Variant (rsID / SNP)

rs3749405

rs3749405 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OSBPL10. Location: chromosome 3, position 31,712,393. The table records no clinical significance for this variant.

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Reference-table entries

OSBPL10Not classified

Variant type: synonymous_variant
Chromosome / position: 3:31712393
HGVS: NM_017784.5,c.1809G>A,p.Pro603Pro
Allele change: Synonymous_P539P

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.