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Variant (rsID / SNP)

rs199645176

LOXHD1

rs199645176 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOXHD1. Location: chromosome 18, position 44,063,648. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LOXHD1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
18:44063648
Cytoband
18q21.1
HGVS
NM_001384474.1(LOXHD1):c.6243T>C (p.Cys2081=)
Allele change
Synonymous_C970C

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 77

Public references

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