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Variant (rsID / SNP)

rs368119524

TRIOBP

rs368119524 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIOBP. Location: chromosome 22, position 38,111,796. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TRIOBPConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
22:38111796
Cytoband
22q13.1
HGVS
NM_001039141.3(TRIOBP):c.483G>A (p.Glu161=)
Allele change
Synonymous_E161E

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.