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: rs1172130
rs1172130
TMCC2
1 205275825 intron variant G/A snv 0.30
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2014
dbSNP: rs1668871
rs1668871
TMCC2
1 205268009 intron variant T/C;G snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 1 2011 2011
dbSNP: rs1668873
rs1668873
TMCC2
1 205266862 intron variant G/A snv 0.27
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2009 2012
dbSNP: rs9660992
rs9660992
TMCC2
1 205280322 intron variant A/G snv 0.43
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2014 2014
dbSNP: rs61823972
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs1151786
rs1151786
TMCC2
1 205258632 intron variant G/A;C;T snv
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1172128
rs1172128
TMCC2
1 205276105 intron variant A/G snv 0.94
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1172129
rs1172129
TMCC2
1 205275844 intron variant T/A snv 0.30
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1172135
rs1172135
TMCC2
1 205278032 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 2018 2018
dbSNP: rs1172149
rs1172149
TMCC2
1 205255630 intron variant A/G snv 0.51
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs61823972
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs61823972
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs61823972
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs748012
rs748012
TMCC2
1 205247445 intron variant G/A snv 0.27
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs896322
rs896322
TMCC2 ; LOC101929459
1 205240617 intron variant A/G snv 0.92
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016