Disease: Cerebral Hemorrhage ×
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: rs2072499
rs2072499 		1.000 0.120 1 156199819 non coding transcript exon variant A/G snv 0.34 0.43
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2241107
rs2241107 		1.000 0.040 1 156212919 upstream gene variant T/C;G snv
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2241108
rs2241108 		1 156211216 3 prime UTR variant C/G snv 0.43
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2253677
rs2253677 		1.000 0.040 1 156201505 intron variant C/G snv 0.42
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2253809
rs2253809 		1 156202334 intron variant T/C;G snv 0.43
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2266514
rs2266514 		1 156203894 intron variant T/C snv 0.42
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2540183
rs2540183 		1 156195094 intron variant C/G snv 0.30
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2736605
rs2736605 		1 156204684 intron variant T/C snv 0.42
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2758619
rs2758619 		1 156192768 upstream gene variant A/G snv 0.42
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2842857
rs2842857 		1 156198945 non coding transcript exon variant T/C snv 0.43
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2842882
rs2842882 		1 156195551 intron variant T/A;G snv
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2853641
rs2853641 		1.000 0.040 1 156211979 3 prime UTR variant A/G snv 0.43
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2984615
rs2984615 		1 156195526 intron variant G/C snv 0.42
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014
dbSNP: rs3001790
rs3001790 		1 156195499 intron variant T/G snv 0.42
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014