Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10188217
PUS10
0.925 0.080 2 60990407 intron variant T/A;C snv 1
rs11552708
TNFSF12-TNFSF13 ; TNFSF13
0.882 0.240 17 7559238 missense variant G/A;C snv 0.13; 4.2E-06 1
rs1359062
LOC105371664
0.925 0.160 1 192572342 intron variant C/A;G;T snv 1
rs1378938 1.000 0.080 15 74804102 downstream gene variant T/A;C snv 1
rs2387397
LINC02649
1.000 0.080 10 6348230 intron variant G/A;C snv 1
rs4558075 1.000 0.080 10 6359663 intergenic variant C/A;G;T snv 1
rs531930
NKAIN2
1.000 0.080 6 124422361 intron variant A/G;T snv 1
rs58911644
GATD3A ; LOC107983952 ; LOC102725065
1.000 0.080 21 44209238 3 prime UTR variant A/T snv 1
rs5979785 0.925 0.160 X 12953405 intergenic variant C/T snv 1
rs6691768
NFIA
1.000 0.080 1 61326191 intron variant G/A;C snv 1
rs7104791 1.000 0.080 11 111326133 downstream gene variant T/A;C snv 1
rs76830965
IL12A-AS1
0.925 0.120 3 159919889 intron variant C/A;G;T snv 1
rs7753008
BACH2
1.000 0.080 6 90099920 intron variant T/A;C snv 1
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 1
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1033180 1.000 0.080 6 383546 regulatory region variant C/T snv 5.4E-02 1
rs6715106
STAT4
1.000 0.080 2 191048308 intron variant A/G snv 6.1E-02 1
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs8081319
ACACA ; C17orf78
1.000 0.080 17 37374139 intron variant A/G snv 6.8E-02 1
rs79758729
ELMO1
1.000 0.080 7 37378851 intron variant A/G snv 7.9E-02 1
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs6806528
FRMD4B
1.000 0.080 3 69203748 intron variant C/T snv 8.7E-02 1
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10