Annotation Detail

Information
Associated Genes
TCF7L2
Associated Variants
TCF7L2 c.451-22060A>G ( ENST00000352065.10, ENST00000369397.8, ENST00000538897.5, ENST00000534894.5, ENST00000355995.9, ENST00000629706.2, ENST00000355717.9, ENST00000545257.6, ENST00000369395.6, ENST00000277945.12, ENST00000627217.3, ENST00000704414.1 )
TCF7L2 c.451-22060A>G ( ENST00000277945.12, ENST00000352065.10, ENST00000355717.9, ENST00000355995.9, ENST00000369395.6, ENST00000369397.8, ENST00000534894.5, ENST00000538897.5, ENST00000545257.6, ENST00000627217.3, ENST00000629706.2, ENST00000704414.1 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_001367943.1(TCF7L2):c.451-22060A>G AND not provided
ClinVar Allele ID
1232008
ClinVar RefSeq Alternation Syntax
NM_001146284.2:c.382-22060A>G
ClinVar RefSeq Alternation Syntax
NM_030756.5:c.382-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001198529.2:c.382-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001363501.2:c.451-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001198526.2:c.382-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001146286.2:c.382-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001198530.2:c.381+66358A>G
ClinVar RefSeq Alternation Syntax
NM_001146285.2:c.382-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001198531.2:c.451-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001146283.2:c.382-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001198525.2:c.382-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001198528.2:c.382-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001146274.2:c.451-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001198527.2:c.382-22060A>G
ClinVar RefSeq Alternation Syntax
NM_001367943.1:c.451-22060A>G
Clinical Significance Description
Benign
Clinical Significance Last Update
2019-06-14
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV001641270
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs