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: rs10044254
rs10044254
0.925 0.080 5 15783487 intron variant A/G snv 0.25
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs12659622
rs12659622
5 15618072 intron variant G/A snv 8.3E-02
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
0.700 1.000 1 2012 2012
dbSNP: rs12659622
rs12659622
5 15618072 intron variant G/A snv 8.3E-02
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs147776718
rs147776718
1.000 0.040 5 15826358 intron variant G/A;T snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.700 1.000 1 2015 2015
dbSNP: rs147776718
rs147776718
1.000 0.040 5 15826358 intron variant G/A;T snv
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
0.700 1.000 1 2015 2015
dbSNP: rs16867528
rs16867528
1.000 0.080 5 15607339 non coding transcript exon variant C/T snv 2.8E-02
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs75002042
rs75002042
1.000 0.080 5 15669858 intron variant T/A snv 7.7E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs76684306
rs76684306
1.000 0.080 5 15616567 intron variant A/G snv 4.5E-02
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs7721607
rs7721607
1.000 5 15652449 intron variant G/A snv 0.17
Adverse effects, not elsewhere classified
0.700 1.000 1 2019 2019
dbSNP: rs80333777
rs80333777
1.000 0.080 5 15524361 intron variant G/A;C;T snv
CUI: C3894553
Disease: response to simvastatin
response to simvastatin
0.700 1.000 1 2018 2018
dbSNP: rs80333777
rs80333777
1.000 0.080 5 15524361 intron variant G/A;C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs10044254
rs10044254
0.925 0.080 5 15783487 intron variant A/G snv 0.25
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs983889
rs983889
5 15555377 intron variant G/T snv 0.55
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities 0.010 1.000 1 2019 2019