Source: ALL
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: rs7085433
rs7085433 		1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2010 2017
dbSNP: rs7085433
rs7085433 		1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs7085433
rs7085433 		1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2010 2010
dbSNP: rs7085433
rs7085433 		1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2010 2010