Source: GWASCAT

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 55
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7