Variant (rsID / SNP)

rs144032672

rs144032672 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNC. Location: chromosome 9, position 117,849,382. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TNCBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:117849382
Cytoband: 9q33.1
HGVS: NM_002160.4(TNC):c.628G>A (p.Gly210Ser)
Allele change: Missense_G210S

Associated conditions / phenotypes

Autosomal dominant nonsyndromic hearing loss 56

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.