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: rs17396340
rs17396340
KIF1B
1 10226118 intron variant G/A;C snv
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs17655730
rs17655730 		11 270715 intergenic variant T/C snv 0.20
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs2227831
rs2227831
F2R
5 76727669 intron variant A/G snv 2.7E-02
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs2393967
rs2393967
JMJD1C ; MIR1296
10 63373396 intron variant A/C snv 0.23
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2009 2012
dbSNP: rs2950390
rs2950390 		12 56661507 downstream gene variant C/G;T snv
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs3000073
rs3000073
BRF1
14 105263455 intron variant G/A snv 0.28
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs342296
rs342296
CTB-30L5.1
7 106732457 intron variant G/A snv 0.41
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2012 2012
dbSNP: rs4305276
rs4305276
ANKMY1
2 240555596 intron variant C/A;G;T snv
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs4521516
rs4521516
MEF2C
5 88804134 intron variant G/C snv 0.15
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs4812048
rs4812048 		20 59012716 intergenic variant C/T snv 0.15
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs6110278
rs6110278
MACROD2
20 14407569 intron variant C/T snv 0.27
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2009 2009
dbSNP: rs6136489
rs6136489 		20 1943088 upstream gene variant T/G snv 0.46
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2009 2012
dbSNP: rs647316
rs647316
EHD3
2 31241963 intron variant A/G snv 0.80
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2009 2012
dbSNP: rs649729
rs649729
EHD3
1.000 0.040 2 31241519 intron variant T/A;C snv
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs7317038
rs7317038
GRTP1 ; GRTP1-AS1
13 113358583 intron variant C/T snv 0.34
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs8076739
rs8076739 		17 29387569 intron variant C/T snv 0.64
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2014
dbSNP: rs893001
rs893001
CD226
18 69849610 intron variant A/C snv 0.18
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2009 2012
dbSNP: rs944002
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
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: rs9900280
rs9900280
TAOK1
17 29442580 intron variant G/A snv 0.58
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2014 2014
dbSNP: rs1001494
rs1001494
ST7L
1 112567997 intron variant T/C snv 0.50
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs10062757
rs10062757 		5 62239297 intergenic variant T/C snv 0.35
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs10072221
rs10072221
IQGAP2
5 76424719 intron variant T/A;C;G snv
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs10220411
rs10220411
ACTN1-AS1
14 68985371 intron variant A/G snv 0.29
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs10274553
rs10274553
CTB-30L5.1
7 106716200 intron variant T/A;C snv
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2019 2019