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
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs121909585
C3
0.925 0.120 19 6692971 missense variant C/T snv 4
rs3092952 0.925 0.160 X 136644791 upstream gene variant A/G snv 0.29 3
rs3092936
CD40LG
1.000 0.040 X 136654046 intron variant T/C snv 8.9E-02 2