Source: CURATED
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1555206402 | 0.790 | 0.320 | 11 | 119093274 | stop lost | GCCCATTAACTGGTTTGTGGGGCACAGATGCCTGGGTTGCTGCTGTCCAGTGCCT/- | delins | 26 | |||
rs1007859875 | 1.000 | 0.160 | 11 | 119092137 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
rs1057521126 | 1.000 | 0.160 | 11 | 119092785 | missense variant | G/A | snv | 1 | |||
rs1165046276 | 1.000 | 0.160 | 11 | 119089992 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
rs118204094 | 1.000 | 0.160 | 11 | 119089991 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs118204095 | 1.000 | 0.160 | 11 | 119091414 | missense variant | G/A;T | snv | 4.5E-05 | 1 | ||
rs118204096 | 1.000 | 0.160 | 11 | 119091432 | missense variant | G/A | snv | 1 | |||
rs118204097 | 1.000 | 0.160 | 11 | 119090230 | stop gained | C/T | snv | 1 | |||
rs118204098 | 1.000 | 0.160 | 11 | 119090213 | missense variant | G/A | snv | 1 | |||
rs118204099 | 1.000 | 0.160 | 11 | 119092486 | missense variant | T/G | snv | 1 | |||
rs118204100 | 1.000 | 0.160 | 11 | 119091507 | stop gained | G/A | snv | 1 | |||
rs118204101 | 1.000 | 0.160 | 11 | 119091413 | missense variant | C/T | snv | 3.8E-05 | 1 | ||
rs118204103 | 1.000 | 0.160 | 11 | 119088298 | missense variant | G/A | snv | 1 | |||
rs118204104 | 1.000 | 0.160 | 11 | 119088638 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs118204105 | 1.000 | 0.160 | 11 | 119088647 | missense variant | C/A | snv | 1 | |||
rs118204106 | 1.000 | 0.160 | 11 | 119089084 | missense variant | G/T | snv | 7.0E-06 | 1 | ||
rs118204107 | 1.000 | 0.160 | 11 | 119089747 | missense variant | G/A | snv | 1 | |||
rs118204108 | 1.000 | 0.160 | 11 | 119091444 | missense variant | T/G | snv | 1 | |||
rs118204109 | 1.000 | 0.160 | 11 | 119091515 | missense variant | C/T | snv | 2.6E-05 | 3.5E-05 | 1 | |
rs118204110 | 1.000 | 0.160 | 11 | 119092419 | stop gained | G/A | snv | 1 | |||
rs118204111 | 1.000 | 0.160 | 11 | 119092491 | missense variant | T/C | snv | 1 | |||
rs118204112 | 1.000 | 0.160 | 11 | 119092500 | missense variant | G/A | snv | 1 | |||
rs118204113 | 1.000 | 0.160 | 11 | 119092506 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |
rs118204114 | 1.000 | 0.160 | 11 | 119092507 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs118204115 | 1.000 | 0.160 | 11 | 119092518 | missense variant | C/A;G | snv | 1 |