Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 5 | |
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
rs3846662 | 0.763 | 0.280 | 5 | 75355259 | non coding transcript exon variant | A/G | snv | 0.50 | 0.58 | 5 | |
rs393152 | 0.851 | 0.160 | 17 | 45641777 | non coding transcript exon variant | A/G | snv | 0.18 | 0.29 | 5 | |
rs241448 | 0.882 | 0.200 | 6 | 32828908 | stop lost | A/G | snv | 0.32 | 0.27 | 5 | |
rs1160985 | 1.000 | 0.080 | 19 | 44900155 | intron variant | C/T | snv | 0.52 | 5 | ||
rs439401 | 0.851 | 0.200 | 19 | 44911194 | non coding transcript exon variant | T/C | snv | 0.68 | 4 | ||
rs6834555 | 0.882 | 0.200 | 4 | 10060702 | regulatory region variant | G/A | snv | 0.74 | 4 | ||
rs714873 | 0.882 | 0.200 | 4 | 10057994 | upstream gene variant | G/A | snv | 0.74 | 4 | ||
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 4 | |
rs12721109 | 1.000 | 0.080 | 19 | 44943964 | intron variant | G/A | snv | 1.3E-02 | 4 | ||
rs769449 | 0.882 | 0.120 | 19 | 44906745 | non coding transcript exon variant | G/A | snv | 8.4E-02 | 4 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 4 | |
rs6499640 | 0.925 | 0.160 | 16 | 53735765 | intron variant | G/A | snv | 0.59 | 4 | ||
rs9268856 | 0.807 | 0.240 | 6 | 32461942 | intron variant | C/A;T | snv | 4 | |||
rs9268877 | 0.827 | 0.200 | 6 | 32463370 | intron variant | A/G;T | snv | 4 | |||
rs13180 | 0.851 | 0.160 | 15 | 78497146 | synonymous variant | C/T | snv | 0.54 | 0.51 | 4 | |
rs688 | 0.742 | 0.400 | 19 | 11116926 | synonymous variant | C/T | snv | 0.39 | 0.34 | 4 | |
rs268 | 0.637 | 0.480 | 8 | 19956018 | missense variant | A/G | snv | 1.3E-02 | 1.3E-02 | 4 | |
rs7232 | 1.000 | 0.080 | 11 | 60173126 | missense variant | T/A | snv | 0.31 | 0.27 | 4 | |
rs387976 | 1.000 | 0.080 | 19 | 44875803 | intron variant | A/C;T | snv | 4 | |||
rs4803763 | 1.000 | 0.080 | 19 | 44854034 | intron variant | G/A;C | snv | 4 | |||
rs8106922 | 1.000 | 0.080 | 19 | 44898409 | intron variant | A/G | snv | 0.36 | 4 | ||
rs1483121 | 1.000 | 0.080 | 11 | 48311808 | downstream gene variant | G/A | snv | 9.7E-02 | 3 | ||
rs3851179 | 0.752 | 0.280 | 11 | 86157598 | downstream gene variant | T/C | snv | 0.70 | 3 |