Variant (rsID / SNP)

rs11739136

rs11739136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNMB1. Location: chromosome 5, position 169,810,796. Clinical significance in the table: protective.

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Reference-table entries

KCNMB1Protective

Clinical significance (as recorded): protective
Variant type: single nucleotide variant
Chromosome / position: 5:169810796
Cytoband: 5q35.1
HGVS: NM_004137.4(KCNMB1):c.193G>A (p.Glu65Lys)
Allele change: Silent

Associated conditions / phenotypes

Hypertension, diastolic, resistance to

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.