KLF2, Kruppel like factor 2, 10365

N. diseases: 132; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11086029
rs11086029
Entrez Id: 10365
Gene Symbol: KLF2
KLF2
CUI: C0026764
Disease:
Multiple Myeloma 		T 0.700 GeneticVariation GWASCAT Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. 30213928 2018
dbSNP: rs3745318
rs3745318
Entrez Id: 10365
Gene Symbol: KLF2
KLF2
CUI: C0428883
Disease:
Diastolic blood pressure 		T 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs1392080411
rs1392080411
Entrez Id: 10365
Gene Symbol: KLF2
KLF2
CUI: C0024301
Disease:
Lymphoma, Follicular 		0.010 GeneticVariation BEFREE The recent surge in next generation sequencing (NGS) technology has shed more light on the genetic landscape of SBCLs through characterization of numerous driver mutations including SF3B1 and NOTCH1 in CLL, ATM and CCND1 in MCL, KMT2D and EPHA7 in FL, MYD88 (L265P) in LPL, KLF2 and NOTCH2 in splenic MZL (SMZL) and BRAF (V600E) in HCL. 27121112 2016
dbSNP: rs1392080411
rs1392080411
Entrez Id: 10365
Gene Symbol: KLF2
KLF2
CUI: C0024419
Disease:
Waldenstrom Macroglobulinemia 		0.010 GeneticVariation BEFREE The recent surge in next generation sequencing (NGS) technology has shed more light on the genetic landscape of SBCLs through characterization of numerous driver mutations including SF3B1 and NOTCH1 in CLL, ATM and CCND1 in MCL, KMT2D and EPHA7 in FL, MYD88 (L265P) in LPL, KLF2 and NOTCH2 in splenic MZL (SMZL) and BRAF (V600E) in HCL. 27121112 2016
dbSNP: rs1392080411
rs1392080411
Entrez Id: 10365
Gene Symbol: KLF2
KLF2
CUI: C0023443
Disease:
Hairy Cell Leukemia 		0.010 GeneticVariation BEFREE The recent surge in next generation sequencing (NGS) technology has shed more light on the genetic landscape of SBCLs through characterization of numerous driver mutations including SF3B1 and NOTCH1 in CLL, ATM and CCND1 in MCL, KMT2D and EPHA7 in FL, MYD88 (L265P) in LPL, KLF2 and NOTCH2 in splenic MZL (SMZL) and BRAF (V600E) in HCL. 27121112 2016
dbSNP: rs1392080411
rs1392080411
Entrez Id: 10365
Gene Symbol: KLF2
KLF2
CUI: C0334633
Disease:
Malignant lymphoma - lymphoplasmacytic 		0.010 GeneticVariation BEFREE The recent surge in next generation sequencing (NGS) technology has shed more light on the genetic landscape of SBCLs through characterization of numerous driver mutations including SF3B1 and NOTCH1 in CLL, ATM and CCND1 in MCL, KMT2D and EPHA7 in FL, MYD88 (L265P) in LPL, KLF2 and NOTCH2 in splenic MZL (SMZL) and BRAF (V600E) in HCL. 27121112 2016
dbSNP: rs1392080411
rs1392080411
Entrez Id: 10365
Gene Symbol: KLF2
KLF2
CUI: C4721414
Disease:
Mantle cell lymphoma 		0.010 GeneticVariation BEFREE The recent surge in next generation sequencing (NGS) technology has shed more light on the genetic landscape of SBCLs through characterization of numerous driver mutations including SF3B1 and NOTCH1 in CLL, ATM and CCND1 in MCL, KMT2D and EPHA7 in FL, MYD88 (L265P) in LPL, KLF2 and NOTCH2 in splenic MZL (SMZL) and BRAF (V600E) in HCL. 27121112 2016
dbSNP: rs3745318
rs3745318
Entrez Id: 10365
Gene Symbol: KLF2
KLF2
CUI: C0028754
Disease:
Obesity 		0.010 GeneticVariation BEFREE These data indicate that the Pro104Leu and 3'UTR 1239C>A polymorphisms in KLF2 are not associated with obesity and obesity-related traits in humans. 16542423 2006