Variant (rsID / SNP)

rs385437

rs385437 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ODF2L. Location: chromosome 1, position 86,822,231. The table records no clinical significance for this variant.

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Reference-table entries

ODF2LNot classified

Variant type: synonymous_variant
Chromosome / position: 1:86822231
HGVS: NM_001366781.1,c.1327T>C,p.Leu443Leu
Allele change: Silent

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.