Variant (rsID / SNP)

rs267606809

rs267606809 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGFR3. Location: chromosome 4, position 1,806,111. Clinical significance in the table: Uncertain significance.

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Reference-table entries

FGFR3Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 4:1806111
Cytoband: 4p16.3
HGVS: NM_000142.5(FGFR3):c.1130T>G (p.Leu377Arg)
Allele change: Missense_L377R

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.