Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 1
rs11206517
PCSK9
1.000 0.120 1 55060755 intron variant T/C;G snv 2
rs11634397 1.000 0.080 15 80139880 downstream gene variant A/G snv 0.57 1
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 2
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 2
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs1558861 11 116736721 regulatory region variant C/G;T snv 3
rs17145738
TBL2
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 6
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 2
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 3
rs2259820
HNF1A
0.882 0.160 12 120997539 synonymous variant C/T snv 0.34 0.26 1
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 3