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
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 6
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 5
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4