Source: GWASDB ×
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 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 4
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 4
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 3
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 3
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 3
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 3
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 3
rs3741414
INHBC
0.925 0.120 12 57450266 3 prime UTR variant C/T snv 0.19 3
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 3
rs12777
MIR3936HG ; SLC22A4
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 3
rs13538
NAT8 ; ALMS1P1
1.000 0.080 2 73641201 missense variant A/G snv 0.21 0.31 3
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 3
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 3
rs6420094
SLC34A1
1.000 0.080 5 177390635 intron variant A/G snv 0.29 3
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 3
rs1913641 0.925 0.120 8 75571004 downstream gene variant T/G snv 0.58 2
rs10821905
A1CF
0.925 0.120 10 50886333 upstream gene variant G/A;T snv 2