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: rs200895692
rs200895692
1 42956286 intron variant GCCTGTAATCCCAG/- delins
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016