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
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 114
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 34
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 22
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 18
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 10
rs1800386
VWF
0.851 0.120 12 6018667 missense variant T/C snv 2.7E-03 2.3E-03 4
rs766182641
AK3
0.882 0.080 9 4719292 missense variant A/G snv 4.0E-06 3
rs137852358
F8
0.882 0.080 X 154861758 missense variant C/A;T snv 2
rs137852403
F8
0.925 0.080 X 154969438 missense variant C/A;T snv 2
rs137852406
F8
0.925 0.080 X 154969400 missense variant T/C snv 5.5E-06 2
rs137852442
F8
0.925 0.080 X 154904998 missense variant C/T snv 2
rs387906475
F9
0.882 0.080 X 139530843 missense variant G/A snv 2
rs772061412
F9
0.925 0.080 X 139561664 missense variant C/G snv 5.5E-06 2
rs3754689
LCT
0.925 0.080 2 135833176 missense variant C/A;G;T snv 4.8E-05; 0.24 2
rs748641905
MCFD2
0.882 0.080 2 46905501 missense variant A/T snv 2
rs1982037 1.000 0.080 18 40854820 intergenic variant C/T snv 0.11 1
rs4833248 1.000 0.080 4 122459250 upstream gene variant G/A;C snv 1
rs17725712
CSF1R
1.000 0.080 5 150111245 intron variant C/T snv 0.11 1
rs111033613
F8
0.925 0.080 X 154928668 missense variant G/A;T snv 1
rs111033615
F8
1.000 0.080 X 154904004 missense variant C/T snv 1