Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9859077
SENP7
3 101417558 intron variant G/A;C snv 0.28 2
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 2
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs7972177
HDAC7
12 47784730 missense variant A/G snv 0.28 0.33 1
rs2748427
TMC6
17 78125783 missense variant A/G snv 0.24 0.29 2
rs60237566
ITM2C
2 230877996 intron variant T/G snv 0.21 0.25 2
rs6121246
DUSP15 ; FOXS1
20 31845549 5 prime UTR variant C/T snv 0.20 0.29 2
rs17116710
KIF4B
5 155015898 missense variant G/A snv 0.18 0.17 1
rs17464525
AP4B1-AS1 ; AP4B1
1 113901277 synonymous variant G/A snv 0.17 0.16 1
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 7
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs35602605
EIF2AK4
15 40016658 missense variant G/A;T snv 7.2E-05; 0.13 1
rs41264487
PABPC4 ; PABPC4-AS1
1 39571682 synonymous variant C/G;T snv 0.13; 4.9E-05 1
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 5
rs2272783
FECH
1.000 18 57571588 synonymous variant A/G snv 0.12 6.3E-02 4
rs34523089
RNF43 ; TSPOAP1-AS1
17 58358748 missense variant C/T snv 0.11 0.11 2
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs7179364
CHD2
15 92904992 missense variant G/A snv 0.10 0.10 1
rs5030755
RPA1
17 1879658 missense variant A/G snv 7.6E-02 7.4E-02 2
rs149290349
ZFP36L2
2 43224818 missense variant G/A;T snv 6.7E-02 3
rs60757417
GFI1B
9 132989049 intron variant C/A;G;T snv 6.3E-02; 4.0E-06 1
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs76242821
NFASC
1 204920781 intron variant G/A snv 5.9E-02 5.1E-02 1
rs74789101
ZNF791 ; ZNF490
19 12609925 missense variant G/A snv 5.9E-02 5.5E-02 1