Variant (rsID / SNP)

rs78648016

rs78648016 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AP4S1. Location: chromosome 14, position 31,494,988. Clinical significance in the table: Benign.

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Reference-table entries

AP4S1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:31494988
Cytoband: 14q12
HGVS: NM_001128126.3(AP4S1):c.-77G>A
Allele change: Silent

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.