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Variant (rsID / SNP)

rs144637717

FOLR1

rs144637717 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOLR1. Location: chromosome 11, position 71,906,793. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FOLR1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:71906793
Cytoband
11q13.4
HGVS
NM_016729.3(FOLR1):c.493+2T>C
Allele change
Silent

Associated conditions / phenotypes

Cerebral folate transport deficiency|History of neurodevelopmental disorder|Seizure

Public references

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