Disease: Chronic Kidney Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs6046
F7
0.925 0.080 13 113118845 missense variant G/A;C;T snv 0.13 5
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 9
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs3834458
FADS1 ; FADS2
0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306