Variant (rsID / SNP)
rs9838238
rs9838238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DCBLD2. Location: chromosome 3, position 98,600,385. The table records no clinical significance for this variant.
Reference-table entries
DCBLD2Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 3:98600385
- HGVS
- NM_080927.4,c.432A>G,p.Ile144Met
- Allele change
- Missense_I144M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.