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Variant (rsID / SNP)

rs140236996

TECTA

rs140236996 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TECTA. Location: chromosome 11, position 121,038,773. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TECTAConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:121038773
Cytoband
11q23.3
HGVS
NM_005422.4(TECTA):c.5597C>T (p.Thr1866Met)
Allele change
Missense_T1866M

Associated conditions / phenotypes

Autosomal dominant nonsyndromic hearing loss 12|Autosomal recessive nonsyndromic hearing loss 21|Inborn genetic diseases|Rare genetic deafness|Sensorineural hearing loss disorder

Public references

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