Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs4645881
BAX
19 48955005 non coding transcript exon variant C/G;T snv 0.83 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs2074585
IQGAP1
0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67 5
rs2856451
TNXB
6 32043581 intron variant A/G;T snv 0.59 3
rs14408
IFITM2
11 308314 missense variant T/C;G snv 0.53 4
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 6
rs3742716
RIN3
14 92652324 synonymous variant G/A snv 0.32 0.25 2
rs725660
BHMG1
19 45759028 missense variant C/A snv 0.32 0.33 2
rs2302006
CCL24
7 75813412 missense variant T/G snv 0.29 0.25 2
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs4807542
GPX4
1.000 0.120 19 1104079 synonymous variant G/A;C snv 0.22; 1.8E-05 3
rs4147915
ABCA7
19 1049306 synonymous variant C/A;G snv 0.18; 4.0E-06 3
rs3209441
DOCK8
9 286491 missense variant G/A snv 0.12 0.11 3
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs34173062
MAF1 ; SHARPIN
8 144103704 missense variant G/A;C snv 7.3E-02 3
rs36084354
ARHGAP45
19 1079960 missense variant G/A snv 5.7E-02 5.9E-02 3
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs11555542
ASB2
14 93951185 missense variant T/C snv 3.3E-02 3.7E-02 2
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs34210653
ALOX15
0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02 4
rs61731111
S1PR4
19 3179519 missense variant C/G;T snv 1.3E-02 2
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 7