rs121912724
|
|
Amyloidosis, familial visceral
|
C |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
rs387906571
|
|
AMYLOIDOSIS, CARDIAC AND CUTANEOUS
|
G |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs28931575
|
|
AMYLOIDOSIS, CARDIAC AND CUTANEOUS
|
G |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs28931574
|
|
Amyloid Polyneuropathy, Iowa Type
|
G |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs28931573
|
|
APOLIPOPROTEIN A-I (MILANO) PHENOTYPE
|
A |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs28929476
|
|
APOLIPOPROTEIN A-I (BALTIMORE) PHENOTYPE
|
A |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912730
|
|
Amyloidosis, familial visceral
|
G |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912729
|
|
Amyloidosis, familial visceral
|
G |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912726
|
|
Amyloidosis, familial visceral
|
G |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912721
|
|
APOLIPOPROTEIN A-I (MUNSTER3B) PHENOTYPE
|
C |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912720
|
|
APOLIPOPROTEIN A-I (MUNSTER3C) PHENOTYPE
|
C |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912719
|
|
APOLIPOPROTEIN A-I (GIESSEN) PHENOTYPE
|
C |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912718
|
|
APOLIPOPROTEIN A-I (NORWAY) PHENOTYPE
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912717
|
|
APOLIPOPROTEIN A-I (MUNSTER4) PHENOTYPE
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912716
|
|
APOLIPOPROTEIN A-I (MARBURG) PHENOTYPE
|
A |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs12721025
|
|
Pyloric Stenosis, Hypertrophic
|
A |
0.800 |
GeneticVariation
|
GWASCAT |
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis.
|
30281099 |
2019 |
rs12721025
|
|
Pyloric Stenosis, Hypertrophic
|
A |
0.800 |
GeneticVariation
|
GWASCAT |
Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis.
|
23989729 |
2013 |
rs7116797
|
|
Systolic Pressure
|
A |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.
|
27841878 |
2017 |
rs7116797
|
|
Diastolic blood pressure
|
A |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.
|
27841878 |
2017 |
rs670
|
|
Blood Protein Measurement
|
T |
0.700 |
GeneticVariation
|
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |
rs12718465
|
|
High density lipoprotein measurement
|
|
0.700 |
GeneticVariation
|
GWASCAT |
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
|
29403010 |
2018 |
rs12721025
|
|
Pyloric Stenosis, Hypertrophic
|
A |
0.800 |
GeneticVariation
|
GWASDB |
Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis.
|
23989729 |
2013 |
rs5072
|
|
Serum albumin measurement
|
|
0.700 |
GeneticVariation
|
GWASDB |
Genome-wide association study identifies multiple loci influencing human serum metabolite levels.
|
22286219 |
2012 |
rs5072
|
|
Serum total cholesterol measurement
|
|
0.700 |
GeneticVariation
|
GWASDB |
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.
|
23063622 |
2012 |
rs5072
|
|
Triglycerides measurement
|
|
0.700 |
GeneticVariation
|
GWASDB |
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.
|
23063622 |
2012 |