Variant (rsID / SNP)

rs7904519

rs7904519 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TCF7L2. Location: chromosome 10, position 114,773,927. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TCF7L2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:114773927
Cytoband: 10q25.2
HGVS: NM_001367943.1(TCF7L2):c.451-25857A>G
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.