Variant (rsID / SNP)
rs1046089
rs1046089 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRRC2A. Location: chromosome 6, position 31,602,967. The table records no clinical significance for this variant.
Reference-table entries
PRRC2ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 6:31602967
- HGVS
- NM_004638.4,c.5219G>A,p.Arg1740His
- Allele change
- Missense_R1740H
Associated conditions / phenotypes
Premature Menopause|Amenorrhea|Malaria|Lipid Metabolism Disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.