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Variant (rsID / SNP)

rs41280102

SCN4A

rs41280102 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN4A. Location: chromosome 17, position 62,028,920. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SCN4ABenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
17:62028920
Cytoband
17q23.3
HGVS
NM_000334.4(SCN4A):c.2717G>C (p.Ser906Thr)
Allele change
Missense_S906T

Associated conditions / phenotypes

Hyperkalemic periodic paralysis|Potassium-aggravated myotonia|Congenital myasthenic syndrome 16|Paramyotonia congenita of Von Eulenburg|Hypokalemic periodic paralysis, type 2

Public references

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