Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 19 | ||
rs17851045 | 0.672 | 0.400 | 12 | 25227341 | missense variant | T/A;G | snv | 4.0E-06 | 15 | ||
rs121913528 | 0.851 | 0.160 | 12 | 25227349 | missense variant | C/A;T | snv | 11 | |||
rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 11 | |||
rs112445441 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 8 | |||
rs121913240 | 0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv | 6 | |||
rs770248150 | 0.807 | 0.240 | 12 | 25225713 | missense variant | T/A;G | snv | 4.0E-06 | 6 | ||
rs121913535 | 0.742 | 0.320 | 12 | 25245348 | missense variant | C/A;G;T | snv | 5 | |||
rs121913238 | 0.732 | 0.240 | 12 | 25227343 | missense variant | G/C;T | snv | 3 | |||
rs1057519725 | 0.851 | 0.320 | 12 | 25225627 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs121913527 | 0.807 | 0.320 | 12 | 25225628 | missense variant | C/A;G;T | snv | 2 | |||
rs121913236 | 0.882 | 0.160 | 12 | 25245321 | missense variant | G/C;T | snv | 1 |