Variant (rsID / SNP)

rs373150395

rs373150395 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN4A. Location: chromosome 17, position 62,025,363. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SCN4AConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 17:62025363
Cytoband: 17q23.3
HGVS: NM_000334.4(SCN4A):c.3205G>A (p.Asp1069Asn)
Allele change: Missense_D1069N

Associated conditions / phenotypes

Hyperkalemic periodic paralysis

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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