Variant (rsID / SNP)

rs13306629

rs13306629 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCNN1B. Location: chromosome 16, position 23,392,103. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SCNN1BUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 16:23392103
Cytoband: 16p12.2
HGVS: NM_000336.3(SCNN1B):c.1904G>A (p.Ser635Asn)
Allele change: Missense_S635N

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.