Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs118203979
CLDN19
0.925 0.080 1 42740005 missense variant C/T snv 9.0E-05 2.8E-05 2
rs3759126
AQP2
0.882 0.080 12 49950079 upstream gene variant A/G snv 0.23 3
rs151340626
CLCN5
0.827 0.200 X 50085987 missense variant C/T snv 5
rs151340624
CLCN5
0.851 0.120 X 50090846 stop gained C/T snv 4
rs121908144
BSND
0.882 0.240 1 54999221 missense variant T/C snv 2.0E-05 3
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
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
rs538166970
ACE
0.925 0.080 17 63496920 missense variant G/A;C snv 1.6E-05; 4.0E-06 2
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7