SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs10782 | snp | A/G | 0.0134861 | 0.0810011 | utr-variant-3-prime | HECW2 | GRCh38.p7 | 2:196199420 | CTGCACTAAAGGCAC[A/G]TACTGCAGTGTGAAG | 57520 |
rs724276 | snp | A/G | 0 | 0 | intron-variant | HECW2 | GRCh38.p7 | 2:196318294 | TAGCTATGTGATTAA[A/G]TCCCAAGGTCTCCCC | 57520 |
rs724277 | snp | A/G | 0 | 0 | intron-variant | HECW2 | GRCh38.p7 | 2:196317964 | ACATCACCTAACTTA[A/G]TTGACATTCCTAAAT | 57520 |
rs729145 | snp | G/T | 0 | 0 | intron-variant | HECW2 | GRCh38.p7 | 2:196232928 | TTTTGGCTTTAGAGG[G/T]GACTCCATCAGTGCT | 57520 |
rs745031 | snp | C/T | 0.369346 | 0.219673 | intron-variant | HECW2 | GRCh38.p7 | 2:196233059 | AGGCATGATGTACCC[C/T]GCTGTGACATGTTTT | 57520 |
rs767620 | snp | A/G | 0.486266 | 0.0817214 | intron-variant | HECW2 | GRCh38.p7 | 2:196214896 | ATGTCACCTTATATA[A/G]TAACAATAATATCAC | 57520 |
rs767621 | snp | G/T | 0.385741 | 0.209939 | intron-variant | HECW2 | GRCh38.p7 | 2:196214922 | ATCACCTAATATCAC[G/T]AATAAAATAGGTTTC | 57520 |
rs767622 | snp | A/C | 0.388021 | 0.208447 | intron-variant | HECW2 | GRCh38.p7 | 2:196215036 | TAGTAAAGTTAGAGG[A/C]AATTTCAGCTCCTTT | 57520 |
rs883289 | snp | C/T | 0.184838 | 0.241358 | intron-variant | HECW2 | GRCh38.p7 | 2:196274333 | GAGTTGAGGCATCCA[C/T]ATTCTTGAGAGGGGC | 57520 |
rs884175 | snp | G/T | 0 | 0 | intron-variant | HECW2 | GRCh38.p7 | 2:196274913 | GCTGTTCTGCTATTG[G/T]CTCAAAAGATTTCTG | 57520 |
rs941373 | snp | C/T | 0.232359 | 0.249377 | intron-variant | HECW2 | GRCh38.p7 | 2:196446805 | TGACTTACATGTGCC[C/T]TTTCTTCCTAATGTG | 57520 |
rs941374 | snp | A/C | 0.388398 | 0.208197 | intron-variant | HECW2 | GRCh38.p7 | 2:196446616 | CCCATGAAATCACTT[A/C]AATTAAAGATCTTAC | 57520 |
rs953179 | snp | A/C | 0.397813 | 0.201621 | intron-variant | HECW2, LOC105373821 | GRCh38.p7 | 2:196469767 | GGTTAACTACTTGTT[A/C]TCTCATATGGATTAT | 57520 |
rs1006800 | snp | A/G | 0.155325 | 0.23138 | intron-variant | HECW2 | GRCh38.p7 | 2:196296655 | TCTTCATCCTTTTGA[A/G]TGATCAGGCCTTGCT | 57520 |
rs1006801 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | HECW2 | GRCh38.p7 | 2:196296568 | taatGAAGCTTAGGA[C/G]ACCCTTGTTCAGTTT | 57520 |
rs1014254 | snp | A/T | 0.455024 | 0.143057 | intron-variant | HECW2 | GRCh38.p7 | 2:196335808 | TGGCAGGTACGTAGT[A/T]AAAATCTTCTGGCCA | 57520 |
rs1014255 | snp | C/T | 0.380138 | 0.213458 | intron-variant | HECW2 | GRCh38.p7 | 2:196335467 | AGAGGAACTCCCTCC[C/T]GTAGCCTAGGATTCT | 57520 |
rs1044148 | snp | A/T | | | utr-variant-3-prime | HECW2 | GRCh38.p7 | 2:196199616 | TGCCCAAACATTTCT[A/T]TGAGATCTATATTTA | 57520 |
rs1110099 | snp | A/G | | | intron-variant | HECW2 | GRCh38.p7 | 2:196275351 | TGATTATCTAAAGGT[A/G]TATTTTTCTTTCCCA | 57520 |
rs1113321 | snp | C/T | 0.430285 | 0.173197 | intron-variant | HECW2 | GRCh38.p7 | 2:196368975 | aactaaataagacac[C/T]ggtgaccaatcctgg | 57520 |
rs1125158 | snp | A/T | 0.481932 | 0.0933148 | intron-variant | HECW2 | GRCh38.p7 | 2:196267272 | CACATTTAAAAATTC[A/T]ATAAAATTTTTAGTA | 57520 |
rs1350102 | snp | A/G | 0.154993 | 0.231244 | intron-variant | HECW2 | GRCh38.p7 | 2:196298078 | TACTAAGAAACTTAA[A/G]CGCTAGAATTAATGT | 57520 |
rs1350103 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | HECW2 | GRCh38.p7 | 2:196238463 | GAAAGCTAAAAAAAA[A/G/T]AAAGAAAGAAAGAAA | 57520 |
rs1358399 | snp | A/G | 0.452597 | 0.146474 | intron-variant | HECW2 | GRCh38.p7 | 2:196528738 | CTGGTTCTTTTCCTA[A/G]TTCTAATAAAAGAAT | 57520 |
rs1358400 | snp | A/G | 0.274661 | 0.248781 | intron-variant | HECW2 | GRCh38.p7 | 2:196563677 | GAAAAGGCACCCACT[A/G]GCTAGATCTGAATAA | 57520 |
rs1358401 | snp | A/G | 0.418007 | 0.185132 | intron-variant, nc-transcript-variant | HECW2, LOC105373821 | GRCh38.p7 | 2:196457103 | TCTTGATTCCATGCC[A/G]TACCTACTCATTAGG | 57520 |
rs1358402 | snp | C/T | 0.325091 | 0.238456 | intron-variant, nc-transcript-variant | HECW2, LOC105373821 | GRCh38.p7 | 2:196457023 | TGCTCCTTCTTTGCT[C/T]GAAGCTTGGTACAGG | 57520 |
rs1358504 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | HECW2 | GRCh38.p7 | 2:196405870 | acccccaccaatcct[A/G]tcaagacaccagccg | 57520 |
rs1358505 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECW2 | GRCh38.p7 | 2:196407002 | gtaagctccacaagt[A/T]gggagacgctctgtt | 57520 |
rs1358506 | snp | C/T | 0.459118 | 0.137002 | intron-variant | HECW2 | GRCh38.p7 | 2:196407435 | tcaaactcctgaact[C/T]acacgatctgcccac | 57520 |
rs1358507 | snp | C/T | 0.163236 | 0.234461 | intron-variant | HECW2 | GRCh38.p7 | 2:196407439 | actcctgaacttaca[C/T]gatctgcccacctca | 57520 |
rs1378621 | snp | C/G | 0.0166199 | 0.089631 | intron-variant | HECW2 | GRCh38.p7 | 2:196278508 | GTCATGCGTTTTGGG[C/G]ACTGACCTGTTGGTT | 57520 |
rs1378622 | snp | A/G | 0.154993 | 0.231244 | intron-variant | HECW2 | GRCh38.p7 | 2:196295593 | CATTGTTCTAAATAG[A/G]TATACCTCTTTATCG | 57520 |
rs1378625 | snp | C/T | 0.361474 | 0.223771 | intron-variant | HECW2 | GRCh38.p7 | 2:196291275 | CTTATCTGTGACATC[C/T]TCCCCAACCACCCTC | 57520 |
rs1378626 | snp | C/T | 0.361474 | 0.223771 | intron-variant | HECW2 | GRCh38.p7 | 2:196291497 | TGCTTAGGCGCTCAA[C/T]AAATATTTGTTGAAC | 57520 |
rs1378627 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW2 | GRCh38.p7 | 2:196237034 | tctgttatgttgtag[C/T]tggtgaaaggtttca | 57520 |
rs1378628 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECW2 | GRCh38.p7 | 2:196349540 | CGCATGTGTGCGCGC[A/G]CACACACACACACAC | 57520 |
rs1401765 | snp | A/G | 0.269809 | 0.249214 | intron-variant | HECW2 | GRCh38.p7 | 2:196588477 | AAAATAGACAAGGTC[A/G]GGAGATGATTTAAAG | 57520 |
rs1401766 | snp | C/T | 0.269809 | 0.249214 | intron-variant | HECW2 | GRCh38.p7 | 2:196588669 | TTGCATACACACACA[C/T]ACACATATACGTTGA | 57520 |
rs1401767 | snp | C/T | 0.27893 | 0.24832 | intron-variant | HECW2 | GRCh38.p7 | 2:196588759 | TTATCACTTGAGTCA[C/T]AGTTAGAACAGCCAT | 57520 |
rs1405882 | snp | C/T | 0.209084 | 0.246629 | intron-variant | HECW2 | GRCh38.p7 | 2:196484958 | TTAGAGGTTCTGTTG[C/T]AGGATTCTAGGTCAA | 57520 |
rs1405883 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | HECW2 | GRCh38.p7 | 2:196484967 | CTGTTGCAGGATTCT[A/C]GGTCAAAAGTGAGGC | 57520 |
rs1405884 | snp | C/T | 0.209084 | 0.246629 | intron-variant | HECW2 | GRCh38.p7 | 2:196485194 | GTTCTATTGGAGCAC[C/T]GAGTGTGAGGTATCT | 57520 |
rs1405885 | snp | A/C | 0.250168 | 0.25 | intron-variant, upstream-variant-2KB | HECW2, LOC105373821 | GRCh38.p7 | 2:196453487 | CTTCCTAATTACAAT[A/C]CTCTCCTTCCTAAGT | 57520 |
rs1405886 | snp | A/G | 0.249886 | 0.25 | intron-variant | HECW2 | GRCh38.p7 | 2:196453381 | GCTTTGAGGCAGTTC[A/G]TTTTCTACTCAAACT | 57520 |
rs1405887 | snp | A/G | 0.097727 | 0.198275 | intron-variant | HECW2, LOC105373822 | GRCh38.p7 | 2:196431146 | AATCCCTTTTGAAAA[A/G]TGATAACTCTTCATC | 57520 |
rs1406213 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | HECW2 | GRCh38.p7 | 2:196421569 | AAATAATTCCTTACT[A/G]TACATACTGATTTTA | 57520 |
rs1406214 | snp | C/T | 0.097727 | 0.198275 | intron-variant | HECW2 | GRCh38.p7 | 2:196421552 | ACATACTGATTTTAT[C/T]GTGTTTGTTATAATT | 57520 |
rs1406215 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | HECW2 | GRCh38.p7 | 2:196421421 | TCTGTTATCAGTTGT[C/T]ACATCAACTTCCTTT | 57520 |
rs1406216 | snp | C/T | 0.401037 | 0.199218 | intron-variant | HECW2 | GRCh38.p7 | 2:196382750 | CAACTGCATTTCCAA[C/T]GGAAATGGCACTTGC | 57520 |
rs1406217 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | HECW2, LOC105373822 | GRCh38.p7 | 2:196430887 | ATATTTGAAGAAATA[A/G]TGGCCAACATTTGTC | 57520 |
rs1406218 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | HECW2, LOC105373822 | GRCh38.p7 | 2:196431032 | AGAAAAATCTTGAAA[A/G]TAGCCAAAGGAGGGG | 57520 |
rs1455814 | snp | A/C/T | 0.609563 | 0.139877 | intron-variant | HECW2 | GRCh38.p7 | 2:196205990 | TTGTTTTTTTCCTGG[A/C/T]CTTGGCTCATAGAGC | 57520 |
rs1455815 | snp | A/C | 0.489376 | 0.0721049 | intron-variant | HECW2 | GRCh38.p7 | 2:196205718 | AAACCTTCTGAATTA[A/C]AATCACAAGGGGTGC | 57520 |
rs1455816 | snp | A/G | 0.491051 | 0.0662916 | intron-variant | HECW2 | GRCh38.p7 | 2:196214157 | TTTCAAATCCACCAG[A/G]TAGATGAGGAAACAG | 57520 |
rs1455817 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | HECW2 | GRCh38.p7 | 2:196324621 | TTGTAGAGTCATAGT[A/G]GGGCCTGAGGCAAGA | 57520 |
rs1455820 | snp | C/G | 0.0298908 | 0.118541 | intron-variant, nc-transcript-variant | HECW2, LOC101927482 | GRCh38.p7 | 2:196263592 | TGAATGATCAGTGCT[C/G]GTCTTCCTTTCTTGA | 57520 |
rs1455821 | snp | A/C | 0.145642 | 0.227177 | intron-variant | HECW2 | GRCh38.p7 | 2:196291376 | TAATCAGCTCTTGGC[A/C]TACAAAGAATAGTAT | 57520 |
rs1455822 | snp | A/C | 0.115438 | 0.210697 | intron-variant | HECW2 | GRCh38.p7 | 2:196313987 | TGCGGCCTCAAACTC[A/C]TGGGCTCAAGTGAAG | 57520 |
rs1527783 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | HECW2 | GRCh38.p7 | 2:196478101 | aACAAACAAAAAAAA[A/C]CTCACAGAGTACACA | 57520 |
rs1527784 | snp | C/T | 0.457853 | 0.138915 | intron-variant | HECW2 | GRCh38.p7 | 2:196483966 | TTTTAGATGTTATAA[C/T]AGTGATGTATGTATG | 57520 |
rs1527785 | snp | A/T | 0 | 0 | intron-variant | HECW2 | GRCh38.p7 | 2:196506420 | ACTAATTTTACCAGC[A/T]GGGGATATATTTTTC | 57520 |
rs1528393 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | HECW2 | GRCh38.p7 | 2:196440912 | ACTCCTTAAAAAATT[A/T]AAAAAAACCCTCCTT | 57520 |
rs1528394 | snp | C/G | 0.0966517 | 0.197444 | intron-variant | HECW2 | GRCh38.p7 | 2:196419961 | CATTACCAGAACCAT[C/G]GTAATGCCTTACCTA | 57520 |
rs1528395 | snp | C/T | | | intron-variant | HECW2 | GRCh38.p7 | 2:196419953 | GAACCATCGTAATGC[C/T]TTACCTACAAACAAG | 57520 |
rs1528396 | snp | C/T | | | intron-variant | HECW2 | GRCh38.p7 | 2:196419948 | ATCGTAATGCCTTAC[C/T]TACAAACAAGCTGGA | 57520 |
rs1528397 | snp | C/T | | | intron-variant | HECW2 | GRCh38.p7 | 2:196419678 | acatttgttgagaac[C/T]tactgtgtggctgcc | 57520 |
rs1528398 | snp | A/G | 0.469642 | 0.119404 | intron-variant | HECW2 | GRCh38.p7 | 2:196446541 | ATTAAGTGAAACATT[A/G]TTCCAGGTGCTCTAC | 57520 |
rs1528400 | snp | C/T | 0.162253 | 0.234095 | intron-variant | HECW2 | GRCh38.p7 | 2:196408653 | GATACAAAGTAGAAG[C/T]AGAAACTTTATGAAC | 57520 |
rs1528401 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | HECW2 | GRCh38.p7 | 2:196351191 | GTGTGTCATTTTTTT[A/T]AAAAAAAAAGAATTA | 57520 |
rs1531106 | snp | A/G | 0.268724 | 0.249298 | intron-variant | HECW2 | GRCh38.p7 | 2:196267399 | TGAAAGAAGATGTTT[A/G]TATGCTATGACACTA | 57520 |
rs1531107 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | HECW2 | GRCh38.p7 | 2:196272041 | TTTCTGACTTGTCAT[A/T]TCTGTGAGGCTGATT | 57520 |
rs1531108 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | HECW2 | GRCh38.p7 | 2:196313246 | AGATGAGTGAAAAAA[C/G]AATCGCCAGCCCAGC | 57520 |
rs1531109 | snp | C/T | 0.127599 | 0.217986 | intron-variant | HECW2 | GRCh38.p7 | 2:196226397 | ATGAGCCAATTAAAC[C/T]TCTTTTCTTTATAAA | 57520 |
rs1531110 | snp | G/T | 0.211516 | 0.24702 | intron-variant | HECW2 | GRCh38.p7 | 2:196226422 | TATAAATTACCAGTC[G/T]CAGGTATTTCTTTAT | 57520 |
rs1531111 | snp | A/G | 0.323578 | 0.238936 | synonymous-codon | HECW2 | GRCh38.p7 | 2:196319597 | TGGCCACTCCAGGCC[A/G]GGGACAGCGACCTGC | 57520 |
rs1531112 | snp | G/T | 0.0513262 | 0.151752 | intron-variant | HECW2 | GRCh38.p7 | 2:196318136 | GTCTCTATTGGAACC[G/T]GGGTTTGTAGATACA | 57520 |
rs1531113 | snp | C/T | 0.534546 | 0.0952719 | intron-variant | HECW2 | GRCh38.p7 | 2:196219863 | CTCCCATCTGACAGA[C/T]GAGGTAATTAGGAAA | 57520 |
rs1531114 | snp | C/T | 0.499575 | 0.0145705 | intron-variant | HECW2 | GRCh38.p7 | 2:196219871 | TGACAGATGAGGTAA[C/T]TAGGAAAAGAAGAGA | 57520 |
rs1531115 | snp | G/T | 0.449726 | 0.150364 | intron-variant | HECW2 | GRCh38.p7 | 2:196290961 | GGCTGGGAATTAGAG[G/T]TTTATTAAAAACACT | 57520 |
rs1531116 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | HECW2 | GRCh38.p7 | 2:196335854 | AAGCAATGTGCCAGA[A/C]AGTGCAAGGGAATCA | 57520 |
rs1531117 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | HECW2 | GRCh38.p7 | 2:196336257 | ATTTCTGAAATAGTA[A/G]TAGCTGGACAGACCT | 57520 |
rs1534382 | snp | C/T | 0.211516 | 0.24702 | intron-variant | HECW2 | GRCh38.p7 | 2:196552408 | caactatttcttact[C/T]tccccattctcctca | 57520 |
rs1534383 | snp | C/T | 0 | 0 | intron-variant | HECW2 | GRCh38.p7 | 2:196552822 | GGGTGAATCTTTCCT[C/T]TTCAGTGAATCAGGG | 57520 |
rs1534384 | snp | A/G | 0.452965 | 0.145963 | intron-variant | HECW2 | GRCh38.p7 | 2:196527445 | CCCTTCTTCTGCGTC[A/G]CTCACGCTGGGAGCT | 57520 |
rs1534536 | snp | C/T | 0.352504 | 0.228019 | intron-variant | HECW2 | GRCh38.p7 | 2:196399154 | CATTAGTAGTGCTTC[C/T]GGAGTGTACATGCTC | 57520 |
rs1534537 | snp | C/T | 0.133777 | 0.221342 | intron-variant | HECW2 | GRCh38.p7 | 2:196398462 | ACTGCTTATGTTTTC[C/T]ACCAGCTCCTGAAAC | 57520 |
rs1534538 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | HECW2 | GRCh38.p7 | 2:196388141 | ctggataattaaaaa[A/T]ttttttttttttagt | 57520 |
rs1534539 | snp | A/T | 0.446641 | 0.154377 | intron-variant | HECW2 | GRCh38.p7 | 2:196388140 | tggataattaaaaat[A/T]tttttttttttagta | 57520 |
rs1548321 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW2 | GRCh38.p7 | 2:196371655 | TATTTTATAGATCTT[A/G]TATTTTATTCCATTT | 57520 |
rs1563377 | snp | A/G | 0.388775 | 0.207946 | intron-variant | HECW2 | GRCh38.p7 | 2:196226303 | CCTTTGCCTTCCACC[A/G]TGATTGAAAAAGCTC | 57520 |
rs1563378 | snp | A/T | 0 | 0 | intron-variant | HECW2 | GRCh38.p7 | 2:196296324 | AATATGGGATCATAA[A/T]AACTCCCTTGCTTTC | 57520 |
rs1563379 | snp | A/G | 0.31721 | 0.240796 | intron-variant | HECW2 | GRCh38.p7 | 2:196246362 | TCTTAAAAGATTTTC[A/G]TTCAGTTCCTTGTTC | 57520 |
rs1563380 | snp | A/G | 0.49995 | 0.00499176 | intron-variant | HECW2 | GRCh38.p7 | 2:196246287 | ATTCATTACAGCTGC[A/G]TTCTGCCCTGTCTGG | 57520 |
rs1563381 | snp | A/T | 0 | 0 | intron-variant | HECW2 | GRCh38.p7 | 2:196335527 | GGGGCTGCTCAATGT[A/T]TTTCCCTAAGGAAGT | 57520 |
rs1569150 | snp | C/T | 0.097727 | 0.198275 | intron-variant | HECW2, LOC105373822 | GRCh38.p7 | 2:196429786 | TGAGTCTGAGTCAAC[C/T]GGAGTACTAGAATCT | 57520 |
rs1569151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW2 | GRCh38.p7 | 2:196378690 | cttctcctcatggct[C/T]gttagtacctttgaa | 57520 |
rs1824019 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW2 | GRCh38.p7 | 2:196237245 | ctaaagaacttactc[A/G]tataaccaaacacca | 57520 |
rs1869792 | snp | A/T | 0.093777 | 0.195178 | intron-variant | HECW2 | GRCh38.p7 | 2:196241318 | CCCTAAAAAATCATC[A/T]GCCTGCCCAAACACC | 57520 |
rs1869793 | snp | C/T | 0.0886136 | 0.19093 | intron-variant | HECW2 | GRCh38.p7 | 2:196217119 | AATCATAAAAGCCCA[C/T]GTTACTTTGACTCTT | 57520 |