Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2
rs11185790
PANK1
10 89612776 intron variant G/A snv 0.15 2
rs2216405 2 210752170 intergenic variant A/G snv 0.15 2
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs9332998
CYP4A11
1 46938514 intron variant T/C snv 0.16 2
rs4481233
SLC2A9
0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs4149081
SLCO1B1
1.000 0.040 12 21225087 intron variant G/A snv 0.18 4
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs2624265
LINC02694
15 38856448 intron variant T/C snv 0.28 2
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 3
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 4
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 4
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs10518693
IVD
15 40407823 intron variant C/T snv 0.37 2
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 3
rs9358356
CDKAL1
1.000 0.080 6 20667151 intron variant T/C snv 0.39 1
rs2652822
LACTB ; RPS27L
15 63130573 3 prime UTR variant T/C snv 0.41 2
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10