PMF1-BGLAP, PMF1-BGLAP readthrough, 100527963

N. diseases: 9; N. variants: 33
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: rs2853646
rs2853646 		1 156219835 intron variant C/T 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: rs3001789
rs3001789 		1 156227823 intron variant T/G snv 0.37
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: rs6427307
rs6427307 		1 156220292 intron variant A/G;T 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: rs7534434
rs7534434 		1 156216824 intron variant A/G;T 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: rs887953
rs887953 		1 156221358 intron variant T/C snv 0.36
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2014 2014