Variant (rsID / SNP)

rs201602333

rs201602333 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAR. Location: chromosome 1, position 154,555,885. Clinical significance in the table: Likely benign.

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Reference-table entries

ADARLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:154555885
Cytoband: 1q21.3
HGVS: NM_001111.5(ADAR):c.*1397C>T
Allele change: Silent

Associated conditions / phenotypes

Symmetrical dyschromatosis of extremities

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.