Source: ALL

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: rs115299243
rs115299243
19 44907291 non coding transcript exon variant A/G snv 7.1E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
dbSNP: rs142480126
rs142480126
19 44907825 missense variant G/A snv 8.0E-06
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.020 1.000 2 2009 2009
dbSNP: rs11542035
rs11542035
19 44908706 missense variant G/A snv 1.9E-05 2.8E-05
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 1.000 1 1995 1995
dbSNP: rs121918395
rs121918395
19 44909032 missense variant C/A;T snv 6.9E-06; 4.2E-05
CUI: C4015869
Disease: APOE2-DUNEDIN PHENOTYPE
APOE2-DUNEDIN PHENOTYPE
0.700 0
dbSNP: rs121918398
rs121918398
19 44909171 missense variant G/A snv 4.5E-06
CUI: C4015878
Disease: APOE4 VARIANT PHENOTYPE
APOE4 VARIANT PHENOTYPE
0.700 0
dbSNP: rs200703101
rs200703101
19 44908757 missense variant G/C;T snv
CUI: C4025650
Disease: Abnormality of lipid metabolism
Abnormality of lipid metabolism
0.700 0
dbSNP: rs28931576
rs28931576
19 44907894 missense variant A/G snv 1.2E-05 1.4E-05
CUI: C4015877
Disease: APOE3(-)-FREIBURG PHENOTYPE
APOE3(-)-FREIBURG PHENOTYPE
0.700 0
dbSNP: rs28931578
rs28931578
19 44908751 missense variant G/A;C;T snv 3.2E-05
CUI: C4015880
Disease: APOE2 VARIANT PHENOTYPE
APOE2 VARIANT PHENOTYPE
0.700 0
dbSNP: rs28931579
rs28931579
19 44909236 missense variant A/C snv 9.5E-05 6.3E-05
CUI: C4015881
Disease: APOE4(+) PHENOTYPE
APOE4(+) PHENOTYPE
0.700 0
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.890 0.933 15 2005 2019
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0750901
Disease: Alzheimer Disease, Early Onset
Alzheimer Disease, Early Onset
0.700 1.000 8 1997 2016
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
0.040 0.750 4 1994 2019
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
High density lipoprotein measurement
0.700 1.000 4 2015 2018
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.040 0.750 4 1993 2004
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.030 1.000 3 2001 2018
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.730 1.000 3 1988 1994
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease
0.700 1.000 3 2014 2019
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0497327
Disease: Dementia
Dementia
0.030 1.000 3 2001 2018
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.720 1.000 3 2006 2018
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.030 1.000 3 2006 2019
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.020 0.500 2 2011 2014
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2018 2018
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2018
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 2 2019 2019
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 1.000 2 2017 2019