Variant (rsID / SNP)

rs201773578

rs201773578 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STRADA. Location: chromosome 17, position 61,784,624. Clinical significance in the table: Uncertain significance.

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Reference-table entries

STRADAUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 17:61784624
Cytoband: 17q23.3
HGVS: NM_001003787.4(STRADA):c.736C>T (p.Pro246Ser)
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.