Variant (rsID / SNP)

rs61753391

rs61753391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAJC6. Location: chromosome 1, position 65,849,887. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DNAJC6Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:65849887
Cytoband: 1p31.3
HGVS: NM_001256864.2(DNAJC6):c.678G>A (p.Ala226=)
Allele change: Synonymous_A169A

Associated conditions / phenotypes

Juvenile onset Parkinson disease 19A

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.