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: rs4848100
rs4848100 		2 111630955 non coding transcript exon variant C/T snv 0.76
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs1044864
rs1044864 		2 111769289 3 prime UTR variant G/A snv 0.20 0.18
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1044864
rs1044864 		2 111769289 3 prime UTR variant G/A snv 0.20 0.18
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs11683361
rs11683361 		2 111622982 intron variant C/G snv 0.70
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs11683361
rs11683361 		2 111622982 intron variant C/G snv 0.70
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs1448190
rs1448190 		1.000 0.040 2 111618386 intron variant A/C snv 0.68
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs17040773
rs17040773 		2 111742458 intron variant A/C snv 0.17
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		0.700 1.000 1 2012 2012
dbSNP: rs4848100
rs4848100 		2 111630955 non coding transcript exon variant C/T snv 0.76
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs4848612
rs4848612 		2 111630961 non coding transcript exon variant G/A snv 0.74
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs66739581
rs66739581 		2 111823394 intron variant T/C snv 0.22
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs78658973
rs78658973 		2 111726948 intron variant T/A snv 0.17
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018