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Variant (rsID / SNP)

rs139769668

SCN3A

rs139769668 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN3A. Location: chromosome 2, position 166,032,861. 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
2:166032861
Cytoband
2q24.3
HGVS
NM_006922.4(SCN3A):c.44G>A (p.Arg15His)
Allele change
Missense_R15H

Public references

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