Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4622308 | 0.925 | 0.160 | 12 | 56075401 | upstream gene variant | C/T | snv | 3 | |||
rs554073050 | 0.925 | 0.040 | 3 | 42263460 | synonymous variant | G/A | snv | 1.2E-05 | 7.0E-06 | 3 | |
rs533123 | 0.882 | 0.160 | 1 | 28814643 | intron variant | G/A;C | snv | 3 | |||
rs1042571 | 0.882 | 0.120 | 2 | 25161018 | 3 prime UTR variant | G/A | snv | 0.16 | 3 | ||
rs10070190 | 0.925 | 0.040 | 5 | 26866262 | intergenic variant | G/A | snv | 0.60 | 2 | ||
rs11783752 | 0.925 | 0.040 | 8 | 20192013 | intergenic variant | G/A;C | snv | 2 | |||
rs12504244 | 0.925 | 0.040 | 4 | 54619021 | intergenic variant | C/A;G;T | snv | 2 | |||
rs2834070 | 0.925 | 0.040 | 21 | 33015144 | intron variant | G/T | snv | 0.24 | 2 | ||
rs75063949 | 0.925 | 0.040 | 6 | 25590813 | intron variant | C/G | snv | 0.14 | 2 | ||
rs929626 | 0.925 | 0.120 | 5 | 158883623 | intron variant | A/G | snv | 0.40 | 2 | ||
rs4825476 | 0.925 | 0.040 | X | 123307628 | intron variant | G/A;C | snv | 2 | |||
rs4869317 | 1.000 | 0.040 | 5 | 96956300 | intron variant | T/A | snv | 0.22 | 2 | ||
rs13338499 | 0.925 | 0.040 | 16 | 67486220 | intron variant | A/G;T | snv | 2 | |||
rs1356639869 | 1.000 | 0.040 | 7 | 24289527 | missense variant | C/A | snv | 2 | |||
rs750136455 | 0.925 | 0.120 | 2 | 25161569 | missense variant | C/T | snv | 2.5E-05 | 7.0E-06 | 2 | |
rs80326661 | 0.925 | 0.120 | 2 | 25161244 | missense variant | T/C | snv | 5.4E-03 | 5.4E-03 | 2 | |
rs11174202 | 0.925 | 0.040 | 12 | 61858476 | intron variant | A/G | snv | 0.49 | 2 | ||
rs10747478 | 1.000 | 0.040 | 1 | 96435899 | intergenic variant | T/A;C;G | snv | 1 | |||
rs1285957 | 1.000 | 0.040 | 7 | 141889478 | downstream gene variant | T/C | snv | 0.86 | 1 | ||
rs13100344 | 1.000 | 0.040 | 3 | 94886263 | intergenic variant | T/A | snv | 0.40 | 1 | ||
rs145241704 | 1.000 | 0.040 | 7 | 141805287 | upstream gene variant | T/G | snv | 7.4E-02 | 1 | ||
rs370838138 | 1.000 | 0.040 | 5 | 25081736 | intergenic variant | G/C | snv | 0.42 | 1 | ||
rs56156506 | 1.000 | 0.040 | X | 38140399 | intron variant | A/T | snv | 0.33 | 1 | ||
rs62090893 | 1.000 | 0.040 | 18 | 75338379 | intergenic variant | G/A | snv | 9.7E-02 | 1 | ||
rs7532266 | 1.000 | 0.040 | 1 | 23225130 | regulatory region variant | A/C | snv | 0.66 | 1 |