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Variant (rsID / SNP)

rs146624492

SCN3A

rs146624492 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN3A. Location: chromosome 2, position 165,946,774. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SCN3AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:165946774
Cytoband
2q24.3
HGVS
NM_006922.4(SCN3A):c.5889T>C (p.Ser1963=)
Allele change
Synonymous_S1914S

Public references

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