Disease: Glomerular Filtration Rate
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 10
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 9
rs2079742
BCAS3
0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 9
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 7
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs3741414
INHBC
0.925 0.120 12 57450266 3 prime UTR variant C/T snv 0.19 7
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 7
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 7
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 6
rs10851885
NRG4
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18 5
rs10994856
A1CF
0.925 0.120 10 50885488 intron variant G/A snv 0.19 5
rs10994860
A1CF
0.925 0.120 10 50885664 5 prime UTR variant C/T snv 0.19 5
rs4971100
TRIM46
0.925 0.120 1 155183255 intron variant G/A snv 0.39 5
rs10821905
A1CF
0.925 0.120 10 50886333 upstream gene variant G/A;T snv 4
rs11858316
IGF1R
0.925 0.120 15 98705800 intron variant C/T snv 0.50 3
rs12989250
ORC4
0.925 0.120 2 148018869 intron variant G/A snv 0.32 3
rs1913641 0.925 0.120 8 75571004 downstream gene variant T/G snv 0.58 3
rs2137683
IGF1R
0.925 0.120 15 98746409 intron variant C/G snv 0.53 3