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Variant (rsID / SNP)

rs149868494

SCN4B

rs149868494 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN4B. Location: chromosome 11, position 118,023,367. 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
11:118023367
Cytoband
11q23.3
HGVS
NM_174934.4(SCN4B):c.22G>A (p.Gly8Ser)
Allele change
Missense_G8S

Associated conditions / phenotypes

Long QT syndrome 10|Cardiovascular phenotype

Public references

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