Variant (rsID / SNP)
rs3795809
rs3795809 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OBSCN. Location: chromosome 1, position 228,525,008. The table records no clinical significance for this variant.
Reference-table entries
OBSCNNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:228525008
- HGVS
- NM_001386125.1,c.19595G>A,p.Arg6532His
- Allele change
- Missense_R6532H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.