Variant (rsID / SNP)

rs62620184

rs62620184 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOCK9. Location: chromosome 13, position 99,554,621. Clinical significance in the table: Benign.

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Reference-table entries

DOCK9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:99554621
Cytoband: 13q32.3
HGVS: NM_001366683.2(DOCK9):c.1301C>T (p.Ala434Val)
Allele change: Missense_A435V

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.