Variant (rsID / SNP)

rs4633660

rs4633660 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR72. Location: chromosome 15, position 53,807,399. Clinical significance in the table: Benign.

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Reference-table entries

WDR72Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:53807399
Cytoband: 15q21.3
HGVS: NM_182758.4(WDR72):c.*2497G>A
Allele change: Silent

Associated conditions / phenotypes

Amelogenesis Imperfecta, Recessive

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.