TNK2, tyrosine kinase non receptor 2, 10188

N. diseases: 59; N. variants: 6
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: rs114951929
rs114951929 		3 195864852 intron variant G/A snv 5.6E-02
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs114951929
rs114951929 		3 195864852 intron variant G/A snv 5.6E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs112384084
rs112384084 		1.000 0.040 3 195867623 missense variant C/T snv 1.4E-02 1.1E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 0
dbSNP: rs113498671
rs113498671 		1.000 0.040 3 195884972 missense variant C/T snv 8.0E-06
CUI: C1335167
Disease: Ovarian Mucinous Adenocarcinoma
Ovarian Mucinous Adenocarcinoma 		Neoplasms 0.700 0
dbSNP: rs970946035
rs970946035 		1.000 0.120 3 195878571 missense variant C/T snv 1.4E-05
CUI: C0346163
Disease: Endometrioid carcinoma ovary
Endometrioid carcinoma ovary 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 0
dbSNP: rs201768983
rs201768983 		0.925 0.080 3 195868640 missense variant C/T snv 1.2E-04 3.5E-05
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2014 2014
dbSNP: rs201768983
rs201768983 		0.925 0.080 3 195868640 missense variant C/T snv 1.2E-04 3.5E-05
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2014 2014
dbSNP: rs2278034
rs2278034 		1.000 0.080 3 195870036 3 prime UTR variant T/C;G snv 0.44; 2.7E-05
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2011 2011
dbSNP: rs970946035
rs970946035 		1.000 0.120 3 195878571 missense variant C/T snv 1.4E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs970946035
rs970946035 		1.000 0.120 3 195878571 missense variant C/T snv 1.4E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2010 2010