CRY2, cryptochrome circadian regulator 2, 1408

N. diseases: 76; N. variants: 9
Disease: Lymphoma, Non-Hodgkin ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11038689
rs11038689
Entrez Id: 1408
Gene Symbol: CRY2
CRY2
CUI: C0024305
Disease:
Lymphoma, Non-Hodgkin 		0.010 GeneticVariation BEFREE Three SNPs were found to be significantly associated with risk of NHL when combining all subtypes [dbSNP IDs, odds ratios (ORs), and 95% confidence intervals: rs11038689, OR, 2.34 (1.28-4.27), P = 0.006; rs7123390, OR, 2.40 (1.39-4.13), P = 0.002; and rs1401417, OR, 2.97 (1.57-5.63, P = 0.001)]. 19318546 2009
dbSNP: rs1401417
rs1401417
Entrez Id: 1408
Gene Symbol: CRY2
CRY2
CUI: C0024305
Disease:
Lymphoma, Non-Hodgkin 		0.010 GeneticVariation BEFREE Three SNPs were found to be significantly associated with risk of NHL when combining all subtypes [dbSNP IDs, odds ratios (ORs), and 95% confidence intervals: rs11038689, OR, 2.34 (1.28-4.27), P = 0.006; rs7123390, OR, 2.40 (1.39-4.13), P = 0.002; and rs1401417, OR, 2.97 (1.57-5.63, P = 0.001)]. 19318546 2009
dbSNP: rs7123390
rs7123390
Entrez Id: 1408
Gene Symbol: CRY2
CRY2
CUI: C0024305
Disease:
Lymphoma, Non-Hodgkin 		0.010 GeneticVariation BEFREE Three SNPs were found to be significantly associated with risk of NHL when combining all subtypes [dbSNP IDs, odds ratios (ORs), and 95% confidence intervals: rs11038689, OR, 2.34 (1.28-4.27), P = 0.006; rs7123390, OR, 2.40 (1.39-4.13), P = 0.002; and rs1401417, OR, 2.97 (1.57-5.63, P = 0.001)]. 19318546 2009