Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs75154329
rs75154329
Entrez Id: 64762
Gene Symbol: GAREM1
GAREM1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8093507
rs8093507
Entrez Id: 64762
Gene Symbol: GAREM1
GAREM1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs117618124
rs117618124
Entrez Id: 64762
Gene Symbol: GAREM1
GAREM1
CUI: C0678222
Disease:
Breast Carcinoma 		T 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs11081761
rs11081761
Entrez Id: 64762
Gene Symbol: GAREM1
GAREM1
CUI: C1821417
Disease:
RESTING HEART RATE 		A 0.700 GeneticVariation GWASCAT Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality. 27798624 2016
dbSNP: rs17744182
rs17744182
Entrez Id: 64762
Gene Symbol: GAREM1
GAREM1
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		A 0.700 GeneticVariation GWASCAT Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians. 25035420 2014
dbSNP: rs554521234
rs554521234
Entrez Id: 64762
Gene Symbol: GAREM1
GAREM1
CUI: C0264694
Disease:
Chronic myocardial ischemia 		0.010 GeneticVariation BEFREE These included signs related to both ATTRm and ATTRwt such as chronic ischaemic heart disease (rs140226130, p = 2.00 × 10<sup>-6</sup>), heart failure (rs73956431, p = 2.74 × 10<sup>-6</sup>), atrial fibrillation (rs10163755, p = 4.63 × 10<sup>-6</sup>), dysphagia (rs2949506, p = 3.95 × 10<sup>-6</sup>), intestine diseases (rs970866, p = 7.14 × 10<sup>-6</sup>) and anxiety (rs554521234, p = 8.85 × 10<sup>-6</sup>). 31659433 2019
dbSNP: rs554521234
rs554521234
Entrez Id: 64762
Gene Symbol: GAREM1
GAREM1
CUI: C0268407
Disease:
Senile cardiac amyloidosis 		0.010 GeneticVariation BEFREE These included signs related to both ATTRm and ATTRwt such as chronic ischaemic heart disease (rs140226130, p = 2.00 × 10<sup>-6</sup>), heart failure (rs73956431, p = 2.74 × 10<sup>-6</sup>), atrial fibrillation (rs10163755, p = 4.63 × 10<sup>-6</sup>), dysphagia (rs2949506, p = 3.95 × 10<sup>-6</sup>), intestine diseases (rs970866, p = 7.14 × 10<sup>-6</sup>) and anxiety (rs554521234, p = 8.85 × 10<sup>-6</sup>). 31659433 2019
dbSNP: rs554521234
rs554521234
Entrez Id: 64762
Gene Symbol: GAREM1
GAREM1
CUI: C2751492
Disease:
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED 		0.010 GeneticVariation BEFREE These included signs related to both ATTRm and ATTRwt such as chronic ischaemic heart disease (rs140226130, p = 2.00 × 10<sup>-6</sup>), heart failure (rs73956431, p = 2.74 × 10<sup>-6</sup>), atrial fibrillation (rs10163755, p = 4.63 × 10<sup>-6</sup>), dysphagia (rs2949506, p = 3.95 × 10<sup>-6</sup>), intestine diseases (rs970866, p = 7.14 × 10<sup>-6</sup>) and anxiety (rs554521234, p = 8.85 × 10<sup>-6</sup>). 31659433 2019
dbSNP: rs554521234
rs554521234
Entrez Id: 64762
Gene Symbol: GAREM1
GAREM1
CUI: C0002726
Disease:
Amyloidosis 		0.010 GeneticVariation BEFREE These included signs related to both ATTRm and ATTRwt such as chronic ischaemic heart disease (rs140226130, p = 2.00 × 10<sup>-6</sup>), heart failure (rs73956431, p = 2.74 × 10<sup>-6</sup>), atrial fibrillation (rs10163755, p = 4.63 × 10<sup>-6</sup>), dysphagia (rs2949506, p = 3.95 × 10<sup>-6</sup>), intestine diseases (rs970866, p = 7.14 × 10<sup>-6</sup>) and anxiety (rs554521234, p = 8.85 × 10<sup>-6</sup>). 31659433 2019