Source: GWASDB

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: rs4656355
rs4656355
NOS1AP ; LOC105371475
1 162154007 intron variant A/C;G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs6427656
rs6427656
NOS1AP ; LOC105371475
1 162164848 intron variant G/A snv 0.45
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs6671817
rs6671817
NOS1AP
1 162183436 intron variant A/G snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs7549718
rs7549718
NOS1AP ; LOC105371475
1 162171072 intron variant A/G snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs945713
rs945713
NOS1AP ; LOC105371475
1 162165880 intron variant G/A snv 0.45
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011