SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3186 | snp | G/T | 0.342582 | 0.232225 | utr-variant-3-prime | SORBS2 | GRCh38.p7 | 4:185587569 | CGCGGGGTGTTTCAG[G/T]CGCGTTGACGCAGGT | 8470 |
rs3651 | snp | C/G | 0.4902 | 0.0693106 | intron-variant | SORBS2 | GRCh38.p7 | 4:185756777 | GTTCCAGGTTTTTTT[C/G]TGAACAAATGATCCT | 8470 |
rs3653 | snp | C/T | 0.439918 | 0.162576 | intron-variant | SORBS2 | GRCh38.p7 | 4:185756864 | CAGTCACCTAAGATA[C/T]CGAGTGGCAAGTCTT | 8470 |
rs724072 | snp | G/T | 0.403158 | 0.197592 | intron-variant | SORBS2 | GRCh38.p7 | 4:185890417 | GAGCCTGCCACACAG[G/T]CTTCTTGTCAGGATA | 8470 |
rs725184 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS2 | GRCh38.p7 | 4:185589479 | AAGCTCGCAGAAAAT[C/T]ACACATAGCTGAAGC | 8470 |
rs725185 | snp | A/G | 0.000971889 | 0.0220227 | missense | SORBS2 | GRCh38.p7 | 4:185589777 | GTATAGTTATACAGA[A/G]CCTGAAACCTTAAAC | 8470 |
rs726466 | snp | C/G | 0.417359 | 0.185718 | intron-variant | SORBS2 | GRCh38.p7 | 4:185624902 | GCCCTATTAAATTGC[C/G]TAAGGGTATAACACT | 8470 |
rs769354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS2 | GRCh38.p7 | 4:185821315 | GCAGGAAGCAGAGGC[C/G]AGGTGGACAGGGTGG | 8470 |
rs870197 | snp | C/T | 0.393434 | 0.20476 | intron-variant | SORBS2 | GRCh38.p7 | 4:185820278 | CAGGCTCCCTGCAAC[C/T]TCACCTGGACAGCGC | 8470 |
rs878356 | snp | C/T | 0.11963 | 0.213316 | intron-variant | SORBS2 | GRCh38.p7 | 4:185808639 | ACATAACTAGTGTAA[C/T]GTAACTAGTGATTTC | 8470 |
rs878357 | snp | A/G | 0.480461 | 0.0968913 | intron-variant | SORBS2 | GRCh38.p7 | 4:185809294 | TCTGTCTGCTGAACC[A/G]TATTGCATTTGTCCC | 8470 |
rs883132 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SORBS2 | GRCh38.p7 | 4:185830088 | TAATCAAATGGCATG[C/T]GATTACAACTGTGCC | 8470 |
rs884993 | snp | A/T | 0.443866 | 0.157848 | intron-variant | SORBS2 | GRCh38.p7 | 4:185708271 | TGTAGTGACAGATAT[A/T]AACTTAAGGAATGAC | 8470 |
rs897194 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SORBS2 | GRCh38.p7 | 4:185925012 | ATTGTTTTAATGCTG[C/T]GTGTATTCACTGAAA | 8470 |
rs897195 | snp | A/G/T | 0.0107246 | 0.0724382 | intron-variant | SORBS2 | GRCh38.p7 | 4:185924913 | ggttcttggtctcac[A/G/T]ccgataggattaatg | 8470 |
rs901094 | snp | A/G | 0.115088 | 0.210473 | intron-variant, upstream-variant-2KB | SORBS2 | GRCh38.p7 | 4:185658916 | GATCAGGACCATCCT[A/G]GCTAGCATGGTGAAA | 8470 |
rs904444 | snp | A/T | 0.030278 | 0.119257 | intron-variant | SORBS2 | GRCh38.p7 | 4:185829601 | CATTTATTCCTTTAA[A/T]GTCATCTCTTGGTTT | 8470 |
rs904445 | snp | C/T | 0.030278 | 0.119257 | intron-variant | SORBS2 | GRCh38.p7 | 4:185829599 | TTTATTCCTTTAATG[C/T]CATCTCTTGGTTTGT | 8470 |
rs904447 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SORBS2 | GRCh38.p7 | 4:185820951 | CCTTAAGGGGCAGAT[A/G]GAATTCATTCACCTG | 8470 |
rs904448 | snp | G/T | 0.401037 | 0.199218 | intron-variant | SORBS2 | GRCh38.p7 | 4:185742271 | TTTATTTAGGCCTGT[G/T]GTTTTTGCTTTGTTT | 8470 |
rs904449 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SORBS2 | GRCh38.p7 | 4:185808283 | ATTTTACTTTCTAAT[C/T]CCAAATATCAGGATA | 8470 |
rs904450 | snp | A/G | 0.490673 | 0.0676508 | intron-variant | SORBS2 | GRCh38.p7 | 4:185808376 | TTTGCTTTCAACACA[A/G]ATATCTTAAAGACAA | 8470 |
rs904451 | snp | A/C | 0.436976 | 0.165952 | intron-variant | SORBS2 | GRCh38.p7 | 4:185709792 | TGCCCTTCATCTGAC[A/C]TTGAATCTAGGCTGT | 8470 |
rs936788 | snp | A/G | 0.5 | 0.00019968 | intron-variant | SORBS2 | GRCh38.p7 | 4:185659729 | CCGTGTCTTAATAAG[A/G]ACTAGCTTAGCCGGG | 8470 |
rs950590 | snp | G/T | 0.135542 | 0.222441 | intron-variant | SORBS2 | GRCh38.p7 | 4:185733223 | AGACTGCACCAGTGC[G/T]ACTTGAAGGGGTAAG | 8470 |
rs955262 | snp | A/G | 0.33875 | 0.233717 | intron-variant | SORBS2 | GRCh38.p7 | 4:185697238 | TCTTAAGACTCAATC[A/G]AAGGTAAAGATCTGC | 8470 |
rs955263 | snp | C/T | 0.487495 | 0.0780784 | intron-variant | SORBS2 | GRCh38.p7 | 4:185697150 | TGCTTTGCTGTCTAG[C/T]GGGGGAGTCGATGAT | 8470 |
rs955264 | snp | A/G | 0.45574 | 0.142025 | intron-variant | SORBS2 | GRCh38.p7 | 4:185697021 | TCAGTTTGCCTATAC[A/G]TGTGTTATAGGGATA | 8470 |
rs959584 | snp | A/G | 0.26518 | 0.249539 | intron-variant | SORBS2 | GRCh38.p7 | 4:185946649 | CTCCTCATCCACCCT[A/G]CTTCTCCTCTAAATG | 8470 |
rs959585 | snp | A/C | 0.280785 | 0.248097 | intron-variant | SORBS2 | GRCh38.p7 | 4:185946908 | AATCATCTTTCATCC[A/C]TGACTATGTGTGCCA | 8470 |
rs959586 | snp | C/T | 0.280256 | 0.248162 | intron-variant | SORBS2 | GRCh38.p7 | 4:185946992 | GCCCATGACTTAGTG[C/T]TCTCACCTCCTCCCA | 8470 |
rs959984 | snp | C/T | 0.108402 | 0.206034 | intron-variant | SORBS2 | GRCh38.p7 | 4:185661377 | TTTTGTGGCCTCCTG[C/T]GAAAGAAGCTTTGCT | 8470 |
rs979922 | snp | A/C | 0.215446 | 0.2476 | intron-variant | SORBS2 | GRCh38.p7 | 4:185779892 | TTTCTATAGGAGAAT[A/C]TGACTGCTGTTTCAA | 8470 |
rs1002601 | snp | A/G | 0.421209 | 0.182174 | intron-variant, upstream-variant-2KB | SORBS2 | GRCh38.p7 | 4:185811536 | GACACATACACACAC[A/G]CATACACACACATTT | 8470 |
rs1003004 | snp | A/G | 0.472522 | 0.113946 | intron-variant | SORBS2 | GRCh38.p7 | 4:185707573 | GAACAAGCATCAAAA[A/G]CAGCAGCTGTCCTAT | 8470 |
rs1014238 | snp | A/C | 0.496649 | 0.0407971 | intron-variant | SORBS2 | GRCh38.p7 | 4:185945525 | AAATTTTCTTCCTAA[A/C]GGTTTACCAAAATTG | 8470 |
rs1021217 | snp | A/G | 0.270621 | 0.249148 | intron-variant | SORBS2 | GRCh38.p7 | 4:185663101 | TGTGGGTAGACAGGC[A/G]TGCTTAATAGTCCTG | 8470 |
rs1021218 | snp | C/T | 0.157311 | 0.232183 | intron-variant | SORBS2 | GRCh38.p7 | 4:185663054 | ACTAAGCCGATTCAG[C/T]TCCATCAGAATAGAT | 8470 |
rs1021678 | snp | C/T | 0.397271 | 0.202018 | intron-variant | SORBS2 | GRCh38.p7 | 4:185757614 | TAATTTCCCAGGACA[C/T]GGAATAACTCTTAAA | 8470 |
rs1026361 | snp | C/T | 0.43598 | 0.167067 | intron-variant | SORBS2 | GRCh38.p7 | 4:185884012 | ccagagacagaagtc[C/T]gatcagttttcatca | 8470 |
rs1026362 | snp | A/G | 0.487368 | 0.0784625 | intron-variant | SORBS2 | GRCh38.p7 | 4:185885354 | TCTTTTCATTTTCTC[A/G]CACTGCTGAATAAAT | 8470 |
rs1027521 | snp | A/G | 0.230603 | 0.249246 | intron-variant | SORBS2 | GRCh38.p7 | 4:185740049 | AGAGCCCAACACGGT[A/G]AGTTTGCTTCCTAGG | 8470 |
rs1027522 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | SORBS2 | GRCh38.p7 | 4:185823517 | AAATGTGTCAATTTA[C/T]TAAAGAATATACAAA | 8470 |
rs1027523 | snp | A/G | 0.409382 | 0.192607 | intron-variant | SORBS2 | GRCh38.p7 | 4:185822973 | ggaacaaaaaggaaa[A/G]gcagcttcctgcatg | 8470 |
rs1027524 | snp | G/T | 0.095934 | 0.196885 | intron-variant | SORBS2 | GRCh38.p7 | 4:185855615 | TAGACCTTTCTTACT[G/T]TGCTTTTAGAAAATG | 8470 |
rs1027525 | snp | A/G | 0.471388 | 0.116136 | intron-variant | SORBS2 | GRCh38.p7 | 4:185855323 | GTATGTACTGGAGCA[A/G]AAGCTTTATCTACGT | 8470 |
rs1031502 | snp | C/T | 0.488118 | 0.0761554 | intron-variant | SORBS2 | GRCh38.p7 | 4:185950810 | CTATGGCCTGCACGG[C/T]GGATATCTGCTCTTT | 8470 |
rs1031503 | snp | C/T | 0.39325 | 0.204889 | intron-variant | SORBS2 | GRCh38.p7 | 4:185950885 | GAAGGGAATAGGGTT[C/T]CCAGATGGTTCCAGA | 8470 |
rs1031504 | snp | A/G | 0.175897 | 0.238765 | intron-variant | SORBS2 | GRCh38.p7 | 4:185951535 | TCCCTGACATTGCAC[A/G]TTCAGGATTAGGCTC | 8470 |
rs1031505 | snp | A/C | 0.396546 | 0.202545 | intron-variant | SORBS2 | GRCh38.p7 | 4:185952690 | GTCCATCATGTATGC[A/C]GACAGCGTTAATTTT | 8470 |
rs1031506 | snp | A/C | 0.435407 | 0.167703 | intron-variant | SORBS2 | GRCh38.p7 | 4:185884560 | GAATGGCAATGAGGG[A/C]CCAGCAGAGCTGAGT | 8470 |
rs1038490 | snp | A/T | 0.434976 | 0.168179 | intron-variant | SORBS2 | GRCh38.p7 | 4:185648819 | tttctgtgtcatatc[A/T]tttgattccgagaac | 8470 |
rs1039233 | snp | A/G | 0.406296 | 0.19512 | intron-variant | SORBS2 | GRCh38.p7 | 4:185753102 | AGATGGAAATTGTTT[A/G]TGGCTAACGTGCTGT | 8470 |
rs1039235 | snp | A/T | 0.400325 | 0.199756 | intron-variant | SORBS2 | GRCh38.p7 | 4:185768859 | TTCACTCTGTAGCTG[A/T]CAATACCTTGATCTG | 8470 |
rs1039236 | snp | A/G | 0.399968 | 0.200024 | intron-variant | SORBS2 | GRCh38.p7 | 4:185767764 | CAGACCCTGTTACAC[A/G]GATGTAACTGAGAAG | 8470 |
rs1039237 | snp | A/G | 0.220843 | 0.248294 | intron-variant | SORBS2 | GRCh38.p7 | 4:185767613 | CTGTAAAATAATTGC[A/G]CCTATAATTTTATTT | 8470 |
rs1039238 | snp | A/G | 0.486855 | 0.0799975 | intron-variant | SORBS2 | GRCh38.p7 | 4:185825802 | CTGGAAACAAAAATT[A/G]TTTCATTAACCTCAG | 8470 |
rs1039239 | snp | C/T | 0.395818 | 0.203069 | intron-variant | SORBS2 | GRCh38.p7 | 4:185746657 | GGCCTGGTCTGGGAC[C/T]GCTAACTCCATTCCC | 8470 |
rs1039240 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SORBS2 | GRCh38.p7 | 4:185744920 | CTCTTCTGAGCCCCC[A/G]ATCCAAAAGAAGGCT | 8470 |
rs1039241 | snp | C/T | 0.341685 | 0.232581 | upstream-variant-2KB, intron-variant | SORBS2 | GRCh38.p7 | 4:185813505 | GCCTACCTTTTCTCA[C/T]TGAAGTTCCCTTCCC | 8470 |
rs1039242 | snp | C/T | 0.206947 | 0.246265 | intron-variant | SORBS2 | GRCh38.p7 | 4:185797170 | GTAGAGCTGTCTGTG[C/T]CGAAGACTGTTTGGC | 8470 |
rs1039243 | snp | A/G | 0.278399 | 0.248382 | intron-variant | SORBS2 | GRCh38.p7 | 4:185797340 | CGACACTATCATTTC[A/G]TAATCTTTTCTTGTG | 8470 |
rs1044197 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | SORBS2 | GRCh38.p7 | 4:185812115 | CAATGGGCATGTTAG[A/T]ATACAATGATCACAG | 8470 |
rs1044198 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | SORBS2 | GRCh38.p7 | 4:185812057 | GACAGGCTGTTGACT[C/G]CCGTTCCAATTAGCT | 8470 |
rs1044199 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | SORBS2 | GRCh38.p7 | 4:185812010 | ATGCAGAGTGATAAT[C/G]CTGCATATCTGCTAT | 8470 |
rs1044200 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | SORBS2 | GRCh38.p7 | 4:185811985 | TGCTATCAGGCAGCA[C/G]CAAAGGTTTTTGTCT | 8470 |
rs1044201 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | SORBS2 | GRCh38.p7 | 4:185811854 | CTGGTCCTGTGCGTG[C/G]CTGTGGCATATGAGC | 8470 |
rs1046236 | snp | C/T | 0.343701 | 0.231776 | utr-variant-3-prime | SORBS2 | GRCh38.p7 | 4:185586033 | AATTTGGTCTTTATC[C/T]TGCGACAACACTTTC | 8470 |
rs1048919 | snp | A/C | 0 | 0 | intron-variant, utr-variant-3-prime | SORBS2 | GRCh38.p7 | 4:185640056 | CACATCACTAAAAAC[A/C]CTGTGAGTATAATTT | 8470 |
rs1057181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SORBS2 | GRCh38.p7 | 4:185642485 | CATAAAAACTCTGCT[A/G]GGATTATATTACTAA | 8470 |
rs1058988 | snp | C/T | 0 | 0 | intron-variant | SORBS2 | GRCh38.p7 | 4:185809427 | CCCCTGAAGAGTCAT[C/T]TCCTTTAAATCTCCC | 8470 |
rs1059036 | snp | C/T | 0 | 0 | intron-variant | SORBS2 | GRCh38.p7 | 4:185730410 | TTAAAATAATACAGT[C/T]TATAATGAAGAAATT | 8470 |
rs1124024 | snp | A/G | 0.251859 | 0.249993 | intron-variant | SORBS2 | GRCh38.p7 | 4:185705068 | CACATACACAAACAC[A/G]TGTGCCCATGCACAG | 8470 |
rs1160906 | in-del | -/AACTC | 0.309103 | 0.242913 | intron-variant | SORBS2 | GRCh38.p7 | 4:185589629 | GGAGTGAGCAAACTC[-/AACTC]AAGCAAATTACAAAA | 8470 |
rs1353801 | snp | A/T | 0.0685596 | 0.171987 | intron-variant | SORBS2 | GRCh38.p7 | 4:185834286 | AGCCTGGTGGGAGGT[A/T]ATTGGCTCACGGGGG | 8470 |
rs1378149 | snp | C/T | 0.407845 | 0.193868 | intron-variant | SORBS2 | GRCh38.p7 | 4:185932875 | GATGTTTAAGGGTCA[C/T]TTTGTAAATTATCCT | 8470 |
rs1378150 | snp | A/G | 0.274661 | 0.248781 | intron-variant | SORBS2 | GRCh38.p7 | 4:185946315 | GCCTAGAAACCTATC[A/G]CAAGGTTATTGCCAT | 8470 |
rs1378151 | snp | C/T | 0.281577 | 0.247998 | intron-variant | SORBS2 | GRCh38.p7 | 4:185946359 | AAATGTGAGTGTGAG[C/T]GAAGGCAATGGTGAG | 8470 |
rs1391866 | snp | A/G | 0.030278 | 0.119257 | intron-variant | SORBS2 | GRCh38.p7 | 4:185828966 | CTGTGTTGTCCCATA[A/G]CATAGCAATGGGACC | 8470 |
rs1391867 | snp | C/T | 0.329783 | 0.236927 | intron-variant | SORBS2 | GRCh38.p7 | 4:185863168 | AAAAATGTTTAATGC[C/T]GTGTTTCCCCTAATG | 8470 |
rs1454745 | snp | A/G | 0.395818 | 0.203069 | intron-variant | SORBS2, LOC101928929 | GRCh38.p7 | 4:185909289 | AAGTGAAACAACTCA[A/G]AACGTCAAATACTTT | 8470 |
rs1471794 | snp | G/T | 0.498756 | 0.0249117 | intron-variant | SORBS2 | GRCh38.p7 | 4:185630470 | CATGATACTCATTAC[G/T]ACTTCACTGAATAAT | 8470 |
rs1471795 | snp | G/T | 0.460702 | 0.134554 | intron-variant | SORBS2 | GRCh38.p7 | 4:185634588 | TTTGCAGAGAGCAGG[G/T]TAACAAGCTTTTGAC | 8470 |
rs1499009 | snp | C/T | 0.495252 | 0.0484902 | intron-variant | SORBS2 | GRCh38.p7 | 4:185840982 | GACATGGCTCAGGTG[C/T]TACCTGCCCCAGGAC | 8470 |
rs1499010 | snp | G/T | 0.435694 | 0.167385 | intron-variant | SORBS2 | GRCh38.p7 | 4:185840484 | GATATTCTACAGACA[G/T]GTTTAGAGGAAATTA | 8470 |
rs1499011 | snp | A/G | 0.143959 | 0.226396 | intron-variant | SORBS2 | GRCh38.p7 | 4:185840439 | GATCAGCTATGCAAG[A/G]TACTAGCATAGTTAT | 8470 |
rs1499012 | snp | C/T | 0.473174 | 0.112665 | intron-variant | SORBS2 | GRCh38.p7 | 4:185838001 | CACAGACTTTCAGAC[C/T]AGAGGAAATGGAAGG | 8470 |
rs1499013 | snp | C/G | 0.309154 | 0.242901 | intron-variant | SORBS2 | GRCh38.p7 | 4:185836556 | GTTCATTGTGAAAAA[C/G]AAATGAGCGATTTCC | 8470 |
rs1499014 | snp | A/T | 0.078151 | 0.181571 | intron-variant | SORBS2 | GRCh38.p7 | 4:185829364 | TGCATTTCACACAGA[A/T]CTCATAGATACTATG | 8470 |
rs1499015 | snp | A/G | 0.167809 | 0.236103 | intron-variant | SORBS2 | GRCh38.p7 | 4:185858549 | AAAGGAAATGTGGCA[A/G]ATGGCAATCTGAAAT | 8470 |
rs1499016 | snp | A/C | 0.0178817 | 0.0928498 | intron-variant | SORBS2 | GRCh38.p7 | 4:185854807 | TAAGGCTCTCTCTCT[A/C]TCTCTCTCTCTCTCT | 8470 |
rs1499017 | snp | C/G | 0.193966 | 0.243639 | intron-variant | SORBS2 | GRCh38.p7 | 4:185779016 | CTGTGAAACACACAA[C/G]GCTCAGGTGCCGCCT | 8470 |
rs1499018 | snp | G/T | 0.206947 | 0.246265 | intron-variant | SORBS2 | GRCh38.p7 | 4:185773514 | AATCTCCAAAGGGGC[G/T]GAGCTGTGGAGAAAG | 8470 |
rs1540711 | snp | A/C | 0.219947 | 0.248187 | intron-variant | SORBS2 | GRCh38.p7 | 4:185710946 | AACAAGGATCCTATT[A/C]ATTAATTTGGGATAA | 8470 |
rs1542847 | snp | A/G | 0.142947 | 0.22592 | intron-variant | SORBS2 | GRCh38.p7 | 4:185700025 | CTGCAGAATCAATAA[A/G]CACACCACTTTGTTT | 8470 |
rs1547908 | snp | A/G | | | intron-variant | SORBS2 | GRCh38.p7 | 4:185701160 | GAGTTTATTTCTGTA[A/G]ATAAAAGGGGGAGAA | 8470 |
rs1547909 | snp | A/G | 0.360421 | 0.224293 | intron-variant | SORBS2 | GRCh38.p7 | 4:185701025 | CGTCAAATAAGTTAG[A/G]GTATTATGAAACAAC | 8470 |
rs1551435 | snp | C/G | 0.498589 | 0.02652 | intron-variant, downstream-variant-500B | SORBS2, LOC101928929 | GRCh38.p7 | 4:185919482 | ATATTATTCTCATTA[C/G]AGAGATCATGAAACT | 8470 |
rs1551436 | snp | G/T | 0.185472 | 0.241529 | intron-variant | SORBS2 | GRCh38.p7 | 4:185945426 | AGGTTAGGTCAAGGG[G/T]AGGCACATTTAATAG | 8470 |
rs1551437 | snp | C/G | 0.39325 | 0.204889 | intron-variant | SORBS2 | GRCh38.p7 | 4:185950792 | GACACTTTGGAAATC[C/G]CACTATGGCCTGCAC | 8470 |