MCPH1, microcephalin 1, 79648

N. diseases: 141; N. variants: 44
Disease: Primary malignant neoplasm of lung ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11137037
rs11137037
Entrez Id: 285;79648
Gene Symbol: ANGPT2;MCPH1
ANGPT2;MCPH1
CUI: C1306460
Disease:
Primary malignant neoplasm of lung 		0.010 GeneticVariation BEFREE Carriers of the variant GT allele of rs12674822 had a higher risk of lung cancer than wild-type (GG) carriers, while the presence of the CC genotype at rs11137037 was associated with higher clinical stage disease compared with having the AA genotype. 31281470 2019
dbSNP: rs12674822
rs12674822
Entrez Id: 285;79648
Gene Symbol: ANGPT2;MCPH1
ANGPT2;MCPH1
CUI: C1306460
Disease:
Primary malignant neoplasm of lung 		0.010 GeneticVariation BEFREE Five Ang2 SNPs (rs2442598, rs734701, rs1823375, 11137037, and rs12674822</span>) were analyzed using TaqMan SNP genotyping in 695 patients with lung cancer and 900 cancer-free controls. 31281470 2019