Variant (rsID / SNP)

rs4961

rs4961 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADD1. Location: chromosome 4, position 2,906,707. Clinical significance in the table: drug response.

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Reference-table entries

ADD1Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 4:2906707
Cytoband: 4p16.3
HGVS: NM_001354761.2(ADD1):c.1378G>T (p.Gly460Trp)
Allele change: Missense_G460W

Associated conditions / phenotypes

Hypertension, salt-sensitive essential, susceptibility to|hydrochlorothiazide response - Efficacy

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.