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: rs3027001
rs3027001
1 159199673 intron variant C/G,T snp 9.6E-05; 0.17
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1 2011 2011
dbSNP: rs3027001
rs3027001
1 159199673 intron variant C/G,T snp 9.6E-05; 0.17
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1 2011 2011
dbSNP: rs3027012
rs3027012
1 159204333 5 prime UTR variant C/T snp 0.13
Soluble Interleukin 6 Receptor Measurement
0.700 1 2012 2012
dbSNP: rs3027012
rs3027012
1 159204333 5 prime UTR variant C/T snp 0.13
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1 2011 2011
dbSNP: rs3027012
rs3027012
1 159204333 5 prime UTR variant C/T snp 0.13
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1 2011 2011
dbSNP: rs3027012
rs3027012
1 159204333 5 prime UTR variant C/T snp 0.13
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1 2013 2013