Variant (rsID / SNP)

rs181271620

rs181271620 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAJC19. Location: chromosome 3, position 180,707,419. Clinical significance in the table: Benign.

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Reference-table entries

DNAJC19Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:180707419
Cytoband: 3q26.33
HGVS: NM_145261.4(DNAJC19):c.-29G>T
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.