Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11190141
rs11190141
1.000 0.040 10 99532633 upstream gene variant C/T snv 0.40
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs6584283
rs6584283
0.776 0.080 10 99530544 intron variant T/C snv 0.56
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018