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Variant (rsID / SNP)

rs351855

FGFR4

rs351855 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGFR4. Location: chromosome 5, position 176,520,243. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FGFR4Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
5:176520243
Cytoband
5q35.2
HGVS
NM_213647.3(FGFR4):c.1162G>A (p.Gly388Arg)
Allele change
Missense_G388R

Associated conditions / phenotypes

Cancer progression and tumor cell motility|See cases

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.