Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10796961
TTC24
1 156586529 synonymous variant G/A snv 0.92 0.79 1
rs4576240
KIAA0319
1.000 0.040 6 24596250 missense variant T/A;G snv 4.0E-06; 0.92 0.91 1
rs12021720
DBT
0.925 0.160 1 100206504 missense variant T/A;C snv 0.92 2
rs6042507
SIRPB2
20 1478415 missense variant T/A;C;G snv 9.6E-05; 4.0E-06; 0.91 1
rs1892251
SLC17A4 ; SLC17A1
0.925 0.120 6 25769121 synonymous variant T/C snv 0.91 0.85 2
rs195162
LOC107984334 ; BEST1
11 61957042 intron variant C/G;T snv 0.91 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89 1
rs1771798
MTHFD1L
6 150960431 intron variant T/C;G snv 0.89 1
rs3134943
AGPAT1 ; MIR6833 ; RNF5
0.882 0.240 6 32179984 intron variant T/A;C snv 0.89 3
rs2228445
ATP2B4
1 203698281 synonymous variant T/A;C snv 0.89 1
rs6537825
TRIM33
1.000 0.040 1 114405659 missense variant A/G snv 0.88 0.92 1
rs1419114
ATP2B4
1 203683316 synonymous variant A/G snv 0.88 0.83 1
rs2576365
ABI3BP
3 100902582 intron variant C/A;G snv 0.88 0.83 1
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs10865030
MRPL30
2 99188179 splice region variant T/C;G snv 0.87 0.83 1
rs501764
GATA3-AS1 ; GATA3
1.000 0.120 10 8051071 non coding transcript exon variant G/T snv 0.87 0.86 1
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 3
rs2011404
UGT1A6 ; UGT1A5 ; UGT1A4 ; UGT1A10 ; UGT1A9 ; UGT1A7 ; UGT1A8
2 233719291 missense variant T/C;G snv 0.87; 2.4E-05 2
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 2
rs3094609
HCG27
0.925 0.080 6 31197789 non coding transcript exon variant T/C snv 0.86 0.89 5
rs562556
PCSK9
0.827 0.280 1 55058564 missense variant G/A snv 0.86 0.83 2
rs2571381
HLA-A
6 29945053 splice region variant T/A;C snv 0.85 1
rs1671152
LOC107985325 ; GP6
0.882 0.160 19 55014977 missense variant T/G snv 0.85 0.81 1