Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 11
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 10
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 8
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 7
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs755249
PPIEL ; BMP8A
1 39529402 3 prime UTR variant C/A;T snv 5
rs10851907
CHRNB4
1.000 0.040 15 78623522 upstream gene variant G/A snv 0.40 4
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 4
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 3
rs6841581
EDNRA
0.882 0.080 4 147480038 upstream gene variant G/A;T snv 3
rs6842241
EDNRA
0.925 0.080 4 147479667 upstream gene variant C/A snv 0.22 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs566125
MMP3
1.000 0.040 11 102839740 intron variant C/T snv 0.10 3
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs4842266 12 79557786 upstream gene variant G/A snv 0.50 2