GC, GC vitamin D binding protein, 2638

N. diseases: 219; N. variants: 17
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: rs2282679
rs2282679 		0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		Nutritional and Metabolic Diseases 0.810 1.000 2 2010 2015
dbSNP: rs2282679
rs2282679 		0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		0.800 1.000 4 2010 2018
dbSNP: rs2282679
rs2282679 		0.645 0.480 4 71742666 intron variant T/G snv 0.21
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		0.800 1.000 4 2010 2018
dbSNP: rs4588
rs4588 		0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		0.700 1.000 2 2017 2018
dbSNP: rs4588
rs4588 		0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		0.700 1.000 2 2017 2018
dbSNP: rs1155563
rs1155563 		0.925 0.080 4 71777771 intron variant T/A;C snv
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		0.700 1.000 1 2014 2014
dbSNP: rs1155563
rs1155563 		0.925 0.080 4 71777771 intron variant T/A;C snv
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		0.700 1.000 1 2014 2014
dbSNP: rs11723621
rs11723621 		4 71749645 intron variant A/G snv 0.21
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1352846
rs1352846 		4 71752058 intron variant A/G snv 0.22
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1352846
rs1352846 		4 71752058 intron variant A/G snv 0.22
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1352846
rs1352846 		4 71752058 intron variant A/G snv 0.22
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs1352846
rs1352846 		4 71752058 intron variant A/G snv 0.22
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs3755967
rs3755967 		0.925 0.080 4 71743681 intron variant C/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs3755967
rs3755967 		0.925 0.080 4 71743681 intron variant C/A;T snv
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3755967
rs3755967 		0.925 0.080 4 71743681 intron variant C/A;T snv
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7041
rs7041 		0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7041
rs7041 		0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7041
rs7041 		0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		0.700 1.000 1 2018 2018
dbSNP: rs705119
rs705119 		4 71747319 intron variant A/C;G snv
CUI: C1285654
Disease: Memory performance
Memory performance 		0.700 1.000 1 2017 2017
dbSNP: rs843005
rs843005 		4 71750610 intron variant C/A;T snv
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		0.700 1.000 1 2018 2018
dbSNP: rs843005
rs843005 		4 71750610 intron variant C/A;T snv
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7041
rs7041 		0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.050 1.000 5 2014 2020
dbSNP: rs4588
rs4588 		0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.040 1.000 4 2010 2019
dbSNP: rs4588
rs4588 		0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		Nutritional and Metabolic Diseases 0.040 1.000 4 2015 2018
dbSNP: rs4588
rs4588 		0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.040 1.000 4 2014 2019