| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs780789264 | snp | C/G | 1.64746e-05 | 0.00287002 | synonymous-codon | FAM63A | GRCh38.p7 | 1:151001304 | GGGCTTGATGGACAG[C/G]AGGCAGTTTCCTACA | 55793 |
| rs780879032 | snp | C/T | 1.74075e-05 | 0.00295016 | missense, intron-variant | FAM63A | GRCh38.p7 | 1:150997778 | AGAGCAATCAGGTAG[C/T]CCTGGGGAGAACAAG | 55793 |
| rs781028977 | snp | A/T | | | intron-variant | FAM63A | GRCh38.p7 | 1:151000648 | AATGATGGAGATTCT[A/T]GCCTTCTCTCCCACC | 55793 |
| rs781092145 | snp | A/G | 1.83643e-05 | 0.00303015 | upstream-variant-2KB, intron-variant | FAM63A, PRUNE1, PRUNE | GRCh38.p7 | 1:151008839 | GAGCGAGGAGCGAGA[A/G]GCCAGTTTAGGAGCG | 55793 |
| rs781098926 | snp | C/T | | | intron-variant | FAM63A | GRCh38.p7 | 1:150998982 | TAGGGGAGGATCATA[C/T]TTTCCTGTCCCATCG | 55793 |
| rs781162463 | snp | C/T | 3.29473e-05 | 0.00405864 | missense | FAM63A | GRCh38.p7 | 1:150999427 | ACGCTAAGTTCACCC[C/T]CCTTAGCAGCTGCTG | 55793 |
| rs781213897 | in-del | -/A | 0.00133822 | 0.0258325 | intron-variant | FAM63A | GRCh38.p7 | 1:151000626 | ACATTCTGGGGGTAG[-/A]AAAAAAAATGATGGA | 55793 |
| rs781248774 | snp | C/G | 1.67694e-05 | 0.00289558 | utr-variant-3-prime | FAM63A | GRCh38.p7 | 1:150997246 | CCAACTAGCCATAGC[C/G]TCTGGAAGAAGGGGC | 55793 |
| rs781261460 | snp | A/C | 1.65132e-05 | 0.00287339 | utr-variant-5-prime, missense, intron-variant | FAM63A | GRCh38.p7 | 1:151002223 | CAAGGGCCGTTAGTG[A/C]TCTGGGTGATGATGG | 55793 |
| rs781360008 | snp | A/G | | | intron-variant | FAM63A | GRCh38.p7 | 1:151004963 | ATTGATTATCCTCTT[A/G]ATTCACATATGTTTA | 55793 |
| rs781429294 | snp | C/T | 1.68738e-05 | 0.00290458 | intron-variant | FAM63A | GRCh38.p7 | 1:150999992 | TGGGATGTGGGATAC[C/T]AAAAAAATTGGGATT | 55793 |
| rs781448566 | snp | C/T | 6.65668e-05 | 0.00576879 | intron-variant | FAM63A | GRCh38.p7 | 1:151001807 | GAAGGGGTGATCACG[C/T]GTGTGCTTTCCTCCA | 55793 |
| rs781517420 | snp | A/G | 7.3177e-05 | 0.0060484 | intron-variant, missense | FAM63A | GRCh38.p7 | 1:150997503 | AGGGGAGAGGGACAG[A/G]CAGGGGAAGGACTCT | 55793 |
| rs781540305 | snp | C/G | | | upstream-variant-2KB, intron-variant | FAM63A, PRUNE1, PRUNE | GRCh38.p7 | 1:151008982 | TCATCTTGGTCAGTT[C/G]CATCAAAAAAACCAG | 55793 |
| rs781578810 | snp | A/G | | | intron-variant | FAM63A | GRCh38.p7 | 1:150999000 | TCCTGTCCCATCGAC[A/G]GCAGGCTTATCCCTT | 55793 |
| rs781716055 | snp | C/T | 0.000506406 | 0.0159043 | intron-variant | FAM63A | GRCh38.p7 | 1:151006096 | TGCCCTGTATACTTG[C/T]TCACAAGGAGAGGGG | 55793 |
| rs781750145 | snp | C/T | 1.78864e-05 | 0.00299046 | intron-variant, missense | FAM63A | GRCh38.p7 | 1:150997579 | CTGGACCCGGCAAAG[C/T]ATGAGGTGGAAACCG | 55793 |
| rs796774415 | snp | C/T | | | utr-variant-3-prime | FAM63A | GRCh38.p7 | 1:150997029 | CAGTCTGTACATACG[C/T]GTGACTATTCAGGGA | 55793 |