Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121918084 | 0.925 | 0.120 | 18 | 31595191 | missense variant | T/C | snv | 1 | |||
rs121918085 | 0.882 | 0.160 | 18 | 31595181 | missense variant | A/T | snv | 1.6E-05 | 3.5E-05 | 1 | |
rs121918086 | 1.000 | 0.120 | 18 | 31595160 | missense variant | G/A | snv | 1 | |||
rs121918087 | 0.882 | 0.120 | 18 | 31598581 | missense variant | C/G | snv | 1 | |||
rs121918089 | 1.000 | 0.120 | 18 | 31598610 | missense variant | A/G | snv | 1 | |||
rs121918090 | 0.790 | 0.240 | 18 | 31593026 | missense variant | G/C | snv | 1 | |||
rs121918093 | 0.882 | 0.200 | 18 | 31592944 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs121918094 | 0.827 | 0.280 | 18 | 31592921 | missense variant | T/C | snv | 1 | |||
rs121918097 | 0.790 | 0.280 | 18 | 31595137 | missense variant | G/A | snv | 1 | |||
rs1555631387 | 1.000 | 0.120 | 18 | 31595125 | missense variant | C/G | snv | 1 | |||
rs1555631402 | 1.000 | 0.120 | 18 | 31595163 | missense variant | G/A | snv | 1 | |||
rs1567945632 | 1.000 | 0.120 | 18 | 31592938 | missense variant | G/A | snv | 1 | |||
rs267607160 | 1.000 | 0.120 | 18 | 31595189 | missense variant | A/C | snv | 1 | |||
rs267607161 | 0.742 | 0.360 | 18 | 31598580 | missense variant | G/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs386134269 | 0.882 | 0.120 | 18 | 31595127 | missense variant | A/C;G | snv | 1 | |||
rs387906523 | 0.882 | 0.160 | 18 | 31593025 | missense variant | G/A;C | snv | 1 | |||
rs876658108 | 1.000 | 0.120 | 18 | 31598649 | missense variant | G/T | snv | 1 | |||
rs121918096 | 1.000 | 0.120 | 18 | 31598652 | inframe deletion | GTC/- | delins | 1 | |||
rs1555631390 | 0.851 | 0.160 | 18 | 31595128 | inframe insertion | -/AGTCTG | delins | 4 |