madd-2
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193343622snpC/T0.0299930.118731intron-variant?WS195V:1224264CTATCTAAGTTCAAC[C/T]CTCCAACAAAAATGA178619
rs193343623snpA/T0.009999750.0699991intron-variant?WS195V:1224459GAATTTTCTAGAATT[A/T]GTTTTTCTCTCTTCC178619
rs193343624snpA/G0.3949650.203679intron-variant?WS195V:1226587GAAGTCACAAAATGG[A/G]TTCATTTTTTGGCAA178619
rs193343625snpA/G0.02969620.118179synonymous-codon?WS195V:1227096TAAACTTGTTGAGCG[A/G]TGGAGAAGGGCGTTG178619
rs193343626snpG/T0.1562590.23176intron-variant?WS195V:1227229TTGAAGTTTCTTACT[G/T]GAAGCCTAAGCTTAA178619
rs193343627snpA/T0.1044420.203256intron-variant?WS195V:1227760TTCATCCCCATTACC[A/T]CATTACATCTGCCAC178619
rs193343628snpC/T0.1562590.23176intron-variant?WS195V:1227846CGTCATCAACCCTGT[C/T]CCCGCTACAAAAAGT178619
rs193343629snpA/G0.07754310.180993intron-variant?WS195V:1227874AGTTTCTTTTACACA[A/G]AGATATACACAGAAA178619
rs193343630snpG/T0.010050.0701712intron-variant?WS195V:1230184CCAGATCCCCAGAAA[G/T]TTGGAAAATGTCTGA178619
rs193343631snpA/G0.0299930.118731intron-variant?WS195V:1230194AGAAAGTTGGAAAAT[A/G]TCTGAGGAAACCTGT178619
rs193343632snpC/T0.02984390.118454intron-variant?WS195V:1230292AGTTCCACCTTTCAA[C/T]TCTTCTCATTTTTCC178619
rs193343633snpC/T0.155550.231472intron-variant?WS195V:1232800AATATTTCCCTTTTC[C/T]AATCCCCAGTCCCGT178619
rs193343634snpA/T0.009999750.0699991intron-variant?WS195V:1232873AATAAACATGTCGTT[A/T]AGTTTACAAAACTTT178619
rs193615350snpC/Tintron-variant?WS195V:1224738AGGCCCAAGTCTAAG[C/T]CTGAGCCTAAACCGA178619
rs193615351snpA/Gsynonymous-codon?WS195V:1225784CGTGAGCCGTTTGCA[A/G]GCAGATCGATTCACT178619
rs193615352snpA/Gintron-variant?WS195V:1227686TAGAGAGTTCTGTCT[A/G]AAAACGCTTTGCTCA178619
rs193615353snpC/Tintron-variant?WS195V:1228936CTCCCAACCAATTTT[C/T]GCGTTTCCATGCGAC178619
rs193615354snpA/Tintron-variant?WS195V:1230454TATGGGGAATGGGGA[A/T]TTGGAACTGTGAGGT178619
rs193615356snpA/Gintron-variant?WS195V:1231045CAGACCACTGTCAAA[A/G]GAGACACACACACAC178619
rs193615357snpA/Tintron-variant?WS195V:1231703CGAGAAAAAGTTTCA[A/T]GGCTCACGCCATTAA178619
rs193615358snpC/Tintron-variant?WS195V:1232072GGTGGCTTTGAAGTT[C/T]TTTGAGACCCCGCGA178619
rs193615359snpC/Tintron-variant?WS195V:1232982TCGATTTCGAAAGCC[C/T]TAGGTCATTAGCCGT178619
rs193615360snpA/Tintron-variant?WS195V:1233160CTGAAGATTTGCGGT[A/T]GAACCTAGCCTCCCC178619
Full records
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