Annotation Detail
Information
- Associated Genes
- PSMA6
- Associated Variants
-
PSMA6 c.-8C>G, ENSG00000258790 c.*891+13751C>G
(
ENST00000627895.2,
ENST00000540871.5,
ENST00000261479.9,
ENST00000555764.5,
ENST00000553809.5,
ENST00000622405.4,
ENST00000628955.1 )
PSMA6 c.-8C>T, ENSG00000258790 c.*891+13751C>T ( ENST00000540871.5, ENST00000627895.2, ENST00000553809.5, ENST00000261479.9, ENST00000555764.5, ENST00000622405.4, ENST00000628955.1 )
PSMA6 c.-8C>G, ENSG00000258790 c.*891+13751C>G ( ENST00000261479.9, ENST00000540871.5, ENST00000553809.5, ENST00000555764.5, ENST00000622405.4, ENST00000627895.2, ENST00000628955.1 )
PSMA6 c.-8C>T, ENSG00000258790 c.*891+13751C>T ( ENST00000261479.9, ENST00000540871.5, ENST00000553809.5, ENST00000555764.5, ENST00000622405.4, ENST00000627895.2, ENST00000628955.1 ) - Associated Disease
- myocardial infarction
- Source Database
- DisGeNET
- Description
- [The functional variant rs1048990 in PSMA6 is associated with susceptibility to myocardial infarction in a Chinese population.]
- Pubmed
- 19272601
- Original source reporting the Gene Disease association
- GAD
- DisGENET score for the Gene Disease association
- 0.259640960834882
- Year of publication
- 2009
Drugs