Variant (rsID / SNP)

rs13306653

rs13306653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCNN1G. Location: chromosome 16, position 23,224,416. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SCNN1GBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:23224416
Cytoband: 16p12.2
HGVS: NM_001039.4(SCNN1G):c.1432-7G>A
Allele change: Silent

Associated conditions / phenotypes

Autosomal recessive pseudohypoaldosteronism type 1|Liddle syndrome 2|Bronchiectasis with or without elevated sweat chloride 3

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.