Variant (rsID / SNP)

rs73162856

rs73162856 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SNAP29. Location: chromosome 22, position 21,244,675. Clinical significance in the table: Benign.

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Reference-table entries

SNAP29Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:21244675
Cytoband: 22q11.21
HGVS: NM_004782.4(SNAP29):c.*2551G>A
Allele change: Silent

Associated conditions / phenotypes

CEDNIK 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.