SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12759 | snp | C/T | 0 | 0 | missense | GRAP2 | GRCh38.p7 | 22:39971046 | CACAACAAGCTGGGC[C/T]TCTTCCCTGCCAACT | 9402 |
rs80400 | snp | C/T | 0.373397 | 0.217424 | intron-variant | GRAP2 | GRCh38.p7 | 22:39955454 | AACCATTCTTCCTTC[C/T]CACCATCTGCTGAGA | 9402 |
rs80403 | snp | A/T | 0.397271 | 0.202018 | intron-variant | GRAP2 | GRCh38.p7 | 22:39918048 | GGCATTATCTGATTT[A/T]TCCTTGCAACAACAG | 9402 |
rs107140 | snp | A/G | 0.41325 | 0.18934 | intron-variant | GRAP2 | GRCh38.p7 | 22:39938923 | TTATAATTCTCGGAC[A/G]AGCTGCAGAGGCCCC | 9402 |
rs137953 | snp | C/T | 0.430434 | 0.173042 | intron-variant | ENTHD1 | GRCh38.p7 | 22:39892381 | gatgatttgtggaaa[C/T]tctcttttgggtgcg | 9402 |
rs137954 | snp | A/G | 0.109814 | 0.206997 | intron-variant | ENTHD1 | GRCh38.p7 | 22:39892826 | AAATGAGCTCTGGCC[A/G]AGAATGCTACGGGAA | 9402 |
rs137955 | snp | C/T | 0.394171 | 0.204242 | upstream-variant-2KB | ENTHD1 | GRCh38.p7 | 22:39895803 | ATTGTAAGTAGTTGC[C/T]ATAATAAAGGCAAAC | 9402 |
rs137956 | snp | C/T | 0.399611 | 0.200291 | | | GRCh38.p7 | 22:39897459 | ccacttcccaccact[C/T]acatcatcctgtttt | 9402 |
rs137957 | snp | A/G | 0.00835141 | 0.0640778 | | | GRCh38.p7 | 22:39897725 | ggtttctccatgttg[A/G]tcaggatggtctcaa | 9402 |
rs137958 | in-del | -/GTT | | | upstream-variant-2KB | GRAP2 | GRCh38.p7 | 22:39899575 | AAGTAGCAAGATGTT[-/GTT]ATTTTTAAATTTTAT | 9402 |
rs137959 | snp | A/G | 0.426047 | 0.177503 | upstream-variant-2KB | GRAP2 | GRCh38.p7 | 22:39900374 | ACTTAGCAAGTAGCA[A/G]TGTCTCTAATTTTCT | 9402 |
rs137960 | snp | A/G | 0.391954 | 0.205789 | intron-variant | GRAP2 | GRCh38.p7 | 22:39905476 | cgaatgaactgggac[A/G]agttattctttttgt | 9402 |
rs137961 | snp | A/G | 0 | 0 | intron-variant | GRAP2 | GRCh38.p7 | 22:39907528 | gattgcttgagcgca[A/G]gagattgagaccagc | 9402 |
rs137962 | snp | A/G | 0.2822 | 0.247918 | intron-variant | GRAP2 | GRCh38.p7 | 22:39907529 | attgcttgagcgcag[A/G]agattgagaccagcc | 9402 |
rs137963 | snp | C/T | 0.13446 | 0.221699 | intron-variant | GRAP2 | GRCh38.p7 | 22:39907930 | GCACCAAGCCTGTCA[C/T]GCTGTAGGCTGGGCC | 9402 |
rs137964 | snp | C/T | 0.446249 | 0.154875 | intron-variant | GRAP2 | GRCh38.p7 | 22:39908577 | CTTGATTTTTTATTA[C/T]GAACAGTTATATCCT | 9402 |
rs137965 | snp | C/T | 0.4021 | 0.198407 | intron-variant | GRAP2 | GRCh38.p7 | 22:39910189 | tcacgggactcagaa[C/T]ggagcaacgctctcc | 9402 |
rs137966 | snp | A/C | 0.397452 | 0.201886 | intron-variant | GRAP2 | GRCh38.p7 | 22:39911383 | TCTCTTCCCTCCATC[A/C]CCTCCCCCAGCCCCA | 9402 |
rs137967 | snp | A/G | 0.494315 | 0.0530107 | intron-variant | GRAP2 | GRCh38.p7 | 22:39911890 | GGGAATTTTTTCACA[A/G]TTTAGATTCTGATTC | 9402 |
rs137968 | snp | C/T | 0.492533 | 0.0606443 | intron-variant | GRAP2 | GRCh38.p7 | 22:39912914 | ACAGGGCTAAAAGGC[C/T]GGTCACGGTGGCTCA | 9402 |
rs137969 | snp | C/T | 0.388964 | 0.20782 | intron-variant | GRAP2 | GRCh38.p7 | 22:39913506 | AGGCATGACCGATGC[C/T]GAGTCAGCCAAGTGT | 9402 |
rs137970 | snp | A/G | 0.400504 | 0.199621 | intron-variant | GRAP2 | GRCh38.p7 | 22:39913852 | TCCATCGAAGTCACA[A/G]CTTCTTCCCCATTTC | 9402 |
rs137971 | in-del | -/TT | 0.401215 | 0.199083 | intron-variant | GRAP2 | GRCh38.p7 | 22:39914483 | ATACTGTCCTGTGGA[-/TT]TTTCATTTCGAATGA | 9402 |
rs137972 | snp | A/G | 0.493013 | 0.058691 | intron-variant | GRAP2 | GRCh38.p7 | 22:39915875 | AATGGGGAGGGGCAC[A/G]GACGCTTCCATCAAC | 9402 |
rs137973 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | GRAP2 | GRCh38.p7 | 22:39917366 | ATTCCAGCCAATTTC[A/C]CTAACAACACGCCTC | 9402 |
rs137974 | in-del | -/CA | | | intron-variant | GRAP2 | GRCh38.p7 | 22:39920989 | acacacacacacaca[-/CA]aTCTGATGTAACGAC | 9402 |
rs137975 | snp | C/T | 0.449599 | 0.150533 | intron-variant | GRAP2 | GRCh38.p7 | 22:39921623 | CAAGTTTCTCTTTTG[C/T]AGTAAATGATCTAGA | 9402 |
rs137977 | snp | A/C | 0.455621 | 0.142197 | intron-variant | GRAP2 | GRCh38.p7 | 22:39924357 | TAGCACTGTGACAAT[A/C]ATCACCACGGTCGTA | 9402 |
rs137978 | snp | A/C | 0.452103 | 0.147154 | upstream-variant-2KB, intron-variant | GRAP2 | GRCh38.p7 | 22:39924754 | ATCAGCAAATATTTA[A/C]TGTGAGCAGGACAAT | 9402 |
rs137979 | snp | A/G | 0.46014 | 0.13543 | utr-variant-5-prime, intron-variant | GRAP2 | GRCh38.p7 | 22:39926680 | CTGTTTGGAAAATTC[A/G]TTGCCATGCATGAGT | 9402 |
rs137980 | snp | C/T | 0.368733 | 0.220005 | intron-variant | GRAP2 | GRCh38.p7 | 22:39929157 | TAGCAATATCAGTTT[C/T]CTAGCTTTGATACTG | 9402 |
rs137981 | snp | A/G | 0.121717 | 0.214577 | intron-variant | GRAP2 | GRCh38.p7 | 22:39931202 | ACTCCTGAGAGAGAG[A/G]AGGTGGGCAAGACAG | 9402 |
rs137982 | in-del | -/A | | | intron-variant | GRAP2 | GRCh38.p7 | 22:39932571 | AAAAAAAAAAAAAAA[-/A]GCTGGATGTGGTGGC | 9402 |
rs137983 | snp | C/T | 0.373397 | 0.217424 | intron-variant | GRAP2 | GRCh38.p7 | 22:39932987 | ggctcatgtgcttGC[C/T]TACCTTACCCAGATG | 9402 |
rs137984 | in-del | -/T | 0.388398 | 0.208197 | intron-variant | GRAP2 | GRCh38.p7 | 22:39933144 | GTGCCTTTGTTTAAG[-/T]GTAAGAAGAATGTGC | 9402 |
rs137985 | snp | A/G | 0.467439 | 0.123371 | intron-variant | GRAP2 | GRCh38.p7 | 22:39937125 | ATGCAAAGGATGATA[A/G]TAACAATAATAAATG | 9402 |
rs137986 | in-del | -/AA | | | intron-variant | GRAP2 | GRCh38.p7 | 22:39939582 | AAAAAAAAAAAAAAA[-/AA]GAAATGGTCCTGCAT | 9402 |
rs137987 | in-del | -/T | 0 | 0 | intron-variant | GRAP2 | GRCh38.p7 | 22:39940384 | TTTGTTTTTTGTTTG[-/T]TTTTTTTTTTTTTTT | 9402 |
rs137988 | snp | A/G | 0.139225 | 0.224118 | intron-variant | GRAP2 | GRCh38.p7 | 22:39940817 | TTCTGTATTTTAAAG[A/G]TTTGAGTCTTTGAAA | 9402 |
rs137989 | snp | C/T | 0.408017 | 0.193729 | intron-variant | GRAP2 | GRCh38.p7 | 22:39940841 | TTTGAAATGTTAAAA[C/T]TGATGCGCCTTAAAA | 9402 |
rs137990 | snp | A/C | 0.209693 | 0.246729 | intron-variant | GRAP2 | GRCh38.p7 | 22:39942280 | TTCGACTGGGGGAGG[A/C]GGCACTCTCCTCTAC | 9402 |
rs137991 | snp | C/T | 0.412416 | 0.190055 | intron-variant | GRAP2 | GRCh38.p7 | 22:39944771 | CATGTTGGAAAGATC[C/T]TCCCCAAATCAAGGT | 9402 |
rs137992 | snp | A/G | 0.446249 | 0.154875 | intron-variant | GRAP2 | GRCh38.p7 | 22:39948039 | GTCCTCAGCAGTCCC[A/G]ATGAGCCTTCTCGGA | 9402 |
rs137993 | snp | G/T | 0.358728 | 0.225118 | intron-variant | GRAP2 | GRCh38.p7 | 22:39952026 | AGTGTGTGGTTTTTT[G/T]TTTTTTTTTTTTCTT | 9402 |
rs137994 | snp | C/T | 0.388587 | 0.208071 | intron-variant | GRAP2 | GRCh38.p7 | 22:39953483 | atatatccTCACCTC[C/T]TCTTAGCCTAGGCCC | 9402 |
rs137995 | in-del | -/A | 0.432651 | 0.170701 | intron-variant | GRAP2 | GRCh38.p7 | 22:39955414 | AGAGAAAAAAAAAAA[-/A]TACACCGTGGAGTAA | 9402 |
rs137996 | snp | A/G | 0.372995 | 0.217652 | intron-variant | GRAP2 | GRCh38.p7 | 22:39956519 | TTGTTTTGAGACAGA[A/G]CCTTGCTCTGTTGCC | 9402 |
rs137997 | snp | A/G | 0.372189 | 0.218105 | intron-variant | GRAP2 | GRCh38.p7 | 22:39956952 | TCTCACCCTTCACTC[A/G]GTGGGTGGACAGACA | 9402 |
rs137998 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | GRAP2 | GRCh38.p7 | 22:39957315 | ctctgcataccccac[C/G]tgctcctcaaacctt | 9402 |
rs137999 | in-del | -/TGAA | | | intron-variant | GRAP2 | GRCh38.p7 | 22:39958545 | GAATGAATGAATGAA[-/TGAA]CGAACGAATATGTAT | 9402 |
rs138000 | snp | A/C | 0.498459 | 0.0277128 | intron-variant | GRAP2 | GRCh38.p7 | 22:39958977 | TCTAGAATTTGGGAA[A/C]CTGAGACATAGGTAG | 9402 |
rs138001 | in-del | -/T | | | intron-variant | GRAP2 | GRCh38.p7 | 22:39960953 | TGTCCCAAGTCTTCT[-/T]TTTTTTTTTTTTTTT | 9402 |
rs138002 | snp | C/T | 0.473081 | 0.112848 | intron-variant | GRAP2 | GRCh38.p7 | 22:39962179 | tctaatcccagcact[C/T]tgggaggctgagttg | 9402 |
rs138003 | snp | C/T | 0.370974 | 0.218781 | intron-variant | GRAP2 | GRCh38.p7 | 22:39963950 | GAACCTGGGAGGTGG[C/T]GCTTGCAGTGAGCAG | 9402 |
rs138004 | in-del | -/A | | | intron-variant | GRAP2 | GRCh38.p7 | 22:39964463 | AAGAGAAGGCTTTCA[-/A]GCAGAAACAAAAAGA | 9402 |
rs138005 | in-del | -/AAAA | | | intron-variant | GRAP2 | GRCh38.p7 | 22:39964734 | AAAAAAAAAAAAAAA[-/AAAA]TCTTCCAGTGGCTCA | 9402 |
rs138006 | snp | A/G | 0.377977 | 0.21476 | intron-variant | GRAP2 | GRCh38.p7 | 22:39966942 | TCTGGTCCATATTAA[A/G]CACTAAGAACATGTT | 9402 |
rs138008 | snp | C/T | 0.385359 | 0.210185 | intron-variant | GRAP2 | GRCh38.p7 | 22:39967546 | ACTTCTTCCCCCACG[C/T]CCAGCCCGGCGGCAG | 9402 |
rs138009 | snp | C/G | 0.494692 | 0.0512434 | intron-variant | GRAP2 | GRCh38.p7 | 22:39968390 | AGACCCTGGACCCCC[C/G]CAAATGGCAGAAATA | 9402 |
rs138010 | in-del | -/AC | 0 | 0 | intron-variant | GRAP2 | GRCh38.p7 | 22:39968459 | ATGGCTCCCACCTGA[-/AC]ACACACACACACACA | 9402 |
rs138011 | snp | C/T | 0.370772 | 0.218893 | utr-variant-3-prime | GRAP2 | GRCh38.p7 | 22:39972225 | TGTCCAAGGGCTCAC[C/T]CTGGAGGTGCACAGC | 9402 |
rs138012 | snp | A/G | 0.375598 | 0.21616 | utr-variant-3-prime | GRAP2 | GRCh38.p7 | 22:39972604 | GGGTTGGGGGCAGCC[A/G]TTATTGAAGGTGATC | 9402 |
rs138013 | snp | G/T | 0 | 0 | downstream-variant-500B | GRAP2 | GRCh38.p7 | 22:39973750 | TCCCCACGGGCCCTA[G/T]TTTCTACCTGACAGC | 9402 |
rs470084 | snp | C/T | 0.396909 | 0.202282 | intron-variant | GRAP2 | GRCh38.p7 | 22:39917352 | ACCCCTAACCTGAAA[C/T]TCCAGCCAATTTCAC | 9402 |
rs713883 | snp | A/G | 0.455144 | 0.142885 | intron-variant | GRAP2 | GRCh38.p7 | 22:39930170 | ACCAAAATATTTAAA[A/G]TGGCATAATGGCTGG | 9402 |
rs713925 | snp | A/C | 0.486595 | 0.0807641 | intron-variant | GRAP2 | GRCh38.p7 | 22:39903154 | GTGTCAGTAAGTGTG[A/C]TTCCATCACGATTTC | 9402 |
rs739090 | snp | C/T | 0.435837 | 0.167226 | intron-variant | GRAP2 | GRCh38.p7 | 22:39918156 | CTCACGGGTTTTTCA[C/T]GCTCCTCCCTGAACA | 9402 |
rs739091 | snp | A/C | 0.383439 | 0.21141 | intron-variant | GRAP2 | GRCh38.p7 | 22:39921122 | GAGCTTAGCTTCAGG[A/C]CTCCATCCCCAGACA | 9402 |
rs1060824 | snp | C/T | 0 | 0 | utr-variant-3-prime | GRAP2 | GRCh38.p7 | 22:39971301 | TTGACACTTGCTTTT[C/T]TGCCCCCCTCAGGGG | 9402 |
rs1135963 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | GRAP2 | GRCh38.p7 | 22:39964341 | AAGAAGTTATCGTCC[A/C/G]GTGGCAGGGTCTGGG | 9402 |
rs2267414 | snp | A/G | 0.357451 | 0.225731 | intron-variant | GRAP2 | GRCh38.p7 | 22:39910650 | CTGACATTGTGATCC[A/G]CCTGCCTCGGCCTCG | 9402 |
rs2267415 | snp | A/G | 0.402277 | 0.198272 | intron-variant | GRAP2 | GRCh38.p7 | 22:39912424 | GAGACCTTGTCTCTG[A/G]AAAAAAAGTACTCTT | 9402 |
rs2267416 | snp | C/G | 0.415891 | 0.18703 | intron-variant | GRAP2 | GRCh38.p7 | 22:39930831 | ACTCCTATTTGCACA[C/G]ACCATTCTCTCTGTG | 9402 |
rs2267417 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | GRAP2 | GRCh38.p7 | 22:39936840 | GAGGTCTGCCAGGTC[G/T]ATTGCAGTCTTTACC | 9402 |
rs2267418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GRAP2 | GRCh38.p7 | 22:39937139 | AGTAACAATAATAAA[C/T]GTTGCAACGGGTGAC | 9402 |
rs2267419 | snp | A/G | 0.479095 | 0.100076 | intron-variant | GRAP2 | GRCh38.p7 | 22:39952192 | CCACCATGCCTGGCT[A/G]ATTTTTGTCTTTATG | 9402 |
rs2267420 | snp | A/G | 0.186421 | 0.24178 | intron-variant | GRAP2 | GRCh38.p7 | 22:39952516 | ACGTGGCTACGAGGC[A/G]CTGCTGCTGGGTTTC | 9402 |
rs2267421 | snp | A/G | 0.112983 | 0.209108 | intron-variant | GRAP2 | GRCh38.p7 | 22:39953349 | TATTTCTGTAAAGCC[A/G]TCACCACCTACTCAG | 9402 |
rs2267423 | snp | A/G | 0.40733 | 0.194287 | intron-variant | GRAP2 | GRCh38.p7 | 22:39968411 | GGCAGAAATAGGGAA[A/G]CTGTTCTTGGCAAAG | 9402 |
rs2284077 | snp | C/T | 0.441295 | 0.160954 | intron-variant | GRAP2 | GRCh38.p7 | 22:39967544 | TTACTTCTTCCCCCA[C/T]GTCCAGCCCGGCGGC | 9402 |
rs2284078 | snp | A/G | 0.390277 | 0.206936 | intron-variant | GRAP2 | GRCh38.p7 | 22:39967774 | AAAAACGAGCGCCCT[A/G]GAAATGGACTAAATG | 9402 |
rs2958646 | snp | C/T | 0.146985 | 0.227789 | | | GRCh38.p7 | 22:39896687 | TTTTGCCAAGCCTAA[C/T]CAACTCCCTCACTGT | 9402 |
rs2958647 | snp | G/T | 0.419296 | 0.183954 | upstream-variant-2KB | ENTHD1 | GRCh38.p7 | 22:39895135 | TTGTAGTATGGATAA[G/T]GTTCTTCATGATCCA | 9402 |
rs2958648 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | ENTHD1 | GRCh38.p7 | 22:39894559 | ATCACGTGCTGGTGG[C/T]ATTTCTAGTCAGTTG | 9402 |
rs2958664 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | GRAP2 | GRCh38.p7 | 22:39924011 | CCATAAAAACTGAAC[A/G]TAGGGGGCCAGAAAT | 9402 |
rs2958666 | snp | C/T | 0.140242 | 0.224618 | intron-variant | GRAP2 | GRCh38.p7 | 22:39951902 | CCAAGCACCAGGTGG[C/T]GGAGAGAAATGGCTG | 9402 |
rs2958667 | snp | A/G | 0.152667 | 0.230274 | intron-variant | GRAP2 | GRCh38.p7 | 22:39967429 | AGAACAGTGCCTGGT[A/G]TATGCTGCCCTCAGG | 9402 |
rs3021213 | snp | A/G | 0.342358 | 0.232314 | intron-variant | GRAP2 | GRCh38.p7 | 22:39955434 | AAAAAAATACACCGT[A/G]GAGTAACCATTCTTC | 9402 |
rs3021226 | snp | A/G | 0.148326 | 0.228391 | intron-variant | GRAP2 | GRCh38.p7 | 22:39915095 | tcaggaggccgaggt[A/G]ggagaatcacttgaa | 9402 |
rs3021227 | snp | A/T | 0.184203 | 0.241186 | intron-variant | GRAP2 | GRCh38.p7 | 22:39951812 | ATGAGAATTTTTTTT[A/T]AAAAAAAACCTCACC | 9402 |
rs3985942 | snp | A/C | | | intron-variant | GRAP2 | GRCh38.p7 | 22:39955011 | AATGAATTTCCA[A/C] | 9402 |
rs3985945 | in-del | -/ACAC | | | intron-variant | GRAP2 | GRCh38.p7 | 22:39920984 | cacacacacacacac[-/ACAC]ACAATCTGATGTAAC | 9402 |
rs4820393 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | GRAP2 | GRCh38.p7 | 22:39969642 | GATCTggctgggcac[A/C/G]gtggctcacacctgt | 9402 |
rs4821918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GRAP2 | GRCh38.p7 | 22:39965316 | aggcggaggttgcag[G/T]gagcagagatcacac | 9402 |
rs5750885 | snp | A/G | | | intron-variant | GRAP2 | GRCh38.p7 | 22:39928752 | CCTGGTTTGTACAGT[A/G]GTGCAGGCTTGGGCA | 9402 |
rs5750889 | snp | C/T | 0.0322114 | 0.122752 | downstream-variant-500B | GRAP2 | GRCh38.p7 | 22:39973439 | TGCAGGAGCTGACCC[C/T]GTAGGCAGGCGGTAT | 9402 |
rs5757805 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GRAP2 | GRCh38.p7 | 22:39902687 | GAGAAGGAGATGATC[A/C]ATCTATTCAATATGA | 9402 |
rs5757806 | snp | A/G | 0.468349 | 0.121752 | intron-variant | GRAP2 | GRCh38.p7 | 22:39922194 | GAGAGAAGACACACA[A/G]GCAAACAAATCATTA | 9402 |
rs5757808 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | GRAP2 | GRCh38.p7 | 22:39929869 | TCCTCTTTCTGTATT[C/T]CCTTATCTCAGAAAA | 9402 |
rs5757810 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | GRAP2 | GRCh38.p7 | 22:39932046 | CATTCTAGAACCTTC[A/C]TACTGCTTATCCCAA | 9402 |