Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6060488
FER1L4
20 35585256 non coding transcript exon variant A/G snv 0.80 0.80 2
rs6060151
TRPC4AP
20 35006423 intron variant G/T snv 0.65 0.58 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs2295887
EDEM2 ; MMP24-AS1-EDEM2
20 35126384 intron variant G/A snv 0.61 0.51 2
rs777435
MYO7B
2 127612321 synonymous variant A/G snv 0.57 0.66 2
rs945959
MMP24-AS1-EDEM2 ; EDEM2
20 35147102 intron variant G/C snv 0.42 0.48 2
rs4662740
MYO7B
2 127581881 intron variant G/T snv 0.41 0.34 2
rs1799810
PROC
1.000 0.040 2 127418464 5 prime UTR variant A/T snv 0.38 0.44 2
rs6087625
NCOA6
20 34754674 intron variant G/A snv 0.35 0.34 2
rs1919127
C2orf16
0.925 0.120 2 27578626 missense variant T/C snv 0.31 0.27 6
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs7568070
CYP27C1
2 127195478 synonymous variant A/C snv 0.26 0.32 2
rs3732209
MAP3K2
2 127322230 synonymous variant A/G snv 0.26 0.27 2
rs2425049
FAM83C
20 35286917 missense variant C/T snv 0.25 0.35 2
rs2250205
EIF6 ; MMP24OS ; MMP24-AS1-EDEM2
20 35280121 splice region variant G/A snv 0.23 0.25 2
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 6
rs3746435
MYH7B
20 34999395 missense variant G/C snv 0.19 0.18 2
rs1178977
BAZ1B
0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21 5
rs3746429
MMP24-AS1-EDEM2 ; EDEM2
20 35115804 missense variant C/T snv 0.16 0.12 2
rs334151
IWS1
2 127495995 splice region variant C/T snv 0.13 0.13 2
rs11906160
MYH7B
20 34977952 missense variant G/A;T snv 0.12 0.16 2
rs8825
ERGIC3
20 35556975 splice region variant A/G snv 0.12 0.15 2
rs1557203
FER1L4
20 35576541 non coding transcript exon variant A/G snv 0.11 0.12 2
rs2275274
MMP24OS ; MMP24-AS1-EDEM2 ; MMP24
20 35269741 intron variant C/A;G;T snv 4.2E-04; 0.11 2
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 5