Variant (rsID / SNP)

rs1617318

rs1617318 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DTNA. Location: chromosome 18, position 32,444,040. Clinical significance in the table: Benign.

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Reference-table entries

DTNABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:32444040
Cytoband: 18q12.1
HGVS: NM_001386795.1(DTNA):c.1743+14G>A
Allele change: Silent

Associated conditions / phenotypes

Left ventricular noncompaction 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.