Variant (rsID / SNP)

rs696

rs696 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NFKBIA. Location: chromosome 14, position 35,871,093. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NFKBIABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:35871093
Cytoband: 14q13.2
HGVS: NM_020529.3(NFKBIA):c.*126G>A
Allele change: Silent

Associated conditions / phenotypes

Ectodermal dysplasia and immunodeficiency 2

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.