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: rs4909945
rs4909945 		11 10652192 missense variant T/A;C snv 0.76
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.800 1.000 1 2013 2013
dbSNP: rs4910165
rs4910165 		11 10652497 intron variant C/G snv 0.78
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.700 1.000 2 2016 2016
dbSNP: rs11042906
rs11042906 		11 10643688 intron variant C/T snv 0.20
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs114527818
rs114527818 		11 10597494 intron variant T/A snv 4.4E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2052690
rs2052690 		0.925 0.080 11 10642486 intron variant G/T snv 0.22
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2052690
rs2052690 		0.925 0.080 11 10642486 intron variant G/T snv 0.22
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4909945
rs4909945 		11 10652192 missense variant T/A;C snv 0.76
CUI: C0018681
Disease: Headache
Headache 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2018 2018
dbSNP: rs4910165
rs4910165 		11 10652497 intron variant C/G snv 0.78
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs6484437
rs6484437 		11 10645728 intron variant A/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs719152
rs719152 		11 10686942 intron variant C/G snv 0.24
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs7936275
rs7936275 		1.000 0.080 11 10639293 intron variant G/T snv 0.24
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs7940646
rs7940646 		11 10647681 intron variant T/A;C;G snv
CUI: C0032176
Disease: Platelet aggregation
Platelet aggregation 		0.700 1.000 1 2010 2010
dbSNP: rs35857561
rs35857561 		0.925 0.160 11 10628820 missense variant G/A snv 5.6E-02 5.0E-02
CUI: C0026654
Disease: Moyamoya Disease
Moyamoya Disease 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs35857561
rs35857561 		0.925 0.160 11 10628820 missense variant G/A snv 5.6E-02 5.0E-02
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases 0.010 1.000 1 2018 2018