SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs16542 | snp | A/G | 0.419616 | 0.183658 | downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39210176 | GGCACCTCTGGGTGG[A/G]CAAGATCGGCCTCGA | 342667 |
rs16543 | snp | C/T | 0.093417 | 0.194889 | downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39210230 | TCCGCCCCTGCGCGA[C/T]TCAGGTGCACATGGA | 342667 |
rs16544 | snp | C/T | 0 | 0 | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39210693 | CAGTGTGGCTTGAGA[C/T]CCCGCTTTGTGGGGG | 342667 |
rs16545 | snp | A/G | 0.0876345 | 0.190099 | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39212161 | AGGCTCCTAAGCCAC[A/G]GTAAGTGGCACCTAG | 342667 |
rs16546 | snp | C/T | 0.0123575 | 0.0776276 | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39212289 | GGGTTCCCTTGGCTC[C/T]TCTCAGATCTCAGTC | 342667 |
rs16547 | snp | C/T | 0.0220715 | 0.102706 | synonymous-codon | STAC2 | GRCh38.p7 | 17:39212322 | GGCGTCGACTGGCAC[C/T]AGGCCCCGCTTCTTG | 342667 |
rs16548 | snp | C/T | 0.00523353 | 0.0508859 | intron-variant | STAC2 | GRCh38.p7 | 17:39212425 | ACATGGAGCTGAGGC[C/T]TGGCATGGCCTGCAG | 342667 |
rs16549 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | STAC2 | GRCh38.p7 | 17:39213321 | GAGCAGAGGGACAAA[A/G]CTGAGGCAAGGAGAG | 342667 |
rs16550 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | STAC2 | GRCh38.p7 | 17:39213326 | GAGGGACAAAGCTGA[A/G]GCAAGGAGAGTCAAA | 342667 |
rs519512 | snp | C/T | 0.0955749 | 0.196603 | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39210735 | AGGGGCCTTTGGGTA[C/T]GAGGGTCTGTGTTTC | 342667 |
rs521397 | snp | G/T | 0.095934 | 0.196885 | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39210953 | CATTCCACCTTCCTT[G/T]TCTGTCTTCCACCCC | 342667 |
rs619741 | snp | C/G | 0.0916144 | 0.193427 | intron-variant, downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39212764 | GTGCTCCTGCGCTAA[C/G]CCAAGCTCCCTCTAA | 342667 |
rs1106769 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | STAC2 | GRCh38.p7 | 17:39224389 | TGGGGTTGGGATAGA[A/C]AGGGCTGTGCCAAGG | 342667 |
rs1457818 | snp | A/C | 0.167158 | 0.235875 | intron-variant | STAC2 | GRCh38.p7 | 17:39218393 | CAGGTGGTTGACCTC[A/C]ATGGAGAAAGGAGTT | 342667 |
rs1673849 | snp | A/G | 0.0858192 | 0.188533 | intron-variant, downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39213966 | CTCCCAGCGGGGCGC[A/G]GTGGCTCACCCTTGT | 342667 |
rs1859262 | snp | A/G | 0.478656 | 0.101077 | intron-variant | STAC2 | GRCh38.p7 | 17:39213163 | GCAATGAACACCCGC[A/G]CCACACCCCACCCCT | 342667 |
rs3025220 | snp | G/T | | | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39210708 | CCCCGCTTTGTGGGG[G/T]AGAAGTGGGGCAGGG | 342667 |
rs3025221 | snp | A/G | | | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39212184 | GCACCTAGGAGAGGG[A/G]CAGAGGGAGGAAGGG | 342667 |
rs3025222 | snp | C/T | | | intron-variant, downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39212584 | GCAGCAAGACCAGCA[C/T]GTCAGCAGACACCCA | 342667 |
rs3025223 | snp | C/T | 0.0248341 | 0.108629 | intron-variant, downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39212965 | TCCCTCCCTCCGCCA[C/T]AGGGCCTGGGCTGGG | 342667 |
rs3889904 | snp | C/T | 0.27893 | 0.24832 | intron-variant | STAC2 | GRCh38.p7 | 17:39216170 | CTCTTAATTTAGAGA[C/T]AGGGTCTCACCATGT | 342667 |
rs4794806 | snp | C/G | 0.490997 | 0.0664859 | intron-variant | STAC2 | GRCh38.p7 | 17:39221316 | GTATTGGCTAGGCTG[C/G]TCTCGAACTCCTGAC | 342667 |
rs4795354 | snp | C/G | 0.13446 | 0.221699 | intron-variant | STAC2 | GRCh38.p7 | 17:39219883 | AGAGGGACTTGGCCA[C/G]GGTTCCCAGCTGGCA | 342667 |
rs5820281 | in-del | -/T/TT | 0.277778 | 0.248452 | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39211290 | TCTTTTTTTTTTTTT[-/T/TT]GAGACGGAGTCTCGC | 342667 |
rs6503496 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | STAC2 | GRCh38.p7 | 17:39218553 | ACTTTTATGTGAAAT[C/T]GGATAGAAACAAGTT | 342667 |
rs7221848 | snp | C/T | 0.167158 | 0.235875 | intron-variant | STAC2 | GRCh38.p7 | 17:39218552 | gacttttatgtgaaa[C/T]cGGATAGAAACAAGT | 342667 |
rs7502074 | snp | C/T | | | intron-variant | STAC2 | GRCh38.p7 | 17:39221203 | caggttcaagcgatt[C/T]tcctgcctcagcctc | 342667 |
rs8070891 | snp | C/G | 0.483477 | 0.0893782 | intron-variant | STAC2 | GRCh38.p7 | 17:39214888 | AGAGGGAAAGGGTGA[C/G]AGGCAGCAGGGAGCA | 342667 |
rs8074753 | snp | A/G | 0.494896 | 0.0502606 | intron-variant | STAC2 | GRCh38.p7 | 17:39222285 | AGAGCCACCTCTGCT[A/G]GGTACCGGAGGCCTC | 342667 |
rs8077497 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | STAC2 | GRCh38.p7 | 17:39222801 | GACAGGGCCTGGCCT[A/G]CCTGTTTCCTCCCCA | 342667 |
rs8080963 | snp | C/G | 0.0528381 | 0.153711 | upstream-variant-2KB | STAC2 | GRCh38.p7 | 17:39226816 | tgctgggaccacagg[C/G]atacgccaccatgcc | 342667 |
rs8081631 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | STAC2 | GRCh38.p7 | 17:39219977 | GGCCCCACCAGCCTC[C/T]GGGAGGCCAGCAGGC | 342667 |
rs8082152 | snp | C/T | 0.0570152 | 0.158924 | intron-variant | STAC2 | GRCh38.p7 | 17:39216790 | TGGGAGCAGGGACTG[C/T]GGCCAGGGGGGGCAC | 342667 |
rs9893784 | snp | A/C | 0.0310518 | 0.120672 | downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39210108 | GCGGGGACGAGGCTG[A/C]CCTCGGATGGGTACT | 342667 |
rs9911410 | snp | C/T | 0.278133 | 0.248412 | intron-variant | STAC2 | GRCh38.p7 | 17:39215771 | tacaatggcacgatc[C/T]tggcttactgcaacc | 342667 |
rs11078892 | snp | C/T | 0.491064 | 0.066244 | intron-variant | STAC2 | GRCh38.p7 | 17:39215266 | AGGCCTGGCTCTGCC[C/T]CAAAGCCCTGCATCT | 342667 |
rs11390252 | in-del | -/A | 0 | 0 | intron-variant | STAC2 | GRCh38.p7 | 17:39218759 | TTAGAAAAAAAAAAA[-/A]TAGGCACGGTATGGT | 342667 |
rs11407976 | in-del | -/T | 0.5 | 0 | intron-variant | STAC2 | GRCh38.p7 | 17:39220483 | CTCTTTTTTTTTTTT[-/T]GATGGAGTCTCACTC | 342667 |
rs11650495 | snp | G/T | | | intron-variant | STAC2 | GRCh38.p7 | 17:39213656 | ACACTGCAGTCCTCA[G/T]CTGGGAGAGACGAtt | 342667 |
rs11650898 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39213910 | tcgaactcctgacct[C/T]aagtgatctgccagc | 342667 |
rs11653147 | snp | G/T | 0.0119091 | 0.0762411 | upstream-variant-2KB | STAC2 | GRCh38.p7 | 17:39226299 | TGATAGATGCCAGAG[G/T]TTGGTGAAGGAAGAA | 342667 |
rs11656897 | snp | C/T | 0.266546 | 0.249452 | intron-variant, downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39214175 | CCCCCTCACACTGTG[C/T]TTCAAGGTCTGGGAG | 342667 |
rs11657409 | snp | G/T | 0.411074 | 0.191194 | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39211903 | TCTGTGGGGAGAGGG[G/T]TGTGCCAGGCATGCG | 342667 |
rs11657506 | snp | C/G | 0.493386 | 0.0571263 | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39211474 | TACTTTTAGTAGAGA[C/G]GGGGTTTCACCATGT | 342667 |
rs11658275 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | STAC2 | GRCh38.p7 | 17:39226421 | CAAAGGCCAGGCCGG[A/G]CAATTCCTCCTTGTG | 342667 |
rs12603328 | snp | C/T | | | intron-variant | STAC2 | GRCh38.p7 | 17:39221882 | tggaagactggccac[C/T]tagagcagtccccaa | 342667 |
rs12950162 | snp | C/T | 0.17332 | 0.23795 | intron-variant | STAC2 | GRCh38.p7 | 17:39223031 | GAGAGGAGGAGGACT[C/T]GCTAGGAAGGTTGCT | 342667 |
rs13342078 | snp | A/G | 0.104504 | 0.2033 | intron-variant | STAC2 | GRCh38.p7 | 17:39220954 | ggcgcccgccaccac[A/G]cctggctaatttttt | 342667 |
rs13342155 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | STAC2 | GRCh38.p7 | 17:39221038 | cctgacctcgtgatc[C/T]gcctgtttcggcctc | 342667 |
rs33910935 | in-del | -/A/AAA | 0.289617 | 0.249907 | intron-variant | STAC2 | GRCh38.p7 | 17:39218752 | TTTACTCAAGTTTAG[-/A/AAA]AAAAAAAAAAATAGG | 342667 |
rs34140015 | in-del | -/G | | | intron-variant | STAC2 | GRCh38.p7 | 17:39220092 | GTCTGGCACACTGAA[-/G]GGCTCAGTGCCTTCC | 342667 |
rs34194643 | in-del | -/C | | | intron-variant, downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39212981 | AGGGCCTGGGCTGGG[-/C]CTCAGGCACTCACCT | 342667 |
rs34227667 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | STAC2 | GRCh38.p7 | 17:39214696 | GCAGTGAATCCCCAC[A/G]CACCATGCTCTTGCC | 342667 |
rs34325637 | snp | C/G | 0.0980852 | 0.198549 | intron-variant | STAC2 | GRCh38.p7 | 17:39221005 | GTTTCACCGTGTTAG[C/G]CAGGATGGTCTCGAT | 342667 |
rs34344310 | snp | C/T | 3.30737e-05 | 0.00406642 | missense | STAC2 | GRCh38.p7 | 17:39214804 | ACCTGCTGTCCAGGA[C/T]TCTTCTCCTCTGGTC | 342667 |
rs34486887 | in-del | -/C | | | intron-variant | STAC2 | GRCh38.p7 | 17:39212481 | CCCCCAGGGGACCCA[-/C]CCTGGGGGATGATGG | 342667 |
rs34533249 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | STAC2 | GRCh38.p7 | 17:39225271 | GCCAACCCACTCCTA[C/G]CCCCGGGAGCGGCGC | 342667 |
rs34545453 | in-del | -/C | | | intron-variant | STAC2 | GRCh38.p7 | 17:39216010 | GCCCTTTCTTTAACT[-/C]CCCTGTCCTTCCTTT | 342667 |
rs34639010 | in-del | -/C | | | intron-variant | STAC2 | GRCh38.p7 | 17:39216118 | CTGGGAAGTCTTCCC[-/C]TGATTTTGCAGATGA | 342667 |
rs34739816 | snp | G/T | 0.128288 | 0.218372 | intron-variant | STAC2 | GRCh38.p7 | 17:39220432 | AAATCACCCCACTTC[G/T]TCTCTCTGAGCCTCA | 342667 |
rs34779735 | in-del | -/A | | | intron-variant | STAC2 | GRCh38.p7 | 17:39214764 | TCCCACCCTGACCTT[-/A]CCGGGCCAATGCCAG | 342667 |
rs34919491 | in-del | -/G | | | intron-variant | STAC2 | GRCh38.p7 | 17:39216188 | GTCTCACCATGTTGC[-/G]CCAGGCTGGACTCCA | 342667 |
rs35137197 | snp | C/G | 0.34437 | 0.231505 | utr-variant-5-prime | STAC2 | GRCh38.p7 | 17:39225598 | CGGGACTCTGAAGCC[C/G]TTCTCCAGAGGCTGC | 342667 |
rs35196013 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | STAC2 | GRCh38.p7 | 17:39225187 | AGTGGCCGCCTCCCC[A/G]GAAGGTCGCGATGGC | 342667 |
rs35272507 | snp | C/G | 0.0001977 | 0.00994037 | synonymous-codon | STAC2 | GRCh38.p7 | 17:39215003 | GCCTTCCCCATCCTC[C/G]GTCAGCTCATCCCGC | 342667 |
rs35290672 | snp | C/G | 0.118235 | 0.212457 | intron-variant | STAC2 | GRCh38.p7 | 17:39219109 | GTTGCGGGGGTGATG[C/G]CTGATCCTGCTAAAA | 342667 |
rs35395054 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | STAC2 | GRCh38.p7 | 17:39224007 | CAAGAGAGAGTCAGG[C/T]GTGCATGTGAAGACT | 342667 |
rs35421081 | snp | G/T | 0.28578 | 0.247426 | intron-variant | STAC2 | GRCh38.p7 | 17:39222106 | TCCAGAAAGGGCTAC[G/T]CCCTCTCATACACTT | 342667 |
rs35712937 | snp | C/G | | | intron-variant | STAC2 | GRCh38.p7 | 17:39216118 | TCTGGGAAGTCTTCC[C/G]TGATTTTGCAGATGA | 342667 |
rs35718597 | snp | A/G | 0.00224004 | 0.0333917 | synonymous-codon | STAC2 | GRCh38.p7 | 17:39214842 | TTCACTCTCTGCTGG[A/G]GCTGTGAATACTGGA | 342667 |
rs35934030 | in-del | -/C | | | intron-variant | STAC2 | GRCh38.p7 | 17:39216642 | AGTCTCACTCTGTAG[-/C]CCCAGGCTGGAGTGC | 342667 |
rs35966204 | in-del | -/G | 0 | 0 | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39210647 | CCCTGGGATATTGCT[-/G]GGGGGGGGGGGCCTC | 342667 |
rs35996049 | snp | A/G | 0.308908 | 0.242961 | intron-variant | STAC2 | GRCh38.p7 | 17:39219101 | ATACAGCTGTTGCGG[A/G]GGTGATGCCTGATCC | 342667 |
rs36063671 | in-del | -/G | | | intron-variant | STAC2 | GRCh38.p7 | 17:39221936 | CACATCCCGTCTCAA[-/G]GAGTTGGTCACCTCT | 342667 |
rs36092397 | snp | C/G | 0.0973687 | 0.197999 | intron-variant | STAC2 | GRCh38.p7 | 17:39220998 | AGACGGGGTTTCACC[C/G]TGTTAGGCAGGATGG | 342667 |
rs36094445 | in-del | -/C | | | intron-variant | STAC2 | GRCh38.p7 | 17:39223741 | TGGGAGGCCCCCAAG[-/C]CCCTGGAGGCAAGCA | 342667 |
rs36106822 | snp | C/T | 0.164873 | 0.23506 | intron-variant | STAC2 | GRCh38.p7 | 17:39222146 | AAATATTTGAAGACA[C/T]CATCAGTCATGTTCC | 342667 |
rs55771778 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | STAC2 | GRCh38.p7 | 17:39218346 | CTCCCCAGGTCCCGA[A/C]GACACTTCGCAATCT | 342667 |
rs56078862 | snp | A/G | 0.130351 | 0.219509 | intron-variant | STAC2 | GRCh38.p7 | 17:39215396 | CATGGTGCCCATGCA[A/G]AAACTTGGAGCATCC | 342667 |
rs56140806 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | STAC2 | GRCh38.p7 | 17:39216061 | ACACCAGTCTTTCCA[C/G]ATCCTAAATGGATGA | 342667 |
rs56213453 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | STAC2 | GRCh38.p7 | 17:39221320 | TGGCTAGGCTGCTCT[C/T]GAACTCCTGACCTCA | 342667 |
rs56282124 | snp | C/T | | | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39211274 | GGCAGCTCTTGGGTT[C/T]CCTTTTCTTTCTTTC | 342667 |
rs57234601 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | STAC2 | GRCh38.p7 | 17:39222910 | TGGGTGGTGGCAGAC[A/G]TGGCACAAGCTGACT | 342667 |
rs57363360 | snp | C/T | 0.101814 | 0.201376 | intron-variant | STAC2 | GRCh38.p7 | 17:39214908 | AGCAGGGAGCACCCT[C/T]CATTGTACCCCATTC | 342667 |
rs57621765 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | STAC2 | GRCh38.p7 | 17:39219089 | CACCTGTCCTCCATA[C/T]AGCTGTTGCGGGGGT | 342667 |
rs57691036 | snp | A/G | 0.206029 | 0.246103 | intron-variant | STAC2 | GRCh38.p7 | 17:39215596 | ACTCTAGCCCTGCCA[A/G]TCCACACAGCAGCCA | 342667 |
rs58343303 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | STAC2 | GRCh38.p7 | 17:39215378 | GATGGCTCTGGGTCC[C/T]CCCATGGTGCCCATG | 342667 |
rs58545654 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | STAC2 | GRCh38.p7 | 17:39213451 | AGTGCCCATTGGGGG[G/T]GGGGGCTGCTGGGGT | 342667 |
rs58969389 | snp | C/T | 0.116838 | 0.211584 | intron-variant | STAC2 | GRCh38.p7 | 17:39221283 | TGTATTTTTTTTTAG[C/T]AGAGATGGGGTTTCA | 342667 |
rs59899545 | snp | A/C | | | intron-variant | STAC2 | GRCh38.p7 | 17:39220566 | TGCAACCTCCACCTC[A/C]TGGGTTCAAGTGATT | 342667 |
rs62074973 | snp | C/T | 0.5 | 0 | intron-variant, synonymous-codon | STAC2 | GRCh38.p7 | 17:39214407 | CTCGCTCTGAGTGTG[C/T]TACCCTGGGGGCTGT | 342667 |
rs62074974 | snp | C/G | 0.5 | 0 | intron-variant | STAC2 | GRCh38.p7 | 17:39216273 | AGGTATGAGCCACCA[C/G]ACCCAGCTTTCAGCA | 342667 |
rs71141788 | in-del | -/G | 0 | 0 | upstream-variant-2KB | STAC2 | GRCh38.p7 | 17:39227016 | AAAAAAAAAAAAAAA[-/G]AAGAAGAAGAAGAGA | 342667 |
rs71369730 | snp | C/T | 0.126909 | 0.217598 | intron-variant | STAC2 | GRCh38.p7 | 17:39215882 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 342667 |
rs71369731 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | STAC2 | GRCh38.p7 | 17:39219733 | AACACACCCTACTGA[A/G]TCTTCCCAGAGAGAG | 342667 |
rs72823355 | snp | C/T | 0.0425829 | 0.139564 | utr-variant-3-prime | STAC2 | GRCh38.p7 | 17:39212065 | TCATTCCCTCCCACC[C/T]CACCCCATCCCCGCC | 342667 |
rs72823358 | snp | C/T | 0.0100487 | 0.0701667 | intron-variant, downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39214191 | TTCAAGGTCTGGGAG[C/T]GCAGAGCTGCCCAGC | 342667 |
rs73306903 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | STAC2 | GRCh38.p7 | 17:39216583 | CCAGTGTGACTCAGG[C/T]ACCCATCTCAGAAAT | 342667 |
rs73983266 | snp | A/G | 0.180064 | 0.240019 | intron-variant, downstream-variant-500B | STAC2 | GRCh38.p7 | 17:39212585 | CAGCAAGACCAGCAC[A/G]TCAGCAGACACCCAG | 342667 |
rs73983270 | snp | A/G | 0.5 | 0 | intron-variant | STAC2 | GRCh38.p7 | 17:39220008 | AGCAAGACAGAGGGG[A/G]AAGCAGAGGGGATGT | 342667 |