Variant (rsID / SNP)

rs2272903

rs2272903 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TFAP2B. Location: chromosome 6, position 50,786,571. Clinical significance in the table: Benign.

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Reference-table entries

TFAP2BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:50786571
Cytoband: 6p12.3
HGVS: NM_003221.3(TFAP2B):c.-34G>A
Allele change: Silent

Associated conditions / phenotypes

Char 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.