Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs9358356
CDKAL1
1.000 0.080 6 20667151 intron variant T/C snv 0.39 1
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs9332998
CYP4A11
1 46938514 intron variant T/C snv 0.16 2
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 3
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs503279
FUT2 ; LOC105447645
19 48705753 3 prime UTR variant T/C snv 0.48 2
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 1
rs10518693
IVD
15 40407823 intron variant C/T snv 0.37 2
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs2652822
LACTB ; RPS27L
15 63130573 3 prime UTR variant T/C snv 0.41 2