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: rs1505307
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2017 2018
dbSNP: rs1505307
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 2 2016 2019
dbSNP: rs1505307
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 2 2016 2019
dbSNP: rs1505307
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 2 2017 2018
dbSNP: rs1505307
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1505307
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2018 2018