RECQL5, RecQ like helicase 5, 9400

N. diseases: 28; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs820196
rs820196
Entrez Id: 9400;643008
Gene Symbol: RECQL5;SMIM5
RECQL5;SMIM5
CUI: C1332986
Disease:
Childhood Osteosarcoma 		0.020 GeneticVariation BEFREE We selected rs820196 in the RECQL5 gene and genotyped 185 patients with osteosarcoma and 201 age- and gender-matched non-cancer controls. 25867335 2015
dbSNP: rs820196
rs820196
Entrez Id: 9400;643008
Gene Symbol: RECQL5;SMIM5
RECQL5;SMIM5
CUI: C0029463
Disease:
Osteosarcoma 		0.020 GeneticVariation BEFREE We selected rs820196 in the RECQL5 gene and genotyped 185 patients with osteosarcoma and 201 age- and gender-matched non-cancer controls. 25867335 2015
dbSNP: rs820196
rs820196
Entrez Id: 9400;643008
Gene Symbol: RECQL5;SMIM5
RECQL5;SMIM5
CUI: C0585442
Disease:
Osteosarcoma of bone 		0.020 GeneticVariation BEFREE We selected rs820196 in the RECQL5 gene and genotyped 185 patients with osteosarcoma and 201 age- and gender-matched non-cancer controls. 25867335 2015
dbSNP: rs820196
rs820196
Entrez Id: 9400;643008
Gene Symbol: RECQL5;SMIM5
RECQL5;SMIM5
CUI: C0029463
Disease:
Osteosarcoma 		0.020 GeneticVariation BEFREE We also found that the C allele of rs820196 (OR = 1.492, 95% CI 1.138 ∼ 1.951; P = 0.004) and A allele of rs4789223 (OR = 1.767, 95% CI: 1.354 ∼ 2.301; P < 0.001) were common in the osteosarcoma patients than those in the control subjects, respectively. 24287950 2014
dbSNP: rs820196
rs820196
Entrez Id: 9400;643008
Gene Symbol: RECQL5;SMIM5
RECQL5;SMIM5
CUI: C0585442
Disease:
Osteosarcoma of bone 		0.020 GeneticVariation BEFREE We also found that the C allele of rs820196 (OR = 1.492, 95% CI 1.138 ∼ 1.951; P = 0.004) and A allele of rs4789223 (OR = 1.767, 95% CI: 1.354 ∼ 2.301; P < 0.001) were common in the osteosarcoma patients than those in the control subjects, respectively. 24287950 2014
dbSNP: rs820196
rs820196
Entrez Id: 9400;643008
Gene Symbol: RECQL5;SMIM5
RECQL5;SMIM5
CUI: C1332986
Disease:
Childhood Osteosarcoma 		0.020 GeneticVariation BEFREE We also found that the C allele of rs820196 (OR = 1.492, 95% CI 1.138 ∼ 1.951; P = 0.004) and A allele of rs4789223 (OR = 1.767, 95% CI: 1.354 ∼ 2.301; P < 0.001) were common in the osteosarcoma patients than those in the control subjects, respectively. 24287950 2014
dbSNP: rs4789223
rs4789223
Entrez Id: 9400;100130933
Gene Symbol: RECQL5;SMIM6
RECQL5;SMIM6
CUI: C1332986
Disease:
Childhood Osteosarcoma 		0.010 GeneticVariation BEFREE We also found that the C allele of rs820196 (OR = 1.492, 95% CI 1.138 ∼ 1.951; P = 0.004) and A allele of rs4789223 (OR = 1.767, 95% CI: 1.354 ∼ 2.301; P < 0.001) were common in the osteosarcoma patients than those in the control subjects, respectively. 24287950 2014
dbSNP: rs4789223
rs4789223
Entrez Id: 9400;100130933
Gene Symbol: RECQL5;SMIM6
RECQL5;SMIM6
CUI: C0029463
Disease:
Osteosarcoma 		0.010 GeneticVariation BEFREE We also found that the C allele of rs820196 (OR = 1.492, 95% CI 1.138 ∼ 1.951; P = 0.004) and A allele of rs4789223 (OR = 1.767, 95% CI: 1.354 ∼ 2.301; P < 0.001) were common in the osteosarcoma patients than those in the control subjects, respectively. 24287950 2014
dbSNP: rs4789223
rs4789223
Entrez Id: 9400;100130933
Gene Symbol: RECQL5;SMIM6
RECQL5;SMIM6
CUI: C0007107
Disease:
Malignant neoplasm of larynx 		0.010 GeneticVariation BEFREE Four polymorphisms of the RECQL5 gene (rs820186, rs820196, rs820200, and rs4789223) were genotyped by the TaqMan method in 275 patients with larynx cancer and 300 age- and sex-matched non-cancer controls. 24213927 2014
dbSNP: rs4789223
rs4789223
Entrez Id: 9400;100130933
Gene Symbol: RECQL5;SMIM6
RECQL5;SMIM6
CUI: C0585442
Disease:
Osteosarcoma of bone 		0.010 GeneticVariation BEFREE We also found that the C allele of rs820196 (OR = 1.492, 95% CI 1.138 ∼ 1.951; P = 0.004) and A allele of rs4789223 (OR = 1.767, 95% CI: 1.354 ∼ 2.301; P < 0.001) were common in the osteosarcoma patients than those in the control subjects, respectively. 24287950 2014
dbSNP: rs820196
rs820196
Entrez Id: 9400;643008
Gene Symbol: RECQL5;SMIM5
RECQL5;SMIM5
CUI: C0007107
Disease:
Malignant neoplasm of larynx 		0.010 GeneticVariation BEFREE We found that rs820196 polymorphism of RECQL5 was associated with larynx cancer, the CC genotype (16.4% vs 9.3%, P = 0.013) and C allele (42% vs 34.2%, P = 0.006) was common in larynx cancer patients than in the control subjects, respectively. 24213927 2014
dbSNP: rs820196
rs820196
Entrez Id: 9400;643008
Gene Symbol: RECQL5;SMIM5
RECQL5;SMIM5
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.010 GeneticVariation BEFREE For rs820196, the CC genotype (16.7 vs 9.4 %, P < 0.001) and C allele (42.5 vs 34.3 %, P < 0.001) were common in the breast cancer patients than in the control subjects, respectively. 25394896 2014
dbSNP: rs820196
rs820196
Entrez Id: 9400;643008
Gene Symbol: RECQL5;SMIM5
RECQL5;SMIM5
CUI: C0678222
Disease:
Breast Carcinoma 		0.010 GeneticVariation BEFREE For rs820196, the CC genotype (16.7 vs 9.4 %, P < 0.001) and C allele (42.5 vs 34.3 %, P < 0.001) were common in the breast cancer patients than in the control subjects, respectively. 25394896 2014