Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs766182641
AK3
0.882 0.080 9 4719292 missense variant A/G snv 4.0E-06 3
rs137852406
F8
0.925 0.080 X 154969400 missense variant T/C snv 5.5E-06 2
rs387906475
F9
0.882 0.080 X 139530843 missense variant G/A snv 2