Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 7
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs3115663
PRRC2A ; MIR6832
0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 6
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 5
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 5
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 5
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 5
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 5
rs12661667
USP49
6 41824807 intron variant C/T snv 0.20 4