Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7643459
LOC101927394 ; LMCD1-AS1
0.925 0.120 3 7963141 intron variant G/C;T snv 1
rs7748275 0.882 0.120 6 3580855 downstream gene variant T/A snv 8.2E-02 1
rs8044477 1.000 0.120 16 58942687 intron variant A/G snv 0.53 1
rs9283636 1.000 0.120 3 166315136 intergenic variant G/A snv 0.46 1
rs9787692 1.000 0.120 10 8603200 intergenic variant T/G snv 0.30 1
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 4
rs183211
LRRC37A2 ; NSF
0.882 0.160 17 46710944 intron variant G/A snv 0.28 0.30 3
rs8170
BABAM1 ; USHBP1
0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 3
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 2
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv 2
rs1834481
IL18
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16 1
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 2
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 1
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 1
rs2070074
GALT
0.742 0.360 9 34649445 missense variant A/G snv 9.2E-02 7.4E-02 1
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1