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Variant (rsID / SNP)

rs61734430

FOLR3

rs61734430 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOLR3. Location: chromosome 11, position 71,850,130. The table records no clinical significance for this variant.

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Reference-table entries

FOLR3Not classified
Variant type
missense_variant
Chromosome / position
11:71850130
HGVS
NM_000804.4,c.292C>T,p.Arg98Cys
Allele change
Missense_R98C

Associated conditions / phenotypes

Benign Mesothelioma

Public references

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