Variant (rsID / SNP)
rs12933808
rs12933808 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNTNAP4. Location: chromosome 16, position 76,532,583. The table records no clinical significance for this variant.
Reference-table entries
CNTNAP4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 16:76532583
- HGVS
- NM_033401.5,c.2354A>G,p.Gln785Arg
- Allele change
- Missense_R786G
Associated conditions / phenotypes
Missense_R785G|Silent|Missense_R786G|Silent|Missense_Q314R|Missense_R736G|Missense_R786G|Missense_Q713R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.