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Variant (rsID / SNP)

rs148261539

TRIP11

rs148261539 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIP11. Location: chromosome 14, position 92,439,151. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TRIP11Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
14:92439151
Cytoband
14q32.12
HGVS
NM_004239.4(TRIP11):c.5629C>A (p.Pro1877Thr)
Allele change
Missense_P1876T

Associated conditions / phenotypes

Achondrogenesis, type IA|Connective tissue disorder

Public references

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