Annotation Detail
Information
- Associated Genes
- AGT
- Associated Variants
-
AGT p.Met259Thr (p.M259T)
(
ENST00000679957.1,
ENST00000681514.1,
ENST00000680041.1,
ENST00000680783.1,
ENST00000681269.1,
ENST00000679684.1,
ENST00000366667.6 )
AGT p.Met259Thr (p.M259T) ( ENST00000366667.6, ENST00000679684.1, ENST00000679957.1, ENST00000680041.1, ENST00000680783.1, ENST00000681269.1, ENST00000681514.1 ) - Associated Disease
- Preeclampsia, susceptibility to
- Source Database
- ClinVar
- Description
- NM_000029.4(AGT):c.803T>C (p.Met268Thr) AND Preeclampsia, susceptibility to
- ClinVar Allele ID
- 33107
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2005-01-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000019692
- ClinVar Disease
- Preeclampsia, susceptibility to
- Observed Origin Sample
- germline
- Pubmed
- 7649545
- Pubmed
- 16059745
- Pubmed
- 8518804
- Pubmed
- 9831339
- Pubmed
- 9421481
- Pubmed
- 1394429
- Pubmed
- 7883995
- Pubmed
- 9259580
- Pubmed
- 8348146
- Pubmed
- 8513325
Drugs