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
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs7081476
ANKRD26
0.851 0.120 10 26969741 intergenic variant G/C;T snv 7
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs74617384
LPA
0.925 0.080 6 160576086 intron variant A/G;T snv 5
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs12922822
UMOD
1.000 0.040 16 20356323 upstream gene variant C/A;T snv 4
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 4
rs10084572
LOC105372829
1.000 0.040 21 43992991 downstream gene variant T/A;C;G snv 3
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 3