Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10220411 | 14 | 68985371 | intron variant | A/G | snv | 0.29 | 2 | ||||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
rs1059196 | 22 | 19724571 | 3 prime UTR variant | C/T | snv | 0.42 | 3 | ||||
rs10761741 | 1.000 | 0.040 | 10 | 63306426 | intron variant | G/T | snv | 0.38 | 3 | ||
rs10876550 | 12 | 54318524 | intron variant | G/A | snv | 0.68 | 2 | ||||
rs10914144 | 1 | 171980610 | intron variant | T/C | snv | 0.78 | 2 | ||||
rs10940072 | 5 | 66620956 | intron variant | G/A | snv | 0.37 | 2 | ||||
rs11071720 | 15 | 63049797 | intron variant | T/C;G | snv | 3 | |||||
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 5 | |||||
rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
rs114694170 | 1.000 | 0.040 | 5 | 88884379 | non coding transcript exon variant | T/C | snv | 3.6E-02 | 4 | ||
rs11471957 | 20 | 59023277 | intron variant | -/AA | ins | 2 | |||||
rs11553699 | 12 | 121779004 | 3 prime UTR variant | A/G | snv | 9.4E-02 | 6 | ||||
rs11602954 | 11 | 202856 | intron variant | G/A | snv | 0.17 | 2 | ||||
rs11604127 | 11 | 196944 | 5 prime UTR variant | C/T | snv | 0.17 | 2 | ||||
rs117672662 | 14 | 68958750 | intron variant | T/C | snv | 7.4E-03 | 3 | ||||
rs12041331 | 0.776 | 0.200 | 1 | 156899922 | intron variant | G/A | snv | 0.19 | 3 | ||
rs12096438 | 1 | 25562931 | non coding transcript exon variant | C/A;T | snv | 2 | |||||
rs13042885 | 20 | 1944061 | upstream gene variant | C/A;T | snv | 2 | |||||
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs1354034 | 3 | 56815721 | intron variant | T/C | snv | 0.49 | 4 | ||||
rs143558304 | 19 | 16102887 | 3 prime UTR variant | -/A | delins | 4.6E-02 | 2 | ||||
rs150813342 | 9 | 132989126 | synonymous variant | C/T | snv | 4.1E-03 | 4.1E-03 | 9 | |||
rs151233 | 16 | 28495107 | synonymous variant | C/T | snv | 0.14 | 0.13 | 2 | |||
rs1716505 | 12 | 64611299 | intron variant | C/G | snv | 0.34 | 2 |