LNX1, ligand of numb-protein X 1, 84708

N. diseases: 17; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12507563
rs12507563
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs62323682
rs62323682
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C2242776
Disease:
Plexiform leiomyoma 		T 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs62323682
rs62323682
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C0042133
Disease:
Uterine Fibroids 		T 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs745398820
rs745398820
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C0042133
Disease:
Uterine Fibroids 		G 0.700 GeneticVariation GWASCAT Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. 30194396 2018
dbSNP: rs745398820
rs745398820
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C2242776
Disease:
Plexiform leiomyoma 		G 0.700 GeneticVariation GWASCAT Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. 30194396 2018
dbSNP: rs1002824
rs1002824
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C0023467
Disease:
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: rs12650358
rs12650358
Entrez Id: 84708;101928879
Gene Symbol: LNX1;LOC101928879
LNX1;LOC101928879
CUI: C0023467
Disease:
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: rs4864471
rs4864471
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C0023467
Disease:
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: rs4864471
rs4864471
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C0023467
Disease:
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: rs6826933
rs6826933
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C0023467
Disease:
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: rs6844977
rs6844977
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C0023467
Disease:
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: rs7685317
rs7685317
Entrez Id: 84708
Gene Symbol: LNX1
LNX1
CUI: C0023467
Disease:
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