Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
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
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 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
rs13220662
HBS1L
6 135074410 intron variant G/A snv 0.41 4
rs1421312
TMPRSS6
22 37091770 intron variant A/G snv 0.45 4
rs2274089
CARMIL1
6 25488355 intron variant C/T snv 5.9E-02 4
rs2856646
H2AC6
6 26135270 intron variant A/G snv 0.73 4
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 4
rs3806113
MED20
6 41908597 intron variant C/T snv 0.18 4
rs5756504
TMPRSS6
22 37071230 intron variant C/G;T snv 4
rs668459 6 139514552 intron variant C/T snv 0.51 4
rs67250268
H2AC6
6 26135269 intron variant A/-;AA delins 4
rs855788
TMPRSS6
22 37078039 intron variant G/A snv 0.51 4
rs10758658
RCL1
9 4856877 intron variant G/A snv 0.15 3
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13 3
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 3