Annotation Detail
Information
- Associated Genes
- FTO
- Associated Variants
-
FTO c.46-30685T>G
(
ENST00000636218.1,
ENST00000636491.1,
ENST00000637001.1,
ENST00000637969.1,
ENST00000471389.6 )
FTO c.46-30685T>G ( ENST00000471389.6, ENST00000636218.1, ENST00000636491.1, ENST00000637001.1, ENST00000637969.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001080432.3(FTO):c.46-30685T>G AND not provided
- ClinVar Allele ID
- 227639
- ClinVar RefSeq Alternation Syntax
- NM_001363899.1:c.46-30685T>G
- ClinVar RefSeq Alternation Syntax
- NM_001363900.1:c.46-30685T>G
- ClinVar RefSeq Alternation Syntax
- NM_001363897.1:c.46-46409T>G
- ClinVar RefSeq Alternation Syntax
- NM_001363988.1:c.46-30685T>G
- ClinVar RefSeq Alternation Syntax
- NM_001363898.1:c.46-30685T>G
- ClinVar RefSeq Alternation Syntax
- NM_001363903.1:c.46-30685T>G
- ClinVar RefSeq Alternation Syntax
- NM_001363891.1:c.46-30685T>G
- ClinVar RefSeq Alternation Syntax
- NM_001363894.1:c.46-30685T>G
- ClinVar RefSeq Alternation Syntax
- NM_001363896.1:c.46-30685T>G
- ClinVar RefSeq Alternation Syntax
- NM_001363905.1:c.-647-30685T>G
- ClinVar RefSeq Alternation Syntax
- NM_001080432.3:c.46-30685T>G
- ClinVar RefSeq Alternation Syntax
- NM_001363901.1:c.46-30685T>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-29
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002057062
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs