Variant (rsID / SNP)

rs61734987

rs61734987 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STRADA. Location: chromosome 17, position 61,787,950. Clinical significance in the table: Likely benign.

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Reference-table entries

STRADALikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:61787950
Cytoband: 17q23.3
HGVS: NM_001003787.4(STRADA):c.482C>T (p.Thr161Ile)
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.