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: rs6584555
rs6584555 		1.000 0.080 10 103539854 intron variant T/C snv 0.27
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.740 0.800 5 2016 2019
dbSNP: rs11598047
rs11598047 		1.000 0.080 10 103582915 non coding transcript exon variant A/G snv 0.16
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 3 2017 2018
dbSNP: rs60572254
rs60572254 		1.000 0.080 10 103565017 intron variant C/T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 2 2017 2018
dbSNP: rs11191732
rs11191732 		1.000 0.040 10 103572004 intron variant G/A snv 0.14
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs11597473
rs11597473 		1.000 0.040 10 103559284 intron variant G/C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs55693294
rs55693294 		1.000 0.080 10 103517717 intron variant C/T snv 4.7E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs60848348
rs60848348 		1.000 0.080 10 103562124 intron variant C/T snv 0.20
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs7071247
rs7071247 		10 103498029 intron variant G/T snv 0.18
CUI: C0032176
Disease: Platelet aggregation
Platelet aggregation 		0.700 1.000 1 2010 2010
dbSNP: rs72848971
rs72848971 		10 103545244 intron variant G/T snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs74154533
rs74154533 		1.000 10 103547967 intron variant G/A snv 0.17
CUI: C1531624
Disease: Cardioembolic stroke
Cardioembolic stroke 		0.700 1.000 1 2018 2018