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: rs769449
rs769449
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2012 2019
dbSNP: rs769449
rs769449
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 2 2008 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: 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: rs769449
rs769449
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs769449
rs769449
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
High density lipoprotein measurement
0.700 1.000 2 2018 2019
dbSNP: rs769449
rs769449
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
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: rs769449
rs769449
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
CUI: C1285654
Disease: Memory performance
Memory performance
0.700 1.000 1 2017 2017
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: C0338656
Disease: Impaired cognition
Impaired cognition
0.010 1.000 1 2014 2014