SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8161628 | snp | C/T | | | utr-variant-3-prime | Faf2 | Rn_Celera | 17:10487180 | TCTCTTGGAGGTGAC[C/T]AACACAAGCTATGCT | 291000 |
rs8163926 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10496725 | AAAAGCATTGACCAT[C/T]CTAGGGTGCTTCTAG | 291000 |
rs104911285 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10493828 | GCTCCTGGCTTCTAC[C/T]TTATTAAATAATCTA | 291000 |
rs104914111 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10492411 | GAAGGTTCCATCCCG[A/G]GGACCCAGACAAAGG | 291000 |
rs104927617 | snp | A/C | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10491309 | GACAAAACACTCACG[A/C]GACACGTGAAATATA | 291000 |
rs104996128 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10495221 | ACACACGTGCAGGTC[A/G]GAGGACACCCTGTGG | 291000 |
rs105002707 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10490150 | GGATGGCTGGCTTTC[A/G]TGTCTTGTGCACATG | 291000 |
rs105076851 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10492204 | AGCACTGGAAATCAA[A/G]ACCCCCAAAGCAGGT | 291000 |
rs105140644 | snp | C/T | 0.498473 | 0.0275894 | synonymous-codon | Faf2 | Rn_Celera | 17:10492621 | GTCATCTGGGGAGGG[C/T]TCAGGGGGCAGGCAC | 291000 |
rs105165837 | snp | C/T | 0 | 0 | upstream-variant-2KB | Faf2 | Rn_Celera | 17:10528527 | ACCTAGACTCGTTTA[C/T]TTTTTGTTGAATGCG | 291000 |
rs105251753 | snp | G/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10503128 | ACAAAACACTGCCTA[G/T]AAAGATGCCAACAAT | 291000 |
rs105316971 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10492917 | ATCGCATACACAGAA[C/T]GGATAAATAAACGCT | 291000 |
rs105529240 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10519981 | AAGCACACACATGCA[C/T]ACCACACATATGAAA | 291000 |
rs105603231 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10493640 | TTTTCCTGGCCGGTG[A/G]TCCTCCTCCTGCTCA | 291000 |
rs105617721 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10498377 | CATACAGAGGTTGCT[A/G]GACAAAACGGCTACA | 291000 |
rs105623716 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10500872 | ACATGAATTGGCTTA[C/T]TGTAGCGCATATGGG | 291000 |
rs105700259 | snp | A/C | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10518098 | AAAAAACAAAAAAAA[A/C]AAAAAACCAAGTATC | 291000 |
rs105746510 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10491801 | TAGAGAAACCCATCT[C/T]GAACCCCCTCCTGCC | 291000 |
rs105762635 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10505115 | AAGGCTTAGTAGCCC[C/T]GGAGTTCAGGGCCTC | 291000 |
rs105806119 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10497197 | CCAAGAGATCAAGCA[C/T]AAGACTTGGGATGCA | 291000 |
rs105878033 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10490931 | GACCTGGACTGTTCT[C/T]AGCACCCACATGGCA | 291000 |
rs105978139 | snp | A/T | 0 | 0 | utr-variant-3-prime | Faf2 | Rn_Celera | 17:10486454 | TCAAGACAGCAGAAC[A/T]GGGGACAGCAAGAAC | 291000 |
rs106147429 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10492891 | CTGGCATGTGTGTAC[C/T]GTGTTCTCACATCGC | 291000 |
rs106150883 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10499294 | AAAGAGGGGAGGGAA[A/G]TGGGGTTGCAAGGGA | 291000 |
rs106208411 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10503897 | GTCAACGGTTTCCCC[A/G]CATAACATATTCATT | 291000 |
rs106226129 | snp | A/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10517011 | TCTTTATCACCTTGA[A/T]TGTTGTTGTAAAAAT | 291000 |
rs106243594 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10506911 | GGGTCACAAATATGC[C/T]CAGAAGCAGCCTTAC | 291000 |
rs106252907 | snp | A/C | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10491557 | AGAAGCCTAAGGCAC[A/C]TTGCTAGGTTTCACA | 291000 |
rs106270805 | snp | A/C | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10518085 | ACCAAAAAAAAAAAA[A/C]AAACAAAAAAAACAA | 291000 |
rs106454726 | snp | C/T | 0 | 0 | utr-variant-3-prime | Faf2 | Rn_Celera | 17:10486708 | GAGTTGTGGCAAGAG[C/T]GGACCCCTTTTTTAT | 291000 |
rs106543371 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10494034 | TAGGCAGGTGGTCTG[A/G]GATGGCATTAGAAAA | 291000 |
rs106551033 | snp | A/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10489577 | ACTACAAAGTTTAAT[A/T]TGCTATCCTTCCATA | 291000 |
rs106614429 | snp | G/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10506887 | CTCCCGTGGCTCGTG[G/T]ACACATGTGGGTCAC | 291000 |
rs106709639 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10492895 | CATGTGTGTACTGTG[C/T]TCTCACATCGCATAC | 291000 |
rs106783262 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10506978 | AAAATGAGGTACAGA[A/G]AACACTTCCTCAGTG | 291000 |
rs106924044 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10500121 | AACGAGCTACCCTGG[A/G]CCTATGGTCTAAATC | 291000 |
rs106975078 | snp | G/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10498580 | GAAGAGGAATGCCTA[G/T]CAAGAGCCTGTTAAA | 291000 |
rs107013027 | snp | A/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10498483 | GTTGCTGCCAGAAAG[A/T]CTGAACTCTCTGTAC | 291000 |
rs107036634 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10506293 | GAGGGGGAGACAGTG[C/T]GGGAGAGAAAAGGAA | 291000 |
rs107053432 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10503757 | CTGTCTCCTAACAAC[A/G]CTCTTCCTGCCAGGG | 291000 |
rs107098473 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10492175 | CTTAATGGGAGACCC[C/T]GACTTCCATTCTAAG | 291000 |
rs107172357 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10493078 | AAGATTAAAGGCCTG[C/T]ACCACTACATCCAGC | 291000 |
rs107181679 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10505293 | TTTAATTTTGTGTAT[A/G]TGGGTGTGCTGCCAG | 291000 |
rs107264595 | snp | C/T | 0 | 0 | utr-variant-3-prime | Faf2 | Rn_Celera | 17:10487010 | CAGCCGGCCTAGCTG[C/T]GCTAACACTTCCCAA | 291000 |
rs107275874 | snp | A/C | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10518101 | AAACAAAAAAAACAA[A/C]AAACCAAGTATCCAA | 291000 |
rs107328239 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10508749 | GGGGTGATGTACTTT[A/G]TCTGAACTTGCACTT | 291000 |
rs107355117 | snp | A/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10497459 | CATGTGGGTGCTGGG[A/T]AATGAACCTGGGTCT | 291000 |
rs107372099 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10525625 | TCTAAACCATCTTTC[C/T]TTCAACATCAAGAAG | 291000 |
rs107393401 | snp | C/G | 0 | 0 | intron-variant, utr-variant-3-prime | Faf2 | Rn_Celera | 17:10487593 | CTCTGCCTCCCAGCA[C/G]ACCACCATGCCTGCG | 291000 |
rs107461437 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10521561 | TCTGTGGTTACTTAC[A/G]CTCATGTTCGTACAG | 291000 |
rs107480797 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10492141 | AAATACATTTAAAAA[C/T]CCAGGGCTGGAGAGA | 291000 |
rs197025112 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10501344 | AATAAATAAATAAAT[A/G]AATGAATAAATAAGA | 291000 |
rs197032850 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10510093 | CAAAAAAAAAAAAAC[C/T]TGTCTTGAAAAAACA | 291000 |
rs197068123 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10504369 | CACAGGCTGGCCCAC[C/T]TCAGGCAGACATTGT | 291000 |
rs197220244 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10502771 | GGATCTGCCAGGGCC[A/G]CTTTGTGTACATTGT | 291000 |
rs197223324 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10489881 | TATTTATGTATATGA[A/G]TACACTGACACTGTC | 291000 |
rs197322138 | snp | C/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10519300 | TTTAGCTCAGTGGTA[C/G]AGCGCTTGCCTAGCA | 291000 |
rs197356959 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10504899 | CTAGAACTGACATGA[C/T]AAAGGGAAACCACAA | 291000 |
rs197442037 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10497668 | AAAAGATAGCTTTCT[A/G]GAGTTGGCCCTCCTC | 291000 |
rs197492278 | snp | A/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10527092 | AGGACCCCCCCCTTT[A/T]AAAAAAAAAACAAAA | 291000 |
rs197559985 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10505687 | TAATTGCTCTAGGAT[C/T]AAATAAAGTGCTTAA | 291000 |
rs197577735 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10496862 | CTATGATGGTCCGCA[C/T]TCTGAACTCTCCTTC | 291000 |
rs197719072 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10501348 | AATAAATAAATGAAT[A/G]AATAAATAAGAAAAA | 291000 |
rs197725347 | snp | A/C | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10507033 | CAGTTCATTAAAAAA[A/C]CTAAGTGGAATGAAG | 291000 |
rs197785023 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10499040 | AAGACAGCGTGAGAG[C/T]AATCTGCCAACTATA | 291000 |
rs197810434 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10511532 | AACACCTATACTCAT[A/G]TGCATACACACATAA | 291000 |
rs197817187 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | Faf2 | Rn_Celera | 17:10487961 | GTGGCAGAAGGAAGC[A/G]CAAATGAGCCCAGGG | 291000 |
rs197843999 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10499730 | ATGGTATGCTCCTAA[C/T]TGCCTGTAATTCCCA | 291000 |
rs197893422 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10493651 | GGTGGTCCTCCTCCT[A/G]CTCACTCATCTCTAG | 291000 |
rs198015731 | snp | C/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10495784 | AGAGAGAGAGACAGA[C/G]ACAGAGAGACAGAGA | 291000 |
rs198122504 | snp | A/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10519301 | TTAGCTCAGTGGTAG[A/T]GCGCTTGCCTAGCAA | 291000 |
rs198140847 | snp | C/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10506500 | GAACTCCCACAGAGT[C/G]TAAGCACTTCCTCAA | 291000 |
rs198170606 | snp | C/G | 0 | 0 | upstream-variant-2KB | Faf2 | Rn_Celera | 17:10529738 | TCTCTGGAGATCTCT[C/G]TCTGTGTGTGTGTGT | 291000 |
rs198283413 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10526576 | CACTCAGAATCTTCC[A/G]AGTCCCCTGAGATTA | 291000 |
rs198332398 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10502484 | ATGTTACGATTCCAC[A/G]TAAAACAGAAATGGC | 291000 |
rs198450394 | snp | A/C | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10501321 | ATAAATAAATAAATA[A/C]ATAAATAAATAAATA | 291000 |
rs198455291 | snp | A/C | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10515182 | TTGCTATACAGTAAG[A/C]TTGTGCCTCAAAACA | 291000 |
rs198509704 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10507484 | CAATGGGAGTCTCAC[A/G]CTTTAGAGGAGAACA | 291000 |
rs198534210 | snp | A/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10507126 | TCATACACAGCTAAC[A/T]AAACTAAATGGGTGA | 291000 |
rs198622599 | snp | C/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10495786 | AGAGAGAGACAGAGA[C/G]AGAGAGACAGAGAGA | 291000 |
rs198641709 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10504424 | GCTATCTACTCTTCT[A/G]CTTCAGTCTCTCTTC | 291000 |
rs198648236 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10522319 | AGCTAGCTTCCATGG[C/T]GCCAGAGGATGCTCT | 291000 |
rs198783349 | snp | C/G | 0 | 0 | upstream-variant-2KB | Faf2 | Rn_Celera | 17:10529740 | TCTGGAGATCTCTCT[C/G]TGTGTGTGTGTGTGT | 291000 |
rs198862427 | snp | C/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10527089 | CTTAGGACCCCCCCC[C/T]TTAAAAAAAAAAACA | 291000 |
rs198889402 | snp | A/G | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10507416 | TGAGTATCATGTGAC[A/G]GCGTACATGATGAGT | 291000 |
rs198946384 | snp | A/G | 0 | 0 | utr-variant-3-prime | Faf2 | Rn_Celera | 17:10488314 | GAAGTCTTCACTGGA[A/G]GATGGAGAGGCGGCT | 291000 |
rs199002534 | snp | A/T | 0 | 0 | utr-variant-3-prime | Faf2 | Rn_Celera | 17:10485905 | GGTGACACCCTCTGA[A/T]TATGTGCTCTGGGGC | 291000 |
rs199088731 | snp | G/T | 0 | 0 | intron-variant | Faf2 | Rn_Celera | 17:10491278 | TACATGCAGAGCACA[G/T]ACATATGTACGGGCA | 291000 |
rs199270471 | snp | A/T | 0 | 0 | utr-variant-3-prime | Faf2 | Rn_Celera | 17:10486380 | TAGGGAGTCCCAGAC[A/T]GAACTGGCCTGGGGG | 291000 |