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: rs2413450
rs2413450
22 37074184 intron variant T/C snv 0.61
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.800 1.000 2 2009 2017
dbSNP: rs855791
rs855791
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 2 2017 2018