Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 9
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 6
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 5
rs12637730
SRPRB ; RAB6B
3 133827453 3 prime UTR variant C/T snv 0.14 3
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 3
rs307412 8 141601769 intron variant A/G;T snv 2
rs7598519 2 239729660 intergenic variant A/C snv 9.3E-02 2
rs10205816
ABCG5 ; DYNC2LI1
2 43817116 intron variant A/G snv 0.39 2
rs6781238
CDV3
3 133579276 intron variant C/T snv 0.47 2
rs799882
LINC00536
8 116248203 intron variant G/A snv 0.99 2
rs7827820
LINC01609
8 111101950 intron variant A/G snv 1.2E-02 2
rs2275335
LINC01710
1 218913054 intron variant T/C snv 6.8E-02 2
rs11022982
LINC02548
11 13841158 intron variant T/C snv 1.9E-02 2
rs7105390
TYR ; LOC107984363
11 89201166 intron variant T/C snv 0.19 2