HOXB3, homeobox B3, 3213

N. diseases: 49; N. variants: 5
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: rs9299
rs9299 		1.000 0.080 17 48592068 3 prime UTR variant C/A;T snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.800 1.000 1 2012 2012
dbSNP: rs2288276
rs2288276 		17 48593060 intron variant G/A;C snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9299
rs9299 		1.000 0.080 17 48592068 3 prime UTR variant C/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs9905793
rs9905793 		1.000 0.040 17 48558287 intron variant A/G snv 0.86
CUI: C0011334
Disease: Dental caries
Dental caries 		Stomatognathic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9906289
rs9906289 		1.000 0.040 17 48567315 intron variant C/T snv 5.9E-02
CUI: C0026603
Disease: Motion Sickness
Motion Sickness 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2015 2015
dbSNP: rs3809783
rs3809783 		1.000 0.080 17 48579816 non coding transcript exon variant A/T snv 5.2E-04; 2.9E-02; 5.9E-06; 5.9E-06 1.8E-02
CUI: C0276138
Disease: Viral myocarditis
Viral myocarditis 		Infections; Cardiovascular Diseases 0.010 1.000 1 2015 2015