SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs64432980 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74984998 | AAAGGGTGGGAGGGA[A/G]AGAAGGAGAAAGAGA | 303412 |
rs64506610 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74984939 | CCAAGGGAAAGGGAA[A/G]AAAGGAAAGTGAAGG | 303412 |
rs65898587 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74984982 | AGAAGGAGAGAGGGA[A/G]AAAGGGTGGGAGGGA | 303412 |
rs104945257 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf43 | Rn_Celera | 10:74995002 | AAGTGATATTTAGGT[C/T]CCATATATCTGAGTT | 303412 |
rs105023501 | snp | C/T | 0.5 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74984528 | TTTTTTTTTTTTTTC[C/T]TTTTTTTTTTTTTTT | 303412 |
rs105197727 | snp | A/G | 0.5 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74989674 | TCTCTGCGTCCTTCC[A/G]ATTTTGGCAGATGAG | 303412 |
rs105210297 | snp | A/G | 0.5 | 0 | downstream-variant-500B | Rnf43 | Rn_Celera | 10:75029092 | CTGTGACCGATAGAA[A/G]TGTGCTGATGGTGGG | 303412 |
rs105306356 | snp | C/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74980664 | ACACATACATACACA[C/G]ATACACACACACACA | 303412 |
rs105454775 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74977995 | TTAAGAATGTAAGAC[A/G]GAATGGCCGCTGGCC | 303412 |
rs105481920 | snp | C/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74984545 | TTTTTTTTTTTTTTC[C/T]TTTTTTTTTTTTTTG | 303412 |
rs105627856 | snp | C/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74981674 | CCTTATATTATCTCC[C/T]CAGAGTGACTAAAGT | 303412 |
rs105717879 | snp | A/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74979585 | TCTTGAACATAAATA[A/T]AAACACACATGTATT | 303412 |
rs105790416 | snp | C/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:75022508 | TGCAAACACAGGTAG[C/T]ACTTTTCACGGCTGC | 303412 |
rs105803017 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74992997 | TGGAGCTCACTGACT[A/G]GAGACCCAGGTTCTA | 303412 |
rs105803975 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74996826 | TGGGCAATGTTAAAG[A/G]GATGTTTTCTTAAAC | 303412 |
rs105889991 | snp | A/C | 0.5 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:75023423 | CAACCAACCAACCAA[A/C]CAAACAAACAAACAA | 303412 |
rs105900777 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:75005303 | TTAGCTCAGTGGTAG[A/G]GCGCTTGCCTAGCAA | 303412 |
rs105906162 | snp | C/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:75022618 | GGGAGGGAAGCCCAG[C/G]GGCTCACGGCTCTCC | 303412 |
rs105906913 | snp | G/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74987545 | TACTTGTTCATGGTG[G/T]ACGGGAGGGCGGTTA | 303412 |
rs105915931 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74970136 | GTTTTGAGCCTAAGT[A/G]CCACATGGGGAAAAA | 303412 |
rs106008169 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf43 | Rn_Celera | 10:74995276 | GCCCAGTCAGCCCAA[C/T]GCGTCACGGACAATG | 303412 |
rs106070634 | snp | C/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:75012266 | GGTGGTCCCTATTGA[C/T]TGACAGCCCCTTCCG | 303412 |
rs106220325 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | Rnf43 | Rn_Celera | 10:74995949 | AGGTAACCTGCCTCG[C/T]GAGGTGGGTGGTGCA | 303412 |
rs106237852 | snp | C/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74983711 | CCTGAGACCAATGTG[C/T]TCTTAATAGGTCATA | 303412 |
rs106302787 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74963800 | TATATATATATATAT[A/G]TATATATATATATAT | 303412 |
rs106315509 | snp | C/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74973936 | TCATTAGTCATCTCA[C/T]GAGAATTGAGGCCGG | 303412 |
rs106318889 | snp | G/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74984883 | TTCACACCTGATTTT[G/T]TTTTTGTTTTTTTTT | 303412 |
rs106364174 | snp | C/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74980666 | ACATACATACACAGA[C/T]ACACACACACACACA | 303412 |
rs106382766 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74981494 | TAAATGCCTTTCAGC[A/G]GGGAGCTAGACCTGT | 303412 |
rs106567598 | snp | C/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:75001951 | GATCTGCAGGGCTTC[C/G]TGGGATTCTTGGAGG | 303412 |
rs106676396 | snp | C/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:75001889 | GACCGAACAGGCCTC[C/T]GGGGCTTTCTGTACT | 303412 |
rs106796162 | snp | C/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74996723 | ACTGGGCCTGGTCAT[C/T]ATAAAATCTTAGTAG | 303412 |
rs106909955 | snp | C/T | 0.277778 | 0.248452 | upstream-variant-2KB, utr-variant-5-prime | Rnf43 | Rn_Celera | 10:74959213 | CTTCATTTTCTGCAC[C/T]GAGGACCTGCCTTCG | 303412 |
rs107005067 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74967988 | TGTGGTGAGCCTGGC[A/G]TTTCCTATGTATGAC | 303412 |
rs107016714 | snp | A/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74979461 | GCCAAGGATGGATGT[A/T]CTGTGACTGATGGGA | 303412 |
rs107059504 | snp | A/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74979536 | CCATCACTCTACCAT[A/G]GGAATATGTATTTGA | 303412 |
rs107093763 | snp | C/T | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74984510 | TAGCCTGTGCCTTTC[C/T]TTTTTTTTTTTTTTT | 303412 |
rs107117146 | snp | C/T | 0.5 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74986214 | GTGAACAGATGTAGG[C/T]TTTGTTTGTACTGCG | 303412 |
rs107132243 | snp | C/T | 0.5 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74986173 | ATCACAAGCGTGACC[C/T]GCCACACCCAGGGTT | 303412 |
rs107134357 | snp | C/T | 0.5 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74983442 | TAATTTCTCTTTAGA[C/T]TGTGAGAGAGCTGAG | 303412 |
rs107180140 | snp | A/C | 0.5 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:75007943 | GGCGATGCTTCTCTG[A/C]TTTGGTCATTCTGCA | 303412 |
rs107216026 | snp | A/G | 0 | 0 | missense | Rnf43 | Rn_Celera | 10:75025833 | GGAATTCAGTAGCCC[A/G]GACCCCAAGACCTAG | 303412 |
rs107348111 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Rnf43 | Rn_Celera | 10:75018671 | TTCTAGCCCGACCCA[A/G]CTCTGTAGAAATCCC | 303412 |
rs107476085 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf43 | Rn_Celera | 10:75019129 | ATCCAAAAAAAAAAA[A/T]TTTTTTTTTTTTGGT | 303412 |
rs197428964 | snp | C/G | 0 | 0 | intron-variant | Rnf43 | Rn_Celera | 10:74980462 | TGCTTACTGCTAAAT[C/G]AATTTTTCTCTCCCT | 303412 |