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
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 7
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 5
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs578776
CHRNA3
0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 3
rs2239803
HLA-DRA
0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 3
rs10483038
KCNJ6
1.000 0.080 21 37652469 intron variant T/C snv 0.26 3
rs111372083
KCNJ6
1.000 0.080 21 37638374 intron variant C/A;T snv 0.27 3
rs111576572
KCNJ6
1.000 0.080 21 37617262 3 prime UTR variant A/G snv 0.32 3
rs1399590
KCNJ6
1.000 0.080 21 37681768 intron variant G/A snv 0.56 3
rs1399591
KCNJ6
1.000 0.080 21 37681654 intron variant C/T snv 0.50 3
rs1399592
KCNJ6
1.000 0.080 21 37681559 intron variant T/A;G snv 0.52 3
rs1475839
KCNJ6
1.000 0.080 21 37649639 intron variant C/T snv 0.31 3
rs1515050
KCNJ6
1.000 0.080 21 37630840 intron variant T/C snv 0.75 3
rs1709817
KCNJ6
1.000 0.080 21 37664047 intron variant T/A;C snv 3
rs1709818
KCNJ6
1.000 0.080 21 37663909 intron variant T/C snv 0.57 3
rs1709819
KCNJ6
1.000 0.080 21 37663813 intron variant A/C snv 0.59 3