Variant (rsID / SNP)

rs2303857

rs2303857 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DYNC1LI1. Location: chromosome 3, position 32,578,505. The table records no clinical significance for this variant.

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Reference-table entries

DYNC1LI1Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 3:32578505
HGVS: NM_016141.4,c.830A>G,p.Gln277Arg
Allele change: Missense_Q161R

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.