Variant (rsID / SNP)

rs3808869

rs3808869 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARID3C, DCTN3. Location: chromosome 9, position 34,622,389. The table records no clinical significance for this variant.

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Reference-table entries

ARID3CNot classified

Variant type: missense_variant
Chromosome / position: 9:34622389
HGVS: NM_001017363.4,c.1003T>G,p.Cys335Gly
Allele change: Missense_C335G

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.