Source: ALL

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: rs1672908
rs1672908
1 52875213 intron variant A/G snv 0.49
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs514406
rs514406
1 52864786 intron variant A/G;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs514406
rs514406
1 52864786 intron variant A/G;T snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2016 2016
dbSNP: rs770551112
rs770551112
1 52849688 intron variant -/CT;CTT ins
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016