Variant (rsID / SNP)

rs117385606

rs117385606 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GJB3. Location: chromosome 1, position 35,250,943. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GJB3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:35250943
Cytoband: 1p34.3
HGVS: NM_024009.3(GJB3):c.580G>A (p.Ala194Thr)
Allele change: Missense_A194T

Associated conditions / phenotypes

Deafness, digenic, GJB2/GJB3|Erythrokeratodermia variabilis et progressiva 1

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.