SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs462 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43263084 | TCTTATCTGCATTTT[C/T]CGCAATTACTTACCT | 23072 |
rs463 | snp | C/T | 0.32885 | 0.23724 | intron-variant | HECW1 | GRCh38.p7 | 7:43263185 | GAAACAGGAATTTTA[C/T]TGAAGCATCTAAAAG | 23072 |
rs2292 | snp | C/T | 0.272241 | 0.249009 | intron-variant | HECW1 | GRCh38.p7 | 7:43503054 | TAGCATTCAGAAGTC[C/T]CTCTTAGAGGTAGTT | 23072 |
rs717486 | snp | C/T | 0.188631 | 0.242351 | intron-variant | HECW1 | GRCh38.p7 | 7:43466921 | TAAAATCATTTTCAC[C/T]GATACAATTTCAAAG | 23072 |
rs718809 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43201594 | ATTTGTGACTTAAGG[G/T]ACCCAAGTGGTAAAG | 23072 |
rs721965 | snp | A/G | 0.394171 | 0.204242 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162143 | CAGCTACTTTTTTTC[A/G]TTTCCTTGTGTTTTG | 23072 |
rs728191 | snp | G/T | 0.49306 | 0.0584955 | intron-variant | HECW1 | GRCh38.p7 | 7:43284726 | TCCCTGAAATAATTT[G/T]TATTCTATTCTTAAT | 23072 |
rs736997 | snp | G/T | 0 | 0 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562310 | AAATGTGAGCATTAA[G/T]CACTCCAGGCTTTCA | 23072 |
rs739982 | snp | C/G | 0.49962 | 0.0137727 | intron-variant | HECW1 | GRCh38.p7 | 7:43282329 | CATCACACTCTTTTT[C/G]GCTGACTTCACTCAT | 23072 |
rs740548 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116325 | TAGAAGGAAACATGG[A/C]CCAAGCACTTTAACC | 23072 |
rs747468 | snp | A/G | 0.0984431 | 0.198823 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512511 | ATTTAGCTCATCAGC[A/G]TTTTACACatttata | 23072 |
rs749844 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43550855 | TCACGTCTGGCACGC[C/T]AGGGTCACATGCCAG | 23072 |
rs755665 | snp | C/T | 0.418007 | 0.185132 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511849 | TAGGAGAGCCCAGAT[C/T]TGGTGATGTGGCTTT | 23072 |
rs755666 | snp | A/G | 0.452227 | 0.146984 | intron-variant, nc-transcript-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512048 | CCACAGCGTGGGCGT[A/G]GCTGCTGCTGATCTC | 23072 |
rs757487 | snp | A/G | 0.43978 | 0.162738 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303163 | ACTTCGCTGCTGAAC[A/G]CCTCCAAACATAAAC | 23072 |
rs757488 | snp | A/G | 0.482534 | 0.0918038 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303209 | GAGCTGCACCAAGCA[A/G]TCCTAGACTTGAGCA | 23072 |
rs757489 | snp | C/T | 0.242775 | 0.249896 | intron-variant | HECW1 | GRCh38.p7 | 7:43308977 | AACAAGAAGGGATAT[C/T]ACTGAATAAAATAAT | 23072 |
rs757490 | snp | A/C | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43312918 | TCAACAGATTCAACA[A/C]CGGGTCATCCGAGGC | 23072 |
rs757491 | snp | A/G | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43313147 | CAGCTTGGTTAGTGC[A/G]TTTATAATACACACA | 23072 |
rs757492 | snp | A/G | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43313182 | TGTAAAGATGGAGGT[A/G]CATAAATTGTTGAAA | 23072 |
rs758272 | snp | A/G | 0.4944 | 0.0526182 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142785 | CCCGCTTCTGAGCAT[A/G]AGGCACAGGAAGCTA | 23072 |
rs758916 | snp | G/T | 0.223225 | 0.248562 | intron-variant | HECW1 | GRCh38.p7 | 7:43386604 | AGAAACATGCAGGGG[G/T]GGCAGGAACATCTCC | 23072 |
rs765558 | snp | C/G | 0.462472 | 0.13174 | intron-variant | HECW1 | GRCh38.p7 | 7:43357651 | agtcactctattgat[C/G]tatcaaacactagat | 23072 |
rs765865 | snp | A/G | 0.471673 | 0.115589 | intron-variant | HECW1 | GRCh38.p7 | 7:43386707 | ATCATCTCAAGTTGT[A/G]AGCCCTCATCTCAGG | 23072 |
rs767666 | snp | C/T | 0.287346 | 0.247195 | intron-variant | HECW1 | GRCh38.p7 | 7:43446299 | AAGAAAGAACATCTT[C/T]GGTTAAAACACAGAA | 23072 |
rs767667 | snp | C/T | 0.484491 | 0.0866827 | intron-variant | HECW1 | GRCh38.p7 | 7:43446239 | TGGATTTGATTCTTA[C/T]TGGAAACAAAGTCAT | 23072 |
rs767668 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43446264 | TTTTAAAACTAATGG[G/T]GGCAGCTTTTGGATT | 23072 |
rs769036 | snp | C/G | 0.497445 | 0.0356514 | intron-variant | HECW1 | GRCh38.p7 | 7:43228822 | AATTTATGAAACTAT[C/G]TTAGAATTTTCAATG | 23072 |
rs886439 | snp | G/T | 0.496175 | 0.0435625 | intron-variant | HECW1 | GRCh38.p7 | 7:43220136 | gtaccccttaggttt[G/T]ctaatttactagaat | 23072 |
rs886549 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269574 | GTGAAGGAAGCTGGA[A/G]AGGATGATTGGAGTG | 23072 |
rs886550 | snp | G/T | 0.44546 | 0.155869 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296644 | TAATTCAGGTTTATG[G/T]CTCCTTTGCATCATT | 23072 |
rs886551 | snp | C/T | 0.464523 | 0.128375 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296926 | GGTGACTATACCTCC[C/T]CTTTGCAGCTTTTTG | 23072 |
rs886552 | snp | A/T | 0.44546 | 0.155869 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297308 | AAATGTCACAATTAC[A/T]CTTGTTTGTTTGTTT | 23072 |
rs917017 | snp | A/G | 0.457037 | 0.140127 | intron-variant | HECW1 | GRCh38.p7 | 7:43325415 | TCAGAATCCTTCCAA[A/G]TCAGGGCTTGGATTG | 23072 |
rs917018 | snp | C/T | 0.390277 | 0.206936 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300882 | GCTGCACACTGTCCC[C/T]GCACCCGCCCAGGAG | 23072 |
rs969023 | snp | C/T | 0.192715 | 0.243348 | intron-variant | HECW1 | GRCh38.p7 | 7:43412105 | gaagtaacgcaaagc[C/T]gtgtacctaaaaatt | 23072 |
rs978056 | snp | A/G | 0.49907 | 0.0215454 | intron-variant | HECW1 | GRCh38.p7 | 7:43339245 | actccaattacatac[A/G]gtggatcattccatt | 23072 |
rs978057 | snp | G/T | 0.17138 | 0.237316 | intron-variant | HECW1 | GRCh38.p7 | 7:43339413 | CATGCATAAAGTTCC[G/T]AATTTCAGCTATTCT | 23072 |
rs1006106 | snp | G/T | 0.453697 | 0.14494 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123456 | AACTTATGTCAAAGC[G/T]CAGGGTCACAGGAGA | 23072 |
rs1006107 | snp | C/T | 0.208169 | 0.246476 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123370 | GGGACCCAAGGTCAA[C/T]GGCAGGTACACTCAG | 23072 |
rs1006108 | snp | A/G | 0.413914 | 0.188765 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123023 | GCTTTGTCTTTGGAC[A/G]TTTTCACCTTTAACC | 23072 |
rs1015561 | snp | A/T | 0.372995 | 0.217652 | intron-variant | HECW1 | GRCh38.p7 | 7:43340231 | CCCCCCACCCCtttt[A/T]tttttctaagacgga | 23072 |
rs1019971 | snp | A/G | 0.190833 | 0.242898 | intron-variant | HECW1 | GRCh38.p7 | 7:43498698 | ACCTGGGGGGTGTTC[A/G]CAGTGGCTTCTTTGA | 23072 |
rs1025540 | snp | A/C | 0.429388 | 0.174127 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519940 | TCATCTCCTGTGACA[A/C]ATATTGATAATCTAA | 23072 |
rs1025541 | snp | C/T | 0.154993 | 0.231244 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519673 | ggatctgctgtaata[C/T]atttaaccattcccc | 23072 |
rs1029479 | snp | A/G | 0.394721 | 0.203852 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155020 | GGTACAGACTACAAC[A/G]CAAGGCTGCAGCTCA | 23072 |
rs1029480 | snp | A/G | 0.420892 | 0.182472 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43214911 | CAGCTGGGAGGCAGC[A/G]GGTGAGGGGGCCCAT | 23072 |
rs1029481 | snp | A/T | 0.371785 | 0.218331 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43214960 | AGCGTCCCAGGACCC[A/T]GGCCAGGAAGAGCAA | 23072 |
rs1029482 | snp | A/C | 0.386504 | 0.209444 | intron-variant | HECW1 | GRCh38.p7 | 7:43215011 | TGCAAGGTAGCCTAC[A/C]CCTTTTGGGTATTTA | 23072 |
rs1072307 | snp | A/G | 0.465683 | 0.126415 | intron-variant | HECW1 | GRCh38.p7 | 7:43395001 | tgtcttcttgcagtg[A/G]gtcagttcctgggtg | 23072 |
rs1072308 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43394734 | AGGGTTCACCTTGCC[C/G]ACTGTCTAGACAGAG | 23072 |
rs1080173 | snp | C/T | 0.49423 | 0.0534032 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149037 | atacaaaattaccat[C/T]agaacacccctgtaa | 23072 |
rs1080174 | snp | A/C | 0.494358 | 0.0528145 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149240 | caattatcaccagta[A/C]taaaacatattgtca | 23072 |
rs1544418 | snp | C/T | 0.473909 | 0.111197 | intron-variant | HECW1 | GRCh38.p7 | 7:43316135 | TGTTTCTGTAAGCTT[C/T]ATTAGACCTTTCTGA | 23072 |
rs1544419 | snp | A/C | 0.474182 | 0.110646 | intron-variant | HECW1 | GRCh38.p7 | 7:43316287 | TTTTCTGTACATGTT[A/C]TGTACAAAATGTACG | 23072 |
rs1557839 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214765 | GGGCACGGGCACTAG[C/T]CCAGAAGGAGGAGGA | 23072 |
rs1560856 | snp | C/T | 0.224709 | 0.248717 | intron-variant | HECW1 | GRCh38.p7 | 7:43498558 | CTCTGCCTATGTCCT[C/T]AACCCCAGCCCTGGG | 23072 |
rs1560857 | snp | A/C | 0.424037 | 0.179474 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517159 | TGATTAACAGCATCA[A/C]ATCTGAAATCTGGCC | 23072 |
rs1560858 | snp | C/T | 0.423257 | 0.180228 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517144 | AATCTGAAATCTGGC[C/T]CTGAAAATCCTTCTC | 23072 |
rs1859403 | snp | C/T | 0.442791 | 0.15916 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302503 | GTGGTGCCCTGGTTA[C/T]GGGAAGAGGCACAGT | 23072 |
rs1860754 | snp | G/T | 0.495521 | 0.0471118 | intron-variant | HECW1 | GRCh38.p7 | 7:43434686 | CCCCACCAGGCCCTT[G/T]TCTCCATGCCATGGT | 23072 |
rs1860755 | snp | C/T | 0.16911 | 0.236552 | intron-variant | HECW1 | GRCh38.p7 | 7:43434275 | TCTCCTTTTGACTCT[C/T]TGGTTATTGAACTTT | 23072 |
rs1860756 | snp | C/T | 0.198634 | 0.244666 | intron-variant | HECW1 | GRCh38.p7 | 7:43391457 | GGTATCATTCACTCC[C/T]ACTCCTGCTTACAAA | 23072 |
rs1865317 | snp | C/T | 0.185788 | 0.241613 | intron-variant | HECW1 | GRCh38.p7 | 7:43458215 | GGAGCTTATCATTTT[C/T]GGCAAGACAGACCTA | 23072 |
rs1963417 | snp | A/G | 0.410061 | 0.192043 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519399 | aattagccgggtgtg[A/G]tagtgggcgcctgta | 23072 |
rs1978232 | snp | C/T | 0.493969 | 0.05458 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133481 | AGATAATTTATTTGT[C/T]TCAACTAGAAATAAA | 23072 |
rs2002505 | snp | A/G | 0.402982 | 0.197728 | intron-variant | HECW1 | GRCh38.p7 | 7:43190153 | GAGTCATGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 23072 |
rs2005721 | snp | A/G | 0.424968 | 0.178567 | intron-variant | HECW1 | GRCh38.p7 | 7:43240313 | ACTACACTCCAGCCT[A/G]GGCGACAGAGCAAGA | 23072 |
rs2017735 | snp | G/T | 0.0908922 | 0.192833 | intron-variant | HECW1 | GRCh38.p7 | 7:43282970 | TAAAAATACATAAGT[G/T]AGCTGAGCGCAGTGG | 23072 |
rs2024125 | snp | C/T | 0.479421 | 0.0993283 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118878 | TTTATAAATGTCATA[C/T]ATCACAGTACCATTT | 23072 |
rs2024267 | snp | C/T | 0.486133 | 0.082104 | intron-variant | HECW1 | GRCh38.p7 | 7:43372014 | GCCAACATGGTGAAA[C/T]CCCATCTCTACTAAA | 23072 |
rs2024268 | snp | G/T | 0.367091 | 0.220884 | intron-variant | HECW1 | GRCh38.p7 | 7:43371938 | CAGCTACTAGGGAGG[G/T]TGAGGCAGGAGAATC | 23072 |
rs2024269 | snp | A/C | 0.482083 | 0.0929373 | intron-variant | HECW1 | GRCh38.p7 | 7:43434218 | GGCCCTTAATGGCCA[A/C]TAATCCTATACAGCT | 23072 |
rs2024270 | snp | C/T | 0.297128 | 0.245518 | intron-variant | HECW1 | GRCh38.p7 | 7:43433130 | ATGGAAGTGAATctc[C/T]acccattagatgcca | 23072 |
rs2040761 | snp | C/T | 0.4983 | 0.0291038 | intron-variant | HECW1 | GRCh38.p7 | 7:43189465 | TACAAAAAGAGATTG[C/T]GTGCAGGTCGCTTTG | 23072 |
rs2040840 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43234840 | AGTTGGCCCACCACA[A/G]ACATTTGCTGAGTGA | 23072 |
rs2052147 | snp | C/T | 0.0663309 | 0.169604 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359498 | ACAACTGAATAGATT[C/T]ACACATTGCAAATAT | 23072 |
rs2052148 | snp | A/G | 0.493748 | 0.0555599 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359364 | CTAGATACCTACCCG[A/G]CATCCATTCTACCTT | 23072 |
rs2057744 | snp | A/T | 0.49533 | 0.0480965 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150160 | aataaccctattatt[A/T]tcactattttacaga | 23072 |
rs2057745 | snp | A/T | 0.494442 | 0.0524218 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150324 | ACCAATTGATTTCAG[A/T]TAGATTTGCTTTAAC | 23072 |
rs2057746 | snp | G/T | 0.495291 | 0.0482933 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150593 | cattctggccaggct[G/T]gttttgaactcctga | 23072 |
rs2057809 | snp | A/G | 0.386694 | 0.20932 | intron-variant | HECW1 | GRCh38.p7 | 7:43326220 | ATATTTTAAAAACAC[A/G]CAGGGGCTCCTGATG | 23072 |
rs2057810 | snp | A/G | 0.493969 | 0.05458 | intron-variant | HECW1 | GRCh38.p7 | 7:43329013 | CCGTCCCTGCATGCC[A/G]AGGTTCTGGCATTAC | 23072 |
rs2079259 | snp | A/T | 0.248471 | 0.249995 | intron-variant | HECW1 | GRCh38.p7 | 7:43342467 | TTTCTCTAAAAGTAC[A/T]GCTCTTATTGTTTCC | 23072 |
rs2079260 | snp | A/C | 0 | 0 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296962 | ACCACCAATTAGAGA[A/C]AGTGATGGCCTCCTT | 23072 |
rs2079261 | snp | A/C | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296978 | AGTGATGGCCTCCTT[A/C]TGAGTGcttgcctgc | 23072 |
rs2079262 | snp | C/G | 0.394721 | 0.203852 | intron-variant | HECW1 | GRCh38.p7 | 7:43305885 | cctgcctcagcctcc[C/G]aagtagctgggatta | 23072 |
rs2079263 | snp | A/G | 0.464096 | 0.129085 | intron-variant | HECW1 | GRCh38.p7 | 7:43306417 | TACCCACCTGGTGGC[A/G]TAACAAAGCCGAGTG | 23072 |
rs2079264 | snp | C/T | 0.278664 | 0.248351 | intron-variant | HECW1 | GRCh38.p7 | 7:43231946 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 23072 |
rs2107270 | snp | A/C | 0.368119 | 0.220336 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154173 | ATCTTTCCAAGTAGT[A/C]ATGTGTTTACATGTC | 23072 |
rs2107271 | snp | A/G | 0.47023 | 0.118317 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156688 | AATATTGTACCAGAT[A/G]TTTCTGGTTCTCCAT | 23072 |
rs2107272 | snp | A/G | 0.390277 | 0.206936 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156788 | GTGGAAGTGATGTGT[A/G]TTACCTCTAGGTTGA | 23072 |
rs2107273 | snp | A/G | 0.453209 | 0.145623 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156974 | TATCAGATTAAGTCA[A/G]TGAGATTTGAGGGGC | 23072 |
rs2107274 | snp | G/T | 0.398534 | 0.201091 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157049 | GTTCATTCGCAAACC[G/T]GGGCTTTGTGCTAGG | 23072 |
rs2107554 | snp | A/G | 0.317451 | 0.240729 | intron-variant | HECW1 | GRCh38.p7 | 7:43347702 | aggtatgttccttct[A/G]tgacgattttcctga | 23072 |
rs2107555 | snp | C/T | 0.486332 | 0.08153 | intron-variant | HECW1 | GRCh38.p7 | 7:43347736 | ttttaatcataaatg[C/T]tggattttgtcaaat | 23072 |
rs2109808 | snp | A/T | 0.435407 | 0.167703 | intron-variant | HECW1 | GRCh38.p7 | 7:43405353 | cataccacgagtata[A/T]ctagatgctgagtct | 23072 |
rs2109809 | snp | C/T | 0.257454 | 0.249889 | intron-variant | HECW1 | GRCh38.p7 | 7:43371109 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 23072 |
rs2109810 | snp | C/T | 0.428333 | 0.175206 | intron-variant | HECW1 | GRCh38.p7 | 7:43371045 | aaaaaattagccaga[C/T]gtggtggcgggcacc | 23072 |
rs2109811 | snp | C/G | 0.472241 | 0.114494 | intron-variant | HECW1 | GRCh38.p7 | 7:43370991 | ctgaggcagtagaat[C/G]gcgagaacccaggaa | 23072 |