Variant (rsID / SNP)

rs376618

rs376618 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGFR4. Location: chromosome 5, position 176,517,797. The table records no clinical significance for this variant.

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Reference-table entries

FGFR4Not classified

Variant type: missense_variant
Chromosome / position: 5:176517797
HGVS: NM_001354984.2,c.407C>T,p.Pro136Leu
Allele change: Missense_P136L

Associated conditions / phenotypes

Liver Cirrhosis

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.