PKN2, protein kinase N2, 5586

N. diseases: 29; N. variants: 7
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: rs10801682
rs10801682 		1 88708570 intron variant A/T snv 0.50
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs305221
rs305221 		1.000 0.040 1 88733302 intron variant G/A snv 0.59
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs305221
rs305221 		1.000 0.040 1 88733302 intron variant G/A snv 0.59
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs35424856
rs35424856 		1 88723411 intron variant CC/-;C;CCC;CCCC;CCCCC;CCCCCC;CCCCCCC delins
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs786906
rs786906 		1 88805891 splice region variant T/C snv 0.56 0.51
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs786906
rs786906 		1 88805891 splice region variant T/C snv 0.56 0.51
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs786914
rs786914 		1 88830082 intron variant C/A;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs786919
rs786919 		1 88815846 intron variant A/G snv 0.58
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs305217
rs305217 		1.000 0.080 1 88754789 intron variant G/A snv 8.6E-02
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs305217
rs305217 		1.000 0.080 1 88754789 intron variant G/A snv 8.6E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 < 0.001 1 2012 2012