Variant "LPA:c.3947+467T>C"
Search results: 2 records
Variant information
Gene:
Variant:
LPA:c.3947+467T>C
Genomic location:
chr6:161010118(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_005577.2:c.3947+467T>C |
dbSNP ID:
GWAS trait:
lipoprotein-associated phospholipase A(2) measurement,acute coronary syndrome,coronary heart disease,coronary artery disease,aortic stenosis,stroke,large artery stroke,response to statin,LDL cholesterol change measurement,low density lipoprotein cholesterol measurement,aortic valve calcification,myocardial infarction,lipoprotein measurement,blood metabolite measurement,apolipoprotein A 1 measurement,total cholesterol measurement,parental longevity
Modifier statisitcs
Record:
2
Disorder:
1
Reference:
2
Effect type:
Expressivity(1)
,Penetrance(1)
Modifier effect:
Altered incidence(1)
,Risk factor(1)
Details: