Variant (rsID / SNP)

rs61734984

rs61734984 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STRADA. Location: chromosome 17, position 61,787,924. Clinical significance in the table: Benign.

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Reference-table entries

STRADABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:61787924
Cytoband: 17q23.3
HGVS: NM_001003787.4(STRADA):c.508C>G (p.Leu170Val)
Allele change: Silent

Associated conditions / phenotypes

Polyhydramnios, megalencephaly, and symptomatic epilepsy

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.