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
rs41507953
EPHX2
0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs46522
UBE2Z
0.807 0.120 17 48911235 non coding transcript exon variant C/T snv 0.40 8
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
rs3834458
FADS1 ; FADS2
0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs7195830
CYBA
0.851 0.080 16 88643304 3 prime UTR variant A/G snv 0.62 0.69 6
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157