Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs112635299
SERPINA2
1.000 0.040 14 94371805 downstream gene variant G/T snv 1.3E-02 7
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 6
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 5
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 5
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 5
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 5
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 5
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 5
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 4
rs7953249
HNF1A-AS1
0.882 0.160 12 120965921 splice region variant G/A snv 0.59 4
rs61812598
IL6R
1.000 0.080 1 154447611 intron variant G/A snv 0.31 4
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34 4
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 4
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 4
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 4