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Variant (rsID / SNP)

rs777218649

SCN4B

rs777218649 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN4B. Location: chromosome 11, position 118,023,403. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SCN4BConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:118023403
Cytoband
11q23.3
HGVS
NM_174934.4(SCN4B):c.-15G>A
Allele change
Silent

Associated conditions / phenotypes

Congenital long QT syndrome

Public references

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