Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs774870551 | 0.925 | 0.160 | 10 | 74070712 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 3 | |
rs150385900 | 1.000 | 0.080 | 10 | 74107316 | missense variant | G/C | snv | 1.1E-03 | 5.2E-04 | 1 | |
rs755660650 | 0.827 | 0.120 | 5 | 102498596 | missense variant | G/C | snv | 4.0E-06 | 5 | ||
rs140704891 | 1.000 | 0.080 | 17 | 8289059 | stop gained | G/A;T | snv | 4.0E-06; 4.0E-03 | 1 | ||
rs370613922 | 1.000 | 0.080 | 17 | 8289425 | missense variant | G/A;C | snv | 1.6E-05 | 1 | ||
rs751751942 | 1.000 | 0.080 | 17 | 8289312 | missense variant | G/A;C | snv | 4.0E-06; 3.2E-05 | 1 | ||
rs1805124 | 0.742 | 0.280 | 3 | 38603929 | missense variant | T/C | snv | 0.22 | 0.25 | 16 | |
rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 15 | ||
rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 15 | ||
rs41261344 | 0.763 | 0.120 | 3 | 38575385 | missense variant | C/T | snv | 5.4E-03 | 2.2E-03 | 11 | |
rs137854601 | 0.776 | 0.120 | 3 | 38551022 | stop gained | C/A;T | snv | 4.0E-06 | 10 | ||
rs199473097 | 0.763 | 0.120 | 3 | 38606710 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 9 | |
rs757532106 | 0.763 | 0.120 | 3 | 38550500 | stop gained | G/A | snv | 4.5E-05 | 4.9E-05 | 9 | |
rs199473605 | 0.851 | 0.120 | 3 | 38560374 | missense variant | C/G;T | snv | 4.8E-05; 4.0E-06 | 7 | ||
rs11708996 | 0.925 | 0.120 | 3 | 38592432 | intron variant | G/C | snv | 0.11 | 6 | ||
rs137854600 | 0.807 | 0.120 | 3 | 38551504 | missense variant | C/A;T | snv | 6 | |||
rs199473225 | 0.851 | 0.120 | 3 | 38560397 | missense variant | G/A;C | snv | 6 | |||
rs137854602 | 0.925 | 0.080 | 3 | 38555664 | missense variant | G/A | snv | 5.6E-05 | 1.4E-05 | 5 | |
rs137854607 | 0.882 | 0.120 | 3 | 38554309 | missense variant | C/G;T | snv | 5 | |||
rs199473062 | 0.827 | 0.120 | 3 | 38622401 | stop gained | C/A;G;T | snv | 4.1E-06 | 5 | ||
rs199473072 | 0.827 | 0.160 | 3 | 38613773 | missense variant | G/A | snv | 1.2E-05 | 8.4E-05 | 5 | |
rs199473282 | 0.827 | 0.120 | 3 | 38551513 | missense variant | G/A;T | snv | 4.0E-06 | 5 | ||
rs137854612 | 0.851 | 0.120 | 3 | 38560170 | missense variant | C/T | snv | 4 | |||
rs137854615 | 0.851 | 0.120 | 3 | 38550989 | missense variant | A/G | snv | 4 | |||
rs185638763 | 0.882 | 0.120 | 3 | 38599001 | missense variant | G/A;T | snv | 1.2E-05 | 4 |