Variant (rsID / SNP)

rs34562867

rs34562867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGFLR1. Location: chromosome 19, position 36,230,767. The table records no clinical significance for this variant.

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Reference-table entries

IGFLR1Not classified

Variant type: missense_variant
Chromosome / position: 19:36230767
HGVS: NM_024660.4,c.565T>C,p.Trp189Arg
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.