Variant (rsID / SNP)

rs2133173

rs2133173 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DYNLT5. Location: chromosome 1, position 67,243,024. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DYNLT5Not classified

Variant type: missense_variant
Chromosome / position: 1:67243024
HGVS: NM_152665.3,c.427C>A,p.Leu143Ile
Allele change: Missense_L143I

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.