Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1799987
CCR5AS ; CCR5
0.763 0.200 3 46370444 intron variant A/G snv 0.49 10
rs868
TGFBR1
0.851 0.160 9 99149374 3 prime UTR variant A/G snv 0.17 4