Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1816537
rs1816537
NCAM1
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
NCAM1
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
NCAM1
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
NCAM1
11 113073328 intron variant C/A;G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs11214489
rs11214489
NCAM1
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
NCAM1
1.000 0.040 11 113046389 intron variant C/T snv 0.19
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs12574893
rs12574893
NCAM1
1.000 0.040 11 113046389 intron variant C/T snv 0.19
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs1273044
rs1273044
NCAM1
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
NCAM1
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
NCAM1
1.000 0.080 11 113120896 intron variant G/T snv 8.5E-02
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy 		0.700 1.000 1 2011 2011
dbSNP: rs1940709
rs1940709
NCAM1
1.000 0.040 11 112978997 intron variant G/A snv 0.30
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs1940709
rs1940709
NCAM1
1.000 0.040 11 112978997 intron variant G/A snv 0.30
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs1940728
rs1940728
NCAM1
1.000 0.040 11 112981473 intron variant G/A;T snv 0.44
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs1940728
rs1940728
NCAM1
1.000 0.040 11 112981473 intron variant G/A;T snv 0.44
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs2155292
rs2155292
NCAM1
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
NCAM1
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
NCAM1
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
NCAM1
11 113094434 intron variant T/C snv 0.20
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs3802850
rs3802850
NCAM1
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
NCAM1
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
NCAM1 ; LOC101928847
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
dbSNP: rs5794844
rs5794844
NCAM1
11 113089378 intron variant TT/-;T;TTT delins 0.54
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs61902492
rs61902492
NCAM1
11 113121199 intron variant A/G;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs668204
rs668204
NCAM1
1.000 0.040 11 113278920 intron variant T/C snv 0.93
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs7111153
rs7111153
NCAM1 ; LOC101928847
11 112963431 non coding transcript exon variant T/A;C snv 0.47
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018