Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16347 | 0.925 | 0.080 | 2 | 112774138 | 3 prime UTR variant | -/TGAA | delins | 0.70 | 2 | ||
rs17709344 | 0.925 | 0.080 | 15 | 93608310 | intron variant | G/A | snv | 4.0E-02 | 2 | ||
rs183962941 | 0.925 | 0.080 | 16 | 20343125 | intron variant | G/A | snv | 1.1E-02 | 2 | ||
rs2391335 | 0.925 | 0.080 | 13 | 106519637 | non coding transcript exon variant | T/C;G | snv | 0.50 | 2 | ||
rs2413396 | 0.925 | 0.080 | 22 | 36312039 | intron variant | C/G;T | snv | 0.88 | 2 | ||
rs2802723 | 0.925 | 0.080 | 1 | 243335010 | intron variant | T/C;G | snv | 2 | |||
rs281874682 | 0.925 | 0.080 | X | 108598805 | missense variant | C/A;T | snv | 5.5E-06 | 2 | ||
rs2838302 | 0.925 | 0.080 | 21 | 43419273 | intron variant | A/G | snv | 1.0E-01 | 2 | ||
rs301640 | 0.925 | 0.080 | 13 | 60885853 | intron variant | C/G;T | snv | 2 | |||
rs370819889 | 0.925 | 0.080 | 4 | 73416353 | missense variant | C/A;T | snv | 8.0E-06; 9.6E-05 | 2 | ||
rs373971520 | 0.925 | 0.080 | 19 | 2568808 | intron variant | CA/-;CACA | delins | 2 | |||
rs374118649 | 0.925 | 0.080 | 3 | 58097965 | missense variant | A/G;T | snv | 3.6E-05 | 2 | ||
rs4253373 | 0.925 | 0.080 | 4 | 186250250 | missense variant | C/A | snv | 6.7E-04 | 2.5E-03 | 2 | |
rs4714384 | 0.925 | 0.080 | 6 | 12297620 | downstream gene variant | T/C | snv | 0.45 | 2 | ||
rs6936632 | 0.925 | 0.080 | 6 | 47588297 | intron variant | G/A | snv | 7.6E-02 | 2 | ||
rs6954996 | 0.925 | 0.080 | 7 | 6401627 | non coding transcript exon variant | G/A;T | snv | 2 | |||
rs702483 | 0.925 | 0.080 | 7 | 6387310 | intron variant | C/A;T | snv | 0.54 | 2 | ||
rs730947 | 0.925 | 0.080 | 2 | 218838575 | upstream gene variant | A/C | snv | 1.0E-01 | 2 | ||
rs7490924 | 0.925 | 0.080 | 13 | 106519396 | non coding transcript exon variant | A/G | snv | 0.51 | 2 | ||
rs752390951 | 0.925 | 0.080 | 19 | 50908408 | missense variant | G/T | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs7583877 | 0.925 | 0.080 | 2 | 99844192 | intron variant | C/T | snv | 0.61 | 2 | ||
rs760452842 | 0.925 | 0.080 | 19 | 50906983 | missense variant | T/G | snv | 4.0E-06 | 2 | ||
rs77113398 | 0.925 | 0.080 | 13 | 106451558 | intergenic variant | G/A | snv | 6.0E-03 | 2 | ||
rs7918972 | 0.925 | 0.080 | 10 | 16828293 | intron variant | T/G | snv | 0.15 | 2 | ||
rs836488 | 0.925 | 0.080 | 7 | 6380162 | intron variant | C/T | snv | 0.13 | 2 |