Annotation Detail
Information
- Associated Genes
- FTO
- Associated Variants
-
FTO c.46-43098T>C
(
ENST00000471389.6,
ENST00000637969.1,
ENST00000637001.1,
ENST00000636491.1,
ENST00000636218.1 )
FTO c.46-43098T>C ( ENST00000471389.6, ENST00000636218.1, ENST00000636491.1, ENST00000637001.1, ENST00000637969.1 ) - Associated Disease
- OBESITY (BMIQ14), SUSCEPTIBILITY TO
- Source Database
- ClinVar
- Description
- NM_001080432.3(FTO):c.46-43098T>C AND OBESITY (BMIQ14), SUSCEPTIBILITY TO
- ClinVar Allele ID
- 214481
- ClinVar RefSeq Alternation Syntax
- NM_001363903.1:c.46-43098T>C
- ClinVar RefSeq Alternation Syntax
- NM_001363988.1:c.46-43098T>C
- ClinVar RefSeq Alternation Syntax
- NM_001363891.1:c.46-43098T>C
- ClinVar RefSeq Alternation Syntax
- NM_001363899.1:c.46-43098T>C
- ClinVar RefSeq Alternation Syntax
- NM_001080432.3:c.46-43098T>C
- ClinVar RefSeq Alternation Syntax
- NM_001363901.1:c.46-43098T>C
- ClinVar RefSeq Alternation Syntax
- NM_001363894.1:c.46-43098T>C
- ClinVar RefSeq Alternation Syntax
- NM_001363897.1:c.46-58822T>C
- ClinVar RefSeq Alternation Syntax
- NM_001363905.1:c.-647-43098T>C
- ClinVar RefSeq Alternation Syntax
- NM_001363896.1:c.46-43098T>C
- ClinVar RefSeq Alternation Syntax
- NM_001363900.1:c.46-43098T>C
- ClinVar RefSeq Alternation Syntax
- NM_001363898.1:c.46-43098T>C
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2015-09-03
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000201907
- ClinVar Disease
- OBESITY (BMIQ14), SUSCEPTIBILITY TO
- Observed Origin Sample
- germline
- Pubmed
- 26287746
- Pubmed
- 19151714
- Pubmed
- 17496892
Drugs