| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs140860 | in-del | -/AATTA | | | intron-variant | SH3GL2 | GRCh38.p7 | 9:17740786 | ATAATCCCTTATTTA[-/AATTA]TGATTTTTGACAGTT | 6456 |
| rs717372 | snp | A/G | 0.330249 | 0.23677 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17699983 | GGAATGTAAACTGGT[A/G]CATCTATTCCAGAAT | 6456 |
| rs717373 | snp | A/G | 0.449473 | 0.150701 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17699911 | TTGATACAGCAACAT[A/G]ACTCCTGAGTGTTAG | 6456 |
| rs717374 | snp | A/T | 0.248755 | 0.249997 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17699849 | CATGTAAAGTGTTCA[A/T]CGTGACACTTTATAA | 6456 |
| rs720268 | snp | A/G | 0.399968 | 0.200024 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17738859 | cttcataatgtgggt[A/G]ggcctcatccaatca | 6456 |
| rs720269 | snp | A/T | 0.174288 | 0.23826 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17739212 | TGTTGACAAGGCCAA[A/T]GCAAGTCAATCAGGA | 6456 |
| rs723941 | snp | A/C | 0.289424 | 0.246872 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17638981 | ATTTTAAAGTACAAC[A/C]AGGGTTAATAATTGA | 6456 |
| rs726306 | snp | C/G | 0 | 0 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17766475 | CCCCGTAAGGCATCA[C/G]AATATGTAAAGAAAA | 6456 |
| rs727112 | snp | A/G | 0.132751 | 0.2208 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17751091 | GAAGGGATTTCCCAC[A/G]ATAATTTTCAGGCTG | 6456 |
| rs766311 | snp | A/G | 0.282632 | 0.247861 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17744568 | ACCAGCCTGGGCAAC[A/G]TAGTAAGACTCTGTC | 6456 |
| rs927300 | snp | A/T | 0.164873 | 0.23506 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17589046 | gtgtgtctgtatatt[A/T]atctatttgtgagct | 6456 |
| rs927301 | snp | C/T | 0.179744 | 0.239925 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17589206 | CTTTTGAAACTGTCG[C/T]CCAGGCTGGGGTATA | 6456 |
| rs941790 | snp | A/G | 0.264632 | 0.249571 | intron-variant, upstream-variant-2KB | SH3GL2 | GRCh38.p7 | 9:17615155 | TTATTGCACAATTTG[A/G]TGAATCAAAGGCTGA | 6456 |
| rs959113 | snp | C/G/T | 0 | 0 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17766216 | GCCTGTGATCCCGCT[C/G/T]ACACTTCCACATCTC | 6456 |
| rs961372 | snp | A/G | 0.48378 | 0.0885831 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17672279 | AAATCTTGGTTTCCA[A/G]GCAACCAAACACACA | 6456 |
| rs975696 | snp | C/T | 0.224709 | 0.248717 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17631145 | AAAAACCCGCAATTA[C/T]TTTTGCACCAACCTA | 6456 |
| rs975697 | snp | A/G | 0.225005 | 0.248747 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17631188 | ATATTTCACATTTGT[A/G]GGCTTGTTTCATCAA | 6456 |
| rs982019 | snp | A/G | 0.288646 | 0.246995 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17613442 | ATAACAACAATGGCA[A/G]TATTTTTGGCAAGAA | 6456 |
| rs982020 | snp | C/T | 0.203267 | 0.245593 | intron-variant, upstream-variant-2KB | SH3GL2 | GRCh38.p7 | 9:17613709 | TTTTATAATGCTCAT[C/T]ATGGGAGGTGACGGG | 6456 |
| rs997141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17601408 | AAAAACCACCAAAAA[C/T]GGAAACATGAGTCAT | 6456 |
| rs998599 | snp | A/G | 0.488606 | 0.0746142 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17700368 | CCCAGTAGCAAAACT[A/G]TAAATTCAGGGTCTT | 6456 |
| rs1000770 | snp | A/G | 0.49334 | 0.057322 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17700648 | TTATTCTTTAGAAAT[A/G]TTTCTCTATTCTGTG | 6456 |
| rs1001155 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17627446 | AAGGCCTGAAACTGT[A/G]ACCTTCTTGGCTATG | 6456 |
| rs1001265 | snp | C/G | 0.424225 | 0.186116 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17628728 | ATACAATTCTCCCTT[C/G]AGCTAGAAAAAAATC | 6456 |
| rs1004021 | snp | A/T | 0.339656 | 0.233371 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17627233 | CTGCAGGATGAAAAC[A/T]GGGAACAGGACAGGA | 6456 |
| rs1008730 | snp | C/T | 0.499933 | 0.00579035 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17602498 | CCAATCTCCTGGAGA[C/T]GGGGGTGAAAGAGGC | 6456 |
| rs1010547 | snp | A/G | 0.400504 | 0.199621 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17599513 | TTAAGGTACTTCTTG[A/G]AATTTATCACAAGTA | 6456 |
| rs1010548 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17599618 | TCATATGATGGAGTT[C/T]TATGAGGCAAATGAT | 6456 |
| rs1022718 | snp | A/G | 0.495445 | 0.0475058 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17595871 | ACCAGGCGTTATGCT[A/G]TATTGTTACAGTAAG | 6456 |
| rs1028594 | snp | A/G | 0.448963 | 0.151372 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17583312 | gaagcttgactgcca[A/G]tgtgacagtattaag | 6456 |
| rs1028595 | snp | A/G | 0.220843 | 0.248294 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17612244 | AGGAAAAGCCCTTCC[A/G]GGAGTGTGCCTGAGT | 6456 |
| rs1033749 | snp | A/G | 0.24134 | 0.24985 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17583290 | gtccctctaaaatac[A/G]tatgttgaagcttga | 6456 |
| rs1049429 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | SH3GL2 | GRCh38.p7 | 9:17796652 | AAACACTAGTAACCA[A/T]CTTTCCACTAGTTCA | 6456 |
| rs1049430 | snp | G/T | 0.454061 | 0.144427 | utr-variant-3-prime, nc-transcript-variant | SH3GL2 | GRCh38.p7 | 9:17796670 | TTCCACTAGTTCATA[G/T]ACTGAGAAACAGTAA | 6456 |
| rs1073417 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | SH3GL2 | GRCh38.p7 | 9:17614114 | AAAGAAATCTGTGAA[A/G]AAAGCATGTCCCCTC | 6456 |
| rs1114790 | snp | C/T | 0.167809 | 0.236103 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17748813 | CTTGACAATGCAGTA[C/T]GGGTGAGTTTCCTCT | 6456 |
| rs1114791 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17748699 | TACGAACTTCATGCA[C/T]TCAGGAACCTTGTCT | 6456 |
| rs1467546 | snp | G/T | 0.365024 | 0.221967 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17627333 | AGAGCTAGCTTGATC[G/T]TTGGGGAATAATGGC | 6456 |
| rs1467547 | snp | A/G | 0.225005 | 0.248747 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17630729 | TATTCTGGAGCTCAA[A/G]TATTTCCTGTTCATT | 6456 |
| rs1535346 | snp | G/T | 0.499954 | 0.00479211 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17602003 | CATTTTAAGGGCATT[G/T]CAGAAAGCCTTCTGG | 6456 |
| rs1536064 | snp | A/G | 0.489376 | 0.0721049 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17655332 | TCCCTCCCTCTTCCT[A/G]TGCCCAACTGGTAAG | 6456 |
| rs1536065 | snp | A/G | 0.483272 | 0.0899109 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17655746 | CTAGCCCCGTGCATC[A/G]TTTTTGAGCACATTT | 6456 |
| rs1536066 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17735907 | ACCCTGTGGGGGCAG[C/T]GGACAAGTACAGTTC | 6456 |
| rs1536067 | snp | C/G | 0.430732 | 0.172731 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17737895 | TTCTGTGTAATAAAG[C/G]TTCTTCCCTAATCCC | 6456 |
| rs1536068 | snp | A/G | 0.318415 | 0.240457 | utr-variant-3-prime, nc-transcript-variant | SH3GL2 | GRCh38.p7 | 9:17795942 | CTTAGCCTGGTGGGC[A/G]TGGCATGTGCTTTTT | 6456 |
| rs1536069 | snp | G/T | 0.499087 | 0.0213463 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17695452 | ACACATAAGGAGTAA[G/T]TGGATTATTTTCCCT | 6456 |
| rs1536070 | snp | A/G | 0.283947 | 0.247685 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17701787 | ATATAACACATGTAT[A/G]ATTTTTCCTAGAAAA | 6456 |
| rs1536071 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17701806 | tttcctagaaaaaga[C/G]atgagaaacagaaaa | 6456 |
| rs1536072 | snp | C/G | 0.36021 | 0.224397 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17701891 | TTTCTCTAAGTTAAA[C/G]TGTAAATGTAATGTG | 6456 |
| rs1536073 | snp | A/G | 0.45235 | 0.146814 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17702076 | ACATAGTGTATTACT[A/G]GTTCATGAAGAAACA | 6456 |
| rs1536074 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17721797 | cagcctccgtaacac[A/T]tgagccaattcccct | 6456 |
| rs1536075 | snp | C/T | 0.489722 | 0.0709447 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17722469 | GCACTCTAAACCTTT[C/T]GTGATTGAGTGTGGC | 6456 |
| rs1536076 | snp | G/T | 0.359998 | 0.2245 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17731923 | ACATACAAAAGACAT[G/T]CAGTGACTATTTTTA | 6456 |
| rs1536077 | snp | G/T | 0.0535932 | 0.154675 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17731973 | TTAGAAGGTAGTCAG[G/T]TTCTGACCTGTGATG | 6456 |
| rs1536078 | snp | C/T | 0.453331 | 0.145452 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17732140 | TCATCATATTCTCAA[C/T]AACAATCATAACAGC | 6456 |
| rs1536079 | snp | C/T | 0.401215 | 0.199083 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17733887 | AAAAAAACCAAACAC[C/T]GCATATTCTCACTGA | 6456 |
| rs1536080 | snp | A/C | 0.401037 | 0.199218 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17734064 | AAATGCACTCTCAGT[A/C]GAGAATTGCATTTTG | 6456 |
| rs1543479 | snp | C/T | 0.460027 | 0.135605 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17604936 | TAGAGCCTGGTATAG[C/T]TTGAGTCAGGGACAG | 6456 |
| rs1548263 | snp | C/G | 0.47885 | 0.100637 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17605242 | TCTTGGCCTCCCAAA[C/G]TACTGGCATTACAGA | 6456 |
| rs1555421 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17599649 | GTGATCTACATTCAC[A/G]TGGAAACCTTTCTTT | 6456 |
| rs1555422 | snp | A/C | 0.340108 | 0.233197 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17621967 | AGTTTTCCACAGTGA[A/C]TGTTCCTAGTTTGTG | 6456 |
| rs1570782 | snp | A/C | 0.16028 | 0.233346 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17684820 | TCAACCCAGATTCCT[A/C]TGTCCTTCAAAATAT | 6456 |
| rs1570783 | snp | A/G | 0.15698 | 0.23205 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17702027 | AACTAGCCCTAATAT[A/G]TATTTAAAAACATTA | 6456 |
| rs1885166 | snp | C/T | 0.44546 | 0.155869 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17610213 | ATGCACATAAGTGTC[C/T]GGCGTAGAGTAAGTG | 6456 |
| rs1886587 | snp | C/T | 0.133093 | 0.220981 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17751805 | CCATAATGTCTCCTT[C/T]ATGGTGTGATGGGAA | 6456 |
| rs1886588 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17751978 | ACATGTTTGCAATAT[A/G]TAGTTCCAAGCTTAT | 6456 |
| rs1886589 | snp | C/T | 0.495927 | 0.0449436 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17761381 | GACTCAACCAAAAAC[C/T]GGTATTCTAAAGCTC | 6456 |
| rs1998246 | snp | A/G | 0.469445 | 0.119766 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17631210 | TTTCATCAACGGAGC[A/G]GTTTCCAAGGCTTCA | 6456 |
| rs1998247 | snp | A/C | 0.428786 | 0.174744 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17631554 | TTTCTATCCTGGAGA[A/C]AACAAAGCCCATCAT | 6456 |
| rs1998248 | snp | A/G | 0.417845 | 0.185278 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17635691 | GCTCTGAGTGTACAC[A/G]ACAGAGGAAATCTGG | 6456 |
| rs2025557 | snp | A/G | 0.493613 | 0.0561475 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17726583 | GAAGAACTACTACAC[A/G]ACACACGAATAAGAA | 6456 |
| rs2025558 | snp | A/G | 0.491783 | 0.0635686 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17726724 | AAAGATATTCCACCT[A/G]TCAGGAATATGACAT | 6456 |
| rs2025559 | snp | A/C | 0.498084 | 0.0308911 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17660561 | TCTATTAGGCTGCTG[A/C]TGATGTAGTGAAGAG | 6456 |
| rs2031456 | snp | A/G | 0.425894 | 0.177655 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17747281 | CTACTTTTCATGTAT[A/G]TTTTAAAACATAAAA | 6456 |
| rs2038518 | snp | C/T | 0.235273 | 0.249566 | intron-variant, upstream-variant-2KB | SH3GL2 | GRCh38.p7 | 9:17615603 | GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 6456 |
| rs2038519 | snp | G/T | 0.492533 | 0.0606443 | intron-variant, utr-variant-5-prime, nc-transcript-variant | SH3GL2 | GRCh38.p7 | 9:17615941 | GATAGAAAAATTGTT[G/T]TTCTGTGAATGAGAA | 6456 |
| rs2038520 | snp | A/T | 0.499996 | 0.00139776 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17618659 | GGCTTGGGGCTTTAT[A/T]TAGTAAATATGCTGT | 6456 |
| rs2038521 | snp | C/T | 0.450609 | 0.149185 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17640024 | aactttttagggtga[C/T]agtattattattaat | 6456 |
| rs2104099 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17592966 | atcagtcatgcctat[A/G]taatgaagcctccat | 6456 |
| rs2145656 | snp | C/T | 0.322483 | 0.239262 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17608786 | GAGGTTGAAATTAGG[C/T]AGGGGGAACATGAAT | 6456 |
| rs2145657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17608817 | TATTTTCTGTAACGT[A/G]CAAGTGGAAACAATT | 6456 |
| rs2145658 | snp | C/T | 0.328616 | 0.237317 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17608818 | ATTTTCTGTAACGTA[C/T]AAGTGGAAACAATTT | 6456 |
| rs2145659 | snp | A/G | 0.416218 | 0.186739 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17609304 | TCTGGATATTTTGCA[A/G]AGAAAGTTTGAGACT | 6456 |
| rs2145660 | snp | C/T | 0 | 0 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17609991 | TCAAGGACTCATTTG[C/T]TAAGTTAGGGGCAGA | 6456 |
| rs2147729 | snp | A/G | 0.488905 | 0.0736498 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17669944 | GGGTCCCAGAAAAAG[A/G]GTTGCCATCCTGTAG | 6456 |
| rs2147730 | snp | A/C | 0.496034 | 0.0443518 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17656788 | AAAAAAAAAAAAAAA[A/C]AAAAAAGGCTTTTCT | 6456 |
| rs2147731 | snp | A/G | 0.156319 | 0.231784 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17705014 | atgcaacaaaggtct[A/G]atatccagaatttat | 6456 |
| rs2147732 | snp | A/C | 0.245916 | 0.249967 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17705060 | acaaacaaaaaaaaa[A/C]cccattaaaaaatgc | 6456 |
| rs2147733 | snp | A/G | 0.21725 | 0.247846 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17713933 | tctactatgtatctg[A/G]caattttctgtccat | 6456 |
| rs2147734 | snp | G/T | 0 | 0 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17716344 | GTTCTGGGACACAGC[G/T]AAATTACATGGAAAC | 6456 |
| rs2147735 | snp | G/T | 0.437824 | 0.164991 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17658672 | GCATAGCAGGCTTTT[G/T]GCTGTGTATTTATTG | 6456 |
| rs2147736 | snp | A/G | 0.472429 | 0.114129 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17658702 | GGGAGGAGAGCTGTT[A/G]GAAATTACAGAGCTG | 6456 |
| rs2180902 | snp | C/G | 0.307919 | 0.243198 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17608993 | TACAGGTGATCCGCT[C/G]TTTCACTGATCCCAG | 6456 |
| rs2180905 | snp | A/G | 0.433236 | 0.170072 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17593260 | CCTGATTTATAGCTG[A/G]TAGGTTAGAAGCACA | 6456 |
| rs2182082 | snp | A/G | 0.305186 | 0.243833 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17784120 | CAGATATGTGAATTA[A/G]TAGGCTTTTTTTAAT | 6456 |
| rs2182083 | snp | C/T | 0.479177 | 0.0998894 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17670335 | TTCTTGGGCTGCTTT[C/T]TGTTAGAAGGGAAGT | 6456 |
| rs2182084 | snp | C/G | 0.474634 | 0.109726 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17683497 | GGAAAATTGCTGTAC[C/G]TTTGGAGGAGGGTCA | 6456 |
| rs2182085 | snp | G/T | 0.432944 | 0.170387 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17655772 | CATTTGAACATGTCT[G/T]ATCCATGTAGTCTGA | 6456 |
| rs2182086 | snp | C/T | 0.481703 | 0.0938806 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17656413 | TTTTTTTACTGGAGA[C/T]GAGAGTTCCATAATT | 6456 |
| rs2182087 | snp | A/G | 0.472241 | 0.114494 | intron-variant | SH3GL2 | GRCh38.p7 | 9:17656902 | TCCAGAAACACTTAA[A/G]AAGTTCTTATAGTGA | 6456 |