RAP1A, RAP1A, member of RAS oncogene family, 5906

N. diseases: 215; N. variants: 7
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: rs494453
rs494453 		1.000 0.080 1 111649500 non coding transcript exon variant T/C snv 0.41
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.800 1.000 1 2010 2010
dbSNP: rs12038204
rs12038204 		1 111715630 3 prime UTR variant A/G snv 0.36
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2477425
rs2477425 		1 111609980 intron variant T/C snv 0.39
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2477432
rs2477432 		1.000 0.040 1 111642655 intron variant T/A snv 0.52
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2477432
rs2477432 		1.000 0.040 1 111642655 intron variant T/A snv 0.52
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs2789546
rs2789546 		1 111601277 intron variant G/C snv 0.80
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9988442
rs9988442 		1 111554040 intron variant C/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6573
rs6573 		1.000 0.080 1 111712767 3 prime UTR variant C/A snv 0.12
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012