Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
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
rs1977412
LOC105373166
0.882 0.160 1 230716523 intron variant T/A;C snv 5
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 5
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 4
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 4
rs261291
ALDH1A2
1.000 0.080 15 58387979 intron variant T/A;C snv 4
rs61812598
IL6R
1.000 0.080 1 154447611 intron variant G/A snv 0.31 4
rs12721109
APOC4 ; APOC4-APOC2
1.000 0.080 19 44943964 intron variant G/A snv 1.3E-02 3
rs17747324
TCF7L2
0.925 0.160 10 112992744 intron variant T/C snv 0.17 3
rs41290120
NECTIN2
1.000 0.080 19 44879418 intron variant G/A;T snv 3
rs727479
MIR4713HG ; CYP19A1 ; MIR4713
0.790 0.240 15 51242350 intron variant C/A;T snv 3
rs759819 1.000 0.080 19 54304302 intron variant C/G;T snv 3
rs7935829
MS4A6A
1.000 0.080 11 60175342 intron variant A/G snv 0.33 3
rs8106922
TOMM40
1.000 0.080 19 44898409 intron variant A/G snv 0.36 3
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 3
rs10207628
BIN1
0.925 0.120 2 127094445 intron variant G/A;C snv 2
rs10401176
BCL3
1.000 0.080 19 44750234 intron variant C/G;T snv 0.17 2
rs10426401
LOC107985305 ; PVR
1.000 0.080 19 44644419 intron variant T/G snv 0.32 2
rs10808026
EPHA1
1.000 0.080 7 143402040 intron variant C/A snv 0.19 2
rs117834366
CNTNAP2
0.925 0.120 7 147937799 intron variant G/A snv 1.2E-02 2