555790541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051210 | AAGCCCTCTTATATG[C/T]AGGGCCCTTGAGCAG | 26524 |
rs555813634 | in-del | -/CC | 0.00953873 | 0.0683987 | intron-variant | LATS2 | GRCh38.p7 | 13:21030150 | GAAAAAAGAAATCCA[-/CC]CCCATGGTCTAATCA | 26524 |
rs555897956 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973595 | TACTTTTTATTTCAA[G/T]GTCATTTTGAAGAAT | 26524 |
rs555901648 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016575 | ATGAACCACCATGCT[C/T]AGCCAGTTCATTCCT | 26524 |
rs555908856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20994383 | CATATACATAGAGCT[A/G]TGTTTTAAACACTGA | 26524 |
rs555923539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057041 | TAAGAATGGAGTTAA[C/T]TAGTAATGAACCATG | 26524 |
rs555929927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058603 | ACTTAAACTATTTCA[A/C]ACTCGATGGAGAAGC | 26524 |
rs555987373 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018831 | TTGTATTTTTAGTAG[A/T]GAAAGGGTTTCACCA | 26524 |
rs555991390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21059249 | TTTACCGGCCAAATG[C/T]ATACTCTATGGCTTA | 26524 |
rs556050198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21052955 | AAAAACCGAACGCTG[A/G]GCCGGGCACGGTGGC | 26524 |
rs556095477 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973269 | AAATGTAAACCAGTA[C/T]ACAGGAATCTTTATT | 26524 |
rs556103933 | in-del | -/CAAACAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010196 | GGAGCTAGACTCTGT[-/CAAACAAA]CAAAAAAACAAACAA | 26524 |
rs556120924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999070 | TCCACGCGAGGCAGG[C/G]GCCCCGGTGACCTTG | 26524 |
rs556133756 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992993 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC | 26524 |
rs556154074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20976327 | GTAGTTGTTTTCATA[A/G]AGCTAAAACTGTAGA | 26524 |
rs556174301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991918 | TGCTGGCTATAGCAG[C/T]GGAGGACTGGCCCTT | 26524 |
rs556222834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21018723 | CAGTGGCTCGATCAC[A/G]GCTGACTGCAGCCTC | 26524 |
rs556241233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21027481 | AAAACCCTCAACCTC[C/T]GCCCTTTTCCTCATT | 26524 |
rs556262632 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039907 | AGTGAAATCCCATCT[A/C]TACTAAAAATACAAA | 26524 |
rs556277999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020835 | CCATCCCTGCTGTCA[C/T]GTGGCACAGATGAGC | 26524 |
rs556280576 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059574 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACAAC | 26524 |
rs556305690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21012848 | AGATGAACAAACTGA[A/G]GCTAAAATAGATTAG | 26524 |
rs556343031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982242 | CTATAGGAAATGGAG[C/T]TCAATGATACACTAC | 26524 |
rs556394962 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050913 | GCCCTGGCCCACGCA[C/G/T]AGACATGCCATGATA | 26524 |
rs556410769 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994551 | TGTCAGAGAGATGCA[A/G]CTGAAGCCTGGCCGA | 26524 |
rs556475454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014247 | TCTCCCAAACCCAAG[C/G]CCTTTTCTTCTTGTT | 26524 |
rs556476351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025783 | GAGGAAGTGAAATTA[C/T]TGCTGTGACCCCTCA | 26524 |
rs556488457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986507 | ATTATGTTAAGTGAA[A/G]TAAGCCAGGAACAGA | 26524 |
rs556580210 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046182 | TTTTTGTAGTTCCTA[C/T]AGAGAACCTAAAATT | 26524 |
rs556592825 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974077 | AGATACAATCATAGC[A/G]AAGAGGTCACCCGCA | 26524 |
rs556612943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21000148 | ACACTTTGGGAAGCC[A/G]AGGCGGGCAGATCAC | 26524 |
rs556644690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21057128 | TCCAAACAGAGGCCC[A/G]CTCCTTTCAAAATCC | 26524 |
rs556659230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049694 | AAGAACCATGAGAAA[A/G]TTCCATGTTAAAGCC | 26524 |
rs556685768 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21003846 | CCCAAAGTGCTGGGA[A/G]TACAGGCATGAGCCA | 26524 |
rs556717433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051257 | CCACACAAGGTGACC[C/T]TGTTACTTGGTCCTG | 26524 |
rs556813627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999684 | GCTGGTCTCAAACTC[C/T]GGAGGCCAAGCCATC | 26524 |
rs556878886 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008269 | TGCTGGGGTTCTCAA[A/G]AGGCACCCCCTGCTC | 26524 |
rs556884470 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20986778 | GAAATGCTTCCAACA[A/C]AGAAATGATAAATAC | 26524 |
rs556902823 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21031623 | TTGGGAAGTTGGGGA[G/T]GGGGAGCATGGGATC | 26524 |
rs556959253 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035049 | CAGCCCGAGAAACAT[A/G]GCAAGACTCCATCTC | 26524 |
rs556962321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21036351 | GCCCATTTTAACAGG[A/G]AAGTGGGTCCAGTCT | 26524 |
rs557008254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004475 | ATGCAAGGGAGAATC[A/C]AATTTTAACAGTATA | 26524 |
rs557021352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20980301 | TGTGTGAGGCCCCTA[C/T]GGAGCCGGGCCTTCC | 26524 |
rs557071469 | in-del | -/G | 0.0111196 | 0.0737302 | intron-variant | LATS2 | GRCh38.p7 | 13:21007632 | TATAGTGTATATATA[-/G]TATATATATATAGTG | 26524 |
rs557188038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030229 | TCAACATGAAATTTG[A/G]GTGGGGACAAATATC | 26524 |
rs557205673 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062848 | CTCTTCCAGGGAATC[A/T]TCTCAGATCTCTGTT | 26524 |
rs557221090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20984613 | ATCTAGGAGTAAATT[C/T]AACCAAAAAGTGAAA | 26524 |
rs557228690 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054760 | GGAGTCCTGGTTTTT[C/T]TTTCTTTTTCCATTC | 26524 |
rs557306332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032135 | GATAAAAACAATACT[C/G]TTGATAATACGTTGC | 26524 |
rs557328304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050558 | GCCTGTCAGTTGTCA[C/T]TGCTGCGTAATATCC | 26524 |
rs557415932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997288 | CTTTCCCAAGAGATT[C/T]CTCCTCTTACATTTT | 26524 |
rs557485224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030667 | CATTTAACTCCCCCA[A/C]CTCATAGTGTTGTAT | 26524 |
rs557501002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037893 | GGTCCTGTCCGCCAA[C/T]TCCCAGGCACCATCC | 26524 |
rs557580553 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002924 | CTAGGCTGGTCTCAA[A/T]CTCCTGGCCTCAAGC | 26524 |
rs557626358 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | LATS2 | GRCh38.p7 | 13:21016929 | TAAAACCAACTTGCC[C/T]GATCCATGGCCATGC | 26524 |
rs557690171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037135 | TAGGACCGGGTGTGG[A/C]GGCTCAGGCCTGTAA | 26524 |
rs557727692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20987385 | AATAATTACCTTCTT[C/G]AGCACTTCAGTGTCA | 26524 |
rs557750303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21019006 | CCACTCTCTCACGCC[C/T]CTGTCCTGTAAATGG | 26524 |
rs557770320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044797 | GTGCAGTGGCTATCA[C/T]AGCTCACTGCAGCCA | 26524 |
rs557778141 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21030810 | TACTTATTGATATCT[A/C]CTGTTTCTAGTGCTC | 26524 |
rs557813856 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974217 | GAACTCTGCTCATGC[A/G]GTACTCTCCACACAC | 26524 |
rs557832520 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20989993 | AGGTTCCTTTCATTT[C/T]TTCAGGCCAACTGCT | 26524 |
rs557858237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038228 | TGGAGCCTGTACCGG[A/G]GGCAGGAGAGGCCAG | 26524 |
rs557866448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992917 | GTGTGTGCCTGTAGT[C/T]CCAGCTACTCAGGAG | 26524 |
rs557947078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21032283 | TTTTATTTTATTTTT[C/T]GAGACAGAGTCTCGC | 26524 |
rs557953841 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024370 | GAACCTGGGAGGCGG[A/T]GGTTGCAGTGAGCCG | 26524 |
rs557964787 | in-del | -/TATTAT | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:21058787 | GTATATTCATTACAC[-/TATTAT]TATATTCAGTGCCTT | 26524 |
rs557974436 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007065 | AGGTAATTCGGTAAA[A/G]TATACAAATATTTTA | 26524 |
rs557998826 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063062 | ATTCTGCAATTGAGC[C/T]CTACTGGCATTACCT | 26524 |
rs558040600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017651 | TTTGTTTTTGAGATG[C/G]AGTCTCACTCTGTCA | 26524 |
rs558056698 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972623 | CCCAAAGTGCTGGGA[C/T]TACAGGTGTGAGCCA | 26524 |
rs558211640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009553 | AAAATGTAGGTAACA[A/C]ACACATATATGTGGG | 26524 |
rs558220608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022867 | ATTATTTCCTGCTTT[A/G]AAGGAAATAATCATG | 26524 |
rs558240095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20985425 | AACAGCAAAAAAAAT[A/G]TCAAATAATCCCATT | 26524 |
rs558297682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009933 | GGCCAGGCGTGGTGG[C/G]TCATGCCTGTAATCC | 26524 |
rs558310599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21016060 | AGTGGTATGATCTCG[G/T]CTCACTGCAACCTCC | 26524 |
rs558331566 | snp | A/C | 5.38228e-05 | 0.00518734 | intron-variant | LATS2 | GRCh38.p7 | 13:20979801 | GTTGAGTGTACCCTG[A/C]AAGACAAAGTTCACT | 26524 |
rs558338359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002868 | TAACTTTATTCTTTA[A/C]TTTCTTTTTCATTTT | 26524 |
rs558365937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980226 | GAAGCTGAAGAATAC[A/G]GAGATGAGGAGGAGG | 26524 |
rs558374890 | snp | C/G/T | 5.05029e-05 | 0.00502483 | missense | LATS2 | GRCh38.p7 | 13:20983791 | TCTGCTCCTGCTCAG[C/G/T]TTCACAGAGTCCAGC | 26524 |
rs558405378 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973477 | CACTTTAAATAGGAA[A/T]CATACTAATTTGAAA | 26524 |
rs558417482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20979986 | GGGGGGCGGTGGCCA[C/T]GGCCGCTTAGGTTTT | 26524 |
rs558519071 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050162 | GATACATACATACAT[A/G]CATACATACATAGAT | 26524 |
rs558527530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053452 | ACGAGGGCAGGAGCA[C/T]CCTGTTTGGTTTACC | 26524 |
rs558576354 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061124 | GGCTCCGTACGGCCT[A/G]GACTACGAGCCGCCG | 26524 |
rs558600757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21016697 | TGCAAATACCAAGGC[A/G]CCAAGAGCAGCCTCT | 26524 |
rs558620215 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993648 | GTGGCGCCTGGACTA[C/T]CAGAAAGGGCAAGTG | 26524 |
rs558626555 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018231 | AGTAAACACTTAATT[A/T]AAAAATACTGTATGA | 26524 |
rs558636651 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061907 | GTGAAAGAAAAAAAA[A/G]AGTTAGCAGGCCTGA | 26524 |
rs558638496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21054356 | GGGGCTGCTGTGAGC[C/T]GAGGTCATTCCACTG | 26524 |
rs558708168 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022027 | AGTATAGTGGGCCCT[G/T]GGTGAAATAGAAAGA | 26524 |
rs558710384 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048457 | TACGCAGAGAGTTTC[C/T]TCATGCTCAAAATAC | 26524 |
rs558719074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21047799 | TCTATTGCACAACCA[C/T]ATGCAATAGCAAACA | 26524 |
rs558746237 | snp | A/G | 0.000399281 | 0.0141238 | missense | LATS2 | GRCh38.p7 | 13:20988870 | CGGCAGGGGGTGGGA[A/G]AGCGAGGCCGGCGCC | 26524 |
rs558783218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20989353 | GTGGGTGTGATCAGT[C/G]GGTTCTGGCACTTCC | 26524 |
rs558806883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040988 | TCACCTTTTTTTTTT[C/T]CTGAGGCAGAGTCTC | 26524 |
rs558817250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995887 | ATTATTTACAGAGTA[A/G]TGTGGTAGGCTAACA | 26524 |
rs558835648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043051 | AACAATAAGAACTCT[C/T]GGCCAGACGTGGTGA | 26524 |
rs558887111 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001926 | TTTAAAAATCCATTT[A/T]TTTTTGAGGCGGAGT | 26524 |
rs558914733 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986562 | GTTACTGATATGTGG[A/G]AGCTAAAATAATTGA | 26524 |
rs558918989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001093 | TCCAGATCACAGTTG[G/T]GTCCAATAAAATGGC | 26524 |
rs558924243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002249 | CACTAAAAATTCTGG[A/G]ATGGTCTAAGATGGT | 26524 |
rs558950227 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024036 | CAGGCATCCTCGGGA[-/AG]GGCCCCCCAGGGAGT | 26524 |
rs558953069 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004395 | GCTGAGATTGCGCCA[C/T]TGCACTCTAGCCTGG | 26524 |
rs558962736 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981846 | GGAGACACACGTGGT[A/G]AGGTTGGCGCTAGCA | 26524 |
rs558991048 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20978376 | TCTTAATTTCAATTC[G/T]CAGTTCAACCCTTAG | 26524 |
rs558996619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008711 | GTTGGCAAAGTTAGA[A/G]AGATGCTGCATTTTG | 26524 |
rs559008005 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21047998 | ATATAGTAAAGTCAC[A/T]GAAATGACTGTAAGA | 26524 |
rs559154058 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21035271 | GTGGCATTTTTTTTT[A/T]AATTTTGAAATTCAT | 26524 |
rs559238694 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023842 | GCTGGGCATGGTGGC[G/T]CATGCCTATAATTTC | 26524 |
rs559241324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21029003 | TTAAAAATAGATTCC[C/T]TAAGGTGTTCTATAA | 26524 |
rs559251927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20977503 | TAATGGGTTTGGGAC[A/G]ATTAACACATTTGAA | 26524 |
rs559272876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029811 | AGAAAAAAAAAGATA[C/T]TGGGGATGGGCGTAG | 26524 |
rs559305508 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056330 | GGGCATGAGCCACCA[C/T]GCCCAGCCAGAGTAT | 26524 |
rs559402934 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028482 | TGTGATCAGCAATGC[C/T]TTGCAGTTTTAAGTG | 26524 |
rs559437393 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062264 | GGTGACCTGAGATCG[C/T]ATCATTGCACTCCAG | 26524 |
rs559458842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042138 | AATATTAATCTAGTG[C/G]CCTAGTTTTTTTCTA | 26524 |
rs559496348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20977769 | AAATTTTATGTTATG[C/T]ATATTTTACCAGAAT | 26524 |
rs559501188 | snp | A/T | 7.43025e-05 | 0.00609473 | missense | LATS2 | GRCh38.p7 | 13:20988518 | AGGGAGGGCTCGGCC[A/T]TGCCAGGCGGACCGG | 26524 |
rs559512362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20990672 | AATCCTTTATCACAC[C/T]CCAGGGGCCTCAGGT | 26524 |
rs559528505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21030361 | TTGGGAGGCCGACAC[A/G]GGTGGATCACGAGGT | 26524 |
rs559548036 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:20993770 | CACCACCGCCTACTT[C/T]GGGAGCTATGCGATG | 26524 |
rs559576917 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049328 | AAGGTGGGCTTAGAA[-/G]GGACAAGTGCAACAC | 26524 |
rs559613965 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050223 | AAGGCTTTTGGGGGT[A/G]GAGGGGGTAGGGGCA | 26524 |
rs559728235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20979144 | CTAGCTTGCTTTATT[A/G]TAAGAATACAGGATC | 26524 |
rs559750580 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978480 | AACTACTTTGAATGA[A/G]TATTAGGAATATGCA | 26524 |
rs559766240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020893 | GCCACGCCAGACTGG[A/T]CCAAGGACACACTCT | 26524 |
rs559818979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028648 | CGATCTTGACTCACC[A/G]CAACCTCCGCCTCCC | 26524 |
rs559857800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21052389 | AGAGTCTCACTCTGT[C/T]ACCTAGACTGGAGTG | 26524 |
rs559859246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014786 | ATGTTTGTTGAGTGG[C/T]TTAAGTTTACAGATT | 26524 |
rs559896560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046559 | TTTATTTTGAAACCC[A/G]CAGCTTGAGGAGTAT | 26524 |
rs559909612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029073 | CAATCTGTGTACTTT[C/T]ATTTCTTTTTTCTTT | 26524 |
rs559909696 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21021779 | CAGTCTGTTGTGAAC[A/C]GTGCTGCTCCTGGGG | 26524 |
rs559962380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058662 | CAATGATTCTAGTAA[C/T]TCACCTTGGTAATTT | 26524 |
rs559972368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20985600 | AAAAATTAGCTGAGC[A/G]TGGTGTCGCACACCT | 26524 |
rs560006986 | snp | C/G | | | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045812 | AAGGCTTTCTGATAA[C/G]GTCCGAACTTTGGGG | 26524 |
rs560008957 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011172 | TATCAGGACCATGGC[A/C]GTTTCTACCTCCTCT | 26524 |
rs560018845 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LATS2 | GRCh38.p7 | 13:21053992 | TAGACAGTGGTGATG[C/T]TTGCAGTAATGGTGC | 26524 |
rs560027449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21054393 | AGCCTAGGCAACAGA[C/G]CAAGTCTCCACCTCA | 26524 |
rs560030542 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998644 | GAGGCCCTCCGGGCC[C/T]AGGCCTCCTCTAACC | 26524 |
rs560071015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014131 | GTAGGAAAAACAGAT[A/T]AAAGTATTTTTAAAA | 26524 |
rs560087218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21005046 | CATGGGAAGGACCAT[G/T]TTGGTCCCACAGAAG | 26524 |
rs560117512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20998711 | CTCCCGGCGATCTTG[A/G]GCAGGTGGGGCCCCA | 26524 |
rs560123366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21005851 | GGCGCAGTGGCTTAC[A/G]CCTATTAATCCCAGT | 26524 |
rs560130640 | in-del | -/CGAGGCGGGGCGGGGC | 0.135825 | 0.222405 | intron-variant | LATS2 | GRCh38.p7 | 13:20998745 | CTTGTCAATGCGGGG[-/CGAGGCGGGGCGGGGC]CGAGGCGGGGCGGGG | 26524 |
rs560140437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013331 | TTATCCTGGCTCGAT[C/G]CCTAATAATAATCTC | 26524 |
rs560193438 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993121 | CGTGCAGGGCTGCTC[C/T]GCAGCAGGAAGCCTG | 26524 |
rs560253789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20975859 | CGGCTGATTTTTGTA[G/T]TTTTAGTAGAGACAG | 26524 |
rs560274366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21006546 | ATGAACAGATTAAAT[A/G]TGACTCCGGAAGAGC | 26524 |
rs560310012 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21032678 | AAAAGATTGGACACC[C/G]CTAAATAATCCCTAA | 26524 |
rs560325756 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017053 | CCGGAAACAAATTCA[C/T]CTTCATTAGTGCTTC | 26524 |
rs560326450 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21036139 | ACCTCGGATGATCCA[-/C]CCCCCCTCAGCCTCC | 26524 |
rs560347393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033140 | AAAAAAAAAATAGCA[A/G]GCCACCGGAGAAAGT | 26524 |
rs560349442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026272 | CCCTTTATAGTACTC[A/C]CTCCCTCCACCCCAC | 26524 |
rs560362821 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21040133 | GGCCCACGCCAGTAA[A/T]CCCAGTACTTTGGGA | 26524 |
rs560390834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000711 | TACACTTACCACAGC[C/T]AGAAATAATACTTTC | 26524 |
rs560437020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026752 | TTTGAGCCCAGGAGA[C/T]GGAGACCAGCCTAGG | 26524 |
rs560463239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001235 | GAGGTAAGCACATTC[C/T]ACAGAAACTTAATAT | 26524 |
rs560472376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995437 | GTGAGCAGCCCTGCC[C/G]CAAAGCAAGAGTTCA | 26524 |
rs560509392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025669 | ACCCAGACAGGTTCA[C/G]ATCTTGCCTGACACT | 26524 |
rs560510975 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058043 | CTTCTAGAGGAATTA[C/T]TAAGCAATAGACTTT | 26524 |
rs560535941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20993935 | TCCATCAGCACTAAC[C/T]GTTCAATTGCTTCAT | 26524 |
rs560549738 | in-del | -/A | 0.33693 | 0.2344 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046083 | AGTGTTTTATTATTT[-/A]AAAAAAAAAAACTGT | 26524 |
rs560573366 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052282 | TTTAATGAGGCCAGG[A/G]GATAAGACCACGGAA | 26524 |
rs560587358 | snp | A/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023306 | TCTCACTACGTCCCA[A/T]CCTCCTGCCTCAGTC | 26524 |
rs560601531 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046819 | ATTGCAGTTTCCACA[A/C]ACACATTATGAGACT | 26524 |
rs560665372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20993191 | ACTGAGTGTCCCCCA[C/T]CTCTGGATAGGGCAT | 26524 |
rs560723194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20981204 | AAATCAGGGCTGGAG[C/T]CATTCCCTTGGGTCT | 26524 |
rs560756826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20987082 | CACCTGTAACCCCAA[C/T]TACTCGGGAAGCTGA | 26524 |
rs560798442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008282 | AAGAGGCACCCCCTG[C/G]TCTCACAGGACCTCT | 26524 |
rs560813892 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994581 | AGGAGCTTGGCCACT[A/C]ACCTTCCTTTCTTAA | 26524 |
rs560849629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035456 | AGCCCCCACACAGAA[C/T]TGCATGCAGACTGGA | 26524 |
rs560856965 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038642 | GACAAACTTCATTGG[C/T]TATGACACTGCCACT | 26524 |
rs560858014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047375 | CACAACATCCTCCCT[A/G]TTCTTCACCCCGTGA | 26524 |
rs560859766 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044208 | GCCCTCTATAAAACA[A/G]CAGGATTCATTTCAC | 26524 |
rs560879049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21059589 | GACAGAGCAAGACAA[C/T]GTCTCAAAAAACAAC | 26524 |
rs560918537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20976534 | GAACAGATTTCAAAA[C/T]ATGTATTTGAAAAGG | 26524 |
rs560921050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20999361 | TCTTTTTGAAACGAA[C/T]GAAGAAGAAATTTGG | 26524 |
rs560951362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21052725 | TCTTTTAACTGTAAA[A/G]ACAGAAAAACACAGA | 26524 |
rs560959731 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:20999816 | CTTGCCAATGATCAC[A/G]AGACCAGCCTGGACA | 26524 |
rs561046200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20993990 | TCCTGCAGGGTGAAT[C/T]ACCAGCCTGTGCTCA | 26524 |
rs561061475 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999263 | CCTCCGACCGCTGGT[A/G]GCGCCGCAGGCCCCC | 26524 |
rs561073203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995456 | AGCAAGAGTTCAGCT[A/G]CAAGCCAACTGAAGG | 26524 |
rs561081053 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20994625 | CCAAGCTGGATGTGG[G/T]GGCTCATGCCTATAA | 26524 |
rs561089602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21006349 | CACTCTCTGGCCCTG[A/G]TCCCCAGCGCCCACT | 26524 |
rs561147967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21001820 | GCAGATGGAGGTTGC[A/G]GTGAGCCGAGACAGC | 26524 |
rs561166704 | snp | A/G | 2.47718e-05 | 0.00351927 | missense | LATS2 | GRCh38.p7 | 13:20988615 | CGTGCGCGCGCGGCG[A/G]CGCCTCCAGGCCCGG | 26524 |
rs561166757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996101 | AAGCCTTCTCTTCTA[C/G]ACAGATCTCAATGCT | 26524 |
rs561201579 | snp | A/G | 0.000232693 | 0.0107839 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989021 | CAGGTGCGGCCGCCC[A/G]TAGTGCGCGCCCTGC | 26524 |
rs561242504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038622 | TTAGCAATAATCGCA[A/C]CTTGGACAAACTTCA | 26524 |
rs561288451 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993435 | CACAAAAAACACAGG[C/T]TGTAAACTGTGTTCT | 26524 |
rs561347902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21027666 | TCCAAAGTCAGGTCT[A/C]GCAGTTTTGAAAGTA | 26524 |
rs561368880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21040010 | TCCGGAAGGCAGAGG[C/T]TGCAGTAAGCCGAGA | 26524 |
rs561394363 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034867 | CAAATAAGTCAATTA[C/T]AGAAGATTACAAATT | 26524 |
rs561402991 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991479 | CTCCCATCCCCACTC[C/T]GTGCTGGACTGTGCT | 26524 |
rs561434508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033271 | GGGAGGATGGGAGAG[A/G]ATAGGGGGTAGAGGG | 26524 |
rs561468864 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20987678 | ATCTCTGATTCTTCA[C/G]AAGAGTCAAGGGGAA | 26524 |
rs561488299 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973883 | ACGGACTACAGAAAC[A/G]GACATGTGTCCGTGA | 26524 |
rs561525630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026798 | TCATGTCAATTTTTA[A/G]TTTAAAAAACATTAG | 26524 |
rs561558920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032329 | GGAGTGCAATGGCGC[A/G]ATCTTGGCTCACTGC | 26524 |
rs561580499 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986960 | CACTTGGGGAGGCCG[A/C]GGTGGGCAGATCACC | 26524 |
rs561643646 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21019372 | ACTCTTGTAGCCCAC[G/T]CTGGAGTGCAGTGGC | 26524 |
rs561675205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058720 | TACCTTAAACTGCCT[A/G]AGATTTGGAAAGTTA | 26524 |
rs561684621 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21011900 | GCTACAAACCAGTAC[A/C]GTCCTCACTTAACAT | 26524 |
rs561700164 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017081 | TTCTTACCCAGATTT[C/G/T]TAAGGACTGGGAAGC | 26524 |
rs561780359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21018572 | CAGGAAGACTGTGGT[C/T]GCTTCCCTGATGTCC | 26524 |
rs561780458 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21026053 | CTGGCCATAAAGAGG[G/T]CTGCCCATGAAATCA | 26524 |
rs561786088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017677 | TGTCACCCAGGCTGG[C/G]GTTAGTGGCACCATC | 26524 |
rs561798620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049460 | GCATATGGGACATTT[A/G]CCCGGCCAGAGGCCT | 26524 |
rs561818818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21019110 | TCTAAGGGAGTTCCC[C/T]AATTACTCTGTATTT | 26524 |
rs561966544 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21034408 | CATGACCAAGTAACT[G/T]GGTCCTGACCGGGGA | 26524 |
rs562010784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044093 | TGCTGAAACACTCTG[C/T]ACCACATTACTCACA | 26524 |
rs562045621 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053678 | CAGGTCTAAATGAAA[C/T]GGGCCCAAGGGAGGT | 26524 |
rs562056006 | in-del | -/ACA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009013 | TAGTGTTTTAACAGT[-/ACA]ACAAGGCCCAGGTTG | 26524 |
rs562123639 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063103 | CCACATTTTTTCCTT[C/T]TTTTCTTAGAGACAG | 26524 |
rs562198592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21010996 | GAAGGCTGCAGCTCC[C/G]TGGTTTGCAAACTGC | 26524 |
rs562211177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21057539 | ATCACGTAACAGGCC[A/G]GGCGCGGTGGCTCAT | 26524 |
rs562212349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037470 | GAAAATGTTTATGAC[A/G]TAATGCTTGTCTCTG | 26524 |
rs562249735 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21031072 | TAATGAGAAGTCAGC[G/T]TTTAATCTTATCTTT | 26524 |
rs562356105 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20998634 | CTGGAAGAATGAGGC[C/T]CTCCGGGCCCAGGCC | 26524 |
rs562357909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991947 | TTAGAGATCTGACTC[A/G]TAGAAGAAAGAAAGG | 26524 |
rs562373227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026724 | ACTTTGGAAGACAGA[A/G]GCAAGAGGATTGTTT | 26524 |
rs562406125 | snp | A/G | 3.30551e-05 | 0.00406528 | missense | LATS2 | GRCh38.p7 | 13:20981549 | TGGTGCTGCTTCCGC[A/G]CCCTCTGCTCTAGGG | 26524 |
rs562409462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20976676 | CAAATGACCAATAAG[A/G]ACATGAAAATAAGCT | 26524 |
rs562499048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21018414 | GAAAAACAAAATTCT[A/G]CCCTGGGGCAGATGA | 26524 |
rs562519546 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21013786 | TCCTGGGCAACACAG[C/T]AAGACCCCGTCTCTA | 26524 |
rs562522978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981068 | GCACCCAGCTGCACA[C/T]GGCACAACTCAGCCA | 26524 |
rs562552756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21012699 | GATTTTTTAAGGGAA[C/T]GAGCAGAAAGAGAGG | 26524 |
rs562565936 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974636 | TACTAAATTTTCAAA[A/T]ATATTGTTTTAATGC | 26524 |
rs562574733 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012545 | TGACTGTATTTATTA[C/T]CAGGTGTTTCATTCA | 26524 |
rs562577256 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041011 | AGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTA | 26524 |
rs562584703 | snp | C/T | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21011809 | GTTGTGTGAACATCA[C/T]AGAGTGTACTTACAC | 26524 |
rs562585297 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21016013 | CTATTTTTTTGAGAC[A/G]GACTCTCACTCTGTC | 26524 |
rs562628373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013315 | TGTCCTGGCTCAGTA[A/C]TTATCCTGGCTCGAT | 26524 |
rs562665428 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991021 | AGGTAGGAAGTACTA[A/T]GGTAATTTCAGACAA | 26524 |
rs562666175 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014037 | AGGAAGAGGAGGAGG[A/C]GGAAGAAGGAGAGAG | 26524 |
rs562688659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051404 | TTTGCCCAAAGAATT[A/G]TGGGGATCTGAAATA | 26524 |
rs562725712 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21049938 | CCAGCCTGGCCAACA[C/G]AGTGAAACGCTGTCT | 26524 |
rs562777410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21031829 | CCACTGCACTCCGGC[C/G]TGGGTGACAGAGCAA | 26524 |
rs562783174 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20999909 | GGCACACACCTATAT[A/C]GTCCCAGCTACTAGG | 26524 |
rs562851957 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034553 | TCACTTGCTAAGGGT[A/G]GCAGATAGAGAGAGA | 26524 |
rs562859742 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:21056576 | CAACAGGATGGGCCA[C/T]CTTATATTCAATTTC | 26524 |
rs562864561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032595 | TTTTTTAAGCCCATC[A/G]GCTATCATTAGTATT | 26524 |
rs562950142 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20999278 | GGCGCCGCAGGCCCC[C/G]GAACCTTGGTAAACC | 26524 |
rs562975055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050338 | GCATCCAAATCAAGA[A/C]GTGTATCATTATCAC | 26524 |
rs562991133 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982402 | CCGCAACCTCTGCTT[C/T]CCGGGTTCAAGCGAT | 26524 |
rs562997212 | in-del | -/GGGTAGGGCCAGGGT | 0.00557542 | 0.0525036 | intron-variant | LATS2 | GRCh38.p7 | 13:21037826 | GGTCAGGACCAGGGC[-/GGGTAGGGCCAGGGT]GGGCCTGCCAGCAGC | 26524 |
rs563043181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991061 | GGGCAAGCGCCAGGC[A/G]TGTCCCACGGTCTAC | 26524 |
rs563051772 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21055192 | CATCAGTCAAGACTG[C/T]AGCTGGAAATGAACA | 26524 |
rs563077702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991788 | GAGTCAGGGAACCTG[A/G]CTTTAACCTCAGCTC | 26524 |
rs563083021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992694 | ACTGAAAATGTAGAA[C/T]GGGGAGCTCCGGAAA | 26524 |
rs563108682 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20996986 | GGGCCTGGCAGCCTC[A/G]TCTCTTCTGGAGAGC | 26524 |
rs563171124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20993145 | AAGCCTGGCCATGGT[C/T]ACAGAGCCACTCCGC | 26524 |
rs563206032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21057787 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTCAAA | 26524 |
rs563251089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042845 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGTGCCT | 26524 |
rs563257437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017771 | GCTAGAATTACAGGC[A/G]CCCACCACCACACCC | 26524 |
rs563374637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037275 | CAGGCATGACGGTGG[A/G]TGCCTGTAATTCCAG | 26524 |
rs563405985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060801 | ATTGGCCCGTGGGAC[C/G]ATGGCGCGGCCGGGA | 26524 |
rs563488197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030919 | CCTGGTAACAAATTT[C/T]CTCAGATTTTTGTTC | 26524 |
rs563509784 | in-del | -/AAAAAAAAAAAAAAAAAAG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030594 | GAGACTCCGTCTCAA[-/AAAAAAAAAAAAAAAAAAG]AAAAAAAAAAAGAAA | 26524 |
rs563559579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20979963 | TGGATACTACTGGGT[A/G]GGGTGGTGGGGGGCG | 26524 |
rs563563851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022414 | TTCCTCAAACACAAC[C/T]CCCACTAGCCCCGAA | 26524 |
rs563590445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20977834 | GAGTAGCTCAGCCAT[C/T]CAATTAGGGCGCAGA | 26524 |
rs563732534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21029575 | AGGCAGGCGTATCAC[A/G]AGGTCAGGAGTTCGA | 26524 |
rs563783015 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050271 | ATATTTTTTAAACTG[C/T]ACAGATTGTAAGATT | 26524 |
rs563789247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015736 | ACGGAGTCTCACTCT[A/G]TCACCCAGGCTGGAG | 26524 |
rs563804403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21048770 | TGAACCAGGGAGGCG[A/G]GGGTTGCAGTGAGCC | 26524 |
rs563812379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002270 | CTAAGATGGTTGGTT[A/G]CACAACAGTAGATAA | 26524 |
rs563851245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20978184 | CCTCCCAAAGTGCTG[A/G]GATGACAGGCATGAT | 26524 |
rs563918005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20980321 | CCGGGCCTTCCTCAC[A/G]GGGCTCCCAGCTGTG | 26524 |
rs563949673 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21010093 | AAATCCCAGCTACTC[C/G/T]GGAGGCTGAGGCACG | 26524 |
rs564000375 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010457 | TCCAATCAGCTTTTA[A/G]TACATCACTCCCAAA | 26524 |
rs564048698 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21049302 | GCTAAGGAGTGACAC[A/G]GCCTGAGTGGAAGGT | 26524 |
rs564087389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21017869 | GACCTCAGGTGATCC[A/G]CCTGCCTTGGCCTCC | 26524 |
rs564103508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037341 | CCCCAGAGGGGGAGG[C/T]TGCAGTAAGCCAGAT | 26524 |
rs564217059 | in-del | -/TAG | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21007708 | TATATAGTATGTATA[-/TAG]TATATATATATATAG | 26524 |
rs564235423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025370 | GCACTCCAGCCTGGG[C/T]GACAAGAGTGAGACT | 26524 |
rs564270660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21055145 | TTCATGGCCAAATTA[C/T]GAACTTTTGAAAGAA | 26524 |
rs564281732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023154 | TGCATCGAGGGCTCC[A/G]GGCTCCGAGGGCTCC | 26524 |
rs564314993 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008511 | TGGTTTGGTCTCCTG[A/C]ACATTATGAACATTT | 26524 |
rs564321959 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21049367 | GAGGAGCAGCAGCCC[C/G]GGGGAGCAAGGGGAA | 26524 |
rs564341761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21056635 | AGAAAGCCTTGCCTC[C/T]TCTGCACCCCTCCAA | 26524 |
rs564354969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21018474 | GAAGGGGAAGGGCTG[C/G]CTCCAGCTGGGTCCA | 26524 |
rs564370720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21016424 | GAGTAACTGGGATTA[C/T]AGGTACATACCACCA | 26524 |
rs564391653 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21011860 | CCTACACACCTAGGC[A/T]AGATGGTATAGCATA | 26524 |
rs564403540 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21057320 | TCAAATATTGTCACA[A/C]AAACAAAAAGTATTT | 26524 |
rs564441514 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21031154 | TCTTTGGCTTTCATT[-/A]AGCTTAAATATGATA | 26524 |
rs564494996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20978306 | ATGACCACCAGGGCA[C/T]GTGAAAATTCCAAGG | 26524 |
rs564497921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21050523 | TGCAGATTCATACAC[A/G]TAGTATATATATAGC | 26524 |
rs564509469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008384 | GCCCGCTGGGTGGTG[G/T]TGTTAGAATGACTTC | 26524 |
rs564533148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20978990 | TGGTCTTGAACTCCT[C/G]ACCTCAGGTAATCTG | 26524 |
rs564534763 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21025268 | ATGGTGGCAAGCACC[C/T]ATAATCCCAGCTACT | 26524 |
rs564571455 | in-del | -/ATTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027906 | GAACATACTCTCTCC[-/ATTT]ATTTATTTATTAATT | 26524 |
rs564572675 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062038 | GTTTGCCAGAAGCGG[C/T]GGCTCACGCCTGTAA | 26524 |
rs564586824 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21017022 | AACAACTCCCACAGA[A/G]GAAAATATGGCAGAA | 26524 |
rs564631168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001865 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 26524 |
rs564633560 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21036795 | CAACAACAACAACAA[A/C]AAACAACAACAAAAA | 26524 |
rs564642511 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21010177 | TGCACTCCAGAGTAG[G/T]CCATGGAGCTAGACT | 26524 |
rs564657626 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20991092 | CACTTGGGGCTGCTC[C/T]CGCCAGGGCCTGACT | 26524 |
rs564674771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21003357 | CTCCTAGGTCCAACC[A/G]ATCCTCCTACCTCAG | 26524 |
rs564731829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035576 | CTGTACATGAGTTCC[C/T]GCCTAGATCTCTACA | 26524 |
rs564785282 | in-del | -/AATT | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20978457 | TATTAAATGACTGAC[-/AATT]ATTTAACTACTTTGA | 26524 |
rs564830908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997998 | GTTTGGCTGAAAAAG[G/T]AGAAACGGAGCACTC | 26524 |
rs564837047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041232 | CCGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 26524 |
rs564858742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053719 | CAAAAGTCGCAGAAC[C/T]ATGGCATATTATTCA | 26524 |
rs564882654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047482 | CCGTGCCAAAGCCCT[C/T]AGTGGCTGCCCCTTC | 26524 |
rs564901443 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21001310 | GGTCCTGGATCCTAT[A/T]TTTCTATTCATGTGT | 26524 |
rs564909445 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994664 | CTTTGGGAGACTGAG[G/T]CAGGAAGACTGCTTG | 26524 |
rs565013466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20979196 | TATGTGTTCATTGAC[A/G]CTATGTTACTGGTAA | 26524 |
rs565034655 | snp | A/G | 0.000231252 | 0.0107505 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988148 | GTTGGGGCCCGCACG[A/G]AGGCTCTGCTCCATG | 26524 |
rs565039979 | in-del | -/AAAAATAAAAAAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048839 | CGAAACTCCGTCTCA[-/AAAAATAAAAAAT]AAAAATAAAAATAAA | 26524 |
rs565059647 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022125 | GCCCAGAATCCACCC[C/T]GGACCAATTAAATCA | 26524 |
rs565069404 | snp | G/T | 0.00279162 | 0.0372561 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988391 | CGCGGGCACCCAGGC[G/T]GGGTGCGAGGGCCCC | 26524 |
rs565088291 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21042036 | TGCCAATAACTATCC[A/G]ATGCTCAAAATATGA | 26524 |
rs565104489 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21000490 | TCAAAAGTTATTAAG[A/T]TTTTTTTATCCCGAT | 26524 |
rs565130670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20983899 | CCTGGAACTGAGAGG[A/C]ACCTAGCTCATTTTA | 26524 |
rs565156750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20982876 | CGTGACTGTAATCCC[A/G]GCTACTCGGGAGGCT | 26524 |
rs565212021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20984157 | CAGGCTGGTCTTGAA[C/T]TCCTGACCTCAGGTG | 26524 |
rs565240677 | in-del | -/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973984 | TTCCCCCCCCCCAAA[-/G]GAATCCAATCACAAC | 26524 |
rs565252852 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20994036 | TTGACTGCCAAGGAA[G/T]GGACAGCTCCAGGAC | 26524 |
rs565288544 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20980048 | TTTTTAATTTAAAAA[G/T]ATTATTTTTATTGTT | 26524 |
rs565316072 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21034151 | TACTTTACATTCTTT[A/C]TGGTCAGCGGGAAAA | 26524 |
rs565333184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043246 | GGGAAGCTGAGGCAG[C/G]AGAATCACTTGAACC | 26524 |
rs565371900 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993580 | CCATGTGGGACATGG[A/G]ACATGAAGTGACAGA | 26524 |
rs565379820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049458 | CTGCATATGGGACAT[G/T]TGCCCGGCCAGAGGC | 26524 |
rs565399406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21027748 | ATTCTAGGTACTTTG[C/T]AGTGCCATATGAATT | 26524 |
rs565400614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20976572 | ACCCAGAGAAAATAC[A/G]GAACTCCTACAACTC | 26524 |
rs565438336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029378 | TAATTATATTGATTT[C/T]CTAATGTTTAACCTT | 26524 |
rs565445792 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21038382 | TTTTTTTTTTAATTT[-/A]AAAAAATAGACAGGG | 26524 |
rs565476390 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017727 | GTCTCCGGGGTTCAA[A/G]TGATTCTCCTGCTTC | 26524 |
rs565519815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035040 | GTTTCAGACCAGCCC[A/G]AGAAACATAGCAAGA | 26524 |
rs565527118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022621 | CAGAGGAAAGCTTTT[C/T]GTTTATTGTCAGAGT | 26524 |
rs565558766 | in-del | -/CC | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21011657 | TTTCCTGACTCTGGA[-/CC]AAATATAGGGGCAAA | 26524 |
rs565566238 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999661 | GATGGGCTCTCACTG[C/T]AACCCAGGCTGGTCT | 26524 |
rs565583538 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028463 | AATTTATTTTGATAT[C/T]TAATGTGATCAGCAA | 26524 |
rs565585296 | in-del | -/AAAAATAAAAAT | 0.0236746 | 0.106192 | intron-variant | LATS2 | GRCh38.p7 | 13:21048846 | CCGTCTCAAAAAATA[-/AAAAATAAAAAT]AAAAATAAAAATAAA | 26524 |
rs565605971 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060504 | AACTCGCAGAGTTGG[C/T]GCGGCAGCCGGCCGG | 26524 |
rs565624115 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21053220 | AGCTTGGCAACAGAG[A/T]GAGACTCTGTCTCAA | 26524 |
rs565719171 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992779 | TGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 26524 |
rs565725130 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023841 | AGCTGGGCATGGTGG[C/T]GCATGCCTATAATTT | 26524 |
rs565753575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20975557 | CGATGGCTCACAGCC[C/T]GAGGCCAGGATGACC | 26524 |
rs565792800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20976051 | ACAGGAAAAACTTCA[C/T]AGGGAAGAATAAAGC | 26524 |
rs565850647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009487 | AATTTATACTTATCC[C/T]AAGGGTAAGCTAAAA | 26524 |
rs565900037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20977976 | GTTGGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC | 26524 |
rs565949425 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061711 | CCTGCCTCCGGCCTC[C/G]ACCGCCACCTGCCCA | 26524 |
rs566008052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001375 | TCTCCCATCCCTGTA[C/T]GTACGGGCTGCAGCC | 26524 |
rs566013196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21054772 | TTTCTTTCTTTTTCC[A/G]TTCCCCCCTCAACAT | 26524 |
rs566019037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995214 | TTCTGGGAAAAAAAA[A/C]CATAAAAACTGTAAT | 26524 |
rs566054908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014173 | AGGGTAATATGAGTC[A/G]GGGGCAGGGGGAAAG | 26524 |
rs566069075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21027904 | GTGAACATACTCTCT[C/T]CATTTATTTATTTAT | 26524 |
rs566090871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013678 | ATCACTTAAAAATAA[A/G]ATAAGGGCCAGGTGC | 26524 |
rs566091905 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:21007549 | ATATATATATAGTAT[A/G]TATATATATATATAT | 26524 |
rs566105761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21021305 | TGGTGAAACCCTGTC[C/T]CTACTAAAAATAGGA | 26524 |
rs566166417 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022250 | CCTATGTGTGTGGAC[A/G]TATGCATATGTGCGT | 26524 |
rs566183827 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21045473 | CTTGCCTGAAAAGGA[A/G]AAGCAGCTCAAAAGA | 26524 |
rs566286248 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040882 | AAAAGAATTCTTATC[A/T]GAGGAATCTGAGTCC | 26524 |
rs566291234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047065 | GCATGGAAATGGCCT[C/T]GTTACATGGAACGCG | 26524 |
rs566306961 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059143 | TCAGTATATTTGTTT[A/C]TTATTAAAATACGGG | 26524 |
rs566313872 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974500 | TTTTCCTAAATGTGA[A/G]TAAGTGCTATGGATA | 26524 |
rs566333174 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041206 | CTCGACCTCCTGACC[A/T]CATGATCTGCCCGCC | 26524 |
rs566451054 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015462 | AACAGCTAACTGTAT[A/T]ATTATCCATACTACA | 26524 |
rs566518133 | in-del | -/GTGTGT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044734 | TGTGTGTGTGTGTGT[-/GTGTGT]TTTAAATAGAGATAG | 26524 |
rs566552252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20994181 | GAGACCACAAGTGAA[A/G]ACTCATGTTCAGAAG | 26524 |
rs566605365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21038894 | TGAGGCATGGCGCAT[C/T]GCTTGAACCCGCGAG | 26524 |
rs566616616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21033427 | AGGTAGAGATGTGCA[C/T]GGGAAGACTGGAAAC | 26524 |
rs566634412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21031981 | AAAAACTAACAAAAT[C/T]TGTCATTTTAACCAT | 26524 |
rs566639569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21032950 | CAGACCCAATGAGAA[C/G]AGGAAGGCTGGGCCG | 26524 |
rs566647175 | in-del | -/TAATT | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21028447 | TGGGTATATACCCAG[-/TAATT]TATTTTGATATTTAA | 26524 |
rs566662107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20987396 | TCTTCAGCACTTCAG[C/T]GTCAACTAAGGTATA | 26524 |
rs566677131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21001033 | ATTAAAACAAAACTG[C/T]CTGTACTATCTAGCT | 26524 |
rs566739368 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21031776 | GAGATGGGAGGATTG[C/G]TTGAGCCCGGGAAGG | 26524 |
rs566774886 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21027065 | GCCCATTTTTAAAGG[C/T]TTGCCTTTTTATTAT | 26524 |
rs566837140 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037717 | TCTGAATCACAGACC[A/C]AAAGATGAGCCCTGA | 26524 |
rs566842047 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987113 | GGCAGGAGAATCGCT[A/T]GAACCCAGGAGGCAG | 26524 |
rs566881116 | in-del | -/AGTC | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21022344 | TAAGTGCATGTACTG[-/AGTC]AGGACTGAGAACCAT | 26524 |
rs566997165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980240 | CGGAGATGAGGAGGA[C/G]GTGGGCAAAACCCAC | 26524 |
rs567071902 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | LATS2 | GRCh38.p7 | 13:20996497 | ATTCTCCTGCCTCAG[C/G]TTCCCGAATAGCTGG | 26524 |
rs567073718 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21019331 | ATTATTATTATTATT[A/C]TTATTATTATTTGAG | 26524 |
rs567088734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980653 | GTAGAGGGAAGTAGA[A/C]CTTCACTGGGCACCA | 26524 |
rs567090215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21018717 | GGAGTGCAGTGGCTC[A/G]ATCACGGCTGACTGC | 26524 |
rs567097867 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21057565 | CTCATGCCTGTAGGC[A/G]GGTGGATCACGAGGT | 26524 |
rs567106453 | snp | A/C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039741 | ATGACAATCTGCCAA[A/C/G]ACAATGCCCAATGCA | 26524 |
rs567121317 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973979 | TTTCAGTTCCCCCCC[A/C]CCAAAGAATCCAATC | 26524 |
rs567195689 | in-del | -/TT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042255 | AAATACCCTTGAGTC[-/TT]TTACTTTTTCCAGAA | 26524 |
rs567197006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000103 | ATTATAAAGATAGGC[C/T]GGGCGTGGTGGCTCA | 26524 |
rs567212945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999628 | CTTGGCTAATTTTTT[A/T]AAAAATTTTTTTGTA | 26524 |
rs567253835 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994336 | GTAAGTACTTCCTAT[C/G]TGTACATTAAATCTC | 26524 |
rs567263147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21059239 | ATTTGAATTTTTTAC[C/T]GGCCAAATGTATACT | 26524 |
rs567302395 | snp | A/G | | | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972995 | TGCTGAGAGAGGCAA[A/G]GACTTACAAACTCCA | 26524 |
rs567415179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028052 | GTCATTTAGCATTAG[C/G]TATATCTCCTAATGC | 26524 |
rs567425024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21018739 | GCTGACTGCAGCCTC[C/T]ACCTCCTGGGTTCAA | 26524 |
rs567432492 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21027167 | CATTCTGTGGATTGA[A/G]TTTTGTTGTTTTAAT | 26524 |
rs567442745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20995035 | CCTCTGCTGCTTAGC[A/T]GCTGTGTAACTTTCA | 26524 |
rs567466386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982079 | AAGGTTACTTCAATG[C/T]CAGAAAATGAGAATG | 26524 |
rs567481114 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | LATS2 | GRCh38.p7 | 13:20976245 | GGCTACCAGCTGGGG[G/T]GATGGGACAGCGGAT | 26524 |
rs567493295 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992960 | GAATTGCTTGAAACC[C/T]GGGAGGTGGAGGCTG | 26524 |
rs567512684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21019527 | TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCACC | 26524 |
rs567558890 | snp | A/G | | | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981527 | CAGTGAATGTGCCAG[A/G]CACCTCTGGTGCTGC | 26524 |
rs567571636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21021383 | GAGTCTCAGGCAGGA[A/G]AGCTGCTTGAACCTG | 26524 |
rs567587255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20983171 | TAGTTGCTTGCAATG[C/G]GGTTAGTGACATCTA | 26524 |
rs567628436 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21032072 | TATTGACTGCCTTAG[C/T]TCCTAAGGGTTTCAC | 26524 |
rs567635704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013430 | GTGTTTGCTGATTCC[A/G]GAGTCTGTGGAAAAA | 26524 |
rs567658857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026379 | AGTATGTACTTTTTG[C/T]GTTCAGCATCTTTCG | 26524 |
rs567716359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025761 | GTCTCCTGTCCTCTG[C/T]ACGGAGGAGGAAGTG | 26524 |
rs567747975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980734 | TAGTTAAGTAACTTG[C/T]GCTGGATTACCACAG | 26524 |
rs567792613 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974075 | AGAGATACAATCATA[A/G]CGAAGAGGTCACCCG | 26524 |
rs567844798 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21013205 | TGAGTTAGGCCCATC[C/T]GCTATGGTGACCATG | 26524 |
rs567848928 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | LATS2 | GRCh38.p7 | 13:21057644 | TAAAAGTAAAAAAAA[A/T]AAAAAATTAGCTGGG | 26524 |
rs567879730 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974814 | GGCCTGTGAGGGCAC[C/T]GGCTCCGGGACCCTG | 26524 |
rs567910149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051222 | ATGTAGGGCCCTTGA[A/G]CAGTGCACAACCTGA | 26524 |
rs567913345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051607 | CTGTCTGGGCAATGC[A/G]GCCCACCAGGAGAGC | 26524 |
rs567960353 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20998271 | AGGCAGGAATCACTT[C/T]GAACCTGGGAGGTGG | 26524 |
rs567963692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21055658 | CTTCACAAACCCACA[A/C]TGGCTGCCAAACACA | 26524 |
rs567966498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21006081 | GGCAGAGGTTGCGGT[A/G]GGCCAATATCATGCC | 26524 |
rs567992471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21010701 | CCAAGTGGCCATTTG[C/T]TGACTAGTCGTCACA | 26524 |
rs567999150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20998756 | CGGGGCGAGGCGGGG[C/T]GGGGCCCGACAACCT | 26524 |
rs568022121 | in-del | -/AACAACAACAAAA | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21036784 | TCTCAAAACAACAAC[-/AACAACAACAAAA]AACAACAACAAAAAA | 26524 |
rs568048074 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056245 | GGTTTCGCCATGTCA[C/T]CCAAGCTCGTCTCGA | 26524 |
rs568055944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017445 | CTCTCAAGGTACAGG[A/G]ATTACAGGCATGAGC | 26524 |
rs568088885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017940 | CTGATTCATTTCTTC[A/G]TACTAATAATGTGAG | 26524 |
rs568161642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21011416 | ATGCTAGGAAACTCC[C/T]GTTTTTAAACTGGTC | 26524 |
rs568169029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042494 | GAAGTTCCAGTCCAG[C/T]CTGGGTAACATAGTG | 26524 |
rs568268709 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21022579 | CATTCAAAATGTTTG[-/A]AAAGATCAAATGAAC | 26524 |
rs568275779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043753 | CACTATAATTATCAC[G/T]AATGGATTTTACCCT | 26524 |
rs568310903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044573 | ACATTTCACTAATTA[C/T]ATTTTTACCTGGTTG | 26524 |
rs568312885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037826 | GGTCAGGACCAGGGC[A/G]GGTAGGGCCAGGGTG | 26524 |
rs568360452 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005243 | AGAACTCAAAAGGAG[A/G]CTCGAAAAACTGTCT | 26524 |
rs568389410 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050775 | ACGCTGAAGAGCGAC[G/T]GGCAGAGCCCCTGGA | 26524 |
rs568393904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009842 | CCTGGGTCCTTAGGT[G/T]TCCCCAGGCCCCCGC | 26524 |
rs568403371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038156 | TACTGTGCAGGGAAG[A/G]CCGGAGAAAGACGCA | 26524 |
rs568435921 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040558 | CCAACCAACGAAATC[A/G]TATGTCAGAGAGACC | 26524 |
rs568448688 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20979601 | CCTACCCTACTCAGA[A/G]TAAGAGGGCAAATGC | 26524 |
rs568452841 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062801 | GGTTCATCCTCCTCC[C/G]CTCCCTCTCTTTCAA | 26524 |
rs568468186 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006711 | TCCACTTACTCGACA[A/G]TGGCACATAGGCGTG | 26524 |
rs568516689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21056907 | CTTGGAGCCTGGAAC[A/T]TCCAATGAAAAGGCT | 26524 |
rs568534292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20990224 | AATCAGCACGGAACA[C/T]GGGCCTGGCCTTCCC | 26524 |
rs568583931 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984693 | ACACAAACAAATGAA[A/G]AGAGATCCCATGTTC | 26524 |
rs568614886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037001 | AAATGTATTCTAAGG[A/C]AGTCAGTAATATCCA | 26524 |
rs568644238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997712 | ACTAAGCACAGGGCT[G/T]ACGAGGACGGGTGGG | 26524 |
rs568681088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991198 | CCAGGCCAGGTTGGA[A/C]CCCTCTGCACGTGGT | 26524 |
rs568712693 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044073 | GCCTTTGCTGTCAGC[C/T]TCACTGCTGAAACAC | 26524 |
rs568734603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20985234 | GGCTAAAATCTCAAA[A/C]GCACAGGCAAAAAAA | 26524 |
rs568752178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21056360 | TCACTTCTACATAAG[C/T]TTACAGTCTCGGGGA | 26524 |
rs568783812 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973901 | CATGTGTCCGTGATT[A/G]AACTTTTTGGCATCG | 26524 |
rs568827832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21011561 | TGACACCATGTGATG[A/G]ATGACTGAACAGTGT | 26524 |
rs568867844 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:20989694 | CCCAAATTGTGGGGG[A/G]CTGAGTTTACCGACA | 26524 |
rs568893804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050529 | TTCATACACGTAGTA[C/T]ATATATAGCAGAAGC | 26524 |
rs568901636 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013322 | GCTCAGTACTTATCC[G/T]GGCTCGATGCCTAAT | 26524 |
rs568916044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21012011 | GTGCAAACTCCACAC[A/C]GTGGCCCTGGCCAGG | 26524 |
rs568980325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044667 | GCTAAGAGATCATAA[A/G]TGTATGGCTATGAGG | 26524 |
rs568981690 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014768 | ATACCTTTTTAAAAA[A/T]GAATGTTTGTTGAGT | 26524 |
rs568984402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037059 | GACCAGCTCTTTACA[A/G]TAAATTATGGGACAT | 26524 |
rs569002895 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LATS2 | GRCh38.p7 | 13:20998870 | GCGACATTGTCCACG[A/G]CCTTGTGCACGCGGG | 26524 |
rs569021149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21037593 | ATCTACAAAGGGAGA[C/T]GCACAAACTACTTAA | 26524 |
rs569054720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038217 | AGGAGCAAAGGTGGA[A/G]CCTGTACCGGGGGCA | 26524 |
rs569086532 | in-del | -/AAAT | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21027794 | AATTTCAATTAAAAA[-/AAAT]AAATAAACCTGCTGA | 26524 |
rs569091872 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029522 | GGAATGTCGGGTGCG[A/G]TGGCTCATGCCTGTA | 26524 |
rs569139852 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058651 | GTTCTATAATTCAAT[G/T]ATTCTAGTAATTCAC | 26524 |
rs569187983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21003573 | AGCCTCTCAAGGAGC[G/T]GGGATTACAGGTGCC | 26524 |
rs569225246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21043475 | CCTGAATTTTCTGAA[C/T]GCAAATACATTTTTT | 26524 |
rs569263365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030741 | TTTACTTTAAATATT[A/G]ATGTCTTTTAAAGAG | 26524 |
rs569317874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20989895 | CCTCTACAAATATCC[A/C]GATTGATTTCATCTG | 26524 |
rs569358463 | snp | A/G | 4.95209e-05 | 0.00497574 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20991354 | GATGTACTCCAGGGC[A/G]GCCTCGATGCTCCTG | 26524 |
rs569470763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025623 | TATGCTATGAAACTC[A/T]GTCTCATCGTCATTA | 26524 |
rs569488669 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033750 | AACAGCTTTTATAAG[A/C]CAAATGAAGTTGCTT | 26524 |
rs569519302 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21004627 | CAGTGGGCTTCCTGG[A/C]CCCCTGCCTCCAACC | 26524 |
rs569529304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980164 | AGTGCTATAACCTGT[C/G]AATAGTCAGGTGAGG | 26524 |
rs569543371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21017219 | CTGTGCAGAAAAAGT[C/T]AGCATTCTATCTAGA | 26524 |
rs569545255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009918 | GAAATAACACAGAAG[A/G]GCCAGGCGTGGTGGC | 26524 |
rs569555909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21018087 | CAGCTTCAGTAACAC[A/G]TAGGATCACTGGCTA | 26524 |
rs569570393 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973421 | AGCATCAGATTTTTT[A/T]AAAAGCAAAAAAGAA | 26524 |
rs569583075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022731 | AAACACACACAAGGC[C/T]AATTTAGATATGAGA | 26524 |
rs569666503 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21036121 | GAGTGGTCTCGAACA[A/C]CCGACCTCGGATGAT | 26524 |
rs569667793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029926 | GTCAGGGGTTCAAGA[A/C]CAGCCTGGCCAACAT | 26524 |
rs569694538 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | LATS2 | GRCh38.p7 | 13:21012191 | AAGATAATGTAAAAA[-/T]ATCATATAAAAGATT | 26524 |
rs569702071 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017816 | TTTTTACTAGAGATG[A/G]GGTTTCACCATGTTG | 26524 |
rs569753303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023501 | CGTCCTTGGCCTCTG[C/T]TCTCGAGGCGGGGCC | 26524 |
rs569778685 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21047788 | ATTTACATAGATCTA[C/T]TGCACAACCATATGC | 26524 |
rs569811368 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21049153 | CTCTTCCTGGAGACA[C/T]AGGAGGTCAAAGGAC | 26524 |
rs569868498 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062537 | GGGATGGTGCAAAGA[G/T]TCACAGTAGAAATAA | 26524 |
rs569931365 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21055381 | ACCAATTGATTCACA[C/T]ACATTTTAAGTAACA | 26524 |
rs569959015 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982246 | AGGAAATGGAGTTCA[A/G]TGATACACTACATAG | 26524 |
rs569981414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049612 | AGCAGGGCACAGAAG[A/G]GGCAAGCTGCTTTTC | 26524 |
rs569998651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20996291 | AGGGCTCCCAACCTT[C/G]GAAGCATCTTGACTT | 26524 |
rs570062406 | snp | A/G | 0.001998 | 0.0315437 | intron-variant | LATS2 | GRCh38.p7 | 13:21007571 | TATATATATATATAT[A/G]TATATATATATATAT | 26524 |
rs570082697 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990357 | TGTGTGTCCTTTTAA[C/T]AATGGAGATATAACT | 26524 |
rs570108662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001383 | CCCTGTATGTACGGG[C/T]TGCAGCCCCCAGTGT | 26524 |
rs570127529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20978578 | TTCTTTAGATACAGT[C/T]GACCCTTGAACAACA | 26524 |
rs570140179 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | LATS2 | GRCh38.p7 | 13:20999757 | GCTAGGGTGCCTGGC[C/T]TTAAATTTGTTATAA | 26524 |
rs570163709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20979420 | ATCCTCACTGTTCTT[A/G]CCTGGAAATAGCAAG | 26524 |
rs570171980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026137 | AAGAAGAGAAGGAAA[C/T]GAATTATTTGCATCC | 26524 |
rs570180947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053922 | GAAAGGGGAACAGGG[A/T]ATTTTTACTTAAGGG | 26524 |
rs570276799 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21001952 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 26524 |
rs570349690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023696 | AAACAAACCTCGGCC[A/G]GGCGCAGTGGCTGAC | 26524 |
rs570361377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21003694 | TGATCCAGCCACCTC[A/G]GCCTCCCAAAGTGCT | 26524 |
rs570387918 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:20977785 | ATATTTTACCAGAAT[-/A]AAAAAATCTGAATTA | 26524 |
rs570398138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21004392 | TGAGCTGAGATTGCG[C/T]CATTGCACTCTAGCC | 26524 |
rs570417020 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054442 | ATAAATAAATAAACA[C/T]AGCTACACAATGAGA | 26524 |
rs570509491 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062697 | TGACAAACTCTTGTG[A/G]AATTTTTAAATTTTA | 26524 |
rs570551928 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21017380 | GGGTCTTGCTATGTT[A/T]CCCAGGCTGGTCTCA | 26524 |
rs570632350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997888 | GGAAGGAATTTCCTA[C/T]GGAGATCCTCCCCCA | 26524 |
rs570666613 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21056142 | AGAATTGGGTCTTTT[A/T]TTTTGGTGGGGGGGG | 26524 |
rs570677959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049637 | CTTTTCACTCAGCTA[C/T]GAAAGGACAAGAGCC | 26524 |
rs570701946 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984491 | TAGCATACATTAGAT[A/G]GACTTGTATATGGTG | 26524 |
rs570716187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049974 | AAAAATACAAAAATT[A/G]GCCAGGTGTGACAGC | 26524 |
rs570724849 | in-del | -/TTAT | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21000672 | ACTACTAAACTATAA[-/TTAT]AATTAATATAGTCCT | 26524 |
rs570840040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20984438 | AGGGAAAATGGGAAA[C/G]CAGGAAGAAAAGTCA | 26524 |
rs570863849 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999479 | CACTTTTTCTTTTTC[-/T]TTTTTTTTTGACAGG | 26524 |
rs570902762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21041719 | AAACAAAGTTCTCAC[A/G]TAAGTCTTCCTAGAG | 26524 |
rs570904107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21009385 | AGCTTTGCAGAAACT[A/G]TTCCTGCAAACTGGT | 26524 |
rs570975667 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004567 | GTCAGCATGAACTTG[C/T]GAGTGCACACAGCAT | 26524 |
rs571008013 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21042379 | CTTAGAAATTGTGCA[A/C/T]TTTTAAAGTAAATTT | 26524 |
rs571041032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21035792 | GCTGCAGGGACCAAC[A/G]CCACAGCACGCAAGT | 26524 |
rs571109396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21028834 | TGGCCTCCCAGAGTA[C/T]TGAGATTACAGGTGT | 26524 |
rs571138362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21040359 | CTGCACTACAGCCTC[A/G]GCGACAGACCTTGTC | 26524 |
rs571190046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21060157 | CCATTCCTCGCCTCG[A/C]CCCCCGTTCCCAACC | 26524 |
rs571238692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053467 | TCCTGTTTGGTTTAC[C/T]CCCATCTACTCCCAG | 26524 |
rs571346491 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044432 | TGAAATCTTACTACT[C/T]TTCCAAGGTACCAAA | 26524 |
rs571375575 | in-del | -/GTGTATTTTTTTCTTCA | 0.0020012 | 0.0315689 | intron-variant | LATS2 | GRCh38.p7 | 13:21030999 | GATATAAAATTCTCG[-/GTGTATTTTTTTCTTCA]GCACTTTGTGTCATT | 26524 |
rs571394687 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20982670 | GTTCCCCACAAAGGC[A/C]CCGTGACACCTTGTA | 26524 |
rs571394727 | snp | C/G/T | 4.41708e-05 | 0.00469934 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988628 | CGGCGCCTCCAGGCC[C/G/T]GGCTTCTGCAGGGAG | 26524 |
rs571404133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981896 | GAAGAATCACAGGAC[A/G]CCATGCACCGTGCTG | 26524 |
rs571467414 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21013469 | TTCTGTAGAGAAGAT[C/G]CAAACGGCCAGGAAA | 26524 |
rs571483338 | snp | C/T | 5.02887e-05 | 0.00501416 | missense | LATS2 | GRCh38.p7 | 13:20983238 | CCTTTCTGGTAATAT[C/T]TGGAATTGTGAGTCC | 26524 |
rs571541848 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21022497 | CCTGTATCCTGCAAA[C/G]ATTGGTCCAGGTGGA | 26524 |
rs571668019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033295 | TAGAGGGGCGAGAGA[A/G]CACACGCTCCTGGTG | 26524 |
rs571688039 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21028379 | ATTGTGAATAGTGCC[A/G]CAATAAACATATGTG | 26524 |
rs571711915 | snp | C/T | 6.58892e-05 | 0.00573936 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975056 | ATGCTTGTTATTGGG[C/T]GAGGTGAGTGTGTCC | 26524 |
rs571719928 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042513 | GGTAACATAGTGAGA[C/T]GCCATCTCTAGAAAA | 26524 |
rs571809268 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992019 | GGTAGCTCAAACTGC[C/T]TGTGGGAAGAACACA | 26524 |
rs571811049 | in-del | -/A | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21025219 | ACCCCGTCTCTACTA[-/A]AAAAAAAAAAAAAAA | 26524 |
rs571856966 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048403 | AACACAGCCATACTA[C/T]CTTCACAAGAACAAT | 26524 |
rs571866248 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046202 | AACCTAAAATTTTCC[A/G/T]AAGTCTTCATTTTGA | 26524 |
rs571875799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058938 | ATTACAACGGTTGTT[A/G]CAGAAAAAAAAAAAA | 26524 |
rs571888821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21000152 | TTTGGGAAGCCGAGG[C/T]GGGCAGATCACAAAG | 26524 |
rs571889621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051715 | TGTAATCCTGGCACT[A/T]TGGGAGGCCAAGGTG | 26524 |
rs571906622 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973712 | AAAAGTGAGAGAACC[A/G]TTAGATCACTCAGTT | 26524 |
rs571926722 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21052772 | CTTTCCTCTCTGAAA[C/T]GTGCCTGCAGCCAGG | 26524 |
rs571996532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21047871 | GAAGGGGATTGTAAG[C/T]GTTTTAACTATCCCC | 26524 |
rs572017897 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982710 | CTTAAAAATATAGTA[G/T]GCCAGGCACGGTGGC | 26524 |
rs572037144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041118 | GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCC | 26524 |
rs572043136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982316 | TGACTCTTTTATTTA[C/T]TTTATTTTATTTGAG | 26524 |
rs572046390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21059458 | AAAAATTAGCCGGGC[A/G]TGGTGGCACACGCCT | 26524 |
rs572048571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21014456 | AGTATGAATAAAGCA[C/T]GGCCTTGGCTAAGGA | 26524 |
rs572080198 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:20975860 | GGCTGATTTTTGTAT[C/T]TTTAGTAGAGACAGG | 26524 |
rs572137942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008211 | ACTGTAGGACAGACA[C/G]TCGGGCACCGCATCC | 26524 |
rs572168176 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21060241 | CCATCCCCGAGGGAA[A/C]GCTCCCCAGAAGTTC | 26524 |
rs572194921 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21015105 | ATTCTTCTTGAGTGT[C/G]ACATGCACAGTGTTC | 26524 |
rs572230736 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999776 | AATTTGTTATAAAAT[A/T]AAATGAACATGAAAA | 26524 |
rs572233571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21008815 | AGATGCTGAAATCCT[A/G]CAACCAAGATTCCAC | 26524 |
rs572267587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000337 | AATGAGCCGAGATTG[C/T]ACCACTGTACTCCAG | 26524 |
rs572339824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013152 | GTGCTGGGGTAGGTT[C/G]TTGTATATGAAGGTT | 26524 |
rs572393527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001550 | TCAGATCGCACCATG[A/G]TTGGAGACAGATCCA | 26524 |
rs572448456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21027642 | TAGAGACTACCCACA[A/G]TAGTCTGGTCCAAAG | 26524 |
rs572482784 | in-del | -/TAAAAATAAAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987218 | TTAAAAAATAAAAAA[-/TAAAAATAAAAA]AAACACAAATGAAAA | 26524 |
rs572556258 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978953 | TTTTCAGTAGAGACG[A/G]GTTTCGCCATGTTGC | 26524 |
rs572560673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051860 | TACTCCGGAGGCTGA[A/G]GTGGGAGAATCACTT | 26524 |
rs572563017 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20993958 | TGCTTCATCTGAAAC[G/T]TGACCAACGCTCTGT | 26524 |
rs572601863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21033641 | CAAGGTTGACAGACG[A/G]CACAGAGTACAATTT | 26524 |
rs572703311 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:20980951 | ATCCAGGAGGCAAAT[G/T]TTATGAGCACTAGTC | 26524 |
rs572737235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21034534 | GGTGCACGCCAAGAC[A/G]GAGTCACTTGCTAAG | 26524 |
rs572747878 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040076 | GAAACTCCATCTCAA[A/G]AAAAAAAAAAAGAAA | 26524 |
rs572814474 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21037979 | ATGAGGGGGGCTAGA[C/T]ACGGTGGCCCACGTT | 26524 |
rs572816395 | in-del | -/ATTGATTT | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21025014 | TTTGTTTTTTGATTC[-/ATTGATTT]ATTGATTTTTATATA | 26524 |
rs572827347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20992990 | GCAGTGAGCCGAGAT[C/T]ACGCCACTGCACTCC | 26524 |
rs572838264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20998470 | TGCACTGTCTCTGGC[A/G]GGATCCTGTGCTTGC | 26524 |
rs572866544 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990066 | GCTGGGCCTTGCCCA[C/T]AGGAAGACCACCCCG | 26524 |
rs572879469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023832 | TACAAAATTAGCTGG[A/G]CATGGTGGCGCATGC | 26524 |
rs572881454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030839 | TCTTCATTCCTTCCT[G/T]TATATCCTTTAGCAT | 26524 |
rs572914756 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LATS2 | GRCh38.p7 | 13:21021680 | TTGAAGAATTGAGGA[C/T]ACCTTCCCAACCACT | 26524 |
rs572931525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21031771 | AAGCTGAGATGGGAG[A/G]ATTGCTTGAGCCCGG | 26524 |
rs572965499 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024389 | TGCAGTGAGCCGAGA[G/T]CGCGCCACTGTACCC | 26524 |
rs572969977 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035612 | ATGACAGCAAATAAT[C/G]TCAGCAGTAAACGTT | 26524 |
rs573039758 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057119 | GCTCACTATTCCAAA[C/T]AGAGGCCCACTCCTT | 26524 |
rs573049773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025918 | GACTAGATTAGGGAC[C/G]CCTGTTATAAGGTTT | 26524 |
rs573056605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21019038 | CCAGTAGCTCTGTAC[A/G]TGGGAACCAGACATC | 26524 |
rs573080931 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973542 | TGTGTGTGTATACAC[A/G]CACATACATCTATAC | 26524 |
rs573105188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049782 | GGCTGAAGGAGGTCC[C/T]GGTTGACTCTGAGGC | 26524 |
rs573120642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991519 | CGCCTCTGTACTGCT[G/T]AGAACCTGCGATATG | 26524 |
rs573123209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21056370 | ATAAGCTTACAGTCT[C/T]GGGGAAAAAGACACC | 26524 |
rs573125492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20985196 | ATATACTCCAGGACA[C/T]TGGTTTGAGCAAAGA | 26524 |
rs573138558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21026464 | TCTTTGTTTTGGTTG[A/G]TAGCATTCTATTGTA | 26524 |
rs573177459 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:20987822 | GGATTGTGCGTGCTT[C/T]CTATTGCCAGTAGAG | 26524 |
rs573245172 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982342 | TTGAGACAGAGTTTC[A/G]CTCTTGTTGCCCAGG | 26524 |
rs573271634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21055725 | TCTCATGGGACCTGC[C/G]CTAATGACACATGTT | 26524 |
rs573279477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20979053 | AGGCATGAGCCACTG[C/T]GCCCAGCCTATGATC | 26524 |
rs573285121 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063065 | CTGCAATTGAGCCCT[A/G]CTGGCATTACCTATG | 26524 |
rs573286913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21038912 | TTGAACCCGCGAGGC[A/G]GAGGTTGTAATGAGC | 26524 |
rs573322279 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053843 | AATATTGTATGATTC[C/T]AGTTATGTGAGTTAC | 26524 |
rs573346922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21018235 | AACACTTAATTAAAA[A/C]ATACTGTATGAAAAT | 26524 |
rs573364780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002813 | CCTGCCTCGGCCTCC[A/C]AAGTAGCTAGGATTA | 26524 |
rs573375670 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973541 | GTGTGTGTGTATACA[C/T]GCACATACATCTATA | 26524 |
rs573383726 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21011656 | TCTTTCCTGACTCTG[G/T]AAAATATAGGGGCAA | 26524 |
rs573437361 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21028874 | TACCCGGCCAAATTT[-/C]AACTTTCAAGTGTTC | 26524 |
rs573507530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21044005 | TTCTGTACGTCAAGG[A/G]ATAATGCTTGGCAGC | 26524 |
rs573577365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21058570 | ATTTGCTAAGGAACA[C/T]GTACAGCTCCAATTT | 26524 |
rs573582640 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015595 | TTCCTAGGTAGTTGT[G/T]TTAAATAGGATTTGG | 26524 |
rs573625255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986972 | CCGAGGTGGGCAGAT[A/C]ACCTGAGGTCAAGAG | 26524 |
rs573639659 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20993069 | AAAAAAAATGGGGGG[G/T]TGGAGATACAGAAAG | 26524 |
rs573662054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20981054 | ACGCTGTCACATAAG[C/T]ACCCAGCTGCACACG | 26524 |
rs573677662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21017698 | TGGCACCATCTCAGC[G/T]CACTGCAACCTCCGT | 26524 |
rs573724179 | snp | A/G | 1.6865e-05 | 0.00290383 | missense | LATS2 | GRCh38.p7 | 13:20981472 | CGCATGTACCTTTGC[A/G]GAGGAGCACCTCGGG | 26524 |
rs573848503 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990325 | GGAAGTTCCTTCTCT[A/T]AAGAAGAAAACAAAA | 26524 |
rs573876818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21051389 | GTGTCACAATGAAAG[C/T]TTGCCCAAAGAATTA | 26524 |
rs573886284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21051931 | TACTGCACTCCAGCC[C/T]GGGAGTCAGAGCAAG | 26524 |
rs573887572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21012407 | GCGTAAGTAAGAGTT[G/T]GACTATGAAGTTACA | 26524 |
rs573897606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21006367 | CCCAGCGCCCACTGT[A/G]TACATCCCTTAAAAA | 26524 |
rs573918891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21044146 | CTCGACATAACAATC[C/T]TCACTATATACAAGT | 26524 |
rs573926574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986032 | CTGGGCAACAAGAGC[A/G]AAACTCTGTCTCAAA | 26524 |
rs573929883 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012473 | TCCATCACAATCTCA[C/T]GGGACCATCATCATA | 26524 |
rs573947952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20979886 | AACATACAGATTTCC[C/T]GTTAAGTGGGAAAGC | 26524 |
rs573989658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21013776 | TTTGAGGCCATCCTG[A/G]GCAACACAGCAAGAC | 26524 |
rs574042898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038362 | GTTTAATATATAATT[C/T]CATCTTTTTTTTTTA | 26524 |
rs574059136 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982215 | TGTTTTTGGCTTTTC[C/T]AAATGGCAGAACTAT | 26524 |
rs574061340 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21053064 | ACACGGTGAAACCCT[C/G]TGTCCACCAAATATA | 26524 |
rs574114949 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21050260 | TTATTTAACATATAT[A/T]TTTTAAACTGCACAG | 26524 |
rs574169881 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21004803 | CTCCTTCTAAAACCT[A/G/T]CACCAACCAAGACAT | 26524 |
rs574175572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21050761 | TCGCCGTGCCAAATA[C/T]GCTGAAGAGCGACTG | 26524 |
rs574181527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21005620 | TGGGGTTTTAATTCG[C/T]ACTCTTGCTGGGAAC | 26524 |
rs574250893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20990720 | TGTGCTCCATCTTGG[A/G]AAAGTAACATTCATC | 26524 |
rs574253095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20997926 | CTTCCTGGTAAGGAA[A/G]CATTTTTCAAGCCTT | 26524 |
rs574317315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20998638 | AAGAATGAGGCCCTC[C/T]GGGCCCAGGCCTCCT | 26524 |
rs574338741 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006062 | GAATCGCTGGAACCC[A/G]GAAGGCAGAGGTTGC | 26524 |
rs574406084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20999148 | AGGTGGAGGACAAAT[A/G]GAAGTAGTGGCCTTT | 26524 |
rs574417166 | in-del | -/AAGCAGCAGGTATTTGCCC | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21011652 | GCTTCTTTCCTGACT[-/AAGCAGCAGGTATTTGCCC]CTGGAAAATATAGGG | 26524 |
rs574463687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21003802 | AGGCTGGTCTCTCCT[A/G]GGCTCAAGCACTCTG | 26524 |
rs574546505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21049653 | GAAAGGACAAGAGCC[A/T]CAAGAGACACTGCAG | 26524 |
rs574628610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030888 | ACCCCTTTAATATTT[C/T]TTTTAATACAGGTCC | 26524 |
rs574732006 | snp | A/G | | | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988043 | GCTGTTTTTGCGGAC[A/G]GGAACGGGAGAGGTC | 26524 |
rs574754831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035382 | CTATTTACATCCTTG[C/T]TGGTTTTCTCTATTT | 26524 |
rs574789577 | snp | G/T | 0.000399281 | 0.0141238 | missense | LATS2 | GRCh38.p7 | 13:20988948 | TCTCCGGCGGCGTCT[G/T]GCTCTGGAAGGAGGG | 26524 |
rs574844890 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:20996062 | ATGCTAATCCATTGA[A/G]GTTGGTTACCACGCC | 26524 |
rs574883804 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981153 | CTGAGCAGAGGTCCT[C/G]TGGCCCTCAGAGTGG | 26524 |
rs574947514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061307 | AACTCTCGCCACCCT[C/T]CGAGCTGCCGCCCCG | 26524 |
rs574949845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20984080 | GGACTACATGTGCCC[A/G]CCACCATGACACCTG | 26524 |
rs574973482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20991821 | CTCCAGGCTAACTCT[A/G]GGACTAGGAAACCTG | 26524 |
rs574981412 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993192 | CTGAGTGTCCCCCAC[C/T]TCTGGATAGGGCATT | 26524 |
rs574995539 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | LATS2 | GRCh38.p7 | 13:21009790 | GGATGAGGTATGGGT[C/G]GAAAAAGAGGCCTCC | 26524 |
rs575053772 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061984 | GCAGAAAAGGACAGA[C/T]GGCTATTGGGACAGT | 26524 |
rs575086690 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002648 | CTCCCAAACTGCTGG[G/T]ATTACAGGTGTGAGC | 26524 |
rs575100185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20986190 | ATAATCTCTCCCCAG[C/T]TAGAACGACTATTAT | 26524 |
rs575115910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21054972 | ACAAGGGCTGTCCCT[C/G]TCTTAAGTGAATATG | 26524 |
rs575134734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21003851 | AGTGCTGGGAGTACA[A/G]GCATGAGCCACTGCG | 26524 |
rs575139857 | in-del | -/G | 0.0189856 | 0.0955633 | intron-variant | LATS2 | GRCh38.p7 | 13:21007588 | ATATATATATATATA[-/G]TATATATATATATAG | 26524 |
rs575151903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21016247 | CTACCTTGGCCTCCC[A/C]AAGTGCTGGGATTAC | 26524 |
rs575152529 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | LATS2 | GRCh38.p7 | 13:21050175 | ATACATACATACATA[C/G]ATGGAAAGCTGCTGA | 26524 |
rs575214311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21043333 | CAGAGCAAGACACCG[C/T]CTAAAAAAAAAAAAG | 26524 |
rs575221480 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978538 | TTTGCGAACAATGAT[A/G]TAATATCCAAATAAA | 26524 |
rs575224264 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987502 | TCCCACAATCTCAAT[C/T]TACAAAACCTTAAAC | 26524 |
rs575230017 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:20998373 | CAAACAAACAAAAAT[A/T]AATTAATTAATTAAA | 26524 |
rs575388551 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062000 | GGCTATTGGGACAGT[A/G]GAATCAAACAATTAA | 26524 |
rs575451374 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21055064 | TTCCTTCAGTTTCAT[A/G]GAGAATGAAAGCATT | 26524 |
rs575451455 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062978 | ATTCAATTTAATTTT[G/T]CGATAGTATCCTGTA | 26524 |
rs575460722 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051606 | CCTGTCTGGGCAATG[C/T]GGCCCACCAGGAGAG | 26524 |
rs575462392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21025790 | TGAAATTATTGCTGT[A/G]ACCCCTCAGTGTTCC | 26524 |
rs575477124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20980855 | TTAATTACACCCCAT[C/T]GTCACTGTGGACCAT | 26524 |
rs575487018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20980305 | TGAGGCCCCTACGGA[A/G]CCGGGCCTTCCTCAC | 26524 |
rs575523192 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987088 | TAACCCCAACTACTC[A/G]GGAAGCTGAGGCAGG | 26524 |
rs575537089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21029588 | ACGAGGTCAGGAGTT[C/G]GAGACCAGCCTGGCC | 26524 |
rs575577742 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033601 | AGACACACACGGTAT[C/T]GCTGAAGGCTCTTGT | 26524 |
rs575579618 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21032163 | TGCAGCAACACTGCA[A/T]TCTAATGGGTTAGGT | 26524 |
rs575614533 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035154 | CTAATATATAAAAAA[A/G/T]TGCATGATGAATGTG | 26524 |
rs575668924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21030251 | ACAAATATCCAAACT[A/G]TATCAACAATCTACT | 26524 |
rs575690561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21052965 | CGCTGGGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 26524 |
rs575699404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023764 | GGATCACCTGAGGTC[G/T]GGAATTCAAGACCAG | 26524 |
rs575699783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024624 | ATCACTGACCAGCAC[C/T]GTGCTGTCCCACAGA | 26524 |
rs575729877 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | LATS2 | GRCh38.p7 | 13:21007672 | TATATAGTGTGTATA[-/C]TATATATATAGTATA | 26524 |
rs575743882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024365 | TGTTTGAACCTGGGA[A/G]GCGGAGGTTGCAGTG | 26524 |
rs575759950 | snp | G/T | 6.87876e-05 | 0.00586422 | missense, intron-variant | LATS2 | GRCh38.p7 | 13:20979711 | GCTGGGTTTCTGTGG[G/T]AGTAGGTGCCAAAAA | 26524 |
rs575786156 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21037107 | TACAATGCAAATGTT[-/A]AAAATCATATTTTAG | 26524 |
rs575788722 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21009527 | GACTGTTAAGTAAAA[A/T]CACAACAACAAAAAT | 26524 |
rs575851864 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LATS2 | GRCh38.p7 | 13:21041193 | TAGCCAGGATGGTCT[C/T]GACCTCCTGACCTCA | 26524 |
rs575865849 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005679 | AAAGGAAAGGAAAAC[C/G]TGTAATCCCAGTGCT | 26524 |
rs575869737 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005969 | AAATACAAAATTAGC[C/T]GGGAGTGGTGGCGCA | 26524 |
rs575902148 | snp | A/C/T | 6.58892e-05 | 0.00573936 | missense | LATS2 | GRCh38.p7 | 13:20983632 | TCATGGCGTACAGGG[A/C/T]GTGAGTGTCCACCTT | 26524 |
rs575903288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21016961 | TCTGTTCTCAGACAT[A/G]AGAGGGATTACAGCA | 26524 |
rs575941054 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21017483 | CCTGGATGATTCTTT[A/G]CATTGTTATGTGCAA | 26524 |
rs575963262 | snp | C/T | 0.000399281 | 0.0141238 | missense | LATS2 | GRCh38.p7 | 13:20983487 | ATCACAAAGTACAGG[C/T]TGTCTTTGTCTTGGA | 26524 |
rs575973860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21035956 | CAGGCTGGAGTGCAG[C/T]GGCACGATCTTGGCT | 26524 |
rs575973994 | in-del | -/AAAAACAAA | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023679 | AAAAAAAAAAAAAAA[-/AAAAACAAA]CCTCGGCCGGGCGCA | 26524 |
rs575987161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022249 | GCCTATGTGTGTGGA[C/T]GTATGCATATGTGCG | 26524 |
rs575998826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20977435 | AACTCACAGAGACAG[G/T]AAGCAGAAGAGAGGC | 26524 |
rs576051454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21053646 | CAACAGCAGCACCTT[C/T]TCTGAAGTTTAACAT | 26524 |
rs576062584 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21059609 | CAAAAAACAACAACA[A/G/T]CAACAACAAAAAACA | 26524 |
rs576090357 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LATS2 | GRCh38.p7 | 13:21047945 | GAGAGACTAAATAAA[C/T]TTCTCAACATGAAAT | 26524 |
rs576103534 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018821 | CAGCTAATTTTTGTA[C/T]TTTTAGTAGAGAAAG | 26524 |
rs576112028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001828 | AGGTTGCGGTGAGCC[A/G]AGACAGCGCCCCTGC | 26524 |
rs576129216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21054143 | TCGTGTTTGAACAAT[A/G]GCTCCCTTTTTAAAC | 26524 |
rs576186445 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20995321 | GAAATGTAATGAGTT[A/C]TTTTCCCCAAGCCTC | 26524 |
rs576206566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21048568 | GGACGTGGTGGCTCA[C/T]GTCTGTAATCCCAGC | 26524 |
rs576222992 | in-del | -/ATAG | 0.462472 | 0.13174 | intron-variant | LATS2 | GRCh38.p7 | 13:21050119 | GGGAGACTCTGTCTC[-/ATAG]ATAGACAGATAGATA | 26524 |
rs576274819 | snp | A/G | 0.00398564 | 0.0444627 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988364 | GGGGGCGGGGGCGGG[A/G]GCCGGGGCAGGCGCG | 26524 |
rs576369571 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995204 | TCTTATGTGTTTCTG[A/G]GAAAAAAAAACATAA | 26524 |
rs576390484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21000454 | TATAAACCAAAAATA[C/T]TCAGGGGTGAATATT | 26524 |
rs576412359 | in-del | -/T | 0.375996 | 0.215928 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974423 | GAGCAGAGTGTTATC[-/T]TTTTTTTTTTTTTAC | 26524 |
rs576581591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21002880 | TTAATTTCTTTTTCA[G/T]TTTTAGAGAAAGGGT | 26524 |
rs576630234 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21028469 | TTTTGATATTTAATG[A/T]GATCAGCAATGCTTT | 26524 |
rs576645435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982810 | CAGCCTGACCAACAC[A/G]GAGAAACCCCGTCTC | 26524 |
rs576659852 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21034101 | CATGGCATTGTGGTC[A/T]GACTGCCACCTCTGC | 26524 |
rs576696591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21034591 | TATTCCTGATGACAC[C/T]GTGGACTGCCGTGCC | 26524 |
rs576730124 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061204 | CTCCGTCCGGACAAA[A/C]TTCCTCGGCCGCCCC | 26524 |
rs576739066 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028158 | TTGTTCAATTCCCAT[C/T]TATGAGTGAGAACAT | 26524 |
rs576811324 | in-del | -/ATT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019340 | ATTATTATTATTATT[-/ATT]TGAGACAGAGTTTCA | 26524 |
rs576838167 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029798 | TCTGTCTCAAAAAAG[-/A]AAAAAAAAGATATTG | 26524 |
rs576852528 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020152 | CAGTTCACATAAAAT[A/T]TACCTGAAAACACAC | 26524 |
rs576895903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042046 | TATCCAATGCTCAAA[A/G]TATGATACTCATAAC | 26524 |
rs576983371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21042727 | GGCATGGTAACTCAC[A/G]CCTGTAATCCCAGCA | 26524 |
rs576995329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21054906 | ACCCCACAAGCTGTT[C/G]TGATTTTTTCTCCAT | 26524 |
rs577042431 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LATS2 | GRCh38.p7 | 13:21049172 | AGGTCAAAGGACTCG[A/G]GGGTAGTGGGGGTGT | 26524 |
rs577100515 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050167 | ATACATACATACATA[C/G]ATACATAGATGGAAA | 26524 |
rs577114645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20977516 | ACGATTAACACATTT[G/T]AAAATAGAGGGTGGT | 26524 |
rs577114678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20984033 | CCTCCTGGGTTCCAG[C/T]GATTCTGCTGTCTCA | 26524 |
rs577144587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20978116 | GAGACGGGGTTTCAC[C/T]ACGTTGGCCAGGCTA | 26524 |
rs577222794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21041077 | TCCTGGGTTCACACC[A/G]TTCTCCTGCCTCAGC | 26524 |
rs577244423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21047966 | AACATGAAATCCCTA[C/T]TTTAATACACAATAT | 26524 |
rs577302405 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999987 | GTGAGTCAAGATCAC[A/G]CAGCAGAGCAAGTCT | 26524 |
rs577327794 | in-del | -/AGAG | 0.00398564 | 0.0444627 | intron-variant | LATS2 | GRCh38.p7 | 13:21051419 | ATGGGGATCTGAAAT[-/AGAG]AGCAGTTACAGGATA | 26524 |
rs577331900 | snp | C/T | 0.000811479 | 0.0201266 | missense | LATS2 | GRCh38.p7 | 13:20988879 | GTGGGAAAGCGAGGC[C/T]GGCGCCTGGCGGTCC | 26524 |
rs577344953 | snp | A/G | 7.06951e-05 | 0.00594496 | synonymous-codon, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21045691 | TGTACCCACCTGGTC[A/G]CATCCTGCGTTCACC | 26524 |
rs577349983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21001487 | AGTGCTGCTGTGCCA[A/G]TTCTGAGCCTCACCC | 26524 |
rs577397232 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:21015167 | AATATTTAGATTCCT[A/G]TTGAAATGAGCTATC | 26524 |
rs577407185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20993013 | TGCACTCCAGCCTGG[C/T]GACAAAGTGTGACTC | 26524 |
rs577430534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022307 | GTGTGAGTGTGCATG[C/T]GTGTGAATATCTGTA | 26524 |
rs577443424 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994594 | CTCACCTTCCTTTCT[C/T]AAGCATGTATGGAGA | 26524 |
rs577448008 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040376 | GACAGACCTTGTCTC[-/A]AAAAAAAAAAAAAAA | 26524 |
rs577454649 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LATS2 | GRCh38.p7 | 13:21035304 | TAACCCTAGTAAAAA[C/T]AGTTCTAAAAGAGAG | 26524 |
rs577465281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060585 | CCAGGGTCCGGTGGC[C/T]TCTGAGGGGCTGACT | 26524 |
rs577469332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21015276 | TGCCATCAGCCTCTG[A/G]TGTGAGTGGGATTTG | 26524 |
rs577476540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21022875 | CTGCTTTAAAGGAAA[A/T]AATCATGTTTCCTAG | 26524 |
rs577491827 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:21029037 | GGATCATGTCAAATG[C/G]AAATTGTTATACTTC | 26524 |
rs577509023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21052962 | GAACGCTGGGCCGGG[A/C]ACGGTGGCTCACGCC | 26524 |
rs577577642 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022476 | CTGCACGGTTAGAAG[G/T]TTCTTCCTGTATCCT | 26524 |
rs577613391 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998306 | TGCAGTGAGCTGAGA[C/T]CATGCCACTGCACTC | 26524 |
rs577617380 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024202 | ACTTTGGGAGGCTGA[A/G/T]GGGGAGGGATCACTT | 26524 |
rs577675048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21020839 | CCCTGCTGTCATGTG[A/G]CACAGATGAGCACAC | 26524 |
rs577691348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20975808 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 26524 |
rs577735209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21012850 | ATGAACAAACTGAGG[C/T]TAAAATAGATTAGCT | 26524 |
rs577803815 | snp | C/G | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21014260 | AGGCCTTTTCTTCTT[C/G]TTCTCCCACAGATGC | 26524 |
rs577804644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:20982255 | AGTTCAATGATACAC[C/T]ACATAGATGCAGGTT | 26524 |
rs577874427 | snp | A/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973389 | AAATATGTGGAATAA[A/T]ATAATGAAAATTATG | 26524 |
rs577971767 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974150 | ACACTCAGTAAAAAC[A/G]TATTCACAGGACCTG | 26524 |
rs578044358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21050921 | CCACGCATAGACATG[C/T]CATGATACCACAGCC | 26524 |
rs578070535 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21045114 | AGTGAGACTGTGTTG[A/C]CACAATTTTGACGAT | 26524 |
rs578139213 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LATS2 | GRCh38.p7 | 13:20999685 | CTGGTCTCAAACTCC[A/G]GAGGCCAAGCCATCC | 26524 |
rs578152738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LATS2 | GRCh38.p7 | 13:21038946 | GATCACCCCACTGCA[C/T]TCCAGCCTAGGCACA | 26524 |
rs578172465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LATS2 | GRCh38.p7 | 13:20993876 | AGCTTTTGGCGCCCA[C/T]TAAAAAAATGTGCCA | 26524 |
rs578225874 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059598 | AGACAACGTCTCAAA[A/C]AACAACAACAACAAC | 26524 |
rs578242353 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982012 | AACAACTGCCTGACA[C/T]ATGTTTTAAGATGAG | 26524 |
rs745306395 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052634 | TGGGATAACAGGCGC[C/G]GGCTACCATGCCCAG | 26524 |
rs745332556 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20980348 | TGTGCTGGGTCAGGG[A/C]TGGCCTCTGGGAGGC | 26524 |
rs745355677 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004415 | CTCTAGCCTGGGCAA[A/C]AAGAGCGAAACACTG | 26524 |
rs745371213 | snp | C/T | 4.94597e-05 | 0.00497266 | missense | LATS2 | GRCh38.p7 | 13:20988107 | CCCTTGGCGCTTTTG[C/T]GGCTCTTGTCGCCGC | 26524 |
rs745392188 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059184 | TTAAAAATGTACGTA[-/T]TTTGTTGAATACTTT | 26524 |
rs745422991 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053592 | CCTGCCAGTGCCACC[A/C]CAAAGGTCTAAGGTG | 26524 |
rs745426595 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052127 | AAGGGTCTAACACCC[A/G]CTACTGTCTACCTGA | 26524 |
rs745459466 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991771 | AAGGGGAAGAACTGT[A/G]GGAGTCAGGGAACCT | 26524 |
rs745496081 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021657 | GCCCATGGTCAGCAG[C/T]TTAATTTTTGAAGAA | 26524 |
rs745579207 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979981 | GTGGTGGGGGGCGGT[C/G]GCCATGGCCGCTTAG | 26524 |
rs745587830 | snp | A/G | 4.94189e-05 | 0.00497062 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983507 | TTTGTCTTGGAAGGA[A/G]TAGTAGAGTTTGACC | 26524 |
rs745629360 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033963 | CCATGTGATTTCTGT[A/G]GGACAGGGGACCAGT | 26524 |
rs745659309 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034821 | CAGGAAAGTCATCAA[G/T]AACTCTTAGGAAAAA | 26524 |
rs745687369 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990768 | AGGGGTTTGGTGCGG[C/T]GCCTCAGGCCCATCA | 26524 |
rs745750926 | in-del | -/CCGGGCT | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023152 | GCTGCATCGAGGGCT[-/CCGGGCT]CCGAGGGCTCCGAAG | 26524 |
rs745775225 | in-del | -/GTGTGTGTGT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044706 | TGTGTGTGTGTGTGT[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 26524 |
rs745776774 | snp | C/T | 1.66211e-05 | 0.00288275 | missense | LATS2 | GRCh38.p7 | 13:20989251 | ACGCAAACGAATCGC[C/T]GGTTCCTTCGAAGCT | 26524 |
rs745779618 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045579 | TAGAAACACTTGTAT[A/T]AGTAGTAACCAATTC | 26524 |
rs745781371 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057786 | GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA | 26524 |
rs745859546 | snp | C/T | 0.000296484 | 0.0121719 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988418 | CCCCACAGCCGTCTG[C/T]GGCTCCGGCCTCAGC | 26524 |
rs745876198 | snp | A/G | 1.80221e-05 | 0.00300179 | missense | LATS2 | GRCh38.p7 | 13:20988230 | AGGTGCTTCGGGTAG[A/G]GCGGAGGCGGGCACC | 26524 |
rs745891213 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039520 | TATCCCGAGGAGATC[C/T]GCATTTCTGGTTAGC | 26524 |
rs745891382 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026026 | ACCATCTTTAAGCCA[C/G]CTCTGAAAGCACTGG | 26524 |
rs745937589 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013451 | TGTGGAAAAAGTCCA[A/G]TTTTCTGTAGAGAAG | 26524 |
rs745938198 | in-del | -/GCC | 2.01924e-05 | 0.00317739 | intron-variant | LATS2 | GRCh38.p7 | 13:20979836 | CCTACACAGGCATGA[-/GCC]ATTCTCCTCCGAGGT | 26524 |
rs745944693 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027361 | TTTAGTTCTACAATC[C/T]ATTTTGACTTAATTT | 26524 |
rs745970962 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057167 | TTCTTAAGATCCTTA[A/C]CATCCTAACTGATCA | 26524 |
rs745979163 | snp | C/T | 3.37769e-05 | 0.00410942 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981632 | GGGCTCCATGCTGTC[C/T]TGTCTGACATGGCTC | 26524 |
rs746029039 | snp | G/T | 1.68216e-05 | 0.00290009 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975292 | AGCAGCACAGCTTGG[G/T]GATGAGGTCCCTGGC | 26524 |
rs746080359 | snp | A/C | 3.52734e-05 | 0.00419946 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989000 | CAGGGGTTCCCCAGG[A/C]ACCAGCAGGTGCGGC | 26524 |
rs746143601 | snp | A/G | 1.67565e-05 | 0.00289447 | missense | LATS2 | GRCh38.p7 | 13:20989064 | GCCCCTGCTGCCTCT[A/G]CGCTGGCACCGTAGC | 26524 |
rs746207138 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978038 | CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGAGAC | 26524 |
rs746235580 | snp | A/T | 1.65389e-05 | 0.00287562 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974913 | GTCTGATCCACCAGA[A/T]CAGAGCTTTCTAAAT | 26524 |
rs746253067 | snp | C/G | 1.65899e-05 | 0.00288005 | missense | LATS2 | GRCh38.p7 | 13:20987895 | CTTTGGCCATTTCTT[C/G]CTCCAGCTGCAGCCT | 26524 |
rs746305345 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037512 | TAGGTGTTTTTGAGA[A/G]CTTGCACAGTTCTGG | 26524 |
rs746313454 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987087 | GTAACCCCAACTACT[C/T]GGGAAGCTGAGGCAG | 26524 |
rs746349266 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017100 | GGACTGGGAAGCATC[C/T]CAGTGGTGGTTACTG | 26524 |
rs746380429 | snp | A/T | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062632 | TATCTGTGGCAAGTG[A/T]TGCTGAGGGTCAATA | 26524 |
rs746402291 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050984 | ATGGAAGGCGTGAAC[A/G]GGACCTCTGAGGCAT | 26524 |
rs746424000 | in-del | -/G | 4.98931e-05 | 0.00499441 | frameshift-variant | LATS2 | GRCh38.p7 | 13:20988748 | GTGAGCAGGCTCTGC[-/G]GGGGGGCTGTCGCTG | 26524 |
rs746429950 | snp | A/G | 1.72273e-05 | 0.00293485 | intron-variant | LATS2 | GRCh38.p7 | 13:20983220 | GGCACACTTCAGACA[A/G]TACCTTTCTGGTAAT | 26524 |
rs746430074 | snp | A/C/T | 9.10881e-05 | 0.00674813 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974827 | ACCGGCTCCGGGACC[A/C/T]TGACCTGGGAGGCAG | 26524 |
rs746455173 | snp | C/T | 1.70874e-05 | 0.00292291 | missense, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21045699 | CCTGGTCGCATCCTG[C/T]GTTCACCAGTTCCTG | 26524 |
rs746465470 | snp | A/G | 1.71873e-05 | 0.00293144 | intron-variant | LATS2 | GRCh38.p7 | 13:20987869 | AATAGTAAAAATGAA[A/G]TGTGAAATTACTTTG | 26524 |
rs746527743 | snp | C/G | 3.29451e-05 | 0.00405851 | missense | LATS2 | GRCh38.p7 | 13:20988021 | ACTCTCTCTTCTCTT[C/G]GTCTCTGCTGTTTTT | 26524 |
rs746542589 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986205 | TTAGAACGACTATTA[C/T]CAAAAAGGAAAAAAA | 26524 |
rs746549030 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998454 | GGCTGGCAGAGGAGG[A/C]TGCACTGTCTCTGGC | 26524 |
rs746562263 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043534 | GGGGAAAGGTGGAGG[C/T]ACAGCTGTTTTAAGT | 26524 |
rs746578150 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034082 | TTTCTGAGCACTAAT[A/G]ACACATGGCATTGTG | 26524 |
rs746620390 | snp | A/G | 5.21716e-05 | 0.00510716 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974876 | GGCCCCCATCTACAC[A/G]TACACAGGCTGGCAG | 26524 |
rs746627789 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010898 | TTCATTTGCATAAAT[A/G]GACCTGAGTGAGAAC | 26524 |
rs746637377 | snp | C/T | 1.86416e-05 | 0.00305294 | intron-variant | LATS2 | GRCh38.p7 | 13:21045682 | GCAGAGGTCTGTACC[C/T]ACCTGGTCGCATCCT | 26524 |
rs746669102 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044314 | TTTGGAAATAACAAA[C/T]AACACTGTTAGCCTT | 26524 |
rs746678645 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997615 | GCTGGCCTCACCCAG[A/C]TCTCCAGCTGCTGAC | 26524 |
rs746685365 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053733 | CTATGGCATATTATT[C/G]AGCTATAAAAAGGAA | 26524 |
rs746710757 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011989 | TTTTACCATACAGAG[A/G]GAGAATGTGCAAACT | 26524 |
rs746740960 | snp | C/T | 1.92688e-05 | 0.00310387 | missense | LATS2 | GRCh38.p7 | 13:20988674 | GTGGCAGCCGGCCAC[C/T]GCTGGACGGAGGTGC | 26524 |
rs746751970 | snp | A/G | 4.26485e-05 | 0.00461762 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988300 | CGCCTGCGCCGCCCA[A/G]CGCCAGGGCATGCTC | 26524 |
rs746754142 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035831 | ATTCCTAGAGCCCAC[C/G]TAGGACCTGCGCCAC | 26524 |
rs746785463 | in-del | -/AAAAAAAAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021478 | GAGACTCTGTCTCAA[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 26524 |
rs746792483 | snp | C/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023363 | TCGCCCCCTCTCCAG[C/G]CCCAATTTTCAGTGT | 26524 |
rs746799271 | in-del | -/ACTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018223 | ACTTAGAAAGTAAAC[-/ACTT]AATTAAAAAATACTG | 26524 |
rs746807189 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022425 | CAACCCCCACTAGCC[C/G]CGAAAGCCTAAAATC | 26524 |
rs746807536 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992593 | ACAAGGGCAAAAACA[A/G]GCAAAGGCCACAAAA | 26524 |
rs746825689 | snp | A/C | 0.000161225 | 0.00897701 | missense | LATS2 | GRCh38.p7 | 13:20988372 | GGGCGGGGGCCGGGG[A/C]AGGCGCGGGCACCCA | 26524 |
rs746861687 | in-del | -/ATA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000378 | GAGCAAGACTCTGTC[-/ATA]ATAATAATAATAATA | 26524 |
rs746863385 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052946 | CTCAGCTAGAAAAAC[C/T]GAACGCTGGGCCGGG | 26524 |
rs746873175 | in-del | -/CTAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021951 | AAATCTTTACTTAGA[-/CTAT]CTGTTTCCACACTTT | 26524 |
rs746896733 | in-del | -/TGTG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022287 | GTATTTGTATGTGCA[-/TGTG]TGTGTGAGTGTGCAT | 26524 |
rs746934854 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002865 | GGCTAACTTTATTCT[G/T]TAATTTCTTTTTCAT | 26524 |
rs746947082 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017784 | GCGCCCACCACCACA[C/G]CCAACTAATTTTTAT | 26524 |
rs746988155 | snp | A/G | 2.62312e-05 | 0.00362145 | intron-variant | LATS2 | GRCh38.p7 | 13:20979642 | TTCATGGGTACATGA[A/G]CAAATCAGATGTCTA | 26524 |
rs746989618 | snp | C/T | 1.70136e-05 | 0.00291659 | missense | LATS2 | GRCh38.p7 | 13:20989173 | GCATCTCCTCCAGCG[C/T]CGTGGGGCCGTCAGC | 26524 |
rs746991718 | snp | A/G | 3.6485e-05 | 0.00427097 | missense | LATS2 | GRCh38.p7 | 13:20988969 | GGAAGGAGGGGCTGC[A/G]CTGCACTCCGTAGCC | 26524 |
rs747084524 | snp | C/T | 1.64993e-05 | 0.00287218 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975233 | GAAGAAGGGGTGGGC[C/T]TTCAGGTCATCGGCC | 26524 |
rs747096391 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21001763 | ATGTGCCTGTAGTCC[C/T]AGTTACTCCAGAGGC | 26524 |
rs747112935 | in-del | -/TTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978762 | ACCTATTTTCTCTTC[-/TTT]ATGATTTTTTTTCTT | 26524 |
rs747132216 | snp | A/G | 0.000169434 | 0.00920263 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989042 | CGCGCCCTGCAGCGG[A/G]AAGTGTGCCCCTGCT | 26524 |
rs747196427 | in-del | -/C | 1.64732e-05 | 0.0028699 | frameshift-variant | LATS2 | GRCh38.p7 | 13:20983483 | GTCCATCACAAAGTA[-/C]AGGCTGTCTTTGTCT | 26524 |
rs747231843 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985447 | AATCCCATTAAAAAG[G/T]AAGCCAAAAGGCCAG | 26524 |
rs747232165 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027574 | TTTTTGTACTCTGTT[C/T]CACTACCTGTCTATC | 26524 |
rs747275813 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038676 | CAAAGCTTTATCTAT[C/T]TTTGTAATTAGAAAA | 26524 |
rs747278695 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975151 | TCGAGGTGTCCATGG[G/T]GTGGCTGATGGTGGG | 26524 |
rs747281695 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052209 | CTGTAATGCATGATA[C/T]ACTGATCAATTATCA | 26524 |
rs747289564 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056380 | AGTCTCGGGGAAAAA[C/G]ACACCATCACATTCT | 26524 |
rs747337030 | snp | A/G | 7.30087e-05 | 0.00604144 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974821 | GAGGGCACCGGCTCC[A/G]GGACCCTGACCTGGG | 26524 |
rs747471079 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039746 | AATCTGCCAACACAA[A/T]GCCCAATGCATGGAG | 26524 |
rs747516315 | in-del | -/TTCTA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032240 | CACATACAAACTGAT[-/TTCTA]CTCTGTTCTTATGGC | 26524 |
rs747539045 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050356 | GTATCATTATCACAA[C/T]CCCAGAAGCCTCCAG | 26524 |
rs747572454 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973549 | GTATACACGCACATA[C/T]ATCTATACTTCTAAG | 26524 |
rs747584993 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978887 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC | 26524 |
rs747591469 | snp | C/T | 1.65269e-05 | 0.00287457 | missense | LATS2 | GRCh38.p7 | 13:20981546 | CTCTGGTGCTGCTTC[C/T]GCGCCCTCTGCTCTA | 26524 |
rs747638434 | snp | C/T | 5.27927e-05 | 0.00513747 | missense | LATS2 | GRCh38.p7 | 13:20988608 | AAGGCCACGTGCGCG[C/T]GCGGCGGCGCCTCCA | 26524 |
rs747642074 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017363 | AATTTTTGTAGAAAT[-/G]GGGGTCTTGCTATGT | 26524 |
rs747647509 | snp | A/G | 5.9022e-05 | 0.00543208 | missense | LATS2 | GRCh38.p7 | 13:20988665 | CGGGCCAGGGTGGCA[A/G]CCGGCCACTGCTGGA | 26524 |
rs747657256 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987856 | TGAGCCGGGAACAAA[C/T]AGTAAAAATGAAGTG | 26524 |
rs747688669 | in-del | -/TGTA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022277 | GCGTGTGCATGTATT[-/TGTA]TGTGCATGTGTGTGT | 26524 |
rs747694955 | snp | A/T | 1.71038e-05 | 0.00292431 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983804 | AGCTTCACAGAGTCC[A/T]GCCTGTGTAGAAGGA | 26524 |
rs747697311 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018121 | TTGATCTGAGACTTT[C/T]AGGTAGAATACATGT | 26524 |
rs747782482 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043905 | GGAGAAGATTTTAAG[C/T]TCTGCTGTTGGCCTG | 26524 |
rs747807123 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023709 | CCGGGCGCAGTGGCT[A/G]ACGCCTGTAATTCCA | 26524 |
rs747873424 | snp | A/G | 4.57718e-05 | 0.0047837 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989075 | CTCTACGCTGGCACC[A/G]TAGCCCTTGGGTGGG | 26524 |
rs747887177 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999697 | TCCGGAGGCCAAGCC[A/G]TCCTCCTGCCTCAGC | 26524 |
rs747942359 | in-del | -/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024201 | ACTTTGGGAGGCTGA[-/G]GGGGGAGGGATCACT | 26524 |
rs747960003 | snp | C/G | 1.83065e-05 | 0.00302538 | missense | LATS2 | GRCh38.p7 | 13:20988236 | TTCGGGTAGGGCGGA[C/G]GCGGGCACCTCCGGT | 26524 |
rs747961930 | snp | G/T | 1.71161e-05 | 0.00292536 | missense | LATS2 | GRCh38.p7 | 13:20989163 | TACGGCCGCGGCATC[G/T]CCTCCAGCGCCGTGG | 26524 |
rs747972492 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20980451 | ATCGTCTTCATGTCA[A/C]CTAATCCTTGCTAAG | 26524 |
rs748054096 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022612 | TACCAAAGTCAGAGG[A/G]AAGCTTTTTGTTTAT | 26524 |
rs748060450 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003302 | CTCAGAGTTCGGGCT[A/G]GAGTGCAGTGGCCCA | 26524 |
rs748096042 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037035 | GAAGGTGTGTAGAAG[A/T]ATGTTCATGACCAGC | 26524 |
rs748107274 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21060578 | GGCGCCCCCAGGGTC[C/T]GGTGGCCTCTGAGGG | 26524 |
rs748147200 | snp | A/G | 3.48772e-05 | 0.00417581 | intron-variant | LATS2 | GRCh38.p7 | 13:20987854 | GATGAGCCGGGAACA[A/G]ATAGTAAAAATGAAG | 26524 |
rs748148536 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993782 | CTTCGGGAGCTATGC[A/G]ATGAGATCACGTCTA | 26524 |
rs748171849 | snp | C/G | | | missense | LATS2 | GRCh38.p7 | 13:20981541 | GGCACCTCTGGTGCT[C/G]CTTCCGCGCCCTCTG | 26524 |
rs748177586 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045943 | CGAAGACTTGGATGG[C/T]TGTTTTAACCCCTCA | 26524 |
rs748195196 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020832 | CCTCCATCCCTGCTG[A/T]CATGTGGCACAGATG | 26524 |
rs748209345 | snp | C/G | 4.94181e-05 | 0.00497057 | missense | LATS2 | GRCh38.p7 | 13:20983611 | CATCCTTTTTCCTTA[C/G]GGTCTTCATGGCGTA | 26524 |
rs748263686 | snp | A/G | 3.5598e-05 | 0.00421873 | missense | LATS2 | GRCh38.p7 | 13:20988863 | AGCCCGGCGGCAGGG[A/G]GTGGGAAAGCGAGGC | 26524 |
rs748311543 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974035 | CTTCTCAGTTACACA[C/T]CTGCATTTCTTTAAC | 26524 |
rs748339386 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973682 | ATACTTCAAAGTACA[C/T]TAAAAGAACAAAAAA | 26524 |
rs748343730 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985998 | GTGGTGAGCTGAGAT[C/T]GTGCCATTGCACTCC | 26524 |
rs748353030 | in-del | -/TT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996380 | GAGTGGTAGAAGATT[-/TT]TTTTTTTTTTTTTTT | 26524 |
rs748359156 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016936 | AACTTGCCCGATCCA[C/T]GGCCATGCATCTGTT | 26524 |
rs748401705 | snp | A/G | 1.65875e-05 | 0.00287984 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988169 | CTGCTCCATGCCTGC[A/G]CACAGGCTGTCCAGG | 26524 |
rs748407739 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | LATS2 | GRCh38.p7 | 13:20983478 | ATGTAGTCCATCACA[A/G]AGTACAGGCTGTCTT | 26524 |
rs748445519 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045835 | CTTTGGGGTGGCTCT[C/T]ATCTGCTGCTGCTGC | 26524 |
rs748449125 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20975785 | GCCTCCTGGGTTCAA[A/G]CGATTCTCCTGCCTC | 26524 |
rs748464572 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041133 | GCCCGCCACCATGCC[C/T]GGCTAATTTTTTGTA | 26524 |
rs748491679 | snp | A/C | 1.65356e-05 | 0.00287533 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981509 | GTAGTTTGGAGTCCC[A/C]ACCAGTGAATGTGCC | 26524 |
rs748542423 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985442 | CAAATAATCCCATTA[A/G]AAAGTAAGCCAAAAG | 26524 |
rs748622407 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039940 | TAGCTGGGCGTGGTG[A/G]CGCATGCCTGTAATC | 26524 |
rs748632128 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012507 | GTGGCCCGTGGTTGC[C/T]CGAAACATCGTTATG | 26524 |
rs748632179 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052422 | GTGGCTCAATCTCAG[C/T]TCACTGCAACCTCCA | 26524 |
rs748635204 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009700 | AATACAGAAACCAGA[C/T]GGAGGAACAGCTGCT | 26524 |
rs748727513 | snp | C/G | 1.87036e-05 | 0.00305802 | missense | LATS2 | GRCh38.p7 | 13:20988952 | CGGCGGCGTCTTGCT[C/G]TGGAAGGAGGGGCTG | 26524 |
rs748732052 | snp | C/T | 1.64928e-05 | 0.00287161 | missense | LATS2 | GRCh38.p7 | 13:20988123 | GGCTCTTGTCGCCGC[C/T]CTCGGGCTCGTTGGG | 26524 |
rs748749814 | snp | A/G | 1.69335e-05 | 0.00290972 | intron-variant | LATS2 | GRCh38.p7 | 13:20989330 | AAAAACAGGAAGACA[A/G]CATCAGAGTGGGTGT | 26524 |
rs748771775 | in-del | -/ATAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010931 | GACAGAAACTTTATA[-/ATAT]AAACACAAACACTCC | 26524 |
rs748793724 | snp | A/G | 3.36287e-05 | 0.00410039 | missense | LATS2 | GRCh38.p7 | 13:20981475 | ATGTACCTTTGCGGA[A/G]GAGCACCTCGGGTGC | 26524 |
rs748799507 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979017 | TCTGCCCACCTTGGC[A/C]TTCCAAAGTGGTGGG | 26524 |
rs748829851 | snp | C/T | 8.31705e-05 | 0.00644812 | missense | LATS2 | GRCh38.p7 | 13:20988513 | CGGGCAGGGAGGGCT[C/T]GGCCTTGCCAGGCGG | 26524 |
rs748865218 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051347 | GGCAGAGGAGAAAAT[C/G]AATTATTTAAATACA | 26524 |
rs748868918 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049164 | GACATAGGAGGTCAA[A/C]GGACTCGGGGGTAGT | 26524 |
rs748873575 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21001149 | CAAAGTTCCTTTTAT[A/C]TGTAAAATTCCAGGA | 26524 |
rs748881098 | in-del | -/AAAAAAAAAAAA | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024093 | AGTGTCTCGCTGTGC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 26524 |
rs748888962 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055583 | AATTCCAACCCTCAA[-/T]TCCAATCCTGGAAAA | 26524 |
rs748927965 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033869 | TACATGATTAATAAT[A/T]CTTCTAATGTCATAA | 26524 |
rs749005656 | snp | A/G | 1.66228e-05 | 0.0028829 | missense | LATS2 | GRCh38.p7 | 13:20989263 | CGCCGGTTCCTTCGA[A/G]GCTGGGCCTCCGCGT | 26524 |
rs749019063 | in-del | -/CTAC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027698 | GGTAGTTTAAGGACT[-/CTAC]CTGTGTTCTTTTTTA | 26524 |
rs749025517 | snp | C/T | 3.29522e-05 | 0.00405894 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975171 | CTGATGGTGGGAACG[C/T]AGGGGGCTGGCTGCT | 26524 |
rs749027289 | in-del | -/A | 6.93489e-05 | 0.00588809 | intron-variant | LATS2 | GRCh38.p7 | 13:21045644 | CCCCAGCTGTCCCAT[-/A]AGCTGCCTCTGCACA | 26524 |
rs749044837 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044102 | ACTCTGCACCACATT[A/G]CTCACAACCCTGTGC | 26524 |
rs749061074 | in-del | -/AAAAAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993038 | TGACTCCATCTCCAA[-/AAAAAAA]AAAAAAAAAAAAAAA | 26524 |
rs749096860 | snp | C/T | 1.67798e-05 | 0.00289648 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983786 | CCGCATCTGCTCCTG[C/T]TCAGCTTCACAGAGT | 26524 |
rs749105936 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061321 | TCCGAGCTGCCGCCC[C/T]GACCCCAGCTCCCAG | 26524 |
rs749117314 | snp | C/G/T | 9.91206e-05 | 0.00703933 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975244 | GGGCCTTCAGGTCAT[C/G/T]GGCCCCATTCCGCCC | 26524 |
rs749172685 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012498 | ATCATACATGTGGCC[C/T]GTGGTTGCCCGAAAC | 26524 |
rs749228491 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041634 | ACAGGCAGGATACAG[C/G]TCATCCACAGAGAAA | 26524 |
rs749239408 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21025861 | CCATACGGCCCTGTA[C/T]GTCTGGGTTGATTTT | 26524 |
rs749280010 | snp | C/G | 2.87882e-05 | 0.00379384 | missense | LATS2 | GRCh38.p7 | 13:20988592 | TGGGCAGTCAGGCCG[C/G]AAGGCCACGTGCGCG | 26524 |
rs749288607 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013362 | ATTTCTTGGACTATG[A/G]CTAATGTGCATGAGG | 26524 |
rs749296230 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984164 | GTCTTGAACTCCTGA[C/T]CTCAGGTGATCTGCC | 26524 |
rs749315535 | snp | A/C | 1.65603e-05 | 0.00287747 | missense | LATS2 | GRCh38.p7 | 13:20983254 | TGGAATTGTGAGTCC[A/C]CCTGAACCCAGTGCA | 26524 |
rs749333942 | snp | C/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024231 | TTGAGGTCAGGAGTT[C/G]AAGACCAGCCTGGCC | 26524 |
rs749334072 | snp | A/T | 1.6476e-05 | 0.00287014 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974945 | TGAGCTCTCAGCCTG[A/T]GAAGCTTCTGCTCCT | 26524 |
rs749334843 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037291 | TGCCTGTAATTCCAG[C/G]TACTCAGGAGGCTGA | 26524 |
rs749349382 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993984 | TCTGTCTCCTGCAGG[G/T]TGAATCACCAGCCTG | 26524 |
rs749391853 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983456 | GCTCATCATGTCCCC[A/G]CCAGGGATGTAGTCC | 26524 |
rs749423745 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018818 | GCCCAGCTAATTTTT[-/G]TATTTTTAGTAGAGA | 26524 |
rs749491909 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051865 | GGAGGCTGAGGTGGG[-/A]AGAATCACTTAAACC | 26524 |
rs749509866 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017817 | TTTTACTAGAGATGG[A/G]GTTTCACCATGTTGG | 26524 |
rs749523070 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005328 | TTGACAGGGTGTAGC[A/G]TAAGCCAGAGGGATG | 26524 |
rs749559845 | snp | C/T | 3.12534e-05 | 0.00395294 | missense | LATS2 | GRCh38.p7 | 13:20988855 | GCACGTAGAGCCCGG[C/T]GGCAGGGGGTGGGAA | 26524 |
rs749573432 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992863 | AACATGGTGAAATCC[C/T]GTCTCTGCTAAAAAT | 26524 |
rs749588481 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012708 | AGGGAACGAGCAGAA[A/G]GAGAGGAAGATGGAA | 26524 |
rs749597666 | snp | A/T | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20988041 | CTGCTGTTTTTGCGG[A/T]CGGGAACGGGAGAGG | 26524 |
rs749648130 | snp | A/G | 3.33244e-05 | 0.0040818 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975275 | CAGGCGGTGGTCTGC[A/G]GAGCAGCACAGCTTG | 26524 |
rs749681245 | in-del | -/GTGGG | 1.86946e-05 | 0.00305727 | intron-variant | LATS2 | GRCh38.p7 | 13:20979818 | GACAAAGTTCACTCA[-/GTGGG]ATCCCTACACAGGCA | 26524 |
rs749692731 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998880 | CCACGACCTTGTGCA[-/C]GCGGGGCGGGGGCCC | 26524 |
rs749695347 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986988 | ACCTGAGGTCAAGAG[C/T]TCGAGACCAGTCTGA | 26524 |
rs749770895 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045822 | GATAAGGTCCGAACT[G/T]TGGGGTGGCTCTCAT | 26524 |
rs749777356 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029310 | TTTCTGAAATGCTTA[A/C]TCTATCTATTGAGAT | 26524 |
rs749808684 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997496 | GGCTGGTCCTCTCAA[C/T]TGCAAGGACCACACC | 26524 |
rs749809080 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986030 | GCCTGGGCAACAAGA[C/G]CGAAACTCTGTCTCA | 26524 |
rs749867787 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045927 | CGGGTAGCCCCTGAA[C/T]CGAAGACTTGGATGG | 26524 |
rs749874418 | snp | A/G | 1.83464e-05 | 0.00302868 | missense | LATS2 | GRCh38.p7 | 13:20988795 | GGGAGCCCAGCACAT[A/G]CAGCTGGTGGGCCGC | 26524 |
rs749922228 | snp | C/T | 1.90903e-05 | 0.00308947 | missense | LATS2 | GRCh38.p7 | 13:20988926 | GGCAGGCTGGCGTAA[C/T]CCCCGGTCTCCGGCG | 26524 |
rs749922275 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035097 | CAAACAAAACCAAAA[-/C]AAAACAAAAAAGCAA | 26524 |
rs749940600 | snp | C/T | 1.6519e-05 | 0.00287388 | missense | LATS2 | GRCh38.p7 | 13:20988146 | TCGTTGGGGCCCGCA[C/T]GGAGGCTCTGCTCCA | 26524 |
rs749998754 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997183 | GTTTCACTGGTTTAC[-/T]GCTGCTACTGACAGC | 26524 |
rs750050823 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048774 | CCAGGGAGGCGGGGG[A/T]TGCAGTGAGCCGAGA | 26524 |
rs750082382 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055845 | CTAAATCAGGCAGAC[A/G]GGCCAGGCCTCCAGC | 26524 |
rs750091868 | snp | A/G | 0.00056296 | 0.0167679 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046009 | ATAAGTCGTGGCAGG[A/G]AAAGTCTTTGGCCTC | 26524 |
rs750137189 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992464 | CCCAGTGGCGCGGGG[C/T]GGTGAGGCTCTGATG | 26524 |
rs750153923 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059148 | ATATTTGTTTCTTAT[C/T]AAAATACGGGCAAAC | 26524 |
rs750159534 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974592 | AAGAAAAAATGGATA[C/T]AAACAAAATAAGTGC | 26524 |
rs750176654 | snp | G/T | 1.64958e-05 | 0.00287187 | missense | LATS2 | GRCh38.p7 | 13:20991318 | CTGCTCATTCCTCGG[G/T]TCCAGGTAGCCCATC | 26524 |
rs750262336 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016753 | TGCTTTTCCAAACCA[A/G]GGGCAGGCAACTGAT | 26524 |
rs750264804 | snp | A/C | 1.66291e-05 | 0.00288345 | intron-variant | LATS2 | GRCh38.p7 | 13:20991446 | GTGCATGTCATCCTA[A/C]AACAAAGCCACCAAA | 26524 |
rs750280455 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21047758 | ACTATGTGTCAGGTG[C/T]GGTTCAAAGAATTAA | 26524 |
rs750320471 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985190 | ATGAAAATATACTCC[A/G]GGACATTGGTTTGAG | 26524 |
rs750324988 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041846 | GACTCATAGGCACCA[A/T]CCTGAGTGCTATAAT | 26524 |
rs750368852 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028823 | TCCACCCGCCTTGGC[C/T]TCCCAGAGTACTGAG | 26524 |
rs750425852 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029835 | GGCGTAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 26524 |
rs750461080 | snp | C/T | 1.83791e-05 | 0.00303137 | missense | LATS2 | GRCh38.p7 | 13:20989139 | ACTCCGGGGAAAAGG[C/T]AGTCCACGTACGGCC | 26524 |
rs750464042 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030344 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGACA | 26524 |
rs750529314 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995889 | TATTTACAGAGTAAT[A/G]TGGTAGGCTAACAAG | 26524 |
rs750596929 | in-del | -/AAAAAAAAAAAAAAAAAC | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023667 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAC]AAACCTCGGCCGGGC | 26524 |
rs750600828 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982780 | GCGGATCACCTGAGG[C/T]TGGGAGTTTGAGACC | 26524 |
rs750604597 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020945 | TTCACTTTATTATCT[C/T]TAAGCCACACATCCG | 26524 |
rs750620465 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991148 | TGCCTGTTAACTGAA[C/T]GAGGCAATGTGCCAG | 26524 |
rs750628413 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20987983 | GAACTTAAAGGCGTA[C/T]GGCGAGTAGCTCTTG | 26524 |
rs750644391 | snp | G/T | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062951 | AAAGAAACCATCATC[G/T]TGCAGCTTAGAATTC | 26524 |
rs750688373 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009063 | GCTCTTTCTTCACAG[C/T]CTTGCCCCCTTGTCC | 26524 |
rs750758299 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033490 | TCACAGGGTGGGGCT[G/T]CTTACTCTAACAGTT | 26524 |
rs750781702 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20989671 | TGCTTTTTCAAAACC[C/T]TATCATGCCCAAATT | 26524 |
rs750798997 | snp | C/T | 3.81061e-05 | 0.00436482 | missense | LATS2 | GRCh38.p7 | 13:20988468 | GGTGCAAGATGTGCG[C/T]GGCCGTGACAGCCGT | 26524 |
rs750808017 | in-del | -/GT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022208 | TGTGCAACTACGTAA[-/GT]GTGTGAATATGTGCA | 26524 |
rs750813337 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019037 | CCCAGTAGCTCTGTA[C/T]GTGGGAACCAGACAT | 26524 |
rs750816560 | snp | C/T | 0.000131781 | 0.00811621 | missense | LATS2 | GRCh38.p7 | 13:20983430 | GGGAAGACCTCCATC[C/T]GGATCAGCAGGCTCA | 26524 |
rs750825968 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999433 | GCTAATCTCTGTATC[A/G]TTCCAATTTTCATAT | 26524 |
rs750826165 | in-del | -/AG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034506 | CTGGAACACCACTGC[-/AG]AGGTGCCGTCTGGTG | 26524 |
rs750829854 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045912 | CACTGTTTGGTCCTG[C/T]GGGTAGCCCCTGAAC | 26524 |
rs750830955 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983570 | CCTCTCGGCCTTGAC[A/G]TGGGCCACCTGATTC | 26524 |
rs750834638 | snp | A/T | 3.29451e-05 | 0.00405851 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975049 | GCTCAGGATGCTTGT[A/T]ATTGGGCGAGGTGAG | 26524 |
rs750931152 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044970 | TGGCCTCAAGTGATC[A/T]TCTTGACTGGCCTCC | 26524 |
rs750941303 | snp | A/G | 9.8256e-05 | 0.00700845 | missense | LATS2 | GRCh38.p7 | 13:20988345 | AGCCCTCCGCAGCCG[A/G]GGCGGGGGCGGGGGC | 26524 |
rs750967838 | in-del | -/A | 1.80994e-05 | 0.00300822 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974845 | ACCTGGGAGGCAGCG[-/A]GTGGTGGGGGTGCCT | 26524 |
rs750989061 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020214 | AAGATTCTTCATCAA[A/G]GCAAGGAGCTTCTGA | 26524 |
rs751006272 | snp | G/T | 4.94181e-05 | 0.00497057 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045893 | TTGGCATCCAGGGAA[G/T]TGTCACTGTTTGGTC | 26524 |
rs751008064 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984079 | GGGACTACATGTGCC[C/T]GCCACCATGACACCT | 26524 |
rs751010495 | snp | A/G | 1.86579e-05 | 0.00305428 | missense | LATS2 | GRCh38.p7 | 13:20988764 | GGGGGGCTGTCGCTG[A/G]CGAACACCTGGCTGC | 26524 |
rs751051318 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012953 | AGTACTTGTTTCTAT[G/T]GCAAAGCAATTAGTT | 26524 |
rs751051817 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054477 | TGGACCTAGGGACTG[C/G]GTAGGATATAGCAGG | 26524 |
rs751075564 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058475 | TGGCTATTTACAACA[G/T]AGCATTTAAAATAAC | 26524 |
rs751120247 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21025218 | AACCCCGTCTCTACT[-/AA]AAAAAAAAAAAAAAA | 26524 |
rs751131540 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20977048 | CCCTGAGGACATTAC[A/G]CTAAGTGAAATAAAC | 26524 |
rs751176682 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055896 | CATAAACCACTATGT[A/G]GATGTACCACACCAG | 26524 |
rs751234294 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011953 | TGCAAGTTTAAGCAA[A/G]ATGATGTCTAACAAA | 26524 |
rs751239712 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994564 | CAGCTGAAGCCTGGC[C/T]GAGGAGCTTGGCCAC | 26524 |
rs751274094 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049021 | AATAAAAAAGAAAGA[C/G]CTCTAGAAATAATTA | 26524 |
rs751290209 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20983206 | TAGAAAGTGCATGTG[A/G]CACACTTCAGACAAT | 26524 |
rs751295450 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973138 | TCCTGAGAAAGAACC[C/T]ACCACATGAAAGTAT | 26524 |
rs751330930 | snp | A/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063139 | CACTCCATTGCCCAC[A/G]CTGGAGTGCAGTGGC | 26524 |
rs751345722 | snp | A/G | 1.67666e-05 | 0.00289534 | intron-variant | LATS2 | GRCh38.p7 | 13:20989310 | AGCCCCTTTCCTGCA[A/G]TGGAAAAAACAGGAA | 26524 |
rs751353738 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20977148 | CACCTATAATCCCAA[C/T]ATTTTGGGAGGCTGA | 26524 |
rs751361530 | snp | A/G | 3.5859e-05 | 0.00423417 | intron-variant | LATS2 | GRCh38.p7 | 13:20979800 | AGTTGAGTGTACCCT[A/G]CAAGACAAAGTTCAC | 26524 |
rs751389167 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048473 | TCATGCTCAAAATAC[A/G]TTCACTCGGCCATCT | 26524 |
rs751434182 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005003 | TAGCCAGGAAGCCTT[A/C]AGCAGAGAGCACAGG | 26524 |
rs751447916 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032084 | TAGTTCCTAAGGGTT[C/T]CACTTTCCGTTTTCT | 26524 |
rs751456234 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20975833 | GGATTACAGGCGCCT[A/G]CCACCACACCCGGCT | 26524 |
rs751564042 | snp | C/G | | | missense | LATS2 | GRCh38.p7 | 13:20988098 | CCTTTGTCCCCCTTG[C/G]CGCTTTTGCGGCTCT | 26524 |
rs751609425 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041954 | CAACCAGAGAGAAAA[C/T]AAGTCCCAGGCTTCC | 26524 |
rs751650182 | snp | C/T | | | missense | LATS2 | GRCh38.p7 | 13:20983739 | GCCCTCTTTAACCTG[C/T]TGTAATTAGACTCTT | 26524 |
rs751656446 | snp | G/T | 1.75758e-05 | 0.00296438 | intron-variant | LATS2 | GRCh38.p7 | 13:20987838 | CTATTGCCAGTAGAG[G/T]GATGAGCCGGGAACA | 26524 |
rs751672737 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029876 | CCAGGGTGGGTGGAT[C/T]ATGAGGTCAGGAGAT | 26524 |
rs751732345 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059330 | TGGCTGGGTGCGGTG[G/T]CTTACGCCTGTAATC | 26524 |
rs751775751 | snp | C/G | 1.66239e-05 | 0.00288299 | missense | LATS2 | GRCh38.p7 | 13:20983772 | TGGTAGAGGATCTTC[C/G]GCATCTGCTCCTGCT | 26524 |
rs751840171 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997060 | GCCCTGGACCAGATA[C/G]AAGGAATTCTTCCCA | 26524 |
rs751858648 | snp | C/G | 2.06759e-05 | 0.0032152 | missense | LATS2 | GRCh38.p7 | 13:20988643 | CGGCTTCTGCAGGGA[C/G]TCCCGGCGGGCCAGG | 26524 |
rs751866991 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011790 | ATCATTAGGTGATTT[C/T]GTTGTTGTGTGAACA | 26524 |
rs751950050 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990012 | AGGCCAACTGCTCCA[C/G]TTGGCTCGGCTTAGC | 26524 |
rs751957428 | snp | A/C/G | 4.53507e-05 | 0.00476169 | stop-gained, synonymous-codon | LATS2 | GRCh38.p7 | 13:20988262 | CCGGTCTGGGCCTCC[A/C/G]TACTCCACGTCCAGC | 26524 |
rs751975912 | snp | C/G/T | 4.41472e-05 | 0.00469805 | missense | LATS2 | GRCh38.p7 | 13:20988336 | TGGCGTCCAAGCCCT[C/G/T]CGCAGCCGGGGCGGG | 26524 |
rs752026330 | snp | A/G | 3.68392e-05 | 0.00429165 | intron-variant | LATS2 | GRCh38.p7 | 13:20975384 | GGAAACAACAGAGCC[A/G]ACAGGTTAGTTTCTC | 26524 |
rs752045866 | snp | A/G | 7.85345e-05 | 0.00626587 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989129 | GTGGGGGCCGACTCC[A/G]GGGAAAAGGTAGTCC | 26524 |
rs752046570 | in-del | -/TAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020315 | TTGCACGAACAATTC[-/TAT]TATTATCCTATTATT | 26524 |
rs752048513 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002183 | CTCCTAAAGTGCTGG[G/T]ATTACACGTGTGAGC | 26524 |
rs752077857 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20975500 | AGACACAAGCAGCAG[C/T]TGTTGATCTCAGCAG | 26524 |
rs752078406 | snp | C/G | 1.99003e-05 | 0.00315432 | intron-variant | LATS2 | GRCh38.p7 | 13:21045673 | CATGGCCCTGCAGAG[C/G]TCTGTACCCACCTGG | 26524 |
rs752100551 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034602 | ACACTGTGGACTGCC[A/G]TGCCACCACAGCCTG | 26524 |
rs752127840 | snp | C/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973221 | TGACAGTCACGACGA[C/G]AGGCACAGCAGACTT | 26524 |
rs752143953 | snp | A/G | 1.77467e-05 | 0.00297876 | intron-variant | LATS2 | GRCh38.p7 | 13:20983194 | GACATCTACACATAG[A/G]AAGTGCATGTGGCAC | 26524 |
rs752153759 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035465 | ACAGAATTGCATGCA[G/T]ACTGGAGACCCAGAA | 26524 |
rs752182817 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000913 | AGGGCTTGATTAGAA[C/T]ATGAAAAAAATTAAA | 26524 |
rs752216344 | snp | C/G | 1.76839e-05 | 0.00297349 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974865 | TGGGGGTGCCTGGCC[C/G]CCATCTACACGTACA | 26524 |
rs752232946 | in-del | -/GCGCCTGCGCCGCCCAGC | 3.08024e-05 | 0.00392432 | cds-indel | LATS2 | GRCh38.p7 | 13:20988284 | ACGTCCAGCGGGAAG[-/GCGCCTGCGCCGCCCAGC]GCCAGGGCATGCTCC | 26524 |
rs752236817 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015357 | TGCAGACACACGAAG[A/G]ACCAGGACCCTAGTG | 26524 |
rs752250610 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040439 | CTGTGGAAGTTTGAA[G/T]AGGAACAGCTCGATC | 26524 |
rs752338072 | snp | A/G | 3.96762e-05 | 0.00445382 | missense | LATS2 | GRCh38.p7 | 13:20988249 | GAGGCGGGCACCTCC[A/G]GTCTGGGCCTCCGTA | 26524 |
rs752343187 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026586 | GTGTACAAGTCTTTT[C/T]GTAGACATGTTTTCA | 26524 |
rs752398703 | in-del | -/TCCTCC | 1.81368e-05 | 0.00301132 | intron-variant | LATS2 | GRCh38.p7 | 13:20979805 | GTGTACCCTGCAAGA[-/TCCTCC]CAAAGTTCACTCAAT | 26524 |
rs752418117 | snp | C/T | 7.13988e-05 | 0.00597447 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988838 | CTTGTGGTGTGGGTG[C/T]GGCACGTAGAGCCCG | 26524 |
rs752428329 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051706 | GCTCACACATGTAAT[-/C]CTGGCACTTTGGGAG | 26524 |
rs752447213 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017305 | TCATAAAAACACTTC[C/T]CTTACATAGAGGTGA | 26524 |
rs752486076 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050932 | CATGCCATGATACCA[C/T]AGCCACGTGAGGGGG | 26524 |
rs752541920 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | LATS2 | GRCh38.p7 | 13:20988090 | CCTTTCCGCCTTTGT[C/T]CCCCTTGGCGCTTTT | 26524 |
rs752544052 | snp | C/T | 1.85603e-05 | 0.00304628 | intron-variant | LATS2 | GRCh38.p7 | 13:20975408 | GTTTCTCCTCACATC[C/T]TGGGCAGTTCTGGGA | 26524 |
rs752546501 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049999 | GACAGCACACCCCTG[C/T]AGTCCAGCTACTCGG | 26524 |
rs752551406 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039064 | TTGCTTGTGTCTTGT[A/C]AAAGTAATTTAAATT | 26524 |
rs752584377 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20977451 | AAGCAGAAGAGAGGC[A/G]AGCAGGTGCTGAAAA | 26524 |
rs752614553 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005177 | CACTAAGTTAGAGAG[A/G]AACCCACTTTAAAAG | 26524 |
rs752615675 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005915 | GGTCAGGAGTTCAAG[A/C]CCAGCCTGACTGACA | 26524 |
rs752615895 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033297 | GAGGGGCGAGAGAAC[A/G]CACGCTCCTGGTGTA | 26524 |
rs752636706 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006588 | GTTTGGGCTCCAAGC[C/T]ACTCCTGGCTCCTGA | 26524 |
rs752698814 | snp | C/T | | | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972661 | AGGCCTCATCAACAA[C/T]TTAAAATGCAAGGTC | 26524 |
rs752716919 | snp | A/G | 1.86799e-05 | 0.00305608 | missense | LATS2 | GRCh38.p7 | 13:20988752 | AGCAGGCTCTGCGGG[A/G]GGCTGTCGCTGGCGA | 26524 |
rs752778622 | snp | A/C/G | 3.30749e-05 | 0.00406652 | stop-gained, synonymous-codon | LATS2 | GRCh38.p7 | 13:20983759 | ATTAGACTCTTTCTG[A/C/G]TAGAGGATCTTCCGC | 26524 |
rs752792340 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987668 | ATGCACAGCTATCTC[C/T]GATTCTTCAGAAGAG | 26524 |
rs752807024 | snp | A/T | 3.86108e-05 | 0.00439362 | missense | LATS2 | GRCh38.p7 | 13:20988555 | GCTGGTGGCTGTTGA[A/T]GGAGTTGGTCCTGCT | 26524 |
rs752809879 | in-del | -/AAAAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987220 | AAAAAATAAAAAATA[-/AAAAT]AAAAAAAACACAAAT | 26524 |
rs752909480 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043103 | CCTTGGGAGGCCGAA[C/T]GAAGCAGGCAGATCA | 26524 |
rs752928808 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986742 | TATTCAATATTTCAA[A/C]ATAGCTAGAAGAGAG | 26524 |
rs752942223 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21047997 | AATATAGTAAAGTCA[C/T]TGAAATGACTGTAAG | 26524 |
rs752942283 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022859 | TTTTGCAGATTATTT[C/G]CTGCTTTAAAGGAAA | 26524 |
rs752954404 | snp | C/T | 0.000122317 | 0.00781942 | missense | LATS2 | GRCh38.p7 | 13:20988492 | CAGCCGTCACGGTGT[C/T]GGGGGCGGGCAGGGA | 26524 |
rs752960432 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032418 | GATTATGGCGCCCAC[C/T]ACCACGTCTGGCTAA | 26524 |
rs753016623 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054116 | TCTCCTAACTACTCC[C/T]ATTTAGCAAACTCGT | 26524 |
rs753021165 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998842 | GACATTGTGCACGCC[A/G]GGTGGGGGCCCTGCG | 26524 |
rs753026198 | snp | A/G | 3.32066e-05 | 0.00407458 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975265 | CATTCCGCCCCAGGC[A/G]GTGGTCTGCGGAGCA | 26524 |
rs753049071 | snp | A/G | 8.83509e-05 | 0.00664588 | missense | LATS2 | GRCh38.p7 | 13:20989040 | TGCGCGCCCTGCAGC[A/G]GGAAGTGTGCCCCTG | 26524 |
rs753082832 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974691 | GAAAGCGATGCTGAG[C/T]CCTGTTTTCAAAAGT | 26524 |
rs753088545 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979923 | AAGCATCGCACTGTG[C/T]GCAAGATGGACCTAT | 26524 |
rs753092502 | snp | C/T | 6.59381e-05 | 0.00574149 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975214 | TGGAGAAGTCAATGG[C/T]GCTGAAGAAGGGGTG | 26524 |
rs753096733 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979251 | TAAAGTTTTTGGGGA[A/G]TTGAAAGTTATGCAG | 26524 |
rs753133972 | snp | C/G | 1.72068e-05 | 0.00293311 | missense | LATS2 | GRCh38.p7 | 13:20988216 | TGCTGCGCAGCAGCA[C/G]GTGCTTCGGGTAGGG | 26524 |
rs753145161 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011839 | CAAACCTAGATGCTA[C/T]AGCCCCCTACACACC | 26524 |
rs753146534 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992376 | GGTCAGGCTGGGGGC[A/G]GCTGTGGGTGCAGAG | 26524 |
rs753152787 | snp | A/G | 5.58332e-05 | 0.00528332 | intron-variant | LATS2 | GRCh38.p7 | 13:20983855 | CATTAGAGAAGTCCC[A/G]TGATAACAAATGACT | 26524 |
rs753246414 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036631 | TACAAAAATTAGCCC[A/G]GCATGGTGGCGCGTG | 26524 |
rs753259829 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007177 | TTTGAAATATATACA[C/T]ATTATGGGTTTAATT | 26524 |
rs753286419 | snp | G/T | 1.68801e-05 | 0.00290512 | missense | LATS2 | GRCh38.p7 | 13:20988201 | CGTACTGCTCCGACT[G/T]GCTGCGCAGCAGCAG | 26524 |
rs753308714 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023371 | TCTCCAGGCCCAATT[C/T]TCAGTGTGAAAGCTC | 26524 |
rs753361598 | snp | A/C/T | 3.31786e-05 | 0.00407289 | missense | LATS2 | GRCh38.p7 | 13:20981585 | AGCCTGTCCCCACAC[A/C/T]GACAGTTAGACACAT | 26524 |
rs753375698 | in-del | -/TATAGT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007641 | ATATATATATATATA[-/TATAGT]GTGTGTATATATATA | 26524 |
rs753391804 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019897 | GAGAATTGCTTGAAC[C/T]CAGGAGGTGGAGTTC | 26524 |
rs753428765 | snp | C/T | 1.65064e-05 | 0.00287279 | missense | LATS2 | GRCh38.p7 | 13:20991353 | TGATGTACTCCAGGG[C/T]GGCCTCGATGCTCCT | 26524 |
rs753447426 | snp | G/T | | | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972765 | ACCCACCATATTTAT[G/T]TGACATCCCACTTAA | 26524 |
rs753453827 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059065 | CCTCATCTTCTAAGT[C/T]AAAATTTTAAGCAAA | 26524 |
rs753486909 | snp | A/G | 0.000103471 | 0.00719201 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989030 | CCGCCCGTAGTGCGC[A/G]CCCTGCAGCGGGAAG | 26524 |
rs753492271 | snp | C/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973539 | GTGTGTGTGTGTATA[C/G]ACGCACATACATCTA | 26524 |
rs753522258 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015695 | ATCAGTTCATCCCTC[A/T]TTTTATTTATTTATT | 26524 |
rs753549394 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974303 | AGATATGCAAAAAGC[C/T]AAAAAAAGCAGCTTT | 26524 |
rs753567261 | snp | A/T | 6.59663e-05 | 0.00574272 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045742 | GTTCACTTCTGCAGC[A/T]GCAGAGGTGCCCGAT | 26524 |
rs753574373 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994657 | CCCAACACTTTGGGA[A/G]ACTGAGGCAGGAAGA | 26524 |
rs753575292 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033521 | CCAGCCTAAAATGCC[-/A]GAAAAATAGTGGAAA | 26524 |
rs753583711 | snp | A/G | 8.78002e-05 | 0.00662513 | intron-variant | LATS2 | GRCh38.p7 | 13:20987842 | TGCCAGTAGAGGGAT[A/G]AGCCGGGAACAAATA | 26524 |
rs753597550 | snp | G/T | 1.80292e-05 | 0.00300238 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974851 | GAGGCAGCGAGTGGT[G/T]GGGGTGCCTGGCCCC | 26524 |
rs753702341 | in-del | -/AA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036784 | TCTCAAAACAACAAC[-/AA]CAACAACAAAAAACA | 26524 |
rs753724836 | snp | C/G | 1.7835e-05 | 0.00298617 | intron-variant | LATS2 | GRCh38.p7 | 13:20983184 | TGGGGTTAGTGACAT[C/G]TACACATAGAAAGTG | 26524 |
rs753741011 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994780 | GTAATCCCAGCTACT[A/G]AAGAGGTTGAGGCAG | 26524 |
rs753758967 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011156 | CCATCAAATCATCTT[A/G]TATCAGGACCATGGC | 26524 |
rs753776424 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995740 | AACATTATCAACAGC[A/G]GCAACTTCCAAGTTT | 26524 |
rs753816666 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039158 | AGAAAAAAAAAGGGG[A/G]AAAGGCAAGGAACTG | 26524 |
rs753860632 | snp | C/T | 4.62337e-05 | 0.00480778 | intron-variant | LATS2 | GRCh38.p7 | 13:21045644 | GCCCCAGCTGTCCCA[C/T]AGCTGCCTCTGCACA | 26524 |
rs753871561 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040579 | CAGAGAGACCCAAAG[C/T]AAGCAAGCGGGAAGA | 26524 |
rs753896872 | in-del | -/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063326 | CCAAGCCACATGGCT[-/G]GCTAATCTTTTTTTG | 26524 |
rs753933515 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020760 | GACATAAGCTGACAA[C/T]TACCCTACATGGAAC | 26524 |
rs753951508 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20988032 | TCTTCGTCTCTGCTG[C/T]TTTTGCGGACGGGAA | 26524 |
rs754027352 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027614 | GCCAATGCCACACTG[A/T]CTTGCTTAGCTTTAG | 26524 |
rs754042853 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033324 | TGTAGAGGAAAGAAT[C/T]TGGAAACTACCAAGG | 26524 |
rs754115426 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055772 | GGATTTCTTGAACCT[A/G]AAATTCCAGCTATTA | 26524 |
rs754159698 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20989559 | CAAGGGCAGAAGAGA[A/C]GACTGCGTCCACATC | 26524 |
rs754165821 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987081 | GCACCTGTAACCCCA[A/G]CTACTCGGGAAGCTG | 26524 |
rs754283453 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999258 | GGCCGCCTCCGACCG[C/T]TGGTGGCGCCGCAGG | 26524 |
rs754335873 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054169 | TAAACATAGCTACAC[A/G]GCTGGGTGCAGTGGC | 26524 |
rs754362058 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024898 | GGCCTCCAAAGCCAC[A/G]CATGGCCTGGGGCTG | 26524 |
rs754388230 | snp | A/G | 0.000246554 | 0.0111003 | missense | LATS2 | GRCh38.p7 | 13:20988539 | GGCGGACCGGGCCGC[A/G]GCTGGTGGCTGTTGA | 26524 |
rs754499289 | in-del | -/AAAAATAAAAAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987212 | ATAAATTAAAAAATA[-/AAAAATAAAAAT]AAAAATAAAAATAAA | 26524 |
rs754532751 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055917 | ACCACACCAGCACTG[C/T]CAAGCCAGGAAGCCA | 26524 |
rs754533161 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043552 | AGCTGTTTTAAGTTA[C/T]AAAGTAACACCACAC | 26524 |
rs754554285 | in-del | -/AAC | 3.6505e-05 | 0.00427214 | intron-variant | LATS2 | GRCh38.p7 | 13:20975372 | TTGATCACCTGAGGA[-/AAC]AACAGAGCCAACAGG | 26524 |
rs754558907 | snp | C/T | 3.30825e-05 | 0.00406696 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988157 | CGCACGGAGGCTCTG[C/T]TCCATGCCTGCGCAC | 26524 |
rs754564305 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035937 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 26524 |
rs754586728 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999461 | TATCTGCTGCAGAAG[C/T]GAGCACTTTTTCTTT | 26524 |
rs754616027 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012109 | TGTTGCACAGCCTGA[A/G]ATTGTAGTGAATACT | 26524 |
rs754631706 | snp | A/C | 0.000398287 | 0.0141062 | missense | LATS2 | GRCh38.p7 | 13:20989032 | GCCCGTAGTGCGCGC[A/C]CTGCAGCGGGAAGTG | 26524 |
rs754654769 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21025604 | TTCATGACACGTGAG[A/G]TAGTATGCTATGAAA | 26524 |
rs754677875 | in-del | -/TAC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017272 | AGTTTTTTTCTTTTG[-/TAC]TACTATGACTCACAA | 26524 |
rs754694537 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054481 | CCTAGGGACTGGGTA[A/G]GATATAGCAGGGCAA | 26524 |
rs754749973 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992740 | CCAGACAGCAGAGAA[G/T]AAAGGGGTGGAGATG | 26524 |
rs754762909 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036964 | AATGCTCTCAACATT[C/T]ACGCTAGTAATTCCA | 26524 |
rs754775962 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005082 | ATTCTAGGAAAAATC[C/T]GGGAACCATTAGTCA | 26524 |
rs754784249 | snp | A/C | 1.75585e-05 | 0.00296293 | intron-variant | LATS2 | GRCh38.p7 | 13:20987843 | GCCAGTAGAGGGATG[A/C]GCCGGGAACAAATAG | 26524 |
rs754827442 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993739 | TGACCCCACCTGGGA[C/T]AGGAGATAAGACTCC | 26524 |
rs754855459 | snp | C/G/T | 4.26979e-05 | 0.00462033 | intron-variant | LATS2 | GRCh38.p7 | 13:21045664 | GCCTCTGCACATGGC[C/G/T]CTGCAGAGGTCTGTA | 26524 |
rs754895490 | snp | C/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061631 | GCCGCATACCAGTCC[C/G]GGCGGGGCGCCTGCG | 26524 |
rs754913744 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017610 | CCTTCCCTTCAAAAG[A/G]TGACTCATTTCTTTC | 26524 |
rs754938751 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004082 | AAGCAGCACACAAAG[A/T]ACTTTAAAATGAATA | 26524 |
rs754949444 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049131 | ATTCAGGTCTGTGCA[A/G]TGCAGGCTCTTCCTG | 26524 |
rs754963258 | snp | C/G | 2.72885e-05 | 0.00369371 | missense | LATS2 | GRCh38.p7 | 13:20988603 | GCCGGAAGGCCACGT[C/G]CGCGCGCGGCGGCGC | 26524 |
rs754966041 | in-del | -/AT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986864 | GTAACAAAATATCAC[-/AT]GTTCCCCACAAATCT | 26524 |
rs754974571 | snp | A/G | 1.79544e-05 | 0.00299615 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974855 | CAGCGAGTGGTGGGG[A/G]TGCCTGGCCCCCATC | 26524 |
rs754974924 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | LATS2 | GRCh38.p7 | 13:20983461 | TCATGTCCCCACCAG[A/G]GATGTAGTCCATCAC | 26524 |
rs754981700 | snp | A/G | 3.97812e-05 | 0.00445971 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988658 | GTCCCGGCGGGCCAG[A/G]GTGGCAGCCGGCCAC | 26524 |
rs754984666 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043334 | GAGCAAGACACCGTC[-/T]TAAAAAAAAAAAAGA | 26524 |
rs754998895 | snp | A/G | 1.824e-05 | 0.00301988 | missense | LATS2 | GRCh38.p7 | 13:20988488 | GTGACAGCCGTCACG[A/G]TGTTGGGGGCGGGCA | 26524 |
rs755007059 | in-del | -/GAACAAAC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009165 | TGGTGAGTGATGAAT[-/GAACAAAC]GAACAAATGAATGAA | 26524 |
rs755009205 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985975 | CTTGAACCCGGGAGG[C/T]GGAGGTTGTGGTGAG | 26524 |
rs755062247 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986687 | ACAGCTGGATAGAAG[A/G]AACAAACTCTAACTA | 26524 |
rs755064183 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975110 | GGCATCGTTCCAAGG[A/G]CTTTCTTCATCTACG | 26524 |
rs755169631 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016872 | AGAGTCCTTAACTGC[C/T]TACCTTGTTCCTGTT | 26524 |
rs755209445 | snp | C/G | 0.000918105 | 0.0214058 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988367 | GGCGGGGGCGGGGGC[C/G]GGGGCAGGCGCGGGC | 26524 |
rs755211321 | snp | A/G | 1.66891e-05 | 0.00288864 | missense | LATS2 | GRCh38.p7 | 13:20989296 | CTGGGGTTGGCATGA[A/G]CCCCTTTCCTGCAGT | 26524 |
rs755228774 | snp | A/C/T | 3.54869e-05 | 0.00421218 | synonymous-codon, intron-variant | LATS2 | GRCh38.p7 | 13:20979796 | ACAGAGTTGAGTGTA[A/C/T]CCTGCAAGACAAAGT | 26524 |
rs755230492 | snp | A/C | 1.64789e-05 | 0.0028704 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975202 | TCCGGATGTCACTGG[A/C]GAAGTCAATGGCGCT | 26524 |
rs755244621 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009184 | AAACGAACAAATGAA[C/T]GAATGAATAAAGAAG | 26524 |
rs755249711 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028908 | GCTAGTTCACAAAAA[A/G]ACTACTGATTTTTGC | 26524 |
rs755252753 | snp | A/C | 1.90496e-05 | 0.00308617 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988943 | CCCGGTCTCCGGCGG[A/C]GTCTTGCTCTGGAAG | 26524 |
rs755263255 | in-del | -/CAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976587 | AGAACTCCTACAACT[-/CAA]CAACAATAACAAAAC | 26524 |
rs755332165 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052106 | TTCAAGCTCCTGCAC[A/G]GTACCAAGGGTCTAA | 26524 |
rs755337151 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022219 | GTAAGTGTGTGAATA[C/T]GTGCATGCATGTGTG | 26524 |
rs755367521 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996010 | TTAATTTAGGAAAGC[G/T]TAATTTAGGATTGGG | 26524 |
rs755383286 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053342 | AGGACCTTCCTGACC[A/T]CCCCAATCTAAGGGA | 26524 |
rs755426636 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991474 | AAAGACTCCCATCCC[C/T]ACTCCGTGCTGGACT | 26524 |
rs755431012 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024094 | AGTGTCTCGCTGTGC[-/AA]AAAAAAAAAAAAAAA | 26524 |
rs755441778 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010299 | ACTGGCTTCAACTCT[C/G]CTCCCCTGCCAACCC | 26524 |
rs755483976 | in-del | -/TTTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003435 | TTTTGTCTGTCTTTC[-/TTTT]TTTTCCTTTTTTTTT | 26524 |
rs755534479 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045928 | GGGTAGCCCCTGAAC[C/T]GAAGACTTGGATGGC | 26524 |
rs755582869 | snp | A/G | 3.30387e-05 | 0.00406427 | missense | LATS2 | GRCh38.p7 | 13:20988147 | CGTTGGGGCCCGCAC[A/G]GAGGCTCTGCTCCAT | 26524 |
rs755583254 | snp | C/G | 1.93399e-05 | 0.0031096 | intron-variant | LATS2 | GRCh38.p7 | 13:20979830 | CTCAATCCCTACACA[C/G]GCATGAATTCTCCTC | 26524 |
rs755670085 | in-del | -/CTT | 1.77307e-05 | 0.00297742 | cds-indel | LATS2 | GRCh38.p7 | 13:20988319 | CAGGGCATGCTCCTC[-/CTT]GGCGTCCAAGCCCTC | 26524 |
rs755675791 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056102 | ACTGAGCATTGTGCT[A/G]GACACTATAAGGTCT | 26524 |
rs755693910 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014286 | GATGCCAGCAAACCA[C/G]GGAGGACAATTAGCA | 26524 |
rs755769191 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992770 | GGCTGGGCGTGGTGG[C/T]TCACGCCTGTAATCC | 26524 |
rs755891065 | snp | A/G | 3.42366e-05 | 0.00413729 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988571 | GGAGTTGGTCCTGCT[A/G]GGCACTGGGCAGTCA | 26524 |
rs755932669 | snp | C/T | | | missense | LATS2 | GRCh38.p7 | 13:20983569 | CCCTCTCGGCCTTGA[C/T]GTGGGCCACCTGATT | 26524 |
rs755932798 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994685 | AGACTGCTTGAGCCC[A/G]GGAGTTTGAGGCCAG | 26524 |
rs755934489 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003614 | ACCCGGCTAATTTTT[G/T]TATTTTTAGTAGAGA | 26524 |
rs755976636 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990469 | ACTAGGATTTTTTTT[-/T]TTTTTTTTTTTTTTT | 26524 |
rs755985643 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984136 | ACAGCGTTTCATCAT[A/G]TTGGCCAGGCTGGTC | 26524 |
rs756015566 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039696 | GGCCTCCAGAGACAC[C/T]GCCTAAGACAGGGAG | 26524 |
rs756027275 | snp | C/T | 0.000304481 | 0.0123348 | missense | LATS2 | GRCh38.p7 | 13:20981471 | GCGCATGTACCTTTG[C/T]GGAGGAGCACCTCGG | 26524 |
rs756093791 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017711 | GCTCACTGCAACCTC[C/T]GTCTCCGGGGTTCAA | 26524 |
rs756096841 | in-del | -/CA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036721 | GAGGTTACAGTGAGC[-/CA]AGATGGCACCACTGC | 26524 |
rs756098345 | snp | C/T | 2.81583e-05 | 0.00375211 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988277 | GTACTCCACGTCCAG[C/T]GGGAAGGCGCCTGCG | 26524 |
rs756099339 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993901 | GTGCCAATTGGGGCT[A/G]ACTCTAACCACAAGC | 26524 |
rs756099892 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038223 | AAAGGTGGAGCCTGT[A/G]CCGGGGGCAGGAGAG | 26524 |
rs756117480 | snp | A/G | 1.69103e-05 | 0.00290773 | intron-variant | LATS2 | GRCh38.p7 | 13:20989326 | TGGAAAAAACAGGAA[A/G]ACAGCATCAGAGTGG | 26524 |
rs756133873 | snp | A/G | 1.64972e-05 | 0.00287199 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20991323 | CATTCCTCGGGTCCA[A/G]GTAGCCCATCTTGCT | 26524 |
rs756133955 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005943 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 26524 |
rs756171433 | in-del | -/TT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058499 | AAATAACAAGGAATC[-/TT]ATTGTAAAATCATTC | 26524 |
rs756258396 | snp | C/T | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063274 | ATGCTTGGCCTTCTT[C/T]TCACTCTTAAGCTGA | 26524 |
rs756335536 | snp | C/T | 7.22661e-05 | 0.00601064 | missense | LATS2 | GRCh38.p7 | 13:20989143 | CGGGGAAAAGGTAGT[C/T]CACGTACGGCCGCGG | 26524 |
rs756338635 | snp | C/G | 1.68337e-05 | 0.00290114 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975293 | GCAGCACAGCTTGGT[C/G]ATGAGGTCCCTGGCC | 26524 |
rs756338747 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986891 | AATCTACAAATACTA[C/T]GTATAAATAAAAAAT | 26524 |
rs756359871 | snp | A/G | 1.85444e-05 | 0.00304498 | intron-variant | LATS2 | GRCh38.p7 | 13:20975405 | TTAGTTTCTCCTCAC[A/G]TCTTGGGCAGTTCTG | 26524 |
rs756362357 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032509 | TGGCCTCAAGCAATC[A/G]CCCACCTCAGCCTCC | 26524 |
rs756368023 | snp | A/C | 1.64732e-05 | 0.0028699 | missense | LATS2 | GRCh38.p7 | 13:20983578 | CCTTGACGTGGGCCA[A/C]CTGATTCCGGTTCAG | 26524 |
rs756369801 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036406 | ACTCACCGCCAAAAT[A/G]AGAGCTTTCTAGTAC | 26524 |
rs756442095 | in-del | -/A | 1.81592e-05 | 0.00301318 | intron-variant | LATS2 | GRCh38.p7 | 13:20979806 | TGTACCCTGCAAGAC[-/A]AAAGTTCACTCAATC | 26524 |
rs756454532 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042083 | ACTTACCTTTCCAAT[A/T]CCTTAAATCTATATT | 26524 |
rs756481455 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975051 | TCAGGATGCTTGTTA[C/T]TGGGCGAGGTGAGTG | 26524 |
rs756507577 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043193 | AAATACAAAAATTAG[C/G]CAGGCGTGGTGTTGC | 26524 |
rs756521585 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030243 | GGGTGGGGACAAATA[G/T]CCAAACTATATCAAC | 26524 |
rs756540056 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000165 | GGCGGGCAGATCACA[A/C]AGTTAGGAGATCGAG | 26524 |
rs756566294 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981069 | CACCCAGCTGCACAC[A/G]GCACAACTCAGCCAG | 26524 |
rs756569960 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20975882 | AGAGACAGGGTTTCA[A/C]CACGTTGGCCAGGCT | 26524 |
rs756594539 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052543 | TTTAGCAGAGATGGG[C/G]GTTTCACCCTGTTGC | 26524 |
rs756616768 | snp | A/G | 0.00858353 | 0.0649468 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988349 | CTCCGCAGCCGGGGC[A/G]GGGGCGGGGGCGGGG | 26524 |
rs756666534 | snp | C/T | 4.94189e-05 | 0.00497062 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045816 | CTTTCTGATAAGGTC[C/T]GAACTTTGGGGTGGC | 26524 |
rs756702960 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | LATS2 | GRCh38.p7 | 13:20983431 | GGAAGACCTCCATCC[A/G]GATCAGCAGGCTCAT | 26524 |
rs756709543 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991618 | GCACAAGCCACACCA[G/T]AGACTATTTAGCCTT | 26524 |
rs756716690 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023385 | TTTCAGTGTGAAAGC[C/T]CTTGGTTCTTAAAAG | 26524 |
rs756763606 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021633 | TTCTTGTCAGCATTG[C/T]TCAAAGCTGCCCATG | 26524 |
rs756766482 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992414 | CACTCAGATGGGGGA[A/G]ACAGAATAGGCAGGA | 26524 |
rs756797795 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979977 | TGGGGTGGTGGGGGG[C/G]GGTGGCCATGGCCGC | 26524 |
rs756830452 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992966 | CTTGAAACCTGGGAG[A/G]TGGAGGCTGCAGTGA | 26524 |
rs756833597 | snp | C/G | 1.67281e-05 | 0.00289202 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974900 | CTGGCAGCCTTCAGT[C/G]TGATCCACCAGATCA | 26524 |
rs756870991 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002524 | GGACTACAGGTGCGT[G/T]ACCACCACACCCAGC | 26524 |
rs756888274 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022327 | GAATATCTGTATATG[A/C]CTAAGTGCATGTACT | 26524 |
rs756898869 | in-del | -/TAC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058914 | GAATATTTTTTCTGT[-/TAC]TACCTTATTACAACG | 26524 |
rs756901277 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045793 | GGAATATCTGATTTC[C/T]CTCAAGGCTTTCTGA | 26524 |
rs756905759 | snp | A/C | 1.86083e-05 | 0.00305021 | missense | LATS2 | GRCh38.p7 | 13:20988770 | CTGTCGCTGGCGAAC[A/C]CCTGGCTGCGGGAGC | 26524 |
rs756917621 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045896 | GCATCCAGGGAAGTG[C/T]CACTGTTTGGTCCTG | 26524 |
rs756933412 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028711 | AATTAGCTGGGATTA[C/G]AGGCATGCACCACCA | 26524 |
rs756968058 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974310 | CAAAAAGCCAAAAAA[A/G]GCAGCTTTTAACATT | 26524 |
rs757005967 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975040 | AAAATGCGTGCTCAG[A/G]ATGCTTGTTATTGGG | 26524 |
rs757012449 | snp | C/T | 1.71047e-05 | 0.00292439 | intron-variant | LATS2 | GRCh38.p7 | 13:20981459 | TGGCTGGCCATGGCG[C/T]ATGTACCTTTGCGGA | 26524 |
rs757040672 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985073 | ACATGCTGGGAAAAC[C/T]AGATATCCATATGCA | 26524 |
rs757048305 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046773 | CACAAAGCCTGTCAC[A/G]TTAAAACTGTCCCAT | 26524 |
rs757056437 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015723 | ATTTATTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 26524 |
rs757079568 | snp | C/T | | | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972726 | ATGCTGGGGAATTAG[C/T]TCTTATTCATGATTT | 26524 |
rs757089362 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059072 | TTCTAAGTTAAAATT[A/T]TAAGCAAAACACTTG | 26524 |
rs757117301 | snp | A/T | 5.04528e-05 | 0.00502234 | intron-variant | LATS2 | GRCh38.p7 | 13:20989318 | TCCTGCAGTGGAAAA[A/T]ACAGGAAGACAGCAT | 26524 |
rs757194565 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995744 | TTATCAACAGCAGCA[A/G]CTTCCAAGTTTTACT | 26524 |
rs757199803 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056236 | ATGAGATGGGGTTTC[A/G]CCATGTCACCCAAGC | 26524 |
rs757296078 | in-del | -/TTT/TTTTTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019493 | ACCACGCCCAGCTAA[-/TTT/TTTTTT]TTTTTTTTTTTTTGT | 26524 |
rs757325184 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21025209 | ACATGGCGAAACCCC[A/G]TCTCTACTAAAAAAA | 26524 |
rs757361474 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044690 | CTATGAGGTGTAGGG[-/GTGTGTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 26524 |
rs757393621 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008846 | TTCCACCCCCTAGAT[A/C]AGTTCCCCACCTTTG | 26524 |
rs757395941 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051066 | CTGCCCTCTAGAAGA[C/T]GTGTGACGCATACGC | 26524 |
rs757412184 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038458 | TCCTCCTGCCTCAGC[C/T]GACCAGACTGTTGAG | 26524 |
rs757448278 | snp | A/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063552 | CCCAAATGTCCAGTC[A/G]AGGGGTAGGAAAATG | 26524 |
rs757463851 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978513 | ACTAGCCTGACCACA[C/T]AGCTGACAGTTTGCG | 26524 |
rs757465555 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039209 | AATACAATTTCCTGT[C/T]ACATGACCGACATTC | 26524 |
rs757472527 | snp | A/G | 3.32546e-05 | 0.00407752 | missense | LATS2 | GRCh38.p7 | 13:20983773 | GGTAGAGGATCTTCC[A/G]CATCTGCTCCTGCTC | 26524 |
rs757536873 | snp | C/T | 1.65026e-05 | 0.00287246 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975235 | AGAAGGGGTGGGCCT[C/T]CAGGTCATCGGCCCC | 26524 |
rs757579118 | in-del | -/T | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062741 | CAGTAGTAAAGGTCA[-/T]TATCTGTGCACTATT | 26524 |
rs757642545 | in-del | -/CCC | 1.88018e-05 | 0.00306603 | intron-variant | LATS2 | GRCh38.p7 | 13:20979821 | CAAAGTTCACTCAAT[-/CCC]TACACAGGCATGAAT | 26524 |
rs757644100 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999306 | ACCAGACACACGCCC[A/G]GAAGACACCTGCTCG | 26524 |
rs757654065 | snp | A/C/T | 3.52878e-05 | 0.00420035 | intron-variant | LATS2 | GRCh38.p7 | 13:20983202 | CACATAGAAAGTGCA[A/C/T]GTGGCACACTTCAGA | 26524 |
rs757658067 | snp | A/G | 0.000100145 | 0.00707549 | missense | LATS2 | GRCh38.p7 | 13:20988338 | GCGTCCAAGCCCTCC[A/G]CAGCCGGGGCGGGGG | 26524 |
rs757658445 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014618 | TGACCATCCATGCAG[C/G]AACTGAAACAAGCTC | 26524 |
rs757793180 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054170 | AAACATAGCTACACG[A/G]CTGGGTGCAGTGGCT | 26524 |
rs757807180 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998220 | TTAGCTGGGCATGGT[C/G]GTGGGTGCCTGTAGT | 26524 |
rs757833559 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033975 | TGTGGGACAGGGGAC[C/T]AGTCGCACCCAGGCT | 26524 |
rs757855419 | snp | C/T | 1.75854e-05 | 0.00296519 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974869 | GGTGCCTGGCCCCCA[C/T]CTACACGTACACAGG | 26524 |
rs757866261 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981186 | TCCATCATCTGACTG[G/T]GAAAATCAGGGCTGG | 26524 |
rs757873625 | in-del | -/AT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022286 | TGTATTTGTATGTGC[-/AT]GTGTGTGTGAGTGTG | 26524 |
rs757955227 | snp | C/T | 1.66454e-05 | 0.00288486 | missense | LATS2 | GRCh38.p7 | 13:20981604 | AGTTAGACACATCAT[C/T]CCAGAGGTCGCTGGG | 26524 |
rs758066332 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036739 | GATGGCACCACTGCA[C/T]TCCAGCCTGGGCGAC | 26524 |
rs758078480 | snp | C/T | 1.9679e-05 | 0.00313674 | intron-variant | LATS2 | GRCh38.p7 | 13:21045675 | TGGCCCTGCAGAGGT[C/T]TGTACCCACCTGGTC | 26524 |
rs758091658 | snp | C/T | 2.07717e-05 | 0.00322264 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988253 | CGGGCACCTCCGGTC[C/T]GGGCCTCCGTACTCC | 26524 |
rs758123390 | snp | C/G | 7.08918e-05 | 0.00595322 | intron-variant | LATS2 | GRCh38.p7 | 13:20983197 | ATCTACACATAGAAA[C/G]TGCATGTGGCACACT | 26524 |
rs758149930 | snp | A/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047109 | ATTTTCCAATAGTAA[A/T]TTCTACCTACCCCAG | 26524 |
rs758188971 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21047872 | AAGGGGATTGTAAGC[A/G]TTTTAACTATCCCCT | 26524 |
rs758190025 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003923 | AGGCCCTAAAGTAAA[C/T]AATTGGTTGGGTTAA | 26524 |
rs758206067 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016818 | CCTCTCACTAATAAA[A/T]CTCCACACAACACCT | 26524 |
rs758226580 | snp | G/T | 1.8583e-05 | 0.00304814 | intron-variant | LATS2 | GRCh38.p7 | 13:20975409 | TTTCTCCTCACATCT[G/T]GGGCAGTTCTGGGAC | 26524 |
rs758240394 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048799 | CCGAGATCGCACCAT[C/T]GCACTCCAGCCTGGG | 26524 |
rs758257680 | snp | G/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973805 | TCTGTCAGTAAAAAG[G/T]TAAGTAGTAGGGTCA | 26524 |
rs758259741 | snp | A/C | 1.8697e-05 | 0.00305747 | missense | LATS2 | GRCh38.p7 | 13:20988759 | TCTGCGGGGGGCTGT[A/C]GCTGGCGAACACCTG | 26524 |
rs758259880 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048326 | CCTATAGGAATTCAC[A/G]CAAATCACTTTGTTT | 26524 |
rs758282786 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991839 | ACTAGGAAACCTGTC[C/T]CCAGGGAGAGGGTGC | 26524 |
rs758348290 | in-del | -/CGGGCT | | | intron-variant, cds-indel | LATS2 | GRCh38.p7 | 13:21023153 | CTGCATCGAGGGCTC[-/CGGGCT]CCGAGGGCTCCGAAG | 26524 |
rs758401309 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040815 | CTGATAAACTCCATG[A/C]CCCACAGACATGAGG | 26524 |
rs758415673 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985249 | AGCACAGGCAAAAAA[A/G]CCCCAAAGTAGACAA | 26524 |
rs758420428 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995891 | TTTACAGAGTAATGT[A/G]GTAGGCTAACAAGAC | 26524 |
rs758457062 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005802 | GAGTGAGACCCCTAC[C/T]CTATAAAAAAAAAAA | 26524 |
rs758481913 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996895 | AATATTAAATGAAAA[A/G]TTATTTTGTCAGATT | 26524 |
rs758519441 | in-del | -/GGGTGC | 0.000185436 | 0.00962723 | cds-indel | LATS2 | GRCh38.p7 | 13:20989087 | CCGTAGCCCTTGGGT[-/GGGTGC]GGGTGCTGGTGCTGG | 26524 |
rs758543844 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027506 | CTCATTGAATTTTCA[A/T]GGTACTTGTGTTGAA | 26524 |
rs758556640 | snp | A/C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051915 | TGAGTCAAGGTCACA[A/C/T]TACTGCACTCCAGCC | 26524 |
rs758560733 | snp | A/G | 3.83178e-05 | 0.00437692 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988556 | CTGGTGGCTGTTGAA[A/G]GAGTTGGTCCTGCTG | 26524 |
rs758585092 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009068 | TTCTTCACAGTCTTG[C/T]CCCCTTGTCCTGCCA | 26524 |
rs758599748 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028859 | AGGTGTGAGCCACCG[C/T]ACCCGGCCAAATTTC | 26524 |
rs758628208 | snp | A/G | 4.94181e-05 | 0.00497057 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983612 | ATCCTTTTTCCTTAG[A/G]GTCTTCATGGCGTAC | 26524 |
rs758639228 | snp | A/C | 0.000111626 | 0.00746997 | missense | LATS2 | GRCh38.p7 | 13:20988498 | TCACGGTGTTGGGGG[A/C]GGGCAGGGAGGGCTC | 26524 |
rs758657521 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039602 | ACAGAACTTTCACTG[A/G]TGAGCAAGCACTGAT | 26524 |
rs758685795 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037455 | CTATTCAATGGAATG[-/A]AAAATGTTTATGACG | 26524 |
rs758737831 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043060 | AACTCTCGGCCAGAC[A/G]TGGTGACGCACGCCT | 26524 |
rs758742881 | in-del | -/AGG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043889 | CTGCAAGTGATTTAC[-/AGG]AGAAGATTTTAAGCT | 26524 |
rs758765234 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009861 | CCAGGCCCCCGCCCC[-/A]ACACCAAATCAGACT | 26524 |
rs758782062 | snp | A/G | 3.44116e-05 | 0.00414784 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988217 | GCTGCGCAGCAGCAG[A/G]TGCTTCGGGTAGGGC | 26524 |
rs758843168 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978749 | ATTAAAATAGTAAAC[C/T]TATTTTCTCTTCTTT | 26524 |
rs758906063 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052160 | GGCTTGCCTTGAGGA[A/T]CACAGTGGTGCTGTG | 26524 |
rs758926751 | snp | A/T | 1.9549e-05 | 0.00312636 | missense | LATS2 | GRCh38.p7 | 13:20988246 | GCGGAGGCGGGCACC[A/T]CCGGTCTGGGCCTCC | 26524 |
rs758948258 | snp | A/G | | | missense | LATS2 | GRCh38.p7 | 13:20988129 | TGTCGCCGCCCTCGG[A/G]CTCGTTGGGGCCCGC | 26524 |
rs758956734 | snp | A/G | 1.85252e-05 | 0.0030434 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988961 | CTTGCTCTGGAAGGA[A/G]GGGCTGCGCTGCACT | 26524 |
rs758967547 | snp | C/T | 1.66007e-05 | 0.00288098 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975267 | TTCCGCCCCAGGCGG[C/T]GGTCTGCGGAGCAGC | 26524 |
rs758975100 | snp | A/G/T | 0.000172314 | 0.00928077 | missense | LATS2 | GRCh38.p7 | 13:20989041 | GCGCGCCCTGCAGCG[A/G/T]GAAGTGTGCCCCTGC | 26524 |
rs758990811 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984799 | CAAAATACCAATGAT[A/G]TTTTTCACATTACTA | 26524 |
rs759028523 | in-del | -/GATTGTG | 2.15789e-05 | 0.00328466 | frameshift-variant | LATS2 | GRCh38.p7 | 13:20988257 | ACCTCCGGTCTGGGC[-/GATTGTG]CTCCGTACTCCACGT | 26524 |
rs759029789 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002189 | AAGTGCTGGGATTAC[A/G]CGTGTGAGCCACTGC | 26524 |
rs759037938 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013931 | AGCTATGATTGCACC[A/G]CTGTACTCCAGCCTG | 26524 |
rs759055573 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054083 | TTTTCCTCAATTTTT[-/A]AAAAATGGGGAAAAA | 26524 |
rs759073395 | snp | C/T | 3.37206e-05 | 0.00410599 | missense | LATS2 | GRCh38.p7 | 13:20989188 | CCGTGGGGCCGTCAG[C/T]GCCGAAGCTTGGGCC | 26524 |
rs759114360 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027785 | CAGCTTGTCAATTTC[A/T]ATTAAAAAAAATAAA | 26524 |
rs759119902 | snp | C/T | 2.5891e-05 | 0.00359789 | missense | LATS2 | GRCh38.p7 | 13:20989112 | TGCTGGTGGCCGGGC[C/T]CGTGGGGGCCGACTC | 26524 |
rs759167381 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056971 | AAAAAATGTTGGGGA[A/G]GGTGCAGGTGTCGTC | 26524 |
rs759199737 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045858 | GCTGCTGCCTGGTGG[C/G]ATCTTTGCTCCCCAG | 26524 |
rs759207855 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018503 | CACCTGGCCTTTGAT[G/T]AAAGGACAAGCAGGA | 26524 |
rs759238945 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049887 | GCTCTTTCGGATGCC[A/G]AGGCAGGCAGATCAC | 26524 |
rs759251801 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994620 | GGAGACCAAGCTGGA[G/T]GTGGTGGCTCATGCC | 26524 |
rs759286630 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981656 | ATGGCTCCCTTCACC[C/G]AGGAATCAGGGATAG | 26524 |
rs759355501 | snp | A/T | 4.94173e-05 | 0.00497053 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975082 | TGTCCCAGGCCTTGG[A/T]GCTACCTTCGCTGGC | 26524 |
rs759368766 | snp | A/G | 3.7428e-05 | 0.0043258 | missense | LATS2 | GRCh38.p7 | 13:20988749 | GTGAGCAGGCTCTGC[A/G]GGGGGCTGTCGCTGG | 26524 |
rs759411221 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006545 | CATGAACAGATTAAA[C/T]GTGACTCCGGAAGAG | 26524 |
rs759465941 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987615 | CTAATTTACCTACAA[G/T]GTAAATTGTAGATTA | 26524 |
rs759496187 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997972 | TAAAGTTTTAACATT[C/T]CAACTATGAGGTTTG | 26524 |
rs759500955 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994193 | GAAGACTCATGTTCA[C/G]AAGGGAGTTTCAAGT | 26524 |
rs759518316 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045748 | TTCTGCAGCTGCAGA[A/G]GTGCCCGATTCATTA | 26524 |
rs759583857 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983357 | GATGAAGCCCATCTT[A/G]TGGACACTCTCAATG | 26524 |
rs759624422 | snp | A/G | 1.65315e-05 | 0.00287498 | intron-variant | LATS2 | GRCh38.p7 | 13:20991260 | CCCACTATGCTGCAG[A/G]CCTGGGCTCACCTGG | 26524 |
rs759625572 | in-del | -/TCTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013607 | TATGTTGGAACGTTC[-/TCTT]TATTTACTCTCTGAA | 26524 |
rs759628142 | snp | C/T | 1.65304e-05 | 0.00287488 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981551 | GTGCTGCTTCCGCGC[C/T]CTCTGCTCTAGGGTC | 26524 |
rs759710814 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986816 | AATGGATACTCTAAA[C/T]ACCTTGACTTGATCA | 26524 |
rs759721927 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032334 | GCAATGGCGCGATCT[G/T]GGCTCACTGCAACCT | 26524 |
rs759760041 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008099 | TCTGGCTCCACCGTG[A/G]GGAGCCAGGTATGAG | 26524 |
rs759786158 | in-del | -/AAAG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032752 | AAATGGGAATTCAGA[-/AAAG]AAAGAACTTAGCGGG | 26524 |
rs759818155 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21025255 | AAATTAGACGGGTAT[A/G]GTGGCAAGCACCTAT | 26524 |
rs759819941 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018818 | CCCAGCTAATTTTTG[-/T]TATTTTTAGTAGAGA | 26524 |
rs759825868 | snp | A/G | 1.76005e-05 | 0.00296647 | intron-variant | LATS2 | GRCh38.p7 | 13:20983824 | GTGTAGAAGGAAAAG[A/G]AAGGAGGAAGAATCA | 26524 |
rs759831265 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992936 | GCTACTCAGGAGGCT[A/G]AGGCAGGTGAATTGC | 26524 |
rs759852402 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004545 | GCACTGACCAGCACA[C/T]GTGTGTGTCAGCATG | 26524 |
rs759940007 | snp | G/T | 1.65814e-05 | 0.00287931 | intron-variant | LATS2 | GRCh38.p7 | 13:20991427 | GGAAGTAAAGGAGAG[G/T]TAAGTGCATGTCATC | 26524 |
rs760003572 | snp | A/T | 9.07194e-05 | 0.00673435 | missense | LATS2 | GRCh38.p7 | 13:20988542 | GGACCGGGCCGCGGC[A/T]GGTGGCTGTTGAAGG | 26524 |
rs760024209 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003598 | GGTGCCTCGCCACCA[C/T]ACCCGGCTAATTTTT | 26524 |
rs760026476 | snp | A/G | 8.88707e-05 | 0.00666539 | missense, synonymous-codon | LATS2 | GRCh38.p7 | 13:20975345 | GCTGGAATGTGGAGC[A/G]TGTTCTCCCAGTTGA | 26524 |
rs760089773 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | LATS2 | GRCh38.p7 | 13:20983728 | TGTCCATCTTGGCCC[C/T]CTTTAACCTGTTGTA | 26524 |
rs760125990 | snp | C/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974199 | GGTAATTTTATAATA[C/G]AAGAACTCTGCTCAT | 26524 |
rs760130517 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015612 | TAAATAGGATTTGGG[G/T]AACTGTGAAAAATTA | 26524 |
rs760140371 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047544 | CAATGAGCAGATTTC[A/G]AAGGATAATCATTTT | 26524 |
rs760153697 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035484 | GGAGACCCAGAACTC[A/G]GAGCCCCTCTCCCAG | 26524 |
rs760185410 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016508 | TGGTCTCAAACTGCT[G/T]ACCTCAAGTGATCTG | 26524 |
rs760187832 | in-del | -/TCCC | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047496 | TTAGTGGCTGCCCCT[-/TCCC]TCACCCACTCCCCCT | 26524 |
rs760190495 | in-del | -/TTTAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982312 | GCTGTGACTCTTTTA[-/TTTAT]TTTATTTTATTTGAG | 26524 |
rs760203072 | snp | A/C/T | 3.30744e-05 | 0.00406649 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975252 | AGGTCATCGGCCCCA[A/C/T]TCCGCCCCAGGCGGT | 26524 |
rs760217856 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041513 | GGGAAAGAACTGGAT[A/T]AATCAGGATTAGGAA | 26524 |
rs760268008 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059902 | CCTGGGAGACGGAGG[C/T]TGCAGTGAGCCGAGA | 26524 |
rs760309651 | snp | A/G | 1.72713e-05 | 0.0029386 | intron-variant | LATS2 | GRCh38.p7 | 13:20983813 | GAGTCCAGCCTGTGT[A/G]GAAGGAAAAGGAAGG | 26524 |
rs760359990 | snp | C/T | 1.65861e-05 | 0.00287972 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046018 | GGCAGGAAAAGTCTT[C/T]GGCCTCATTGTTAGT | 26524 |
rs760363121 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996573 | TTTAGTAGAGGTGGC[A/G]TTTTGCCATGTTGGC | 26524 |
rs760382408 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019636 | GTGTGAGCCACCGCA[C/T]CCAGCTGGATTTGTT | 26524 |
rs760391059 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984907 | GACTTCAAAATATGT[G/T]ACAAGCCTAGAGTAA | 26524 |
rs760406321 | snp | G/T | 1.64944e-05 | 0.00287175 | intron-variant | LATS2 | GRCh38.p7 | 13:20981697 | GAACAAAATATAAAG[G/T]GAATTTTCACTCTTC | 26524 |
rs760418287 | snp | C/T | 1.81306e-05 | 0.00301081 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974843 | TGACCTGGGAGGCAG[C/T]GAGTGGTGGGGGTGC | 26524 |
rs760432773 | snp | A/C | | | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972671 | AACAATTTAAAATGC[A/C]AGGTCAGGAGCTCTA | 26524 |
rs760446066 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975189 | GGGGCTGGCTGCTTC[C/T]GGATGTCACTGGAGA | 26524 |
rs760484600 | in-del | -/CT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013062 | CCAAGCAGTGTAAGG[-/CT]CTGTTCTAAGCACTG | 26524 |
rs760486874 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051646 | TGGTGGAGGAGGAAG[G/T]CAGTGACCAAAGGTG | 26524 |
rs760495945 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020580 | ACAGCTAGATGGCCA[C/T]AAATGTTGTCCTGCT | 26524 |
rs760505593 | snp | A/G | 2.3391e-05 | 0.00341979 | intron-variant | LATS2 | GRCh38.p7 | 13:21045634 | CATTCTGACTGCCCC[A/G]GCTGTCCCATAGCTG | 26524 |
rs760523262 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009516 | AACAATTAACAGACT[A/G]TTAAGTAAAAACACA | 26524 |
rs760581826 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979273 | GTTATGCAGATTTTT[G/T]ACTGTGCAGGGGGTT | 26524 |
rs760642024 | snp | C/G | 3.51105e-05 | 0.00418975 | missense | LATS2 | GRCh38.p7 | 13:20989092 | AGCCCTTGGGTGGGT[C/G]CTGGTGCTGGTGGCC | 26524 |
rs760674320 | snp | A/G | 1.89234e-05 | 0.00307593 | missense | LATS2 | GRCh38.p7 | 13:20988240 | GGTAGGGCGGAGGCG[A/G]GCACCTCCGGTCTGG | 26524 |
rs760677949 | in-del | -/A | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063116 | TTTTTTCTTAGAGAC[-/A]AGAGTCTCACTCCAT | 26524 |
rs760692992 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033276 | GATGGGAGAGAATAG[C/G]GGGTAGAGGGGCGAG | 26524 |
rs760739279 | snp | C/T | 1.73498e-05 | 0.00294527 | synonymous-codon, intron-variant | LATS2 | GRCh38.p7 | 13:20979787 | CCACCAGTCACAGAG[C/T]TGAGTGTACCCTGCA | 26524 |
rs760785195 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999055 | TGGTCCACAACCTTG[C/T]CCACGCGAGGCAGGG | 26524 |
rs760795772 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000336 | CAATGAGCCGAGATT[A/G]CACCACTGTACTCCA | 26524 |
rs760814272 | snp | A/G | | | missense | LATS2 | GRCh38.p7 | 13:20988962 | TTGCTCTGGAAGGAG[A/G]GGCTGCGCTGCACTC | 26524 |
rs760824668 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20989506 | TTGCCCTAATGTGTT[A/C]GCAGAGTGGAGACAA | 26524 |
rs760866787 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006530 | TCATCAGAGCTGAAG[-/C]ATGAACAGATTAAAT | 26524 |
rs760905234 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044567 | CTTGTTACATTTCAC[A/T]AATTACATTTTTACC | 26524 |
rs760944913 | snp | A/T | 2.05408e-05 | 0.00320468 | missense | LATS2 | GRCh38.p7 | 13:20988824 | GCGGGACCGGCCTGC[A/T]TGTGGTGTGGGTGCG | 26524 |
rs760957245 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013655 | GTCCTCCCAATAAAT[C/T]TGTACAGATCACTTA | 26524 |
rs760977592 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002366 | AAATTAACTAACTAA[C/T]TAATTAACTTTTTTT | 26524 |
rs760983609 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055473 | TAAATCCAGAGCTGA[C/G]ACAACTACTAAATCC | 26524 |
rs761008370 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026093 | CCTGGAATACCCATC[A/G]GATGCCCCACCCTCC | 26524 |
rs761033135 | snp | A/G | 5.30743e-05 | 0.00515115 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988874 | AGGGGGTGGGAAAGC[A/G]AGGCCGGCGCCTGGC | 26524 |
rs761038230 | snp | A/G | 5.59112e-05 | 0.00528701 | missense | LATS2 | GRCh38.p7 | 13:20988533 | TTGCCAGGCGGACCG[A/G]GCCGCGGCTGGTGGC | 26524 |
rs761054380 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20983953 | GGGTCTCATATACTA[C/T]AGAGTCTCGCTCTGT | 26524 |
rs761060096 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024862 | CACTGCACACCTCAA[C/T]TGAGATGAGCCCCAT | 26524 |
rs761126356 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | LATS2 | GRCh38.p7 | 13:20983682 | CCAAAGGCACCGATC[C/G]CCAGGGTTTTGATCT | 26524 |
rs761146064 | snp | C/G | 1.66543e-05 | 0.00288563 | missense | LATS2 | GRCh38.p7 | 13:20989283 | GGCCTCCGCGTCACT[C/G]GGGTTGGCATGAGCC | 26524 |
rs761147095 | snp | G/T | 1.89181e-05 | 0.0030755 | missense | LATS2 | GRCh38.p7 | 13:20988470 | TGCAAGATGTGCGCG[G/T]CCGTGACAGCCGTCA | 26524 |
rs761179859 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017430 | TCCACCAGCCTCGGC[C/T]TCTCAAGGTACAGGG | 26524 |
rs761207565 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994422 | GGAATCCACTTCTAA[A/G]TCCATCAGAAATACA | 26524 |
rs761234102 | snp | A/G | 3.32055e-05 | 0.00407451 | intron-variant | LATS2 | GRCh38.p7 | 13:20991238 | CTTAAGCCACAAACC[A/G]TCTTTGCCCACTATG | 26524 |
rs761301898 | snp | C/T | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062819 | CCCTCTCTTTCAATC[C/T]CTTAAGGCCTCAGCT | 26524 |
rs761336728 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003734 | TGCGAGAGCCACCAT[A/G]CCAGGCCTAATTTTT | 26524 |
rs761356934 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049530 | TGGCTGAGGCCCTCC[A/C]GGCTCACTCACATTC | 26524 |
rs761440689 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975177 | GTGGGAACGTAGGGG[A/G]CTGGCTGCTTCCGGA | 26524 |
rs761443465 | snp | C/T | 6.01956e-05 | 0.00548582 | missense | LATS2 | GRCh38.p7 | 13:20988530 | GCCTTGCCAGGCGGA[C/T]CGGGCCGCGGCTGGT | 26524 |
rs761449978 | snp | C/G | 1.66671e-05 | 0.00288674 | missense | LATS2 | GRCh38.p7 | 13:20988184 | GCACAGGCTGTCCAG[C/G]TCGTACTGCTCCGAC | 26524 |
rs761481661 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059951 | GCCTGGGAGACAGAG[C/T]GAGATCTTGTCTTAA | 26524 |
rs761494486 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016628 | CTAAGAGACTTGATA[C/T]GAAATTTCTTACACT | 26524 |
rs761504627 | snp | C/G | 0.000310414 | 0.0124544 | missense | LATS2 | GRCh38.p7 | 13:20988454 | CACGCTCTTCACCGG[C/G]TGCAAGATGTGCGCG | 26524 |
rs761527026 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996811 | CAATGGTTACAAAAT[-/A]AAGAGTCTGACGGGC | 26524 |
rs761532481 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058075 | TAAAAGGAAGAAGAT[C/T]CAGAGAATGTTTAGA | 26524 |
rs761537939 | snp | C/T | 1.65479e-05 | 0.0028764 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981566 | CCTCTGCTCTAGGGT[C/T]TTCAGCCTGTCCCCA | 26524 |
rs761568212 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999249 | CCCAGCCGTGGCCGC[C/T]TCCGACCGCTGGTGG | 26524 |
rs761584705 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20980355 | GGTCAGGGCTGGCCT[C/T]TGGGAGGCTGTAGGC | 26524 |
rs761628306 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983561 | CAGGATGTCCCTCTC[A/G]GCCTTGACGTGGGCC | 26524 |
rs761630356 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041800 | ATGGGCCTCCCCTGG[A/G]AGTTACTGAATTGGA | 26524 |
rs761664849 | in-del | -/ATA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000379 | GAGCAAGACTCTGTC[-/ATA]ATAATAATAATAATA | 26524 |
rs761666490 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011381 | TACTTTGCTACAAAT[G/T]ATCTAGACATATATT | 26524 |
rs761723150 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974568 | CAAAGTTAATCCCTA[C/T]AATTTAGTAAGAAAA | 26524 |
rs761754714 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029624 | GGTGAAACCCCATTG[C/T]TACTAAAAATACAAA | 26524 |
rs761798256 | snp | A/C/T | 0.000118127 | 0.00768435 | missense | LATS2 | GRCh38.p7 | 13:20989020 | GCAGGTGCGGCCGCC[A/C/T]GTAGTGCGCGCCCTG | 26524 |
rs761824101 | snp | A/G/T | 0.000115304 | 0.0075921 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988049 | TTTGCGGACGGGAAC[A/G/T]GGAGAGGTCTGAATC | 26524 |
rs761861034 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040588 | CCAAAGTAAGCAAGC[A/G]GGAAGAGCTGTCTGG | 26524 |
rs761866363 | snp | C/T | 1.65132e-05 | 0.00287339 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988142 | GGGCTCGTTGGGGCC[C/T]GCACGGAGGCTCTGC | 26524 |
rs761886665 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | LATS2 | GRCh38.p7 | 13:20987961 | TCTCCACGTGCTGCT[C/G]CATGAAGAACTTAAA | 26524 |
rs761912214 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012288 | GGGTGAGTGAGTGAG[-/T]TGAGTGGTGAGGGAA | 26524 |
rs761920534 | snp | A/G | 1.95242e-05 | 0.00312437 | missense | LATS2 | GRCh38.p7 | 13:20988812 | AGCTGGTGGGCCGCG[A/G]GACCGGCCTGCTTGT | 26524 |
rs761947403 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021837 | CTCACAGAGCCCCAG[A/G]GCACCTTTCACAGTG | 26524 |
rs761972484 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979435 | GCCTGGAAATAGCAA[A/G]GTGGCAGATGGCCAA | 26524 |
rs761978716 | snp | C/G/T | 5.52882e-05 | 0.00525752 | intron-variant | LATS2 | GRCh38.p7 | 13:20975386 | AAACAACAGAGCCAA[C/G/T]AGGTTAGTTTCTCCT | 26524 |
rs762102440 | snp | A/G | 1.65367e-05 | 0.00287543 | missense, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21045726 | CCTGCAGCATTTGCC[A/G]GTTCACTTCTGCAGC | 26524 |
rs762135360 | snp | A/C | 3.29489e-05 | 0.00405874 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974958 | TGTGAAGCTTCTGCT[A/C]CTGAAGGCTTTGGGC | 26524 |
rs762186521 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013832 | AGGAATTAGCCAGGT[A/G]TGACCACACATGCCT | 26524 |
rs762240840 | snp | C/G | 1.67522e-05 | 0.0028941 | missense | LATS2 | GRCh38.p7 | 13:20989206 | CGAAGCTTGGGCCCT[C/G]GTAGGGGGTACCGCT | 26524 |
rs762259528 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056557 | TTCCTAATAGCAAGC[A/G]ACCCAACAGGATGGG | 26524 |
rs762300108 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983390 | CAAAGTCAGCTCTGC[A/G]ATGTAGAACCGGGCC | 26524 |
rs762319686 | snp | A/C | | | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975247 | CCTTCAGGTCATCGG[A/C]CCCATTCCGCCCCAG | 26524 |
rs762332774 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006294 | GTGAGCAGAGAAAGA[A/C]GACCAGGCCCAAGAC | 26524 |
rs762336361 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984590 | ATTTACAACAGCTAT[-/A]AAAAAAAATCTAGGA | 26524 |
rs762348293 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026251 | ATCCCCAAATTTTCT[C/T]AGTGCCCCTTTATAG | 26524 |
rs762352987 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984563 | GGATTTCTGTACACC[A/C]ATAATGAATGCCATT | 26524 |
rs762386237 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994460 | TGGGCACAAAGTACA[C/T]GCAGAGTCACAGAGT | 26524 |
rs762387982 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975014 | AAAGAACCTTCGGAA[A/G]GTGAATTCGTAAAAT | 26524 |
rs762394486 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042933 | AAGTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 26524 |
rs762417232 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21055793 | CCAGCTATTATTTAA[A/G]TCATATCCCTACTAT | 26524 |
rs762480973 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993635 | CCTGTTTGTTAAAGT[G/T]GCGCCTGGACTACCA | 26524 |
rs762484566 | snp | A/C/T | 0.00176991 | 0.0296955 | missense | LATS2 | GRCh38.p7 | 13:20988437 | TCCGGCCTCAGCACA[A/C/T]GCACGCTCTTCACCG | 26524 |
rs762544451 | snp | G/T | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20983534 | GACCACCCACTCATT[G/T]TCTGCCTCGGCCAGG | 26524 |
rs762599541 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976975 | AGAACCGGAAGCAGG[A/G]ACTCATACAGTGGAA | 26524 |
rs762614289 | snp | A/G | 0.000148467 | 0.00861461 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988880 | TGGGAAAGCGAGGCC[A/G]GCGCCTGGCGGTCCT | 26524 |
rs762642278 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004962 | GAGACCAGCCCCGGC[A/G]TTCTAAATGCCTGGG | 26524 |
rs762687013 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039420 | GGCAGGATCTTGTCA[C/T]CAAGACAAAGGGCTA | 26524 |
rs762751990 | snp | C/T | 1.7731e-05 | 0.00297744 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988319 | CAGGGCATGCTCCTC[C/T]TTGGCGTCCAAGCCC | 26524 |
rs762778383 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21031726 | TGAGCTGAGCGTGGC[A/G]AAGTGTGCCTGTAGT | 26524 |
rs762794701 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049976 | AAATACAAAAATTAG[-/C]CAGGTGTGACAGCAC | 26524 |
rs762812425 | in-del | -/ATG | 3.68813e-05 | 0.0042941 | intron-variant | LATS2 | GRCh38.p7 | 13:20983855 | CATTAGAGAAGTCCC[-/ATG]ATAACAAATGACTGG | 26524 |
rs762821349 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042804 | CCATCCTGGCTAACA[C/T]GAAACCCGTCTCTAC | 26524 |
rs762855641 | snp | G/T | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063069 | AATTGAGCCCTACTG[G/T]CATTACCTATGTACT | 26524 |
rs762862480 | in-del | -/TCA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000377 | CAGAGCAAGACTCTG[-/TCA]TAATAATAATAATAA | 26524 |
rs762867365 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997792 | AGCTGGGCTTGCAAT[G/T]TCTAAGCAGCAGAAG | 26524 |
rs762892798 | snp | C/T | 1.6819e-05 | 0.00289987 | missense, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21045705 | CGCATCCTGCGTTCA[C/T]CAGTTCCTGCAGCAT | 26524 |
rs762905878 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017525 | GATTATTTGATCTAC[C/T]CAAGGATCTTACTGT | 26524 |
rs762909566 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032893 | AGCGAACCCAGTGTG[A/G]GAGAAAACCTCATAG | 26524 |
rs762957882 | snp | G/T | 2.432e-05 | 0.00348703 | missense | LATS2 | GRCh38.p7 | 13:20988839 | TTGTGGTGTGGGTGC[G/T]GCACGTAGAGCCCGG | 26524 |
rs762984472 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975092 | CTTGGTGCTACCTTC[A/G]CTGGCATCGTTCCAA | 26524 |
rs763015525 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029836 | GCGTAGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 26524 |
rs763028949 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011405 | ATATATTTCTCATGC[G/T]AGGAAACTCCTGTTT | 26524 |
rs763041640 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022740 | CAAGGCCAATTTAGA[C/T]ATGAGAGTGGGGATT | 26524 |
rs763091275 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007515 | TAAGGGAAGGAGTAG[A/T]TAGTCGTAGGGGATG | 26524 |
rs763115573 | snp | C/T | 5.45827e-05 | 0.00522383 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974833 | TCCGGGACCCTGACC[C/T]GGGAGGCAGCGAGTG | 26524 |
rs763135051 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041917 | ACCCACACCATGCAG[A/C]TGTTCCCCCTATAAC | 26524 |
rs763154528 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981805 | CGCTGAGCTGCTCCA[C/T]AGGGGCAGCCTGCTG | 26524 |
rs763166797 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030422 | GTGAAACCCCGTCTC[C/T]ACTAAAAATGCACAA | 26524 |
rs763204526 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036061 | GTGACACCACACCTG[C/G]ATAATTTTTGTATTT | 26524 |
rs763241909 | snp | A/T | 1.65946e-05 | 0.00288046 | intron-variant | LATS2 | GRCh38.p7 | 13:20991435 | AGGAGAGGTAAGTGC[A/T]TGTCATCCTAAAACA | 26524 |
rs763242362 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003340 | GTCACTGCAAACCCT[A/G]CCTCCTAGGTCCAAC | 26524 |
rs763249026 | snp | C/T | 1.83656e-05 | 0.00303026 | intron-variant | LATS2 | GRCh38.p7 | 13:20975377 | CACCTGAGGAAACAA[C/T]AGAGCCAACAGGTTA | 26524 |
rs763280656 | snp | C/T | 1.87996e-05 | 0.00306586 | intron-variant | LATS2 | GRCh38.p7 | 13:20981669 | CCCAGGAATCAGGGA[C/T]AGTGAAAGAAAAGAA | 26524 |
rs763285477 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035289 | TTTTGAAATTCATCA[C/T]AACCCTAGTAAAAAT | 26524 |
rs763336893 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045142 | GATTTCTCAAGCTTT[A/T]TCTTTCTAGTTTTTC | 26524 |
rs763352394 | snp | G/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047392 | TCTTCACCCCGTGAT[G/T]AATGTTTATATAACC | 26524 |
rs763358548 | snp | C/T | 2.19527e-05 | 0.00331298 | missense | LATS2 | GRCh38.p7 | 13:20989122 | CGGGCCCGTGGGGGC[C/T]GACTCCGGGGAAAAG | 26524 |
rs763426034 | snp | C/T | 3.71941e-05 | 0.00431227 | intron-variant | LATS2 | GRCh38.p7 | 13:20983856 | ATTAGAGAAGTCCCA[C/T]GATAACAAATGACTG | 26524 |
rs763520138 | snp | C/T | 8.23879e-05 | 0.00641772 | missense | LATS2 | GRCh38.p7 | 13:20987930 | TTAACCTTCTGCTGG[C/T]AGGTTTTGATGACAT | 26524 |
rs763571852 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974089 | AGCGAAGAGGTCACC[C/T]GCACAATACATTATC | 26524 |
rs763587142 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046320 | TAAACAGTGATCGTG[A/G]AAATATACCGCTTGG | 26524 |
rs763587367 | snp | A/C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058503 | AACAAGGAATCTTAT[A/C/T]GTAAAATCATTCCCC | 26524 |
rs763635321 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047610 | GAGTACCCTCTAAAC[A/G]GGGATGGGCAGAGGG | 26524 |
rs763640510 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974204 | TTTTATAATAGAAGA[A/G]CTCTGCTCATGCAGT | 26524 |
rs763662441 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045890 | ACTTTGGCATCCAGG[A/G]AAGTGTCACTGTTTG | 26524 |
rs763752179 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015624 | GGGGAACTGTGAAAA[A/C]TTAATTTGATTTTTT | 26524 |
rs763779658 | snp | A/G | 4.24556e-05 | 0.00460717 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988331 | CTCCTTGGCGTCCAA[A/G]CCCTCCGCAGCCGGG | 26524 |
rs763808711 | snp | C/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974289 | CTTCCTATTATACTA[C/G]ATATGCAAAAAGCCA | 26524 |
rs763816466 | in-del | -/GCCGGGGCGGGGGCGGGGGCGGGG | 0.00209132 | 0.032269 | cds-indel | LATS2 | GRCh38.p7 | 13:20988341 | TCCAAGCCCTCCGCA[-/GCCGGGGCGGGGGCGGGGGCGGGG]GCCGGGGCAGGCGCG | 26524 |
rs763870231 | snp | A/C/G | 8.31067e-05 | 0.00644574 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988847 | TGGGTGCGGCACGTA[A/C/G]AGCCCGGCGGCAGGG | 26524 |
rs763871877 | snp | A/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973375 | AGAACTTCAAGGAAA[A/T]ATATGTGGAATAATA | 26524 |
rs763871975 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985731 | CAATAGAGCAAGACT[C/G]CGTCTTAATTAAAAA | 26524 |
rs763873400 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058974 | AAAGCAGCTTACCAA[A/G]AATATACAACAAGAT | 26524 |
rs763911116 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035061 | CATAGCAAGACTCCA[C/T]CTCTATTGACAAGAA | 26524 |
rs763930918 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026738 | AGGCAAGAGGATTGT[C/T]TGAGCCCAGGAGATG | 26524 |
rs763944820 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995585 | GTGACATAGGATAGA[C/T]GAAAGGAAGAAAGAG | 26524 |
rs763963151 | snp | A/G | 1.65029e-05 | 0.00287248 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045998 | CTATTTCCAGAATAA[A/G]TCGTGGCAGGAAAAG | 26524 |
rs763963747 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040551 | GATACTTCCAACCAA[C/T]GAAATCATATGTCAG | 26524 |
rs763977052 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020732 | GGCTTTTTTCCACTA[C/G]GAAGGCTGTGGGGAC | 26524 |
rs763977795 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053579 | ACTGAGGACAAAGCC[A/T]GCCAGTGCCACCCCA | 26524 |
rs764015668 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20989510 | CCTAATGTGTTAGCA[A/G]AGTGGAGACAAGCTG | 26524 |
rs764063607 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979401 | CAGCAGCACACCTTT[A/G]CTGATCCTCACTGTT | 26524 |
rs764089367 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048220 | ACATTCCGACAAAAA[C/T]GGAGAGGTTCTCAAG | 26524 |
rs764104427 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008779 | ACAGGAGAATATTTT[G/T]ACCATATCTAGTAAA | 26524 |
rs764122265 | snp | A/G | 1.85758e-05 | 0.00304755 | intron-variant | LATS2 | GRCh38.p7 | 13:20983858 | TAGAGAAGTCCCATG[A/G]TAACAAATGACTGGG | 26524 |
rs764132931 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034264 | GACACAGCCAAGGTG[A/G]CACATGGCTACACTA | 26524 |
rs764140992 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978505 | TATGCACAACTAGCC[C/T]GACCACATAGCTGAC | 26524 |
rs764237058 | snp | C/G | 1.81717e-05 | 0.00301422 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974836 | GGGACCCTGACCTGG[C/G]AGGCAGCGAGTGGTG | 26524 |
rs764244799 | snp | C/T | 2.12069e-05 | 0.00325622 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988634 | CTCCAGGCCCGGCTT[C/T]TGCAGGGAGTCCCGG | 26524 |
rs764275044 | snp | A/G | 1.86538e-05 | 0.00305394 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988712 | TTCATACAGGTCCAC[A/G]TTGAGGCTGTTCCGC | 26524 |
rs764310023 | snp | A/G | 3.67006e-05 | 0.00428357 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988562 | GCTGTTGAAGGAGTT[A/G]GTCCTGCTGGGCACT | 26524 |
rs764332528 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044647 | TGTATTCAGGTATAC[A/G]AATTGCTAAGAGATC | 26524 |
rs764363947 | in-del | -/A | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024761 | AAATATTAACATTTC[-/A]AACAAGTAAGCAATG | 26524 |
rs764432062 | in-del | -/AGAC/AGACAGAC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050121 | GAGACTCTGTCTCAT[-/AGAC/AGACAGAC]AGACAGATAGATAGA | 26524 |
rs764450588 | snp | A/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21063470 | GTGCATAAAATACCT[A/G]ATAAAAATGTTGCAG | 26524 |
rs764457385 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037933 | AGAAAAGGTTTCCAG[A/C]AGGGAAATGACAGAA | 26524 |
rs764530088 | snp | A/G | 8.3647e-05 | 0.00646657 | missense | LATS2 | GRCh38.p7 | 13:20989124 | GGCCCGTGGGGGCCG[A/G]CTCCGGGGAAAAGGT | 26524 |
rs764573947 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054162 | CCCTTTTTAAACATA[C/G]CTACACGGCTGGGTG | 26524 |
rs764574613 | snp | A/C/T | 9.99746e-05 | 0.0070696 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975274 | CCAGGCGGTGGTCTG[A/C/T]GGAGCAGCACAGCTT | 26524 |
rs764591645 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999125 | CGAGCCAATTATGAC[C/T]GGAAAACAGGTGGAG | 26524 |
rs764592742 | snp | C/G | 1.83727e-05 | 0.00303085 | intron-variant | LATS2 | GRCh38.p7 | 13:20975379 | CCTGAGGAAACAACA[C/G]AGCCAACAGGTTAGT | 26524 |
rs764610447 | snp | C/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023435 | AAACTTGTAAGACAC[C/G]GTGTGGGTAGAATAG | 26524 |
rs764619872 | snp | A/G | 1.67713e-05 | 0.00289575 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989201 | AGCGCCGAAGCTTGG[A/G]CCCTCGTAGGGGGTA | 26524 |
rs764619975 | snp | C/T | 0.000135719 | 0.00823657 | missense | LATS2 | GRCh38.p7 | 13:20988261 | TCCGGTCTGGGCCTC[C/T]GTACTCCACGTCCAG | 26524 |
rs764633061 | in-del | -/CTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014849 | CAAATACCATGCAAC[-/CTT]CTTTTTCCAGCTGGG | 26524 |
rs764657352 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982583 | TTCAAAGTGCTAGGA[C/T]TACAGGCGTGAGCCA | 26524 |
rs764757324 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016717 | GAGCAGCCTCTCAGG[C/T]AACCCAGAGCAAAAA | 26524 |
rs764768818 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036686 | GCTGAAGCAGGAGAA[C/T]TGCTTGAACCTGGGA | 26524 |
rs764772539 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993452 | GTAAACTGTGTTCTT[A/T]GCAATGCAGGCGTGG | 26524 |
rs764794905 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004843 | TAAGGACAACAGGTA[C/T]ACTAAAATTTGGTTT | 26524 |
rs764808852 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003762 | TTTGTCTTTTTGGTA[A/G]AGAGAGGGTTTCACC | 26524 |
rs764833775 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994756 | GCTGGGTGTTGATGG[C/T]GCATGCCTGTAATCC | 26524 |
rs764871364 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022297 | GTGCATGTGTGTGTG[A/T]GTGTGCATGTGTGTG | 26524 |
rs764949303 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20975568 | AGCCTGAGGCCAGGA[C/T]GACCAGTCAAATACA | 26524 |
rs764960515 | snp | C/T | 1.98281e-05 | 0.0031486 | missense | LATS2 | GRCh38.p7 | 13:20988248 | GGAGGCGGGCACCTC[C/T]GGTCTGGGCCTCCGT | 26524 |
rs764995344 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986397 | CTGATGAACAGATAA[A/G]GAAAATGTGGTCTGT | 26524 |
rs765035554 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059102 | GTGCAAGATCACACA[C/T]ATTTTTGTGATTTCC | 26524 |
rs765054900 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045879 | TGCTCCCCAGGACTT[C/T]GGCATCCAGGGAAGT | 26524 |
rs765072692 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983363 | GCCCATCTTGTGGAC[A/G]CTCTCAATGGCCAAA | 26524 |
rs765083407 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035452 | ATGAAGCCCCCACAC[A/T]GAATTGCATGCAGAC | 26524 |
rs765113610 | snp | G/T | 3.73727e-05 | 0.00432261 | missense | LATS2 | GRCh38.p7 | 13:20988750 | TGAGCAGGCTCTGCG[G/T]GGGGCTGTCGCTGGC | 26524 |
rs765124666 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976268 | CAGCGGATAAGGCAT[A/G]GAAGTTAGTGGGTGT | 26524 |
rs765142695 | snp | A/T | 4.35996e-05 | 0.00466882 | missense | LATS2 | GRCh38.p7 | 13:20988830 | CCGGCCTGCTTGTGG[A/T]GTGGGTGCGGCACGT | 26524 |
rs765143917 | snp | G/T | 5.43592e-05 | 0.00521312 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974856 | AGCGAGTGGTGGGGG[G/T]GCCTGGCCCCCATCT | 26524 |
rs765160402 | snp | A/C/G | 3.29453e-05 | 0.00405854 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975005 | ATTGTCATCAAAGAA[A/C/G]CTTCGGAAGGTGAAT | 26524 |
rs765165962 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20987997 | ATGGCGAGTAGCTCT[C/T]GATGCGTGACTCTCT | 26524 |
rs765203476 | snp | A/C/G | 3.30542e-05 | 0.00406524 | intron-variant | LATS2 | GRCh38.p7 | 13:20991262 | CACTATGCTGCAGGC[A/C/G]TGGGCTCACCTGGGG | 26524 |
rs765234533 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027755 | GTACTTTGCAGTGCC[A/G]TATGAATTCACAATC | 26524 |
rs765258918 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051784 | GGCAACAGAGGCAGA[C/T]GGCATTTCTAAAAGT | 26524 |
rs765273645 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011738 | TATTAATACAGTCAT[C/G]CATTCCTTAAATATG | 26524 |
rs765286789 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021870 | ACAGAGACCAGTTCT[G/T]TCACCAAGCAGCACA | 26524 |
rs765329451 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041837 | CCCTCACAGGACTCA[C/T]AGGCACCATCCTGAG | 26524 |
rs765347840 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979651 | ACATGAGCAAATCAG[A/G]TGTCTACAGCAAGCA | 26524 |
rs765364739 | snp | C/T | 4.17023e-05 | 0.00456611 | missense | LATS2 | GRCh38.p7 | 13:20988548 | GGCCGCGGCTGGTGG[C/T]TGTTGAAGGAGTTGG | 26524 |
rs765435539 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002969 | CAGCTTCCCAAAGTG[C/T]TGGGATTATAGGCAT | 26524 |
rs765450288 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020862 | GAGCACACCTACTAC[A/G]TCACAATGCAGTGTA | 26524 |
rs765454834 | snp | C/T | 1.67133e-05 | 0.00289074 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989300 | GGTTGGCATGAGCCC[C/T]TTTCCTGCAGTGGAA | 26524 |
rs765536839 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973162 | AAAGTATGTCAGAGC[A/G]CTGTGAGTAACAACA | 26524 |
rs765558689 | snp | C/G | 1.65356e-05 | 0.00287533 | missense | LATS2 | GRCh38.p7 | 13:20981554 | CTGCTTCCGCGCCCT[C/G]TGCTCTAGGGTCTTC | 26524 |
rs765566250 | snp | C/T | 1.66078e-05 | 0.00288161 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975264 | CCATTCCGCCCCAGG[C/T]GGTGGTCTGCGGAGC | 26524 |
rs765583469 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991093 | ACTTGGGGCTGCTCC[C/T]GCCAGGGCCTGACTC | 26524 |
rs765615303 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046248 | GAAAAAGAAAATAAA[C/T]GGGAGAGAAATGTTC | 26524 |
rs765671499 | snp | C/T | 1.6504e-05 | 0.00287258 | missense | LATS2 | GRCh38.p7 | 13:20983746 | TTAACCTGTTGTAAT[C/T]AGACTCTTTCTGGTA | 26524 |
rs765673390 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013886 | TAAGATGGGAGGATC[A/G]CTTGAGCCCAGGAGA | 26524 |
rs765688623 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000764 | CTACCACTGTTCTAG[A/G]TGGTATGTAGCAAAA | 26524 |
rs765731914 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012863 | GGCTAAAATAGATTA[A/G]CTTTTTACCTAAAGT | 26524 |
rs765734459 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044938 | TCGCTATGTTGTCCA[A/G]GCTGGTCTCAAACTC | 26524 |
rs765750027 | snp | A/C | 0.000490605 | 0.0156544 | missense | LATS2 | GRCh38.p7 | 13:20989033 | CCCGTAGTGCGCGCC[A/C]TGCAGCGGGAAGTGT | 26524 |
rs765750558 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044920 | TTGTAGAGATGGGGA[A/G]TCTCGCTATGTTGTC | 26524 |
rs765763855 | snp | A/T | 1.78816e-05 | 0.00299006 | intron-variant | LATS2 | GRCh38.p7 | 13:20983837 | AGGAAGGAGGAAGAA[A/T]CACATTAGAGAAGTC | 26524 |
rs765853420 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038931 | GTTGTAATGAGCTGA[A/G]ATCACCCCACTGCAC | 26524 |
rs765889644 | snp | C/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21025063 | ATTATAATCAGTATT[C/G]CTTTATGGCTGATCT | 26524 |
rs765917652 | snp | A/G | 1.68451e-05 | 0.00290211 | missense | LATS2 | GRCh38.p7 | 13:20988197 | AGGTCGTACTGCTCC[A/G]ACTTGCTGCGCAGCA | 26524 |
rs765937065 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056046 | TCTCCAATAGCAGCA[C/T]CATCACAAGGCCTCA | 26524 |
rs765973333 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993681 | TACAACCTGGAAGAG[A/T]TGCAGAGAGAAGGCA | 26524 |
rs766001272 | in-del | -/AAAAAAAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993036 | TGTGACTCCATCTCC[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 26524 |
rs766080720 | snp | C/T | 0.00010614 | 0.00728415 | missense | LATS2 | GRCh38.p7 | 13:20989029 | GCCGCCCGTAGTGCG[C/T]GCCCTGCAGCGGGAA | 26524 |
rs766149898 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974844 | GACCTGGGAGGCAGC[A/G]AGTGGTGGGGGTGCC | 26524 |
rs766153701 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20977142 | GGCTCACACCTATAA[A/T]CCCAACATTTTGGGA | 26524 |
rs766176215 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029840 | AGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG | 26524 |
rs766186007 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048894 | CTACTGAATCTCAGG[C/G]ACTGATAGGATAAAT | 26524 |
rs766227035 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20983858 | AGAGAAGTCCCATGA[-/T]TAACAAATGACTGGG | 26524 |
rs766244161 | snp | A/C | 2.34717e-05 | 0.00342568 | intron-variant | LATS2 | GRCh38.p7 | 13:21045636 | TTCTGACTGCCCCAG[A/C]TGTCCCATAGCTGCC | 26524 |
rs766266362 | snp | A/C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017600 | GCAACCAGTGCCTTC[A/C/T]CTTCAAAAGATGACT | 26524 |
rs766291894 | snp | C/T | 3.31521e-05 | 0.00407123 | missense | LATS2 | GRCh38.p7 | 13:20981582 | TTCAGCCTGTCCCCA[C/T]ACCGACAGTTAGACA | 26524 |
rs766293973 | snp | A/C | 1.91265e-05 | 0.00309239 | missense | LATS2 | GRCh38.p7 | 13:20988242 | TAGGGCGGAGGCGGG[A/C]ACCTCCGGTCTGGGC | 26524 |
rs766310501 | snp | A/G | 3.57264e-05 | 0.00422634 | intron-variant | LATS2 | GRCh38.p7 | 13:20983176 | GCTTGCAATGGGGTT[A/G]GTGACATCTACACAT | 26524 |
rs766319766 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004996 | AGCAGCATAGCCAGG[A/G]AGCCTTCAGCAGAGA | 26524 |
rs766329035 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042996 | CTCAAAAAAAAAACC[-/A]AAAAACAAAAAACAG | 26524 |
rs766332009 | snp | C/T | 1.65031e-05 | 0.00287251 | synonymous-codon, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21045736 | TTGCCGGTTCACTTC[C/T]GCAGCTGCAGAGGTG | 26524 |
rs766332713 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986538 | AGTTCGGTTAGAACA[C/T]CACACACTGTTACTG | 26524 |
rs766346109 | snp | A/C | 2.03901e-05 | 0.0031929 | missense | LATS2 | GRCh38.p7 | 13:20988650 | TGCAGGGAGTCCCGG[A/C]GGGCCAGGGTGGCAG | 26524 |
rs766368292 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011496 | TACTTTACAGTTCCT[C/T]AGGTCCAGCAACACT | 26524 |
rs766421693 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016823 | CACTAATAAAACTCC[A/G]CACAACACCTGAACT | 26524 |
rs766424408 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008023 | CTCAGCCTCCCAAAG[A/T]GTTGGGATCACAGGC | 26524 |
rs766497064 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997813 | GCAGCAGAAGTATTT[C/T]ACGTGCATTGCCATG | 26524 |
rs766523938 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022834 | GATCCTCATTATGTT[C/T]ATAAAGGGATTTTGC | 26524 |
rs766538188 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013401 | ATGATTATACCTTAT[-/A]AAAGTAAAAATTAGT | 26524 |
rs766567305 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051999 | AAAACTGGGTGTGCA[A/G]TGCTAAAGTGGCTGG | 26524 |
rs766573697 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043111 | GGCCGAACGAAGCAG[A/G]CAGATCACTTGAGGT | 26524 |
rs766615062 | snp | A/C | 1.75363e-05 | 0.00296106 | intron-variant | LATS2 | GRCh38.p7 | 13:20981435 | AAGGGAAGGAGACCT[A/C]CTGCGGGGTGGCTGG | 26524 |
rs766647771 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988082 | CTTTTTATCCTTTCC[A/G]CCTTTGTCCCCCTTG | 26524 |
rs766657150 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045199 | ACCCCCTGTAACAGC[-/A]ATATACACTAATTGT | 26524 |
rs766676131 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20980575 | CACCTCTTCCTGTCC[A/G]AGTTTGGCAACAGAG | 26524 |
rs766703964 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986625 | CCAGAGGTGGGAAAG[G/T]GTGTGTGTGTGTTGA | 26524 |
rs766718464 | snp | C/T | 5.0491e-05 | 0.00502424 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046038 | TCATTGTTAGTCCAG[C/T]TTCCTTTTACCATAA | 26524 |
rs766767257 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974155 | CAGTAAAAACGTATT[C/T]ACAGGACCTGCTGTG | 26524 |
rs766801338 | snp | C/T | 3.31153e-05 | 0.00406898 | intron-variant | LATS2 | GRCh38.p7 | 13:20991252 | CATCTTTGCCCACTA[C/T]GCTGCAGGCCTGGGC | 26524 |
rs766828593 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035409 | ATTTACATCCACAAA[C/T]GGTTTGGCAATGACA | 26524 |
rs766855723 | snp | C/T | 0.000189843 | 0.00974093 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988472 | CAAGATGTGCGCGGC[C/T]GTGACAGCCGTCACG | 26524 |
rs766891263 | snp | A/G | 5.50888e-05 | 0.00524799 | missense | LATS2 | GRCh38.p7 | 13:20988534 | TGCCAGGCGGACCGG[A/G]CCGCGGCTGGTGGCT | 26524 |
rs766905467 | in-del | -/TTATTA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019302 | CACTTGGATTTGTTA[-/TTATTA]TTATTATTATTATTA | 26524 |
rs766937031 | in-del | -/TGTG | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973516 | TTGTGTTTATCTCTG[-/TGTG]TGTGTGTGTGTGTGT | 26524 |
rs766963768 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997313 | CATTTTGTCAACAAA[C/T]TGATGTTCGCTTAAA | 26524 |
rs767001893 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027834 | ATTTGGATTCTGCTG[G/T]ATCCACAGATAACTG | 26524 |
rs767021401 | snp | A/G | 3.30077e-05 | 0.00406236 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046001 | TTTCCAGAATAAGTC[A/G]TGGCAGGAAAAGTCT | 26524 |
rs767028106 | snp | A/T | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045903 | GGGAAGTGTCACTGT[A/T]TGGTCCTGCGGGTAG | 26524 |
rs767056907 | in-del | -/GTGCT | 2.15915e-05 | 0.00328562 | frameshift-variant | LATS2 | GRCh38.p7 | 13:20988258 | CCTCCGGTCTGGGCC[-/GTGCT]TCCGTACTCCACGTC | 26524 |
rs767057484 | in-del | -/ATA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000381 | CAAGACTCTGTCATA[-/ATA]ATAATAATAATAATA | 26524 |
rs767078332 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056983 | GGAGGGTGCAGGTGT[C/T]GTCCGGGTACATTTA | 26524 |
rs767081472 | snp | C/T | 0.000156801 | 0.00885302 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988913 | CTGGCCCTTCGTGGG[C/T]AGGCTGGCGTAACCC | 26524 |
rs767087998 | snp | A/T | 0.000181241 | 0.00951777 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975183 | ACGTAGGGGGCTGGC[A/T]GCTTCCGGATGTCAC | 26524 |
rs767105444 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984108 | CTGGCTAATTTTTGT[A/C]TTTTTAGTAGAAACA | 26524 |
rs767119587 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973203 | ATAAAATAGCGAGAA[C/T]ACTGACAGTCACGAC | 26524 |
rs767138604 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042903 | GCAGGAGAATTGCTT[-/G]AACCTGGGAGGCAGA | 26524 |
rs767147084 | in-del | -/CGCCCAGCCTAT | 1.80078e-05 | 0.0030006 | intron-variant | LATS2 | GRCh38.p7 | 13:20979803 | GAGTGTACCCTGCAA[-/CGCCCAGCCTAT]GACAAAGTTCACTCA | 26524 |
rs767161343 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026449 | GTGGTCCCTCGGGTT[G/T]CTTTGTTTTGGTTGG | 26524 |
rs767165796 | in-del | -/C | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061868 | GTTAAAGCCACTATT[-/C]TTAAGTATCTCATAC | 26524 |
rs767270051 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | LATS2 | GRCh38.p7 | 13:20983563 | GGATGTCCCTCTCGG[A/C]CTTGACGTGGGCCAC | 26524 |
rs767322862 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992577 | TGAGGCTGGCTGTGG[A/G]ACAAGGGCAAAAACA | 26524 |
rs767417071 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006553 | GATTAAATGTGACTC[C/T]GGAAGAGCAGACTTT | 26524 |
rs767430546 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998816 | TGTCCACACGGGGCG[A/G]GGGCCGCAGCGACAT | 26524 |
rs767452489 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033220 | AAGCTAGGAACCTTT[A/G]TTAGACCAGACCTGG | 26524 |
rs767473722 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032382 | AAGCAATTCTCCTGC[C/T]TGAGCCTCCTGAGTA | 26524 |
rs767487018 | snp | C/T | 1.64917e-05 | 0.00287151 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20991315 | AATCTGCTCATTCCT[C/T]GGGTCCAGGTAGCCC | 26524 |
rs767507677 | snp | A/C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018546 | ACCACACCCTGCTTG[A/C/T]GCAGCAGGTCCAGGA | 26524 |
rs767518840 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986704 | ACAAACTCTAACTAG[G/T]ATGACTATGGTTAGT | 26524 |
rs767556914 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049952 | ACAGTGAAACGCTGT[A/C]TCTACTAAAAATACA | 26524 |
rs767601503 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051574 | GGTGGTGCCATTCTC[C/T]GAGCCAGGAAACCTC | 26524 |
rs767633481 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987665 | ATTATGCACAGCTAT[C/G]TCTGATTCTTCAGAA | 26524 |
rs767657460 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012615 | TCCTATCTTATGATT[A/C]TTTTCTCCTAGAAAA | 26524 |
rs767659882 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054034 | CTTAACTGAACTGTA[C/T]ACTTAAGAATGGTTA | 26524 |
rs767667887 | snp | C/G | 3.29451e-05 | 0.00405851 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20987977 | CATGAAGAACTTAAA[C/G]GCGTATGGCGAGTAG | 26524 |
rs767708795 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20980693 | ACAACCTCTCAAGGT[C/T]GTTATTGCTATGTCT | 26524 |
rs767716835 | in-del | -/AAAAC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000008 | AGCAAGTCTCCATCA[-/AAAAC]AAAACAAAACAAAAC | 26524 |
rs767749098 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057635 | CGTCTCTACTAAAAG[-/T]AAAAAAAAAAAAAAA | 26524 |
rs767782841 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043067 | GGCCAGACGTGGTGA[C/T]GCACGCCTGTAATCC | 26524 |
rs767793375 | snp | C/G | 1.87092e-05 | 0.00305848 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988739 | CCGCGAGGGAGTGAG[C/G]AGGCTCTGCGGGGGG | 26524 |
rs767801193 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993279 | AGAAGAACCTGGCAG[A/G]GCCTGAATCCATGTT | 26524 |
rs767812842 | snp | C/T | 1.9331e-05 | 0.00310888 | missense | LATS2 | GRCh38.p7 | 13:20988462 | TCACCGGGTGCAAGA[C/T]GTGCGCGGCCGTGAC | 26524 |
rs767815541 | in-del | -/TC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026962 | GTTTTAATTTGCATT[-/TC]TCTGATGATGAATGA | 26524 |
rs767903864 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024391 | CAGTGAGCCGAGATC[A/G]CGCCACTGTACCCCA | 26524 |
rs767966217 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011793 | ATTAGGTGATTTCGT[C/T]GTTGTGTGAACATCA | 26524 |
rs767983842 | snp | C/T | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023153 | CTGCATCGAGGGCTC[C/T]GGGCTCCGAGGGCTC | 26524 |
rs767989086 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998496 | CTTGCTTGGAGGATT[A/G]CCAGCAGGGTGGTCT | 26524 |
rs768002766 | snp | A/G | 1.67413e-05 | 0.00289316 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989207 | GAAGCTTGGGCCCTC[A/G]TAGGGGGTACCGCTC | 26524 |
rs768008944 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058548 | AGCCCCTCCCACCAA[-/C]CCTGTGATTTGCTAA | 26524 |
rs768025927 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059919 | GCAGTGAGCCGAGAT[C/G]GCGCCACTCCCCTCC | 26524 |
rs768036053 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21031012 | CGGTGTATTTTTTTC[G/T]TCAGCACTTTGTGTC | 26524 |
rs768066235 | snp | A/G | 3.4219e-05 | 0.00413622 | synonymous-codon, intron-variant | LATS2 | GRCh38.p7 | 13:20979778 | TCCAACACTCCACCA[A/G]TCACAGAGTTGAGTG | 26524 |
rs768066331 | in-del | -/AG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034560 | CTAAGGGTGGCAGAT[-/AG]AGAGAGAAGGTGCCT | 26524 |
rs768066493 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002190 | AGTGCTGGGATTACA[A/C]GTGTGAGCCACTGCG | 26524 |
rs768087455 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017164 | TTGAATGGCAGCCAG[C/T]ACAGTGAAATAAAAC | 26524 |
rs768093071 | snp | C/G | 0.000104455 | 0.0072261 | missense | LATS2 | GRCh38.p7 | 13:20988344 | AAGCCCTCCGCAGCC[C/G]GGGCGGGGGCGGGGG | 26524 |
rs768214090 | snp | A/C | 1.6943e-05 | 0.00291053 | intron-variant | LATS2 | GRCh38.p7 | 13:20989332 | AAACAGGAAGACAGC[A/C]TCAGAGTGGGTGTGA | 26524 |
rs768225372 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986232 | AAAAAGAAACTAAAA[A/C]TAGAACTACCATACA | 26524 |
rs768227371 | in-del | -/AG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011700 | TGTTGTAGACTTAAC[-/AG]AGTTTCAAAAATGAT | 26524 |
rs768267604 | snp | A/C | 2.09861e-05 | 0.00323923 | intron-variant | LATS2 | GRCh38.p7 | 13:20979840 | ACACAGGCATGAATT[A/C]TCCTCCGAGGTGAAT | 26524 |
rs768269096 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998852 | ACGCCGGGTGGGGGC[A/C]CTGCGACATTGTCCA | 26524 |
rs768297258 | snp | A/G | 1.66252e-05 | 0.00288311 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989264 | GCCGGTTCCTTCGAA[A/G]CTGGGCCTCCGCGTC | 26524 |
rs768351824 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987110 | TGAGGCAGGAGAATC[G/T]CTTGAACCCAGGAGG | 26524 |
rs768370299 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041549 | AGCTGACACAATATT[C/T]AGGACCAGGAAAATG | 26524 |
rs768375606 | snp | C/G | 1.75613e-05 | 0.00296316 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989006 | TTCCCCAGGCACCAG[C/G]AGGTGCGGCCGCCCG | 26524 |
rs768388955 | snp | C/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047318 | CAGTGGTGAGCACCG[C/G]GTCAGATGACAAGGG | 26524 |
rs768402707 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030603 | CTCAAAAAAAAAAAA[-/G]AAAAAAAAGAAAAAA | 26524 |
rs768439789 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042559 | CCAGACGTGGTGGCA[C/T]GCCTGTAGTCCCAGC | 26524 |
rs768537849 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035077 | CTCTATTGACAAGAA[C/G]AAACCAAACAAAACC | 26524 |
rs768542289 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010901 | ATTTGCATAAATGGA[C/T]CTGAGTGAGAACATG | 26524 |
rs768589242 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021681 | TGAAGAATTGAGGAC[A/G]CCTTCCCAACCACTG | 26524 |
rs768593110 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035902 | TCCTCAAAAGCCCCC[A/T]TCCCCTTTTTTCGGG | 26524 |
rs768622025 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21001140 | AGCTAATCCCAAAGT[G/T]CCTTTTATCTGTAAA | 26524 |
rs768630177 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057347 | ATTTGTGAATTAACT[C/T]AAAACACTTGTCACA | 26524 |
rs768694273 | in-del | -/AGTGGGTGTGATC | 1.69954e-05 | 0.00291503 | intron-variant | LATS2 | GRCh38.p7 | 13:20989337 | GGAAGACAGCATCAG[-/AGTGGGTGTGATC]AGTGGGTTCTGGCAC | 26524 |
rs768696379 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056464 | AATGGCATAAAAAAA[C/T]TGAGCTACAGAAGTC | 26524 |
rs768701244 | in-del | -/TTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996379 | AGAGTGGTAGAAGAT[-/TTT]TTTTTTTTTTTTTTT | 26524 |
rs768711180 | snp | G/T | 8.23608e-05 | 0.00641667 | missense | LATS2 | GRCh38.p7 | 13:20983634 | ATGGCGTACAGGGCG[G/T]GAGTGTCCACCTTAC | 26524 |
rs768744616 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974953 | CAGCCTGTGAAGCTT[C/T]TGCTCCTGAAGGCTT | 26524 |
rs768757439 | snp | A/C | 1.97506e-05 | 0.00314243 | intron-variant | LATS2 | GRCh38.p7 | 13:20981680 | GGGATAGTGAAAGAA[A/C]AGAACAAAATATAAA | 26524 |
rs768786760 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016240 | GATTCACCTACCTTG[A/G]CCTCCCAAAGTGCTG | 26524 |
rs768842218 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985398 | ATTCAGAATATACAA[A/G]GAACTCAACTCAACA | 26524 |
rs768842751 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990951 | AAAAGACCATTTTTA[C/T]GCCCGCTTTGCTGAC | 26524 |
rs768847336 | in-del | -/TTTTTTTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990462 | TGCTAATTACTAGGA[-/TTTTTTTT]TTTTTTTTTTTTTTT | 26524 |
rs768856635 | in-del | -/TT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018662 | TTCTCAGAGTCCCTC[-/TT]TTTTTTTTGACACGT | 26524 |
rs768866769 | snp | G/T | 3.19821e-05 | 0.00399875 | missense | LATS2 | GRCh38.p7 | 13:20988284 | ACGTCCAGCGGGAAG[G/T]CGCCTGCGCCGCCCA | 26524 |
rs768905193 | snp | A/C | 4.94181e-05 | 0.00497057 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045831 | CGAACTTTGGGGTGG[A/C]TCTCATCTGCTGCTG | 26524 |
rs768941710 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027611 | TATGCCAATGCCACA[C/T]TGTCTTGCTTAGCTT | 26524 |
rs768946991 | in-del | -/A | 1.6473e-05 | 0.00286988 | frameshift-variant | LATS2 | GRCh38.p7 | 13:20983511 | CTTGGAAGGAGTAGT[-/A]AGAGTTTGACCACCC | 26524 |
rs768955024 | snp | C/T | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:20995194 | CACAAAGGTATCTTA[C/T]GTGTTTCTGGGAAAA | 26524 |
rs768984229 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057996 | ACAATGGGAACGATG[C/T]CCCTGGACTTGTGTA | 26524 |
rs769017966 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014574 | AATGCTGAGGATGGA[C/T]GCTAGGAGGACATGA | 26524 |
rs769023154 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975059 | CTTGTTATTGGGCGA[A/G]GTGAGTGTGTCCCAG | 26524 |
rs769031740 | snp | G/T | 0.00014662 | 0.00856086 | missense | LATS2 | GRCh38.p7 | 13:20988804 | GCACATGCAGCTGGT[G/T]GGCCGCGGGACCGGC | 26524 |
rs769047956 | snp | A/C | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20988042 | TGCTGTTTTTGCGGA[A/C]GGGAACGGGAGAGGT | 26524 |
rs769071614 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984477 | CATACAAAAATCAGT[A/G]GCATACATTAGATAG | 26524 |
rs769071759 | in-del | -/AA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052250 | TTAAAGATTTATAAT[-/AA]GTTAGGCAAAAAAGG | 26524 |
rs769072103 | in-del | -/GTGGGAC | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993568 | ATGTTGCCTGCCCAT[-/GTGGGAC]GTGGGACATGGGACA | 26524 |
rs769114461 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050556 | AAGCCTGTCAGTTGT[C/T]ATTGCTGCGTAATAT | 26524 |
rs769146985 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007046 | CCTCAAAGAGTCACT[A/G]ACAAGGTAATTCGGT | 26524 |
rs769177924 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994447 | AATACATGGCCTCTG[A/G]GCACAAAGTACATGC | 26524 |
rs769180944 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018366 | GGCATGCTACTGTCC[A/C]TCTGGCAAGATGAGG | 26524 |
rs769188772 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978137 | GGCCAGGCTAGTCTC[A/G]ATCTCCTGACCTCGT | 26524 |
rs769212994 | snp | A/G | 3.22732e-05 | 0.00401691 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988856 | CACGTAGAGCCCGGC[A/G]GCAGGGGGTGGGAAA | 26524 |
rs769348251 | snp | A/G | 2.5181e-05 | 0.00354822 | intron-variant | LATS2 | GRCh38.p7 | 13:20979660 | AATCAGATGTCTACA[A/G]CAAGCAGATGCGTGG | 26524 |
rs769375665 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976834 | TGAACACTCAGTCAC[C/T]GTTGGTGGGAATGTA | 26524 |
rs769397012 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019219 | AAATGTTAGCTATTA[C/T]ATAGTCACAACATAC | 26524 |
rs769413532 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997741 | GGAACTGGAAGACAC[G/T]CCTTCAATCTACCGC | 26524 |
rs769433391 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20988038 | TCTCTGCTGTTTTTG[C/T]GGACGGGAACGGGAG | 26524 |
rs769440196 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978395 | TTCAACCCTTAGTAA[C/T]TCATTTCAGAAAGCA | 26524 |
rs769467425 | snp | C/G | 1.66219e-05 | 0.00288283 | missense | LATS2 | GRCh38.p7 | 13:20989260 | AATCGCCGGTTCCTT[C/G]GAAGCTGGGCCTCCG | 26524 |
rs769480912 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005572 | GCCCTGTCTGCTGGA[-/G]GCTCTAGCAGCAGAA | 26524 |
rs769506765 | snp | A/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062843 | CTCAGCTCTTCCAGG[A/G]AATCTTCTCAGATCT | 26524 |
rs769522771 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043958 | CCAGATTTCCCCAGG[A/G]CTGCTCCTTCCCTAC | 26524 |
rs769527254 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975086 | CCAGGCCTTGGTGCT[A/G]CCTTCGCTGGCATCG | 26524 |
rs769528970 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21031718 | TTAAAAAGTGAGCTG[A/G]GCGTGGCGAAGTGTG | 26524 |
rs769538257 | snp | A/G | 3.29636e-05 | 0.00405964 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045981 | CTTGCAGTCGCTGCC[A/G]GCTATTTCCAGAATA | 26524 |
rs769590508 | snp | A/G | 1.68508e-05 | 0.0029026 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989189 | CGTGGGGCCGTCAGC[A/G]CCGAAGCTTGGGCCC | 26524 |
rs769622780 | snp | A/C | 9.97357e-05 | 0.00706101 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988502 | GGTGTTGGGGGCGGG[A/C]AGGGAGGGCTCGGCC | 26524 |
rs769757498 | snp | A/G | 0.00451465 | 0.0472963 | missense | LATS2 | GRCh38.p7 | 13:20988419 | CCCACAGCCGTCTGC[A/G]GCTCCGGCCTCAGCA | 26524 |
rs769771909 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | LATS2 | GRCh38.p7 | 13:20983528 | GAGTTTGACCACCCA[C/G]TCATTGTCTGCCTCG | 26524 |
rs769805312 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037199 | CACCTGAGGTCAGGA[C/G]TTCTAGACCAGCCTG | 26524 |
rs769830939 | snp | G/T | 3.31159e-05 | 0.00406901 | missense | LATS2 | GRCh38.p7 | 13:20981571 | GCTCTAGGGTCTTCA[G/T]CCTGTCCCCACACCG | 26524 |
rs769868574 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047312 | TTAGGACAGTGGTGA[A/G]CACCGGGTCAGATGA | 26524 |
rs769872217 | snp | A/C/G | 3.64726e-05 | 0.00427027 | intron-variant | LATS2 | GRCh38.p7 | 13:20981663 | CCTTCACCCAGGAAT[A/C/G]AGGGATAGTGAAAGA | 26524 |
rs769911689 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035162 | TAAAAAATTGCATGA[C/T]GAATGTGGCTTTAAT | 26524 |
rs769923703 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973719 | AGAGAACCATTAGAT[C/T]ACTCAGTTTCCTGAC | 26524 |
rs769942784 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003104 | AAAAGGTAAATTTTC[A/G]AATAGGTAAGATGAC | 26524 |
rs769988987 | snp | A/G | | | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975226 | TGGCGCTGAAGAAGG[A/G]GTGGGCCTTCAGGTC | 26524 |
rs769989453 | in-del | -/GTTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041425 | ATAATCAGTTTATCA[-/GTTT]GTTTGTTTACATTTC | 26524 |
rs769991034 | snp | C/G | 5.80333e-05 | 0.0053864 | missense | LATS2 | GRCh38.p7 | 13:20989065 | CCCCTGCTGCCTCTA[C/G]GCTGGCACCGTAGCC | 26524 |
rs770075801 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007407 | TCTAAATGCCAAAAA[C/T]TGTGTCTACAGACCA | 26524 |
rs770108766 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016345 | GCTCAGTACAGTGGC[A/G]TGATCTCGGCTCACT | 26524 |
rs770154749 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048093 | CATATCAGAAGCCTA[C/G]AGCTCTGCTTAATTG | 26524 |
rs770191896 | snp | A/G | 1.65086e-05 | 0.00287298 | stop-gained | LATS2 | GRCh38.p7 | 13:20987904 | TTTCTTGCTCCAGCT[A/G]CAGCCTCCGGTTAAC | 26524 |
rs770192145 | snp | A/G | 1.84783e-05 | 0.00303954 | missense | LATS2 | GRCh38.p7 | 13:20988780 | CGAACACCTGGCTGC[A/G]GGAGCCCAGCACATG | 26524 |
rs770193042 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014961 | GCAGGTTGATGAGCC[C/T]CAACTGTGAGCTCCG | 26524 |
rs770275664 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986024 | ACTCCAGCCTGGGCA[A/G]CAAGAGCGAAACTCT | 26524 |
rs770296932 | snp | A/G | 1.76886e-05 | 0.00297389 | synonymous-codon, missense | LATS2 | GRCh38.p7 | 13:20975341 | CTGGGCTGGAATGTG[A/G]AGCGTGTTCTCCCAG | 26524 |
rs770299070 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979070 | CCCAGCCTATGATCC[C/T]CCCAAAGTAGTGGGA | 26524 |
rs770300330 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041159 | TTGTATTTTTAGTAC[A/C]GACAGGGTTTCACCA | 26524 |
rs770315196 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051364 | ATTATTTAAATACAC[A/T]ATAGGGTATGTGTCA | 26524 |
rs770372276 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026510 | TCATCCATTCAACTG[C/T]TGATGGACACTGGGG | 26524 |
rs770377047 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:20989558 | CCAAGGGCAGAAGAG[-/A]AGACTGCGTCCACAT | 26524 |
rs770391008 | snp | A/G | 2.79755e-05 | 0.00373992 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989108 | CTGGTGCTGGTGGCC[A/G]GGCCCGTGGGGGCCG | 26524 |
rs770407387 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995369 | TCTTCCAGCTTACCT[C/T]AGGCTGCTGTGTAAA | 26524 |
rs770483804 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974927 | ATCAGAGCTTTCTAA[A/G]TCTGAGCTCTCAGCC | 26524 |
rs770490765 | snp | G/T | 1.71605e-05 | 0.00292915 | intron-variant | LATS2 | GRCh38.p7 | 13:20987870 | ATAGTAAAAATGAAG[G/T]GTGAAATTACTTTGG | 26524 |
rs770558742 | in-del | -/CGTG | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973893 | AAACGGACATGTGTC[-/CGTG]CGTGATTAAACTTTT | 26524 |
rs770603771 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061418 | TCGCGCCGGGAGACC[A/G]GGCACTGGTGGCTGG | 26524 |
rs770622977 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009207 | TAAAGAAGCAGATGT[A/G]CAAAGGTACAGCTCT | 26524 |
rs770675403 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050771 | AAATACGCTGAAGAG[C/T]GACTGGCAGAGCCCC | 26524 |
rs770756388 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974242 | ACACACCAGACGTCG[A/G]AAATCACAGCCACAT | 26524 |
rs770760278 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | LATS2 | GRCh38.p7 | 13:20983339 | AGGCTTGATGTCTCG[C/G]TGGATGAAGCCCATC | 26524 |
rs770769931 | in-del | -/AAAAAAAAAAAAACAAA | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023671 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAACAAA]CCTCGGCCGGGCGCA | 26524 |
rs770778568 | snp | A/G | 0.000874083 | 0.0208873 | missense | LATS2 | GRCh38.p7 | 13:20988890 | AGGCCGGCGCCTGGC[A/G]GTCCTCCCTGGCCCT | 26524 |
rs770785455 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044261 | AAATTCTCTATTTAA[C/G]GTCTATGGTAATAAA | 26524 |
rs770800340 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033870 | ACATGATTAATAATT[A/C]TTCTAATGTCATAAC | 26524 |
rs770807523 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013376 | GACTAATGTGCATGA[A/G]GGAATATTAATGATT | 26524 |
rs770812427 | in-del | -/CCCT | 2.17896e-05 | 0.00330065 | intron-variant | LATS2 | GRCh38.p7 | 13:21045662 | TGCCTCTGCACATGG[-/CCCT]CCCTGCAGAGGTCTG | 26524 |
rs770839178 | snp | A/G | 1.69315e-05 | 0.00290955 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989180 | CTCCAGCGCCGTGGG[A/G]CCGTCAGCGCCGAAG | 26524 |
rs770852020 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018766 | TCAAGTGATTCTCCT[C/G]CTTCAGCCTCCTGAG | 26524 |
rs770865744 | snp | C/T | 2.57152e-05 | 0.00358566 | intron-variant | LATS2 | GRCh38.p7 | 13:20979652 | CATGAGCAAATCAGA[C/T]GTCTACAGCAAGCAG | 26524 |
rs770890762 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018454 | CATGAGGCAGCTAGA[A/G]TTCAGAAGGGGAAGG | 26524 |
rs770929099 | snp | C/T | 1.70714e-05 | 0.00292154 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988301 | GCCTGCGCCGCCCAG[C/T]GCCAGGGCATGCTCC | 26524 |
rs770958277 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20975998 | ATTCAAATACTTATT[A/G]CGGTCAAAAAACGGC | 26524 |
rs770969294 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21025873 | GTACGTCTGGGTTGA[C/T]TTTTTCACCAACCGT | 26524 |
rs770984282 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994021 | TTAACCCAGTACCTG[C/T]TGACTGCCAAGGAAG | 26524 |
rs770997883 | snp | C/G | 5.49768e-05 | 0.00524265 | missense | LATS2 | GRCh38.p7 | 13:20988876 | GGGGTGGGAAAGCGA[C/G]GCCGGCGCCTGGCGG | 26524 |
rs771028282 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992907 | GGGTATGGTGGTGTG[C/T]GCCTGTAGTTCCAGC | 26524 |
rs771043141 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024453 | AATAATAATAAATGA[C/T]AATAAATAATATAAA | 26524 |
rs771045242 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054980 | TGTCCCTGTCTTAAG[C/T]GAATATGAAAAAATA | 26524 |
rs771046319 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998518 | GGGTGGTCTTCAAAA[A/G]AATCTCTGACCCAAA | 26524 |
rs771082758 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981118 | AAAGCTAGAGCCCGG[-/A]AATGTGTGGTCTGGG | 26524 |
rs771084727 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982196 | AAAGAAGATAATAAT[C/T]AGCTGTTTTTGGCTT | 26524 |
rs771107817 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975158 | GTCCATGGGGTGGCT[A/G]ATGGTGGGAACGTAG | 26524 |
rs771183010 | snp | A/G | 1.66125e-05 | 0.00288201 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988174 | CCATGCCTGCGCACA[A/G]GCTGTCCAGGTCGTA | 26524 |
rs771214840 | snp | C/G | 1.79968e-05 | 0.00299968 | missense | LATS2 | GRCh38.p7 | 13:20988977 | GGGCTGCGCTGCACT[C/G]CGTAGCCCAGGGGTT | 26524 |
rs771239970 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036088 | ATTTTTAATAGACGG[G/T]TTTCACCATGTTGGC | 26524 |
rs771276886 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036607 | GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 26524 |
rs771278507 | snp | A/G | | | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975299 | CAGCTTGGTGATGAG[A/G]TCCCTGGCCTCAGGG | 26524 |
rs771282680 | snp | C/T | 1.82254e-05 | 0.00301867 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974825 | GCACCGGCTCCGGGA[C/T]CCTGACCTGGGAGGC | 26524 |
rs771295061 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037307 | TACTCAGGAGGCTGA[C/T]GGGGGAGAATCGCTT | 26524 |
rs771305486 | snp | A/T | 1.64966e-05 | 0.00287194 | missense | LATS2 | GRCh38.p7 | 13:20988131 | TCGCCGCCCTCGGGC[A/T]CGTTGGGGCCCGCAC | 26524 |
rs771320435 | snp | C/T | 2.32043e-05 | 0.00340611 | missense | LATS2 | GRCh38.p7 | 13:20988621 | CGCGCGGCGGCGCCT[C/T]CAGGCCCGGCTTCTG | 26524 |
rs771336625 | snp | C/T | 1.78131e-05 | 0.00298433 | missense, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21045690 | CTGTACCCACCTGGT[C/T]GCATCCTGCGTTCAC | 26524 |
rs771389282 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048437 | TGCAAGGGAGGGCCT[C/G]ACAATACGCAGAGAG | 26524 |
rs771414976 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010761 | ACCTCTGCTTAACTT[A/G]GGGACTTTCATAGCT | 26524 |
rs771415091 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981850 | ACACACGTGGTGAGG[C/T]TGGCGCTAGCACCAA | 26524 |
rs771463308 | snp | A/G | 8.27931e-05 | 0.00643348 | intron-variant | LATS2 | GRCh38.p7 | 13:20991413 | CCATCTCCTGGGAGG[A/G]AAGTAAAGGAGAGGT | 26524 |
rs771525769 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059726 | ATCCCAGCACTCTGG[C/G]AGACGGAGGCAGGTG | 26524 |
rs771534648 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986123 | GCTAAGAGGTGCATG[C/G]AAAGATGCTCATTAA | 26524 |
rs771556703 | snp | C/T | 8.26276e-05 | 0.00642705 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981548 | CTGGTGCTGCTTCCG[C/T]GCCCTCTGCTCTAGG | 26524 |
rs771575305 | snp | A/G | 1.67164e-05 | 0.00289101 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981614 | ATCATCCCAGAGGTC[A/G]CTGGGCTCCATGCTG | 26524 |
rs771614643 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029323 | TACTCTATCTATTGA[A/G]ATGATGAAATGGTTT | 26524 |
rs771615379 | snp | A/G | 1.65222e-05 | 0.00287417 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20991387 | GCCAGTCTGCTTGAG[A/G]GCTCGGCCAGCCATC | 26524 |
rs771631605 | snp | A/G | 1.71669e-05 | 0.00292971 | missense | LATS2 | GRCh38.p7 | 13:20988612 | CCACGTGCGCGCGCG[A/G]CGGCGCCTCCAGGCC | 26524 |
rs771708949 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990801 | GGGGATGCTGAGGGG[A/G]GCCCAGCGCTCTGCC | 26524 |
rs771745531 | in-del | -/C | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047247 | TGACCCTGGACCAGT[-/C]CCTTCGCCTCCCTCA | 26524 |
rs771762456 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020474 | GGAAGTAAACTTTTG[C/T]AACCAAAATAGCATT | 26524 |
rs771765141 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997539 | CTCCCCATGGGATGG[G/T]CCAGGCCTCTGTTGC | 26524 |
rs771789026 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044117 | ACTCACAACCCTGTG[A/C]TTTATCAAAGCAGCT | 26524 |
rs771871763 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009397 | ACTATTCCTGCAAAC[A/T]GGTTCCAATTTGCTG | 26524 |
rs771906845 | snp | C/T | 1.70752e-05 | 0.00292187 | missense | LATS2 | GRCh38.p7 | 13:20989167 | GCCGCGGCATCTCCT[C/T]CAGCGCCGTGGGGCC | 26524 |
rs771907039 | snp | C/T | 3.78408e-05 | 0.00434959 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988238 | CGGGTAGGGCGGAGG[C/T]GGGCACCTCCGGTCT | 26524 |
rs771921540 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033969 | GATTTCTGTGGGACA[A/G]GGGACCAGTCGCACC | 26524 |
rs771928210 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019621 | GTGCTGGGATTATAG[G/T]TGTGAGCCACCGCAT | 26524 |
rs771938833 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021666 | CAGCAGCTTAATTTT[G/T]GAAGAATTGAGGACA | 26524 |
rs771943905 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045599 | GTAACCAATTCAAAG[C/T]CTTCAAGTAGTTGCC | 26524 |
rs772031398 | snp | C/T | 0.000116607 | 0.00763477 | missense | LATS2 | GRCh38.p7 | 13:20989083 | TGGCACCGTAGCCCT[C/T]GGGTGGGTGCTGGTG | 26524 |
rs772096823 | snp | C/T | 3.29489e-05 | 0.00405874 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975137 | TACGGGGTCGAAATT[C/T]GAGGTGTCCATGGGG | 26524 |
rs772105424 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056365 | TCTACATAAGCTTAC[A/G]GTCTCGGGGAAAAAG | 26524 |
rs772106533 | snp | A/C | 1.65378e-05 | 0.00287552 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975248 | CTTCAGGTCATCGGC[A/C]CCATTCCGCCCCAGG | 26524 |
rs772125060 | in-del | -/GT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012668 | TGGTAAACAAGTATG[-/GT]ATAAGCGCTTTGCAG | 26524 |
rs772129050 | snp | A/G | 1.73909e-05 | 0.00294875 | intron-variant | LATS2 | GRCh38.p7 | 13:20987858 | AGCCGGGAACAAATA[A/G]TAAAAATGAAGTGTG | 26524 |
rs772144893 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984324 | CTAGGATACTTTTGG[C/T]TCTAAAAACTAAGGG | 26524 |
rs772220905 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037126 | ATCATATTTTAGGAC[C/T]GGGTGTGGCGGCTCA | 26524 |
rs772243099 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000147 | AACACTTTGGGAAGC[C/T]GAGGCGGGCAGATCA | 26524 |
rs772248213 | snp | C/G | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:20995168 | TCACTTAAGGGTTAG[C/G]TGTTACAGTTCACAA | 26524 |
rs772276792 | snp | A/T | 3.29462e-05 | 0.00405857 | missense | LATS2 | GRCh38.p7 | 13:20983481 | TAGTCCATCACAAAG[A/T]ACAGGCTGTCTTTGT | 26524 |
rs772276927 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974973 | CCTGAAGGCTTTGGG[C/T]ATCGAAAGGGGTAGC | 26524 |
rs772331591 | snp | A/G | 9.168e-05 | 0.0067699 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988871 | GGCAGGGGGTGGGAA[A/G]GCGAGGCCGGCGCCT | 26524 |
rs772333844 | in-del | -/CTGCGCCTGGCCAGCATT | 2.04192e-05 | 0.00319518 | intron-variant | LATS2 | GRCh38.p7 | 13:20979837 | CTACACAGGCATGAA[-/CTGCGCCTGGCCAGCATT]TTCTCCTCCGAGGTG | 26524 |
rs772350192 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045853 | CTGCTGCTGCTGCCT[A/G]GTGGCATCTTTGCTC | 26524 |
rs772373138 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003458 | CCTTTTTTTTTTTTT[-/A]AAGACAGAGTCTTGC | 26524 |
rs772385361 | in-del | -/GACA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978518 | CCTGACCACATAGCT[-/GACA]GTTTGCGAACAATGA | 26524 |
rs772431354 | snp | C/T | 1.65214e-05 | 0.0028741 | missense | LATS2 | GRCh38.p7 | 13:20981519 | GTCCCCACCAGTGAA[C/T]GTGCCAGGCACCTCT | 26524 |
rs772434676 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026036 | AGCCACCTCTGAAAG[C/T]ACTGGCCATAAAGAG | 26524 |
rs772456666 | snp | A/C/G | 8.24782e-05 | 0.0064213 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988127 | CTTGTCGCCGCCCTC[A/C/G]GGCTCGTTGGGGCCC | 26524 |
rs772459145 | snp | C/T | 1.97959e-05 | 0.00314604 | missense | LATS2 | GRCh38.p7 | 13:20988816 | GGTGGGCCGCGGGAC[C/T]GGCCTGCTTGTGGTG | 26524 |
rs772472407 | snp | C/T | 2.17536e-05 | 0.00329792 | intron-variant | LATS2 | GRCh38.p7 | 13:20979843 | CAGGCATGAATTCTC[C/T]TCCGAGGTGAATTTC | 26524 |
rs772475723 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037594 | TCTACAAAGGGAGAC[A/G]CACAAACTACTTAAC | 26524 |
rs772480447 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994315 | CCATCAACCCTTCTT[A/T]AGCAAGTAAGTACTT | 26524 |
rs772525162 | snp | A/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062667 | GTTTAAAGTCAACTC[A/G]ATTTCCTCTTTAATT | 26524 |
rs772590422 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004595 | CATGCTGTTCTGGGC[A/G]TAGGAAACCAGCAAT | 26524 |
rs772612351 | snp | C/T | | | missense | LATS2 | GRCh38.p7 | 13:20991382 | CTGCTGCCAGTCTGC[C/T]TGAGAGCTCGGCCAG | 26524 |
rs772643289 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049370 | GAGCAGCAGCCCCGG[A/G]GAGCAAGGGGAAGGG | 26524 |
rs772651577 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017930 | CATGTCCAGCCTGAT[G/T]CATTTCTTCATACTA | 26524 |
rs772697305 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987390 | TTACCTTCTTCAGCA[A/C]TTCAGTGTCAACTAA | 26524 |
rs772703569 | snp | A/C | 3.29462e-05 | 0.00405857 | missense | LATS2 | GRCh38.p7 | 13:20983674 | ACACTTCTCCAAAGG[A/C]ACCGATCCCCAGGGT | 26524 |
rs772713657 | snp | C/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062861 | TCTTCTCAGATCTCT[C/G]TTTTCTCTCTTCTTT | 26524 |
rs772750384 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976867 | ATGGTGCAGCCACTA[C/T]GGCAAACAGTTTGGG | 26524 |
rs772751433 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006284 | GCTGTCATTAGTGAG[C/G]AGAGAAAGAAGACCA | 26524 |
rs772790311 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037981 | GAGGGGGGCTAGACA[C/T]GGTGGCCCACGTTTG | 26524 |
rs772826137 | in-del | -/A | 1.74382e-05 | 0.00295276 | intron-variant | LATS2 | GRCh38.p7 | 13:20983819 | AGCCTGTGTAGAAGG[-/A]AAAGGAAGGAGGAAG | 26524 |
rs772828618 | snp | C/G | 1.64776e-05 | 0.00287028 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975188 | GGGGGCTGGCTGCTT[C/G]CGGATGTCACTGGAG | 26524 |
rs772915138 | in-del | -/TATATATATATATATATAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007558 | TAGTATATATATATA[-/TATATATATATATATATAT]ATATATATATAGTAT | 26524 |
rs772919502 | in-del | -/A | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062308 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 26524 |
rs772925377 | snp | A/G | 1.65381e-05 | 0.00287555 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975251 | CAGGTCATCGGCCCC[A/G]TTCCGCCCCAGGCGG | 26524 |
rs772931594 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017510 | GCAACCCACAAAACT[C/G]ATTATTTGATCTACT | 26524 |
rs772931648 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032892 | GAGCGAACCCAGTGT[C/G]GGAGAAAACCTCATA | 26524 |
rs772963885 | snp | A/G | 1.89263e-05 | 0.00307617 | missense | LATS2 | GRCh38.p7 | 13:20988239 | GGGTAGGGCGGAGGC[A/G]GGCACCTCCGGTCTG | 26524 |
rs772971782 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998665 | TCCTCTAACCGCCCC[A/T]CCATTGCGTGCCCCT | 26524 |
rs772976930 | snp | C/T | 3.56284e-05 | 0.00422054 | missense | LATS2 | GRCh38.p7 | 13:20989091 | TAGCCCTTGGGTGGG[C/T]GCTGGTGCTGGTGGC | 26524 |
rs773037587 | in-del | -/CTTTTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999466 | CTGCAGAAGCGAGCA[-/CTTTTT]CTTTTTCTTTTTCTT | 26524 |
rs773054368 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018373 | TACTGTCCATCTGGC[A/T]AGATGAGGAGACAAG | 26524 |
rs773078128 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011393 | AATGATCTAGACATA[C/T]ATTTCTCATGCTAGG | 26524 |
rs773118467 | snp | G/T | 4.02188e-05 | 0.00448417 | intron-variant | LATS2 | GRCh38.p7 | 13:20981682 | GATAGTGAAAGAAAA[G/T]AACAAAATATAAAGT | 26524 |
rs773197913 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022626 | GAAAGCTTTTTGTTT[A/G]TTGTCAGAGTGCTTT | 26524 |
rs773204697 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012477 | TCACAATCTCATGGG[A/G]CCATCATCATACATG | 26524 |
rs773251517 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042772 | AGAGGGCGGATCACA[A/G]GGTCAGGAGATTGAG | 26524 |
rs773354669 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975064 | TATTGGGCGAGGTGA[A/G]TGTGTCCCAGGCCTT | 26524 |
rs773397864 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988076 | AATCTGCTTTTTATC[C/T]TTTCCGCCTTTGTCC | 26524 |
rs773426949 | snp | G/T | 1.65206e-05 | 0.00287403 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20981521 | CCCCACCAGTGAATG[G/T]GCCAGGCACCTCTGG | 26524 |
rs773445986 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007514 | ATAAGGGAAGGAGTA[G/T]TTAGTCGTAGGGGAT | 26524 |
rs773465558 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981710 | AGTGAATTTTCACTC[A/T]TCAATAACTCAACAG | 26524 |
rs773465849 | in-del | -/TCA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21000379 | AGCAAGACTCTGTCA[-/TCA]TAATAATAATAATAA | 26524 |
rs773478606 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035184 | GGCTTTAATTCAAGA[A/G]CTATGAATTTCTGGC | 26524 |
rs773522644 | snp | A/G | 1.99015e-05 | 0.00315442 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988817 | GTGGGCCGCGGGACC[A/G]GCCTGCTTGTGGTGT | 26524 |
rs773530007 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021960 | CTTAGACTATCTGTT[C/T]CCACACTTTCTTCGT | 26524 |
rs773533803 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032844 | GGGTGGACCACGGCT[G/T]GCTGGGGAATGCACT | 26524 |
rs773548921 | snp | A/G | 1.66139e-05 | 0.00288213 | intron-variant | LATS2 | GRCh38.p7 | 13:20991231 | TGTTGTCCTTAAGCC[A/G]CAAACCATCTTTGCC | 26524 |
rs773553595 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048110 | GCTCTGCTTAATTGG[C/T]GTAAAATGGGGCATA | 26524 |
rs773553661 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996131 | TGGAGTTGAAGCCAT[C/T]ATATGAGCACCAGAT | 26524 |
rs773569941 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992174 | AGCCCTGGGAGAGAA[A/G]AGGCATTCCTGGCAG | 26524 |
rs773599405 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016353 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAACCTC | 26524 |
rs773605214 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985495 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 26524 |
rs773654040 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014976 | TCAACTGTGAGCTCC[A/G]GGAGGGCAGGCCAGG | 26524 |
rs773717069 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047388 | CTATTCTTCACCCCG[C/T]GATGAATGTTTATAT | 26524 |
rs773728066 | snp | A/G | 2.25568e-05 | 0.00335826 | intron-variant | LATS2 | GRCh38.p7 | 13:20979847 | CATGAATTCTCCTCC[A/G]AGGTGAATTTCATTA | 26524 |
rs773809416 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21039919 | TCTCTACTAAAAATA[C/T]AAAATTAGCTGGGCG | 26524 |
rs773819441 | in-del | -/AGAG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034560 | CTAAGGGTGGCAGAT[-/AGAG]AGAGAAGGTGCCTAT | 26524 |
rs773855939 | in-del | -/AT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030671 | TAACTCCCCCAACTC[-/AT]AGTGTTGTATATCAG | 26524 |
rs773873684 | snp | A/T | 1.65021e-05 | 0.00287241 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045999 | TATTTCCAGAATAAG[A/T]CGTGGCAGGAAAAGT | 26524 |
rs773888902 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061446 | TGGAGCTGCTGCTGG[C/T]CCCGCAGGGACGGGG | 26524 |
rs773944543 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004264 | ACATGGTGAAACCCC[A/G]TCTCTGTTAAACATA | 26524 |
rs773970142 | snp | A/T | 1.75072e-05 | 0.00295859 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988529 | GGCCTTGCCAGGCGG[A/T]CCGGGCCGCGGCTGG | 26524 |
rs773970528 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983548 | TGTCTGCCTCGGCCA[A/G]GATGTCCCTCTCGGC | 26524 |
rs774008101 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979159 | GTAAGAATACAGGAT[C/T]TAATACATATAAAAT | 26524 |
rs774013358 | snp | A/G | 1.69911e-05 | 0.00291466 | intron-variant | LATS2 | GRCh38.p7 | 13:20989337 | GGAAGACAGCATCAG[A/G]GTGGGTGTGATCAGT | 26524 |
rs774048510 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033882 | ATTCTTCTAATGTCA[C/T]AACCACCCAAATATA | 26524 |
rs774063705 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20983635 | TGGCGTACAGGGCGT[A/G]AGTGTCCACCTTACA | 26524 |
rs774093409 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975176 | GGTGGGAACGTAGGG[A/G]GCTGGCTGCTTCCGG | 26524 |
rs774094311 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21020231 | CAAGGAGCTTCTGAC[A/G]TGAGCAAGTCTAGCT | 26524 |
rs774100473 | snp | C/T | 0.000360166 | 0.0134147 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988451 | ACGCACGCTCTTCAC[C/T]GGGTGCAAGATGTGC | 26524 |
rs774120765 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016708 | AGGCGCCAAGAGCAG[C/G]CTCTCAGGCAACCCA | 26524 |
rs774127148 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981393 | GTCCTTGGAAAGCTA[C/G]AGCCAGCGAGACTCA | 26524 |
rs774128777 | snp | A/G | 3.48189e-05 | 0.00417232 | missense | LATS2 | GRCh38.p7 | 13:20989013 | GGCACCAGCAGGTGC[A/G]GCCGCCCGTAGTGCG | 26524 |
rs774211442 | snp | C/T | 1.66493e-05 | 0.0028852 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988181 | TGCGCACAGGCTGTC[C/T]AGGTCGTACTGCTCC | 26524 |
rs774243239 | in-del | -/CTG | 1.64732e-05 | 0.0028699 | cds-indel, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045837 | TGGGGTGGCTCTCAT[-/CTG]CTGCTGCTGCTGCCT | 26524 |
rs774275931 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987525 | CCTTAAACTTTGTTT[C/T]TACTCATTCAAATGT | 26524 |
rs774291933 | snp | A/G | 1.86754e-05 | 0.0030557 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988718 | CAGGTCCACGTTGAG[A/G]CTGTTCCGCGAGGGA | 26524 |
rs774319858 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018462 | AGCTAGAGTTCAGAA[A/G]GGGAAGGGCTGGCTC | 26524 |
rs774333346 | in-del | -/CGCTTTTGCGGCTCTTGT | 1.64821e-05 | 0.00287067 | cds-indel | LATS2 | GRCh38.p7 | 13:20988099 | CTTTGTCCCCCTTGG[-/CGCTTTTGCGGCTCTTGT]CGCCGCCCTCGGGCT | 26524 |
rs774363917 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054011 | CAGTAATGGTGCATT[C/T]AATGCCACTTAACTG | 26524 |
rs774383041 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051427 | CTGAAATAGAGAGCA[C/G]TTACAGGATAGAGAA | 26524 |
rs774459468 | snp | A/C | 3.295e-05 | 0.00405881 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974956 | CCTGTGAAGCTTCTG[A/C]TCCTGAAGGCTTTGG | 26524 |
rs774491904 | snp | G/T | 1.6483e-05 | 0.00287076 | missense | LATS2 | GRCh38.p7 | 13:20983283 | CAGAGGCCGAAATCT[G/T]TGAGTTTAATGTGAC | 26524 |
rs774556590 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992249 | CAGCAGCACGCAAGG[A/G]TAGGTGGAGATGGGG | 26524 |
rs774557203 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045833 | AACTTTGGGGTGGCT[C/T]TCATCTGCTGCTGCT | 26524 |
rs774568224 | snp | C/T | 1.81516e-05 | 0.00301255 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974840 | CCCTGACCTGGGAGG[C/T]AGCGAGTGGTGGGGG | 26524 |
rs774584474 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992914 | GTGGTGTGTGCCTGT[A/G]GTTCCAGCTACTCAG | 26524 |
rs774609901 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012207 | ATCATATAAAAGATT[-/A]AAAAAAATGCATATC | 26524 |
rs774639626 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982205 | AATAATCAGCTGTTT[C/T]TGGCTTTTCCAAATG | 26524 |
rs774651148 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037395 | GCAACACAGCAAGAC[G/T]CCATCTCAAAAATCA | 26524 |
rs774676269 | snp | C/T | 5.06804e-05 | 0.00503365 | synonymous-codon, intron-variant | LATS2 | GRCh38.p7 | 13:20979730 | AGGTGCCAAAAAGGG[C/T]GGCTGCCCCACCAGC | 26524 |
rs774753719 | in-del | -/AG | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999366 | TGAAACGAATGAAGA[-/AG]AGAAATTTGGCATAA | 26524 |
rs774774482 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011498 | CTTTACAGTTCCTCA[C/G]GTCCAGCAACACTTT | 26524 |
rs774784195 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016440 | AGGTACATACCACCA[C/T]GCCTAATTTTTGTAT | 26524 |
rs774883033 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974183 | GTGAATGGCAAGATA[C/T]GGTAATTTTATAATA | 26524 |
rs774884992 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026515 | CATTCAACTGTTGAT[A/G]GACACTGGGGTTGTT | 26524 |
rs774885199 | snp | A/C | 8.23608e-05 | 0.00641667 | missense | LATS2 | GRCh38.p7 | 13:20988048 | TTTTGCGGACGGGAA[A/C]GGGAGAGGTCTGAAT | 26524 |
rs774905195 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003552 | CTCAAGCAGTCCTCC[C/T]GCCTCAGCCTCTCAA | 26524 |
rs774959810 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986182 | AATGAGATATAATCT[A/C]TCCCCAGTTAGAACG | 26524 |
rs774967454 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019632 | ATAGGTGTGAGCCAC[C/T]GCATCCAGCTGGATT | 26524 |
rs775004082 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040307 | CGGAGAATTGCTTGA[A/G]CCCAGGTCAAGGCTA | 26524 |
rs775057424 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027843 | CTGCTGGATCCACAG[A/G]TAACTGTGAGAACTG | 26524 |
rs775057450 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042180 | GTAAGTTTTCAGTAA[C/T]TTATGTGCAAAAGAC | 26524 |
rs775060105 | snp | C/T | 0.000114063 | 0.00755105 | intron-variant | LATS2 | GRCh38.p7 | 13:20979671 | TACAGCAAGCAGATG[C/T]GTGGTTCCTCTCACA | 26524 |
rs775075244 | snp | C/T | 6.58968e-05 | 0.00573969 | missense | LATS2 | GRCh38.p7 | 13:20983389 | CCAAAGTCAGCTCTG[C/T]GATGTAGAACCGGGC | 26524 |
rs775077265 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21058549 | GCCCCTCCCACCAAC[A/C]CTGTGATTTGCTAAG | 26524 |
rs775115185 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997551 | TGGTCCAGGCCTCTG[G/T]TGCAGGTACATCACC | 26524 |
rs775115919 | multinucleotide-polymorphism | CA/TG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041223 | ATGATCTGCCCGCCT[CA/TG]GCCTCCCAAAGTGCT | 26524 |
rs775118892 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985716 | GCACTCCAGCCTGGG[C/T]AATAGAGCAAGACTC | 26524 |
rs775135248 | snp | A/G | 1.66219e-05 | 0.00288283 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989261 | ATCGCCGGTTCCTTC[A/G]AAGCTGGGCCTCCGC | 26524 |
rs775135313 | snp | A/T | 7.24927e-05 | 0.00602006 | missense | LATS2 | GRCh38.p7 | 13:20988317 | GCCAGGGCATGCTCC[A/T]CCTTGGCGTCCAAGC | 26524 |
rs775151766 | snp | C/T | 4.95835e-05 | 0.00497888 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988424 | AGCCGTCTGCGGCTC[C/T]GGCCTCAGCACACGC | 26524 |
rs775173102 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044221 | CAGCAGGATTCATTT[C/T]ACAAACATCTCCTCT | 26524 |
rs775175958 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021673 | TTAATTTTTGAAGAA[C/T]TGAGGACACCTTCCC | 26524 |
rs775247544 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | LATS2 | GRCh38.p7 | 13:20983532 | TTGACCACCCACTCA[C/T]TGTCTGCCTCGGCCA | 26524 |
rs775256441 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979198 | TGTGTTCATTGACGC[A/T]ATGTTACTGGTAAGG | 26524 |
rs775264550 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052735 | GTAAAGACAGAAAAA[C/T]ACAGAGAAGAAAAGC | 26524 |
rs775326823 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008643 | GAAAAAATAAGAGAG[C/G]ACTTCACACCCATTA | 26524 |
rs775335330 | snp | A/C/G | 0.00014825 | 0.00860854 | missense, synonymous-codon | LATS2 | GRCh38.p7 | 13:20983633 | CATGGCGTACAGGGC[A/C/G]TGAGTGTCCACCTTA | 26524 |
rs775342052 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045887 | AGGACTTTGGCATCC[A/T]GGGAAGTGTCACTGT | 26524 |
rs775348642 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996658 | GGTGCTGGGATTATA[A/G]GTGTGAGCCACCGTG | 26524 |
rs775349223 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029797 | TCTGTCTCAAAAAAG[-/A]AAAAAAAAAGATATT | 26524 |
rs775353796 | snp | A/C | 1.64855e-05 | 0.00287097 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045989 | CGCTGCCGGCTATTT[A/C]CAGAATAAGTCGTGG | 26524 |
rs775410514 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978398 | AACCCTTAGTAACTC[A/G]TTTCAGAAAGCAAAT | 26524 |
rs775425216 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975170 | GCTGATGGTGGGAAC[A/G]TAGGGGGCTGGCTGC | 26524 |
rs775426416 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051637 | CAGTGTCAGTGGTGG[A/C]GGAGGAAGGCAGTGA | 26524 |
rs775429622 | snp | A/G | 1.65858e-05 | 0.00287969 | intron-variant | LATS2 | GRCh38.p7 | 13:20991431 | GTAAAGGAGAGGTAA[A/G]TGCATGTCATCCTAA | 26524 |
rs775429967 | snp | A/G | | | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972910 | CCCCAAGACATTCCT[A/G]AGACAGCCCTGTCTG | 26524 |
rs775445789 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21001624 | GGTATTCAGCCCCAG[A/C]TGAGTTCCCAGTGGA | 26524 |
rs775451432 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034846 | GAAAAAAAAGGCATC[C/T]GCTAACAAATAAGTC | 26524 |
rs775504826 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990856 | ACTCTCAGAAGCTAC[A/G]ATGTGAGAGAGGTGT | 26524 |
rs775508994 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053275 | CAACTCAACCCCACC[C/T]GCCTGGCTCACTCCT | 26524 |
rs775535885 | snp | A/G | 1.81401e-05 | 0.0030116 | missense | LATS2 | GRCh38.p7 | 13:20988233 | TGCTTCGGGTAGGGC[A/G]GAGGCGGGCACCTCC | 26524 |
rs775573915 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045666 | CTCTGCACATGGCCC[C/T]GCAGAGGTCTGTACC | 26524 |
rs775593160 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984351 | AGGGAAACTTCTATT[A/T]ACACAAATCTGTGGA | 26524 |
rs775620113 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056372 | AAGCTTACAGTCTCG[A/G]GGAAAAAGACACCAT | 26524 |
rs775653875 | snp | C/T | 1.69476e-05 | 0.00291093 | missense, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21045701 | TGGTCGCATCCTGCG[C/T]TCACCAGTTCCTGCA | 26524 |
rs775670145 | snp | C/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974711 | TTTTCAAAAGTGTCC[C/T]GTTTGGGTTTTCTTG | 26524 |
rs775697303 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982409 | CTCTGCTTCCCGGGT[C/T]CAAGCGATTCTCATG | 26524 |
rs775735281 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044560 | TGTTTTACTTGTTAC[A/G]TTTCACTAATTACAT | 26524 |
rs775743967 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20983888 | GATGGGGATGCCCTG[A/G]AACTGAGAGGAACCT | 26524 |
rs775781939 | snp | G/T | 7.2808e-05 | 0.00603313 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974829 | CGGCTCCGGGACCCT[G/T]ACCTGGGAGGCAGCG | 26524 |
rs775798832 | snp | C/G | 1.65075e-05 | 0.00287289 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20987905 | TTCTTGCTCCAGCTG[C/G]AGCCTCCGGTTAACC | 26524 |
rs775802023 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017945 | TCATTTCTTCATACT[A/C]ATAATGTGAGACTAT | 26524 |
rs775804937 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051084 | GTGACGCATACGCCG[C/T]GTCAGGGGAGGTGAG | 26524 |
rs775806160 | snp | C/T | | | missense | LATS2 | GRCh38.p7 | 13:20991404 | CTCGGCCAGCCATCT[C/T]CTGGGAGGGAAGTAA | 26524 |
rs775817720 | in-del | -/CT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015732 | TGAGACGGAGTCTCA[-/CT]CTGTCACCCAGGCTG | 26524 |
rs775860882 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21049413 | GAATGAAAGGCACAG[A/G]TGGGGGATGGTGGGG | 26524 |
rs775892552 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20988039 | CTCTGCTGTTTTTGC[A/G]GACGGGAACGGGAGA | 26524 |
rs775894375 | snp | C/T | 3.54264e-05 | 0.00420856 | missense | LATS2 | GRCh38.p7 | 13:20988893 | CCGGCGCCTGGCGGT[C/T]CTCCCTGGCCCTTCG | 26524 |
rs775897822 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037602 | GGGAGACGCACAAAC[C/T]ACTTAACAGCAGATT | 26524 |
rs775917304 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004630 | TGGGCTTCCTGGCCC[C/T]CTGCCTCCAACCTGG | 26524 |
rs775942256 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038670 | ACTGTGCAAAGCTTT[A/G]TCTATTTTTGTAATT | 26524 |
rs776015793 | snp | A/T | 1.859e-05 | 0.00304871 | stop-gained | LATS2 | GRCh38.p7 | 13:20988700 | GGTGCTGCCCAATTC[A/T]TACAGGTCCACGTTG | 26524 |
rs776021607 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029561 | ACTTTGGGAGGCCAA[A/G]GCAGGCGTATCACGA | 26524 |
rs776066723 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21059945 | CCTCCAGCCTGGGAG[A/G]CAGAGCGAGATCTTG | 26524 |
rs776086204 | snp | A/C | 0.000148301 | 0.00860978 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974941 | AATCTGAGCTCTCAG[A/C]CTGTGAAGCTTCTGC | 26524 |
rs776134094 | snp | A/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21062743 | GTAGTAAAGGTCATT[A/G]TCTGTGCACTATTTT | 26524 |
rs776141033 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21029594 | TCAGGAGTTCGAGAC[C/G]AGCCTGGCCAATATG | 26524 |
rs776187556 | snp | C/G | 7.98882e-05 | 0.00631963 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20989111 | GTGCTGGTGGCCGGG[C/G]CCGTGGGGGCCGACT | 26524 |
rs776195777 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987132 | CCCAGGAGGCAGAGG[C/T]TGCAGCGAGCCAAGA | 26524 |
rs776205810 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048715 | GGTGGCGGGTGCCTA[C/T]AATCCCAGCTACTTG | 26524 |
rs776206124 | snp | A/G | 1.92121e-05 | 0.0030993 | missense | LATS2 | GRCh38.p7 | 13:20988243 | AGGGCGGAGGCGGGC[A/G]CCTCCGGTCTGGGCC | 26524 |
rs776232474 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017174 | GCCAGCACAGTGAAA[C/T]AAAACGGACGATAGC | 26524 |
rs776254240 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21011022 | ACTGCTCATTGGAGT[A/G]AAGTCTTTTTAAATT | 26524 |
rs776273141 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044467 | CTTAGCTTATTTCCG[C/T]TTCATGCAACTGTAA | 26524 |
rs776302950 | in-del | -/AG | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974413 | TCCGTGACATTGAGC[-/AG]AGTGTTATCTTTTTT | 26524 |
rs776306238 | snp | A/G | 1.70801e-05 | 0.00292229 | intron-variant | LATS2 | GRCh38.p7 | 13:20987873 | GTAAAAATGAAGTGT[A/G]AAATTACTTTGGCCA | 26524 |
rs776318009 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976797 | AAAAACAGGAAAATA[C/G]TTATTGAGGATGTAG | 26524 |
rs776378570 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | LATS2 | GRCh38.p7 | 13:20983349 | TCTCGGTGGATGAAG[C/T]CCATCTTGTGGACAC | 26524 |
rs776382278 | snp | C/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21023608 | TCAAAAGGATGGGAG[C/G]GAGGTCCACCAAATG | 26524 |
rs776391625 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21031160 | GGCTTTCATTAGCTT[A/C]AATATGATAGGCCTA | 26524 |
rs776395915 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979408 | ACACCTTTGCTGATC[C/T]TCACTGTTCTTGCCT | 26524 |
rs776412950 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042573 | ACGCCTGTAGTCCCA[C/G]CTACTTCAGAGGCTG | 26524 |
rs776454083 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996705 | ATTCTGGATACTTTG[A/T]AGGCAGAACTGATAC | 26524 |
rs776466850 | snp | C/T | 0.000131778 | 0.00811614 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974976 | GAAGGCTTTGGGCAT[C/T]GAAAGGGGTAGCCAT | 26524 |
rs776467267 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983489 | CACAAAGTACAGGCT[A/G]TCTTTGTCTTGGAAG | 26524 |
rs776495511 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999062 | CAACCTTGTCCACGC[C/G]AGGCAGGGGCCCCGG | 26524 |
rs776495638 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045855 | GCTGCTGCTGCCTGG[C/T]GGCATCTTTGCTCCC | 26524 |
rs776575412 | snp | G/T | | | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975207 | ATGTCACTGGAGAAG[G/T]CAATGGCGCTGAAGA | 26524 |
rs776576646 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041639 | CAGGATACAGGTCAT[C/T]CACAGAGAAAAAGCC | 26524 |
rs776666363 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991946 | CTTAGAGATCTGACT[C/T]GTAGAAGAAAGAAAG | 26524 |
rs776667323 | snp | A/G | 1.777e-05 | 0.00298072 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988988 | CACTCCGTAGCCCAG[A/G]GGTTCCCCAGGCACC | 26524 |
rs776684800 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009693 | CTTTTAAAATACAGA[A/C]ACCAGATGGAGGAAC | 26524 |
rs776702476 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051757 | TGAGCCCAGGAGCTG[C/G]AGACCAACCTGGGCA | 26524 |
rs776718134 | snp | A/G | 1.65427e-05 | 0.00287595 | intron-variant | LATS2 | GRCh38.p7 | 13:20991256 | TTTGCCCACTATGCT[A/G]CAGGCCTGGGCTCAC | 26524 |
rs776817232 | snp | C/T | 1.75225e-05 | 0.00295989 | intron-variant | LATS2 | GRCh38.p7 | 13:20981439 | GAAGGAGACCTCCTG[C/T]GGGGTGGCTGGCCAT | 26524 |
rs776821247 | snp | A/C | 1.66316e-05 | 0.00288367 | missense | LATS2 | GRCh38.p7 | 13:20988176 | ATGCCTGCGCACAGG[A/C]TGTCCAGGTCGTACT | 26524 |
rs776833654 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991007 | ACACACCTTCCCCTA[C/G]GTAGGAAGTACTAAG | 26524 |
rs776851102 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21014577 | GCTGAGGATGGATGC[C/T]AGGAGGACATGAGAA | 26524 |
rs776861049 | in-del | -/A | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047704 | TTTTTCAAGTGGATT[-/A]AAAAAAAAAAAAAGG | 26524 |
rs776870058 | snp | C/G | 1.74199e-05 | 0.00295121 | intron-variant | LATS2 | GRCh38.p7 | 13:20983817 | CCAGCCTGTGTAGAA[C/G]GAAAAGGAAGGAGGA | 26524 |
rs776888458 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013801 | CAAGACCCCGTCTCT[A/G]CAAAACAATTTAAAA | 26524 |
rs776956274 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008049 | CAGGCGTGAGCCACC[A/G]TACCCAGCCCTGACT | 26524 |
rs776967645 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005061 | GTTGGTCCCACAGAA[A/G]ATGCAATTCTAGGAA | 26524 |
rs776979582 | in-del | -/C | 1.6599e-05 | 0.00288084 | intron-variant | LATS2 | GRCh38.p7 | 13:20991240 | TAAGCCACAAACCAT[-/C]TTTGCCCACTATGCT | 26524 |
rs776992329 | snp | A/C/T | 7.54167e-05 | 0.00614032 | missense | LATS2 | GRCh38.p7 | 13:20988690 | GCTGGACGGAGGTGC[A/C/T]GCCCAATTCATACAG | 26524 |
rs777010853 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004951 | TCCAAGGGACAGAGA[C/G]CAGCCCCGGCGTTCT | 26524 |
rs777016907 | snp | C/T | | | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20973006 | GCAAGGACTTACAAA[C/T]TCCAGTAAGACATGA | 26524 |
rs777054050 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21026181 | CGTTCAAGTATGAAA[C/G]ATGTATACACCAGTA | 26524 |
rs777056755 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21001827 | GAGGTTGCGGTGAGC[C/T]GAGACAGCGCCCCTG | 26524 |
rs777083780 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21027624 | CACTGTCTTGCTTAG[C/T]TTTAGAGACTACCCA | 26524 |
rs777102261 | in-del | -/TTC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032639 | TGTGGTCCAAGACAA[-/TTC]TTCTTCTAATGTGGC | 26524 |
rs777111663 | snp | A/G | 1.95158e-05 | 0.0031237 | missense | LATS2 | GRCh38.p7 | 13:20988668 | GCCAGGGTGGCAGCC[A/G]GCCACTGCTGGACGG | 26524 |
rs777162020 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007114 | AAAAACTGAAATTCC[C/T]TGGCTATGCAGTTTT | 26524 |
rs777166025 | snp | G/T | 1.65765e-05 | 0.00287888 | intron-variant | LATS2 | GRCh38.p7 | 13:20991422 | GGGAGGGAAGTAAAG[G/T]AGAGGTAAGTGCATG | 26524 |
rs777203386 | snp | C/T | 1.72761e-05 | 0.002939 | intron-variant | LATS2 | GRCh38.p7 | 13:20987865 | AACAAATAGTAAAAA[C/T]GAAGTGTGAAATTAC | 26524 |
rs777218062 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042866 | GTGGGTGCCTGTAAT[A/C]CCAGCTACTCAGGAG | 26524 |
rs777282059 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992781 | GTGGCTCACGCCTGT[A/G]ATCCCAGCACTTTGG | 26524 |
rs777296126 | snp | C/G | 1.82158e-05 | 0.00301787 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974826 | CACCGGCTCCGGGAC[C/G]CTGACCTGGGAGGCA | 26524 |
rs777319923 | snp | A/C | 1.74439e-05 | 0.00295325 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974875 | TGGCCCCCATCTACA[A/C]GTACACAGGCTGGCA | 26524 |
rs777354670 | snp | A/C | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046563 | TTTTGAAACCCACAG[A/C]TTGAGGAGTATTTAA | 26524 |
rs777368593 | snp | G/T | 1.93827e-05 | 0.00311303 | intron-variant | LATS2 | GRCh38.p7 | 13:21045677 | GCCCTGCAGAGGTCT[G/T]TACCCACCTGGTCGC | 26524 |
rs777388440 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019301 | TCACTTGGATTTGTT[A/G]TTATTATTATTATTA | 26524 |
rs777388539 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034650 | TCTTACTCTGCCTCT[C/G]GGGGTTAGGCCTCTG | 26524 |
rs777392012 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991505 | GTGCTGGGACACTTC[A/G]CCTCTGTACTGCTGA | 26524 |
rs777397200 | snp | A/G | 1.86496e-05 | 0.0030536 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988763 | CGGGGGGCTGTCGCT[A/G]GCGAACACCTGGCTG | 26524 |
rs777423592 | snp | C/T | 5.4793e-05 | 0.00523388 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974820 | TGAGGGCACCGGCTC[C/T]GGGACCCTGACCTGG | 26524 |
rs777425651 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045321 | GAAAAGGGAAGCCAG[A/T]CTCTTTCCACGATAG | 26524 |
rs777437817 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21031389 | TTCAATTTTTTTCTA[A/T]GATTTTTGGATTGGG | 26524 |
rs777439645 | in-del | -/TTAATCCCAGTACTTTGGGAGGCCGAGG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005856 | AGTGGCTTACGCCTA[-/TTAATCCCAGTACTTTGGGAGGCCGAGG]TTGGTGGATCACCTG | 26524 |
rs777491849 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045367 | ATAAACACCAAAAAA[-/A]GGGGCTAAGCACGAA | 26524 |
rs777520691 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028837 | CCTCCCAGAGTACTG[A/G]GATTACAGGTGTGAG | 26524 |
rs777523098 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21013336 | CTGGCTCGATGCCTA[A/G]TAATAATCTCATTTC | 26524 |
rs777622007 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054875 | TGGTTTTGTTTGGTA[A/C]GGAGGGAGGGGGAGG | 26524 |
rs777634015 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20980808 | AAAGGACTTTAAACA[A/T]CATGTGATGGCAGGG | 26524 |
rs777648050 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041555 | CACAATATTCAGGAC[C/G]AGGAAAATGTATCAA | 26524 |
rs777696058 | snp | G/T | 6.58892e-05 | 0.00573936 | missense | LATS2 | GRCh38.p7 | 13:20988017 | CGTGACTCTCTCTTC[G/T]CTTCGTCTCTGCTGT | 26524 |
rs777813908 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017040 | AAATATGGCAGAACC[A/G]GAAACAAATTCATCT | 26524 |
rs777837966 | in-del | -/CTCCGGG | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023150 | GCGCTGCATCGAGGG[-/CTCCGGG]CTCCGAGGGCTCCGA | 26524 |
rs777864982 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004366 | TTGAACCCAGGAGGT[A/G]GAGGTTGCAGTGAGC | 26524 |
rs777868701 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975231 | CTGAAGAAGGGGTGG[A/G]CCTTCAGGTCATCGG | 26524 |
rs777926713 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032535 | CCTCCCAAAGTGCTG[C/G]GATTATAGGGGTGAG | 26524 |
rs777957695 | in-del | -/TCACTC | 1.83545e-05 | 0.00302934 | intron-variant | LATS2 | GRCh38.p7 | 13:20979812 | CCTGCAAGACAAAGT[-/TCACTC]AATCCCTACACAGGC | 26524 |
rs777979479 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21017718 | GCAACCTCCGTCTCC[A/G]GGGTTCAAGTGATTC | 26524 |
rs777989771 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975138 | ACGGGGTCGAAATTC[A/G]AGGTGTCCATGGGGT | 26524 |
rs777991905 | snp | A/G | 1.65515e-05 | 0.00287671 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983762 | AGACTCTTTCTGGTA[A/G]AGGATCTTCCGCATC | 26524 |
rs778020436 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050017 | TCCAGCTACTCGGAA[C/G]GCTGAGGCAGGAGAA | 26524 |
rs778029181 | in-del | -/CAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998354 | CAAGAGACCCTGTCT[-/CAAA]CAAACAAACAAAAAT | 26524 |
rs778039858 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986935 | TGGTGGCTCACACGT[A/G]TAATTCCAGCACTTG | 26524 |
rs778073485 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21056597 | ATTCAATTTCATAGC[C/T]CAGCAGGGGTTCTCA | 26524 |
rs778075235 | in-del | -/TAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987356 | TGTTACATTTTAATT[-/TAAA]TAGTTTCATCAATAA | 26524 |
rs778111112 | snp | A/T | 1.65378e-05 | 0.00287552 | missense | LATS2 | GRCh38.p7 | 13:20991400 | AGAGCTCGGCCAGCC[A/T]TCTCCTGGGAGGGAA | 26524 |
rs778187529 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20986010 | GATCGTGCCATTGCA[C/T]TCCAGCCTGGGCAAC | 26524 |
rs778262618 | snp | A/G | 1.651e-05 | 0.0028731 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20991360 | CTCCAGGGCGGCCTC[A/G]ATGCTCCTGCTGCCA | 26524 |
rs778266923 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022332 | TCTGTATATGCCTAA[A/G]TGCATGTACTGAGTC | 26524 |
rs778269734 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20998111 | GCTGACGCCTGTAAT[C/T]CCAGGGCTTTGGGAG | 26524 |
rs778281615 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053585 | GACAAAGCCTGCCAG[C/T]GCCACCCCAAAGGTC | 26524 |
rs778315916 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052633 | CTGGGATAACAGGCG[C/T]GGGCTACCATGCCCA | 26524 |
rs778317216 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042121 | CAGCTCCTCCCATAA[C/G]AAATATTAATCTAGT | 26524 |
rs778322373 | snp | A/C | | | missense | LATS2 | GRCh38.p7 | 13:20988212 | GACTTGCTGCGCAGC[A/C]GCAGGTGCTTCGGGT | 26524 |
rs778386367 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010718 | GACTAGTCGTCACAC[A/G]TGTACTTTGAATTCC | 26524 |
rs778414719 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012663 | TTGGATGGTAAACAA[A/G]TATGGTATAAGCGCT | 26524 |
rs778446455 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981121 | GCTAGAGCCCGGAAA[C/T]GTGTGGTCTGGGCAG | 26524 |
rs778450722 | snp | A/G | 3.31824e-05 | 0.00407309 | missense | LATS2 | GRCh38.p7 | 13:20981586 | GCCTGTCCCCACACC[A/G]ACAGTTAGACACATC | 26524 |
rs778494526 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21038651 | CATTGGCTATGACAC[C/T]GCCACTGTGCAAAGC | 26524 |
rs778497546 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990690 | AGGGGCCTCAGGTAC[C/G]AATCACAGGGCCCAT | 26524 |
rs778499998 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035656 | CAGGCATTAAGTGAA[C/T]AATATTTATGATCTC | 26524 |
rs778545901 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009294 | GCTGCACATTCAACC[C/T]GGAGCCTTGGAGCAC | 26524 |
rs778552334 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991717 | AACTTTTGTGGTTGG[A/G]CTGGTGAGTTCAGGA | 26524 |
rs778572163 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034815 | ACAGTACAGGAAAGT[A/C]ATCAAGAACTCTTAG | 26524 |
rs778573603 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008636 | CTTCACTGAAAAAAT[A/T]AGAGAGCACTTCACA | 26524 |
rs778586179 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002607 | GGTCTGGAACTCCTG[A/G]GCTCAAGCAATCTGC | 26524 |
rs778616143 | snp | A/G | 1.68977e-05 | 0.00290665 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975298 | ACAGCTTGGTGATGA[A/G]GTCCCTGGCCTCAGG | 26524 |
rs778627422 | snp | C/T | 2.69473e-05 | 0.00367055 | missense | LATS2 | GRCh38.p7 | 13:20988606 | GGAAGGCCACGTGCG[C/T]GCGCGGCGGCGCCTC | 26524 |
rs778693659 | snp | C/T | 5.02071e-05 | 0.00501009 | missense | LATS2 | GRCh38.p7 | 13:20989071 | CTGCCTCTACGCTGG[C/T]ACCGTAGCCCTTGGG | 26524 |
rs778696672 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021647 | GCTCAAAGCTGCCCA[C/T]GGTCAGCAGCTTAAT | 26524 |
rs778698464 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21031825 | GCACCCACTGCACTC[C/T]GGCCTGGGTGACAGA | 26524 |
rs778699538 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046816 | TCAATTGCAGTTTCC[A/G]CACACACATTATGAG | 26524 |
rs778753355 | snp | A/G | | | | | GRCh38.p7 | 13:21045524 | AGAACCTTCAATTGT[A/G]AGTTCAATTATGTGT | 26524 |
rs778777286 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021184 | TTCCATAATTAAAAG[C/T]TTTCTTGGTCAGGTG | 26524 |
rs778787084 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973651 | ATATGTATTGTTTAA[A/G]CCAAGTTAAGATTTG | 26524 |
rs778818452 | in-del | -/AAAAAAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993037 | GTGACTCCATCTCCA[-/AAAAAAAA]AAAAAAAAAAAAAAA | 26524 |
rs778871420 | in-del | -/GTGTGTGT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044708 | TGTGTGTGTGTGTGT[-/GTGTGTGT]GTGTGTGTGTGTGTG | 26524 |
rs778931991 | snp | G/T | 1.68493e-05 | 0.00290248 | missense | LATS2 | GRCh38.p7 | 13:20983792 | CTGCTCCTGCTCAGC[G/T]TCACAGAGTCCAGCC | 26524 |
rs778932047 | snp | A/G | 1.96562e-05 | 0.00313492 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988664 | GCGGGCCAGGGTGGC[A/G]GCCGGCCACTGCTGG | 26524 |
rs778936935 | snp | C/T | 0.000619617 | 0.0175905 | missense | LATS2 | GRCh38.p7 | 13:20988491 | ACAGCCGTCACGGTG[C/T]TGGGGGCGGGCAGGG | 26524 |
rs779016113 | snp | C/G | | | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972751 | TGATTTACTTGATCA[C/G]CCACCATATTTATTT | 26524 |
rs779019947 | snp | A/G | 1.74778e-05 | 0.00295611 | intron-variant | LATS2 | GRCh38.p7 | 13:20987851 | AGGGATGAGCCGGGA[A/G]CAAATAGTAAAAATG | 26524 |
rs779028626 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | LATS2 | GRCh38.p7 | 13:20983602 | GGTTCAGGACATCCT[C/T]TTTCCTTAGGGTCTT | 26524 |
rs779035690 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20994983 | GCAGTGGTACAGGGC[A/G]CAGATAGGGAGGCCA | 26524 |
rs779048855 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985652 | CTGAGGCAGGAGAAT[A/G]GCTTGAATCCAGAAG | 26524 |
rs779063612 | snp | A/G | 8.53643e-05 | 0.0065326 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988370 | GGGGGCGGGGGCCGG[A/G]GCAGGCGCGGGCACC | 26524 |
rs779091122 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20984296 | AGTTAAGATAAAAAA[G/T]AAAGTTCTTTCTCTA | 26524 |
rs779107948 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21025886 | GATTTTTTCACCAAC[C/T]GTGACTCTCTGACTA | 26524 |
rs779112301 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006786 | TAGCTGTGTGTGTTT[A/G]GGACTTTTTAAGAGA | 26524 |
rs779129215 | snp | A/G | 1.64923e-05 | 0.00287156 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988121 | GCGGCTCTTGTCGCC[A/G]CCCTCGGGCTCGTTG | 26524 |
rs779162360 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978148 | TCTCGATCTCCTGAC[C/G]TCGTAATCTGCCCGC | 26524 |
rs779228067 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975128 | TTCTTCATCTACGGG[A/G]TCGAAATTCGAGGTG | 26524 |
rs779239293 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051079 | GATGTGTGACGCATA[C/T]GCCGTGTCAGGGGAG | 26524 |
rs779264890 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993140 | GCAGGAAGCCTGGCC[A/G]TGGTCACAGAGCCAC | 26524 |
rs779274889 | in-del | -/GGGGCG | 0.00180505 | 0.0299878 | cds-indel | LATS2 | GRCh38.p7 | 13:20988344 | AAGCCCTCCGCAGCC[-/GGGGCG]GGGGCGGGGGCGGGG | 26524 |
rs779335443 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20976362 | CTAGAAGAAAACATA[A/G]GGTGAAATCTTCATG | 26524 |
rs779402447 | snp | A/G | 0.000202491 | 0.01006 | missense | LATS2 | GRCh38.p7 | 13:20988944 | CCGGTCTCCGGCGGC[A/G]TCTTGCTCTGGAAGG | 26524 |
rs779411298 | in-del | -/GAATG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009181 | AACAAACGAACAAAT[-/GAATG]AATGAATAAAGAAGC | 26524 |
rs779429900 | in-del | -/GCC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041090 | CATTCTCCTGCCTCA[-/GCC]GCCTCCAGAGTAGCT | 26524 |
rs779479305 | in-del | -/AC | 1.90874e-05 | 0.00308923 | intron-variant | LATS2 | GRCh38.p7 | 13:20979825 | GTTCACTCAATCCCT[-/AC]ACAGGCATGAATTCT | 26524 |
rs779494814 | in-del | -/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21037469 | GAAAATGTTTATGAC[-/G]GTAATGCTTGTCTCT | 26524 |
rs779509504 | snp | A/T | 1.77514e-05 | 0.00297916 | utr-variant-5-prime, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21046058 | TTTTACCATAAATAC[A/T]ATCTTCTTAAAGTGT | 26524 |
rs779525816 | snp | C/G | 3.39023e-05 | 0.00411704 | missense | LATS2 | GRCh38.p7 | 13:20988861 | AGAGCCCGGCGGCAG[C/G]GGGTGGGAAAGCGAG | 26524 |
rs779528339 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032588 | TTCGTTCTTTTTTAA[G/T]CCCATCAGCTATCAT | 26524 |
rs779538689 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991053 | GCTGGATGGGGCAAG[C/T]GCCAGGCGTGTCCCA | 26524 |
rs779551921 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034061 | GCTCTCCAGCAACTT[C/T]ACAAGTTTCTGAGCA | 26524 |
rs779572652 | in-del | -/TC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21044757 | TAAATAGAGATAGGG[-/TC]TCGCTCAGCTAACCA | 26524 |
rs779621749 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036818 | AACAAAAAAGCCAAC[C/T]ATTAAACTGACAGTT | 26524 |
rs779703425 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20991847 | ACCTGTCCCCAGGGA[A/G]AGGGTGCAGCTGCCG | 26524 |
rs779706029 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20981216 | GAGTCATTCCCTTGG[A/G]TCTAGGTAGAGCCCG | 26524 |
rs779707935 | snp | A/G | 5.84767e-05 | 0.00540693 | intron-variant | LATS2 | GRCh38.p7 | 13:20979831 | TCAATCCCTACACAG[A/G]CATGAATTCTCCTCC | 26524 |
rs779716343 | snp | C/T | 1.69172e-05 | 0.00290832 | intron-variant | LATS2 | GRCh38.p7 | 13:20989328 | GAAAAAACAGGAAGA[C/T]AGCATCAGAGTGGGT | 26524 |
rs779742135 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987539 | TCTACTCATTCAAAT[A/G]TTCTATTATTAATCC | 26524 |
rs779823280 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010878 | AACTAAGCAAGTTTG[A/C]CTCCTTCATTTGCAT | 26524 |
rs779853028 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21035823 | AGCCAGTGATTCCTA[A/G]AGCCCACCTAGGACC | 26524 |
rs779858503 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21002819 | TCGGCCTCCCAAGTA[G/T]CTAGGATTACAGGTG | 26524 |
rs779957444 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21047066 | CATGGAAATGGCCTC[A/G]TTACATGGAACGCGA | 26524 |
rs779973966 | snp | C/G | 1.71979e-05 | 0.00293235 | missense | LATS2 | GRCh38.p7 | 13:20988576 | TGGTCCTGCTGGGCA[C/G]TGGGCAGTCAGGCCG | 26524 |
rs779988925 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21025630 | TGAAACTCTGTCTCA[A/T]CGTCATTAGGTCTGC | 26524 |
rs780010287 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21047878 | ATTGTAAGCGTTTTA[A/T]CTATCCCCTTTCTCA | 26524 |
rs780069056 | snp | A/G | 0.0114282 | 0.0747228 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988361 | GGCGGGGGCGGGGGC[A/G]GGGGCCGGGGCAGGC | 26524 |
rs780087067 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21015978 | TGTTGGGATTACAGG[C/T]GTGAACCACCACGCT | 26524 |
rs780090868 | snp | A/G | 1.65031e-05 | 0.00287251 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20991342 | GCCCATCTTGCTGAT[A/G]TACTCCAGGGCGGCC | 26524 |
rs780099132 | snp | A/G | 8.96097e-05 | 0.00669304 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988508 | GGGGGCGGGCAGGGA[A/G]GGCTCGGCCTTGCCA | 26524 |
rs780099732 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985253 | CAGGCAAAAAAACCC[C/T]AAAGTAGACAAATGG | 26524 |
rs780102705 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009085 | CCCTTGTCCTGCCAG[A/C]GATTTGGGCCAGAAC | 26524 |
rs780161498 | snp | A/G | 5.63396e-05 | 0.00530722 | missense | LATS2 | GRCh38.p7 | 13:20988278 | TACTCCACGTCCAGC[A/G]GGAAGGCGCCTGCGC | 26524 |
rs780190244 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057933 | GGGGCCATCACAGGG[A/C]ACTCTATGTAATAAA | 26524 |
rs780211635 | snp | A/G | 1.72169e-05 | 0.00293396 | missense | LATS2 | GRCh38.p7 | 13:20989158 | CCACGTACGGCCGCG[A/G]CATCTCCTCCAGCGC | 26524 |
rs780234119 | in-del | -/GGTGCT | 7.29315e-05 | 0.00603825 | cds-indel | LATS2 | GRCh38.p7 | 13:20989088 | CGTAGCCCTTGGGTG[-/GGTGCT]GGTGCTGGTGCTGGT | 26524 |
rs780251206 | snp | C/G | 5.51526e-05 | 0.00525103 | missense | LATS2 | GRCh38.p7 | 13:20988789 | GGCTGCGGGAGCCCA[C/G]CACATGCAGCTGGTG | 26524 |
rs780316499 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21051185 | AATGTGTATACATGT[A/G]ATGTGAGACAAGCCC | 26524 |
rs780367764 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | LATS2 | GRCh38.p7 | 13:20983449 | TCAGCAGGCTCATCA[C/T]GTCCCCACCAGGGAT | 26524 |
rs780372533 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007059 | CTGACAAGGTAATTC[A/G]GTAAAGTATACAAAT | 26524 |
rs780380172 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040911 | CCTTTTAAATTATTA[C/G]GCCCAGAGAGACATT | 26524 |
rs780441890 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21045925 | TGCGGGTAGCCCCTG[A/G]ACCGAAGACTTGGAT | 26524 |
rs780495505 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032209 | TAAGAGCTATGTGCT[A/G]CAATTTGACTAAATT | 26524 |
rs780495811 | snp | A/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978812 | TGTCACCCAGGCTGG[A/C]CTGCAGTGGTGTGAT | 26524 |
rs780545279 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | LATS2 | GRCh38.p7 | 13:20988023 | TCTCTCTTCTCTTCG[C/T]CTCTGCTGTTTTTGC | 26524 |
rs780596632 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21032768 | AAGAAAGAACTTAGC[A/G]GGCACTGGGATGAAT | 26524 |
rs780614508 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975124 | GGCTTTCTTCATCTA[C/T]GGGGTCGAAATTCGA | 26524 |
rs780629896 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20989847 | TATTAAAACAAAGCA[A/G]TATATACACAATAAT | 26524 |
rs780631250 | snp | A/C/T | 5.07914e-05 | 0.00503921 | intron-variant | LATS2 | GRCh38.p7 | 13:20979658 | CAAATCAGATGTCTA[A/C/T]AGCAAGCAGATGCGT | 26524 |
rs780649276 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21033610 | CGGTATCGCTGAAGG[C/T]TCTTGTAAGCGTCTC | 26524 |
rs780671828 | snp | G/T | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973235 | ACAGGCACAGCAGAC[G/T]TGAGTATGCCACTCA | 26524 |
rs780672524 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21052171 | AGGATCACAGTGGTG[C/T]TGTGTGTGACAGCAG | 26524 |
rs780676724 | snp | G/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019094 | CTTTCTCCCTATGTG[G/T]TCTAAGGGAGTTCCC | 26524 |
rs780726732 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20978119 | ACGGGGTTTCACTAC[A/G]TTGGCCAGGCTAGTC | 26524 |
rs780744866 | snp | C/T | 1.64846e-05 | 0.0028709 | missense | LATS2 | GRCh38.p7 | 13:20988104 | TCCCCCTTGGCGCTT[C/T]TGCGGCTCTTGTCGC | 26524 |
rs780761513 | in-del | -/TAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:20995265 | GATATTTAATGGCTC[-/TAA]TGTTTTACTGTGTAT | 26524 |
rs780771422 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012206 | TATCATATAAAAGAT[A/T]AAAAAAAATGCATAT | 26524 |
rs780775452 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21025629 | ATGAAACTCTGTCTC[A/G]TCGTCATTAGGTCTG | 26524 |
rs780781517 | snp | A/C | 1.6617e-05 | 0.00288239 | missense | LATS2 | GRCh38.p7 | 13:20988771 | TGTCGCTGGCGAACA[A/C]CTGGCTGCGGGAGCC | 26524 |
rs780795874 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20989744 | CTCCCTCACAGAAAG[A/G]GCAGAACTGTATCCA | 26524 |
rs780829531 | snp | A/T | 3.3695e-05 | 0.00410443 | intron-variant | LATS2 | GRCh38.p7 | 13:20989319 | CCTGCAGTGGAAAAA[A/T]CAGGAAGACAGCATC | 26524 |
rs780834836 | in-del | -/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004059 | AAAAACATACGCCAA[-/T]TTTTAAAAAGCAGCA | 26524 |
rs780873713 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21045040 | CTCTGTAAGCTGTGT[A/G]TTAATGTATAACTGG | 26524 |
rs780883501 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20987827 | GTGCGTGCTTCCTAT[C/T]GCCAGTAGAGGGATG | 26524 |
rs780905308 | snp | G/T | 0.000213904 | 0.0103395 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20988499 | CACGGTGTTGGGGGC[G/T]GGCAGGGAGGGCTCG | 26524 |
rs780980451 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975041 | AAATGCGTGCTCAGG[A/C]TGCTTGTTATTGGGC | 26524 |
rs781033538 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21043643 | GCAATTAACATAAAT[C/T]AAATGTTGATGGAAA | 26524 |
rs781050017 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036967 | GCTCTCAACATTTAC[A/G]CTAGTAATTCCATTC | 26524 |
rs781089418 | snp | A/G | 0.000181361 | 0.0095209 | synonymous-codon | LATS2 | GRCh38.p7 | 13:20983276 | CCCAGTGCAGAGGCC[A/G]AAATCTGTGAGTTTA | 26524 |
rs781116052 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21036029 | TCAGCCTCCTGAGTA[C/G]CTGGGACTACAAGCG | 26524 |
rs781124167 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant | LATS2 | GRCh38.p7 | 13:20979828 | CACTCAATCCCTACA[C/T]AGGCATGAATTCTCC | 26524 |
rs781132546 | snp | A/G | 1.66261e-05 | 0.00288319 | missense | LATS2 | GRCh38.p7 | 13:20989242 | GGTGGTAGGACGCAA[A/G]CGAATCGCCGGTTCC | 26524 |
rs781143637 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21053894 | GAGACAGAAAGAAGA[C/G]AGATTACCAGAAGAA | 26524 |
rs781187608 | snp | A/G | 1.84858e-05 | 0.00304016 | missense | LATS2 | GRCh38.p7 | 13:20989137 | CGACTCCGGGGAAAA[A/G]GTAGTCCACGTACGG | 26524 |
rs781187633 | in-del | -/TAACATA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050250 | GGCAATCCACTTATT[-/TAACATA]TATTTTTTAAACTGC | 26524 |
rs781216256 | snp | G/T | 0.000115635 | 0.00760289 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975243 | TGGGCCTTCAGGTCA[G/T]CGGCCCCATTCCGCC | 26524 |
rs781238217 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21004150 | AAATGCTTCTGTAAC[A/G]GTGGCTGGGTGCAGT | 26524 |
rs781313774 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21016897 | CCTGTTGTTAAGTCC[A/G]GTTCCCCAAAGATAA | 26524 |
rs781346843 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21018593 | CCTGATGTCCTTCAC[C/T]CAGGTGCCTGAGAGT | 26524 |
rs781366840 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048069 | ATCCCCTGGGGCCTG[C/T]ACTGGCCACATATCA | 26524 |
rs781398659 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21010356 | TCTTCTGGTAAAACC[A/G]AAAGGCCCCAGGGAC | 26524 |
rs781452039 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997182 | GGTTTCACTGGTTTA[C/G]TGCTGCTACTGACAG | 26524 |
rs781454442 | snp | C/G | | | upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21061679 | GCCGCTCCGCCCAGC[C/G]CCGCCCGGCCGTGCT | 26524 |
rs781486621 | snp | A/T | 2.26426e-05 | 0.00336464 | missense | LATS2 | GRCh38.p7 | 13:20988263 | CGGTCTGGGCCTCCG[A/T]ACTCCACGTCCAGCG | 26524 |
rs781512146 | snp | A/G | 1.67652e-05 | 0.00289522 | synonymous-codon, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20975286 | CTGCGGAGCAGCACA[A/G]CTTGGTGATGAGGTC | 26524 |
rs781538087 | in-del | -/TTTT | | | intron-variant | LATS2 | GRCh38.p7 | 13:20996378 | TAGAGTGGTAGAAGA[-/TTTT]TTTTTTTTTTTTTTT | 26524 |
rs781567974 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21041032 | GGCTGGAGTACAGTG[A/G]CACGATCTGGGCTCA | 26524 |
rs781574049 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20985422 | CTCAACAGCAAAAAA[A/T]ATATCAAATAATCCC | 26524 |
rs781598182 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21054478 | GGACCTAGGGACTGG[A/G]TAGGATATAGCAGGG | 26524 |
rs781647384 | snp | C/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20997798 | GCTTGCAATGTCTAA[C/G]CAGCAGAAGTATTTC | 26524 |
rs781716101 | snp | A/C | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973567 | CTATACTTCTAAGAA[A/C]ATACGTATGGCTTAC | 26524 |
rs781721101 | snp | C/T | 1.65883e-05 | 0.00287991 | missense, utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974908 | CTTCAGTCTGATCCA[C/T]CAGATCAGAGCTTTC | 26524 |
rs781735616 | snp | A/G | 1.6768e-05 | 0.00289546 | missense | LATS2 | GRCh38.p7 | 13:20981619 | CCCAGAGGTCGCTGG[A/G]CTCCATGCTGTCCTG | 26524 |
rs781737819 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20979900 | CTGTTAAGTGGGAAA[A/G]CGCGTTGAAGCATCG | 26524 |
rs781742179 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21034260 | GGTTGACACAGCCAA[A/G]GTGACACATGGCTAC | 26524 |
rs781746591 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021337 | AATTAGACGGGTGTG[A/G]TGGTGCGTGCCTGTA | 26524 |
rs796067008 | in-del | A/CC | | | intron-variant | LATS2 | GRCh38.p7 | 13:21012787 | TGGGTGAATCACACC[A/CC]CCCCCCACCTCCTAG | 26524 |
rs796131175 | snp | A/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974145 | TAAAGACACTCAGTA[A/G]AAACGTATTCACAGG | 26524 |
rs796146007 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20980881 | ACCATGCAGGATCAC[C/T]GAAGGATTCCTCCTA | 26524 |
rs796158489 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21007573 | TATATATATATATAT[A/T]TATATATATATATAG | 26524 |
rs796182911 | in-del | -/AAAG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030613 | AAAAAAAAAAAAAGA[-/AAAG]AAAAAAAAAAGAAAA | 26524 |
rs796204259 | multinucleotide-polymorphism | AA/TT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21005807 | GACCCCTACTCTATA[AA/TT]AAAAAAAAAAAAAAA | 26524 |
rs796250615 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20999119 | CGTGTGCGAGCCAAT[A/T]ATGACTGGAAAACAG | 26524 |
rs796256509 | snp | A/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024133 | AAAAGAAAAAACAGC[A/T]TGAAAAATAACAGGA | 26524 |
rs796334372 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21009155 | CAGTCACGTGTGGTG[A/G]GTGATGAATGAACAA | 26524 |
rs796342242 | multinucleotide-polymorphism | CA/TG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030038 | TGACTCAGGAGAATT[CA/TG]TTGAACCTGGGAGGG | 26524 |
rs796392534 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21030482 | TAGTCCCAGCTACTC[A/G]GCAGGCTGAGGCAGG | 26524 |
rs796437651 | in-del | -/AAAAAAAAAAAA | | | intron-variant | LATS2 | GRCh38.p7 | 13:21021493 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]GCTTTGTAAAAGGCA | 26524 |
rs796453925 | in-del | -/AAAT | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040413 | AAAAGAAAAAGAAAG[-/AAAT]GTCTTTGCTGTGGAA | 26524 |
rs796481651 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982372 | GCTGGGGCGCAATGG[C/T]GCGATCTCAGCTCAC | 26524 |
rs796513091 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21003214 | TGGTGTGATCAGTGA[-/A]TTTTGAGAACCTAAA | 26524 |
rs796517941 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21022818 | CTGCGAGAGAATAAA[-/A]GATCCTCATTATGTT | 26524 |
rs796525819 | in-del | -/TA | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973535 | GTGTGTGTGTGTGTG[-/TA]TACACGCACATACAT | 26524 |
rs796599917 | snp | C/T | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024129 | AAGAAAAAGAAAAAA[C/T]AGCTTGAAAAATAAC | 26524 |
rs796658767 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20982961 | CACGCCATTGCACTC[C/T]AGCCTGGGCAACAAG | 26524 |
rs796683745 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21028826 | ACCCGCCTTGGCCTC[C/T]CAGAGTACTGAGATT | 26524 |
rs796722822 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20993106 | GACAGTGGGGGAGGC[C/T]GTGCAGGGCTGCTCT | 26524 |
rs796735802 | in-del | CTCCGGGC/T | | | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023150 | CGCTGCATCGAGGGC[CTCCGGGC/T]CCGAGGGCTCCGAAG | 26524 |
rs796772427 | in-del | -/A | | | intron-variant | LATS2 | GRCh38.p7 | 13:21057815 | AAAAATAAAAAAAAA[-/A]TGAAAAATAAAAATC | 26524 |
rs796789358 | in-del | -/ATAGACAGATAGATAG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21050120 | GGGAGACTCTGTCTC[-/ATAGACAGATAGATAG]ATAGATAGATAGATA | 26524 |
rs796789550 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21008696 | CTGACAACAGCAAGT[A/G]TTGGCAAAGTTAGAG | 26524 |
rs796798848 | in-del | -/GAAAG | | | intron-variant | LATS2 | GRCh38.p7 | 13:21040392 | AAAAAAAAAAAAAAA[-/GAAAG]AAAAAGAAAAAGAAA | 26524 |
rs796823106 | in-del | -/C | | | intron-variant | LATS2 | GRCh38.p7 | 13:21042995 | TCTCAAAAAAAAAAC[-/C]AAAAAACAAAAAACA | 26524 |
rs796844529 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21048151 | ACTCATTTCAGTGAC[C/T]TTGTGCTCTAAGCAT | 26524 |
rs796959487 | in-del | -/C | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973971 | ACAAATGTTTCAGTT[-/C]CCCCCCCCCCAAAGA | 26524 |
rs797001899 | in-del | -/G | | | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20974587 | TTAGTAAGAAAAAAT[-/G]GATATAAACAAAATA | 26524 |
rs797005222 | snp | A/G | | | intron-variant, upstream-variant-2KB | LATS2 | GRCh38.p7 | 13:21024122 | AAAAAAAAAGAAAAA[A/G]AAAAAACAGCTTGAA | 26524 |