Variant (rsID / SNP)

rs8191933

rs8191933 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGF2R. Location: chromosome 6, position 160,517,472. Clinical significance in the table: Benign.

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Reference-table entries

IGF2RBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:160517472
Cytoband: 6q25.3
HGVS: NM_000876.4(IGF2R):c.6657C>T (p.Asp2219=)
Allele change: Synonymous_D2219D

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.