Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2629540
rs2629540
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0600427
Disease:
Cocaine Dependence
0.810 GeneticVariation BEFREE We evaluated, in a Spanish sample of 1711 subjects with substance dependence (1011 of them cocaine dependent) and 1719 control individuals, three SNPs identified as GWS in previous studies: rs1868152 and rs2952621 (located near LINC02052 and LINC01854, respectively), associated with substance dependence, and rs2629540 (in the first intron of FAM53B), associated with cocaine dependence. 29715653 2018
dbSNP: rs2629540
rs2629540
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0600427
Disease:
Cocaine Dependence
0.810 GeneticVariation GWASCAT Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. 23958962 2014
dbSNP: rs2629540
rs2629540
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0600427
Disease:
Cocaine Dependence
0.810 GeneticVariation GWASDB Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. 23958962 2014
dbSNP: rs11245333
rs11245333
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11245344
rs11245344
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0017654
Disease:
Glomerular Filtration Rate
C 0.700 GeneticVariation GWASCAT Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. 31015462 2019
dbSNP: rs36053385
rs36053385
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0017654
Disease:
Glomerular Filtration Rate
CA 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs3781466
rs3781466
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4962691
rs4962691
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0017654
Disease:
Glomerular Filtration Rate
T 0.700 GeneticVariation GWASCAT Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. 30604766 2019
dbSNP: rs2629540
rs2629540
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0596887
Disease:
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: rs2629540
rs2629540
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0596887
Disease:
mathematical ability
G 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: rs3781452
rs3781452
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C4049090
Disease:
Alopecia, Androgenetic, 1
C 0.700 GeneticVariation GWASCAT GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. 29146897 2017
dbSNP: rs3781452
rs3781452
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C4083212
Disease:
Alopecia, Male Pattern
C 0.700 GeneticVariation GWASCAT GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. 29146897 2017
dbSNP: rs3781452
rs3781452
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0002170
Disease:
Alopecia
T 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs3781452
rs3781452
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0162311
Disease:
Androgenetic Alopecia
C 0.700 GeneticVariation GWASCAT GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. 29146897 2017
dbSNP: rs3781452
rs3781452
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C2676272
Disease:
Alopecia, Androgenetic, 3
C 0.700 GeneticVariation GWASCAT GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. 29146897 2017
dbSNP: rs3781452
rs3781452
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C2678038
Disease:
Alopecia, Androgenetic, 2
C 0.700 GeneticVariation GWASCAT GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. 29146897 2017
dbSNP: rs3781452
rs3781452
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0029489
Disease:
Other alopecia
C 0.700 GeneticVariation GWASCAT GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. 29146897 2017
dbSNP: rs3781458
rs3781458
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0002170
Disease:
Alopecia
T 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs1998418
rs1998418
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0200665
Disease:
Platelet mean volume determination (procedure)
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3781454
rs3781454
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0023508
Disease:
White Blood Cell Count procedure
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3781458
rs3781458
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C4083212
Disease:
Alopecia, Male Pattern
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs3781458
rs3781458
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C4049090
Disease:
Alopecia, Androgenetic, 1
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs3781458
rs3781458
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C0162311
Disease:
Androgenetic Alopecia
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs3781458
rs3781458
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C2678038
Disease:
Alopecia, Androgenetic, 2
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs3781458
rs3781458
Entrez Id: 9679
Gene Symbol: FAM53B
FAM53B
CUI: C2676272
Disease:
Alopecia, Androgenetic, 3
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016