Variant (rsID / SNP)
rs3617
rs3617 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITIH3. Location: chromosome 3, position 52,833,805. The table records no clinical significance for this variant.
Reference-table entries
ITIH3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:52833805
- HGVS
- NM_001392019.1,c.943C>A,p.Gln315Lys
- Allele change
- Missense_Q315K
Associated conditions / phenotypes
Schizophrenia|Autism|Autism Spectrum Disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.