SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs478243 | snp | C/T | 0.499776 | 0.0105807 | intron-variant | LATS2 | GRCh38.p7 | 13:21004478 | CAAGGGAGAATCAAA[C/T]TTTAACAGTATACAT | 26524 |
rs481485 | snp | A/G | 0.361263 | 0.223876 | intron-variant | LATS2 | GRCh38.p7 | 13:21025763 | TTCACTTCCTCCTCC[A/G]TGCAGAGGACAGGAG | 26524 |
rs492809 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | LATS2 | GRCh38.p7 | 13:20986257 | catacaatctaccaa[A/T]cccattattgggtat | 26524 |
rs498032 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | LATS2 | GRCh38.p7 | 13:20997234 | GGTGTGTGAATTACA[C/T]ATGAATAAAGCAGTT | 26524 |
rs501811 | snp | A/G | 0.254944 | 0.249951 | intron-variant | LATS2 | GRCh38.p7 | 13:20984125 | CCAACATGATGAAAC[A/G]CTGTTTCTACTAAAA | 26524 |
rs503606 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | LATS2 | GRCh38.p7 | 13:20990121 | TGCCTGTGACCTTTG[C/T]TCAGTGCCAGGCTGT | 26524 |
rs503777 | snp | C/T | 0.307423 | 0.243316 | intron-variant | LATS2 | GRCh38.p7 | 13:21006823 | GTGCATGTTTGGGGG[C/T]TCTGGGGCTCTCCGT | 26524 |
rs504308 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | LATS2 | GRCh38.p7 | 13:20990152 | TTCTGGGCCCAGGGA[A/G]AACAAAGCCTTGGTG | 26524 |
rs507186 | snp | C/T | 0.109108 | 0.206518 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973887 | TTAATCACGGACACA[C/T]GTCCGTTTCTGTAGT | 26524 |
rs507272 | snp | A/G | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:20990507 | agcctgggcaacaga[A/G]ggagacctcgtctgt | 26524 |
rs512199 | snp | A/G | 0.35894 | 0.225016 | intron-variant | LATS2 | GRCh38.p7 | 13:21000253 | gctggggctacaggc[A/G]catgctaccactccc | 26524 |
rs519593 | snp | G/T | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21010201 | TTTGTTTGTTTGTTT[G/T]TTTGACAGAGTCTAG | 26524 |
rs531985 | snp | C/T | 0.359364 | 0.22481 | intron-variant | LATS2 | GRCh38.p7 | 13:21006069 | gcccaccgcaacctc[C/T]gccttccgggttcca | 26524 |
rs533896 | snp | C/G | 0.0941369 | 0.195465 | intron-variant | LATS2 | GRCh38.p7 | 13:21005853 | gtactgggattaata[C/G]gcgtaagccaccgcg | 26524 |
rs535233 | snp | A/G | 0.338069 | 0.233974 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973178 | TTTTATAGTCGTGCC[A/G]TGTTGTTACTCACAG | 26524 |
rs539841 | snp | C/G | 0.0644693 | 0.167566 | intron-variant | LATS2 | GRCh38.p7 | 13:21000993 | TACATGTGTAAGCAT[C/G]TTATTGTCATGCTCT | 26524 |
rs553089 | snp | C/T | 0.499846 | 0.00878459 | intron-variant | LATS2 | GRCh38.p7 | 13:21022381 | TCAAGGCCATGCATG[C/T]ACCTAGATGGCCTCA | 26524 |
rs555919 | snp | A/G | 0.109108 | 0.206518 | intron-variant | LATS2 | GRCh38.p7 | 13:20975999 | GGCCGTTTTTTGACC[A/G]CAATAAGTATTTGAA | 26524 |
rs558614 | snp | C/T | 0.390056 | 0.207085 | missense | LATS2 | GRCh38.p7 | 13:20988809 | AGCAGGCCGGTCCCG[C/T]GGCCCACCAGCTGCA | 26524 |
rs563001 | snp | A/C | 0.465263 | 0.127129 | intron-variant | LATS2 | GRCh38.p7 | 13:20991992 | CCCATGGAGCCACAC[A/C]GGTCCAGGACAGGTA | 26524 |
rs567322 | snp | A/C | 0.485731 | 0.0832509 | intron-variant | LATS2 | GRCh38.p7 | 13:21025413 | AAAAAAAAAAAAAAA[A/C]ATTATGGTCATGAGT | 26524 |
rs570061 | snp | C/T | 0.351635 | 0.228408 | intron-variant | LATS2 | GRCh38.p7 | 13:21025685 | AAATAATGTTGTGAG[C/T]AGTGTCAGGCAAGAT | 26524 |
rs571032 | snp | C/T | 0.337158 | 0.234315 | intron-variant | LATS2 | GRCh38.p7 | 13:20978129 | actacgttggccagg[C/T]tagtctcgatctcct | 26524 |
rs572224 | snp | A/C | 0.36021 | 0.224397 | intron-variant | LATS2 | GRCh38.p7 | 13:21011905 | tgatgatgttaagtg[A/C]ggactgtactggttt | 26524 |
rs573049 | snp | G/T | 0.0829062 | 0.185956 | intron-variant | LATS2 | GRCh38.p7 | 13:21011845 | agcctaggtgtgtag[G/T]gggctgtagcatcta | 26524 |
rs579097 | snp | G/T | 0.361053 | 0.22398 | intron-variant | LATS2 | GRCh38.p7 | 13:21017652 | GTGACAGAGTGAGAC[G/T]CCATCTCAAAAACAA | 26524 |
rs580636 | snp | C/T | 0.271194 | 0.2491 | intron-variant, utr-variant-5-prime | LATS2 | GRCh38.p7 | 13:21023150 | GCGCTGCATCGAGGG[C/T]TCCGGGCTCCGAGGG | 26524 |
rs584299 | snp | A/G | 0.338069 | 0.233974 | downstream-variant-500B | LATS2 | GRCh38.p7 | 13:20972988 | TACAACATGCTGAGA[A/G]AGGCAAGGACTTACA | 26524 |
rs585980 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | LATS2 | GRCh38.p7 | 13:21009202 | TGTACCTTTGCACAT[C/T]TGCTTCTTTATTCAT | 26524 |
rs586567 | snp | A/G | 0.315273 | 0.241329 | intron-variant | LATS2 | GRCh38.p7 | 13:21027649 | tacccacaatagtct[A/G]gtccaaagtcaggtc | 26524 |
rs587289 | snp | C/T | 0.481627 | 0.0940692 | intron-variant | LATS2 | GRCh38.p7 | 13:21022044 | TCTTTTCTCCTATTT[C/T]ATCTTTCTATTTCAC | 26524 |
rs593390 | snp | A/G | 0.349452 | 0.229367 | intron-variant | LATS2 | GRCh38.p7 | 13:20980645 | TGCACGTGGTAGAGG[A/G]AAGTAGACCTTCACT | 26524 |
rs594273 | snp | A/G | 0.464203 | 0.128908 | intron-variant | LATS2 | GRCh38.p7 | 13:20994632 | GTTGGGATTATAGGC[A/G]TGAGCCACCACATCC | 26524 |
rs594669 | snp | C/T | 0.439502 | 0.163061 | intron-variant | LATS2 | GRCh38.p7 | 13:20980921 | AGATGTTGCATTTGA[C/T]AGAATGAAGCATCCA | 26524 |
rs600422 | snp | C/T | 0.359152 | 0.224913 | intron-variant | LATS2 | GRCh38.p7 | 13:21001380 | ctgggggctgcaGCC[C/T]GTACATACAGGGATG | 26524 |
rs600426 | snp | A/G | 0.499683 | 0.0125759 | intron-variant | LATS2 | GRCh38.p7 | 13:21008305 | TAGTCTGGAGCAGCA[A/G]GAGCCAAAGAGGTCC | 26524 |
rs609980 | snp | A/G | 0.464947 | 0.127663 | intron-variant | LATS2 | GRCh38.p7 | 13:20993432 | CAGCACAAAAAACAC[A/G]GGCTGTAAACTGTGT | 26524 |
rs610312 | snp | C/T | 0.479502 | 0.0991411 | intron-variant | LATS2 | GRCh38.p7 | 13:20993400 | CATTCTGCTGGCATA[C/T]GGCCAGGACTGGAAA | 26524 |
rs613375 | snp | C/T | 0.31503 | 0.241394 | intron-variant | LATS2 | GRCh38.p7 | 13:21000770 | CTGTTCTAGATGGTA[C/T]GTAGCAAAAATAAGC | 26524 |
rs614674 | snp | C/T | 0.364401 | 0.222289 | intron-variant | LATS2 | GRCh38.p7 | 13:21000489 | TCGGGataaaaaaaa[C/T]ttaataacttttgat | 26524 |
rs615142 | snp | G/T | 0.346368 | 0.23068 | intron-variant | LATS2 | GRCh38.p7 | 13:21000381 | tattattattattat[G/T]atgacagagtcttgc | 26524 |
rs616495 | snp | C/G | 0.358515 | 0.225221 | intron-variant | LATS2 | GRCh38.p7 | 13:21006984 | CCTTCTTGGGTGAAC[C/G]TATAATTTGCCAGAT | 26524 |
rs628621 | snp | A/C | 0.469049 | 0.120489 | intron-variant | LATS2 | GRCh38.p7 | 13:20975926 | TGACCTCAGGTGATC[A/C]GCTAAAGTTATTTCT | 26524 |
rs632050 | snp | C/T | 0.358303 | 0.225323 | intron-variant | LATS2 | GRCh38.p7 | 13:21005841 | ATAGGCGTAAGCCAC[C/T]GCGCCTGGCCTCCGT | 26524 |
rs632084 | snp | C/G | 0.499879 | 0.0077866 | intron-variant | LATS2 | GRCh38.p7 | 13:21018980 | AGTGGCTGCAGAAAA[C/G]TAGAAAGGAAAATTA | 26524 |
rs642826 | snp | C/T | 0.109108 | 0.206518 | intron-variant | LATS2 | GRCh38.p7 | 13:20976830 | aaactgaacactcag[C/T]cactgttggtgggaa | 26524 |
rs643284 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | LATS2 | GRCh38.p7 | 13:20998648 | GGGCGGTTAGAGGAG[C/G]CCTGGGCCCGGAGGG | 26524 |
rs644431 | snp | A/C | 0.0652144 | 0.168387 | intron-variant | LATS2 | GRCh38.p7 | 13:21018555 | CCACAGTCTTCCTGG[A/C]CCTGCTGCGCAAGCA | 26524 |
rs649363 | snp | C/T | 0.464735 | 0.128019 | intron-variant | LATS2 | GRCh38.p7 | 13:20985148 | ttatttctaggtctt[C/T]aatctgttttaagtt | 26524 |
rs651670 | snp | C/T | 0.436976 | 0.165952 | intron-variant | LATS2 | GRCh38.p7 | 13:20984671 | tgtttgtgtcctctt[C/T]agtttctttcttcag | 26524 |
rs660787 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | LATS2 | GRCh38.p7 | 13:21003968 | ACAAAAGCATTTAAA[C/T]ATTAATAAAAGTAAT | 26524 |
rs663599 | snp | G/T | 0.253544 | 0.249975 | intron-variant | LATS2 | GRCh38.p7 | 13:20984315 | GTTCTTTCTCTAGGA[G/T]ACTTTTGGCTCTAAA | 26524 |
rs670631 | snp | C/T | 0.464523 | 0.128375 | intron-variant | LATS2 | GRCh38.p7 | 13:20997118 | ATCTCTTAGTTTTAG[C/T]CATGAGGCAGAAAAC | 26524 |
rs673314 | snp | A/G | 0.464416 | 0.128553 | intron-variant | LATS2 | GRCh38.p7 | 13:20996529 | GCCAGGTATGGTGGT[A/G]GTTCATGCATGTAAT | 26524 |
rs673716 | snp | C/T | 0.337841 | 0.23406 | intron-variant | LATS2 | GRCh38.p7 | 13:20979095 | gtgggattacaggca[C/T]gagccactgcgcctg | 26524 |
rs674533 | snp | A/C | 0.312348 | 0.242101 | intron-variant | LATS2 | GRCh38.p7 | 13:21003240 | ataataaatttaaaa[A/C]tacatatttatttaG | 26524 |
rs685167 | snp | A/G | 0.254664 | 0.249956 | intron-variant | LATS2 | GRCh38.p7 | 13:20989576 | GCAGGGACGCACCTC[A/G]GGATGTGGACGCAGT | 26524 |
rs688663 | snp | A/T | 0.430434 | 0.173042 | intron-variant | LATS2 | GRCh38.p7 | 13:20980078 | TAGCAAATAGTTACT[A/T]GCCAGAATTTTATGT | 26524 |
rs693784 | snp | C/T | 0.316968 | 0.240864 | intron-variant | LATS2 | GRCh38.p7 | 13:21021319 | cacccgtctaatttt[C/T]ctatttttagtagag | 26524 |
rs870846 | snp | C/G | 0.487933 | 0.0767327 | intron-variant | LATS2 | GRCh38.p7 | 13:20981405 | CTAGAGCCAGCGAGA[C/G]TCAGCTCACGTCTGA | 26524 |
rs870847 | snp | A/T | 0.487933 | 0.0767327 | intron-variant | LATS2 | GRCh38.p7 | 13:20981406 | TAGAGCCAGCGAGAC[A/T]CAGCTCACGTCTGAA | 26524 |
rs870848 | snp | A/G | 0.492779 | 0.0596531 | intron-variant | LATS2 | GRCh38.p7 | 13:20981415 | CGAGACTCAGCTCAC[A/G]TCTGAAGGGAAGGAG | 26524 |
rs877923 | snp | A/G | 0.27278 | 0.24896 | intron-variant | LATS2 | GRCh38.p7 | 13:20991927 | TAGCAGCGGAGGACT[A/G]GCCCTTAGAGATCTG | 26524 |
rs935136 | snp | C/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:20992963 | ctgcagcctccacct[C/T]ccaggtttcaagcaa | 26524 |
rs958260 | snp | C/T | 0.093777 | 0.195178 | intron-variant | LATS2 | GRCh38.p7 | 13:21047928 | TTATTTAGTCTCTCT[C/T]TTATCTTCTAAATGG | 26524 |
rs999325 | snp | A/G | 0.47885 | 0.100637 | intron-variant | LATS2 | GRCh38.p7 | 13:21038113 | CCTGTCTCAAAAACC[A/G]AAACAAAACAAATCA | 26524 |
rs1003966 | snp | C/T | 0.171057 | 0.237209 | intron-variant | LATS2 | GRCh38.p7 | 13:21038020 | gctacctgggtggac[C/T]gcttgagcccaggag | 26524 |
rs1050345 | snp | A/C | 0 | 0 | utr-variant-3-prime | LATS2 | GRCh38.p7 | 13:20973065 | AAAGCTTCTACTGGC[A/C]CAATTTATTATTAAA | 26524 |
rs1199734 | snp | A/C | 0.464841 | 0.127841 | intron-variant | LATS2 | GRCh38.p7 | 13:20996107 | AACTCCAGCATTGAG[A/C]TCTGTCTAGAAGAGA | 26524 |
rs1199735 | snp | C/G | 0.254385 | 0.249962 | intron-variant | LATS2 | GRCh38.p7 | 13:20996063 | GGGCGTGGTAACCAA[C/G]TTCAATGGATTAGCA | 26524 |
rs1199736 | snp | C/T | 0.122411 | 0.214991 | intron-variant | LATS2 | GRCh38.p7 | 13:20996042 | TGGATTAGCATCCTT[C/T]TTCTATGAGACATTA | 26524 |
rs1209727 | snp | C/T | 0 | 0 | intron-variant | LATS2 | GRCh38.p7 | 13:21012676 | AAAAAATCTGCAAAG[C/T]GCTTATACCATACTT | 26524 |
rs1212480 | snp | A/T | 0.358728 | 0.225118 | intron-variant | LATS2 | GRCh38.p7 | 13:21001766 | TTAGCCTCTGGAGTA[A/T]CTGGGACTACAGGCA | 26524 |
rs1308408 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:21019435 | ggaggctgaggcagg[A/G]gaatcgcttgaaccc | 26524 |
rs1345067 | snp | A/G | 0.472335 | 0.114312 | intron-variant | LATS2 | GRCh38.p7 | 13:20996171 | GATGAAGGAAGTGTT[A/G]AACACTGCAGGTATC | 26524 |
rs1550633 | snp | A/C | 0.254105 | 0.249966 | intron-variant | LATS2 | GRCh38.p7 | 13:20995450 | GTTGGCTTGCAGCTG[A/C]ACTCTTGCTTTGGGG | 26524 |
rs1753891 | snp | C/T | 0.253824 | 0.249971 | intron-variant | LATS2 | GRCh38.p7 | 13:20985912 | agctgggcgtggtgg[C/T]gcatgcctgtaatcc | 26524 |
rs1764538 | snp | C/T | 0.358515 | 0.225221 | intron-variant | LATS2 | GRCh38.p7 | 13:21003400 | ctgggactacaggtg[C/T]gccaccacacacaac | 26524 |
rs1887894 | snp | A/G | 0.49263 | 0.0602539 | intron-variant | LATS2 | GRCh38.p7 | 13:21033461 | CACACCGAGTTCAAT[A/G]CAGAAATACCCAGTC | 26524 |
rs1887895 | snp | A/G | 0.499563 | 0.0147699 | intron-variant | LATS2 | GRCh38.p7 | 13:21033621 | AAGGCTCTTGTAAGC[A/G]TCTCCAAGGTTGACA | 26524 |
rs1928268 | snp | A/C | 0.344815 | 0.231323 | intron-variant | LATS2 | GRCh38.p7 | 13:21030869 | tttttccccccatac[A/C]cccacccctttaata | 26524 |
rs1928269 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | LATS2 | GRCh38.p7 | 13:21047895 | TATCCCCTTTCTCAA[C/T]GTAATTGTGAGAAGA | 26524 |
rs1928270 | snp | C/T | 0.266546 | 0.249452 | intron-variant | LATS2 | GRCh38.p7 | 13:21048082 | TGTACTGGCCACATA[C/T]CAGAAGCCTAGAGCT | 26524 |
rs1984160 | snp | C/T | 0.497558 | 0.0348586 | intron-variant | LATS2 | GRCh38.p7 | 13:21002205 | GGCTTTTTggccggg[C/T]gcagtggctcacacg | 26524 |
rs1984161 | snp | A/G | 0.067446 | 0.170804 | intron-variant | LATS2 | GRCh38.p7 | 13:21002074 | tacaaaaaattagcc[A/G]ggcatggtggtgggc | 26524 |
rs2003291 | snp | A/G | 0.162253 | 0.234095 | intron-variant | LATS2 | GRCh38.p7 | 13:20992784 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 26524 |
rs2018227 | snp | A/G | 0.498852 | 0.0239341 | intron-variant | LATS2 | GRCh38.p7 | 13:21038066 | AGCCATGATCATGCC[A/G]CCACACTCCAGTCTG | 26524 |
rs2050576 | snp | C/T | 0.282369 | 0.247896 | intron-variant | LATS2 | GRCh38.p7 | 13:21013328 | ATTATTATTAGGCAT[C/T]GAGCCAGGATAAGTA | 26524 |
rs2065889 | snp | C/T | 0.361053 | 0.22398 | intron-variant | LATS2 | GRCh38.p7 | 13:21019292 | taataataacaaATC[C/T]AAGTGAGAATACAAA | 26524 |
rs2253147 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | LATS2 | GRCh38.p7 | 13:21012508 | tggcccgtggttgcc[C/T]gaaacatcgttatgc | 26524 |
rs2275234 | snp | A/G | 0.216407 | 0.247733 | intron-variant | LATS2 | GRCh38.p7 | 13:20979832 | CGGAGGAGAATTCAT[A/G]CCTGTGTAGGGATTG | 26524 |
rs2480170 | snp | C/T | 0.437965 | 0.164831 | intron-variant | LATS2 | GRCh38.p7 | 13:20982948 | agtgagccgagatca[C/T]gccattgcactccag | 26524 |
rs2480171 | snp | C/T | 0.253824 | 0.249971 | intron-variant | LATS2 | GRCh38.p7 | 13:20985719 | ctccagcctgggcaa[C/T]agagcaagactccgt | 26524 |
rs2480172 | snp | A/T | 0.35809 | 0.225425 | intron-variant | LATS2 | GRCh38.p7 | 13:21012207 | atcatataaaagatt[A/T]aaaaaaatgcatatc | 26524 |
rs2585890 | snp | A/G | 0.499853 | 0.008585 | | | GRCh38.p7 | 13:21007300 | GCTGTTACCCTACCA[A/G]TTGGAATTTCTTCTT | 26524 |
rs2585893 | snp | A/G | 0.00496275 | 0.0495656 | | | GRCh38.p7 | 13:20975458 | TTTCAAATATGTTTA[A/G]TTTCACAATAGGAGA | 26524 |
rs2770924 | snp | A/T | | | intron-variant | LATS2 | GRCh38.p7 | 13:21006133 | tctttttttttgaga[A/T]gcagttttgctcttg | 26524 |
rs2770926 | snp | A/G | | | intron-variant | LATS2 | GRCh38.p7 | 13:20990548 | gggaggctgaggcca[A/G]aggatggaggcagga | 26524 |
rs2770927 | snp | A/T | 0.494057 | 0.0541878 | intron-variant | LATS2 | GRCh38.p7 | 13:20990488 | GACCTCGTCTGTATT[A/T]AAAAAAAAAAAAAAA | 26524 |
rs2770928 | snp | A/G | 0.221828 | 0.248408 | missense | LATS2 | GRCh38.p7 | 13:20988693 | GACCTGTATGAATTG[A/G]GCAGCACCTCCGTCC | 26524 |