Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2352028 | 0.851 | 0.080 | 13 | 91792975 | intron variant | C/G;T | snv | 6 | |||
rs2564978 | 0.827 | 0.080 | 1 | 207321071 | upstream gene variant | T/C | snv | 0.77 | 6 | ||
rs2835267 | 0.827 | 0.080 | 21 | 36074727 | intron variant | T/C | snv | 0.63 | 6 | ||
rs4513061 | 0.807 | 0.080 | 15 | 86428401 | intron variant | G/A;T | snv | 6 | |||
rs503464 | 0.851 | 0.080 | 15 | 78565554 | 5 prime UTR variant | T/A | snv | 0.28 | 6 | ||
rs7177514 | 0.882 | 0.080 | 15 | 78615064 | intron variant | C/G;T | snv | 6 | |||
rs767935771 | 0.827 | 0.080 | 19 | 41259690 | missense variant | T/C | snv | 1.6E-05 | 5.6E-05 | 6 | |
rs772399455 | 0.851 | 0.080 | 2 | 15942096 | missense variant | G/A;C | snv | 4.0E-06 | 6 | ||
rs78768932 | 0.882 | 0.080 | 12 | 120222977 | missense variant | C/G;T | snv | 5.4E-03 | 5.4E-03 | 6 | |
rs7937 | 0.851 | 0.080 | 19 | 40796801 | 3 prime UTR variant | C/A;T | snv | 0.49 | 6 | ||
rs8042059 | 0.882 | 0.080 | 15 | 78615517 | intron variant | A/C;T | snv | 6 | |||
rs9895829 | 0.807 | 0.080 | 17 | 7675361 | 5 prime UTR variant | A/G | snv | 7.4E-02 | 6 | ||
rs1019340046 | 0.882 | 0.080 | 17 | 7674225 | missense variant | C/T | snv | 5 | |||
rs10254120 | 0.851 | 0.080 | 7 | 6005996 | missense variant | C/A;G;T | snv | 7.2E-02 | 5 | ||
rs1026411 | 0.827 | 0.080 | 8 | 127014165 | intron variant | G/A;C | snv | 0.25 | 5 | ||
rs121917737 | 0.827 | 0.080 | 10 | 79557264 | missense variant | C/A | snv | 5 | |||
rs121917738 | 0.827 | 0.080 | 10 | 79557363 | missense variant | A/G | snv | 5 | |||
rs12587742 | 0.851 | 0.080 | 14 | 72926683 | intron variant | G/A | snv | 0.18 | 5 | ||
rs1275824108 | 0.851 | 0.080 | 14 | 54399922 | missense variant | A/G | snv | 7.0E-06 | 5 | ||
rs1329032366 | 0.882 | 0.080 | 4 | 94654530 | missense variant | A/G | snv | 4.0E-06 | 5 | ||
rs1330189219 | 0.882 | 0.080 | 6 | 31573570 | synonymous variant | C/T | snv | 4.0E-06 | 5 | ||
rs1423493595 | 0.851 | 0.080 | 20 | 50082836 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 5 | |
rs1454694 | 0.827 | 0.080 | 4 | 181276794 | intergenic variant | T/C | snv | 0.20 | 5 | ||
rs1487151044 | 0.851 | 0.080 | 10 | 31510817 | missense variant | T/C | snv | 5 | |||
rs3124599 | 0.851 | 0.080 | 9 | 136509318 | intron variant | G/A | snv | 0.13 | 5 |