NCALD, neurocalcin delta, 83988

N. diseases: 18; N. variants: 4
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: rs1074703
rs1074703 		8 101803258 intron variant C/A snv 0.63
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs12544026
rs12544026 		0.925 0.080 8 101819970 intron variant G/A snv 0.85
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs12544026
rs12544026 		0.925 0.080 8 101819970 intron variant G/A snv 0.85
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		Chemically-Induced Disorders 0.700 1.000 1 2017 2017
dbSNP: rs12544026
rs12544026 		0.925 0.080 8 101819970 intron variant G/A snv 0.85
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs12544026
rs12544026 		0.925 0.080 8 101819970 intron variant G/A snv 0.85
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs142449193
rs142449193 		8 101738369 intron variant C/T snv 6.9E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs636089
rs636089 		8 102065562 intron variant T/C snv 0.28
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs636089
rs636089 		8 102065562 intron variant T/C snv 0.28
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019