Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1557551678
CLDN19
0.882 0.160 1 42738421 missense variant C/A snv 9
rs138308105
CLDN16
0.925 0.200 3 190408323 missense variant G/A;C snv 6.8E-05 2.6E-04 7
rs200817545
SLC12A3
0.925 0.160 16 56879168 missense variant A/C;G;T snv 4.0E-06; 1.6E-04 6
rs2274924
TRPM6
0.851 0.160 9 74761731 missense variant T/C snv 0.20 0.23 6
rs199473648
LOC105372791 ; KCNE2
1.000 0.080 21 34370507 missense variant C/T snv 2.5E-04 2.4E-04 4
rs104893701
CASR
0.925 0.120 3 122284317 missense variant T/G snv 3
rs28938168
FXYD6-FXYD2 ; FXYD2
1.000 0.160 11 117822424 missense variant C/T snv 3
rs752010
HIVEP3
0.925 0.080 1 41627344 intron variant C/T snv 0.59 3
rs121909267
CASR
1.000 3 122257288 missense variant C/G snv 2
rs1043614377
CNNM2
1.000 0.040 10 103049727 missense variant G/A snv 2
rs3750425
TRPM6
1.000 0.080 9 74762494 missense variant C/A;T snv 8.0E-06; 0.12 2