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
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 7
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs3819299
HLA-B
1.000 6 31354590 non coding transcript exon variant T/G snv 7.7E-02 2.3E-02 5
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 3
rs6065
CHRNE ; GP1BA
0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 3
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 3
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 3
rs13300663
RCL1
9 4814948 intron variant G/A;C snv 3
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 3
rs6141
THPO
0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 3
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 3
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 2