Variant (rsID / SNP)

rs1886176

rs1886176 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GJA3. Location: chromosome 13, position 20,715,801. Clinical significance in the table: Benign.

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Reference-table entries

GJA3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:20715801
Cytoband: 13q12.11
HGVS: NM_021954.4(GJA3):c.*319G>T
Allele change: Silent

Associated conditions / phenotypes

Cataract 14 multiple types

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.