Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs1999594 1 11899159 regulatory region variant G/A;C;T snv 2
rs2639453
KIAA2013
1 11922487 3 prime UTR variant T/C snv 0.77 0.81 2
rs11194787 10 109674583 intergenic variant G/A snv 1.4E-02 1
rs12611820 2 2479854 intergenic variant T/G snv 0.33 1
rs17393539 7 31301873 intergenic variant T/A snv 6.0E-02 1
rs2670029
LOC101929415
8 56472437 intron variant C/A snv 0.45 1