Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.800 1.000 1 2011 2011
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis
0.710 1.000 1 2015 2015
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement
0.700 1.000 2 2011 2015
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement
0.700 1.000 2 2011 2015
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
Iron binding capacity total measurement
0.700 1.000 1 2011 2011
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
HFE-Associated Hereditary Hemochromatosis
0.700 1.000 1 2015 2015
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement
0.700 1.000 1 2015 2015
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders
0.700 1.000 1 2015 2015
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
Total iron binding capacity function
0.700 1.000 1 2011 2011
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1
0.700 1.000 1 2015 2015