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: rs9310736
rs9310736
THRB
3 24309320 intron variant A/G snv 0.69
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.800 1.000 3 2010 2017
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: 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: 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: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 2 2016 2019
dbSNP: rs113700287
rs113700287
THRB
3 24293020 intron variant -/GTT delins
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs113700287
rs113700287
THRB
3 24293020 intron variant -/GTT delins
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs113700287
rs113700287
THRB
3 24293020 intron variant -/GTT delins
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs113700287
rs113700287
THRB
3 24293020 intron variant -/GTT delins
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1349265
rs1349265
THRB
1.000 0.040 3 24117896 3 prime UTR variant A/C;G snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs1349265
rs1349265
THRB
1.000 0.040 3 24117896 3 prime UTR variant A/C;G snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
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
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: rs2044753
rs2044753
THRB
3 24251510 intron variant T/C snv 0.14
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs35601156
rs35601156
THRB
3 24345531 intron variant T/A snv 0.18
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3749376
rs3749376
THRB ; THRB-AS1
3 24496776 non coding transcript exon variant G/C;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs6792725
rs6792725
THRB
3 24478792 intron variant A/G snv 0.71
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs73032363
rs73032363
THRB
1.000 0.080 3 24431375 intron variant A/G snv 0.24
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2018 2018
dbSNP: rs73041705
rs73041705
THRB
1.000 0.080 3 24421744 intron variant T/C snv 0.25
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2018 2018
dbSNP: rs76247835
rs76247835
THRB
1.000 0.080 3 24465348 intron variant T/C snv 2.7E-03
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2018 2018
dbSNP: rs7652234
rs7652234
THRB
3 24148968 intron variant C/G snv 0.11
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs826220
rs826220
THRB
1.000 0.040 3 24227186 intron variant C/T snv 0.70
CUI: C0027092
Disease: Myopia
Myopia 		0.700 1.000 1 2016 2016
dbSNP: rs869784
rs869784
THRB
3 24306517 intron variant T/C snv 0.68
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs869784
rs869784
THRB
3 24306517 intron variant T/C snv 0.68
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs869784
rs869784
THRB
3 24306517 intron variant T/C snv 0.68
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016