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: rs1934363
rs1934363
LINC02652
1.000 0.120 10 28484549 intron variant G/C snv 0.18
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2019 2019
dbSNP: rs2807743
rs2807743
LINC02652
10 28491364 intron variant C/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs2807743
rs2807743
LINC02652
10 28491364 intron variant C/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2998286
rs2998286
LINC02652
10 28491444 intron variant T/C snv 0.73
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2998286
rs2998286
LINC02652
10 28491444 intron variant T/C snv 0.73
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs2998286
rs2998286
LINC02652
10 28491444 intron variant T/C snv 0.73
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs2998286
rs2998286
LINC02652
10 28491444 intron variant T/C snv 0.73
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs2998286
rs2998286
LINC02652
10 28491444 intron variant T/C snv 0.73
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016