Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7698623
MEPE
4 87834676 intron variant T/A;C snv 6.1E-05; 0.94 1
rs289714
CETP
16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70 5
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs4950806
RNPEP
1 201983446 5 prime UTR variant T/C snv 0.58 0.60 1
rs2469953
RAPH1
2 203457575 synonymous variant T/C snv 0.58 0.61 1
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs3731694
CYP20A1
2 203251937 intron variant A/T snv 0.50 1
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 3
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs11754288
SLC17A4 ; SLC17A1
0.925 0.120 6 25776721 missense variant G/A snv 0.36 0.32 4
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs3213545
OASL
12 121033534 synonymous variant G/A snv 0.32 0.26 2
rs16890979
SLC2A9
0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 4
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 5
rs1803274
BCHE
0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs283813
NECTIN2
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16 6
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10