Variant (rsID / SNP)

rs55770488

rs55770488 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGF1R. Location: chromosome 15, position 99,250,921. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

IGF1RBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:99250921
Cytoband: 15q26.3
HGVS: NM_000875.5(IGF1R):c.225C>T (p.Phe75=)
Allele change: Synonymous_F75F

Associated conditions / phenotypes

Growth delay due to insulin-like growth factor I resistance

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.