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: rs1867503
rs1867503
TF ; INHCAP
3 133691804 non coding transcript exon variant G/A snv 0.60
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2015 2015
dbSNP: rs190500289
rs190500289
TF ; INHCAP
1.000 0.080 3 133712051 intron variant G/A snv 2.6E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2016 2016
dbSNP: rs8177179
rs8177179
TF ; INHCAP
0.925 0.080 3 133744613 intron variant G/A snv 0.58
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		0.700 1.000 1 2014 2014
dbSNP: rs8177179
rs8177179
TF ; INHCAP
0.925 0.080 3 133744613 intron variant G/A snv 0.58
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		0.700 1.000 1 2014 2014
dbSNP: rs8177318
rs8177318
TF ; INHCAP
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs8177318
rs8177318
TF ; INHCAP
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs8177318
rs8177318
TF ; INHCAP
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs8177318
rs8177318
TF ; INHCAP
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs8177318
rs8177318
TF ; INHCAP
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs9872999
rs9872999
TF ; INHCAP
3 133738670 intron variant C/G;T snv
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0.700 1.000 1 2015 2015
dbSNP: rs9872999
rs9872999
TF ; INHCAP
3 133738670 intron variant C/G;T snv
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0.700 1.000 1 2015 2015