Variant (rsID / SNP)

rs3735802

rs3735802 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAPPC9. Location: chromosome 8, position 141,461,185. Clinical significance in the table: Benign.

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Reference-table entries

TRAPPC9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:141461185
Cytoband: 8q24.3
HGVS: NM_001160372.4(TRAPPC9):c.288T>C (p.Phe96=)
Allele change: Synonymous_F96F

Associated conditions / phenotypes

Intellectual Disability, Recessive|History of neurodevelopmental disorder|Intellectual disability, autosomal recessive 13

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.