Variant (rsID / SNP)
rs1134767
rs1134767 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PATJ. Location: chromosome 1, position 62,456,014. The table records no clinical significance for this variant.
Reference-table entries
PATJNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:62456014
- HGVS
- NM_001350145.3,c.3845G>A,p.Arg1282His
- Allele change
- Missense_R1282H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.