Disease: Autoantibody measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs12518099
LINC01339
0.925 0.120 5 90250292 intron variant A/G;T snv 3
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3
rs4689388
WFS1
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 3
rs4712523
CDKAL1
0.925 0.120 6 20657333 intron variant A/G snv 0.41 3