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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs61747728
NPHS2
0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs121908144
BSND
0.882 0.240 1 54999221 missense variant T/C snv 2.0E-05 3
rs118203979
CLDN19
0.925 0.080 1 42740005 missense variant C/T snv 9.0E-05 2.8E-05 2
rs188942711
COL4A3 ; MFF-DT
0.763 0.200 2 227253336 missense variant G/A;T snv 2.8E-05; 4.0E-06 9
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 9
rs3024912
LOC105373805
0.925 0.120 2 191028361 intron variant A/C snv 0.29 2
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
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs11739136
KCNIP1 ; KCNMB1
0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs760336723
PODXL
0.882 0.240 7 131506292 missense variant G/A snv 2.8E-05 5.6E-05 3
rs367825197
PODXL
0.925 0.080 7 131509412 stop gained G/A snv 4.0E-06 2
rs4281481
CCDC179 ; GAS2
0.882 0.080 11 22859013 intron variant C/G snv 0.36 3
rs200640958
TRPC6
1.000 0.080 11 101471303 synonymous variant G/A;C snv 8.0E-06; 1.6E-05 1
rs754919065
TRPC6
1.000 0.080 11 101504767 missense variant G/A snv 6.1E-05; 4.1E-06 7.0E-06 1
rs3759126
AQP2
0.882 0.080 12 49950079 upstream gene variant A/G snv 0.23 3
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4