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
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs7493
PON2
0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs1194897557
MTHFR
0.827 0.240 1 11796276 missense variant A/G snv 8.0E-06 7
rs769737896
LDLR
0.851 0.080 19 11110759 stop gained C/A;G;T snv 4.0E-06; 4.0E-06; 8.0E-06 5
rs2454727
HCAR2
0.925 0.040 12 122702333 missense variant C/T snv 3
rs7314976
HCAR2
0.925 0.040 12 122702353 missense variant G/A;C snv 3.9E-02; 4.5E-06 3
rs773371778
CETP
0.925 0.080 16 56972000 missense variant C/T snv 4.0E-06 2