SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2617 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | ZFYVE21, PPP1R13B | GRCh38.p7 | 14:103733971 | CTCATACATGAAAAA[A/C/T]AGAGCCTAAGGGCCT | 23368 |
rs722637 | snp | G/T | 0.411578 | 0.190768 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103795386 | ATTTACCGTGGCTTT[G/T]GTACATGCTCCTTCG | 23368 |
rs730114 | snp | G/T | 0.143959 | 0.226396 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103739474 | CTGGGTGGGAGGTCA[G/T]TGTTGACGGAGCAGA | 23368 |
rs876002 | snp | A/G | 0.48491 | 0.0855403 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103773360 | agagaatgttccaga[A/G]ctgttgacagatgcc | 23368 |
rs879724 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103774438 | agcttccaagatgtc[C/T]ccaggttccgtggtt | 23368 |
rs941473 | snp | C/G | 0.483995 | 0.0880135 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103735532 | AGCTGCCAGGGGCTT[C/G]CTGTTGAGCCAACGT | 23368 |
rs941475 | snp | G/T | 0.482534 | 0.0918038 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103774281 | TTCTCAGCCAAGCAG[G/T]TTTAAAATCTGAGTC | 23368 |
rs1040813 | snp | A/G | 0.485324 | 0.0843964 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103840359 | ATTTTTAGCAAAATA[A/G]GAACTTAAAATATCA | 23368 |
rs1058080 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | ZFYVE21, PPP1R13B | GRCh38.p7 | 14:103733414 | TAGGAACTCAGGCTT[C/T]TGGTCTGCAGTGGAG | 23368 |
rs1155751 | snp | C/G | 0.463343 | 0.130326 | intron-variant, upstream-variant-2KB | PPP1R13B | GRCh38.p7 | 14:103820210 | TGGACCTGGTGGGGT[C/G]GTGAGAAGGGAGGGG | 23368 |
rs1187416 | snp | C/T | 0.485255 | 0.0845871 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103845128 | GTTTGTGTAGAGcag[C/T]actgtccaataaaaa | 23368 |
rs1187417 | snp | A/G | 0.369754 | 0.219451 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103843688 | ggataacaggcgtat[A/G]ccactgcgctctgcc | 23368 |
rs1187418 | snp | C/T | 0 | 0 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103842367 | tgcagtgagccgaga[C/T]agtgccactgcactc | 23368 |
rs1187419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103835476 | accactgtacttcag[C/T]ctgggcaacagagca | 23368 |
rs1187420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103827059 | gggattactggcgtg[C/T]gccaccgtgcccagc | 23368 |
rs1475007 | snp | C/T | 0.48491 | 0.0855403 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103830810 | ggcttaaccataccc[C/T]aggttctcaatagcc | 23368 |
rs1535096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103765370 | AAACTAAGTGCAAAA[A/G]GGAACGAGCATGAAA | 23368 |
rs1535097 | snp | A/G | 0.485187 | 0.0847778 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103750312 | TTTGGTCCTTTTTGA[A/G]TTTCCTGCTGCCTCC | 23368 |
rs1535098 | snp | A/T | 0.485187 | 0.0847778 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103750176 | GTAATCATCATTGGC[A/T]CTAGTCATTTCGTGT | 23368 |
rs1547604 | snp | A/T | 0.482757 | 0.0912364 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103804322 | AAAATATCTGTGTGG[A/T]TTACTTAAATTAGTG | 23368 |
rs1950301 | snp | C/T | | | intron-variant | PPP1R13B | GRCh38.p7 | 14:103775051 | TTGATGAAGTTTTTT[C/T]TTGTTAATAAGGAGA | 23368 |
rs1955660 | snp | A/G | 0.495483 | 0.0473088 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103763648 | gtaaattatgcctca[A/G]ttaaCTCTAAAAAAG | 23368 |
rs1980620 | snp | C/G | 0 | 0 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103817959 | AGATTATTTCCTGTA[C/G]TTTCATCAAGATGAA | 23368 |
rs1997913 | snp | A/G | 0.483345 | 0.0897213 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103747623 | AATTGTGTGCAGTGT[A/G]CACTGCTAGAGTGCA | 23368 |
rs2024667 | snp | A/C | 0.483199 | 0.0901004 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103745192 | AAGAGCATCACCAGC[A/C]CTTGTGAGCCACAAG | 23368 |
rs2024668 | snp | C/G | 0.0998734 | 0.199905 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103744816 | GCTCACCTTCAGAGT[C/G]GGGGCAGCAGCTCAG | 23368 |
rs2024669 | snp | C/G | 0.481473 | 0.0944461 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103809265 | ATGTGAAATTATTAA[C/G]GCAAGTAAAACAGTG | 23368 |
rs2144079 | snp | A/G | 0.481473 | 0.0944461 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103792547 | tttctactttaaaac[A/G]aaaattatgttcagt | 23368 |
rs2144080 | snp | G/T | 0.481473 | 0.0944461 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103792424 | acttgaggccaaggc[G/T]ggcagattgcttgag | 23368 |
rs2179947 | snp | A/T | | | intron-variant | PPP1R13B | GRCh38.p7 | 14:103802825 | TAAGTTATTTGGGTG[A/T]TCTTCGCTTTTAAAA | 23368 |
rs2179948 | snp | A/G | | | intron-variant | PPP1R13B | GRCh38.p7 | 14:103763675 | AGTTACAATGGGTGA[A/G]TTTTAGGATATGTAA | 23368 |
rs2223937 | snp | C/T | 0.482905 | 0.0908579 | intron-variant, upstream-variant-2KB | PPP1R13B | GRCh38.p7 | 14:103820043 | TGGCAGGTAGAGGAC[C/T]ACTCAAGGCCTTGGA | 23368 |
rs2295140 | snp | A/G | 0.499934 | 0.00575657 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103749956 | AACACAAATCATAAA[A/G]GTTGTATTTTGTGGT | 23368 |
rs2295141 | snp | A/G | 0.485255 | 0.0845871 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103746612 | CAGTCTCTTGCACTA[A/G]GCTTAGGACTTCTTT | 23368 |
rs2295142 | snp | A/G | 0.000150823 | 0.00868268 | synonymous-codon, nc-transcript-variant | PPP1R13B | GRCh38.p7 | 14:103742663 | AGCACTGGGACCCAC[A/G]GAGAAGCCGGTAGGC | 23368 |
rs2295143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103738590 | GACAATTAGGAAGCA[C/T]GGAAGAGAGAATTAG | 23368 |
rs2295144 | snp | C/T | 0.181528 | 0.24044 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103736236 | GCTGCAGGCCACCCT[C/T]TGCTGAGGCCTGACC | 23368 |
rs2295145 | snp | C/T | 0.490778 | 0.0672751 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103735967 | CTGGGAAACTAGCTG[C/T]CCGTGTCTCTGTACA | 23368 |
rs2307733 | in-del | -/GTAT | 0.455263 | 0.142713 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103845237 | AATATTTTAAACTAT[-/GTAT]CCAAAAATGTAAATA | 23368 |
rs2368558 | snp | A/G | 0.481396 | 0.0946345 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103764181 | TGTTTAGCTTTTTAA[A/G]AGACTGCCAAACTGT | 23368 |
rs2368559 | snp | C/T | 0.481396 | 0.0946345 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103764198 | GACTGCCAAACTGTT[C/T]TCCAAAGCGATTGCA | 23368 |
rs2368560 | snp | C/T | 0.464203 | 0.128908 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103806974 | CATTCAAAACCTTCC[C/T]GTGGTTTCCTCTCTG | 23368 |
rs2368561 | snp | A/C | 0.293294 | 0.246223 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103816767 | CTGCAAATACCAAAA[A/C]TTCAGTATTAATCCA | 23368 |
rs2887282 | snp | C/T | 0.48491 | 0.0855403 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103814397 | aatttgtcccaagtc[C/T]gctgaactaataaat | 23368 |
rs3035519 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103792202 | tgtgtgtgtgtgtgt[A/G]tatttttttaaagac | 23368 |
rs3222998 | microsatellite | (CA)25/26/27/28/29/30/31/32/33 | 0.806882 | 0.0828657 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103748062 | gccaattccttaaaT[(CA)25/26/27/28/29/30/31/32/33]CGCTACTGGTTCTCT | 23368 |
rs3742367 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | ZFYVE21, PPP1R13B | GRCh38.p7 | 14:103733829 | GGCCATGCTCCTGTG[C/G]TCGGGCTGCTCTACA | 23368 |
rs3742368 | snp | C/G/T | 0.00485709 | 0.0490403 | synonymous-codon, nc-transcript-variant | PPP1R13B | GRCh38.p7 | 14:103740517 | AGGCTGTGGTGTGCC[C/G/T]GTGGACAGTGACCCG | 23368 |
rs3742369 | snp | C/T | 0.473369 | 0.112278 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103784939 | AGACCACATCTTTTT[C/T]ACTCCAGAATTAAAA | 23368 |
rs3818085 | snp | A/G | 0.485187 | 0.0847778 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103749648 | AAAAATGACAGAACA[A/G]AGTTCCTTCTCCCAG | 23368 |
rs3825550 | snp | A/G | 0.160143 | 0.233293 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103735212 | TCCTGTCCTGACGCG[A/G]CTCCGTTGCTTCCCA | 23368 |
rs4344667 | snp | A/C | 0 | 0 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103766871 | AAAAAATGATCAAAC[A/C]TCAACAATTTCACAT | 23368 |
rs4641668 | snp | A/T | 0.104504 | 0.2033 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103755915 | AAACAAGTCCAACCC[A/T]AATTATTATTTACAT | 23368 |
rs4900594 | snp | C/T | 0.461037 | 0.134028 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103784669 | AACATGGGATACCAA[C/T]TTTCCCTCTAGCCAC | 23368 |
rs4900595 | snp | A/G | 0.485049 | 0.0851591 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103791717 | acagagcaagactcc[A/G]tctcaaaacaaacaa | 23368 |
rs4900596 | snp | A/C | 0.00649344 | 0.0566088 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103793537 | ctgtgagtaaattaa[A/C]cctttttcctttata | 23368 |
rs4900597 | snp | C/T | 0.367297 | 0.220775 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103800327 | tAAAATCTCTGCATT[C/T]GAGTAAGCATATGAT | 23368 |
rs4900598 | snp | C/T | 0.485049 | 0.0851591 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103815204 | catattatatgattc[C/T]gtttttataaaatgt | 23368 |
rs4900599 | snp | G/T | 0.367091 | 0.220884 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103817107 | GTGGAAAACAAAATT[G/T]CAAGTGCCTGGAGAT | 23368 |
rs4900600 | snp | A/G | 0.482609 | 0.0916147 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103825502 | acacacaaatgataa[A/G]agcctgaaacagcct | 23368 |
rs4906363 | snp | A/G | 0.348354 | 0.22984 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103743902 | TGACCCGATGCAGCC[A/G]CACCGCAACCCCAGC | 23368 |
rs4906364 | snp | C/G | 0.374 | 0.217081 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103748005 | CCACGCTGCCGGCCG[C/G]CCTCACAGATTCTGG | 23368 |
rs4906365 | snp | C/G | 0.480144 | 0.097642 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103762893 | GACACAGTGGAATCA[C/G]AGCAAATTTCCATCA | 23368 |
rs4906368 | snp | A/C | 0.481473 | 0.0944461 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103776060 | TCTACAGACAAAGCA[A/C]AAAAGGTTTATAGTT | 23368 |
rs4906369 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103776121 | TACAACATGAAAGTC[C/T]GGTACAGCTGCAAGA | 23368 |
rs4906371 | snp | A/G | 0.485049 | 0.0851591 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103790595 | cagcctgggcaacat[A/G]gcaaaaccccatctt | 23368 |
rs4906372 | snp | A/C | 0.484841 | 0.0857308 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103799326 | tgggactacaggcgc[A/C]cgtcactacgcccgg | 23368 |
rs4906373 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103803471 | ACACAGTGAAACCCC[A/G]TCTCTATTAAAAATA | 23368 |
rs4906374 | snp | A/T | 0.483923 | 0.0882034 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103803663 | TAAATAAATAAATAA[A/T]TAATTAATTAATAAA | 23368 |
rs4906375 | snp | A/G | 0 | 0 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103805351 | CAACGGTGGCAGATT[A/G]CTTGAGCTCAAGAGT | 23368 |
rs4906376 | snp | A/C | 0.367503 | 0.220665 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103805828 | gcccaaaacagtcaa[A/C]tccatagagaaagaa | 23368 |
rs4906377 | snp | A/G | 0.367708 | 0.220556 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103812519 | ctgcctcctgggttc[A/G]agcgattctcgtgac | 23368 |
rs4906378 | snp | C/T | 0.367091 | 0.220884 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103817108 | TGGAAAACAAAATTG[C/T]AAGTGCCTGGAGATT | 23368 |
rs4906379 | snp | A/G | 0.367503 | 0.220665 | upstream-variant-2KB, intron-variant | PPP1R13B, LINC00637 | GRCh38.p7 | 14:103849154 | CTCTTCTGGGAGCAG[A/G]GTTTGGAGAGAAGAG | 23368 |
rs5811117 | in-del | -/G | 0.485187 | 0.0847778 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103750199 | TGATTACAGGAGACT[-/G]AGTGCGGTGTTTGGG | 23368 |
rs5811119 | in-del | -/T | 0.484841 | 0.0857308 | intron-variant, upstream-variant-2KB | PPP1R13B | GRCh38.p7 | 14:103820446 | TCACAAGGACCCGTA[-/T]TTTTGACACAAAAAT | 23368 |
rs6575997 | snp | A/G | 0.488363 | 0.0753851 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103762209 | GAGCTAAGCTACAGC[A/G]TAAACGATGGAGGTT | 23368 |
rs6575998 | snp | A/G | 0.499816 | 0.0095829 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103784080 | actcgggaggctgaa[A/G]caggagaatcgcttg | 23368 |
rs6575999 | snp | C/G | 0.485596 | 0.0836329 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103784272 | TGAGAAGGAAAGAAG[C/G]GTTGGTGCCTAAAAA | 23368 |
rs6576000 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103787942 | ggcgtgagccgccgc[A/G]cccagcctccttttt | 23368 |
rs6576001 | snp | C/G | 0.0681886 | 0.171594 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103799063 | ggaatgcaatgtcgc[C/G]atcttggttcactgc | 23368 |
rs6576003 | snp | A/C | 0.482683 | 0.0914256 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103824993 | accctgtgtcaagca[A/C]gtctactggtgccat | 23368 |
rs6576005 | snp | C/T | 0.48155 | 0.0942576 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103826032 | gtatttttattttta[C/T]tattatttttaattt | 23368 |
rs7141473 | snp | A/C | 0.484841 | 0.0857308 | intron-variant, upstream-variant-2KB | LINC00637, PPP1R13B | GRCh38.p7 | 14:103849718 | GCCCCCACCATTCCC[A/C]ACACGCCCCTGCCCT | 23368 |
rs7141928 | snp | C/T | 0.485049 | 0.0851591 | intron-variant, upstream-variant-2KB | PPP1R13B | GRCh38.p7 | 14:103753612 | ACTTATCTTAATGCA[C/T]GGATACAAGTTAAGT | 23368 |
rs7142679 | snp | C/G | | | intron-variant | PPP1R13B | GRCh38.p7 | 14:103746615 | GAAGTCCTAAGCTTA[C/G]TGCAAGAGACTGCCA | 23368 |
rs7142769 | snp | C/T | 0.341235 | 0.232758 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103762504 | CCTAATGTTAAATGA[C/T]GAGTTAATGGGTGCA | 23368 |
rs7143669 | snp | C/T | 0 | 0 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103762238 | TTTAACTATGAATGG[C/T]GCTTTTTCCTTCAAT | 23368 |
rs7145899 | snp | A/C | | | intron-variant, upstream-variant-2KB | PPP1R13B, LINC00637 | GRCh38.p7 | 14:103847284 | CGCCGCCACCTCCCG[A/C]CCGCCCTCACCCACC | 23368 |
rs7147171 | snp | A/G | 0.48491 | 0.0855403 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103798520 | TATTACAAATACAAA[A/G]CTAATCCCCTCAATA | 23368 |
rs7147292 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103768442 | gctggaactacaggc[A/G]tgcgccaccacgccc | 23368 |
rs7147662 | snp | A/T | | | intron-variant | PPP1R13B | GRCh38.p7 | 14:103825862 | ttttttttttttttt[A/T]gagagagagtctcgc | 23368 |
rs7149024 | snp | C/T | 0.461592 | 0.133149 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103756341 | ATGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 23368 |
rs7150438 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103838997 | CACTGTGTTTCAttt[A/C]tttttctttttttct | 23368 |
rs7152148 | snp | G/T | 0.48491 | 0.0855403 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103768753 | tttttgtatttttag[G/T]agagatggggtttca | 23368 |
rs7152309 | snp | A/G | 0.00335611 | 0.0408264 | synonymous-codon, nc-transcript-variant | PPP1R13B | GRCh38.p7 | 14:103738753 | GTGATGGTGGCCGGC[A/G]CAGACGGCGTTGTGC | 23368 |
rs7155786 | snp | C/T | 0.101658 | 0.201233 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103751706 | tacgtggggacacag[C/T]gagaaggcggctctc | 23368 |
rs7156450 | snp | A/G | | | intron-variant | PPP1R13B | GRCh38.p7 | 14:103736444 | GGACAGACAGGACAA[A/G]CGAGCTCCTGAGCCC | 23368 |
rs7156697 | snp | A/G | 0.461592 | 0.133149 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103744799 | CCAGCTCCACCTCTG[A/G]GCTGAGCTGCTGCCC | 23368 |
rs7156834 | snp | A/G | 0.46137 | 0.133501 | intron-variant | PPP1R13B | GRCh38.p7 | 14:103744843 | GAGCACAGGTTCCCC[A/G]TGTCCATGACTTTCA | 23368 |