Variant (rsID / SNP)

rs2615489

rs2615489 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSPP. Location: chromosome 4, position 88,537,737. Clinical significance in the table: Benign.

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Reference-table entries

DSPPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:88537737
Cytoband: 4q22.1
HGVS: NM_014208.3(DSPP):c.*17G>A
Allele change: Silent

Associated conditions / phenotypes

Denticles|Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1|Dentinogenesis imperfecta type 3|Dentinogenesis imperfecta type 2

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.