Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs12124078
DNAJC16
1 15543404 intron variant A/G snv 0.32 1
rs1933182 1.000 0.080 1 109457216 intergenic variant A/C snv 0.63 1
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 1
rs3093058
CRP
1 159715525 upstream gene variant T/A;C;G snv 1
rs6428106
LOC105371664
1 192585301 intron variant G/T snv 0.14 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 1
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
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs13538
NAT8 ; ALMS1P1
1.000 0.080 2 73641201 missense variant A/G snv 0.21 0.31 3
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 3
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 3
rs16864170 1.000 0.080 2 5767748 intergenic variant T/C snv 3.8E-02 1
rs2887915 2 210689850 intergenic variant C/G;T snv 1
rs3764913
ACADL
1.000 0.080 2 210210185 non coding transcript exon variant T/C snv 0.30 0.27 1
rs6431731
LINC01804
1.000 0.080 2 15722878 intron variant C/T snv 0.97 1
rs6546837
ALMS1
2 73450771 missense variant G/C;T snv 0.27 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs347685
TFDP2
1.000 0.080 3 142088295 intron variant C/A snv 0.74 1
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 4
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34 2
rs6420094
SLC34A1
1.000 0.080 5 177390635 intron variant A/G snv 0.29 3
rs10068737 5 118700852 intergenic variant T/A;C snv 1