Source: CURATED

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: rs769449
rs769449
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2012 2012
dbSNP: rs769449
rs769449
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs769450
rs769450
0.925 0.120 19 44907187 non coding transcript exon variant G/A snv 0.39
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs769452
rs769452
0.925 0.160 19 44907853 missense variant T/C snv 2.5E-03 1.9E-03
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
Hyperlipoproteinemia Type IIa
0.700 1.000 3 2013 2016
dbSNP: rs769455
rs769455
0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
Hyperlipoproteinemia Type IIa
0.700 1.000 3 2013 2016
dbSNP: rs7259620
rs7259620
0.925 0.120 19 44904531 upstream gene variant G/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 2 2013 2019
dbSNP: rs769449
rs769449
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 2 2013 2019
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
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: rs769455
rs769455
0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
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: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.710 1.000 1 2014 2019
dbSNP: rs769449
rs769449
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
0.710 1.000 1 2014 2014
dbSNP: rs769455
rs769455
0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2014 2014
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: rs7412
rs7412
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02
Red cell distribution width determination
0.700 1.000 2 2016 2019
dbSNP: rs7412
rs7412
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02
RDW - Red blood cell distribution width result
0.700 1.000 2 2016 2019
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C2237660
Disease: exudative macular degeneration
exudative macular degeneration
0.700 1.000 1 2016 2016
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
Exudative age-related macular degeneration
0.700 1.000 1 2016 2016
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
RDW - Red blood cell distribution width result
0.700 1.000 1 2016 2016
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy
0.700 1.000 1 2016 2016
dbSNP: rs7412
rs7412
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.710 1.000 1 2016 2019
dbSNP: rs7412
rs7412
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs7412
rs7412
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02
High density lipoprotein measurement
0.700 1.000 4 2017 2019