Variant (rsID / SNP)

rs139339332

rs139339332 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TFAP2B. Location: chromosome 6, position 50,807,934. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TFAP2BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:50807934
Cytoband: 6p12.3
HGVS: NM_003221.4(TFAP2B):c.1006G>A (p.Val336Ile)
Allele change: Missense_V336I

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.