Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs34517439 | 0.882 | 0.120 | 1 | 77984833 | intron variant | C/A | snv | 7.3E-02 | 7 | ||
rs34720381 | 1 | 171486183 | intron variant | C/T | snv | 7.3E-02 | 4 | ||||
rs6422513 | 1 | 92566910 | intron variant | G/A;C | snv | 2 | |||||
rs7534091 | 1 | 118321993 | intergenic variant | A/G | snv | 0.23 | 2 | ||||
rs1541777 | 2 | 218722568 | intron variant | A/G | snv | 0.51 | 2 | ||||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 35 | ||
rs9880211 | 3 | 136388707 | intron variant | G/A | snv | 0.19 | 2 | ||||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
rs6823268 | 4 | 145061411 | intron variant | A/G | snv | 0.28 | 2 | ||||
rs1582931 | 5 | 123321505 | intergenic variant | G/A;T | snv | 2 | |||||
rs6234 | 0.851 | 0.160 | 5 | 96393270 | missense variant | G/C | snv | 0.27 | 0.24 | 4 | |
rs6569648 | 1.000 | 0.080 | 6 | 130027974 | intron variant | C/T | snv | 0.84 | 5 | ||
rs7740107 | 1.000 | 0.080 | 6 | 130053316 | intron variant | T/A;G | snv | 6 | |||
rs1167827 | 7 | 75533848 | 3 prime UTR variant | G/A | snv | 0.37 | 5 | ||||
rs7826312 | 8 | 32542597 | intron variant | T/C | snv | 0.57 | 2 | ||||
rs1064939 | 11 | 118525616 | 3 prime UTR variant | A/T | snv | 1.4E-02 | 2 | ||||
rs174547 | 0.742 | 0.240 | 11 | 61803311 | intron variant | T/C | snv | 0.28 | 20 | ||
rs145878042 | 12 | 47749532 | missense variant | A/G | snv | 7.3E-03 | 7.6E-03 | 3 | |||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 21 | |
rs76895963 | 1.000 | 0.080 | 12 | 4275678 | intron variant | T/G | snv | 1.5E-02 | 6 | ||
rs76929617 | 12 | 120429995 | intergenic variant | A/G | snv | 3.7E-02 | 2 | ||||
rs7141420 | 1.000 | 0.080 | 14 | 79433111 | intron variant | C/T | snv | 0.56 | 5 | ||
rs72755233 | 1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 | 5 |