Variant (rsID / SNP)

rs34723936

rs34723936 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOXHD1. Location: chromosome 18, position 44,146,287. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LOXHD1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:44146287
Cytoband: 18q21.1
HGVS: NM_001384474.1(LOXHD1):c.2370C>T (p.Asp790=)
Allele change: Synonymous_D790D

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.