Source: GWASCAT ×
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 61
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 8
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 7
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 6
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 6
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 5
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5