Variant (rsID / SNP)

rs121913479

rs121913479 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGFR3. Location: chromosome 4, position 1,806,089. Clinical significance in the table: Pathogenic.

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Reference-table entries

FGFR3Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 4:1806089
Cytoband: 4p16.3
HGVS: NM_000142.5(FGFR3):c.1108G>T (p.Gly370Cys)
Allele change: Missense_G370C

Associated conditions / phenotypes

Thanatophoric dysplasia type 1|Epidermal nevus|Urinary bladder carcinoma

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.