SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs42857 | snp | A/T | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87357333 | tcaaaaaaaaaaaaa[A/T]aaaaagaaCCGAATT | 79791 |
rs189703 | snp | C/T | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87332746 | CACAGGCCCAGCTCC[C/T]GGAGGGGGTTTGGAT | 79791 |
rs190434 | snp | C/G | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87349709 | Atttttttttttttt[C/G]agatggagtcttgct | 79791 |
rs194198 | snp | C/T | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87349697 | tttcagatggagtct[C/T]gctctgttgcccagg | 79791 |
rs254300 | snp | A/C | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87349515 | accatgttggccagg[A/C]tggtctcgaactcct | 79791 |
rs254301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO31 | GRCh38.p7 | 16:87349539 | tattttaagtagaga[C/T]ggggtttcaccatgt | 79791 |
rs254302 | snp | A/T | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87349548 | aattttttgtatttt[A/T]agtagagacggggtt | 79791 |
rs254303 | snp | C/T | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87349560 | ctatgcctggctaat[C/T]ttttgtattttaagt | 79791 |
rs254304 | snp | C/T | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87349614 | aagtgattctcctgc[C/T]tcagcctcccgagta | 79791 |
rs254305 | snp | C/T | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87349689 | ggagtcttgctctgt[C/T]gcccaggctggagtg | 79791 |
rs737682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO31 | GRCh38.p7 | 16:87370275 | CCAGTGTGCTGAGTG[C/T]GGGCTCGGCCACGCT | 79791 |
rs745280 | snp | A/G | 0.424348 | 0.179172 | intron-variant | FBXO31 | GRCh38.p7 | 16:87363682 | ATGGTTAAGTGCTAC[A/G]GGGAAATCAAAGAAT | 79791 |
rs750956 | snp | C/T | 0.188631 | 0.242351 | intron-variant | FBXO31 | GRCh38.p7 | 16:87387163 | TTGCTGAAGCGCTCA[C/T]GGTCATTCTtttctt | 79791 |
rs750957 | snp | C/T | 0.474091 | 0.11083 | intron-variant | FBXO31 | GRCh38.p7 | 16:87386776 | CCTGCAATCATAAGT[C/T]TGATGTACTAGTTAC | 79791 |
rs750958 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | FBXO31 | GRCh38.p7 | 16:87386771 | AATCATAAGTCTGAT[A/G]TACTAGTTACATGTC | 79791 |
rs751405 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | FBXO31 | GRCh38.p7 | 16:87332082 | CTAAATTCTTCCAAC[A/G]GATGACGAGAAGTAA | 79791 |
rs873222 | snp | C/T | 0.229429 | 0.249152 | intron-variant | FBXO31 | GRCh38.p7 | 16:87368527 | GTAGGCAGCACAGGT[C/T]GTGCTGGCCGTCTGG | 79791 |
rs889600 | snp | A/C | 0.406814 | 0.194704 | intron-variant | FBXO31 | GRCh38.p7 | 16:87357024 | GCCAAGGTGGGAGGA[A/C]TGAATGAGCCCAAGA | 79791 |
rs889601 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | FBXO31 | GRCh38.p7 | 16:87363474 | ACCTGGGGCATCTGA[C/G]GCTTGCCTGCCAAGG | 79791 |
rs889602 | snp | C/G | 0.490453 | 0.0684267 | intron-variant | FBXO31 | GRCh38.p7 | 16:87370411 | TTGAGAAAGGCACCA[C/G]ACTAAGATGCCATCT | 79791 |
rs889603 | snp | C/G | 0.493201 | 0.0579089 | intron-variant | FBXO31 | GRCh38.p7 | 16:87370482 | CCCAGCCCTGGGGCA[C/G]TCGACACCAGGGACT | 79791 |
rs889604 | snp | A/T | 0.476052 | 0.106772 | intron-variant | FBXO31 | GRCh38.p7 | 16:87377201 | AGTAATCCTAGCACT[A/T]TGGGAGGCCGAGGCG | 79791 |
rs891093 | snp | A/G | 0.4973 | 0.0366419 | intron-variant | FBXO31 | GRCh38.p7 | 16:87344298 | AAACCGAAGTGCAGG[A/G]GAGGAGAGAGACGCC | 79791 |
rs891094 | snp | C/G | 0.453939 | 0.144598 | intron-variant | FBXO31 | GRCh38.p7 | 16:87344395 | TGTCCGGGCGCCGAT[C/G]GTGCAAATGCAGAGG | 79791 |
rs891095 | snp | A/C | 0.497959 | 0.0318836 | intron-variant | FBXO31 | GRCh38.p7 | 16:87344482 | GCCTAGCCTCACCCC[A/C]TTCTGGGAGAGCTGG | 79791 |
rs933717 | snp | C/T | 0.48178 | 0.0936921 | intron-variant | FBXO31 | GRCh38.p7 | 16:87381644 | CTCATGCAGACCTCC[C/T]TGGGGTGCAAACTCA | 79791 |
rs980304 | snp | C/T | 0.469247 | 0.120128 | upstream-variant-2KB, intron-variant | FBXO31, MAP1LC3B | GRCh38.p7 | 16:87393061 | AACACCGCTGTGGGC[C/T]GTCCCGGGCGCGGCG | 79791 |
rs980305 | snp | A/C | 0.466824 | 0.124448 | upstream-variant-2KB, intron-variant | FBXO31, MAP1LC3B | GRCh38.p7 | 16:87392799 | GGTACGGCAGGCACC[A/C]CGCCGCGGAGGGCGC | 79791 |
rs1062746 | snp | A/G | 0.363776 | 0.222609 | utr-variant-3-prime | FBXO31 | GRCh38.p7 | 16:87331044 | GAGAGAACGAGCCTG[A/G]ATACAGCAGATGTAG | 79791 |
rs1808437 | snp | C/G | 0.295854 | 0.245759 | intron-variant | FBXO31 | GRCh38.p7 | 16:87387717 | CGGGTTCACACCATT[C/G]TCCTGCTTCAGCCTC | 79791 |
rs1834022 | snp | C/T | 0.357451 | 0.225731 | intron-variant | FBXO31 | GRCh38.p7 | 16:87360780 | GCACAGGGAAGTACA[C/T]GGGGTGGACTGGCCT | 79791 |
rs1971728 | snp | A/G | 0.208169 | 0.246476 | intron-variant | FBXO31 | GRCh38.p7 | 16:87348564 | GACTACAGACCTGGC[A/G]GGAGGATAAGCCAAC | 79791 |
rs2007193 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO31 | GRCh38.p7 | 16:87377281 | AAAAATCTGTCTCTA[C/T]AAAAAGATACAAAAA | 79791 |
rs2007266 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FBXO31 | GRCh38.p7 | 16:87332421 | GCTGCAGCACGTGCT[A/G]TGACTCGCAAACTGG | 79791 |
rs2007286 | snp | G/T | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87332722 | TTTGGATGTCTGGGT[G/T]GGGGGAAGGGTGCCA | 79791 |
rs2059259 | snp | A/C | 0.46703 | 0.124089 | intron-variant, upstream-variant-2KB | FBXO31, MAP1LC3B | GRCh38.p7 | 16:87391029 | ATCTAATACTTTGAA[A/C]GAGCCCCATAGTTCC | 79791 |
rs2278270 | snp | A/G | 0.277067 | 0.24853 | utr-variant-3-prime | FBXO31 | GRCh38.p7 | 16:87327787 | GACAGGTTGGGCCAC[A/G]TTAACACTGGACTTG | 79791 |
rs2278271 | snp | A/G | 0.275999 | 0.248644 | utr-variant-3-prime | FBXO31 | GRCh38.p7 | 16:87328197 | CTGAAGGGCCCTTGC[A/G]TGCGGCTGCAGCACA | 79791 |
rs2278272 | snp | C/T | 0.284995 | 0.247539 | utr-variant-3-prime | FBXO31 | GRCh38.p7 | 16:87328396 | GGGATGCCACAGAGC[C/T]GCAGGCAGACTGAAG | 79791 |
rs2278273 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | FBXO31 | GRCh38.p7 | 16:87358485 | CGTCCCGACTTCACG[C/G/T]GAGGGTTTATACCTG | 79791 |
rs2278274 | snp | C/T | 0.226188 | 0.248863 | intron-variant | FBXO31 | GRCh38.p7 | 16:87364254 | CACCGCACAGGAGGG[C/T]TGACCCCAGGGAAAC | 79791 |
rs2288482 | snp | C/G | 0.288906 | 0.246954 | utr-variant-3-prime | FBXO31 | GRCh38.p7 | 16:87331057 | ATTCAGGCTCGTTCT[C/G]TCTGTTTTTGGTAAG | 79791 |
rs2288483 | snp | C/G | 0.274393 | 0.248807 | intron-variant | FBXO31 | GRCh38.p7 | 16:87389464 | TTATGGATGCCCAAG[C/G]GTGGGAAAATATGAG | 79791 |
rs2303763 | snp | C/T | 0.449303 | 0.150925 | intron-variant | FBXO31 | GRCh38.p7 | 16:87342999 | GTGAGGAACAGAGTC[C/T]ATCACAGCATCCCCC | 79791 |
rs2303764 | snp | C/G | 0.449599 | 0.150533 | intron-variant | FBXO31 | GRCh38.p7 | 16:87343849 | TCCCCGCACTGCAAT[C/G]GCACAGAGAAGCTCC | 79791 |
rs2318446 | snp | A/G | 0.336702 | 0.234484 | intron-variant | FBXO31 | GRCh38.p7 | 16:87331616 | GCAAGAGCCACATCC[A/G]CTGTTCATCAGCCAG | 79791 |
rs2318447 | snp | A/G | | | intron-variant | FBXO31 | GRCh38.p7 | 16:87344984 | GCCCATCCCTGCCCC[A/G]AACCCCACCTGGGGG | 79791 |
rs2318448 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | FBXO31 | GRCh38.p7 | 16:87350480 | GTTACTTTACGGTCA[C/T]ACCTAGACGGGTGTG | 79791 |
rs2318449 | snp | A/G | 0.0857041 | 0.19211 | intron-variant | FBXO31 | GRCh38.p7 | 16:87379576 | CAGCTCCAGCTTCTC[A/G]GGGCTGCTCTCTGGC | 79791 |
rs2318450 | snp | A/G | 0.47709 | 0.104548 | intron-variant, upstream-variant-2KB | FBXO31 | GRCh38.p7 | 16:87384015 | TGCCGAGTGCAAAAC[A/G]TTAGACTGCCCCGTG | 79791 |
rs3076211 | in-del | -/ACA | 0 | 0 | intron-variant | FBXO31 | GRCh38.p7 | 16:87363837 | ATAACTGGAGCAACA[-/ACA]TCTTCATTTTTCATC | 79791 |
rs3748394 | snp | C/G | 0.496245 | 0.0431677 | downstream-variant-500B | FBXO31 | GRCh38.p7 | 16:87326894 | TCCTCAAGAAGCTGG[C/G]AAGTCTGGGTTCCCA | 79791 |
rs3748395 | snp | A/G | 0.28578 | 0.247426 | utr-variant-3-prime | FBXO31 | GRCh38.p7 | 16:87327021 | ACTTGAAACTGTGAG[A/G]AGAAACAAGTGCACG | 79791 |
rs3748396 | snp | G/T | 0.426966 | 0.176587 | utr-variant-3-prime | FBXO31 | GRCh38.p7 | 16:87327143 | CAGGGGGTGCAGAGG[G/T]GCTCATGATCAGATG | 79791 |
rs3748397 | snp | A/G | | | upstream-variant-2KB, intron-variant | FBXO31, MAP1LC3B | GRCh38.p7 | 16:87392507 | GGTGCGGCGGGGCCG[A/G]GGTCCGAGCTGTGGA | 79791 |
rs4240793 | snp | A/C | 0.472616 | 0.113763 | intron-variant | FBXO31 | GRCh38.p7 | 16:87355350 | TTCCGAAAGGTTTGG[A/C]TGCTGTGAGAGAACA | 79791 |
rs4294823 | snp | A/G | 0.479095 | 0.100076 | intron-variant | FBXO31 | GRCh38.p7 | 16:87387836 | AAGAAAGAAAGCCAC[A/G]TTAACTGTATCCCAA | 79791 |
rs4843236 | snp | C/T | 0.108402 | 0.206034 | intron-variant | FBXO31 | GRCh38.p7 | 16:87334734 | TCGGGGAATAGGCTT[C/T]GCCCCTTCAGGCGCT | 79791 |
rs4843237 | snp | C/G | 0.100944 | 0.200705 | intron-variant | FBXO31 | GRCh38.p7 | 16:87343017 | CACAGCATCCCCCAC[C/G]CCAGGCAGGTGGCCA | 79791 |
rs4843238 | snp | C/T | 0.350109 | 0.229081 | intron-variant | FBXO31 | GRCh38.p7 | 16:87356549 | CTCAACAAGGCAGTG[C/T]TGTTAGCAGGCGTGT | 79791 |
rs4843239 | snp | A/G | 0.4582 | 0.138394 | intron-variant | FBXO31 | GRCh38.p7 | 16:87365847 | AGCCTGGCCAACATG[A/G]TGAAACCCGGTCTCT | 79791 |
rs4843240 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | FBXO31 | GRCh38.p7 | 16:87374986 | TCAGGAGTTCAAGAC[C/T]AGCCTGGCCAACATA | 79791 |
rs4843241 | snp | A/G | 0.116488 | 0.211364 | intron-variant | FBXO31 | GRCh38.p7 | 16:87386666 | CTTGAATTCCTGACC[A/G]GAGGCGATCCACCCA | 79791 |
rs4843597 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | FBXO31 | GRCh38.p7 | 16:87347753 | AAATGAGTCTCCCAT[A/G]AAGTGATGAGCCTCC | 79791 |
rs4843598 | snp | A/C | 0.162909 | 0.23434 | intron-variant | FBXO31 | GRCh38.p7 | 16:87350032 | ACCACATGCACAGTC[A/C]ACATGTTGGCGAACA | 79791 |
rs4843599 | snp | A/G | 0.370365 | 0.219117 | intron-variant | FBXO31 | GRCh38.p7 | 16:87350103 | GAGCATGTGTGACTG[A/G]ACGAATGGGCAGGAT | 79791 |
rs4843600 | snp | C/G | 0.0541208 | 0.156047 | intron-variant | FBXO31 | GRCh38.p7 | 16:87351409 | ATTGGGCTCTGGTGG[C/G]GGGGGAAAGGAGCCA | 79791 |
rs4843601 | snp | C/T | 0.491051 | 0.0662916 | intron-variant | FBXO31 | GRCh38.p7 | 16:87351439 | AGGAACAACGTTCCC[C/T]GCACTTCAGTGCCCC | 79791 |
rs4843602 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FBXO31 | GRCh38.p7 | 16:87352491 | GGGTAAAGGCTAAAA[C/T]GAAAGAAAATAATCC | 79791 |
rs4843603 | snp | A/G | 0.475348 | 0.108251 | intron-variant | FBXO31 | GRCh38.p7 | 16:87370544 | GCTGCGCCAGCCACC[A/G]GGCCGCCAGACCCAG | 79791 |
rs4843604 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | FBXO31 | GRCh38.p7 | 16:87370695 | TGGGACACTGCTGGG[C/T]CTCAGCCTCCCTGGA | 79791 |
rs4843605 | snp | C/T | 0.469049 | 0.120489 | intron-variant | FBXO31 | GRCh38.p7 | 16:87375439 | GAGGATGAAGTGAGC[C/T]GAGATCACGCCACTG | 79791 |
rs4843606 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | FBXO31 | GRCh38.p7 | 16:87378945 | CCAGCCAGGGCGACA[A/G]AGCAAGACTCCATCT | 79791 |
rs6419429 | snp | A/G | 0.040671 | 0.13668 | intron-variant | FBXO31 | GRCh38.p7 | 16:87356385 | TGGTCAGTCTAGAAC[A/G]GCACAAATGTCTTCA | 79791 |
rs6540040 | snp | A/G | 0.447421 | 0.153379 | intron-variant | FBXO31 | GRCh38.p7 | 16:87353727 | CGGGAGCAGGGCCCC[A/G]GACACCTTGTCTTGA | 79791 |
rs6540041 | snp | A/T | 0.469937 | 0.118861 | intron-variant | FBXO31 | GRCh38.p7 | 16:87370769 | ACCTGCTGGCTGGTG[A/T]CCTACCCGCTTTACA | 79791 |
rs6540042 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | FBXO31, MAP1LC3B | GRCh38.p7 | 16:87391559 | TGGGGCAGGCCTGGC[A/G]GTCGCCACAGACGAC | 79791 |
rs7184449 | snp | A/C/G | 0.0111196 | 0.0737302 | intron-variant | FBXO31 | GRCh38.p7 | 16:87370280 | GGCCGAGCCCGCACT[A/C/G]AGCACACTGGGATGG | 79791 |
rs7186855 | snp | C/G | 0.0916144 | 0.193427 | utr-variant-3-prime | FBXO31 | GRCh38.p7 | 16:87328225 | ACAACTGCAGGTTCT[C/G]AGAGAAAAATCTCCA | 79791 |
rs7187315 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FBXO31 | GRCh38.p7 | 16:87372586 | TTTTTTTAGAGGTAG[A/G]GTCTCACTCCATCAC | 79791 |
rs7194065 | snp | C/T | 0.130351 | 0.219509 | utr-variant-5-prime | FBXO31 | GRCh38.p7 | 16:87389796 | TAGCCATCTTCTGAA[C/T]GCTGTCCTAGATCAT | 79791 |
rs7194495 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | FBXO31 | GRCh38.p7 | 16:87377551 | ATTAAACAATCCAGA[G/T]GCAGCAGCTCACGCC | 79791 |
rs7201507 | snp | G/T | 0.410399 | 0.191761 | intron-variant | FBXO31 | GRCh38.p7 | 16:87339005 | AGTTCTCTCTTTTTT[G/T]GCCTGCCGCCATGTA | 79791 |
rs7498213 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | FBXO31 | GRCh38.p7 | 16:87363933 | acgattctaGTTGGA[G/T]ATAAAAGAATATTCA | 79791 |
rs7501336 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXO31 | GRCh38.p7 | 16:87384160 | CTCGCGCCCGTGCGT[C/T]CCGCTTCCGGCGCCC | 79791 |
rs8043569 | snp | C/T | 0.00571624 | 0.0531549 | upstream-variant-2KB, utr-variant-5-prime | FBXO31, MAP1LC3B | GRCh38.p7 | 16:87392422 | CGCCGCCCAGATCCC[C/T]GCACCATGCCGTCGG | 79791 |
rs8043667 | snp | A/T | 0.471958 | 0.115042 | intron-variant | FBXO31 | GRCh38.p7 | 16:87354159 | GCTAAAATGAATTGG[A/T]GTTTTACATATTTTA | 79791 |
rs8043703 | snp | A/T | 0.0456336 | 0.143994 | intron-variant | FBXO31 | GRCh38.p7 | 16:87345682 | GAAAACAAGAAAAAG[A/T]AAAAAAGACTGAACA | 79791 |
rs8043933 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | FBXO31 | GRCh38.p7 | 16:87370335 | CTATTCTGTGCACGG[C/T]ACTGGCACTAGGGGG | 79791 |
rs8046273 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | FBXO31 | GRCh38.p7 | 16:87342675 | GCAGGGGGAGGGGAC[C/T]GGCAACCTGCCCGCC | 79791 |
rs8047558 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FBXO31 | GRCh38.p7 | 16:87336879 | GCTGAGGATATTTCG[C/T]GCTTAATGGTTTGAT | 79791 |
rs8048240 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | FBXO31 | GRCh38.p7 | 16:87375852 | GGAACTCCCTTCACC[C/T]GCCCAAAGAAACACT | 79791 |
rs8048834 | snp | C/T | 0.464841 | 0.127841 | intron-variant | FBXO31 | GRCh38.p7 | 16:87376770 | GCACCTCCCAGGCAG[C/T]CCAAGCTCTGCTCCT | 79791 |
rs8050303 | snp | C/T | 0.399432 | 0.200425 | intron-variant | FBXO31 | GRCh38.p7 | 16:87342147 | CATAGCTCACTGCAG[C/T]CTCCACCTCCTGGGC | 79791 |
rs8052244 | snp | C/G | 0.2768 | 0.248559 | intron-variant | FBXO31 | GRCh38.p7 | 16:87368655 | TTGCCTTTATAAGAG[C/G]AAGTGTGCTGGGTAA | 79791 |
rs8052386 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FBXO31 | GRCh38.p7 | 16:87368714 | GAACAGATAACCTCA[A/G]TCCAACATGATTGGA | 79791 |
rs8052807 | snp | C/T | 0.221439 | 0.248363 | intron-variant, upstream-variant-2KB | FBXO31, MAP1LC3B | GRCh38.p7 | 16:87391088 | gggagcagtggctca[C/T]gcctgtaatcccaac | 79791 |
rs8054103 | snp | A/G | 0.295088 | 0.245901 | intron-variant | FBXO31 | GRCh38.p7 | 16:87386576 | GTAGCTGGGATTACA[A/G]GCGAGTGCCACCACA | 79791 |
rs8056833 | snp | C/G | 0.453209 | 0.145623 | intron-variant | FBXO31 | GRCh38.p7 | 16:87344782 | AAAAGCAAGGCTGGA[C/G]CACGCGACGCCCAAC | 79791 |
rs8057105 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | FBXO31 | GRCh38.p7 | 16:87353390 | tccctcaaaattcac[A/G]tcccctagaacctca | 79791 |