Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10994856
A1CF
0.925 0.120 10 50885488 intron variant G/A snv 0.19 2
rs10994860
A1CF
0.925 0.120 10 50885664 5 prime UTR variant C/T snv 0.19 2
rs10206899
ALMS1P1
2 73673773 intron variant T/C;G snv 0.21; 3.9E-05 2
rs2079742
BCAS3
0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 2
rs7208487
FBXL20
0.925 0.080 17 39387196 intron variant T/A;G snv 2
rs11858316
IGF1R
0.925 0.120 15 98705800 intron variant C/T snv 0.50 2
rs2137683
IGF1R
0.925 0.120 15 98746409 intron variant C/G snv 0.53 2
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 2
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 2
rs10851885
NRG4
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18 2
rs12989250
ORC4
0.925 0.120 2 148018869 intron variant G/A snv 0.32 2
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 2
rs7805747
PRKAG2
1.000 0.080 7 151710715 intron variant G/A snv 0.26 2
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 2
rs4760355
R3HDM2
0.925 0.120 12 57331414 intron variant G/A snv 0.20 2
rs6933716
RREB1
0.925 0.120 6 7125476 intron variant T/C snv 0.53 2
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34 2
rs6066043
SLC13A3
1.000 0.080 20 46659814 intron variant G/A;T snv 2
rs4971100
TRIM46
0.925 0.120 1 155183255 intron variant G/A snv 0.39 2
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 2
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 1
rs17536527 15 45426989 upstream gene variant G/A;C snv 1
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 1
rs227731 0.882 0.120 17 56695877 intergenic variant T/A;G snv 1
rs2453533 1.000 0.080 15 45349027 intergenic variant C/A snv 0.56 1