Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 5
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 5
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 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
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 4
rs1569534 6 135130442 intergenic variant C/T snv 0.21 4
rs17064262 6 135144336 intergenic variant T/C snv 0.18 4
rs198833 6 26114280 downstream gene variant G/A snv 0.87 4
rs2050019 6 135142809 intergenic variant C/T snv 0.27 4
rs218237 4 54528005 intergenic variant C/T snv 0.18 4
rs6569992 6 135131014 intergenic variant G/A;C;T snv 4
rs668459 6 139514552 intron variant C/T snv 0.51 4
rs932316 6 25640972 upstream gene variant T/C;G snv 4
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 4
rs2274089
CARMIL1
6 25488355 intron variant C/T snv 5.9E-02 4
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 4
rs2856646
H2AC6
6 26135270 intron variant A/G snv 0.73 4
rs67250268
H2AC6
6 26135269 intron variant A/-;AA delins 4
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 4
rs13220662
HBS1L
6 135074410 intron variant G/A snv 0.41 4
rs9402686
LOC105378010
6 135106679 upstream gene variant G/A snv 0.20 4