EPHA5, EPH receptor A5, 2044

N. diseases: 61; N. variants: 9
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: rs1057520012
rs1057520012 		1.000 0.040 4 65404419 missense variant C/T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.800 1.000 1 2005 2005
dbSNP: rs11735820
rs11735820 		1.000 0.080 4 65633298 intron variant T/G snv 0.33
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs13145146
rs13145146 		1.000 0.040 4 65564907 intron variant A/G snv 4.3E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs13145146
rs13145146 		1.000 0.040 4 65564907 intron variant A/G snv 4.3E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs28535294
rs28535294 		4 65604825 intron variant G/A snv 0.31
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs60178806
rs60178806 		4 65615276 intron variant T/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7659227
rs7659227 		1.000 0.080 4 65630452 intron variant A/G snv 0.34
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7659227
rs7659227 		1.000 0.080 4 65630452 intron variant A/G snv 0.34
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs7692430
rs7692430 		0.790 0.080 4 65354979 intron variant T/C snv 0.16
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2018 2018
dbSNP: rs7692430
rs7692430 		0.790 0.080 4 65354979 intron variant T/C snv 0.16
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs7692430
rs7692430 		0.790 0.080 4 65354979 intron variant T/C snv 0.16
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs7692430
rs7692430 		0.790 0.080 4 65354979 intron variant T/C snv 0.16
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs7692430
rs7692430 		0.790 0.080 4 65354979 intron variant T/C snv 0.16
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs7692430
rs7692430 		0.790 0.080 4 65354979 intron variant T/C snv 0.16
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2018 2018
dbSNP: rs7692430
rs7692430 		0.790 0.080 4 65354979 intron variant T/C snv 0.16
CUI: C0037274
Disease: Dermatologic disorders
Dermatologic disorders 		Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7692430
rs7692430 		0.790 0.080 4 65354979 intron variant T/C snv 0.16
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs7692430
rs7692430 		0.790 0.080 4 65354979 intron variant T/C snv 0.16
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2018 2018
dbSNP: rs7692430
rs7692430 		0.790 0.080 4 65354979 intron variant T/C snv 0.16
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs199614818
rs199614818 		1.000 0.040 4 65490529 missense variant C/A;T snv 4.0E-06; 2.4E-05
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.700 0
dbSNP: rs7349683
rs7349683 		0.925 0.080 4 65332086 synonymous variant C/A;T snv 0.35
CUI: C0442874
Disease: Neuropathy
Neuropathy 		Nervous System Diseases 0.020 1.000 2 2013 2019
dbSNP: rs7349683
rs7349683 		0.925 0.080 4 65332086 synonymous variant C/A;T snv 0.35
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs7349683
rs7349683 		0.925 0.080 4 65332086 synonymous variant C/A;T snv 0.35
CUI: C3873567
Disease: Peripheral neuropathy due to and following chemotherapy
Peripheral neuropathy due to and following chemotherapy 		Nervous System Diseases 0.010 1.000 1 2019 2019