Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 3
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 2
rs12282742
SAA2-SAA4 ; SAA2
11 18244252 intron variant C/G;T snv 2
rs1992044
LOC105375856 ; LINC01602
8 57928349 intron variant G/A;T snv 2
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 2
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 2
rs7065696
PHF8
X 53947621 intron variant C/G;T snv 2
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs9960767
TCF4
0.925 0.040 18 55487771 intron variant A/C;G snv 1
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 2
rs17512836
TCF4
0.925 0.040 18 55527730 intron variant T/C snv 2.2E-02 1
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 2
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 3
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
rs1992045
LOC105375856 ; LINC01602
8 57928365 intron variant C/T snv 0.14 2