Variant (rsID / SNP)

rs2396092

rs2396092 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CUL3. Location: chromosome 2, position 225,335,290. Clinical significance in the table: Benign.

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Reference-table entries

CUL3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:225335290
Cytoband: 2q36.2
HGVS: NM_003590.5(CUL3):c.*3672T>C
Allele change: Silent

Associated conditions / phenotypes

Autosomal dominant pseudohypoaldosteronism type 1|Pseudohypoaldosteronism type 2E

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.