Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7643459
rs7643459
LMCD1-AS1 ; LOC101927394
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer 		T 0.710 GeneticVariation GWASCAT We identified four novel loci with suggestive evidence of association with EOC (p < 1 × 10<sup>-6</sup> ), including rs4525119 (intronic to AKR1C3), rs7643459 (intronic to LOC101927394), rs4286604 (12 kb 3' of UGT2A2) and rs142091544 (5 kb 5' of WWC1). 31469419

2019
dbSNP: rs10510388
rs10510388
LMCD1-AS1
CUI: C0596887
Disease: mathematical ability
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018
dbSNP: rs1157280
rs1157280
LMCD1-AS1 ; LOC101927394
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs13317787
rs13317787
LMCD1-AS1
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of acute kidney injury after coronary bypass graft surgery identifies susceptibility loci. 26083657

2015
dbSNP: rs1485149
rs1485149
LMCD1-AS1 ; LOC101927394
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs1485149
rs1485149
LMCD1-AS1 ; LOC101927394
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs1554194
rs1554194
LMCD1-AS1
CUI: C1305855
Disease: Body mass index
Body mass index 		C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722

2019
dbSNP: rs17048879
rs17048879
LMCD1-AS1
CUI: C0596887
Disease: mathematical ability
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018
dbSNP: rs171408
rs171408
LMCD1 ; LMCD1-AS1
CUI: C0026267
Disease: Mitral Valve Prolapse Syndrome
Mitral Valve Prolapse Syndrome 		G 0.700 GeneticVariation GWASCAT Genetic association analyses highlight biological pathways underlying mitral valve prolapse. 26301497

2015
dbSNP: rs1994876
rs1994876
LMCD1 ; LMCD1-AS1
CUI: C0005890
Disease: Body Height
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs35144233
rs35144233
LMCD1-AS1 ; LOC101927394
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of familial lung cancer. 29924316

2018
dbSNP: rs359027
rs359027
LMCD1-AS1
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		G 0.700 GeneticVariation GWASCAT A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs. 26879886

2016
dbSNP: rs388458
rs388458
LMCD1-AS1
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566

2018
dbSNP: rs4349489
rs4349489
LMCD1 ; LMCD1-AS1
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs4686203
rs4686203
LMCD1-AS1 ; LOC101927394
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs4686205
rs4686205
LMCD1-AS1 ; LOC101927394
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs543719221
rs543719221
LMCD1-AS1
CUI: C0005890
Disease: Body Height
Body Height 		A 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017
dbSNP: rs6777332
rs6777332
LMCD1-AS1
CUI: C0596887
Disease: mathematical ability
mathematical ability 		C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018
dbSNP: rs7624284
rs7624284
LMCD1-AS1 ; LOC101927394
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs7624374
rs7624374
LMCD1-AS1 ; LOC101927394
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs9816551
rs9816551
LMCD1-AS1
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of familial lung cancer. 29924316

2018
dbSNP: rs9846963
rs9846963
LMCD1-AS1 ; LOC101927394
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs9847133
rs9847133
LMCD1-AS1
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of type 2 diabetes in Africa. 31049640

2019
dbSNP: rs9862842
rs9862842
LMCD1-AS1
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs9872473
rs9872473
LMCD1-AS1 ; LOC101927394
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017