SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1133478 | snp | A/T | 0.330947 | 0.236533 | utr-variant-3-prime, nc-transcript-variant | STAM2 | GRCh38.p7 | 2:152117740 | CTTAGGGATTTTTTT[A/T]AAAAAGGTTTTCTTA | 10254 |
rs1137674 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | STAM2 | GRCh38.p7 | 2:152120020 | AAATATGCTGGCAAG[C/G/T]TAAATGCTTACACAC | 10254 |
rs2002247 | snp | C/T | 0.345482 | 0.231048 | intron-variant | STAM2 | GRCh38.p7 | 2:152169064 | CACCACACTCAGCCC[C/T]GAAGCCTTTCTTAAG | 10254 |
rs2345639 | snp | A/G | 0.39979 | 0.200158 | intron-variant, upstream-variant-2KB | STAM2, LOC105373689 | GRCh38.p7 | 2:152174599 | GCACATCTCAGCAGT[A/G]ATTCCCCTGTTTCAT | 10254 |
rs2345640 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | STAM2 | GRCh38.p7 | 2:152169337 | gtgagccatgattgc[A/G]tcactgcactccagc | 10254 |
rs2345641 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | STAM2 | GRCh38.p7 | 2:152169151 | TTCTGTTTGTTTCTG[C/G]TGTCTTTTATTGTAA | 10254 |
rs3045386 | in-del | -/AT | | | intron-variant | STAM2 | GRCh38.p7 | 2:152132787 | TGTTAACTTCATAAC[-/AT]AGTCAATTGATGCAT | 10254 |
rs3768648 | snp | A/G | 0.323434 | 0.238972 | intron-variant | STAM2 | GRCh38.p7 | 2:152146898 | GCAAAAGGCATAGGT[A/G]TATGACATACCCCTT | 10254 |
rs3768649 | snp | C/G | 0.367091 | 0.220884 | intron-variant | STAM2 | GRCh38.p7 | 2:152146590 | CAAGACTTGTTTGTT[C/G]AAGAGTGAATATGCC | 10254 |
rs3768650 | snp | C/T | 0.490119 | 0.0695896 | intron-variant | STAM2 | GRCh38.p7 | 2:152134418 | TATAATTTTATTCCT[C/T]TTAACTGACTCTCTA | 10254 |
rs3768651 | snp | A/C | 0.328507 | 0.240584 | intron-variant | STAM2 | GRCh38.p7 | 2:152134207 | TTGAAATAAATGACT[A/C]ACAGTTGGGATTTAA | 10254 |
rs3820702 | snp | A/T | 0.490007 | 0.0699769 | intron-variant | STAM2 | GRCh38.p7 | 2:152124339 | TTGGATGAGTCATCC[A/T]GGGATGAGGGTAAAG | 10254 |
rs3835745 | in-del | -/A | 0.393065 | 0.205018 | intron-variant | STAM2 | GRCh38.p7 | 2:152135402 | TAACTTTTGTTTTAA[-/A]TCATTTCTTTATAGG | 10254 |
rs3835746 | in-del | -/C | 0.367503 | 0.220665 | intron-variant | STAM2 | GRCh38.p7 | 2:152134105 | ATTCTAGCAATACTC[-/C]AGGGAACATTTAAAT | 10254 |
rs3963509 | snp | C/T | 0.416545 | 0.186448 | intron-variant | STAM2 | GRCh38.p7 | 2:152161260 | aagcacatcttgcac[C/T]gcccttaatccattc | 10254 |
rs4036223 | snp | C/G | 0.322959 | 0.239117 | intron-variant | STAM2 | GRCh38.p7 | 2:152161307 | GGTGATGACTCTTAA[C/G]GAGCATGCTGCCTTC | 10254 |
rs4036224 | snp | A/G | 0.323197 | 0.239044 | intron-variant | STAM2 | GRCh38.p7 | 2:152161278 | TCAAGCATCTGTTTA[A/G]CAAAGCACATCTTGC | 10254 |
rs4368329 | snp | A/G | 0.34101 | 0.232846 | upstream-variant-2KB, nc-transcript-variant | STAM2, LOC105373689 | GRCh38.p7 | 2:152176079 | GGCGCGGTTACCCGT[A/G]GTTTTTCGCGTTGGA | 10254 |
rs4471888 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | STAM2 | GRCh38.p7 | 2:152128022 | GATTTGTCACTTTTC[C/T]TCTACTAGAGTCTGT | 10254 |
rs4473376 | snp | C/T | 0.367708 | 0.220556 | intron-variant | STAM2 | GRCh38.p7 | 2:152128051 | GTTATGTCTGAACTA[C/T]AACAACGAAAAGTCT | 10254 |
rs4611639 | snp | C/G | 0.324619 | 0.238604 | intron-variant | STAM2 | GRCh38.p7 | 2:152168516 | ACAAAAGCCATGCTA[C/G]AGACACATCCACCTA | 10254 |
rs4664079 | snp | A/C | 0.499673 | 0.0127754 | intron-variant | STAM2 | GRCh38.p7 | 2:152121770 | ATACTTTTGGCTGGA[A/C]GCGGTGGCTCACACC | 10254 |
rs4664080 | snp | A/G | 0.421526 | 0.181876 | intron-variant | STAM2 | GRCh38.p7 | 2:152121827 | AGGAGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 10254 |
rs4664081 | snp | A/C | 0.0759472 | 0.179459 | intron-variant | STAM2 | GRCh38.p7 | 2:152122049 | TGAGACTCCGTCCCC[A/C]AAAAAAAAATATATA | 10254 |
rs4664082 | snp | A/G | 0.49975 | 0.0111793 | intron-variant | STAM2 | GRCh38.p7 | 2:152135998 | GGGAGGCTGAGGCAG[A/G]AGAATCGCTTAAACC | 10254 |
rs4664083 | snp | C/T | 0.392325 | 0.205532 | intron-variant | STAM2 | GRCh38.p7 | 2:152164693 | TATATTTAAGAGCTG[C/T]TTCCTCTGATGGAAT | 10254 |
rs4664084 | snp | C/T | 0.345482 | 0.231048 | intron-variant | STAM2 | GRCh38.p7 | 2:152165557 | CCATTATGCACACTC[C/T]GTATGCACCTGTGGA | 10254 |
rs4664085 | snp | G/T | 0.343924 | 0.231686 | intron-variant | STAM2 | GRCh38.p7 | 2:152167236 | AAAGGCCTCCCTGAA[G/T]GCAACAGAGATCGCC | 10254 |
rs4664530 | snp | C/T | 0.368119 | 0.220336 | intron-variant | STAM2 | GRCh38.p7 | 2:152122525 | CCAGTTTTTTCTCCA[C/T]AGTTCCTAGTGTTAC | 10254 |
rs4664531 | snp | C/T | 0.384209 | 0.210922 | intron-variant | STAM2 | GRCh38.p7 | 2:152129527 | AATAAGATTAAATTG[C/T]CATAGTTTCTGCCTT | 10254 |
rs4664532 | snp | C/T | 0.296873 | 0.245566 | intron-variant | STAM2 | GRCh38.p7 | 2:152136897 | AAACATTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 10254 |
rs4664533 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | STAM2 | GRCh38.p7 | 2:152143481 | CAAGGGTATATTGCT[A/G]TATTTCTTCCTAAAG | 10254 |
rs4664534 | snp | C/T | 0.490063 | 0.0697833 | intron-variant | STAM2 | GRCh38.p7 | 2:152144607 | ACAGTGGTGCCATCT[C/T]GGCTCACTGCAACCT | 10254 |
rs4664535 | snp | A/G | 0.367503 | 0.220665 | intron-variant | STAM2 | GRCh38.p7 | 2:152147739 | AATCTAATGCTCCAA[A/G]GGTAGTTAAGAGCAT | 10254 |
rs4664536 | snp | A/C | 0.418007 | 0.185132 | intron-variant | STAM2 | GRCh38.p7 | 2:152147871 | GTTTTTGGTGCTACA[A/C]ATTAAAAAATCAAAT | 10254 |
rs4664537 | snp | C/T | 0.367708 | 0.220556 | intron-variant | STAM2 | GRCh38.p7 | 2:152148453 | GGCGGGAGGATCACT[C/T]GAGCCCATGAATTTG | 10254 |
rs4664540 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | STAM2 | GRCh38.p7 | 2:152170028 | TTTTCAGTAGAGACA[C/G]GTTTCATCATGTTGG | 10254 |
rs5835408 | in-del | -/T | 0.490569 | 0.0680199 | intron-variant | STAM2 | GRCh38.p7 | 2:152132096 | TATACTTTTTATTCC[-/T]TGCACGAAAAATCTC | 10254 |
rs5835409 | in-del | -/TA | 0.400504 | 0.199621 | intron-variant | STAM2 | GRCh38.p7 | 2:152132786 | CATGCATCAATTGAC[-/TA]TGTTATGAAGTTAAC | 10254 |
rs6650771 | snp | A/G | 0.418007 | 0.185132 | intron-variant | STAM2 | GRCh38.p7 | 2:152152617 | GCGATGAACATTCAT[A/G]TACAAGTCTCTGTGT | 10254 |
rs6650779 | snp | A/G | 0.367708 | 0.220556 | intron-variant | STAM2 | GRCh38.p7 | 2:152150520 | AAAGATGTATAATCC[A/G]GGCCGGGCATGGTGG | 10254 |
rs6711725 | snp | A/C | | | intron-variant | STAM2 | GRCh38.p7 | 2:152123409 | TGAACTACAAATTCC[A/C]CAGTTCAAACGCCCT | 10254 |
rs6726066 | snp | C/T | 0.0356815 | 0.128715 | upstream-variant-2KB, intron-variant | STAM2, LOC105373689 | GRCh38.p7 | 2:152176704 | TGGTCACTACTATAT[C/T]CCCAGCGTCTAAAAC | 10254 |
rs6731625 | snp | A/G | 0.420096 | 0.183214 | intron-variant | STAM2 | GRCh38.p7 | 2:152164098 | acttgctgattttgc[A/G]gctctggtggggcat | 10254 |
rs6738680 | snp | A/G | 0.415727 | 0.187175 | intron-variant | STAM2 | GRCh38.p7 | 2:152167599 | AAAAACACTTTTAAA[A/G]ACTTTGTAACTTAGG | 10254 |
rs6740224 | snp | A/C | 0.48818 | 0.0759629 | upstream-variant-2KB, nc-transcript-variant | STAM2, LOC105373689 | GRCh38.p7 | 2:152176276 | GACTGCTCTTCAACA[A/C]TTATTGTGTTGCACC | 10254 |
rs6747861 | snp | C/T | 0.110519 | 0.207473 | intron-variant | STAM2 | GRCh38.p7 | 2:152147700 | TTTATAAAATAAGAA[C/T]GATAAGGGAATCTAA | 10254 |
rs6750749 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM2 | GRCh38.p7 | 2:152170642 | gtagtatagtatcac[A/G]cagccattaaaattt | 10254 |
rs6753703 | snp | C/T | 0.110872 | 0.20771 | intron-variant | STAM2 | GRCh38.p7 | 2:152144081 | AACATTAGATGACAA[C/T]GTAAAATTTAATAAG | 10254 |
rs6757260 | snp | G/T | 0.0337553 | 0.125452 | upstream-variant-2KB, intron-variant | STAM2, LOC105373689 | GRCh38.p7 | 2:152177242 | ggcatggtggcgcaa[G/T]cctgtaatgccaact | 10254 |
rs7369093 | snp | A/G | 0.490063 | 0.0697833 | intron-variant | STAM2 | GRCh38.p7 | 2:152159999 | gcctcccgaggtgcc[A/G]ggattgcagacggag | 10254 |
rs7371111 | snp | A/T | 0.49931 | 0.0185575 | intron-variant | STAM2 | GRCh38.p7 | 2:152173406 | TACATATATATATAT[A/T]TTTTTTTTCGAGACG | 10254 |
rs7420568 | snp | C/T | | | intron-variant | STAM2 | GRCh38.p7 | 2:152153885 | CTTCCAGACATTaca[C/T]acacacacacacaca | 10254 |
rs7590270 | snp | A/G | 0.116838 | 0.211584 | upstream-variant-2KB, intron-variant | STAM2, LOC105373689 | GRCh38.p7 | 2:152176997 | GTGGTTGCATTTTAT[A/G]AAGTTCGGGGCACAA | 10254 |
rs7598163 | snp | C/T | 0.039522 | 0.134904 | intron-variant | STAM2 | GRCh38.p7 | 2:152128000 | AGCCTGGACTGAGTC[C/T]TATCAAGATTTGTCA | 10254 |
rs7600978 | snp | C/T | 0.111576 | 0.20818 | intron-variant | STAM2 | GRCh38.p7 | 2:152173395 | atatatatgtataca[C/T]atatatatatatttt | 10254 |
rs7603232 | snp | C/T | 0.417683 | 0.185425 | intron-variant | STAM2 | GRCh38.p7 | 2:152124869 | GTAGCCTACACAATA[C/T]AACTAATGTGTTACC | 10254 |
rs7605123 | snp | C/G | 0.0633504 | 0.166319 | upstream-variant-2KB, intron-variant | STAM2, LOC105373689 | GRCh38.p7 | 2:152177179 | ttcaagaccagactg[C/G]ctaacatggcgaaaa | 10254 |
rs7605808 | snp | C/G | 0.0419574 | 0.139363 | utr-variant-3-prime, nc-transcript-variant | STAM2 | GRCh38.p7 | 2:152117596 | GAAAAAGTACCTTCC[C/G]ATAGAAATAAAGCAT | 10254 |
rs9917176 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | STAM2 | GRCh38.p7 | 2:152162913 | gatctgcccgcctca[C/G]cctcccaaagtgctg | 10254 |
rs9917198 | snp | G/T | 0.366679 | 0.221102 | intron-variant | STAM2 | GRCh38.p7 | 2:152163610 | ctgactgcctgcggg[G/T]tagggcaaaaagagc | 10254 |
rs9917346 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | STAM2 | GRCh38.p7 | 2:152163350 | agttcccaaataata[C/G]tcttataatttctta | 10254 |
rs10166701 | snp | C/T | 0.111576 | 0.20818 | intron-variant | STAM2 | GRCh38.p7 | 2:152142082 | GTTTGCATTTGTCTA[C/T]CAGCGATTACCAATC | 10254 |
rs10177222 | snp | C/T | 0.367091 | 0.220884 | intron-variant | STAM2 | GRCh38.p7 | 2:152146113 | CGTCTCTACTAAAAA[C/T]ACAAAAAATTAGCCG | 10254 |
rs10178907 | snp | A/C | 0.490063 | 0.0697833 | intron-variant | STAM2 | GRCh38.p7 | 2:152156790 | TCTATCAGTAATAAA[A/C]AACTTAACTACATAA | 10254 |
rs10182220 | snp | G/T | 0.496874 | 0.0394129 | intron-variant | STAM2 | GRCh38.p7 | 2:152145280 | CACTATGTTTCCTGG[G/T]CTGATCTGCAACTCT | 10254 |
rs10184862 | snp | A/G | 0.499872 | 0.0079862 | intron-variant | STAM2 | GRCh38.p7 | 2:152149330 | CTCTTTTTCATGTAA[A/G]TTAATCCCATAAATC | 10254 |
rs10187630 | snp | C/T | 0.367708 | 0.220556 | intron-variant | STAM2 | GRCh38.p7 | 2:152149525 | TTTTTTGAGACAGAG[C/T]CTCGCTCTACCGTCC | 10254 |
rs10194016 | snp | A/G | 0 | 0 | intron-variant | STAM2 | GRCh38.p7 | 2:152133362 | ATAGTACATTTAAAT[A/G]TCTTGATAGTTTAAC | 10254 |
rs10200655 | snp | A/T | 0.484632 | 0.086302 | utr-variant-3-prime, nc-transcript-variant | STAM2 | GRCh38.p7 | 2:152118446 | ATATATACTATATAT[A/T]TATATATATATATAT | 10254 |
rs10202920 | snp | C/T | 0.110519 | 0.207473 | intron-variant | STAM2 | GRCh38.p7 | 2:152123646 | GGTAACACCATTCCA[C/T]TTCACAGGATTATGA | 10254 |
rs10203589 | snp | C/T | 0.110872 | 0.20771 | intron-variant | STAM2 | GRCh38.p7 | 2:152124954 | ATATTTCAAATGCTC[C/T]TGAGTGAACAGTGTA | 10254 |
rs10209826 | snp | C/T | 0.110872 | 0.20771 | intron-variant | STAM2 | GRCh38.p7 | 2:152126570 | ATAGCTAGGCTGATA[C/T]tgaggcaggagaata | 10254 |
rs10427181 | snp | C/G | 0.418491 | 0.184691 | intron-variant | STAM2 | GRCh38.p7 | 2:152166646 | TATCAGGTAACTTAA[C/G]AGAACCTAATAAGGT | 10254 |
rs10469642 | snp | G/T | 0.323908 | 0.238825 | intron-variant | STAM2 | GRCh38.p7 | 2:152125910 | CCATATTTACAAAAA[G/T]GATTTATGTTTACAT | 10254 |
rs10497094 | snp | C/G | 0.387642 | 0.208697 | utr-variant-3-prime, nc-transcript-variant | STAM2 | GRCh38.p7 | 2:152119488 | TTAGCAACGGTACTT[C/G]AATCACCTCTTTAAA | 10254 |
rs10497095 | snp | A/G | 0.345037 | 0.231231 | intron-variant | STAM2 | GRCh38.p7 | 2:152121474 | GCCCTGGCTCAAGAT[A/G]CCACTTTCAGCCCAT | 10254 |
rs10497096 | snp | C/T | 0.345925 | 0.230864 | intron-variant | STAM2 | GRCh38.p7 | 2:152168591 | TCATTCTCTTCTTGA[C/T]TTACTTACAAATTAT | 10254 |
rs10497097 | snp | A/G | 0.34303 | 0.232046 | intron-variant, upstream-variant-2KB | STAM2, LOC105373689 | GRCh38.p7 | 2:152174355 | AGAATACTGCAATGA[A/G]GCGTTCCAAAAGGAA | 10254 |
rs10524193 | in-del | -/AT/ATATATAT | 0.229429 | 0.249152 | intron-variant | STAM2 | GRCh38.p7 | 2:152159094 | AGCCAAAAAAAAACC[-/AT/ATATATAT]ATATATATATATATA | 10254 |
rs10580213 | snp | A/G | 0.347253 | 0.230308 | intron-variant | STAM2 | GRCh38.p7 | 2:152122076 | tatatatatatatat[A/G]tgtgtgtgtgtgtgt | 10254 |
rs10627182 | in-del | -/ACAG | 0.0138799 | 0.0821421 | intron-variant | STAM2 | GRCh38.p7 | 2:152136620 | CAAGTCCATATAGAA[-/ACAG]AACAGACACAGATGC | 10254 |
rs10714838 | in-del | -/A | | | intron-variant | STAM2 | GRCh38.p7 | 2:152161516 | AAAAAAAAAAAAAAA[-/A]CATTATATATACTTA | 10254 |
rs10718793 | in-del | -/A | 0.5 | 0 | intron-variant | STAM2 | GRCh38.p7 | 2:152161495 | AAAAAAAAAAAAAAA[-/A]ACATTATATATACTT | 10254 |
rs10803946 | snp | A/C | 0.482309 | 0.0923707 | upstream-variant-2KB, intron-variant | STAM2, LOC105373689 | GRCh38.p7 | 2:152177003 | GCATTTTATAAAGTT[A/C]GGGGCACAAATGAGA | 10254 |
rs10930939 | snp | C/T | 0.421526 | 0.181876 | intron-variant | STAM2 | GRCh38.p7 | 2:152123419 | ATTCCACAGTTCAAA[C/T]GCCCTTCTTAAGGGT | 10254 |
rs10930958 | snp | C/T | 0.416055 | 0.186885 | intron-variant | STAM2 | GRCh38.p7 | 2:152152895 | CAAACTTGAGGGGGG[C/T]TCAAAAGAAGACAGG | 10254 |
rs10930959 | snp | A/G | 0.367708 | 0.220556 | intron-variant | STAM2 | GRCh38.p7 | 2:152152955 | AGTTGTACAGTATGT[A/G]TGTAGAAAATATTTT | 10254 |
rs10930967 | snp | C/T | 0.47885 | 0.100637 | upstream-variant-2KB, intron-variant | STAM2, LOC105373689 | GRCh38.p7 | 2:152177106 | GGGCATGGTGGCTCA[C/T]GCATGTAATCCCAGC | 10254 |
rs10930968 | snp | A/T | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | STAM2, LOC105373689 | GRCh38.p7 | 2:152177951 | atcccttcgtttccc[A/T]taagggatactttta | 10254 |
rs11300791 | in-del | -/A | 0 | 0 | intron-variant | STAM2 | GRCh38.p7 | 2:152130996 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 10254 |
rs11384182 | in-del | -/A | 0.490673 | 0.0676508 | intron-variant | STAM2 | GRCh38.p7 | 2:152167731 | ATTTCTAGAAAAAAA[-/A]TAAATAAATAAATAA | 10254 |
rs11424941 | in-del | -/T | 0.456568 | 0.140818 | intron-variant | STAM2 | GRCh38.p7 | 2:152162807 | ATTTTTTTTTTTTTT[-/T]AATTTTTGTATTTTT | 10254 |
rs11673722 | snp | C/T | 0 | 0 | intron-variant | STAM2 | GRCh38.p7 | 2:152131376 | aagaattgcttgaac[C/T]ggggaggcagaggtt | 10254 |
rs11673814 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | STAM2 | GRCh38.p7 | 2:152159940 | ttcgctgtgttggcc[A/G]ggctggtctccagct | 10254 |
rs11683326 | snp | C/T | 0.178465 | 0.239547 | intron-variant | STAM2 | GRCh38.p7 | 2:152173365 | GCGtatatacacaca[C/T]atatatacatatata | 10254 |
rs11684002 | snp | A/G | 0.180383 | 0.240111 | intron-variant | STAM2 | GRCh38.p7 | 2:152141212 | TGTAGAAAGTAAAAC[A/G]CTTTTCTTGATATAC | 10254 |
rs11684622 | snp | C/G | 0.178785 | 0.239642 | intron-variant | STAM2 | GRCh38.p7 | 2:152131755 | TTGGCCAAAACTGCT[C/G]TCCATCACTACAGTG | 10254 |
rs11693948 | snp | A/T | 0.478354 | 0.101757 | utr-variant-3-prime, nc-transcript-variant | STAM2 | GRCh38.p7 | 2:152120189 | AAGTATGAGATACTT[A/T]TGACAAACTCACTCT | 10254 |
rs11694120 | snp | C/T | 0.345037 | 0.231231 | intron-variant | STAM2 | GRCh38.p7 | 2:152170444 | gctgagatcgcgcca[C/T]tgcactccagcctgg | 10254 |