Variant (rsID / SNP)
rs3743599
rs3743599 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAT1. Location: chromosome 16, position 75,646,576. The table records no clinical significance for this variant.
Reference-table entries
ADAT1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 16:75646576
- HGVS
- NM_001324445.2,c.608C>A,p.Thr203Asn
- Allele change
- Missense_T203N
Associated conditions / phenotypes
Missense_T54N|Missense_T116N|Missense_T203N|Missense_T203N|Missense_T203N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.