Variant (rsID / SNP)

rs61752191

rs61752191 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIKFYVE. Location: chromosome 2, position 209,204,738. Clinical significance in the table: Benign.

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Reference-table entries

PIKFYVEBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:209204738
Cytoband: 2q34
HGVS: NM_015040.4(PIKFYVE):c.4814T>G (p.Val1605Gly)
Allele change: Missense_V1605G

Associated conditions / phenotypes

Fleck corneal dystrophy

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.