Variant (rsID / SNP)

rs10163657

rs10163657 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOXHD1. Location: chromosome 18, position 44,181,227. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

LOXHD1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:44181227
Cytoband: 18q21.1
HGVS: NM_001384474.1(LOXHD1):c.1087G>A (p.Val363Ile)
Allele change: Missense_V363I

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 77

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.