SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs193336396 | snp | C/G | 0.059645 | 0.162065 | intron-variant | npp-20 | WS195 | IV:1493698 | AAATATCCAAAACCT[C/G]GAAATTTTGAATTTA | 176957 |
rs193336397 | snp | G/T | 0.0747531 | 0.178293 | intron-variant | npp-20 | WS195 | IV:1494134 | GCTTAGGCTAAGGCT[G/T]AGGCCTTAAAAAAAA | 176957 |
rs193336398 | snp | A/G | 0.161167 | 0.233685 | intron-variant | npp-20 | WS195 | IV:1494136 | TTAGGCTAAGGCTTA[A/G]GCCTTAAAAAAAATC | 176957 |
rs193336399 | snp | A/T | 0.204142 | 0.245758 | intron-variant | npp-20 | WS195 | IV:1494142 | TAAGGCTTAGGCCTT[A/T]AAAAAAATCCGAATT | 176957 |
rs193336400 | snp | A/T | 0.15201 | 0.229996 | intron-variant | npp-20 | WS195 | IV:1494161 | AAAATCCGAATTTAA[A/T]TTTTATTTTGCGAAT | 176957 |
rs193603915 | snp | C/G | | | intron-variant | npp-20 | WS195 | IV:1491729 | CTCATGCCTACTGCG[C/G]CTAGAGGTAGGTAAG | 176957 |
rs193603916 | snp | A/C | | | intron-variant | npp-20 | WS195 | IV:1491829 | TTTCTAGGTTTTGCT[A/C]GAAAAATCATAATTT | 176957 |
rs193603917 | snp | A/G | | | intron-variant | npp-20 | WS195 | IV:1493319 | TTCGAATTTTCACCA[A/G]CAATTTTGTTTGTAG | 176957 |
rs193603920 | snp | A/T | | | intron-variant | npp-20 | WS195 | IV:1495484 | AATTTTTGGCAAAAA[A/T]CCCAAAAAATGAGCT | 176957 |