Variant (rsID / SNP)
rs10221698
rs10221698 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIAA2012. Location: chromosome 2, position 202,939,654. The table records no clinical significance for this variant.
Reference-table entries
KIAA2012Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:202939654
- HGVS
- NM_001277372.4,c.125T>C,p.Val42Ala
- Allele change
- Missense_V42A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
