SCARB1, scavenger receptor class B member 1, 949

N. diseases: 116; N. variants: 34
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: rs57276302
rs57276302
12 124879441 intron variant C/A;T snv
High density lipoprotein measurement
0.700 1.000 1 2019 2019
dbSNP: rs57276302
rs57276302
12 124879441 intron variant C/A;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs61005347
rs61005347
12 124841232 intron variant C/T snv 2.2E-02
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs67053123
rs67053123
12 124869264 intron variant T/A snv 0.11
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs67053123
rs67053123
12 124869264 intron variant T/A snv 0.11
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs7137923
rs7137923
12 124822302 intron variant G/T snv 3.1E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs7137923
rs7137923
12 124822302 intron variant G/T snv 3.1E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs7485656
rs7485656
12 124831101 intron variant A/G snv 0.26
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs7485656
rs7485656
12 124831101 intron variant A/G snv 0.26
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs78194510
rs78194510
1.000 0.080 12 124853790 intron variant T/C snv 8.2E-02
High density lipoprotein measurement
0.700 1.000 1 2019 2019
dbSNP: rs78194510
rs78194510
1.000 0.080 12 124853790 intron variant T/C snv 8.2E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs838880
rs838880
12 124777047 3 prime UTR variant C/T snv 0.55
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs838886
rs838886
12 124779741 intron variant T/A;G snv
High density lipoprotein measurement
0.700 1.000 1 2015 2015
dbSNP: rs865716
rs865716
12 124806310 intron variant A/T snv 0.58
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs865716
rs865716
12 124806310 intron variant A/T snv 0.58
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs187831231
rs187831231
12 124814309 missense variant T/C snv 1.1E-04 2.0E-04
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6
0.700 0
dbSNP: rs387906791
rs387906791
12 124807881 missense variant G/A snv 8.0E-06 6.3E-05
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6
0.700 0
dbSNP: rs397514572
rs397514572
12 124815064 missense variant G/A snv
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6
0.700 0
dbSNP: rs74830677
rs74830677
0.882 0.080 12 124800125 missense variant G/A snv 9.9E-04 6.7E-04
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6
0.700 0
dbSNP: rs10846744
rs10846744
0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.040 0.750 4 2010 2018
dbSNP: rs10846744
rs10846744
0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.040 0.750 4 2010 2018
dbSNP: rs10846744
rs10846744
0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C3266262
Disease: Multiple Chronic Conditions
Multiple Chronic Conditions
Pathological Conditions, Signs and Symptoms 0.030 1.000 3 2010 2018
dbSNP: rs5888
rs5888
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.030 1.000 3 2013 2018
dbSNP: rs5888
rs5888
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.030 0.333 3 2013 2018
dbSNP: rs10846744
rs10846744
0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.020 1.000 2 2017 2018