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: rs2011503
rs2011503 		1.000 0.040 19 19333177 intron variant T/C;G snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.800 1.000 1 2014 2014
dbSNP: rs8102280
rs8102280 		19 19344941 non coding transcript exon variant G/A snv 2.8E-02 1.5E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 3 2016 2019
dbSNP: rs73001065
rs73001065 		19 19349732 intron variant G/C snv 4.8E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2015 2018
dbSNP: rs140868651
rs140868651 		19 19321482 intron variant G/- delins 4.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2285627
rs2285627 		19 19357128 3 prime UTR variant T/C;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2285627
rs2285627 		19 19357128 3 prime UTR variant T/C;G snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs2285628
rs2285628 		19 19357187 3 prime UTR variant T/A snv 0.22
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2285628
rs2285628 		19 19357187 3 prime UTR variant T/A snv 0.22
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2285628
rs2285628 		19 19357187 3 prime UTR variant T/A snv 0.22
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2285628
rs2285628 		19 19357187 3 prime UTR variant T/A snv 0.22
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3764567
rs3764567 		1.000 0.040 19 19329257 intron variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs73001065
rs73001065 		19 19349732 intron variant G/C snv 4.8E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs73001065
rs73001065 		19 19349732 intron variant G/C snv 4.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs8102280
rs8102280 		19 19344941 non coding transcript exon variant G/A snv 2.8E-02 1.5E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2019 2019
dbSNP: rs8102280
rs8102280 		19 19344941 non coding transcript exon variant G/A snv 2.8E-02 1.5E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2019 2019