Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35457250 | 0.925 | 0.080 | 3 | 186620775 | missense variant | C/T | snv | 9.0E-03 | 8.1E-03 | 5 | |
rs7141420 | 1.000 | 0.080 | 14 | 79433111 | intron variant | C/T | snv | 0.56 | 5 | ||
rs8057044 | 0.882 | 0.080 | 16 | 53778702 | intron variant | G/A | snv | 0.54 | 5 | ||
rs9816226 | 1.000 | 0.080 | 3 | 186116710 | intron variant | A/T | snv | 0.82 | 5 | ||
rs11152213 | 1.000 | 0.080 | 18 | 60185715 | intergenic variant | A/C;T | snv | 4 | |||
rs12444979 | 1.000 | 0.080 | 16 | 19922278 | intergenic variant | C/T | snv | 0.11 | 4 | ||
rs12463617 | 1.000 | 0.080 | 2 | 629244 | regulatory region variant | A/C;T | snv | 4 | |||
rs12955983 | 1.000 | 0.080 | 18 | 60205756 | intergenic variant | A/G | snv | 0.20 | 4 | ||
rs12969709 | 1.000 | 0.080 | 18 | 60192330 | upstream gene variant | C/A | snv | 0.21 | 4 | ||
rs1330 | 1.000 | 0.080 | 11 | 17294482 | intron variant | C/T | snv | 0.30 | 4 | ||
rs1514175 | 1.000 | 0.080 | 1 | 74525960 | intron variant | A/G | snv | 0.48 | 4 | ||
rs17700144 | 1.000 | 0.080 | 18 | 60144750 | intron variant | G/A | snv | 0.14 | 4 | ||
rs2206277 | 0.925 | 0.080 | 6 | 50830813 | intron variant | C/T | snv | 0.19 | 4 | ||
rs2207139 | 1.000 | 0.080 | 6 | 50877777 | intergenic variant | A/G | snv | 0.16 | 4 | ||
rs4771122 | 1.000 | 0.080 | 13 | 27446043 | intron variant | G/A;C | snv | 4 | |||
rs4929949 | 1.000 | 0.080 | 11 | 8583046 | intron variant | T/C | snv | 0.46 | 4 | ||
rs62033400 | 1.000 | 0.080 | 16 | 53777876 | intron variant | A/G | snv | 0.30 | 4 | ||
rs7001819 | 0.925 | 0.080 | 8 | 11792966 | upstream gene variant | T/C | snv | 0.35 | 4 | ||
rs7132908 | 1.000 | 0.080 | 12 | 49869365 | 3 prime UTR variant | G/A | snv | 0.31 | 4 | ||
rs939583 | 1.000 | 0.080 | 2 | 622531 | intergenic variant | C/T | snv | 0.85 | 4 | ||
rs9939973 | 1.000 | 0.080 | 16 | 53766656 | intron variant | G/A | snv | 0.42 | 4 | ||
rs10182181 | 1.000 | 0.080 | 2 | 24927427 | intergenic variant | A/G | snv | 0.57 | 3 | ||
rs10835211 | 1.000 | 0.080 | 11 | 27679818 | intron variant | G/A | snv | 0.19 | 3 | ||
rs11042023 | 1.000 | 0.080 | 11 | 8640969 | missense variant | T/C | snv | 0.60 | 0.59 | 3 | |
rs11075985 | 1.000 | 0.080 | 16 | 53771295 | intron variant | C/A | snv | 0.42 | 3 |