Variant (rsID / SNP)

rs12195525

rs12195525 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOX3. Location: chromosome 6, position 155,775,980. The table records no clinical significance for this variant.

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Reference-table entries

NOX3Not classified

Variant type: synonymous_variant
Chromosome / position: 6:155775980
HGVS: NM_015718.3,c.220C>A,p.Arg74Arg
Allele change: Synonymous_R74R

Associated conditions / phenotypes

Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus|Hearing Loss, Noise-Induced

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.