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
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;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
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
rs1532085
ALDH1A2
0.882 0.080 15 58391167 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
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 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
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6