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: rs2290547
rs2290547
SETD2
3 47019693 intron variant G/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2013 2017
dbSNP: rs114151323
rs114151323
SETD2
3 47142565 intron variant C/T snv 1.2E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs13063578
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs13063578
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs13063578
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs13063578
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs13063578
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs17784127
rs17784127
SETD2
3 47020210 intron variant T/C snv 0.35
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs543811905
rs543811905
SETD2
3 47029484 intron variant AA/-;A;AAA;AAAA;AAAAA delins
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs62246406
rs62246406
SETD2
3 47056495 intron variant G/A snv 0.14
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018