Annotation Detail
Information
- Associated Genes
- PPARG
- Associated Variants
-
PPARG p.Pro40Ala (p.P40A)
(
ENST00000287820.10,
ENST00000309576.11,
ENST00000397000.6,
ENST00000397010.7,
ENST00000397015.7,
ENST00000397026.7,
ENST00000643197.2,
ENST00000643888.2,
ENST00000644622.2,
ENST00000651735.1,
ENST00000652098.1,
ENST00000652431.1,
ENST00000681982.1,
ENST00000682446.1,
ENST00000683586.1,
ENST00000683699.1 )
PPARG p.Pro40Ala (p.P40A) ( ENST00000287820.10, ENST00000309576.11, ENST00000397000.6, ENST00000397010.7, ENST00000397015.7, ENST00000397026.7, ENST00000643197.2, ENST00000643888.2, ENST00000644622.2, ENST00000651735.1, ENST00000652098.1, ENST00000652431.1, ENST00000681982.1, ENST00000682446.1, ENST00000683586.1, ENST00000683699.1 ) - Associated Disease
- Intimal medial thickness of internal carotid artery, modifier of
- Source Database
- ClinVar
- Description
- NM_138711.6(PPARG):c.28C>G (p.Pro10Ala) AND Intimal medial thickness of internal carotid artery, modifier of
- ClinVar Allele ID
- 23170
- ClinVar RefSeq Alternation Syntax
- NM_001354670.2:c.34C>G
- ClinVar RefSeq Alternation Syntax
- NM_001374262.3:c.28C>G
- ClinVar RefSeq Alternation Syntax
- NM_001374263.2:c.28C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354669.2:c.-400C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354666.3:c.28C>G
- ClinVar RefSeq Alternation Syntax
- NM_001374261.3:c.28C>G
- ClinVar RefSeq Alternation Syntax
- NM_138711.6:c.28C>G
- ClinVar RefSeq Alternation Syntax
- NM_005037.7:c.28C>G
- ClinVar RefSeq Alternation Syntax
- NM_001374264.2:c.28C>G
- ClinVar RefSeq Alternation Syntax
- NM_015869.5:c.118C>G
- ClinVar RefSeq Alternation Syntax
- NM_001374266.1:c.34C>G
- ClinVar RefSeq Alternation Syntax
- NM_001374265.1:c.118C>G
- ClinVar RefSeq Alternation Syntax
- NM_001330615.4:c.28C>G
- ClinVar RefSeq Alternation Syntax
- NM_138712.5:c.28C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354668.2:c.118C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354667.3:c.28C>G
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2007-06-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000008607
- ClinVar Disease
- Intimal medial thickness of internal carotid artery, modifier of
- Observed Origin Sample
- germline
- Pubmed
- 15562023
- Pubmed
- 14569127
- Pubmed
- 11158005
- Pubmed
- 17213274
- Pubmed
- 15367918
- Pubmed
- 10523018
- Pubmed
- 12161548
- Pubmed
- 10843155
- Pubmed
- 17463249
- Pubmed
- 17463246
- Pubmed
- 17463248
- Pubmed
- 9425261
- Pubmed
- 10843190
- Pubmed
- 12096349
- Pubmed
- 10973253
- Pubmed
- 9918859
- Pubmed
- 11836319
- Pubmed
- 12679463
- Pubmed
- 14671186
- Pubmed
- 9806549
- Pubmed
- 9792554
- Pubmed
- 15562396
- Pubmed
- 12524541
- Pubmed
- 15356014
- Pubmed
- 14506127
- Pubmed
- 12974743
- Pubmed
- 16822823
- Pubmed
- 10364535
- Pubmed
- 15797964
Drugs