Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs11154178
LOC105377982 ; TRDN
0.807 0.240 6 123540174 intron variant T/A;C snv 7
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs80028505
MAPK14
0.807 0.240 6 36030611 intron variant C/G;T snv 7
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 6
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 5
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs1333062
ITLN1
0.807 0.200 1 160876494 downstream gene variant T/C;G snv 5
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 5
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5