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: rs1434282
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 3 2016 2019
dbSNP: rs1434282
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 3 2016 2019
dbSNP: rs1036332
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs1434282
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 2 2016 2018
dbSNP: rs1036332
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs115858175
rs115858175
LINC01221
1.000 0.040 1 199032122 intron variant C/A;G snv
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder 		0.700 1.000 1 2019 2019
dbSNP: rs1434282
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1434282
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs6427756
rs6427756
LINC01221
1 199031598 intron variant A/G snv 0.71
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2018 2018
dbSNP: rs7529925
rs7529925
LINC01221
1 199038079 intron variant C/T snv 0.77
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7529925
rs7529925
LINC01221
1 199038079 intron variant C/T snv 0.77
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7529925
rs7529925
LINC01221
1 199038079 intron variant C/T snv 0.77
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2017 2017
dbSNP: rs781255974
rs781255974
LINC01221
1 199025568 intron variant AAA/-;A;AA;AAAA;AAAAA delins
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016