Variant (rsID / SNP)

rs73429414

rs73429414 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CARD14. Location: chromosome 17, position 78,172,328. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CARD14Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:78172328
Cytoband: 17q25.3
HGVS: NM_001366385.1(CARD14):c.1789C>T (p.Arg597Trp)
Allele change: Silent

Associated conditions / phenotypes

Pityriasis rubra pilaris|Psoriasis 2|Autoinflammatory syndrome

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.