Source: CURATED
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs702859 | 1.000 | 0.080 | 21 | 37625399 | synonymous variant | G/A | snv | 0.71 | 0.72 | 3 | |
rs10483038 | 1.000 | 0.080 | 21 | 37652469 | intron variant | T/C | snv | 0.26 | 3 | ||
rs111372083 | 1.000 | 0.080 | 21 | 37638374 | intron variant | C/A;T | snv | 0.27 | 3 | ||
rs111576572 | 1.000 | 0.080 | 21 | 37617262 | 3 prime UTR variant | A/G | snv | 0.32 | 3 | ||
rs12482570 | 1.000 | 0.080 | 21 | 37705475 | intron variant | A/G | snv | 0.30 | 3 | ||
rs1399590 | 1.000 | 0.080 | 21 | 37681768 | intron variant | G/A | snv | 0.56 | 3 | ||
rs1399591 | 1.000 | 0.080 | 21 | 37681654 | intron variant | C/T | snv | 0.50 | 3 | ||
rs1399592 | 1.000 | 0.080 | 21 | 37681559 | intron variant | T/A;G | snv | 0.52 | 3 | ||
rs1475839 | 1.000 | 0.080 | 21 | 37649639 | intron variant | C/T | snv | 0.31 | 3 | ||
rs1515050 | 1.000 | 0.080 | 21 | 37630840 | intron variant | T/C | snv | 0.75 | 3 | ||
rs1515056 | 1.000 | 0.080 | 21 | 37710283 | intron variant | C/G;T | snv | 0.28 | 3 | ||
rs1709817 | 1.000 | 0.080 | 21 | 37664047 | intron variant | T/A;C | snv | 3 | |||
rs1709818 | 1.000 | 0.080 | 21 | 37663909 | intron variant | T/C | snv | 0.57 | 3 | ||
rs1709819 | 1.000 | 0.080 | 21 | 37663813 | intron variant | A/C | snv | 0.59 | 3 | ||
rs1709820 | 1.000 | 0.080 | 21 | 37663669 | intron variant | A/C | snv | 0.57 | 3 | ||
rs1709826 | 1.000 | 0.080 | 21 | 37677171 | intron variant | G/A;C | snv | 3 | |||
rs1709832 | 1.000 | 0.080 | 21 | 37665865 | intron variant | T/G | snv | 0.57 | 3 | ||
rs1709833 | 1.000 | 0.080 | 21 | 37665503 | intron variant | A/G | snv | 0.57 | 3 | ||
rs1709835 | 1.000 | 0.080 | 21 | 37665334 | intron variant | A/C;G | snv | 0.57 | 3 | ||
rs17814920 | 1.000 | 0.080 | 21 | 37643595 | intron variant | G/A | snv | 0.27 | 3 | ||
rs1787330 | 1.000 | 0.080 | 21 | 37630485 | intron variant | G/A | snv | 0.74 | 3 | ||
rs1787331 | 1.000 | 0.080 | 21 | 37631223 | intron variant | T/G | snv | 0.68 | 3 | ||
rs1787394 | 1.000 | 0.080 | 21 | 37663874 | intron variant | C/A | snv | 0.58 | 3 | ||
rs1787395 | 1.000 | 0.080 | 21 | 37664176 | intron variant | A/C;T | snv | 3 | |||
rs1787396 | 1.000 | 0.080 | 21 | 37664185 | intron variant | A/C | snv | 0.57 | 3 |