SNP - dbSNP | dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene | rs8161095 | snp | C/T | 0 | 0 | missense, intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12628975 | CACACACACGAGCCA[C/T]GGTGCAGGGTGACAG | 299607 | rs8163032 | snp | A/C | | | utr-variant-3-prime, intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12632179 | GGTCCCAAAGGGAAA[A/C]TGAGGCAGATACCCC | 299607 | rs106095187 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant, utr-variant-3-prime | Med16, Arhgap45, R3hdm4 | Rn_Celera | 7:12618219 | GTTTGCGCGCGCGCG[C/T]GTGTGTGTGTGTGTG | 299607 | rs106315113 | snp | C/T | 0 | 0 | intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12623176 | AGAGCAAGTGGATCT[C/T]TGAGTTGAGACCAGC | 299607 | rs106949390 | snp | A/G | 0 | 0 | intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12624360 | GTGAAACCAGGTCTG[A/G]AGGATGCAGGTAAAT | 299607 | rs107306134 | snp | C/T | 0 | 0 | intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12626825 | GACTGACCCCAGGGC[C/T]TTGCGCTTGCTAGGC | 299607 | rs107550580 | snp | A/G | 0 | 0 | intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12624342 | CCTGCCTCACCTTCC[A/G]TGGTGAAACCAGGTC | 299607 | rs197256260 | snp | C/T | 0 | 0 | intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12622044 | GTTTTTGGAGCCTAA[C/T]GGCTTTCACATTGCC | 299607 | rs197448267 | snp | C/G | 0 | 0 | intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12622595 | CAGCATTGAGCTCAA[C/G]GATGCCATGTAAGGT | 299607 | rs198088998 | snp | A/G | 0 | 0 | intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12624311 | GGGGTGCCTTCCTCC[A/G]TCTGCCTCTTGCCCT | 299607 | rs198250250 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | Med16, Arhgap45, R3hdm4 | Rn_Celera | 7:12618949 | GGTCTACATAGCCAG[G/T]GCCACACAGTGACCC | 299607 | rs198256446 | snp | A/C | 0 | 0 | intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12626286 | ACACACACGTGCGCG[A/C]GCACCTCCCACAGAT | 299607 | rs198338963 | snp | A/T | 0 | 0 | downstream-variant-500B, intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12632505 | TACCACTAATAGGGA[A/T]AAGGGGTAACGTTGT | 299607 | rs198748822 | snp | C/G | 0 | 0 | synonymous-codon, intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12631585 | GGGTGCCTACCCCAC[C/G]GAGGAGTGCAAAGCC | 299607 | rs198831598 | snp | C/T | 0 | 0 | intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12626824 | GGACTGACCCCAGGG[C/T]TTTGCGCTTGCTAGG | 299607 | rs199131811 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12619503 | GCGAGCACGAACTAC[A/G]GGCTTACCCAAGACA | 299607 | rs199231920 | snp | C/T | 0 | 0 | intron-variant | Med16, Arhgap45 | Rn_Celera | 7:12622541 | CAGGAACCTCAGGAG[C/T]AGTTCTTGGCTGACT | 299607 | |