NCAM1, neural cell adhesion molecule 1, 4684

N. diseases: 445; N. variants: 34
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: rs1816537
rs1816537 		11 113097929 intron variant A/C snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs10891483
rs10891483 		11 112967156 intron variant C/G;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018
dbSNP: rs10891499
rs10891499 		11 113053392 intron variant G/A snv 0.43
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs11214475
rs11214475 		11 113073328 intron variant C/A;G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs11214489
rs11214489 		11 113105212 intron variant C/T snv 0.22
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12574893
rs12574893 		1.000 0.040 11 113046389 intron variant C/T snv 0.19
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs12574893
rs12574893 		1.000 0.040 11 113046389 intron variant C/T snv 0.19
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs1273044
rs1273044 		11 113123126 intron variant T/C;G snv 0.70
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1436109
rs1436109 		1.000 0.080 11 113120896 intron variant G/T snv 8.5E-02
CUI: C0011904
Disease: Diagnostic Techniques, Cardiovascular
Diagnostic Techniques, Cardiovascular 		0.700 1.000 1 2011 2011
dbSNP: rs1436109
rs1436109 		1.000 0.080 11 113120896 intron variant G/T snv 8.5E-02
CUI: C0455825
Disease: Left ventricular mass
Left ventricular mass 		0.700 1.000 1 2011 2011
dbSNP: rs1436109
rs1436109 		1.000 0.080 11 113120896 intron variant G/T snv 8.5E-02
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1940700
rs1940700 		11 113032833 intron variant A/T snv 1.3E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1940700
rs1940700 		11 113032833 intron variant A/T snv 1.3E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1940709
rs1940709 		1.000 0.040 11 112978997 intron variant G/A snv 0.30
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs1940709
rs1940709 		1.000 0.040 11 112978997 intron variant G/A snv 0.30
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs1940728
rs1940728 		1.000 0.040 11 112981473 intron variant G/A;T snv 0.44
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs1940728
rs1940728 		1.000 0.040 11 112981473 intron variant G/A;T snv 0.44
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs2155287
rs2155287 		11 112976484 intron variant G/A snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2155292
rs2155292 		11 113040061 intron variant A/G snv 0.45
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2155645
rs2155645 		11 113042225 intron variant C/T snv 0.25
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2288158
rs2288158 		11 113262954 3 prime UTR variant T/G snv 0.15 0.13
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2885208
rs2885208 		11 113094434 intron variant T/C snv 0.20
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs3802850
rs3802850 		11 113041796 intron variant A/C snv 0.45
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4471463
rs4471463 		1.000 11 113112873 intron variant C/T snv 0.57
CUI: C3160814
Disease: Cannabis use
Cannabis use 		0.700 1.000 1 2016 2016
dbSNP: rs4533068
rs4533068 		11 112962896 intron variant G/A snv 0.11
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019