Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 26 | |
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 13 | ||
rs2740488 | 0.827 | 0.120 | 9 | 104899461 | intron variant | A/C | snv | 0.29 | 9 | ||
rs17231506 | 0.851 | 0.040 | 16 | 56960616 | upstream gene variant | C/G;T | snv | 0.28 | 8 | ||
rs10737680 | 0.827 | 0.080 | 1 | 196710325 | intron variant | A/C | snv | 0.44 | 7 | ||
rs2070895 | 0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 | 7 | ||
rs2043085 | 0.827 | 0.080 | 15 | 58388755 | intron variant | T/C | snv | 0.54 | 6 | ||
rs10922109 | 0.827 | 0.080 | 1 | 196735502 | intron variant | C/A | snv | 0.46 | 6 | ||
rs1142 | 0.851 | 0.040 | 7 | 105115879 | intron variant | C/T | snv | 0.31 | 6 | ||
rs72802342 | 0.851 | 0.040 | 16 | 75200974 | downstream gene variant | C/A | snv | 6.2E-02 | 5 | ||
rs62358361 | 0.851 | 0.040 | 5 | 39327786 | intron variant | G/C;T | snv | 5 | |||
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 5 | |
rs570618 | 0.827 | 0.040 | 1 | 196687934 | intron variant | T/G | snv | 0.69 | 5 | ||
rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 5 | |
rs10033900 | 0.807 | 0.040 | 4 | 109737911 | intron variant | T/C | snv | 0.54 | 5 | ||
rs73036519 | 0.851 | 0.040 | 19 | 45245104 | intron variant | G/A;C | snv | 5 | |||
rs3138141 | 0.827 | 0.040 | 12 | 55721994 | 3 prime UTR variant | C/A | snv | 0.19 | 0.16 | 5 | |
rs11080055 | 0.851 | 0.040 | 17 | 28322698 | intron variant | A/C | snv | 0.54 | 5 | ||
rs10781182 | 0.851 | 0.040 | 9 | 74002804 | intergenic variant | T/G | snv | 0.54 | 4 | ||
rs114092250 | 0.851 | 0.040 | 5 | 35494346 | intergenic variant | G/A;T | snv | 4 | |||
rs142450006 | 0.851 | 0.040 | 20 | 45986353 | regulatory region variant | TTCT/-;TTCTTTCT | delins | 2.0E-02 | 4 | ||
rs148553336 | 0.851 | 0.040 | 1 | 196644043 | intergenic variant | T/C | snv | 7.7E-03 | 4 | ||
rs1626340 | 0.827 | 0.120 | 9 | 99161090 | intergenic variant | G/A;T | snv | 4 | |||
rs201459901 | 0.851 | 0.040 | 20 | 58078668 | regulatory region variant | -/A | delins | 0.21 | 4 | ||
rs61818925 | 0.851 | 0.040 | 1 | 196846320 | upstream gene variant | T/G | snv | 0.67 | 4 |