EVL, Enah/Vasp-like, 51466

N. diseases: 23; N. variants: 7
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: rs10148930
rs10148930
14 100134466 intron variant A/G;T snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs11621315
rs11621315
14 100060318 intron variant C/T snv 0.61
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs12588659
rs12588659
14 100121476 intron variant C/A snv 6.6E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
Behavior and Behavior Mechanisms 0.700 1.000 1 2010 2010
dbSNP: rs7158754
rs7158754
14 100117012 intron variant A/G snv 0.81
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs367737727
rs367737727
1.000 0.080 14 100128600 missense variant C/T snv 1.1E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs1190983
rs1190983
0.925 0.080 14 100031649 intron variant T/C snv 0.61
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1190983
rs1190983
0.925 0.080 14 100031649 intron variant T/C snv 0.61
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs941898
rs941898
1.000 0.040 14 100133100 intron variant G/T snv 0.81
CUI: C1456784
Disease: Paranoia
Paranoia
Mental Disorders 0.010 1.000 1 2011 2011