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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs198388
NPPB
0.851 0.160 1 11857283 downstream gene variant C/G;T snv 4
rs632793 0.882 0.120 1 11850620 upstream gene variant A/G snv 0.45 3
rs8450
DENND4B ; CRTC2
1.000 0.040 1 153947810 3 prime UTR variant G/A snv 0.27 2
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 7
rs886916693
KIDINS220
1.000 0.040 2 8806360 missense variant T/C snv 4.1E-06 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs4973768
SLC4A7
0.807 0.120 3 27374522 3 prime UTR variant C/T snv 0.44 7
rs7744
MYD88
0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs2222823
MYLK
0.925 0.080 3 123885940 upstream gene variant T/A snv 0.14 4
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs3816873
MTTP
0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs920435389
FGFR4
1.000 0.040 5 177091064 missense variant G/C snv 3
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226