Variant (rsID / SNP)

rs13333226

rs13333226 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UMOD. Location: chromosome 16, position 20,365,654. Clinical significance in the table: association.

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Reference-table entries

UMODAssociation

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 16:20365654
Cytoband: 16p12.3
HGVS: NM_003361.3(UMOD):c.-1746T>C

Associated conditions / phenotypes

Essential hypertension

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.