SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs488133 | snp | C/T | 0.256061 | 0.249927 | upstream-variant-2KB, intron-variant | ESR1 | GRCh38.p7 | 6:151804309 | CTGTGAGGAGACAGC[C/T]AACCTTCTTATTCTT | 2099 |
rs523736 | snp | A/G | 0.466204 | 0.125522 | intron-variant | ESR1 | GRCh38.p7 | 6:151802760 | TTGGGAGGTTGAGGC[A/G]GGTGGATCACCTGTG | 2099 |
rs528529 | snp | A/C | 0.483126 | 0.0902898 | intron-variant | ESR1 | GRCh38.p7 | 6:151781804 | AAAAAGTATTGTGCA[A/C]AAAAAAAAAAACTAC | 2099 |
rs532010 | snp | C/T | 0.485799 | 0.0830599 | intron-variant | ESR1 | GRCh38.p7 | 6:151809783 | CCAACCTTTAAAAGT[C/T]TTGTTCATTGTTTGT | 2099 |
rs532062 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | ESR1 | GRCh38.p7 | 6:151792585 | gggtgcagtagtgta[C/T]gtctgcagtaccagc | 2099 |
rs538098 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ESR1 | GRCh38.p7 | 6:151799734 | aggagtagcactcaa[C/T]aggaaatcaaggaag | 2099 |
rs543648 | snp | C/T | 0.443598 | 0.158176 | intron-variant, upstream-variant-2KB | ESR1 | GRCh38.p7 | 6:151789809 | ACCATCTTCCTCCAT[C/T]ACACTGCAGGCAGCG | 2099 |
rs543650 | snp | A/C | 0.443598 | 0.158176 | intron-variant, upstream-variant-2KB | ESR1 | GRCh38.p7 | 6:151789808 | CCATCTTCCTCCATT[A/C]CACTGCAGGCAGCGG | 2099 |
rs575708 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ESR1 | GRCh38.p7 | 6:151784458 | AAATGAAGTCAACAG[A/G]ATAAAATATTTTTAA | 2099 |
rs576330 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ESR1 | GRCh38.p7 | 6:151811040 | ACATCCAGTGGGACA[C/T]TCGGGAGGACAGTCC | 2099 |
rs655459 | snp | G/T | 0.455502 | 0.142369 | intron-variant | ESR1 | GRCh38.p7 | 6:151781147 | AAACTGAGACTCAAA[G/T]ATATTAATTAATTTA | 2099 |
rs655890 | snp | A/G | 0.456685 | 0.140646 | intron-variant | ESR1 | GRCh38.p7 | 6:151781217 | CATACTTGAGACTGG[A/G]TAATTTATATTGAAC | 2099 |
rs712221 | snp | A/T | 0.499891 | 0.00738737 | intron-variant | ESR1 | GRCh38.p7 | 6:151859106 | AGGACTTCATGTTCA[A/T]TAACTTTTCCTTTTT | 2099 |
rs722029 | snp | C/G | 0 | 0 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ESR1 | GRCh38.p7 | 6:152102286 | TATGCCACTGGCTTA[C/G]AGTACTCCTTCCCCT | 2099 |
rs722207 | snp | A/G | 0.486595 | 0.0807641 | intron-variant | ESR1 | GRCh38.p7 | 6:152002057 | CCTTGTAAAACTCCC[A/G]TTTCGACATTCTGAA | 2099 |
rs722208 | snp | A/G | 0.497502 | 0.035255 | intron-variant | ESR1 | GRCh38.p7 | 6:152001750 | GGTGGGGTGGAAGAC[A/G]CTGAAATGAATTTTT | 2099 |
rs722209 | snp | C/T | 0.286564 | 0.247312 | intron-variant | ESR1 | GRCh38.p7 | 6:152002061 | GTAAAACTCCCGTTT[C/T]GACATTCTGAACTTA | 2099 |
rs722210 | snp | G/T | 0.0659589 | 0.169201 | intron-variant | ESR1 | GRCh38.p7 | 6:152001928 | CTTGGACCCCAAAGG[G/T]CTCCTGACTGGCTGG | 2099 |
rs726281 | snp | A/G | 0.494976 | 0.0498674 | intron-variant | ESR1 | GRCh38.p7 | 6:151981443 | GAATTTGTTCTTAGA[A/G]TAAATGACAATAAAG | 2099 |
rs726282 | snp | A/C | 0.293551 | 0.246177 | intron-variant | ESR1 | GRCh38.p7 | 6:151981519 | TAAAGTTGCTATATT[A/C]TTTTTCTTCTGATGG | 2099 |
rs726283 | snp | A/G | 0.494976 | 0.0498674 | intron-variant | ESR1 | GRCh38.p7 | 6:151981874 | CATGTTCCTAAACAT[A/G]TTTTCCTCAAAAGGG | 2099 |
rs728523 | snp | A/T | 0.170084 | 0.236883 | intron-variant | ESR1 | GRCh38.p7 | 6:151982056 | ACAATCTCACTTTAT[A/T]CATTCACTCTGTTTA | 2099 |
rs728524 | snp | A/G | 0.239326 | 0.249772 | intron-variant | ESR1 | GRCh38.p7 | 6:151982302 | TTTTTAAAGGCGCTT[A/G]TGTTTCCTTTCTGGT | 2099 |
rs746432 | snp | C/G | 0.177183 | 0.23916 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ESR1 | GRCh38.p7 | 6:151808173 | GTTGGAGCCGAACGC[C/G]GCAGCCTCAGACCCG | 2099 |
rs749491 | snp | C/T | 0.498693 | 0.0255257 | intron-variant | ESR1 | GRCh38.p7 | 6:152087751 | TCTTGAAAACATGGA[C/T]TGTATCCTTGTTTTG | 2099 |
rs750686 | snp | A/G | 0.499776 | 0.0105807 | intron-variant | ESR1 | GRCh38.p7 | 6:152086991 | CTTTATTCAACTCAC[A/G]TAATGAGAAGTCAGT | 2099 |
rs827417 | snp | A/G | 0.275732 | 0.248672 | intron-variant | ESR1 | GRCh38.p7 | 6:151868129 | aaaaacaaacaaaca[A/G]aaaaaaacaaagaaa | 2099 |
rs827418 | snp | G/T | 0.49681 | 0.0398085 | intron-variant | ESR1 | GRCh38.p7 | 6:151857493 | gtgtgtgtgtgtgtg[G/T]gtgggtgggtgtgtt | 2099 |
rs827419 | snp | G/T | 0.283684 | 0.24772 | intron-variant | ESR1 | GRCh38.p7 | 6:151856528 | TGAGATCAGTTTTAC[G/T]GCCACAATTTTAAAA | 2099 |
rs827420 | snp | C/T | 0.499913 | 0.00658888 | intron-variant | ESR1 | GRCh38.p7 | 6:151856394 | CCTTTCATAAATATC[C/T]CATAGAAGTAAAGCC | 2099 |
rs827421 | snp | C/T | 0.499053 | 0.0217445 | intron-variant | ESR1 | GRCh38.p7 | 6:151835987 | TGTCATAAAGTACAA[C/T]GTTCTCCTTTGAATA | 2099 |
rs827422 | snp | C/T | 0.49925 | 0.0193545 | intron-variant | ESR1 | GRCh38.p7 | 6:151835593 | TCCAGACAATTTATA[C/T]GACTTATCTTAAGTA | 2099 |
rs827423 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | ESR1 | GRCh38.p7 | 6:151835062 | CTTAAACTGCATTTC[C/T]TCCAGGGAGCTTTGC | 2099 |
rs827424 | snp | A/T | 0.283684 | 0.24772 | intron-variant | ESR1 | GRCh38.p7 | 6:151834592 | cccgtcatctacatt[A/T]ggtatttctcctaat | 2099 |
rs827425 | snp | A/T | | | intron-variant | ESR1 | GRCh38.p7 | 6:151863178 | ctaccaatgactttc[A/T]tcacagaattttaaa | 2099 |
rs851975 | snp | A/G | 0.300421 | 0.244863 | intron-variant | ESR1 | GRCh38.p7 | 6:151710168 | TAATCAAAGCAATAC[A/G]TCTCAGGCCTGGCAA | 2099 |
rs851976 | snp | A/G | 0.393619 | 0.204631 | intron-variant | ESR1 | GRCh38.p7 | 6:151708873 | CGATATTGATATATC[A/G]AGATATATGTATATC | 2099 |
rs851977 | snp | A/G | 0.393619 | 0.204631 | intron-variant | ESR1 | GRCh38.p7 | 6:151708473 | caatagaaatgtaaa[A/G]atacacatacctttt | 2099 |
rs851978 | snp | A/C | 0.393065 | 0.205018 | intron-variant | ESR1 | GRCh38.p7 | 6:151708421 | ggacttacaccataa[A/C]aataaaacccccaat | 2099 |
rs851979 | snp | A/G | 0 | 0 | intron-variant | ESR1 | GRCh38.p7 | 6:151706905 | GGACAAATCCTTCCA[A/G]TAGGCAGCTCTCAGA | 2099 |
rs851980 | snp | A/G | 0.310386 | 0.242597 | intron-variant | ESR1 | GRCh38.p7 | 6:151706820 | TTTTACTTCTACTGA[A/G]TAGCAGTCATGATTT | 2099 |
rs851981 | snp | A/T | 0.291235 | 0.246576 | intron-variant | ESR1 | GRCh38.p7 | 6:151705939 | TAGTATAATCCACTG[A/T]GTGACCTTGTTAGGT | 2099 |
rs851982 | snp | C/T | 0.366266 | 0.221319 | intron-variant | ESR1 | GRCh38.p7 | 6:151703850 | CTTAGATCCAAAACT[C/T]TGATTCCAGAAAGGT | 2099 |
rs851983 | snp | C/T | 0.384017 | 0.211044 | intron-variant | ESR1 | GRCh38.p7 | 6:151703280 | AGCTAAGCCTGGAAG[C/T]GGTGACTTTATTTAC | 2099 |
rs851984 | snp | C/T | 0.370974 | 0.218781 | intron-variant | ESR1 | GRCh38.p7 | 6:151702056 | TAGATCTTATCAATT[C/T]ACGGACAAAGTCAGG | 2099 |
rs851985 | snp | G/T | 0.417621 | 0.193535 | intron-variant | ESR1 | GRCh38.p7 | 6:151699255 | ATGTAGCAGTACAAA[G/T]CTTTTCCCCTACTAA | 2099 |
rs851986 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ESR1 | GRCh38.p7 | 6:151698532 | TCCCATAACTGTAAA[C/G]CATTTTAGGCAACTG | 2099 |
rs851996 | snp | A/G | 0.457037 | 0.140127 | intron-variant | ESR1 | GRCh38.p7 | 6:151695668 | GGTGTCCTTAGTAAC[A/G]TTCCAAAAGGAATTA | 2099 |
rs862346 | snp | A/T | 0.459914 | 0.13578 | intron-variant | ESR1 | GRCh38.p7 | 6:151695234 | AAATAGGAGACTAAA[A/T]CCAAATGAAGTTATT | 2099 |
rs867239 | snp | C/G | 0.208169 | 0.246476 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | ESR1 | GRCh38.p7 | 6:151807496 | GCCTCTATCCAGCAG[C/G]GACGACAAGTAAAGT | 2099 |
rs867240 | snp | A/G | 0.0744748 | 0.178019 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | ESR1 | GRCh38.p7 | 6:151807507 | GCAGCGACGACAAGT[A/G]AAGTAAAGTTCAGGG | 2099 |
rs872921 | snp | G/T | 0.0198 | 0.0975087 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | ESR1 | GRCh38.p7 | 6:151807804 | GTTAGAGGCGACGCA[G/T]CGCATGTCCCGCCGA | 2099 |
rs926681 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | ESR1 | GRCh38.p7 | 6:151743853 | actctacgattaatt[C/T]gtggtgaaagctgca | 2099 |
rs926777 | snp | A/C | 0.483199 | 0.0901004 | intron-variant | ESR1 | GRCh38.p7 | 6:151983912 | TTAGAGAGTCCTCAG[A/C]ATGTTGCTTATTTTT | 2099 |
rs926778 | snp | A/C | 0.49168 | 0.063958 | intron-variant | ESR1 | GRCh38.p7 | 6:152034647 | GCAACTAACTCTTTC[A/C]AAGCATTGACCAGAT | 2099 |
rs926779 | snp | A/G | 0.491629 | 0.0641526 | intron-variant | ESR1 | GRCh38.p7 | 6:152034785 | CATAGATCTTAACGA[A/G]GTTTTTACTAACGAC | 2099 |
rs932477 | snp | A/G | 0.335559 | 0.234904 | intron-variant | ESR1 | GRCh38.p7 | 6:151983461 | AGAAAGGATGGATAT[A/G]TGTGTGATCCTGGGT | 2099 |
rs932479 | snp | C/T | 0.399611 | 0.200291 | intron-variant | ESR1 | GRCh38.p7 | 6:151966902 | TTCTTTTGTTCTATC[C/T]CTCACTTCCAAATGA | 2099 |
rs932480 | snp | G/T | 0.399611 | 0.200291 | intron-variant | ESR1 | GRCh38.p7 | 6:151967106 | TTGCAGTTTTCTCCT[G/T]TTTTATGGATGCAAT | 2099 |
rs957428 | snp | C/T | 0 | 0 | intron-variant | ESR1 | GRCh38.p7 | 6:151781019 | TGAAACTAATTTTTT[C/T]TTTTGCTTTCAAACT | 2099 |
rs974276 | snp | A/G | 0.400682 | 0.199487 | intron-variant | ESR1 | GRCh38.p7 | 6:152061285 | TGCAGATTCCTTATA[A/G]AGGTAGAACCATGCT | 2099 |
rs974277 | snp | C/T | 0.400325 | 0.199756 | intron-variant | ESR1 | GRCh38.p7 | 6:152061686 | GTCTGATTCTACTGC[C/T]CCTTCGTATTTATTT | 2099 |
rs977532 | snp | A/G | 0.499609 | 0.0139722 | intron-variant | ESR1 | GRCh38.p7 | 6:151747748 | tgaaataagccagac[A/G]caaaagaccgcatat | 2099 |
rs977533 | snp | C/T | 0.498964 | 0.02274 | intron-variant | ESR1 | GRCh38.p7 | 6:151747739 | ccagacgcaaaagac[C/T]gcatattgtattgtt | 2099 |
rs985191 | snp | A/C | 0.290718 | 0.246662 | intron-variant | ESR1 | GRCh38.p7 | 6:151962323 | GTTTCTTAAAACCCA[A/C]GTGGGTTACCTAAGC | 2099 |
rs985192 | snp | A/C | 0.437683 | 0.165152 | intron-variant | ESR1 | GRCh38.p7 | 6:151962343 | GTTACCTAAGCCATC[A/C]TAGTTCTGCCCCCTG | 2099 |
rs985694 | snp | C/T | 0.398894 | 0.200825 | intron-variant | ESR1 | GRCh38.p7 | 6:151965490 | GCTTTATATAATACA[C/T]CCCTGAAGTTTAGAT | 2099 |
rs985695 | snp | C/T | 0.352938 | 0.227824 | intron-variant | ESR1 | GRCh38.p7 | 6:151965570 | CTTTCCTTTCACTTT[C/T]CTACCCTCTACCTAC | 2099 |
rs988328 | snp | A/G | 0.346147 | 0.230772 | intron-variant | ESR1 | GRCh38.p7 | 6:151920015 | GCTTAAAAAGCCTTT[A/G]TCTCCACCTTCATGG | 2099 |
rs1018442 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ESR1 | GRCh38.p7 | 6:151720809 | TAAATTATGTCCTCA[C/T]GTCCTTCATGTCTTG | 2099 |
rs1033181 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | ESR1 | GRCh38.p7 | 6:151873686 | TAAAACTAAAATGTC[A/G]TAGGTTTTCCTTTGG | 2099 |
rs1033182 | snp | A/G | 0.261884 | 0.249717 | intron-variant | ESR1 | GRCh38.p7 | 6:151873899 | AAATATTCGATGAGT[A/G]CCTTTAATAAGGAGA | 2099 |
rs1062577 | snp | A/T | 0.245631 | 0.249962 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ESR1 | GRCh38.p7 | 6:152102770 | GAAAAATTTCTATTC[A/T]TTTTTTTGCATCCAA | 2099 |
rs1101080 | snp | A/C | 0.392881 | 0.205147 | intron-variant | ESR1 | GRCh38.p7 | 6:151712508 | ctgctcaaggaaaaa[A/C]gagaggacacaaaga | 2099 |
rs1101081 | snp | A/G | 0.330714 | 0.236612 | intron-variant | ESR1 | GRCh38.p7 | 6:151711782 | aacctacagaatggg[A/G]gaaaaatttcgtaat | 2099 |
rs1101082 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ESR1 | GRCh38.p7 | 6:151711637 | tcatttatgcggcca[A/G]caaacatatgaaaaa | 2099 |
rs1124674 | snp | A/C | 0.493703 | 0.0557558 | intron-variant | ESR1 | GRCh38.p7 | 6:151759600 | CTAAGGAGATACTAA[A/C]CTAGCTTCAATTATT | 2099 |
rs1159327 | snp | A/G | 0.396909 | 0.202282 | intron-variant | ESR1 | GRCh38.p7 | 6:151726887 | tcttcccattgtagt[A/G]aaggatcctagtcaa | 2099 |
rs1285054 | snp | G/T | 0.482159 | 0.0927485 | intron-variant | ESR1 | GRCh38.p7 | 6:151778458 | tcatccaggctggat[G/T]gcggtggcatgatct | 2099 |
rs1285055 | snp | C/T | 0.397452 | 0.201886 | intron-variant | ESR1 | GRCh38.p7 | 6:151778564 | gtgtgtgccaccatg[C/T]ctggctaatttttgt | 2099 |
rs1285056 | snp | C/G | 0.491732 | 0.0637633 | intron-variant | ESR1 | GRCh38.p7 | 6:151779871 | cgccactgcactcca[C/G]cctgggcgacagagc | 2099 |
rs1285057 | snp | C/T | 0.439224 | 0.163383 | intron-variant | ESR1 | GRCh38.p7 | 6:151782657 | GTGCACATTTTAACA[C/T]TCCTCATTATTCTGG | 2099 |
rs1285058 | snp | C/G | 0.311859 | 0.242226 | intron-variant | ESR1 | GRCh38.p7 | 6:151787904 | aggagtggtgagaga[C/G]ggcatcattttcttg | 2099 |
rs1285060 | snp | C/T | 0 | 0 | intron-variant | ESR1 | GRCh38.p7 | 6:151798214 | GAATTCTAATCAAAA[C/T]CCACAGCAGAAAAAA | 2099 |
rs1290387 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | ESR1 | GRCh38.p7 | 6:151787562 | tagagaatttcacct[C/G]ccgggttagctgtat | 2099 |
rs1293935 | snp | C/G | 0.448195 | 0.152377 | intron-variant | ESR1 | GRCh38.p7 | 6:151696823 | GAAATACCTTCTTCT[C/G]TTTACACTTCCTCAC | 2099 |
rs1293936 | snp | A/C | 0.461813 | 0.132798 | intron-variant | ESR1 | GRCh38.p7 | 6:151696556 | GGCACAGGGTAGAAA[A/C]CTGAACAACCCCATC | 2099 |
rs1336981 | snp | A/G | 0.406641 | 0.194842 | intron-variant | ESR1 | GRCh38.p7 | 6:151761234 | AAATAAGGCTAAAAC[A/G]TAAATATTTTAAATA | 2099 |
rs1336983 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | ESR1 | GRCh38.p7 | 6:151737967 | TTCTAAGACTGCTCA[A/G]AGAACACTGGCAAGT | 2099 |
rs1336984 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ESR1 | GRCh38.p7 | 6:151732247 | GTAAATTATCCGCCT[A/G]ATGAGACTCATGCCC | 2099 |
rs1355930 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ESR1 | GRCh38.p7 | 6:151915857 | ATagagagagagaga[A/G]agagagagaaagaga | 2099 |
rs1361024 | snp | C/T | 0.158632 | 0.232706 | intron-variant | ESR1 | GRCh38.p7 | 6:151749793 | GTTCTTTTTCCCCCA[C/T]GGAGCTAAAAATATC | 2099 |
rs1415193 | snp | A/T | 0.378372 | 0.214524 | intron-variant, upstream-variant-2KB | ESR1, LOC107986529 | GRCh38.p7 | 6:151771503 | CATGTAGTTACACCT[A/T]TTGTTGCTATTTCAC | 2099 |
rs1415194 | snp | C/T | 0.49706 | 0.0382258 | intron-variant | ESR1 | GRCh38.p7 | 6:151742863 | ACATATTTCTTTGTA[C/T]ATATAACATCTAGCC | 2099 |
rs1514347 | snp | A/G | 0.408359 | 0.193449 | intron-variant | ESR1 | GRCh38.p7 | 6:151908310 | TACAATAATGATAAT[A/G]CACACAGGTATTAAA | 2099 |
rs1514348 | snp | A/C | 0.499809 | 0.00978247 | intron-variant | ESR1 | GRCh38.p7 | 6:151861180 | AGCAGGCTGAATGGA[A/C]AATGCAGACTTACCC | 2099 |
rs1569788 | snp | C/T | 0.497803 | 0.033074 | intron-variant | ESR1 | GRCh38.p7 | 6:152007481 | AGATTACTGCCCATA[C/T]GCGGGGTGAGGAGTG | 2099 |
rs1606678 | snp | A/G | 0.303938 | 0.244112 | intron-variant | ESR1 | GRCh38.p7 | 6:151888680 | agagttcctgccaga[A/G]caattatgcaagaaa | 2099 |
rs1606680 | snp | C/G | 0.417034 | 0.18601 | intron-variant | ESR1 | GRCh38.p7 | 6:151927396 | aattctctacaatct[C/G]tgttagtaaacaggc | 2099 |
rs1609624 | snp | A/G | 0.462363 | 0.131916 | intron-variant | ESR1 | GRCh38.p7 | 6:151759874 | cgcagttacttttgc[A/G]ccaacctaaTACCTG | 2099 |