Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12007229 1.000 0.120 X 67528513 upstream gene variant C/A snv 0.11 1
rs2497931 1.000 0.120 X 67436434 intergenic variant A/C;T snv 1
rs4485213 1.000 0.120 13 105256524 intergenic variant C/T snv 0.19 1
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs893051
CLDN1
0.807 0.400 3 190321812 intron variant G/A;C snv 7
rs117834366
CNTNAP2
0.925 0.120 7 147937799 intron variant G/A snv 1.2E-02 2
rs4986938
ESR2
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs944050
ESR2
0.827 0.280 14 64233327 splice region variant T/C snv 9.5E-02 7.9E-02 5
rs4925
GSTO1
0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs17501010
LOC107986170 ; CLDN1
0.827 0.320 3 190308865 intron variant G/T snv 0.15 5
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs951660
PHLDB2
1.000 0.120 3 111919285 intron variant A/C snv 0.86 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs7493
PON2
0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs10491487
RASGRF2
1.000 0.120 5 81027549 intron variant T/G snv 8.2E-02 1
rs26906
RASGRF2
1.000 0.120 5 81069068 intron variant T/C snv 0.86 1