EPHA1, EPH receptor A1, 2041

N. diseases: 119; 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: rs10808026
rs10808026
1.000 0.080 7 143402040 intron variant C/A snv 0.19
High density lipoprotein measurement
0.700 1.000 1 2019 2019
dbSNP: rs10808026
rs10808026
1.000 0.080 7 143402040 intron variant C/A snv 0.19
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs3935067
rs3935067
1.000 0.080 7 143407238 intron variant G/C snv 0.27
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs4421280
rs4421280
7 143406124 intron variant G/A snv 0.93
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs4725617
rs4725617
7 143400007 missense variant A/G;T snv 0.93
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs56402156
rs56402156
1.000 0.080 7 143406388 intron variant G/A snv 0.19
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs1298929475
rs1298929475
0.925 0.080 7 143397630 missense variant A/G snv 8.0E-06
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1298929475
rs1298929475
0.925 0.080 7 143397630 missense variant A/G snv 8.0E-06
Amyotrophic Lateral Sclerosis, Familial
Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs202178565
rs202178565
1.000 0.080 7 143398406 missense variant G/A snv 2.1E-04 2.2E-04
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2015 2015