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: rs1539189
rs1539189
20 1966633 intron variant A/G snv 2.0E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs185387034
rs185387034
20 1970274 intron variant A/G snv 4.6E-03
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs4411786
rs4411786
20 1950251 intron variant T/A;C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs4411786
rs4411786
20 1950251 intron variant T/A;C;G snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs4618126
rs4618126
20 1950239 intron variant G/A snv 0.43
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs6045612
rs6045612
20 1950355 intron variant C/T snv 0.43
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016