Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2418736
NFATC3
16 68120959 intron variant G/A snv 0.28 4
rs2856646
H2AC6
6 26135270 intron variant A/G snv 0.73 4
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 4
rs3758348
SURF4
9 133372523 intron variant G/C snv 0.13 4
rs3806113
MED20
6 41908597 intron variant C/T snv 0.18 4
rs5750373
MPST
22 37028990 non coding transcript exon variant G/A snv 0.49 4
rs5756504
TMPRSS6
22 37071230 intron variant C/G;T snv 4
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs6569992 6 135131014 intergenic variant G/A;C;T snv 4
rs668459 6 139514552 intron variant C/T snv 0.51 4
rs67250268
H2AC6
6 26135269 intron variant A/-;AA delins 4
rs763668 22 37115036 intergenic variant C/G;T snv 4
rs8141597
MPST
22 37028807 non coding transcript exon variant T/C snv 0.31 4
rs855788
TMPRSS6
22 37078039 intron variant G/A snv 0.51 4
rs932316 6 25640972 upstream gene variant T/C;G snv 4
rs9357371
MED20
6 41917581 5 prime UTR variant A/C snv 0.20 4
rs9402686
LOC105378010
6 135106679 upstream gene variant G/A snv 0.20 4
rs1010222
CALR
19 12937794 upstream gene variant A/G snv 0.70 3
rs10445937 2 60410521 intron variant G/A snv 0.39 3
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 3
rs10758658
RCL1
9 4856877 intron variant G/A snv 0.15 3
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13 3
rs11085825
GCDH
19 12896644 intron variant C/T snv 0.31 3
rs1109166
LCAT ; SLC12A4
16 67943479 5 prime UTR variant T/C snv 0.32 3
rs11914132 22 37113047 upstream gene variant C/T snv 0.27 3