Variant (rsID / SNP)

rs5729

rs5729 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCNN1G. Location: chromosome 16, position 23,227,396. Clinical significance in the table: Benign.

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Reference-table entries

SCNN1GBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:23227396
Cytoband: 16p12.2
HGVS: NM_001039.4(SCNN1G):c.*606T>A
Allele change: Silent

Associated conditions / phenotypes

Liddle syndrome 2|Autosomal recessive pseudohypoaldosteronism type 1

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.