Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1977412
LOC105373166
0.882 0.160 1 230716523 intron variant T/A;C snv 5
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 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
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 4
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 4
rs4968782 1.000 0.080 17 63471115 upstream gene variant G/A;T snv 4
rs261291
ALDH1A2
1.000 0.080 15 58387979 intron variant T/A;C snv 4
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs5112
APOC1P1
1.000 0.080 19 44927023 non coding transcript exon variant C/G snv 0.55 4
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 4
rs12459419
CD33
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31 4
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 4
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 4
rs9332739
CYP21A2 ; C2-AS1 ; C2
0.763 0.360 6 31936027 missense variant G/A;C snv 4.1E-06; 3.9E-02 4
rs61812598
IL6R
1.000 0.080 1 154447611 intron variant G/A snv 0.31 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs34311866
TMEM175
0.882 0.080 4 958159 missense variant T/C snv 0.18 0.14 4
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 4
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs157595 1.000 0.080 19 44922203 upstream gene variant A/G;T snv 3
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 3
rs75627662 1.000 0.080 19 44910319 non coding transcript exon variant C/T snv 0.17 3