Variant (rsID / SNP)
rs3743598
rs3743598 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAT1. Location: chromosome 16, position 75,646,685. The table records no clinical significance for this variant.
Reference-table entries
ADAT1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 16:75646685
- HGVS
- NM_001324445.2,c.499C>A,p.His167Asn
- Allele change
- Missense_H167N
Associated conditions / phenotypes
Missense_H18N|Missense_H80N|Missense_H167N|Missense_H167N|Missense_H167N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.