Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs760670617
rs760670617
Entrez Id: 9871
Gene Symbol: SEC24D
SEC24D
CUI: C4225382
Disease:
COLE-CARPENTER SYNDROME 2 		0.800 GeneticVariation UNIPROT Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta. 25683121 2015
dbSNP: rs760670617
rs760670617
Entrez Id: 9871
Gene Symbol: SEC24D
SEC24D
CUI: C4225382
Disease:
COLE-CARPENTER SYNDROME 2 		A 0.800 CausalMutation CLINVAR
dbSNP: rs786204846
rs786204846
Entrez Id: 9871
Gene Symbol: SEC24D
SEC24D
CUI: C4225382
Disease:
COLE-CARPENTER SYNDROME 2 		0.800 GeneticVariation UNIPROT
dbSNP: rs786204846
rs786204846
Entrez Id: 9871
Gene Symbol: SEC24D
SEC24D
CUI: C4225382
Disease:
COLE-CARPENTER SYNDROME 2 		G 0.800 CausalMutation CLINVAR
dbSNP: rs10518325
rs10518325
Entrez Id: 9871
Gene Symbol: SEC24D
SEC24D
CUI: C0027051
Disease:
Myocardial Infarction 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery. 25948407 2015
dbSNP: rs6822035
rs6822035
Entrez Id: 9871
Gene Symbol: SEC24D
SEC24D
CUI: C0027051
Disease:
Myocardial Infarction 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery. 25948407 2015
dbSNP: rs730882211
rs730882211
Entrez Id: 9871
Gene Symbol: SEC24D
SEC24D
CUI: C1843367
Disease:
Poor school performance 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs730882211
rs730882211
Entrez Id: 9871
Gene Symbol: SEC24D
SEC24D
CUI: C0014544
Disease:
Epilepsy 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs786204845
rs786204845
Entrez Id: 9871
Gene Symbol: SEC24D
SEC24D
CUI: C4225382
Disease:
COLE-CARPENTER SYNDROME 2 		A 0.700 CausalMutation CLINVAR
dbSNP: rs76459466
rs76459466
Entrez Id: 9871
Gene Symbol: SEC24D
SEC24D
CUI: C0019163
Disease:
Hepatitis B 		0.010 GeneticVariation BEFREE Second, SNP rs76459466 in SEC24D was adversely associated with HBV risk (OR<sub>meta</sub> = 0.82; P<sub>meta</sub> = 0.002), which again indicated that SEC24D represents a novel susceptibility gene for HBV infection. 31530870 2019