Variant (rsID / SNP)

rs1805637

rs1805637 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAJC19. Location: chromosome 3, position 180,705,102. Clinical significance in the table: Likely benign.

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Reference-table entries

DNAJC19Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:180705102
Cytoband: 3q26.33
HGVS: NM_145261.4(DNAJC19):c.130-292T>C
Allele change: Silent

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.