CFL1, cofilin 1, 1072

N. diseases: 153; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17854357
rs17854357
Entrez Id: 1072;254122
Gene Symbol: CFL1;SNX32
CFL1;SNX32
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7102454
rs7102454
Entrez Id: 1072
Gene Symbol: CFL1
CFL1
CUI: C0005612
Disease:
Birth Weight 		C 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs118086960
rs118086960
Entrez Id: 1072
Gene Symbol: CFL1
CFL1
CUI: C0033860
Disease:
Psoriasis 		T 0.700 GeneticVariation GWASCAT Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants. 28537254 2017
dbSNP: rs11227332
rs11227332
Entrez Id: 1072;254122
Gene Symbol: CFL1;SNX32
CFL1;SNX32
CUI: C0080178
Disease:
Spina Bifida 		0.010 GeneticVariation BEFREE Homozygosity for the minor alleles of the SNPs studied (rs652021, rs665306, rs667555, rs4621 and rs11227332) appeared to produce an increased risk for spina bifida. 17352815 2007
dbSNP: rs4621
rs4621
Entrez Id: 1072;254122
Gene Symbol: CFL1;SNX32
CFL1;SNX32
CUI: C0080178
Disease:
Spina Bifida 		0.010 GeneticVariation BEFREE Homozygosity for the minor alleles of the SNPs studied (rs652021, rs665306, rs667555, rs4621 and rs11227332) appeared to produce an increased risk for spina bifida. 17352815 2007
dbSNP: rs667555
rs667555
Entrez Id: 1072
Gene Symbol: CFL1
CFL1
CUI: C0080178
Disease:
Spina Bifida 		0.010 GeneticVariation BEFREE Homozygosity for the minor alleles of the SNPs studied (rs652021, rs665306, rs667555, rs4621 and rs11227332) appeared to produce an increased risk for spina bifida. 17352815 2007