Variant (rsID / SNP)

rs1799998

rs1799998 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP11B2. Location: chromosome 8, position 143,999,600. Clinical significance in the table: association.

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Reference-table entries

CYP11B2Association

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 8:143999600
Cytoband: 8q24.3
HGVS: NM_000498.3(CYP11B2):c.-344T=

Associated conditions / phenotypes

Aldosterone to renin ratio, increased

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.